WO2020083099A1 - 一种发动机排放处理系统和方法 - Google Patents
一种发动机排放处理系统和方法 Download PDFInfo
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- WO2020083099A1 WO2020083099A1 PCT/CN2019/111816 CN2019111816W WO2020083099A1 WO 2020083099 A1 WO2020083099 A1 WO 2020083099A1 CN 2019111816 W CN2019111816 W CN 2019111816W WO 2020083099 A1 WO2020083099 A1 WO 2020083099A1
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- electric field
- present
- exhaust gas
- intake
- dust removal
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- F01N2240/00—Combination or association of two or more different exhaust treating devices, or of at least one such device with an auxiliary device, not covered by indexing codes F01N2230/00 or F01N2250/00, one of the devices being
- F01N2240/38—Combination or association of two or more different exhaust treating devices, or of at least one such device with an auxiliary device, not covered by indexing codes F01N2230/00 or F01N2250/00, one of the devices being an ozone (O3) generator, e.g. for adding ozone after generation of ozone from air
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N2250/00—Combinations of different methods of purification
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N2250/00—Combinations of different methods of purification
- F01N2250/10—Combinations of different methods of purification cooling and filtering
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N2560/00—Exhaust systems with means for detecting or measuring exhaust gas components or characteristics
- F01N2560/02—Exhaust systems with means for detecting or measuring exhaust gas components or characteristics the means being an exhaust gas sensor
- F01N2560/026—Exhaust systems with means for detecting or measuring exhaust gas components or characteristics the means being an exhaust gas sensor for measuring or detecting NOx
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N2570/00—Exhaust treating apparatus eliminating, absorbing or adsorbing specific elements or compounds
- F01N2570/14—Nitrogen oxides
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N2610/00—Adding substances to exhaust gases
- F01N2610/02—Adding substances to exhaust gases the substance being ammonia or urea
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N2610/00—Adding substances to exhaust gases
- F01N2610/06—Adding substances to exhaust gases the substance being in the gaseous form
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N2900/00—Details of electrical control or of the monitoring of the exhaust gas treating apparatus
- F01N2900/04—Methods of control or diagnosing
- F01N2900/0416—Methods of control or diagnosing using the state of a sensor, e.g. of an exhaust gas sensor
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N3/00—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
- F01N3/005—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for draining or otherwise eliminating condensates or moisture accumulating in the apparatus
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N3/00—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
- F01N3/02—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust
- F01N3/0205—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust using heat exchangers
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/20—Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters
- Y02A50/2351—Atmospheric particulate matter [PM], e.g. carbon smoke microparticles, smog, aerosol particles, dust
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E20/00—Combustion technologies with mitigation potential
- Y02E20/12—Heat utilisation in combustion or incineration of waste
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/10—Greenhouse gas [GHG] capture, material saving, heat recovery or other energy efficient measures, e.g. motor control, characterised by manufacturing processes, e.g. for rolling metal or metal working
Definitions
- the invention belongs to the field of environmental protection and relates to an engine emission treatment system and method.
- particulate filtering is usually performed through a diesel particulate filter (DPF).
- DPF diesel particulate filter
- the DPF works in a combustion mode, that is, it uses carbon deposits in the porous structure to be fully blocked and then heated up to the ignition point to burn in a natural or combustion-supporting manner.
- the working principle of the DPF is as follows: the intake air with particulate matter enters the honeycomb carrier of the DPF, the particulate matter is intercepted in the honeycomb loading body, and most of the particulate matter has been filtered out when the intake air flows out of the DPF.
- the carrier materials of DPF are mainly cordierite, silicon carbide, aluminum titanate, etc., which can be selected and used according to the actual situation.
- the above method stores the following defects:
- Electrostatic dust removal is a gas dust removal method, usually used in metallurgy, chemical and other industrial fields to purify gas or recover useful dust particles.
- the particulate matter of the engine intake air cannot be processed based on electrostatic dust removal.
- the engine's environmental pollution mainly comes from the exhaust product of the engine, that is, the engine exhaust.
- the conventional technical route is to use the oxidation catalyst DOC to remove the hydrocarbons THC and CO, and at the same time oxidize the low-valent NO to the high-valent NO 2 ; after the DOC, the particulate matter PM is filtered by the diesel particulate trap DPF; after the diesel particulate trap DPF, urea is injected, and the urea is decomposed into ammonia gas NH 3 in the exhaust gas, and the subsequent selectivity of NH 3 A selective catalytic reduction reaction with NO 2 occurs on the catalyst SCR to produce nitrogen N 2 and water.
- the object of the present invention is to provide an engine emission treatment system and method for solving the prior art dust removal system that requires regular maintenance and the effect is unstable and that a large amount of urea treatment exhaust gas needs to be added and the exhaust gas is purified
- the effect is generally at least one problem.
- the present invention finds new problems in the existing ionization dust removal technology through research and solves it through a series of technical means. For example, when the exhaust gas temperature or the engine temperature is lower than a certain temperature, the engine exhaust gas may contain liquid water.
- the present invention also provides an auxiliary electric field that is not parallel to the ionizing electric field between the anode and the cathode of the intake ionization and dust removal electric field.
- the flow rate is greater than the air flow rate, which plays a role in increasing oxygen, and the oxygen content in the intake air of the engine increases, thereby greatly improving the power of the engine. Therefore, the present invention is suitable for operating under harsh conditions and guarantees dust removal efficiency, so from a commercial point of view, the present invention is fully applicable to engines.
- the invention provides an engine emission treatment system, including at least one of an intake dust removal system, an exhaust gas dust removal system, and an exhaust gas ozone purification system.
- the air intake dust removal system includes an air intake dust removal system inlet, an air intake dust removal system outlet, and an air intake electric field device.
- the exhaust gas dedusting system includes an exhaust gas dedusting system inlet, an exhaust gas dedusting system outlet, and an exhaust gas electric field device.
- the exhaust gas ozone purification system includes a reaction field for mixing and reacting the ozone stream with the exhaust stream.
- the engine emission treatment system can effectively treat engine emissions, making the engine emissions cleaner.
- Example 1 provided by the present invention: an engine emission treatment system.
- Example 2 provided by the present invention: The above example 1 includes an intake air dust removal system including an intake air dust removal system inlet, an intake air dust removal system outlet, and an intake electric field device.
- Example 3 provided by the present invention includes the above example 2, wherein the intake electric field device includes an intake electric field device inlet, an intake electric field device outlet, an intake dust electric field cathode and an intake dust electric field anode, the inlet The cathode of the gas dedusting electric field and the anode of the air inlet dedusting electric field are used to generate an air inlet ionization dedusting electric field.
- the intake electric field device includes an intake electric field device inlet, an intake electric field device outlet, an intake dust electric field cathode and an intake dust electric field anode, the inlet The cathode of the gas dedusting electric field and the anode of the air inlet dedusting electric field are used to generate an air inlet ionization dedusting electric field.
- Example 4 provided by the present invention includes the above example 3, wherein the anode of the intake air dedusting electric field includes a first anode part and a second anode part, the first anode part is close to the inlet of the intake electric field device, the first The two anode portions are close to the outlet of the intake electric field device, and at least one cathode support plate is provided between the first anode portion and the second anode portion.
- Example 5 provided by the present invention includes the above example 4, wherein the intake electric field device further includes an intake insulation mechanism for realizing insulation between the cathode support plate and the anode of the intake dust removal electric field.
- Example 6 provided by the present invention includes the above example 4, wherein an electric field flow path is formed between the anode of the intake air dust removal electric field and the cathode of the intake air dust removal electric field, and the intake air insulation mechanism is provided at the electric field flow Outside the road.
- Example 7 provided by the present invention includes the above example 5 or 6, wherein the intake air insulating mechanism includes an insulating portion and a heat insulating portion; the material of the insulating portion is a ceramic material or a glass material.
- Example 8 provided by the present invention includes the above example 7, wherein the insulating part is an umbrella-shaped string ceramic column, an umbrella-shaped string glass column, a column-shaped string ceramic column or a column-shaped glass column, and the glaze is hung on the inside or outside of the umbrella.
- the insulating part is an umbrella-shaped string ceramic column, an umbrella-shaped string glass column, a column-shaped string ceramic column or a column-shaped glass column, and the glaze is hung on the inside or outside of the umbrella.
- Example 9 provided by the present invention includes the above example 8, wherein the distance between the outer edge of the umbrella-shaped string ceramic column or the umbrella-shaped string glass column and the anode of the intake dust removal electric field is greater than 1.4 times the electric field distance, and the umbrella-shaped string ceramic The sum of the distance between the edge of the umbrella or the glass string of the umbrella-shaped string is 1.4 times greater than the insulation distance of the ceramic string of the umbrella-shaped string or the glass string of the umbrella-shaped string. The insulation distance of the string-shaped ceramic column or the umbrella-shaped string glass column is 1.4 times.
- Example 10 provided by the present invention: including any one of the above examples 4 to 9, wherein the length of the first anode portion is 1/10 to 1/4, 1 of the length of the anode of the intake dust removal electric field / 4 to 1/3, 1/3 to 1/2, 1/2 to 2/3, 2/3 to 3/4, or 3/4 to 9/10.
- Example 11 provided by the present invention: including any one of the above examples 4 to 10, wherein the length of the first anode portion is long enough to remove part of dust and reduce accumulation in the intake insulation mechanism And the dust on the cathode support plate to reduce the electrical breakdown caused by the dust.
- Example 12 provided by the present invention: including any one of the above examples 4 to 11, wherein the second anode portion includes a dust accumulation section and a reserved dust accumulation section.
- Example 13 provided by the present invention: including any one of the above examples 3 to 12, wherein the cathode of the intake air dust removal electric field includes at least one electrode rod.
- Example 14 provided by the present invention includes the above example 13, wherein the diameter of the electrode rod is not greater than 3 mm.
- Example 15 provided by the present invention includes the above example 13 or 14, wherein the electrode rod has a needle shape, a polygonal shape, a burr shape, a threaded rod shape or a column shape.
- Example 16 provided by the present invention: including any one of the above examples 3 to 15, wherein the anode of the intake dust removal electric field is composed of a hollow tube bundle.
- Example 17 provided by the present invention includes the above example 16, wherein the hollow cross-section of the anode tube bundle of the intake air dust removal electric field adopts a circle or a polygon.
- Example 18 provided by the present invention: including the above Example 17, wherein the polygon is a hexagon.
- Example 19 provided by the present invention includes any one of the above Examples 15 to 18, wherein the tube bundle of the anode of the intake air dust removal electric field is in a honeycomb shape.
- Example 20 provided by the present invention includes any one of the above examples 3 to 19, wherein the cathode of the intake dust removal electric field penetrates into the anode of the intake dust removal electric field.
- Example 21 provided by the present invention includes any one of the above Examples 3 to 20, wherein, when the electric field accumulates dust to a certain extent, the intake electric field device performs dust removal processing.
- Example 22 provided by the present invention includes the above example 21, wherein the intake electric field device detects the electric field current to determine whether the dust accumulation is to a certain degree, and the dust removal process is required.
- Example 23 provided by the present invention includes the above example 21 or 22, wherein the intake electric field device increases the electric field voltage to perform the dust removal process.
- Example 24 provided by the present invention includes the above example 21 or 22, wherein the intake electric field device performs a dust removal process using an electric field back-corona discharge phenomenon.
- Example 25 provided by the present invention includes the above example 21 or 22, wherein the intake electric field device utilizes the phenomenon of electric field counter-corona discharge to increase the electric field voltage, limit the injection current, and cause the sharp occurrence of carbon deposition at the anode The discharge generates plasma that deeply oxidizes the organic components of the dust, breaks the polymer bonds, and forms small-molecule carbon dioxide and water for dust removal.
- the intake electric field device utilizes the phenomenon of electric field counter-corona discharge to increase the electric field voltage, limit the injection current, and cause the sharp occurrence of carbon deposition at the anode
- the discharge generates plasma that deeply oxidizes the organic components of the dust, breaks the polymer bonds, and forms small-molecule carbon dioxide and water for dust removal.
- Example 26 provided by the present invention includes any one of the above examples 3 to 25, wherein the intake electric field device further includes an auxiliary electric field unit for generating an auxiliary that is not parallel to the electric field of the intake ionization and dedusting electric field.
- Example 27 provided by the present invention includes any one of the above Examples 3 to 25, wherein the intake electric field device further includes an auxiliary electric field unit, and the intake ionization and dust removal electric field includes a flow channel, the auxiliary electric field The unit is used to generate an auxiliary electric field that is not perpendicular to the flow channel.
- Example 28 provided by the present invention includes the above example 26 or 27, wherein the auxiliary electric field unit includes a first electrode, and the first electrode of the auxiliary electric field unit is disposed at or near the inlet of the intake ionization and dust removal electric field .
- Example 29 provided by the present invention: including the above example 28, wherein the first electrode is a cathode.
- Example 30 provided by the present invention includes the above example 28 or 29, wherein the first electrode of the auxiliary electric field unit is an extension of the cathode of the intake dust removal electric field.
- Example 32 provided by the present invention: including any one of the above examples 26 to 31, wherein the auxiliary electric field unit includes a second electrode, and the second electrode of the auxiliary electric field unit is disposed at or near the intake air The outlet of the ionization dust removal electric field.
- Example 33 provided by the present invention: including the above example 32, wherein the second electrode is an anode.
- Example 34 provided by the present invention: including the above example 32 or 33, wherein the second electrode of the auxiliary electric field unit is an extension of the anode of the intake dust removal electric field.
- Example 36 provided by the present invention includes any one of the above examples 26 to 29, 32 and 33, wherein the electrode of the auxiliary electric field and the electrode of the intake ionization and dedusting electric field are provided independently.
- Example 37 provided by the present invention includes any one of the above Examples 3 to 36, wherein the ratio of the dust accumulation area of the intake air dedusting electric field anode to the discharge area of the intake air dedusting electric field cathode is 1.667: 1-1680: 1.
- Example 38 provided by the present invention includes any one of the above Examples 3 to 36, wherein the ratio of the area of the dust collection anode of the intake air dedusting electric field to the discharge area of the cathode of the intake air dedusting electric field is 6.67: 1-56.67: 1.
- Example 39 provided by the present invention includes any one of the above examples 3 to 38, wherein the cathode of the intake air dedusting electric field has a diameter of 1-3 mm, the anode of the intake air dedusting electric field and the intake air dedusting
- the pole pitch of the electric field cathode is 2.5-139.9 mm; the ratio of the dust accumulation area of the anode of the intake air dedusting electric field to the discharge area of the cathode of the intake air dedusting electric field is 1.667: 1-1680: 1.
- Example 40 provided by the present invention includes any one of the above examples 3 to 38, wherein the electrode separation between the intake air dust removal electric field anode and the intake air dust removal electric field cathode is less than 150 mm.
- Example 41 provided by the present invention: including any one of the above examples 3 to 38, wherein the pole separation between the anode of the intake air dust removal electric field and the cathode of the intake air dust removal electric field is 2.5-139.9 mm.
- Example 42 provided by the present invention: including any one of the above examples 3 to 38, wherein the electrode separation between the anode of the intake air dust removal electric field and the cathode of the intake air dust removal electric field is 5-100 mm.
- Example 43 provided by the present invention: including any one of the above examples 3 to 42, wherein the length of the anode of the intake dust removal electric field is 10-180 mm.
- Example 44 provided by the present invention: including any one of the above examples 3 to 42, wherein the length of the anode of the intake dust removal electric field is 60-180 mm.
- Example 45 provided by the present invention: including any one of the above examples 3 to 44, wherein the cathode length of the air intake dust removal electric field is 30-180 mm.
- Example 46 provided by the present invention: including any one of the above examples 3 to 44, wherein the cathode length of the air intake dust removal electric field is 54-176 mm.
- Example 47 provided by the present invention includes any one of the above examples 37 to 46, wherein, during operation, the coupling number of the electric field of the ionization and dust removal of the intake air is ⁇ 3.
- Example 48 provided by the present invention: including any one of the above examples 26 to 46, wherein, during operation, the coupling number of the electric field of the ionization and dust removal of the intake air is ⁇ 3.
- Example 49 provided by the present invention includes any one of the above examples 3 to 48, wherein the value range of the electric field voltage of the intake ionization and dedusting is 1kv-50kv.
- Example 50 provided by the present invention includes any one of the above examples 3 to 49, wherein the intake electric field device further includes several connection housings, and the series electric field stages are connected through the connection housings.
- Example 51 provided by the present invention includes the above example 50, wherein the distance between adjacent electric field levels is greater than 1.4 times the pole pitch.
- Example 52 provided by the present invention includes any one of the above examples 3 to 51, wherein the intake electric field device further includes an intake front electrode, the intake front electrode is in the intake electric field Between the inlet of the device and the intake ionization and dust removal electric field formed by the anode of the intake dust removal electric field and the cathode of the intake dust removal electric field.
- Example 53 provided by the present invention includes the above example 52, wherein the intake front electrode is dot-shaped, linear, mesh-shaped, orifice-shaped, plate-shaped, needle-rod-shaped, ball cage-shaped, box-shaped, Tube, natural form of material, or material processing form.
- Example 54 provided by the present invention includes the above example 52 or 53, wherein the intake front electrode is provided with an intake through hole.
- Example 55 provided by the present invention includes the above example 54, wherein the air intake through hole is polygonal, circular, elliptical, square, rectangular, trapezoidal, or rhombic.
- Example 56 provided by the present invention includes the above example 54 or 55, wherein the size of the air intake through hole is 0.1-3 mm.
- Example 57 provided by the present invention includes any one of the above examples 52 to 56, wherein the gas inlet front electrode is one or more forms of solid, liquid, gas molecular cluster, or plasma The combination.
- Example 58 provided by the present invention includes any one of the above examples 52 to 57, wherein the intake front electrode is a conductive mixed state substance, a biological natural mixed conductive substance, or an object is artificially processed to form a conductive substance .
- Example 59 provided by the present invention includes any one of the above examples 52 to 58, wherein the intake front electrode is 304 steel or graphite.
- Example 60 provided by the present invention: including any one of the above examples 52 to 58, wherein the intake front electrode is an ion-containing conductive liquid.
- Example 61 provided by the present invention includes any one of the above examples 52 to 60, wherein, during operation, when the gas with pollutants enters the cathode of the intake dust removal electric field and the anode formed by the anode of the intake dust removal electric field Before the gas ionizes the dedusting electric field and the gas with pollutants passes through the intake air front electrode, the intake air front electrode charges the pollutants in the gas.
- Example 62 provided by the present invention includes the above example 61, wherein, when the gas carrying pollutants enters the intake ionization and dust removal electric field, the anode of the intake dust removal electric field exerts an attractive force on the charged pollutants to cause pollution The object moves toward the anode of the intake dust removal electric field until pollutants adhere to the anode of the intake dust removal electric field.
- Example 63 provided by the present invention includes the above example 61 or 62, wherein the intake front electrode introduces electrons into pollutants, and the electrons are located between the intake front electrode and the anode of the intake dust removal electric field. The pollutants are transferred between them, so that more pollutants are charged.
- Example 64 provided by the present invention includes any one of the above examples 61 to 63, wherein between the intake front electrode and the intake dust removal electric field anode, electrons are conducted through pollutants and an electric current is formed.
- Example 65 provided by the present invention includes any one of the above examples 61 to 64, wherein the intake front electrode charges the pollutant by contact with the pollutant.
- Example 66 provided by the present invention includes any one of the above examples 61 to 65, wherein the intake front electrode charges pollutants by way of energy fluctuation.
- Example 67 provided by the present invention includes any one of the above examples 61 to 66, wherein the intake front electrode is provided with an intake through hole.
- Example 68 provided by the present invention includes any one of the above examples 52 to 67, wherein the intake front electrode is linear and the intake dust removal electric field anode is planar.
- Example 69 provided by the present invention includes any one of the above examples 52 to 68, wherein the intake front electrode is perpendicular to the intake dust removal electric field anode.
- Example 70 provided by the present invention includes any one of the above examples 52 to 69, wherein the intake front electrode is parallel to the intake dust removal electric field anode.
- Example 71 provided by the present invention includes any one of the above examples 51 to 69, wherein the intake front electrode is curved or arc-shaped.
- Example 72 provided by the present invention: including any one of the above examples 52 to 71, wherein the intake front electrode adopts a wire mesh.
- Example 73 provided by the present invention: including any one of the above examples 52 to 72, wherein the voltage between the intake front electrode and the intake dust removal electric field anode is different from the intake dust removal electric field The voltage between the cathode and the anode of the intake dust removal electric field.
- Example 74 provided by the present invention includes any one of the above examples 52 to 73, wherein the voltage between the intake front electrode and the intake dust removal electric field anode is less than the initial halo voltage.
- Example 75 provided by the present invention includes any one of the above examples 52 to 74, wherein the voltage between the intake front electrode and the intake dust removal electric field anode is 0.1kv / mm-2kv / mm.
- Example 76 provided by the present invention includes any one of the above examples 52 to 75, wherein the intake electric field device includes an intake runner, and the intake front electrode is located in the intake runner; The ratio of the cross-sectional area of the intake front electrode to the cross-sectional area of the intake runner is 99% -10%, or 90-10%, or 80-20%, or 70-30%, or 60-40%, or 50% .
- Example 77 provided by the present invention includes any one of the above Examples 3 to 76, wherein the intake electric field device includes an intake electret element.
- Example 78 provided by the present invention includes the above example 77, wherein, when the anode of the intake air electric field and the cathode of the intake air electric field are turned on, the intake electret element is ionized at the intake In the dust removal electric field.
- Example 79 provided by the present invention includes the above example 77 or 78, wherein the intake electret element is close to the outlet of the intake electric field device, or the intake electret element is provided at the inlet Gas field device outlet.
- Example 80 provided by the present invention includes any one of the above examples 78 to 79, wherein the anode of the intake air dedusting electric field and the cathode of the intake air dedusting electric field form an intake flow channel, and the intake electret The element is arranged in the intake flow channel.
- Example 81 provided by the present invention includes the above example 80, wherein the intake runner includes an intake runner outlet, the intake electret element is close to the intake runner outlet, or the intake The polar body element is provided at the outlet of the intake flow channel.
- Example 82 provided by the present invention: includes the above example 80 or 81, wherein the cross section of the intake electret element in the intake flow passage accounts for 5% -100% of the cross section of the intake flow passage.
- Example 83 provided by the present invention: including the above example 82, wherein the cross section of the intake electret element in the intake flow passage accounts for 10% -90%, 20% -80% of the cross section of the intake flow passage , Or 40% -60%.
- Example 84 provided by the present invention includes any one of the above examples 77 to 83, wherein the intake air ionization and dust removal electric field charges the intake electret element.
- Example 85 provided by the present invention includes any one of the above examples 77 to 84, wherein the intake electret element has a porous structure.
- Example 86 provided by the present invention: including any one of the above examples 77 to 85, wherein the intake electret element is a fabric.
- Example 87 provided by the present invention includes any one of the above examples 77 to 86, wherein the inside of the anode of the intake dust removal electric field is tubular, and the outside of the intake electret element is tubular, the intake The electret element is externally sheathed inside the anode of the air intake dust removal electric field.
- Example 88 provided by the present invention includes any one of the above examples 77 to 87, wherein the intake electret element and the intake dust removal electric field anode are detachably connected.
- Example 89 provided by the present invention includes any one of the above examples 77 to 88, wherein the material of the intake electret element includes an inorganic compound having electret properties.
- Example 90 provided by the present invention includes the above Example 89, wherein the inorganic compound is selected from one or more combinations of oxygen-containing compounds, nitrogen-containing compounds, or glass fibers.
- Example 91 provided by the present invention includes the above Example 90, wherein the oxygen-containing compound is selected from one or more combinations of metal-based oxides, oxygen-containing complexes, and oxygen-containing inorganic heteropoly acid salts.
- Example 92 provided by the present invention: including the above example 91, wherein the metal-based oxide is selected from aluminum oxide, zinc oxide, zirconium oxide, titanium oxide, barium oxide, tantalum oxide, silicon oxide, lead oxide, tin oxide One or more combinations.
- the metal-based oxide is selected from aluminum oxide, zinc oxide, zirconium oxide, titanium oxide, barium oxide, tantalum oxide, silicon oxide, lead oxide, tin oxide One or more combinations.
- Example 93 provided by the present invention: including the above Example 91, wherein the metal-based oxide is alumina.
- Example 94 provided by the present invention includes the above example 91, wherein the oxygen-containing composite is selected from one or more combinations of titanium zirconium composite oxide or titanium barium composite oxide.
- Example 95 provided by the present invention includes the above Example 91, wherein the oxygen-containing inorganic heteropoly acid salt is selected from one or more combinations of zirconium titanate, lead zirconate titanate, or barium titanate.
- Example 96 provided by the present invention includes the above Example 90, wherein the nitrogen-containing compound is silicon nitride.
- Example 97 provided by the present invention includes any one of the above examples 77 to 96, wherein the material of the intake electret element includes an organic compound having electret properties.
- Example 98 provided by the present invention: including the above example 97, wherein the organic compound is selected from one or more combinations of fluoropolymer, polycarbonate, PP, PE, PVC, natural wax, resin, and rosin .
- Example 99 provided by the present invention includes the above example 98, wherein the fluoropolymer is selected from one or more of polytetrafluoroethylene, polyperfluoroethylene propylene, soluble polytetrafluoroethylene, and polyvinylidene fluoridekinds of combinations.
- Example 100 provided by the present invention: including the above example 98, wherein the fluoropolymer is polytetrafluoroethylene.
- Example 101 includes any one of the above examples 2 to 100, wherein it further includes an air intake equalizing device.
- Example 102 provided by the present invention includes the above example 101, wherein the intake air equalization device forms an inlet formed at the entrance of the intake dust removal system with the anode of the intake dust removal electric field and the cathode of the intake dust removal electric field. Between the gas ionization and dust removal electric field, when the anode of the air intake and dust removal electric field is a cuboid, the air intake equalizing device includes: an air intake pipe provided on one side of the anode of the air intake and dust removal electric field, and an air intake pipe on the other Side air outlet pipe; wherein, the air inlet pipe is opposite to the air outlet pipe.
- Example 103 provided by the present invention includes the above example 101, wherein the inlet air equalization device forms an inlet formed at the inlet of the inlet dust removal system with the anode of the inlet dust removal electric field and the cathode of the inlet dust removal electric field. Between the gas ionization and dedusting electric field, when the anode of the air intake and dust removing electric field is a cylinder, the air intake and air distribution device is composed of several rotatable air distribution blades.
- Example 104 provided by the present invention includes the above example 101, in which the first venturi plate air equalizing mechanism of the intake air equalization device and the second venturi plate provided at the outlet end of the anode of the intake dust removal electric field are both Wind mechanism, the first venturi plate air equalizing mechanism is provided with an air inlet hole, the second venturi plate air equalizing mechanism is provided with an air outlet hole, and the air inlet hole and the air outlet hole are arranged in a staggered arrangement, And the front side air intake and side air exhaust, forming a cyclone structure.
- Example 105 provided by the present invention includes any one of the above examples 2 to 104, further including an ozone removing device for removing or reducing ozone generated by the intake electric field device, the ozone removing device Between the outlet of the intake electric field device and the outlet of the intake dust removal system.
- Example 106 provided by the present invention: includes the above example 105, wherein the ozone removing device further includes an ozone digester.
- Example 107 provided by the present invention includes the above example 106, wherein the ozone digester is selected from at least one of an ultraviolet ozone digester and a catalytic ozone digester.
- Example 108 provided by the present invention includes any one of the above examples 2 to 107, wherein it further includes a centrifugal separation mechanism.
- Example 109 provided by the present invention includes the above example 108, wherein the centrifugal separation mechanism includes an airflow turning channel, and the airflow turning channel can change the flow direction of the airflow.
- Example 110 provided by the present invention includes the above example 109, wherein the gas flow turning channel can guide the gas to flow in the circumferential direction.
- Example 111 provided by the present invention: including the above example 108 or 109, wherein the air flow turning channel is spiral or conical.
- Example 112 provided by the present invention: including any one of the above examples 108 to 111, wherein the centrifugal separation mechanism includes a separation cylinder.
- Example 113 provided by the present invention includes the above example 112, wherein the airflow turning channel is provided in the separation cylinder, and a dust outlet is provided at the bottom of the separation cylinder.
- Example 114 provided by the present invention includes the above example 112 or 113, wherein an air inlet communicating with the first end of the air flow turning channel is provided on the side wall of the separation cylinder.
- Example 115 provided by the present invention includes any one of the above examples 112 to 114, wherein the top of the separation cylinder is provided with an air outlet that communicates with the second end of the air flow turning channel.
- Example 116 provided by the present invention includes any one of the above Examples 1-115, and further includes an exhaust gas dust removal system, the exhaust gas dust removal system includes an exhaust gas dust removal system inlet, an exhaust gas dust removal system outlet, and an exhaust gas electric field device.
- Example 117 provided by the present invention includes the above example 116, wherein the tail gas electric field device includes an tail gas electric field device inlet, a tail gas electric field device outlet, a tail gas dedusting electric field cathode and a tail gas dedusting electric field anode, the tail gas dedusting electric field cathode and all The anode of the exhaust gas dedusting electric field is used to generate the exhaust gas ionization dedusting electric field.
- Example 118 provided by the present invention includes the above example 117, wherein the exhaust gas dedusting electric field anode includes a first anode portion and a second anode portion, the first anode portion is near an exhaust gas electric field device inlet, and the second anode portion is near At the outlet of the exhaust gas electric field device, at least one cathode support plate is provided between the first anode portion and the second anode portion.
- Example 119 provided by the present invention includes the above example 118, wherein the exhaust gas electric field device further includes an exhaust gas insulation mechanism for achieving insulation between the cathode support plate and the anode of the exhaust gas dedusting electric field.
- Example 120 provided by the present invention includes the above example 119, wherein an electric field flow path is formed between the exhaust gas dedusting electric field anode and the exhaust gas dedusting electric field cathode, and the exhaust gas insulation mechanism is provided outside the electric field flow path.
- Example 121 provided by the present invention includes the above example 119 or 120, wherein the exhaust gas insulation mechanism includes an insulating portion and a heat insulating portion; the material of the insulating portion is a ceramic material or a glass material.
- Example 122 provided by the present invention includes the above example 121, wherein the insulating portion is an umbrella-shaped string ceramic column, an umbrella-shaped string glass column, a column-shaped string ceramic column or a column-shaped glass column, and the glaze is hung on the inside or outside of the umbrella.
- the insulating portion is an umbrella-shaped string ceramic column, an umbrella-shaped string glass column, a column-shaped string ceramic column or a column-shaped glass column, and the glaze is hung on the inside or outside of the umbrella.
- Example 123 provided by the present invention includes the above example 122, wherein the distance between the outer edge of the umbrella-shaped string ceramic column or the umbrella-shaped string glass column and the anode of the exhaust gas dedusting electric field is greater than 1.4 times the electric field distance, The total length of the umbrella flanges of the umbrella-shaped string glass column is 1.4 times greater than the insulation distance of the umbrella-shaped string ceramic column or umbrella-shaped string glass column. Insulation distance of string ceramic column or glass string with umbrella shape is 1.4 times.
- Example 124 provided by the present invention: including any one of the above examples 118 to 123, wherein the length of the first anode portion is 1/10 to 1/4, 1/1 of the length of the anode of the exhaust gas dedusting electric field 4 to 1/3, 1/3 to 1/2, 1/2 to 2/3, 2/3 to 3/4, or 3/4 to 9/10.
- Example 125 provided by the present invention includes any one of the above examples 118 to 124, wherein the length of the first anode portion is long enough to remove part of the dust and reduce accumulation in the exhaust gas insulation mechanism and The dust on the cathode support plate reduces the electrical breakdown caused by the dust.
- Example 126 provided by the present invention: including any one of the above examples 118 to 125, wherein the second anode portion includes a dust accumulation section and a reserved dust accumulation section.
- Example 127 provided by the present invention includes any one of the above examples 117 to 126, wherein the exhaust gas dedusting electric field cathode includes at least one electrode rod.
- Example 128 provided by the present invention: including the above example 127, wherein the diameter of the electrode rod is not greater than 3 mm.
- Example 129 provided by the present invention includes the above example 127 or 128, wherein the electrode rod has a needle shape, a polygonal shape, a burr shape, a threaded rod shape or a column shape.
- Example 130 provided by the present invention includes any one of the above examples 117 to 129, wherein the exhaust gas dedusting electric field anode is composed of a hollow tube bundle.
- Example 131 provided by the present invention includes the above example 130, wherein the hollow section of the anode tube bundle of the exhaust gas dedusting electric field adopts a circle or a polygon.
- Example 132 provided by the present invention includes the above example 131, wherein the polygon is a hexagon.
- Example 133 provided by the present invention includes any one of the above examples 130 to 132, wherein the tube bundle of the anode of the exhaust gas dedusting electric field has a honeycomb shape.
- Example 134 provided by the present invention includes any one of the above examples 117 to 133, wherein the exhaust gas dedusting electric field cathode penetrates the exhaust gas dedusting electric field anode.
- Example 135 provided by the present invention includes any one of the above examples 117 to 134, wherein the exhaust gas electric field device performs carbon black removal treatment when the electric field accumulates dust to a certain degree.
- Example 136 provided by the present invention includes the above example 135, wherein the exhaust gas electric field device detects electric field current to determine whether dust accumulation is to a certain degree, and carbon black removal treatment is required.
- Example 137 provided by the present invention includes the above example 135 or 136, wherein the exhaust gas electric field device increases the electric field voltage to perform the carbon black removal treatment.
- Example 138 provided by the present invention includes the above example 135 or 136, wherein the exhaust gas electric field device uses the electric field back-corona discharge phenomenon to perform carbon black removal treatment.
- Example 139 provided by the present invention includes the above example 135 or 136, wherein the exhaust gas electric field device utilizes the phenomenon of electric field back-corona discharge to increase the voltage and limit the injection current to cause the sharp discharge occurring at the position of the anode carbon deposit Plasma, which deeply oxidizes the organic components of carbon black, breaks the polymer bonds, and forms small-molecule carbon dioxide and water for carbon black removal treatment.
- Example 140 provided by the present invention includes any one of the above examples 117 to 139, wherein the length of the tail gas dedusting electric field anode is 10-90 mm, and the length of the tail gas dedusting electric field cathode is 10-90 mm.
- Example 141 provided by the present invention includes the above example 140, wherein when the electric field temperature is 200 ° C, the corresponding dust collection efficiency is 99.9%.
- Example 142 provided by the present invention includes the above example 140 or 141, wherein when the electric field temperature is 400 ° C, the corresponding dust collection efficiency is 90%.
- Example 143 provided by the present invention includes any one of the above examples 140 to 142, wherein when the electric field temperature is 500 ° C., the corresponding dust collection efficiency is 50%.
- Example 144 provided by the present invention includes any one of the above examples 117 to 143, wherein the exhaust gas electric field device further includes an auxiliary electric field unit for generating an auxiliary electric field that is not parallel to the exhaust gas ionization and dust removal electric field.
- Example 145 provided by the present invention includes any one of the above examples 117 to 143, wherein the tail gas electric field device further includes an auxiliary electric field unit, the tail gas ionization and dust removal electric field includes a flow channel, and the auxiliary electric field unit uses To generate an auxiliary electric field that is not perpendicular to the flow channel.
- Example 146 provided by the present invention includes the above example 144 or 145, wherein the auxiliary electric field unit includes a first electrode, and the first electrode of the auxiliary electric field unit is disposed at or near the inlet of the exhaust gas ionization and dust removal electric field.
- Example 147 provided by the present invention: including the above example 146, wherein the first electrode is a cathode.
- Example 148 provided by the present invention includes the above example 146 or 147, wherein the first electrode of the auxiliary electric field unit is an extension of the cathode of the exhaust gas dedusting electric field.
- Example 150 provided by the present invention includes any one of the above examples 144 to 149, wherein the auxiliary electric field unit includes a second electrode, and the second electrode of the auxiliary electric field unit is disposed at or near the exhaust gas ionization The outlet of the dust removal electric field.
- Example 151 provided by the present invention: including the above example 150, wherein the second electrode is an anode.
- Example 152 provided by the present invention includes the above example 150 or 151, wherein the second electrode of the auxiliary electric field unit is an extension of the anode of the exhaust gas dedusting electric field.
- Example 154 provided by the present invention includes any one of the above examples 144 to 147, 150, and 151, wherein the electrode of the auxiliary electric field and the electrode of the exhaust gas ionization and dust removal electric field are provided independently.
- Example 155 provided by the present invention includes any one of the above examples 117 to 154, wherein the ratio of the dust accumulation area of the exhaust gas dedusting electric field anode to the discharge area of the exhaust gas dedusting electric field cathode is 1.667: 1- 1680: 1.
- Example 156 provided by the present invention includes any one of the above examples 117 to 154, wherein the ratio of the dust accumulation area of the exhaust gas dedusting electric field anode to the discharge area of the exhaust gas dedusting electric field cathode is 6.67: 1- 56.67: 1.
- Example 157 provided by the present invention includes any one of the above examples 117 to 156, wherein the diameter of the exhaust gas dedusting electric field cathode is 1-3 mm, and the exhaust gas dedusting electric field anode and the exhaust gas dedusting electric field cathode The pole spacing is 2.5-139.9 mm; the ratio of the dust accumulation area of the exhaust gas dedusting electric field anode to the discharge area of the exhaust gas dedusting electric field cathode is 1.667: 1-1680: 1.
- Example 158 provided by the present invention includes any one of the above examples 117 to 156, wherein the electrode separation between the exhaust gas dedusting electric field anode and the exhaust gas dedusting electric field cathode is less than 150 mm.
- Example 159 provided by the present invention includes any one of the above examples 117 to 156, wherein the pole separation of the exhaust gas dedusting electric field anode and the exhaust gas dedusting electric field cathode is 2.5-139.9 mm.
- Example 160 provided by the present invention: including any one of the above examples 117 to 156, wherein the electrode separation between the anode of the exhaust gas dedusting electric field and the cathode of the exhaust gas dedusting electric field is 5-100 mm.
- Example 161 provided by the present invention: including any one of the above examples 117 to 160, wherein the length of the exhaust gas dedusting electric field anode is 10-180 mm.
- Example 162 provided by the present invention includes any one of the above examples 117 to 160, wherein the length of the exhaust gas dedusting electric field anode is 60-180 mm.
- Example 163 provided by the present invention: including any one of the above examples 117 to 162, wherein the cathode length of the exhaust gas dedusting electric field is 30-180 mm.
- Example 164 provided by the present invention: including any one of the above examples 117 to 162, wherein the cathode length of the exhaust gas dedusting electric field is 54-176 mm.
- Example 165 provided by the present invention includes any one of the above examples 155 to 164, wherein, during operation, the coupling number of the exhaust gas ionization and dust removal electric field is ⁇ 3.
- Example 166 provided by the present invention includes any one of the above examples 144 to 164, wherein, during operation, the coupling number of the exhaust gas ionization and dust removal electric field is ⁇ 3.
- Example 167 provided by the present invention includes any one of the above examples 117 to 166, wherein the exhaust gas ionization dust removal electric field voltage has a value range of 1kv-50kv.
- Example 168 provided by the present invention includes any one of the above examples 117 to 167, wherein the exhaust gas electric field device further includes several connection housings, and the series electric field stages are connected through the connection housings.
- Example 169 provided by the present invention includes the above example 168, wherein the distance between adjacent electric field levels is greater than 1.4 times the pole pitch.
- Example 170 provided by the present invention includes any one of the above examples 117 to 169, wherein the tail gas electric field device further includes a tail gas pre-electrode at the entrance of the tail gas electric field device The exhaust gas ionization and dedusting electric field formed by the anode of the exhaust gas dedusting electric field and the cathode of the exhaust gas dedusting electric field.
- Example 171 provided by the present invention includes the above example 170, wherein the exhaust gas pre-electrode is dot-shaped, linear, mesh-shaped, orifice-shaped, plate-shaped, needle-rod-shaped, ball cage-shaped, box-shaped, tubular , Material natural form, or material processing form.
- Example 172 provided by the present invention includes the above example 170 or 171, wherein the exhaust gas pre-electrode is provided with exhaust gas through holes.
- Example 173 provided by the present invention includes the above example 172, wherein the exhaust gas through-hole is polygonal, circular, elliptical, square, rectangular, trapezoidal, or rhombic.
- Example 174 provided by the present invention includes the above example 172 or 173, wherein the size of the exhaust gas through hole is 0.1-3 mm.
- Example 175 provided by the present invention includes any one of the above examples 170 to 174, wherein the tail gas pre-electrode is in one or more forms of solid, liquid, gas molecular group, or plasma combination.
- Example 176 provided by the present invention includes any one of the above examples 170 to 175, wherein the exhaust gas front electrode is a conductive mixed state substance, a biological natural mixed conductive substance, or an object is artificially processed to form a conductive substance.
- Example 177 provided by the present invention includes any one of the above examples 170 to 176, wherein the exhaust gas front electrode is 304 steel or graphite.
- Example 178 provided by the present invention includes any one of the above examples 170 to 176, wherein the exhaust gas front electrode is an ion-containing conductive liquid.
- Example 179 provided by the present invention includes any one of the above examples 170 to 178, wherein during operation, the exhaust ionized dust formed by the pollutant gas entering the cathode of the exhaust gas dedusting electric field and the anode of the exhaust gas dedusting electric field Before the electric field, and when the pollutant-laden gas passes through the tail gas pre-electrode, the tail gas pre-electrode charges the pollutant in the gas.
- Example 180 provided by the present invention includes the above example 179, wherein, when the gas carrying pollutants enters the tail gas ionization dust removal electric field, the anode of the tail gas dust removal electric field exerts an attractive force on the charged pollutants, causing the pollutants to The anode of the exhaust gas dedusting electric field moves until pollutants adhere to the anode of the exhaust gas dedusting electric field.
- Example 181 provided by the present invention: including the above example 179 or 180, wherein the tail gas pre-electrode introduces electrons into pollutants, and the contamination of electrons between the tail gas pre-electrode and the tail gas dedusting electric field anode Transfer between objects to charge more pollutants.
- Example 182 provided by the present invention includes any one of the above examples 178 to 180, wherein between the exhaust gas front electrode and the exhaust gas dedusting electric field anode conduct electrons through pollutants and form an electric current.
- Example 183 provided by the present invention includes any one of the above examples 179 to 182, wherein the exhaust gas front electrode charges the pollutant by contact with the pollutant.
- Example 184 provided by the present invention includes any one of the above examples 179 to 183, wherein the exhaust gas front electrode charges pollutants by means of energy fluctuation.
- Example 185 provided by the present invention includes any one of the above examples 179 to 184, wherein the exhaust gas pre-electrode is provided with exhaust gas through holes.
- Example 186 provided by the present invention includes any one of the above examples 170 to 185, wherein the tail gas pre-electrode is linear, and the tail gas dedusting electric field anode is planar.
- Example 187 provided by the present invention: including any one of the above examples 170 to 186, wherein the tail gas pre-electrode is perpendicular to the tail gas dedusting electric field anode.
- Example 188 provided by the present invention includes any one of the above examples 170 to 187, wherein the tail gas pre-electrode is parallel to the tail gas dedusting electric field anode.
- Example 189 provided by the present invention: including any one of the above examples 170 to 188, wherein the exhaust gas pre-electrode is curved or arc-shaped.
- Example 190 provided by the present invention: including any one of the above examples 170 to 189, wherein the exhaust gas pre-electrode adopts a wire mesh.
- Example 191 provided by the present invention includes any one of the above examples 170 to 190, wherein the voltage between the exhaust gas front electrode and the exhaust gas dedusting electric field anode is different from the exhaust gas dedusting electric field cathode and the Describe the voltage between the anodes of the exhaust gas dedusting electric field.
- Example 192 provided by the present invention includes any one of the above examples 170 to 191, wherein the voltage between the exhaust gas front electrode and the exhaust gas dedusting electric field anode is less than the initial halo voltage.
- Example 193 provided by the present invention includes any one of the above examples 170 to 192, wherein the voltage between the exhaust gas front electrode and the exhaust gas dedusting electric field anode is 0.1 kv / mm-2 kv / mm.
- Example 194 provided by the present invention includes any one of the above examples 170 to 193, wherein the tail gas electric field device includes a tail gas flow channel, the tail gas pre-electrode is located in the tail gas flow channel; the tail gas front
- the ratio of the cross-sectional area of the disposed electrode to the cross-sectional area of the exhaust gas channel is 99% -10%, or 90-10%, or 80-20%, or 70-30%, or 60-40%, or 50%.
- Example 195 provided by the present invention includes any one of the above examples 117 to 194, wherein the tail gas electric field device includes a tail gas electret element.
- Example 196 provided by the present invention includes the above example 195, wherein when the anode of the exhaust gas dedusting electric field and the cathode of the exhaust gas dedusting electric field are powered on, the exhaust gas electret element is in the exhaust gas ionizing dedusting electric field.
- Example 197 provided by the present invention includes the above example 195 or 196, wherein the exhaust gas electret element is close to the exhaust gas electric field device outlet, or the exhaust gas electret element is provided at the exhaust gas electric field device outlet .
- Example 198 provided by the present invention includes any one of the above examples 195 to 197, wherein the exhaust gas dedusting electric field anode and the exhaust gas dedusting electric field cathode form an exhaust gas flow channel, and the exhaust gas electret element is provided at In the exhaust gas channel.
- Example 199 provided by the present invention includes the above example 198, wherein the exhaust gas channel includes an exhaust gas channel outlet, the exhaust gas electret element is close to the exhaust gas channel outlet, or the exhaust gas electret The element is arranged at the outlet of the tail gas channel.
- Example 200 provided by the present invention includes the above example 198 or 199, wherein the cross-section of the exhaust gas electret element in the exhaust gas flow channel accounts for 5% -100% of the cross-section of the exhaust gas flow channel.
- Example 201 provided by the present invention includes the above example 200, wherein the cross-section of the exhaust electret element in the exhaust gas channel accounts for 10% -90%, 20% -80% of the cross-section of the exhaust gas channel, Or 40% -60%.
- Example 202 provided by the present invention includes any one of the above examples 195 to 201, wherein the exhaust gas ionization and dust removal electric field charges the exhaust gas electret element.
- Example 203 provided by the present invention includes any one of the above examples 195 to 202, wherein the exhaust electret element has a porous structure.
- Example 204 provided by the present invention: including any one of the above examples 195 to 203, wherein the exhaust electret element is a fabric.
- Example 205 provided by the present invention includes any one of the above examples 195 to 204, wherein the anode of the exhaust gas dedusting electric field is tubular, the exterior of the exhaust gas electret element is tubular, and the exhaust gas electret The outside of the element is sheathed inside the anode of the exhaust gas dedusting electric field.
- Example 206 provided by the present invention includes any one of the above examples 195 to 205, wherein the tail gas electret element and the tail gas dedusting electric field anode are detachably connected.
- Example 207 provided by the present invention includes any one of the above examples 195 to 206, wherein the material of the exhaust electret element includes an inorganic compound having electret properties.
- Example 208 provided by the present invention includes the above example 207, wherein the inorganic compound is selected from one or more combinations of oxygen-containing compounds, nitrogen-containing compounds, or glass fibers.
- Example 209 provided by the present invention includes the above example 208, wherein the oxygen-containing compound is selected from one or more combinations of metal-based oxides, oxygen-containing complexes, and oxygen-containing inorganic heteropoly acid salts.
- Example 210 provided by the present invention includes the above example 209, wherein the metal-based oxide is selected from aluminum oxide, zinc oxide, zirconium oxide, titanium oxide, barium oxide, tantalum oxide, silicon oxide, lead oxide, tin oxide One or more combinations.
- the metal-based oxide is selected from aluminum oxide, zinc oxide, zirconium oxide, titanium oxide, barium oxide, tantalum oxide, silicon oxide, lead oxide, tin oxide One or more combinations.
- Example 211 provided by the present invention includes the above example 209, wherein the metal-based oxide is alumina.
- Example 212 provided by the present invention includes the above example 209, wherein the oxygen-containing composite is selected from one or more combinations of titanium zirconium composite oxide or titanium barium composite oxide.
- Example 213 provided by the present invention includes the above example 209, wherein the oxygen-containing inorganic heteropoly acid salt is selected from one or more combinations of zirconium titanate, lead zirconate titanate, or barium titanate.
- Example 214 provided by the present invention: including the above example 208, wherein the nitrogen-containing compound is silicon nitride.
- Example 215 provided by the present invention includes any one of the above examples 195 to 214, wherein the material of the exhaust electret element includes an organic compound having electret properties.
- Example 216 provided by the present invention: including the above example 215, wherein the organic compound is selected from one or more combinations of fluoropolymer, polycarbonate, PP, PE, PVC, natural wax, resin, and rosin .
- Example 217 provided by the present invention includes the above example 216, wherein the fluoropolymer is selected from one or more of polytetrafluoroethylene, polyperfluoroethylene propylene, soluble polytetrafluoroethylene, and polyvinylidene fluoride Kinds of combinations.
- Example 218 provided by the present invention: including the above example 216, wherein the fluoropolymer is polytetrafluoroethylene.
- Example 219 provided by the present invention includes any one of the above examples 116 to 218, and further includes an exhaust air equalizing device.
- Example 220 provided by the present invention includes the above example 219, wherein the exhaust gas equalization device is formed at the entrance of the exhaust gas dedusting system and the exhaust gas ionization and dedusting electric field formed by the exhaust gas dedusting electric field anode and the exhaust gas dedusting electric field cathode
- the exhaust gas equalizing device includes: an air inlet pipe provided on one side of the anode of the exhaust gas dedusting electric field and an air outlet pipe provided on the other side; wherein, The air inlet pipe is opposed to the air outlet pipe.
- Example 221 provided by the present invention includes the above example 219, wherein the tail gas ionization device forms a tail gas ionization and dust removal electric field formed at the entrance of the tail gas removal system and the anode of the tail gas removal electric field and the cathode of the tail gas removal electric field In the meantime, when the anode of the exhaust gas dedusting electric field is a cylinder, the exhaust gas equalizing device is composed of several rotatable air equalizing blades.
- Example 222 provided by the present invention includes the above example 219, wherein the first ventilating device of the exhaust gas equalizing device and the second ventilating device of the second venturi are provided at the outlet end of the anode of the exhaust gas dedusting electric field ,
- the first venturi plate air distribution mechanism is provided with air inlet holes
- the second venturi plate air distribution mechanism is provided with air outlet holes
- the air inlet holes and the air outlet holes are arranged in a staggered arrangement
- the front The air is discharged from the intake side to form a cyclone structure.
- Example 223 provided by the present invention includes any one of the above examples 116 to 222, wherein it further includes an oxygen supplement device for adding a gas including oxygen before the exhaust gas ionization and dedusting electric field.
- Example 224 provided by the present invention includes the above example 223, wherein the oxygen supplementing device adds oxygen by simply increasing oxygen, passing in outside air, passing in compressed air, and / or passing in ozone.
- Example 225 provided by the present invention includes the above examples 223 or 224, wherein the amount of oxygen supplementation is determined at least according to the content of exhaust gas particles.
- Example 226 provided by the present invention includes any one of the above examples 116 to 225, and further includes a water removal device for removing liquid water before the inlet of the exhaust gas electric field device.
- Example 227 provided by the present invention includes the above example 226, wherein, when the exhaust gas temperature or the engine temperature is lower than a certain temperature, the water removal device removes liquid water in the exhaust gas.
- Example 228 provided by the present invention: including the above example 227, wherein the certain temperature is above 90 ° C and below 100 ° C.
- Example 229 provided by the present invention: including the above example 227, wherein the certain temperature is above 80 ° C and below 90 ° C.
- Example 230 provided by the present invention includes the above example 227, wherein the certain temperature is below 80 ° C.
- Example 231 provided by the present invention includes the above examples 226 to 230, wherein the water removal device is an electrocoagulation device.
- Example 232 provided by the present invention includes any one of the above examples 116 to 231, which further includes a tail gas cooling device for reducing the temperature of the tail gas before the inlet of the tail gas electric field device.
- Example 233 provided by the present invention includes the above example 232, wherein the exhaust gas cooling device includes a heat exchange unit for heat exchange with the exhaust gas of the engine to heat the liquid heat exchange medium in the heat exchange unit into a gaseous state Heat exchange medium.
- Example 234 provided by the present invention includes the above example 233, wherein the heat exchange unit includes:
- the exhaust gas passage cavity communicates with the exhaust pipe of the engine, and the exhaust gas passage cavity is used for passing the exhaust gas of the engine;
- a medium gasification chamber which is used to convert a liquid heat exchange medium and tail gas into a gaseous state after heat exchange.
- Example 235 provided by the present invention includes the above example 233 or 234, wherein it further includes a power generation unit for converting the thermal energy of the heat exchange medium and / or the exhaust gas into mechanical energy.
- Example 236 provided by the present invention includes the above example 235, wherein the power generation unit includes a turbofan.
- Example 237 provided by the present invention includes the above example 236, wherein the turbofan includes:
- the medium cavity turbofan assembly is installed on the turbofan shaft, and the medium cavity turbofan assembly is located in the medium gasification cavity.
- Example 238 provided by the present invention includes the above example 237, wherein the medium cavity turbofan assembly includes a medium cavity guide fan and a medium cavity power fan.
- Example 239 provided by the present invention: including any one of the above examples 236 to 238, wherein the turbofan includes:
- the exhaust chamber turbofan assembly is installed on the turbofan shaft, and the exhaust chamber turbofan assembly is located in the exhaust gas passage cavity.
- Example 240 provided by the present invention includes the above example 239, wherein the exhaust chamber turbofan assembly includes an exhaust chamber guide fan and an exhaust chamber power fan.
- Example 241 provided by the present invention includes any one of the above examples 235 to 240, wherein the exhaust gas cooling device further includes a power generation unit for converting mechanical energy generated by the power generation unit into electrical energy.
- Example 242 provided by the present invention includes the above example 241, wherein the power generation unit includes a generator stator and a generator rotor, and the generator rotor is connected to a turbofan shaft of a power generation unit.
- Examples provided by the present invention include the above examples 241 or 242, wherein the power generation unit includes a battery assembly.
- Example 244 provided by the present invention includes any one of the above examples 241 to 243, wherein the power generation unit includes a generator regulation component, and the generator regulation component is used to regulate the electric torque of the generator.
- Example 245 provided by the present invention includes any one of the above examples 235 to 244, wherein the exhaust gas cooling device further includes a medium transmission unit, the medium transmission unit is connected between the heat exchange unit and the power generation unit .
- Example 246 provided by the present invention: includes the above example 245, wherein the medium transmission unit includes a reverse thrust duct.
- Example 247 provided by the present invention includes the above example 245, wherein the medium transmission unit includes a pressure-bearing pipeline.
- Example 248 provided by the present invention includes any one of the above examples 241 to 247, wherein the exhaust gas cooling device further includes a coupling unit electrically connected between the power generation unit and the power generation unit.
- Example 249 provided by the present invention includes the above example 248, wherein the coupling unit includes an electromagnetic coupler.
- Example 250 includes any one of the above examples 233 to 249, wherein the exhaust gas temperature-lowering device further includes a heat insulation pipe connected to the exhaust gas pipe of the engine and the heat exchange unit between.
- Example 251 provided by the present invention: including any one of the above examples 232 to 250, wherein the exhaust gas cooling device includes a fan, which blows air to the exhaust gas before passing the air into the inlet of the exhaust gas electric field device The role of cooling.
- the exhaust gas cooling device includes a fan, which blows air to the exhaust gas before passing the air into the inlet of the exhaust gas electric field device The role of cooling.
- Example 252 provided by the present invention includes the above example 251, wherein the air passed in is 50% to 300% of the exhaust gas.
- Example 253 provided by the present invention includes the above example 251, wherein the air passed in is 100% to 180% of the exhaust gas.
- Example 254 provided by the present invention: including the above example 251, wherein the air passing in is 120% to 150% of the exhaust gas.
- Example 255 provided by the present invention includes the above example 234, wherein the oxygen supplement device includes a fan, and the fan plays a role in cooling the exhaust gas before passing the air into the exhaust gas electric field device inlet.
- Example 256 provided by the present invention: including the above example 255, wherein the air passing in is 50% to 300% of the exhaust gas.
- Example 257 provided by the present invention: including the above example 255, wherein the air passing in is 100% to 180% of the exhaust gas.
- Example 258 provided by the present invention: including the above example 255, wherein the incoming air is 120% to 150% of the exhaust gas.
- Example 259 provided by the present invention: includes any one of the above examples 1-258, and further includes an exhaust gas ozone purification system including a reaction field for mixing and reacting the ozone stream with the exhaust gas stream .
- Example 260 provided by the present invention: includes the above example 259, wherein the reaction field includes pipes and / or reactors.
- Example 261 provided by the present invention: includes the above example 260, in which at least one of the following technical features is also included:
- the pipe section diameter is 100-200 mm
- the length of the pipe is greater than 0.1 times the pipe diameter
- the reactor is selected from at least one of the following:
- Reactor 1 The reactor has a reaction chamber, and tail gas and ozone are mixed and reacted in the reaction chamber;
- the reactor includes a number of honeycomb-shaped cavities for providing a space where tail gas and ozone are mixed and reacted; a gap is provided between the honeycomb-shaped cavities for passing a cold medium to control the tail gas and Ozone reaction temperature;
- Reactor 3 The reactor includes several carrier units, and the carrier unit provides a reaction site;
- Reactor 4 The reactor includes a catalyst unit, and the catalyst unit is used to promote the oxidation reaction of the tail gas;
- the reaction field is provided with an ozone inlet, and the ozone inlet is selected from at least one of a nozzle, a spray grid, a nozzle, a swirl nozzle, and a nozzle provided with a venturi tube;
- the reaction field is provided with an ozone inlet.
- the ozone enters the reaction field through the ozone inlet to contact the exhaust gas.
- the ozone inlet is formed in at least one of the following directions: opposite to the direction of the exhaust gas flow, and The direction is perpendicular, tangent to the direction of exhaust gas flow, inserting the direction of exhaust gas flow, and contacting the exhaust gas in multiple directions.
- Example 262 provided by the present invention: includes any one of the above examples 259 to 261, wherein the reaction field includes an exhaust pipe, a regenerator device, or a catalyst.
- Example 263 provided by the present invention: including any one of the above examples 259 to 262, wherein the temperature of the reaction field is -50-200 ° C.
- Example 264 provided by the present invention: including the above example 263, wherein the temperature of the reaction field is 60-70 ° C.
- Example 265 provided by the present invention: including any one of the above examples 259 to 264, wherein the exhaust gas ozone purification system further includes an ozone source for providing an ozone stream.
- Example 266 provided by the present invention includes the above example 265, wherein the ozone source includes a storage ozone unit and / or an ozone generator.
- Example 267 provided by the present invention includes the above example 266, wherein the ozone generator includes a surface discharge ozone generator, a power frequency arc ozone generator, a high frequency induction ozone generator, a low pressure ozone generator, ultraviolet rays A combination of one or more of an ozone generator, an electrolyte ozone generator, a chemical ozone generator, and a radiation irradiation particle generator.
- the ozone generator includes a surface discharge ozone generator, a power frequency arc ozone generator, a high frequency induction ozone generator, a low pressure ozone generator, ultraviolet rays A combination of one or more of an ozone generator, an electrolyte ozone generator, a chemical ozone generator, and a radiation irradiation particle generator.
- Example 268 provided by the present invention includes the above example 266, wherein the ozone generator includes an electrode, and a catalyst layer is provided on the electrode, and the catalyst layer includes an oxidation catalytic bond cracking selective catalyst layer.
- Example 269 provided by the present invention includes the above example 268, wherein the electrode includes a high-voltage electrode or a high-voltage electrode provided with a barrier dielectric layer, and when the electrode includes a high-voltage electrode, the oxidation catalytic bond cleavage selective catalyst A layer is provided on the surface of the high-voltage electrode.
- the electrode includes the high-voltage electrode of the barrier medium layer, the selective catalytic layer for oxidative catalytic bond cleavage is provided on the surface of the barrier medium layer.
- Example 270 provided by the present invention includes the above example 269, wherein the barrier medium layer is selected from at least one of ceramic plates, ceramic tubes, quartz glass plates, quartz plates, and quartz tubes.
- Example 271 provided by the present invention includes the above example 269, wherein, when the electrode includes a high-voltage electrode, the thickness of the oxidation catalytic bond cleavage selective catalyst layer is 1-3 mm; when the electrode includes a barrier medium layer In the case of high-voltage electrodes, the loading of the selective catalytic layer for the oxidation catalytic bond cleavage includes 1-12 wt% of the barrier medium layer.
- Example 272 provided by the present invention includes any one of the above examples 268 to 271, wherein the oxidation catalytic bond cleavage selective catalyst layer includes the following components in weight percentages:
- the active component is selected from at least one of a compound of metal M and metal element M
- the metal element M is selected from alkaline earth metal elements, transition metal elements, fourth main group metal elements, precious metal elements and lanthanide rare earth elements At least one of
- the coating is selected from at least one of alumina, cerium oxide, zirconia, manganese oxide, metal composite oxides, porous materials, and layered materials.
- the metal composite oxide includes aluminum, cerium, zirconium, and manganese A composite oxide of one or more metals.
- Example 273 provided by the present invention: including the above example 272, wherein the alkaline earth metal element is selected from at least one of magnesium, strontium and calcium.
- Example 274 provided by the present invention includes the above example 272, wherein the transition metal element is selected from at least one of titanium, manganese, zinc, copper, iron, nickel, cobalt, yttrium and zirconium.
- Example 275 provided by the present invention: including the above example 272, wherein the metal element of the fourth main group is tin.
- Example 276 provided by the present invention includes the above example 272, wherein the precious metal element is selected from at least one of platinum, rhodium, palladium, gold, silver, and iridium.
- Example 277 provided by the present invention includes the above example 272, wherein the lanthanide rare earth element is selected from at least one of lanthanum, cerium, praseodymium, and samarium.
- Example 278 provided by the present invention: including the above example 272, wherein the compound of the metal element M is selected from at least one of oxides, sulfides, sulfates, phosphates, carbonates, and perovskites .
- Example 279 provided by the present invention includes the above example 272, wherein the porous material is selected from at least one of molecular sieve, diatomaceous earth, zeolite, and carbon nanotubes.
- Example 280 provided by the present invention: including the above example 272, wherein the layered material is selected from at least one of graphene and graphite.
- Example 281 provided by the present invention includes any one of the above examples 259 to 280, wherein the exhaust gas ozone purification system further includes an ozone amount control device for controlling the amount of ozone so as to effectively oxidize the gas to be treated in the exhaust gas Components, the ozone amount control device includes a control unit.
- Example 282 provided by the present invention includes the above example 281, wherein the ozone amount control device further includes a tail gas component detection unit before ozone treatment, which is used to detect the content of the tail gas component before ozone treatment.
- Example 283 provided by the present invention includes any one of the above examples 281 to 282, wherein the control unit controls the amount of ozone required for the mixing reaction according to the content of the exhaust gas component before the ozone treatment.
- Example 284 provided by the present invention includes the above example 282 or 283, wherein the exhaust gas component detection unit before ozone treatment is selected from at least one of the following detection units:
- the first volatile organic compound detection unit is used to detect the content of volatile organic compounds in the exhaust gas before ozone treatment
- the first CO detection unit is used to detect the CO content in the exhaust gas before ozone treatment
- the first nitrogen oxide detection unit is used to detect the nitrogen oxide content in the exhaust gas before ozone treatment.
- Example 285 provided by the present invention includes the above example 284, wherein the control unit controls the amount of ozone required for the mixed reaction according to the output value of at least one of the exhaust gas component detection units before ozone treatment.
- Example 286 provided by the present invention includes any one of the above examples 281 to 285, wherein the control unit is used to control the amount of ozone required for the mixed reaction according to a preset mathematical model.
- Example 287 provided by the present invention includes any one of the above examples 281 to 286, wherein the control unit is used to control the amount of ozone required for the mixed reaction according to a theoretical estimated value.
- Example 288 provided by the present invention includes any one of the above example 287, wherein the theoretical estimated value is: the molar ratio of ozone flux to the to-be-processed material in the exhaust gas is 2-10.
- Example 289 provided by the present invention includes any one of the above examples 281 to 288, wherein the ozone amount control device includes an ozone-treated tail gas component detection unit for detecting the content of the tail gas component after ozone treatment.
- Example 290 provided by the present invention includes any one of the above examples 281 to 289, wherein the control unit controls the amount of ozone required for the mixing reaction according to the exhaust gas component content after the ozone treatment.
- Example 291 provided by the present invention includes the above-mentioned example 289 or 290, wherein the exhaust gas component detection unit after ozone treatment is selected from at least one of the following detection units:
- the first ozone detection unit is used to detect the ozone content in the exhaust gas after ozone treatment
- the second volatile organic compound detection unit is used to detect the content of volatile organic compounds in the exhaust gas after ozone treatment
- the second CO detection unit is used to detect the CO content in the exhaust gas after ozone treatment
- the second nitrogen oxide detection unit is used to detect the nitrogen oxide content in the exhaust gas after ozone treatment.
- Example 292 provided by the present invention includes the above example 291, wherein the control unit controls the amount of ozone according to at least one output value of the ozone-treated tail gas component detection unit.
- Example 293 provided by the present invention includes any one of the above examples 259 to 292, wherein the exhaust gas ozone purification system further includes a denitration device for removing the mixed reaction product of the ozone stream and the exhaust gas stream Nitric acid.
- Example 294 provided by the present invention includes the above example 293, wherein the denitration device includes an electrocoagulation device, and the electrocoagulation device includes:
- a first electrode, the first electrode is located in the electrocoagulation flow channel
- Example 295 provided by the present invention including the above example 294, wherein the first electrode is a solid, liquid, gas molecular group, plasma, conductive mixed state substance, biological natural mixed conductive substance, or artificially formed by an object A combination of one or more forms in a conductive substance.
- Example 296 provided by the present invention: including the above example 294 or 295, wherein the first electrode is solid metal, graphite, or 304 steel.
- Example 297 provided by the present invention includes any one of the above examples 294 to 296, wherein the first electrode is dot-shaped, wire-shaped, mesh-shaped, orifice-shaped, plate-shaped, needle-rod-shaped, ball cage Shaped, box-shaped, tubular, natural form material, or processed form material.
- Example 298 provided by the present invention includes any one of the above examples 294 to 297, wherein the first electrode is provided with a front through hole.
- Example 299 provided by the present invention includes the above example 298, wherein the shape of the front through hole is polygon, circle, ellipse, square, rectangle, trapezoid, or rhombus.
- Example 300 provided by the present invention: including the above example 298 or 299, wherein the hole diameter of the front through hole is 0.1-3 mm.
- Example 301 provided by the present invention includes any one of the above examples 294 to 300, wherein the second electrode has a multi-layer mesh shape, a mesh shape, a perforated plate shape, a tubular shape, a barrel shape, a ball cage shape, Box-shaped, plate-shaped, granular layered, bent plate-shaped, or panel-shaped.
- Example 302 provided by the present invention includes any one of the above examples 294 to 301, wherein the second electrode is provided with a rear through hole.
- Example 303 provided by the present invention includes the above example 302, wherein the rear through hole is polygonal, circular, elliptical, square, rectangular, trapezoidal, or rhombic.
- Example 304 provided by the present invention includes the above example 302 or 303, wherein the diameter of the rear through hole is 0.1-3 mm.
- Example 305 provided by the present invention includes any one of the above examples 294 to 304, wherein the second electrode is made of a conductive substance.
- Example 306 provided by the present invention includes any one of the above examples 294 to 305, wherein the surface of the second electrode has a conductive substance.
- Example 307 provided by the present invention includes any one of the above examples 294 to 306, wherein there is an electrocoagulation electric field between the first electrode and the second electrode, and the electrocoagulation electric field is a point-surface electric field, a line A combination of one or more electric fields in the surface electric field, mesh surface electric field, dot barrel electric field, line barrel electric field, or mesh barrel electric field.
- Example 308 provided by the present invention includes any one of the above examples 294 to 307, wherein the first electrode is linear and the second electrode is planar.
- Example 309 provided by the present invention includes any one of the above examples 294 to 308, wherein the first electrode is perpendicular to the second electrode.
- Example 310 provided by the present invention includes any one of the above examples 294 to 309, wherein the first electrode is parallel to the second electrode.
- Example 311 provided by the present invention includes any one of the above examples 294 to 310, wherein the first electrode is curved or arc-shaped.
- Example 312 provided by the present invention includes any one of the above examples 294 to 311, wherein the first electrode and the second electrode are both planar, and the first electrode is parallel to the second electrode.
- Example 313 provided by the present invention includes any one of the above examples 294 to 312, wherein the first electrode uses a wire mesh.
- Example 314 provided by the present invention: including any one of the above examples 294 to 313, wherein the first electrode is planar or spherical.
- Example 315 provided by the present invention includes any one of the above examples 294 to 314, wherein the second electrode is curved or spherical.
- Example 316 provided by the present invention includes any one of the above examples 294 to 315, wherein the first electrode has a dot shape, a line shape, or a mesh shape, and the second electrode has a barrel shape.
- the first electrode is located inside the second electrode, and the first electrode is located on the central axis of symmetry of the second electrode.
- Example 317 provided by the present invention includes any one of the above examples 294 to 316, wherein the first electrode is electrically connected to one electrode of the power supply, and the second electrode is electrically connected to the other electrode of the power supply connection.
- Example 318 provided by the present invention includes any one of the above examples 294 to 317, wherein the first electrode is electrically connected to the cathode of the power supply, and the second electrode is electrically connected to the anode of the power supply
- Example 319 provided by the present invention: including the above example 317 or 318, wherein the voltage of the power supply is 5-50KV.
- Example 320 provided by the present invention includes any one of the above examples 317 to 319, wherein the voltage of the power supply is less than the initial halo voltage.
- Example 321 provided by the present invention includes any one of the above examples 317 to 320, wherein the voltage of the power supply is 0.1 kv / mm-2 kv / mm.
- Example 322 provided by the present invention includes any one of the above examples 317 to 321, wherein the voltage waveform of the power supply is a DC waveform, a sine wave, or a modulation waveform.
- Example 323 provided by the present invention includes any one of the above examples 317 to 322, wherein the power supply is an AC power supply, and the frequency conversion pulse range of the power supply is 0.1 Hz to 5 GHz.
- Example 324 provided by the present invention includes any one of the above examples 294 to 323, wherein the first electrode and the second electrode both extend in the left-right direction, and the left end of the first electrode is located on the second electrode Left of the left end.
- Example 325 provided by the present invention includes any one of the above examples 294 to 324, wherein there are two second electrodes, and the first electrode is located between the two second electrodes.
- Example 326 provided by the present invention includes any one of the above examples 294 to 325, wherein the distance between the first electrode and the second electrode is 5-50 mm.
- Example 327 provided by the present invention includes any one of the above examples 294 to 326, wherein the first electrode and the second electrode constitute an adsorption unit, and there are a plurality of adsorption units.
- Example 328 provided by the present invention includes the above example 327, in which all adsorption units are distributed in one or more directions of the left-right direction, the front-rear direction, the oblique direction, or the spiral direction.
- Example 329 provided by the present invention includes any one of the above examples 294 to 328, which further includes an electrocoagulation housing including an electrocoagulation inlet, an electrocoagulation outlet, and the electrocoagulation For the flow channel, the two ends of the electrocoagulation flow channel are respectively connected to the electrocoagulation inlet and the electrocoagulation outlet.
- Example 330 provided by the present invention includes the above example 329, wherein the electrocoagulation inlet is circular, and the diameter of the electrocoagulation inlet is 300-1000 mm, or 500 mm.
- Example 331 provided by the present invention includes the above example 329 or 330, wherein the electrocoagulation outlet is circular, and the diameter of the electrocoagulation outlet is 300-1000 mm, or 500 mm.
- Example 332 provided by the present invention: including any one of the above examples 329 to 331, wherein the electrocoagulation housing includes a first housing portion and a second housing that are sequentially distributed from the electrocoagulation inlet to the electrocoagulation outlet In the housing portion and the third housing portion, the electrocoagulation inlet is located at one end of the first housing portion, and the electrocoagulation outlet is located at the one end of the third housing portion.
- Example 333 provided by the present invention includes the above example 332, wherein the outline size of the first housing portion gradually increases from the direction of the electrocoagulation inlet to the electrocoagulation outlet.
- Example 334 provided by the present invention: including the above example 332 or 333, wherein the first housing portion has a straight tubular shape.
- Example 335 provided by the present invention includes any one of the above examples 332 to 334, wherein the second housing portion has a straight tubular shape, and the first electrode and the second electrode are mounted on the second housing Ministry.
- Example 336 provided by the present invention includes any one of the above examples 332 to 335, wherein the outline size of the third housing portion gradually decreases from the electrocoagulation inlet to the electrocoagulation outlet direction.
- Example 337 provided by the present invention includes any one of the above examples 332 to 336, wherein the first housing portion, the second housing portion, and the third housing portion are all rectangular in cross section.
- Example 338 provided by the present invention includes any one of the above examples 329 to 337, wherein the material of the electrocoagulation shell is stainless steel, aluminum alloy, iron alloy, cloth, sponge, molecular sieve, activated carbon, foamed iron, Or foamed silicon carbide.
- the material of the electrocoagulation shell is stainless steel, aluminum alloy, iron alloy, cloth, sponge, molecular sieve, activated carbon, foamed iron, Or foamed silicon carbide.
- Example 339 provided by the present invention includes any one of the above examples 294 to 338, wherein the first electrode is connected to the electrocoagulation housing through an electrocoagulation insulator.
- Example 340 provided by the present invention includes the above example 339, wherein the material of the electrocoagulation insulating member is insulating mica.
- Example 341 provided by the present invention including the above example 339 or 340, wherein the electrocoagulation insulating member has a column shape or a tower shape.
- Example 342 provided by the present invention includes any one of the above examples 294 to 341, wherein a cylindrical front connection portion is provided on the first electrode, and the front connection portion and the electrocoagulation insulating member Fixed connection.
- Example 343 provided by the present invention includes any one of the above examples 294 to 342, wherein the second electrode is provided with a cylindrical rear connection portion, and the rear connection portion and the electrocoagulation insulating member Fixed connection.
- Example 344 provided by the present invention includes any one of the above examples 294 to 343, wherein the ratio of the cross-sectional area of the first electrode to the cross-sectional area of the electrocoagulation channel is 99% -10%, or 90 10%, or 80-20%, or 70-30%, or 60-40%, or 50%.
- Example 345 provided by the present invention includes any one of the above examples 293 to 344, wherein the denitration device includes a condensing unit for condensing the ozone-treated tail gas to achieve gas-liquid separation.
- Example 346 provided by the present invention includes any one of the above examples 293 to 345, wherein the denitration device includes a leaching unit for rinsing the exhaust gas after ozone treatment.
- Example 347 provided by the present invention includes the above example 346, wherein the denitration device further includes a rinsing liquid unit for supplying the rinsing liquid to the rinsing unit.
- Example 348 provided by the present invention includes the above example 347, wherein the eluent in the eluent unit includes water and / or alkali.
- Example 349 provided by the present invention includes any one of the above examples 293 to 348, wherein the denitration device further includes a denitration liquid collection unit for storing the nitric acid aqueous solution and / or nitrate aqueous solution removed in the tail gas .
- Example 350 provided by the present invention includes the above example 349, wherein, when the nitric acid aqueous solution is stored in the denitration solution collection unit, the denitration solution collection unit is provided with an alkaline solution addition unit for forming nitrate with nitric acid .
- Example 351 provided by the present invention includes any one of the above examples 259 to 350, wherein the exhaust gas ozone purification system further includes an ozone digester for digesting ozone in the exhaust gas treated by the reaction field.
- Example 352 provided by the present invention includes the above example 351, wherein the ozone digester is selected from at least one of an ultraviolet ozone digester and a catalytic ozone digester.
- Example 353 provided by the present invention includes any one of the above examples 259 to 352, wherein the exhaust gas ozone purification system further includes a first denitration device for removing nitrogen oxides in the exhaust gas; the reaction field It is used to mix and react the tail gas processed by the first denitration device with the ozone stream, or to mix and react the tail gas with the ozone stream before being processed by the first denitration device.
- the exhaust gas ozone purification system further includes a first denitration device for removing nitrogen oxides in the exhaust gas; the reaction field It is used to mix and react the tail gas processed by the first denitration device with the ozone stream, or to mix and react the tail gas with the ozone stream before being processed by the first denitration device.
- Example 354 provided by the present invention includes the above example 353, wherein the first denitration device is selected from at least one of a non-catalytic reduction device, a selective catalytic reduction device, a non-selective catalytic reduction device, and an electron beam denitration device Species.
- Example 355 provided by the present invention includes any one of the above examples 1 to 354, in which the engine is also included.
- Example 356 provided by the present invention: a method for dedusting an engine intake electric field, including the following steps:
- Example 357 provided by the present invention: An engine intake electric field dust removal method including Example 356, wherein the dust removal process is completed using the electric field back-corona discharge phenomenon.
- Example 358 provided by the present invention: The engine intake electric field dust removal method including Example 356, wherein the electric field reverse corona discharge phenomenon is used to increase the voltage and limit the injection current to complete the dust removal process.
- Example 359 provided by the present invention: The engine intake electric field dust removal method including Example 356, wherein the electric field reverse corona discharge phenomenon is used to increase the voltage and limit the injection current to cause the rapid discharge occurring at the position of the anode dust to generate plasma The plasma oxidizes the organic components of the dust deeply, breaks the polymer bonds, and forms small molecules of carbon dioxide and water to complete the dust removal process.
- Example 360 provided by the present invention: The engine intake electric field dust removal method including any one of Examples 356 to 359, wherein, when the electric field device detects that the electric field current increases to a given value, the electric field device performs dust removal deal with.
- Example 361 provided by the present invention: The engine intake electric field dust removal method including any one of Examples 356 to 360, wherein the dust removal electric field cathode includes at least one electrode rod.
- Example 362 provided by the present invention: The engine intake electric field dust removal method including Example 361, wherein the diameter of the electrode rod is not greater than 3 mm.
- Example 363 provided by the present invention: An engine intake electric field dust removal method including Example 361 or 362, wherein the electrode rod has a needle shape, a polygonal shape, a burr shape, a threaded rod shape, or a column shape.
- Example 364 provided by the present invention: The engine intake electric field dust removal method including any one of Examples 356 to 363, wherein the dust removal electric field anode is composed of a hollow tube bundle.
- Example 365 provided by the present invention: An engine intake electric field dust removal method including Example 364, wherein the hollow cross section of the anode tube bundle adopts a circle or a polygon.
- Example 366 provided by the present invention: The engine intake electric field dust removal method including Example 365, wherein the polygon is a hexagon.
- Example 367 provided by the present invention: The engine intake electric field dust removal method including any one of Examples 364 to 366, wherein the tube bundle of the dust removal electric field anode is honeycomb-shaped.
- Example 368 provided by the present invention: The engine intake electric field dust removal method including any one of Examples 356 to 367, wherein the dust removal electric field cathode penetrates the dust removal electric field anode.
- Example 369 provided by the present invention: The engine intake electric field dust removal method including any one of Examples 356 to 368, wherein when the detected electric field current increases to a given value, the dust removal process is performed.
- Example 370 provided by the present invention: a method for removing carbon black from an engine exhaust electric field, including the following steps:
- the dust-containing gas passes through the anode of the exhaust gas dedusting electric field and the cathode of the exhaust gas dedusting electric field;
- Example 371 provided by the present invention: a method for removing carbon black from an engine exhaust electric field including Example 370, wherein the carbon black cleaning process is completed using an electric field back-corona discharge phenomenon.
- Example 372 provided by the present invention: An engine exhaust electric field carbon black removal method including Example 370, in which the electric field reverse corona discharge phenomenon is used to increase the voltage and limit the injection current to complete the carbon black cleaning process.
- Example 373 provided by the present invention: The method for removing carbon black from the engine exhaust electric field including Example 370, in which the electric field reverse corona discharge phenomenon is used to increase the voltage and limit the injection current to cause the sharp discharge that occurs at the position of the anode dust Plasma, the plasma deeply oxidizes the organic components of the cleaned carbon black, breaks the polymer bonds, forms small molecule carbon dioxide and water, and completes the cleaned carbon black treatment.
- Example 374 provided by the present invention: A method for removing carbon black from an engine exhaust electric field including any one of Examples 370 to 373, wherein when the electric field device detects that the electric field current increases to a given value, the electric field device performs cleaning Dust treatment.
- Example 375 provided by the present invention: A method for removing carbon black from an engine exhaust electric field including any one of Examples 370 to 374, wherein the dust-removing electric field cathode includes at least one electrode rod.
- Example 376 provided by the present invention: a method for removing carbon black from an engine exhaust electric field including Example 375, wherein the diameter of the electrode rod is not greater than 3 mm.
- Example 377 provided by the present invention: An engine exhaust electric field carbon black removal method including Example 375 or 376, wherein the electrode rod has a needle shape, a polygonal shape, a burr shape, a threaded rod shape, or a column shape.
- Example 378 provided by the present invention: An engine exhaust electric field carbon black removal method including any one of Examples 370 to 377, wherein the dust removal electric field anode is composed of a hollow tube bundle.
- Example 379 provided by the present invention: An engine exhaust electric field carbon black removal method including Example 378, wherein the hollow cross section of the anode tube bundle adopts a circular or polygonal shape.
- Example 380 provided by the present invention: a method for removing carbon black from an engine exhaust electric field including Example 379, wherein the polygon is a hexagon.
- Example 381 provided by the present invention: A method for removing carbon black from an engine exhaust electric field including any one of Examples 378 to 380, wherein the tube bundle of the anode of the dust removal electric field is honeycomb-shaped.
- Example 382 provided by the present invention: An engine exhaust electric field carbon black removal method including any one of Examples 370 to 381, wherein the dust removal electric field cathode penetrates the dust removal electric field anode.
- Example 383 provided by the present invention: An engine exhaust electric field carbon black removal method including any one of Examples 370 to 382, wherein when the detected electric field current increases to a given value, a carbon black cleaning process is performed.
- Example 384 provided by the present invention: A method for adding oxygen to engine intake air, including the following steps:
- An electric field is generated in the flow channel, the electric field is not perpendicular to the flow channel, and the electric field includes an inlet and an outlet.
- Example 385 provided by the present invention: A method of adding oxygen to engine intake air including Example 384, wherein the electric field includes a first anode and a first cathode, the first anode and the first cathode forming the flow channel , The flow channel connects the inlet and the outlet.
- Example 386 provided by the present invention: The method of adding oxygen to an intake air of an engine including any one of Examples 384 to 385, wherein the first anode and the first cathode ionize oxygen in the intake air.
- Example 387 provided by the present invention: The method of adding oxygen to engine intake air, including any of Examples 384 to 386, wherein the electric field includes a second electrode disposed at or near the inlet.
- Example 388 provided by the present invention: The method of adding oxygen to the intake air of the engine including Example 387, wherein the second electrode is a cathode.
- Example 389 provided by the present invention: a method of adding oxygen to engine intake air including example 387 or 388, wherein the second electrode is an extension of the first cathode.
- Example 391 provided by the present invention: the method of adding oxygen to engine intake air including any one of Examples 384 to 390, wherein the electric field includes a third electrode disposed at or near the outlet.
- Example 392 provided by the present invention: the method of adding oxygen to the intake air of the engine including example 391, wherein the third electrode is an anode.
- Example 393 provided by the present invention: a method of adding oxygen to engine intake air including example 391 or 392, wherein the third electrode is an extension of the first anode.
- Example 395 provided by the present invention: The method for adding oxygen to engine intake air according to any one of Examples 389 to 394, wherein the third electrode is provided separately from the first anode and the first cathode.
- Example 396 provided by the present invention: a method for adding oxygen to engine intake air, including any one of Examples 387 to 395, wherein the second electrode is provided separately from the first anode and the first cathode.
- Example 397 provided by the present invention: The method for adding oxygen to engine intake air according to any one of Examples 385 to 396, wherein the first cathode includes at least one electrode rod.
- Example 398 provided by the present invention: a method for adding oxygen to an intake air of an engine including any one of Examples 385 to 397, wherein the first anode is composed of a hollow tube bundle.
- Example 399 provided by the present invention: a method for adding oxygen to engine intake air including Example 398, wherein the hollow cross section of the anode tube bundle adopts a circle or a polygon.
- Example 400 provided by the present invention: a method for adding oxygen to engine intake air including Example 399, wherein the polygon is a hexagon.
- Example 401 provided by the present invention: The method for adding oxygen to engine intake air according to any one of Examples 398 to 400, wherein the tube bundle of the first anode is honeycomb-shaped.
- Example 402 provided by the present invention: The method for adding oxygen to engine intake air according to any one of Examples 385 to 401, wherein the first cathode is penetrated into the first anode.
- Example 403 provided by the present invention: The method for adding oxygen to engine intake air according to any one of Examples 385 to 402, wherein the electric field acts on oxygen ions in the flow channel to increase the flow of oxygen ions and increase the Oxygen content in the outlet intake.
- Example 404 provided by the present invention: A method for reducing electric field coupling of engine intake dust removal, including the following steps:
- Example 405 provided by the present invention: A method for reducing coupling of an engine intake dust removal electric field including Example 404, which includes selecting a ratio of a dust collection area of the intake dust removal electric field anode to a discharge area of the intake dust removal electric field cathode.
- Example 406 provided by the present invention: A method including Example 405 for reducing an electric field of an engine intake dust-removing electric field coupling, including selecting a dust accumulation area of the intake dust-removing electric field anode and a discharge area of the intake dust-removing electric field cathode The ratio is 1.667: 1-1680: 1.
- Example 407 provided by the present invention: a method for reducing coupling of an engine intake dust removal electric field including Example 405, including selecting a dust accumulation area of the intake dust removal electric field anode and a discharge area of the intake dust removal electric field cathode The ratio is 6.67: 1-56.67: 1.
- Example 408 provided by the present invention: a method for reducing coupling of an engine intake dust removal electric field including any one of Examples 404 to 407, wherein the intake dust removal electric field has a cathode diameter of 1-3 mm, and the intake dust removal electric field
- the pole spacing between the anode and the cathode of the intake air dedusting electric field is 2.5-139.9 mm; the ratio of the dust accumulation area of the intake air dedusting electric field anode to the discharge area of the intake air dedusting electric field cathode is 1.667: 1-1680: 1 .
- Example 409 provided by the present invention: A method for reducing coupling of an engine intake dust removal electric field including any one of Examples 404 to 408, including selecting a pole spacing between the intake dust removal electric field anode and the intake dust removal electric field cathode Less than 150mm.
- Example 410 provided by the present invention: A method including any one of Examples 404 to 408 for reducing a coupling of an engine intake dust removal electric field, including selecting a pole interval between the intake dust removal electric field anode and the intake dust removal electric field cathode It is 2.5-139.9mm.
- Example 411 provided by the present invention: A method for reducing coupling of an engine intake dust removal electric field including any one of Examples 404 to 408, including selecting a pole interval between the intake dust removal electric field anode and the intake dust removal electric field cathode 5-100mm.
- Example 412 provided by the present invention: The method for reducing the electric field coupling of engine intake dust removal including any one of Examples 404 to 411, wherein the method includes selecting the anode length of the intake dust removal electric field to be 10-180 mm.
- Example 413 provided by the present invention: The method for reducing the electric field coupling of the engine intake dust removal including any one of Examples 404 to 411, including selecting the anode length of the intake dust removal electric field to be 60-180 mm.
- Example 414 provided by the present invention: The method for reducing the electric field coupling of engine intake dust removal including any one of Examples 404 to 413, which includes selecting the cathode length of the intake dust removal electric field to be 30-180 mm.
- Example 415 provided by the present invention: The method for reducing the electric field coupling of the engine intake dust removal including any one of Examples 404 to 413, including selecting the cathode length of the intake dust removal electric field to be 54-176 mm.
- Example 416 provided by the present invention: The method for reducing the electric field coupling of the engine intake dust removal including any one of Examples 404 to 415, wherein the method includes selecting the cathode of the intake dust removal electric field to include at least one electrode rod.
- Example 417 provided by the present invention: a method for reducing electric field coupling of engine intake dust removal including Example 416, which includes selecting that the diameter of the electrode rod is not greater than 3 mm.
- Example 418 provided by the present invention: a method for reducing electric field coupling of engine intake dust removal including Example 416 or 417, which includes selecting the shape of the electrode rod to be needle, polygon, burr, threaded rod or column .
- Example 419 provided by the present invention: A method for reducing coupling of an engine intake dust removal electric field including any one of Examples 404 to 418, wherein the method includes selecting the intake dust removal electric field anode to be composed of a hollow tube bundle.
- Example 420 provided by the present invention: The method for reducing the electric field coupling of engine intake dust removal including Example 419, wherein the method includes selecting the hollow cross section of the anode tube bundle to adopt a circular or polygonal shape.
- Example 421 provided by the present invention: the method for reducing electric field coupling of engine intake dust removal including Example 420, including selecting the polygon to be a hexagon.
- Example 422 provided by the present invention: The method for reducing the coupling of the electric field of the engine's intake dust removal field including any one of Examples 419 to 421, wherein the tube bundle including the anode of the intake dust removal electric field is honeycomb-shaped.
- Example 423 provided by the present invention: A method for reducing coupling of an engine intake dust removal electric field including any one of Examples 404 to 422, wherein the method includes selecting the intake dust removal electric field cathode to penetrate the intake dust removal electric field anode .
- Example 424 provided by the present invention: A method for reducing coupling of an engine intake dust removal electric field including any one of Examples 404 to 423, wherein the size of the intake dust removal electric field anode or / and the intake dust removal electric field cathode is selected such that The number of electric field couplings ⁇ 3.
- Example 425 provided by the present invention: a method for reducing electric field coupling of engine exhaust dust removal, including the following steps:
- Example 426 provided by the present invention: a method for reducing coupling of an engine exhaust dust electric field including Example 425, which includes selecting a ratio of a dust collecting area of the exhaust gas electric field anode to a discharge area of the exhaust gas electric field cathode.
- Example 427 provided by the present invention: The method for reducing the coupling of the engine exhaust dust electric field including the example 426, wherein the ratio of the dust accumulation area including the anode of the exhaust gas electric field to the discharge area of the cathode of the exhaust gas electric field is 1.667. : 1-1680: 1.
- Example 428 provided by the present invention: The method for reducing the coupling of the engine exhaust dust electric field including the example 426, wherein the ratio of the area of the accumulated dust of the anode of the exhaust gas electric field to the discharge area of the cathode of the exhaust gas electric field is 6.67 : 1-56.67: 1.
- Example 429 provided by the present invention: a method for reducing coupling of an engine exhaust dust electric field including any one of Examples 425 to 428, wherein a diameter of the exhaust gas electric field cathode is 1-3 mm, and an anode of the exhaust gas electric field
- the pole spacing of the cathode of the exhaust gas dedusting electric field is 2.5-139.9 mm; the ratio of the dust accumulation area of the anode of the exhaust gas dedusting electric field to the discharge area of the cathode of the exhaust gas dedusting electric field is 1.667: 1-1680: 1.
- Example 430 provided by the present invention: The method for reducing the coupling of the engine exhaust dust electric field including any one of Examples 425 to 429, wherein the electrode separation between the anode of the exhaust gas electric field and the cathode of the exhaust gas electric field is less than 150mm.
- Example 431 provided by the present invention: a method for reducing coupling of an engine exhaust dust electric field including any one of Examples 425 to 429, wherein the method includes selecting a pole interval of the exhaust gas electric field anode and the exhaust gas electric field cathode of 2.5- 139.9mm.
- Example 432 provided by the present invention: A method for reducing coupling of an engine exhaust dust electric field including any one of Examples 425 to 429, wherein the method includes selecting a pole interval of the exhaust gas electric field anode and an exhaust gas electric field cathode of 5- 100mm.
- Example 433 provided by the present invention: a method for reducing coupling of an engine exhaust dust electric field including any one of Examples 425 to 432, wherein the method includes selecting the anode length of the exhaust gas electric field to be 10-180 mm.
- Example 434 provided by the present invention: The method for reducing the coupling of the engine exhaust dust electric field including any one of Examples 425 to 432, which includes selecting the anode length of the exhaust gas electric field to be 60-180 mm.
- Example 435 provided by the present invention: A method for reducing coupling of an engine exhaust dust electric field including any one of Examples 425 to 434, which includes selecting a cathode length of the exhaust gas electric field cathode of 30-180 mm.
- Example 436 provided by the present invention: a method for reducing coupling of an engine exhaust dust electric field including any one of Examples 425 to 434, which includes selecting a cathode length of the exhaust gas electric field of 54-176 mm.
- Example 437 provided by the present invention: A method for reducing electric field coupling of engine exhaust dust removal including any one of Examples 425 to 436, wherein the method includes selecting the exhaust gas removal electric field cathode to include at least one electrode rod.
- Example 438 provided by the present invention: a method for reducing electric field coupling of engine exhaust dust removal including Example 437, which includes selecting the diameter of the electrode rod to be no greater than 3 mm.
- Example 439 provided by the present invention: A method for reducing electric field coupling of engine exhaust dust removal including Example 437 or 438, which includes selecting the shape of the electrode rod to be needle-shaped, polygonal, burr-shaped, threaded rod-shaped, or cylindrical.
- Example 440 provided by the present invention: A method for reducing coupling of an engine exhaust dust electric field including any one of Examples 425 to 439, wherein the method includes selecting that the exhaust gas electric field anode is composed of a hollow tube bundle.
- Example 441 provided by the present invention: a method for reducing electric field coupling of engine exhaust dust removal including Example 440, wherein the method includes selecting the hollow cross section of the anode tube bundle to adopt a circular or polygonal shape.
- Example 442 provided by the present invention: A method for reducing electric field coupling of engine exhaust dust removal including Example 441, which includes selecting the polygon to be a hexagon.
- Example 443 provided by the present invention: A method for reducing coupling of an engine exhaust dust electric field including any one of Examples 440 to 442, wherein the tube bundle including selecting the anode of the exhaust gas electric field is honeycomb-shaped.
- Example 444 provided by the present invention: A method for reducing coupling of an engine exhaust dust electric field including any one of Examples 425 to 443, wherein the method includes selecting the exhaust gas electric field cathode to penetrate the anode of the exhaust gas electric field.
- Example 445 provided by the present invention: A method for reducing electric field coupling of engine exhaust dust removal including any one of Examples 425 to 444, wherein the size of the exhaust gas removal electric field anode or / and exhaust gas removal electric field cathode is selected such that the number of electric field couplings ⁇ 3.
- Example 446 provided by the present invention: An engine exhaust dust removal method, including the following steps: when the exhaust gas temperature is lower than 100 ° C, the liquid water in the exhaust gas is removed, and then the ionization dust is removed.
- Example 447 provided by the present invention: An engine exhaust dust removal method including Example 446, wherein, when the exhaust gas temperature is ⁇ 100 ° C, the exhaust gas is ionized and dedusted.
- Example 448 provided by the present invention: An engine exhaust dust removal method including Example 446 or 447, wherein, when the exhaust gas temperature is ⁇ 90 ° C, liquid water in the exhaust gas is removed, and then ionized for dust removal.
- Example 449 provided by the present invention: an engine exhaust dust removal method including Example 446 or 447, wherein, when the exhaust gas temperature is ⁇ 80 ° C, liquid water in the exhaust gas is removed, and then ionized for dust removal.
- Example 450 provided by the present invention: The engine exhaust dust removal method including Example 446 or 447, wherein, when the exhaust gas temperature is ⁇ 70 ° C, liquid water in the exhaust gas is removed, and then ionized for dust removal.
- Example 451 provided by the present invention: The engine exhaust dust removal method including Example 446 or 447, wherein the liquid water in the exhaust gas is removed by the electrocoagulation and mist removal method, and then the ionization dust is removed.
- Example 452 provided by the present invention: An engine exhaust dust removal method, including the following steps: adding a gas including oxygen before the exhaust gas ionization dust removal electric field to perform ionization dust removal.
- Example 453 provided by the present invention: An engine exhaust dust removal method including Example 452, wherein oxygen is added by simply adding oxygen, passing in outside air, passing in compressed air, and / or passing in ozone.
- Example 454 provided by the present invention: An engine exhaust dust removal method including Example 452 or 453, wherein the amount of oxygen supplementation is determined based at least on the exhaust particulate content.
- Example 455 provided by the present invention: An engine exhaust dust removal method, including the following steps:
- Example 456 provided by the present invention: An engine exhaust dust removing method including Example 455, wherein the exhaust electret element is close to an exhaust gas electric field device outlet, or the exhaust gas electret element is provided at an exhaust gas electric field device outlet.
- Example 457 provided by the present invention: An engine exhaust dust removal method including Example 455, wherein the exhaust gas dedusting electric field anode and the exhaust gas dedusting electric field cathode form an exhaust gas flow channel, and the exhaust gas electret element is provided in the exhaust gas In the channel.
- Example 458 provided by the present invention: An engine exhaust dust removal method including Example 457, wherein the exhaust gas flow path includes an exhaust gas flow path outlet, and the exhaust gas electret element is close to the exhaust gas flow path outlet, or, the The tail gas electret element is provided at the outlet of the tail gas channel.
- Example 459 provided by the present invention: An engine exhaust dust removal method including any one of Examples 452 to 458, wherein, when the exhaust gas ionization dust removal electric field has no electrified driving voltage, a charged exhaust electret element is used to adsorb particulate matter in the exhaust gas .
- Example 460 provided by the present invention: An engine exhaust dust removal method including Example 458, wherein after the charged exhaust electret element adsorbs certain particulate matter in the exhaust, it is replaced with a new exhaust electret element.
- Example 461 provided by the present invention: an engine exhaust dust removal method including Example 460, wherein the exhaust gas ionization and dust removal electric field is restarted after being replaced with a new exhaust gas electret element to adsorb particulate matter in the exhaust gas and give a new exhaust gas electret Component charging.
- Example 462 provided by the present invention: An engine exhaust dust removing method including any one of Examples 455 to 461, wherein the material of the exhaust electret element includes an inorganic compound having electret properties.
- Example 463 provided by the present invention: An engine exhaust dust removal method including Example 462, wherein the inorganic compound is selected from one or more combinations of oxygen-containing compounds, nitrogen-containing compounds, or glass fibers.
- Example 464 provided by the present invention: An engine exhaust dust removal method including Example 463, wherein the oxygen-containing compound is selected from one of metal-based oxides, oxygen-containing composites, and oxygen-containing inorganic heteropoly acid salts or Various combinations.
- Example 465 provided by the present invention: an engine exhaust dust removal method including Example 464, wherein the metal-based oxide is selected from aluminum oxide, zinc oxide, zirconium oxide, titanium oxide, barium oxide, tantalum oxide, silicon oxide, oxide One or more combinations of lead and tin oxide.
- the metal-based oxide is selected from aluminum oxide, zinc oxide, zirconium oxide, titanium oxide, barium oxide, tantalum oxide, silicon oxide, oxide One or more combinations of lead and tin oxide.
- Example 466 provided by the present invention: An engine exhaust dust removal method including Example 464, wherein the metal-based oxide is alumina.
- Example 467 provided by the present invention: An engine exhaust dust removal method including Example 464, wherein the oxygen-containing composite is selected from one or more combinations of titanium-zirconium composite oxide or titanium-barium composite oxide.
- Example 468 provided by the present invention: an engine exhaust dust removal method including Example 464, wherein the oxygen-containing inorganic heteropoly acid salt is selected from one or more of zirconium titanate, lead zirconate titanate, or barium titanatekinds of combinations.
- Example 469 provided by the present invention: An engine exhaust dust removal method including Example 463, wherein the nitrogen-containing compound is silicon nitride.
- Example 470 provided by the present invention: An engine exhaust dust removal method including any one of Examples 455 to 461, wherein the material of the exhaust electret element includes an organic compound having electret properties.
- Example 471 provided by the present invention: an engine exhaust dust removal method including Example 470, wherein the organic compound is selected from one of fluoropolymer, polycarbonate, PP, PE, PVC, natural wax, resin, and rosin Or multiple combinations.
- the organic compound is selected from one of fluoropolymer, polycarbonate, PP, PE, PVC, natural wax, resin, and rosin Or multiple combinations.
- Example 472 provided by the present invention: An engine exhaust dust removal method including Example 471, wherein the fluoropolymer is selected from polytetrafluoroethylene, polyperfluoroethylene propylene, soluble polytetrafluoroethylene, and polyvinylidene fluoride One or more combinations.
- the fluoropolymer is selected from polytetrafluoroethylene, polyperfluoroethylene propylene, soluble polytetrafluoroethylene, and polyvinylidene fluoride One or more combinations.
- Example 473 provided by the present invention: An engine exhaust dust removal method including Example 471, wherein the fluoropolymer is polytetrafluoroethylene.
- Example 474 provided by the present invention: An engine intake dust removal method, including the following steps:
- Example 475 provided by the present invention: The engine intake dust removal method including Example 474, wherein the intake electret element is close to the outlet of the intake electric field device, or the intake electret element is provided at the intake Electric field device outlet.
- Example 476 provided by the present invention: The engine intake dust removal method including Example 474, wherein the intake dust removal electric field anode and the intake dust removal electric field cathode form an intake flow channel, and the intake electret element is provided In the intake runner.
- Example 477 provided by the present invention: An engine intake dust removal method including Example 476, wherein the intake runner includes an intake runner outlet, and the intake electret element is near the intake runner outlet, or, The intake electret element is provided at the outlet of the intake runner.
- Example 478 provided by the present invention: The engine intake dust removal method including any one of examples 474 to 477, wherein when the intake ionization dust removal electric field has no electrified driving voltage, the charged intake electret element is used to adsorb Particulate matter in the air.
- Example 479 provided by the present invention: An engine intake dust removal method including Example 477, wherein, after the charged intake electret element adsorbs certain particulate matter in the intake, it is replaced with a new intake electret ⁇ ⁇ Body components.
- Example 480 provided by the present invention: The engine intake dust removal method including Example 479, in which the intake air ionization dust removal electric field is restarted after being replaced with a new intake electret element to adsorb particulate matter in the intake air and give a new The air intake electret element is charged.
- Example 481 provided by the present invention: The engine intake dust removal method including any one of Examples 474 to 480, wherein the material of the intake electret element includes an inorganic compound having electret properties.
- Example 482 provided by the present invention: An engine intake dust removal method including Example 481, wherein the inorganic compound is selected from one or more combinations of oxygen-containing compounds, nitrogen-containing compounds, or glass fibers.
- Example 483 provided by the present invention: An engine intake dust removal method including Example 482, wherein the oxygen-containing compound is selected from one of metal-based oxides, oxygen-containing composites, and oxygen-containing inorganic heteropoly acid salts Or multiple combinations.
- Example 484 provided by the present invention: The engine intake dust removal method including Example 483, wherein the metal-based oxide is selected from aluminum oxide, zinc oxide, zirconium oxide, titanium oxide, barium oxide, tantalum oxide, silicon oxide, One or more combinations of lead oxide and tin oxide.
- Example 485 provided by the present invention The engine intake dust removal method including Example 483, wherein the metal-based oxide is alumina.
- Example 486 provided by the present invention: The engine intake dust removal method including Example 483, wherein the oxygen-containing composite is selected from one or more combinations of titanium-zirconium composite oxide or titanium-barium composite oxide.
- Example 487 provided by the present invention: An engine intake dust removal method including Example 483, wherein the oxygen-containing inorganic heteropoly acid salt is selected from one of zirconium titanate, lead zirconate titanate, or barium titanate or Various combinations.
- Example 488 provided by the present invention: An engine intake dust removal method including Example 482, wherein the nitrogen-containing compound is silicon nitride.
- Example 489 provided by the present invention: The engine intake dust removal method including any one of Examples 474 to 480, wherein the material of the intake electret element includes an organic compound having electret properties.
- Example 490 provided by the present invention: The engine intake dust removal method including Example 489, wherein the organic compound is selected from one of fluoropolymer, polycarbonate, PP, PE, PVC, natural wax, resin, and rosin One or more combinations.
- the organic compound is selected from one of fluoropolymer, polycarbonate, PP, PE, PVC, natural wax, resin, and rosin One or more combinations.
- Example 491 provided by the present invention: An engine intake dust removal method including Example 490, wherein the fluoropolymer is selected from polytetrafluoroethylene, polyperfluoroethylene propylene, soluble polytetrafluoroethylene, and polyvinylidene fluoride One or more combinations.
- the fluoropolymer is selected from polytetrafluoroethylene, polyperfluoroethylene propylene, soluble polytetrafluoroethylene, and polyvinylidene fluoride One or more combinations.
- Example 492 provided by the present invention: An engine intake dust removal method including Example 490, wherein the fluoropolymer is polytetrafluoroethylene.
- Example 493 provided by the present invention: An engine intake dust removal method, characterized in that it includes the following steps: the intake air is subjected to intake air ionization and dust removal to remove or reduce ozone generated by the intake air ionization and dust removal.
- Example 494 provided by the present invention: The engine intake air dedusting method including example 493, wherein ozone generated by intake ionization dedusting is subjected to ozone digestion.
- Example 495 provided by the present invention: An engine intake dust removal method including Example 493, wherein the ozone digestion is selected from at least one of ultraviolet digestion and catalytic digestion.
- Example 496 provided by the present invention: an exhaust gas ozone purification method, comprising the following steps: mixing and reacting an ozone stream with an exhaust stream.
- Example 497 provided by the present invention includes the exhaust gas ozone purification method described in Example 496, wherein the exhaust gas stream includes nitrogen oxides and volatile organic compounds.
- Example 498 provided by the present invention includes the exhaust gas ozone purification method described in Example 496 or 497, wherein, in the low temperature section of the exhaust gas, the mixture of the ozone stream and the exhaust gas stream reacts.
- Example 499 provided by the present invention includes the exhaust gas ozone purification method described in any one of Examples 496 to 498, wherein the mixing reaction temperature of the ozone stream and the exhaust gas stream is -50 to 200 ° C.
- Example 500 provided by the present invention includes the exhaust gas ozone purification method described in Example 499, wherein the mixing reaction temperature of the ozone stream and the exhaust gas stream is 60-70 ° C.
- Example 501 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 496 to 500, wherein the mixing method of the ozone stream and the exhaust stream is selected from Venturi mixing, positive pressure mixing, insertion mixing, At least one of dynamic mixing and fluid mixing.
- Example 502 provided by the present invention includes the exhaust gas ozone purification method described in Example 501, wherein when the mixing mode of the ozone stream and the exhaust gas stream is positive pressure mixing, the pressure of the ozone inlet gas is greater than the pressure of the exhaust gas.
- Example 503 provided by the present invention includes the exhaust gas ozone purification method described in Example 496, wherein, before the ozone stream and the exhaust gas stream are mixed and reacted, the exhaust gas stream velocity is increased and the ozone stream is mixed using the Venturi principle.
- Example 504 provided by the present invention includes the exhaust gas ozone purification method described in Example 496, wherein the mixing method of the ozone stream and the exhaust gas stream is selected from the reverse flow inlet of the exhaust gas outlet, the mixing in the front section of the reaction field, the insertion of the dust collector before and after, and denitration At least one of mixing back and forth of the device, mixing back and forth of the catalytic device, mixing back and forth of the washing device, mixing back and forth of the filtering device, mixing back and forth of the muffler device, mixing in the exhaust pipe, mixing externally by the adsorption device and mixing back and forth of the condensation device.
- Example 505 provided by the present invention includes the exhaust gas ozone purification method described in Example 496, wherein the reaction field in which the ozone stream and the exhaust gas stream are mixed and reacted includes pipes and / or reactors.
- Example 506 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 496 to 505, wherein the reaction field includes an exhaust pipe, a regenerator device, or a catalyst.
- Example 507 provided by the present invention includes the exhaust gas ozone purification method described in Example 506, wherein the exhaust gas ozone purification method further includes at least one of the following technical features:
- the pipe section diameter is 100-200 mm
- the length of the pipe is greater than 0.1 times the pipe diameter
- the reactor is selected from at least one of the following:
- Reactor 1 The reactor has a reaction chamber, and tail gas and ozone are mixed and reacted in the reaction chamber;
- the reactor includes a number of honeycomb-shaped cavities for providing a space where tail gas and ozone are mixed and reacted; a gap is provided between the honeycomb-shaped cavities for passing a cold medium to control the tail gas and Ozone reaction temperature;
- Reactor 3 The reactor includes several carrier units, and the carrier unit provides a reaction site;
- Reactor 4 The reactor includes a catalyst unit, and the catalyst unit is used to promote the oxidation reaction of the tail gas;
- the reaction field is provided with an ozone inlet, and the ozone inlet is selected from at least one of a nozzle, a spray grid, a nozzle, a swirl nozzle, and a nozzle provided with a venturi tube;
- the reaction field is provided with an ozone inlet.
- the ozone enters the reaction field through the ozone inlet to contact the exhaust gas.
- the ozone inlet is formed in at least one of the following directions: opposite to the direction of the exhaust gas flow, and The direction is perpendicular, tangent to the direction of exhaust gas flow, inserting the direction of exhaust gas flow, and contacting the exhaust gas in multiple directions.
- Example 508 provided by the present invention: The exhaust gas ozone purification method according to any one of Examples 496 to 507, wherein the ozone stream is provided by a storage ozone unit and / or an ozone generator.
- Example 509 provided by the present invention includes the exhaust gas ozone purification method described in Example 508, wherein the ozone generator includes a surface discharge ozone generator, a power frequency arc ozone generator, a high frequency induction ozone generator, a low One or more combinations of air pressure ozone generator, ultraviolet ozone generator, electrolyte ozone generator, chemical agent ozone generator and radiation irradiation particle generator.
- the ozone generator includes a surface discharge ozone generator, a power frequency arc ozone generator, a high frequency induction ozone generator, a low One or more combinations of air pressure ozone generator, ultraviolet ozone generator, electrolyte ozone generator, chemical agent ozone generator and radiation irradiation particle generator.
- Example 510 provided by the present invention includes the exhaust gas ozone purification method described in Example 508, wherein the ozone stream providing method: under the action of an electric field and an oxidation catalytic bond cracking selective catalyst, a gas containing oxygen generates ozone, A selective catalyst for oxidative catalytic bond cleavage is supported on the electrode forming the electric field.
- Example 511 provided by the present invention includes the exhaust gas ozone purification method described in Example 510, wherein the electrode includes a high-voltage electrode or an electrode provided with a barrier medium layer, and when the electrode includes a high-voltage electrode, the oxidation catalysis A selective catalyst for bond cleavage is supported on the surface of the high-voltage electrode. When the electrode includes a high-voltage electrode for the barrier medium layer, the selective catalyst for bond cleavage of the oxidation catalyst is supported on the surface of the barrier medium layer.
- Example 512 provided by the present invention includes the exhaust gas ozone purification method described in Example 510, wherein, when the electrode includes a high-voltage electrode, the thickness of the oxidation catalytic bond cracking selective catalyst is 1 to 3 mm; when the When the electrode includes a high-voltage electrode that blocks the dielectric layer, the loading of the selective catalyst for oxidative catalytic bond cleavage includes 1 to 10 wt% of the blocking dielectric layer.
- Example 513 provided by the present invention: The exhaust gas ozone purification method according to any one of Examples 510 to 512, wherein the oxidation catalytic bond cracking selective catalyst includes the following components in weight percentages:
- the active component is selected from at least one of a compound of metal M and metal element M
- the metal element M is selected from alkaline earth metal elements, transition metal elements, fourth main group metal elements, precious metal elements and lanthanide rare earth elements At least one of
- the coating is selected from at least one of alumina, cerium oxide, zirconia, manganese oxide, metal composite oxides, porous materials, and layered materials.
- the metal composite oxide includes aluminum, cerium, zirconium, and manganese A composite oxide of one or more metals.
- Example 514 provided by the present invention includes the exhaust gas ozone purification method described in Example 513, wherein the alkaline earth metal element is selected from at least one of magnesium, strontium, and calcium.
- Example 515 provided by the present invention includes the exhaust gas ozone purification method described in Example 513, wherein the transition metal element is selected from at least one of titanium, manganese, zinc, copper, iron, nickel, cobalt, yttrium, and zirconium Species.
- Example 516 provided by the present invention includes the exhaust gas ozone purification method described in Example 513, wherein the fourth main group metal element is tin.
- Example 517 provided by the present invention includes the exhaust gas ozone purification method described in Example 513, wherein the precious metal element is selected from at least one of platinum, rhodium, palladium, gold, silver, and iridium.
- Example 518 provided by the present invention: includes the exhaust gas ozone purification method described in Example 513, wherein the lanthanide rare earth element is selected from at least one of lanthanum, cerium, praseodymium, and samarium.
- Example 519 provided by the present invention includes the exhaust gas ozone purification method described in Example 513, wherein the compound of the metal element M is selected from oxides, sulfides, sulfates, phosphates, carbonates, and calcium titanium At least one of the mines.
- Example 520 provided by the present invention includes the exhaust gas ozone purification method described in Example 513, wherein the porous material is selected from at least one of molecular sieve, diatomaceous earth, zeolite, and carbon nanotubes.
- Example 521 provided by the present invention includes the exhaust gas ozone purification method described in Example 513, wherein the layered material is selected from at least one of graphene and graphite.
- Example 522 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 510 to 512, wherein the electrode is loaded with an oxygen double catalytic bond cracking selective catalyst by a method of impregnation and / or spraying.
- Example 523 provided by the present invention includes the exhaust gas ozone purification method described in Example 522, which includes the following steps:
- the slurry of the coating material is loaded on the surface of the high-voltage electrode or the surface of the barrier medium layer, dried, and calcined to obtain the coated high-voltage electrode or the barrier medium layer;
- the raw material solution or slurry containing the metal element M is loaded onto the step 1) to obtain the coating, dried, and calcined.
- the barrier The medium layer is provided with a high-voltage electrode relative to the other side of the loaded coating, to obtain the electrode for the ozone generator; or, according to the catalyst composition ratio, the raw material solution or slurry containing the metal element M is loaded to step 1) to obtain a coating
- drying, calcining and post-processing when the coating layer is loaded on the surface of the barrier medium layer, after post-processing, a high-voltage electrode is provided on the other side of the barrier medium layer relative to the load coating layer to obtain the electrode for the ozone generator;
- the control of the morphology of the active component in the catalyst for electrodes is achieved through the calcination temperature and atmosphere, and post-treatment.
- Example 524 provided by the present invention includes the exhaust gas ozone purification method described in Example 522, which includes the following steps:
- the raw material solution or slurry containing the metal element M is loaded on the coating raw material, dried and calcined to obtain the coating material loaded with the active component;
- the coating material loaded with active components obtained in step 1) is made into a slurry, which is loaded on the surface of the high-voltage electrode or the surface of the barrier medium layer, dried, calcined, when the coating is loaded When it is on the surface of the barrier medium layer, after calcination, a high-voltage electrode is provided on the other side of the barrier medium layer relative to the supporting coating layer, that is, the electrode for the ozone generator; or, according to the catalyst composition ratio, obtained in step 1)
- the coating material loaded with the active component is made into a slurry, which is loaded on the surface of the high-voltage electrode or the surface of the barrier medium layer, dried, calcined and post-treated. When the coating layer is loaded on the surface of the barrier medium layer, the post-treatment Then, a high-voltage electrode is provided on the other side of the barrier medium layer relative to the load coating layer to obtain the electrode for the ozone generator;
- the control of the morphology of the active component in the catalyst for electrodes is achieved through the calcination temperature and atmosphere, and post-treatment.
- Example 525 provided by the present invention includes the exhaust gas ozone purification method described in any one of Examples 496 to 524, which includes: controlling the amount of ozone in the ozone stream so as to effectively oxidize the gas component to be treated in the exhaust gas.
- Example 526 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 496 to 525, wherein controlling the amount of ozone in the ozone stream to achieve the following removal efficiency:
- Nitrogen oxide removal efficiency 60-99.97%
- Example 527 provided by the present invention includes the exhaust gas ozone purification method described in Example 525 or 526, which includes: detecting the content of exhaust gas components before ozone treatment.
- Example 528 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 525 to 527, wherein the amount of ozone required for the mixing reaction is controlled according to the content of the exhaust gas component before the ozone treatment.
- Example 529 provided by the present invention includes the exhaust gas ozone purification method described in Example 527 or 528, wherein the content of the exhaust gas component before the ozone treatment is selected from at least one of the following:
- Example 530 provided by the present invention includes the exhaust gas ozone purification method described in Example 529, wherein the amount of ozone required for the mixed reaction is controlled according to at least one output value that detects the content of the exhaust gas component before ozone treatment.
- Example 531 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 525 to 530, wherein the amount of ozone required for the mixed reaction is controlled according to a preset mathematical model.
- Example 532 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 525 to 531, wherein the amount of ozone required for the mixed reaction is controlled according to a theoretical estimated value.
- Example 533 provided by the present invention includes the method for purifying ozone in exhaust gas as described in Example 532, wherein the theoretical estimated value is: the molar ratio of ozone flux to the to-be-processed material in the exhaust gas is 2-10.
- Example 534 provided by the present invention includes the exhaust gas ozone purification method described in any one of Examples 525 to 533, which includes: detecting the content of exhaust gas components after ozone treatment.
- Example 535 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 525 to 534, wherein the amount of ozone required for the mixing reaction is controlled according to the content of the exhaust gas component after the ozone treatment.
- Example 536 provided by the present invention includes the exhaust gas ozone purification method described in Example 534 or 535, wherein the content of the exhaust gas component after the ozone treatment is detected is selected from at least one of the following:
- Example 537 provided by the present invention includes the exhaust gas ozone purification method described in Example 536, wherein the amount of ozone is controlled according to at least one output value that detects the content of the exhaust gas component after ozone treatment.
- Example 538 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 496 to 537, wherein the exhaust gas ozone purification method further includes the following steps: removing mixed reaction products of the ozone stream and the exhaust gas stream Nitric acid.
- Example 539 provided by the present invention includes the exhaust gas ozone purification method described in Example 538, wherein the gas with nitric acid mist flows through the first electrode;
- the first electrode charges the nitric acid mist in the gas, and the second electrode applies an attractive force to the charged nitric acid mist, so that the nitric acid mist moves toward the second electrode until the nitric acid mist adheres to On the second electrode.
- Example 540 provided by the present invention includes the exhaust gas ozone purification method described in Example 539, wherein the first electrode introduces electrons into the nitric acid mist, and the electrons are transferred between mist droplets between the first electrode and the second electrode, Charge more droplets.
- Example 541 provided by the present invention: includes the exhaust gas ozone purification method described in Example 539 or 540, wherein electrons are conducted between the first electrode and the second electrode through nitric acid mist and an electric current is formed.
- Example 542 includes the exhaust gas ozone purification method according to any one of Examples 539-541, wherein the first electrode charges the nitric acid mist by contact with the nitric acid mist.
- Example 543 provided by the present invention: including the exhaust gas ozone purification method according to any one of Examples 539-542, wherein the first electrode charges the nitric acid mist by means of energy fluctuation.
- Example 544 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 539-543, wherein the nitric acid mist attached to the second electrode forms water droplets, and the water droplets on the second electrode flow into the collection tank.
- Example 545 provided by the present invention includes the exhaust gas ozone purification method described in Example 544, wherein water droplets on the second electrode flow into the collection tank under the action of gravity.
- Example 546 provided by the present invention: includes the exhaust gas ozone purification method described in Example 544 or 545, wherein, when the gas flows, blowing water droplets flow into the collection tank.
- Example 547 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 539-546, wherein the first electrode is a solid, a liquid, a gas molecular group, a plasma, a conductive mixed state substance, a biological body Naturally mixed conductive substances, or objects are artificially processed to form a combination of one or more forms of conductive substances.
- Example 548 provided by the present invention: including the exhaust gas ozone purification method according to any one of Examples 539-547, wherein the first electrode is solid metal, graphite, or 304 steel.
- Example 549 provided by the present invention: including the exhaust gas ozone purification method according to any one of Examples 539-548, wherein the first electrode is dot-shaped, wire-shaped, mesh-shaped, orifice-shaped, plate-shaped, needle-rod-shaped , Ball cage, box, tube, natural form material, or processed form material.
- Example 550 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 539-549, wherein the first electrode is provided with a front through hole.
- Example 551 includes the exhaust gas ozone purification method of Example 550, wherein the shape of the front through hole is polygon, circle, ellipse, square, rectangle, trapezoid, or diamond.
- Example 552 provided by the present invention includes the exhaust gas ozone purification method described in Example 550 or 551, wherein the pore diameter of the front through hole is 0.1-3 mm.
- Example 553 includes the exhaust gas ozone purification method of any one of Examples 539-552, wherein the second electrode is in the form of a multi-layer mesh, mesh, orifice, tube, barrel, Ball cage, box shape, plate shape, particle accumulation layer shape, bent plate shape, or panel shape.
- Example 554 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 539 to 553, wherein a rear through hole is provided on the second electrode.
- Example 555 provided by the present invention: including the exhaust gas ozone purification method of Example 554, wherein the rear through hole is polygonal, circular, elliptical, square, rectangular, trapezoidal, or rhombic.
- Example 556 provided by the present invention includes the exhaust gas ozone purification method described in Example 554 or 555, wherein the diameter of the rear through hole is 0.1-3 mm.
- Example 557 provided by the present invention: includes the exhaust gas ozone purification method of any one of Examples 539 to 556, wherein the second electrode is made of a conductive substance.
- Example 558 provided by the present invention: including the exhaust gas ozone purification method according to any one of Examples 539 to 557, wherein the surface of the second electrode has a conductive substance.
- Example 559 provided by the present invention: including the exhaust gas ozone purification method according to any one of Examples 539 to 558, wherein an electrocoagulation electric field is provided between the first electrode and the second electrode, and the electrocoagulation electric field is a point surface A combination of one or more electric fields in the electric field, line-area electric field, mesh-area electric field, dot-barrel electric field, wire-barrel electric field, or wire-barrel electric field.
- Example 560 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 539 to 559, wherein the first electrode is linear and the second electrode is planar.
- Example 561 provided by the present invention: includes the exhaust gas ozone purification method of any one of Examples 539 to 560, wherein the first electrode is perpendicular to the second electrode.
- Example 562 provided by the present invention: includes the exhaust gas ozone purification method of any one of Examples 539 to 561, wherein the first electrode is parallel to the second electrode.
- Example 563 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 539 to 562, wherein the first electrode is curved or arc-shaped.
- Example 564 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 539 to 563, wherein the first electrode and the second electrode are both planar, and the first electrode and the second electrode Parallel.
- Example 565 provided by the present invention: including the exhaust gas ozone purification method according to any one of Examples 539 to 564, wherein the first electrode uses a wire mesh.
- Example 566 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 539 to 565, wherein the first electrode is planar or spherical.
- Example 567 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 539 to 566, wherein the second electrode is curved or spherical.
- Example 568 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 539 to 567, wherein the first electrode has a dot shape, a line shape, or a mesh shape, and the second electrode has a barrel shape , The first electrode is located inside the second electrode, and the first electrode is located on the central axis of symmetry of the second electrode.
- Example 569 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 539 to 568, wherein the first electrode is electrically connected to one electrode of the power supply, and the second electrode is connected to the other of the power supply The electrodes are electrically connected.
- Example 570 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 539 to 569, wherein the first electrode is electrically connected to the cathode of the power supply, and the second electrode is electrically connected to the anode of the power supply connection.
- Example 571 provided by the present invention includes the exhaust gas ozone purification method described in Example 569 or 570, wherein the voltage of the power supply is 5-50KV.
- Example 572 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 569 to 571, wherein the voltage of the power supply is less than the initial halo voltage.
- Example 573 provided by the present invention: including any of the exhaust gas ozone purification methods of Examples 569 to 572, wherein the voltage of the power supply is 0.1 kv / mm-2 kv / mm.
- Example 574 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 569 to 573, wherein the voltage waveform of the power supply is a DC waveform, a sine wave, or a modulated waveform.
- Example 575 includes the exhaust gas ozone purification method according to any one of Examples 569 to 574, wherein the power supply is an AC power supply, and the frequency conversion pulse range of the power supply is 0.1 Hz to 5 GHz.
- Example 576 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 539 to 575, wherein the first electrode and the second electrode both extend in the left-right direction, and the left end of the first electrode is located at the The left end of the left end of the two electrodes.
- Example 577 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 539 to 576, wherein there are two second electrodes, and the first electrode is located between the two second electrodes.
- Example 578 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 539 to 577, wherein the distance between the first electrode and the second electrode is 5-50 mm.
- Example 579 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 539 to 578, wherein the first electrode and the second electrode constitute an adsorption unit, and there are a plurality of adsorption units.
- Example 580 provided by the present invention includes the exhaust gas ozone purification method described in Example 579, wherein all adsorption units are distributed in one or more directions of the left-right direction, the front-rear direction, the oblique direction, or the spiral direction.
- Example 581 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 539 to 580, wherein the first electrode is installed in an electrocoagulation housing, and the electrocoagulation housing has an electrocoagulation inlet and Electrocoagulation outlet.
- Example 582 provided by the present invention: including the exhaust gas ozone purification method of Example 581, wherein the electrocoagulation inlet is circular, and the diameter of the electrocoagulation inlet is 300-1000 mm, or 500 mm.
- Example 583 provided by the present invention: includes the exhaust gas ozone purification method described in Example 581 or 582, wherein the electrocoagulation outlet is circular, and the diameter of the electrocoagulation outlet is 300-1000 mm, or 500 mm.
- Example 584 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 581 to 583, wherein the electrocoagulation housing includes a first housing portion sequentially distributed from the electrocoagulation inlet to the electrocoagulation outlet In the second casing portion and the third casing portion, the electrocoagulation inlet is located at one end of the first casing portion, and the electrocoagulation outlet is located at one end of the third casing portion.
- Example 585 provided by the present invention: including the exhaust gas ozone purification method of Example 584, wherein the outline size of the first housing portion gradually increases from the electrocoagulation inlet to the electrocoagulation outlet direction.
- Example 586 provided by the present invention includes the exhaust gas ozone purification method described in Example 584 or 585, wherein the first housing portion has a straight tubular shape.
- Example 587 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 584 to 586, wherein the second housing portion has a straight tube shape, and the first electrode and the second electrode are installed at the first In the second housing part.
- Example 588 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 584 to 587, wherein the outline size of the third housing portion gradually decreases from the electrocoagulation inlet to the electrocoagulation outlet direction.
- Example 589 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 584 to 588, wherein the cross sections of the first shell portion, the second shell portion, and the third shell portion are all rectangle.
- Example 590 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 581 to 589, wherein the material of the electrocoagulation shell is stainless steel, aluminum alloy, iron alloy, cloth, sponge, molecular sieve, activated carbon, Foam iron, or foam silicon carbide.
- the material of the electrocoagulation shell is stainless steel, aluminum alloy, iron alloy, cloth, sponge, molecular sieve, activated carbon, Foam iron, or foam silicon carbide.
- Example 591 provided by the present invention: includes the exhaust gas ozone purification method according to any one of Examples 539 to 590, wherein the first electrode is connected to an electrocoagulation housing through an electrocoagulation insulator.
- Example 592 provided by the present invention includes the exhaust gas ozone purification method described in Example 591, wherein the material of the electrocoagulation insulator is insulating mica.
- Example 593 provided by the present invention: includes the exhaust gas ozone purification method described in Example 591 or 592, wherein the electrocoagulation insulator is in the shape of a column or tower.
- Example 594 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 539 to 593, wherein a cylindrical front connection portion is provided on the first electrode, and the front connection portion is Condensation insulation is fixed.
- Example 595 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 539 to 594, wherein the second electrode is provided with a cylindrical rear connection portion, and the rear connection portion is Condensation insulation is fixed.
- Example 596 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 539 to 595, wherein the first electrode is located in the electrocoagulation flow channel; the gas with nitric acid mist flows along the electrocoagulation flow channel, and Flowing through the first electrode; the ratio of the cross-sectional area of the first electrode to the cross-sectional area of the electrocoagulation flow channel is 99% -10%, or 90-10%, or 80-20%, or 70-30%, or 60 ⁇ 40%, or 50%.
- Example 597 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 538 to 596, wherein the method for removing nitric acid in the mixed reaction product of the ozone stream and the exhaust gas stream: combining the ozone stream with The tail gas stream mixes the reaction product and condenses.
- Example 598 provided by the present invention includes the exhaust gas ozone purification method described in any one of Examples 538 to 597, wherein the method for removing nitric acid in the mixed reaction product of the ozone stream and the exhaust gas stream: combining the ozone stream with The tail gas stream mixes the reaction product for rinsing.
- Example 599 provided by the present invention includes the exhaust gas ozone purification method described in Example 598, wherein the method for removing nitric acid in the mixed reaction product of the ozone stream and the exhaust gas stream further includes: to the ozone stream and the exhaust gas stream The mixed reaction products provide eluent.
- Example 600 provided by the present invention: includes the method for purifying ozone in exhaust gas as described in Example 599, wherein the eluent is water and / or alkali.
- Example 601 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 538 to 600, wherein the method for removing nitric acid in the mixed reaction product of the ozone stream and the exhaust gas stream further includes: storing the exhaust gas The removed nitric acid aqueous solution and / or nitrate aqueous solution.
- Example 602 provided by the present invention includes the exhaust gas ozone purification method described in Example 601, wherein when an aqueous solution of nitric acid is stored, an alkaline solution is added to form nitrate with nitric acid.
- Example 603 includes the exhaust gas ozone purification method according to any one of Examples 496 to 602, wherein the exhaust gas ozone purification method further includes the following step: performing ozone digestion on the nitric acid-removed exhaust gas.
- Example 604 provided by the present invention includes the exhaust gas ozone purification method described in Example 603, wherein the ozone digestion is selected from at least one of ultraviolet digestion and catalytic digestion.
- Example 605 provided by the present invention includes the exhaust gas ozone purification method according to any one of Examples 496 to 604, wherein the exhaust gas ozone purification method further includes the following steps: removing nitrogen oxides from the exhaust gas for the first time; The tail gas stream after one-time removal of nitrogen oxides is mixed and reacted with the ozone stream, or, before the first removal of nitrogen oxides in the tail gas, it is mixed and reacted with the ozone stream first.
- Example 606 provided by the present invention: includes the exhaust gas ozone purification method described in Example 605, wherein the first removal of nitrogen oxides in the exhaust gas is selected from a non-catalytic reduction method, a selective catalytic reduction method, and a non-selective method At least one of a catalytic reduction method, an electron beam denitration method, and the like.
- FIG. 1 is a schematic diagram of the exhaust gas ozone purification system of the present invention.
- FIG. 2 is a schematic diagram 1 of an electrode for an ozone generator of the present invention.
- FIG 3 is a schematic diagram 2 of the electrode for the ozone generator of the present invention.
- Fig. 4 is a structural schematic diagram of a discharge type ozone generator in the prior art.
- FIG. 5 is a schematic structural diagram of an intake dust removal system in an engine-based gas treatment system of the present invention.
- FIG. 6 is a structural diagram of another embodiment of a first water filtering mechanism provided in an intake device in an engine-based gas treatment system of the present invention.
- FIG 7A is an implementation structure diagram of an air intake equalizing device of an air intake device in an engine-based gas processing system of the present invention.
- FIG. 7B is another implementation structure diagram of the intake air equalization device of the intake device in the engine-based gas treatment system of the present invention.
- 7C is another embodiment structure diagram of the intake air equalizing device of the intake device in the engine-based gas treatment system of the present invention.
- FIG. 7D is a top structural view of the middle and second venturi plate air equalizing mechanism of the air intake device in the engine-based gas processing system of the present invention.
- FIG. 8 is a schematic diagram 1 of an intake electric field device according to Embodiment 2 of the present invention.
- FIG. 9 is a schematic diagram 2 of an intake electric field device according to Embodiment 3 of the present invention.
- FIG. 10 is a top view of the intake electric field device of FIG. 5 of the present invention.
- FIG. 11 is a schematic diagram of the cross section of the intake electret element in the intake runner in Embodiment 3 accounting for the cross section of the intake runner.
- FIG. 12 is a schematic diagram of an intake dust removal system according to Embodiment 4 of the present invention.
- FIG. 13 is a schematic diagram of an exhaust gas dust removal system according to Embodiment 5 of the present invention.
- FIG. 14 is a schematic diagram of an exhaust gas dust removal system according to Embodiment 6 of the present invention.
- 15 is a schematic perspective view of an embodiment of an exhaust gas treatment device in an engine-based gas treatment system of the present invention.
- FIG. 16 is a schematic structural view of an exhaust gas insulation mechanism in an umbrella shape of an exhaust gas treatment device in an engine-based gas treatment system of the present invention.
- FIG. 17A is an implementation structure diagram of an intake air equalization device of an exhaust gas treatment device in an engine-based gas treatment system of the present invention.
- FIG. 17B is another implementation structure diagram of the exhaust gas equalizing device of the exhaust gas treatment device in the engine-based gas treatment system of the present invention.
- FIG. 17C is another embodiment structure diagram of the exhaust gas equalizing device of the exhaust gas treatment device in the engine-based gas treatment system of the present invention.
- FIG. 18 is a schematic diagram of an exhaust gas ozone purification system according to Embodiment 8 of the present invention.
- FIG. 19 is a plan view of a reaction field in an exhaust gas ozone purification system according to Embodiment 8 of the present invention.
- Fig. 20 is a schematic diagram of the ozone quantity control device of the present invention.
- 21 is a schematic diagram of the structure of the electric field generating unit.
- Fig. 22 is an A-A view of the electric field generating unit of Fig. 21.
- Fig. 23 is an A-A view of the electric field generating unit of Fig. 21 labeled with length and angle.
- 24 is a schematic diagram of the structure of an electric field device with two electric field levels.
- Embodiment 30 is a schematic structural diagram of an electric field device in Embodiment 30 of the present invention.
- FIG. 26 is a schematic structural diagram of an electric field device in Embodiment 32 of the present invention.
- FIG. 27 is a schematic structural diagram of an electric field device in Embodiment 33 of the present invention.
- FIG. 28 is a schematic structural diagram of an exhaust gas dust removal system in Embodiment 36 of the present invention.
- FIG. 29 is a schematic structural diagram of an impeller duct in Embodiment 36 of the present invention.
- FIG. 30 is a schematic structural diagram of an electrocoagulation device in Embodiment 37 of the present invention.
- FIG. 31 is a left side view of the electrocoagulation device in Embodiment 37 of the present invention.
- FIG. 32 is a perspective view of an electrocoagulation device in Embodiment 37 of the present invention.
- Embodiment 38 is a schematic structural diagram of an electrocoagulation device in Embodiment 38 of the present invention.
- Embodiment 34 is a plan view of the electrocoagulation device in Embodiment 38 of the present invention.
- Embodiment 39 is a schematic structural diagram of an electrocoagulation device in Embodiment 39 of the present invention.
- FIG. 36 is a schematic structural diagram of an electrocoagulation device in Embodiment 40 of the present invention.
- FIG. 37 is a schematic structural diagram of an electrocoagulation device in Embodiment 41 of the present invention.
- Embodiment 38 is a schematic structural diagram of an electrocoagulation device in Embodiment 42 of the present invention.
- Embodiment 43 of the present invention is a schematic structural diagram of an electrocoagulation device in Embodiment 43 of the present invention.
- FIG. 40 is a schematic structural diagram of an electrocoagulation device in Embodiment 44 of the present invention.
- Example 41 is a schematic structural diagram of an electrocoagulation device in Example 45 of the present invention.
- Embodiment 46 is a schematic structural diagram of an electrocoagulation device in Embodiment 46 of the present invention.
- Embodiment 47 is a schematic structural diagram of an electrocoagulation device in Embodiment 47 of the present invention.
- FIG. 44 is a schematic structural diagram of an electrocoagulation device in Embodiment 48 of the present invention.
- Embodiment 45 is a schematic structural diagram of an electrocoagulation device in Embodiment 49 of the present invention.
- Embodiment 50 is a schematic structural diagram of an electrocoagulation device in Embodiment 50 of the present invention.
- Embodiment 47 is a schematic structural diagram of an engine emission treatment system in Embodiment 51 of the present invention.
- Embodiment 48 is a schematic structural diagram of an engine emission treatment system in Embodiment 52 of the present invention.
- Embodiment 53 is a schematic structural diagram of an engine emission treatment system in Embodiment 53 of the present invention.
- Embodiment 50 is a schematic structural diagram of an engine emission treatment system in Embodiment 54 of the present invention.
- Embodiment 51 is a schematic structural diagram of an engine emission treatment system in Embodiment 55 of the present invention.
- FIG. 52 is a schematic structural diagram of an engine emission treatment system in Embodiment 56 of the present invention.
- Embodiment 53 is a schematic structural diagram of an engine emission treatment system in Embodiment 57 of the present invention.
- Embodiment 54 is a schematic structural diagram of an engine emission treatment system in Embodiment 58 of the present invention.
- Embodiment 55 is a schematic structural diagram of an engine emission treatment system in Embodiment 59 of the present invention.
- Embodiment 60 of the present invention is a schematic structural diagram of an intake electric field device in Embodiment 60 of the present invention.
- FIG. 57 is a schematic structural diagram of an exhaust gas cooling device in Embodiment 61 of the present invention.
- FIG. 58 is a schematic structural diagram of an exhaust gas cooling device in Embodiment 62 of the present invention.
- FIG. 59 is a schematic structural diagram of an exhaust gas temperature-lowering device in Embodiment 63 of the present invention.
- FIG. 60 is a schematic structural diagram of a heat exchange unit in Embodiment 63 of the present invention.
- 61 is a schematic structural diagram of an exhaust gas temperature-lowering device in Embodiment 64 of the present invention.
- the engine emission treatment system includes an intake dust removal system, an exhaust gas dust removal system, and an exhaust gas ozone purification system.
- the engine emission treatment system and method can be applied to technical fields such as engines, power stations, brick kilns, steel making, cement, chemical industry, oil refining, etc., which will generate exhaust gas due to the combustion of hydrocarbon fuel.
- the intake air dust removal system includes a centrifugal separation mechanism.
- the centrifugal separation mechanism includes an airflow turning channel, which can change the flow direction of the airflow.
- the flow direction of the gas will change; and the particulate matter in the gas will continue to move in the original direction under the action of inertia until the side wall of the gas flow turning channel, that is, the centrifugal separation mechanism
- the inner wall of the collision the particles can not continue to move in the original direction, and fall down under the action of gravity, so that the particles are separated from the gas.
- the gas flow turning channel can guide the gas to flow in the circumferential direction.
- the air flow deflecting channel may be spiral or conical.
- the centrifugal separation mechanism includes a separation cylinder.
- the air separation channel is provided in the separation cylinder, and a dust outlet can be provided at the bottom of the separation cylinder.
- An air inlet communicating with the first end of the air flow steering channel may be provided on the side wall of the separation cylinder.
- the top of the separation cylinder may be provided with an air outlet communicating with the second end of the air flow steering channel.
- the air outlet is also called an exhaust port, and the size of the exhaust port can be set according to the required amount of intake air.
- the gas After the gas flows into the separation cylinder from the air inlet and turns into the channel, the gas will change from linear motion to circular motion, and the particles in the gas will continue to move in a linear direction under the action of inertia until the particles collide with the inner wall of the separation cylinder
- the particulate matter sinks under the force of gravity, so that the particulate matter is separated from the gas, and the particulate matter is finally discharged from the dust outlet at the bottom, and the gas is finally discharged from the exhaust outlet at the top.
- the inlet of the intake electric field device communicates with the exhaust port of the centrifugal separation mechanism.
- the air outlet of the separation cylinder is located at the connection between the separation cylinder and the intake electric field device.
- the centrifugal separation mechanism may have a bent structure.
- the shape of the centrifugal separation mechanism may be one shape or a combination of multiple shapes among a ring shape, a zigzag shape, a cross shape, a T shape, an L shape, a concave shape, or a folded shape.
- the air flow steering channel of the centrifugal separation mechanism has at least one turn. When the gas flows through the turn, the flow direction will change, and the particles in the gas will continue to move in the original direction under the inertia until the particles collide with the inner wall of the centrifugal separation mechanism. When sinking, the particles are detached from the gas and finally discharged from the powder outlet at the lower end, and the gas finally flows out from the exhaust outlet.
- a first filter layer may be provided at the exhaust port of the centrifugal separation mechanism.
- the first filter layer may include a metal mesh sheet, and the metal mesh sheet may be disposed perpendicular to the airflow direction. The metal mesh will filter the gas discharged from the exhaust port to filter out the particles that have not been separated from the gas.
- the air intake and dust removal system may include an air intake equalizing device.
- the air intake equalizing device is arranged before the air intake electric field device, and can evenly pass the airflow entering the air intake electric field device.
- the anode of the air intake electric field device of the air intake electric field device may be a cube
- the air intake equalization device may include an air intake pipe on one side of the cathode support plate and an outlet on the other side of the cathode support plate
- the trachea and the cathode support plate are located at the intake end of the anode of the intake dust removal electric field; wherein, the side where the intake pipe is installed is opposite to the side where the outlet pipe is installed.
- the air intake equalizing device can make the air flow entering the air intake electric field device evenly pass through the electrostatic field.
- the anode of the intake dust removal electric field may be a cylinder
- the intake air equalization device is formed at the inlet of the intake dust removal system and the anode of the intake dust removal electric field and the cathode of the intake dust removal electric field.
- the intake air is ionized between the dust removal electric field, and the intake air equalizing device includes a number of air equalizing blades rotating around the inlet center of the intake electric field device.
- the air intake air-equalizing device can make all kinds of changing air intake uniformly pass through the electric field generated by the anode of the air intake dust removal electric field. At the same time, it can keep the internal temperature of the anode of the air intake dust removal electric field constant, and the oxygen is sufficient.
- the air intake equalizing device can make the air flow entering the air intake electric field device evenly pass through the electrostatic field.
- the air intake equalizing device includes an air inlet plate provided at the air inlet end of the anode of the air intake dust removal electric field and an air outlet plate provided at the air outlet end of the anode of the air intake dust removal electric field.
- the air outlet is provided with air outlet holes, the air inlet holes and the air outlet holes are arranged in a staggered arrangement, and the front air inlet and the side air outlet form a cyclone structure.
- the air intake equalizing device can make the air flow entering the air intake electric field device evenly pass through the electrostatic field.
- the air intake system may include an air intake dust inlet, an air intake dust outlet, and an air intake electric field device.
- the intake electric field device may include an intake electric field device inlet, an intake electric field device outlet, and an intake front electrode between the intake electric field device inlet and the intake electric field device outlet. When the inlet electric field device inlet flows through the inlet front electrode, the particulate matter in the gas will be charged.
- the intake electric field device includes an intake front electrode.
- the intake front electrode is formed at the inlet of the intake electric field device and the anode of the intake dust removal electric field and the cathode of the intake dust removal electric field. between.
- the shape of the intake front electrode may be dot-shaped, linear, mesh-shaped, orifice-shaped, plate-shaped, needle-rod-shaped, ball-cage-shaped, box-shaped, tubular, natural form of substance, or substance Processing form.
- the intake front electrode has a hole structure, one or more intake through holes are provided on the intake front electrode.
- the shape of the air intake through hole may be polygon, circle, ellipse, square, rectangle, trapezoid, or rhombus.
- the outline size of the air intake through hole may be 0.1 to 3 mm, 0.1 to 0.2 mm, 0.2 to 0.5 mm, 0.5 to 1 mm, 1 to 1.2 mm, 1.2 to 1.5 mm, 1.5 to 2 mm, 2 to 2.5mm, 2.5 ⁇ 2.8mm, or 2.8 ⁇ 3mm.
- the shape of the intake front electrode may be one of solid, liquid, gas molecular group, plasma, conductive mixed state substance, biological natural mixed conductive substance, or artificially processed object to form conductive substance Or a combination of multiple forms.
- the intake front electrode is solid, solid metal, such as 304 steel, or other solid conductors, such as graphite, can be used.
- the intake front electrode is a liquid, it may be a conductive liquid containing ions.
- the air intake front electrode Charge the pollutants in the gas.
- the anode of the intake dust removal electric field exerts an attractive force on the charged pollutants, so that the pollutants move toward the anode of the intake dust removal electric field until the pollutants adhere to the anode of the intake dust removal electric field .
- the intake front electrode introduces electrons into the pollutants, and the electrons are transferred between the pollutants between the intake front electrode and the anode of the intake dust removal electric field, so that more pollutants are charged. Between the air intake front electrode and the air intake dedusting electric field anode, electrons are conducted through pollutants and an electric current is formed.
- the intake front electrode charges the pollutants by contact with the pollutants. In an embodiment of the invention, the intake front electrode charges pollutants by means of energy fluctuations. In an embodiment of the present invention, the intake front electrode transfers electrons to the pollutant by contacting the pollutant and charges the pollutant. In an embodiment of the invention, the intake front electrode transfers electrons to the pollutants by means of energy fluctuations, and charges the pollutants.
- the intake front electrode is linear, and the anode of the intake dust removal electric field is planar. In an embodiment of the present invention, the intake front electrode is perpendicular to the anode of the intake dust removal electric field. In an embodiment of the present invention, the intake front electrode is parallel to the anode of the intake dust removal electric field. In an embodiment of the invention, the intake front electrode is curved or arc-shaped. In an embodiment of the present invention, the air intake front electrode uses a wire mesh. In an embodiment of the present invention, the voltage between the intake front electrode and the anode of the intake dust removal electric field is different from the voltage between the cathode of the intake dust removal electric field and the anode of the intake dust removal electric field.
- the voltage between the air intake front electrode and the air intake dust removal electric field anode is less than the initial halo voltage.
- the initial halo voltage is the minimum value of the voltage between the cathode of the intake dust removal electric field and the anode of the intake dust removal electric field.
- the voltage between the air intake front electrode and the air intake dust removal electric field anode may be 0.1-2 kV / mm.
- the intake electric field device includes an intake runner, and the intake front electrode is located in the intake runner.
- the ratio of the cross-sectional area of the intake front electrode to the cross-sectional area of the intake runner is 99% -10%, or 90-10%, or 80-20%, or 70-30%, or 60 ⁇ 40%, or 50%.
- the cross-sectional area of the air intake front electrode refers to the sum of the areas of the air intake front electrode along the solid part of the cross section.
- the intake front electrode has a negative potential.
- the metal powder, mist, or aerosol pollutants with strong conductivity in the gas are in contact with the intake front electrode. Or when the distance to the front electrode of the intake air reaches a certain range, it will be directly negatively charged. Then, all pollutants will enter the intake ionization and dust removal electric field with the airflow. The anode of the intake air removal electric field will give negatively charged metal dust, mist droplets, or air. The sol, etc.
- the intake ionization and dust removal electric field formed between the anode and the cathode of the intake dust removal electric field obtains oxygen ions by ionizing the oxygen in the gas.
- the anode of the electric field exerts an attractive force on the negatively charged dust and other pollutants, so that the dust and other pollutants move to the anode of the air intake dust removal electric field until this part
- the pollutants are attached to the anode of the air intake dust removal electric field, so that some common dust and other pollutants are also collected, thereby collecting the pollutants with stronger conductivity and weaker conductivity in the gas, and making the air intake dust removal electric field
- the anode can collect a wider range of pollutants in the gas, and the collection ability is stronger and the collection efficiency is higher.
- the inlet of the intake electric field device communicates with the exhaust port of the separation mechanism.
- the air intake electric field device may include an air intake dust removal electric field cathode and an air intake dust removal electric field anode, and an ionization dust removal electric field is formed between the air intake dust removal electric field cathode and the air intake dust removal electric field anode.
- an ionization dust removal electric field is formed between the air intake dust removal electric field cathode and the air intake dust removal electric field anode.
- the cathode of the air intake dust removal electric field includes a plurality of cathode wires.
- the diameter of the cathode wire can be 0.1mm-20mm, and the size parameter can be adjusted according to the application and dust accumulation requirements. In an embodiment of the invention, the diameter of the cathode wire is not greater than 3 mm.
- the cathode wire uses a metal wire or an alloy wire that is easy to discharge, is temperature resistant, can support its own weight, and is electrochemically stable.
- the material of the cathode wire is titanium. The specific shape of the cathode wire is adjusted according to the shape of the anode of the intake dust removal electric field.
- the cross section of the cathode wire is circular;
- the cathode wire needs to be designed into a polyhedron shape. The length of the cathode wire is adjusted according to the anode of the intake dust removal electric field.
- the cathode of the air intake dust removal electric field includes a plurality of cathode rods.
- the diameter of the cathode rod is not greater than 3 mm.
- a metal rod or an alloy rod that is easy to discharge is used as the cathode rod.
- the shape of the cathode rod may be needle-shaped, polygonal, burr-shaped, threaded rod-shaped, columnar or the like. The shape of the cathode rod can be adjusted according to the shape of the anode of the intake air dedusting electric field.
- the cross section of the cathode rod needs to be designed to be circular;
- the dust surface is a circular arc surface, and the cathode rod needs to be designed into a polyhedron shape.
- the cathode of the intake air dedusting electric field passes through the anode of the intake air dedusting electric field.
- the anode of the air intake dust removal electric field includes one or more empty anode tubes arranged in parallel.
- all the hollow anode tubes constitute a honeycomb-shaped anode for the electric field of air intake dust removal.
- the hollow anode tube may have a circular or polygonal cross section. If the cross section of the hollow anode tube is circular, a uniform electric field can be formed between the anode of the air intake dust removal electric field and the cathode of the air intake dust removal electric field, and the inner wall of the hollow anode tube is not easy to accumulate dust.
- the cross section of the hollow anode tube is a triangular shape, three dust accumulation surfaces and three distant dust holding angles can be formed on the inner wall of the hollow anode tube.
- This structure of the hollow anode tube has the highest dust holding rate. If the cross section of the hollow anode tube is quadrangular, 4 dust-collecting surfaces and 4 dust-holding angles can be obtained, but the grouping structure is unstable. If the cross section of the hollow anode tube is hexagonal, 6 dust accumulation surfaces and 6 dust accumulation angles can be formed, and the dust accumulation surface and the dust accumulation rate are balanced. If the cross section of the hollow anode tube is more polygonal, more dust accumulation edges can be obtained, but the dust holding rate is lost.
- the diameter of the inscribed circle diameter of the hollow anode tube ranges from 5 mm to 400 mm.
- the cathode of the intake air dust removal electric field is installed on a cathode support plate, and the cathode support plate and the anode of the intake air dust removal electric field are connected by an intake insulation mechanism.
- the intake air insulation mechanism is used to achieve insulation between the cathode support plate and the anode of the intake dust removal electric field.
- the anode of the intake air dust removal electric field includes a first anode portion and a second anode portion, that is, the first anode portion is close to the inlet of the intake dust removal device, and the second anode portion is close to the outlet of the intake dust removal device.
- the cathode support plate and the air intake insulation mechanism are between the first anode part and the second anode part, that is, the air intake insulation mechanism is installed in the middle of the ionization electric field or the air intake dust removal electric field cathode, which can play a good role in the air intake dust removal electric field cathode It supports the cathode of the intake air dedusting electric field relative to the anode of the intake air dedusting electric field anode, and maintains the set distance between the intake air dedusting electric field cathode and the intake air dedusting electric field anode.
- the support point of the cathode is at the end of the cathode, and it is difficult to maintain the distance between the cathode and the anode.
- the air intake insulation mechanism is provided outside the dust removal flow path, that is, outside the second-stage flow path, to prevent or reduce the accumulation of dust in the gas on the air intake insulation mechanism, causing the intake air insulation mechanism to break down or conduct electricity .
- the intake air insulation mechanism uses a high-voltage resistant ceramic insulator to insulate the intake air dedusting electric field cathode and the intake air dedusting electric field anode.
- the anode of the air intake dust removal electric field is also called a kind of shell.
- the first anode portion is located before the cathode support plate and the intake insulation mechanism in the gas flow direction, and the first anode portion can remove water from the gas and prevent water from entering the intake insulation mechanism, causing intake air Insulation mechanism short circuit and fire.
- the first positive stage can remove a considerable part of the dust in the gas. When the gas passes through the intake insulation mechanism, a considerable part of the dust has been eliminated, reducing the possibility of the dust causing the intake insulation mechanism to short circuit.
- the air intake insulation mechanism includes an insulating ceramic post. The design of the first anode part is mainly to protect the insulating ceramic column from being polluted by particles in the gas.
- the gas pollutes the insulating ceramic column it will cause the anode of the intake air dedusting electric field and the cathode of the intake air dedusting electric field to conduct, thus making the intake air dedusting
- the dust accumulation function of the anode of the electric field fails, so the design of the first anode part can effectively reduce the pollution of the insulating ceramic column and improve the service time of the product.
- the first anode part and the cathode of the intake dust removal electric field first contact with the polluting gas, and the intake insulation mechanism contacts the gas, so as to achieve the purpose of removing dust first and then passing through the intake insulation mechanism.
- the length of the first anode part is long enough to remove part of the dust, reduce the dust accumulated on the intake insulation mechanism and the cathode support plate, and reduce the electrical breakdown caused by the dust.
- the length of the first anode portion accounts for 1/10 to 1/4, 1/4 to 1/3, 1/3 to 1/2, 1/2 to 2 of the total length of the anode of the intake dust removal electric field / 3, 2/3 to 3/4, or 3/4 to 9/10.
- the second anode portion is located behind the cathode support plate and the intake insulation mechanism in the gas flow direction.
- the second anode part includes a dust accumulation section and a reserved dust accumulation section.
- the dust accumulation section utilizes static electricity to adsorb particulate matter in the gas.
- the dust accumulation section is used to increase the dust accumulation area and prolong the service time of the intake electric field device.
- the reserved dust accumulation section can provide failure protection for the dust accumulation section.
- the dust accumulation section is reserved to further increase the dust accumulation area and improve the dust removal effect under the premise of meeting the design dust removal requirements.
- the dust accumulation section is reserved for supplementing the dust accumulation in the previous section.
- different power sources can be used for the first anode portion and the second anode portion.
- the intake air insulation mechanism is provided at The second-stage flow channel between the cathode of the intake air dust removal electric field and the anode of the intake air dust removal electric field. Therefore, the intake insulation mechanism is suspended outside the anode of the intake dust removal electric field.
- the air intake insulation mechanism may use non-conductor temperature-resistant materials, such as ceramics and glass.
- completely sealed air-free material insulation requires an insulation isolation thickness> 0.3 mm / kv; air insulation requirements> 1.4 mm / kv.
- the insulation distance can be set according to 1.4 times the pole spacing between the cathode of the intake air dust removal electric field and the anode of the intake air dust removal electric field.
- the air intake insulation mechanism uses ceramics and the surface is glazed; the connection cannot be filled with glue or organic materials, and the temperature resistance is greater than 350 degrees Celsius.
- the intake insulation mechanism includes an insulation portion and a heat insulation portion.
- the material of the insulation part adopts ceramic material or glass material.
- the insulating portion may be an umbrella-shaped string ceramic column or a glass column, and the umbrella is glazed inside and outside.
- the distance between the outer edge of the umbrella-shaped string ceramic column or glass column and the anode of the air intake dust removal electric field is greater than 1.4 times the electric field distance, that is, greater than 1.4 times the pole spacing.
- the sum of the umbrella flange spacing of the umbrella-shaped string ceramic column or glass column is greater than 1.4 times the insulation spacing of the umbrella-shaped string ceramic column.
- the total length of the inner depth of the umbrella-shaped string ceramic column or glass column is 1.4 times greater than the insulation distance of the umbrella-shaped string ceramic column.
- the insulating part can also be a columnar string ceramic column or a glass column with glaze inside and outside. In an embodiment of the present invention, the insulating portion may also have a tower shape.
- a heating rod is provided in the insulating portion.
- the heating rod is activated and heated. Due to the temperature difference between the inside and outside of the insulating part during use, condensation is likely to occur inside and outside of the insulating part and outside.
- the outer surface of the insulation may spontaneously or be heated by gas to generate high temperature, which requires necessary isolation and protection to prevent burns.
- the heat insulation part includes a protective baffle located outside the insulation part and a denitration purification reaction chamber.
- the tail portion of the insulating portion needs to be insulated at the same location to prevent the environment and heat dissipation from heating the condensation component.
- the lead-out line of the power supply of the intake electric field device uses an umbrella-shaped string of ceramic columns or glass columns to pass through the wall connection, an elastic contact is used in the wall to connect the cathode support plate, and a sealed insulating protective wiring cap is used for plugging out
- the insulation distance between the lead-out conductor and the wall is greater than that of the umbrella-shaped string ceramic column or glass column.
- the high-voltage part is eliminated from the lead, and directly installed on the end to ensure safety.
- the overall outer insulation of the high-voltage module is protected by ip68, and the medium is used for heat dissipation.
- an asymmetric structure is adopted between the cathode of the intake air dust removal electric field and the anode of the intake air dust removal electric field.
- polar particles are subjected to a force of the same size but in opposite directions, and polar particles reciprocate in the electric field; in an asymmetric electric field, polar particles are subjected to two forces of different sizes, and polar particles act Moving in the direction of high force can avoid coupling.
- the ionization dust removal electric field is formed between the cathode of the air intake dust removal electric field and the anode of the air intake dust removal electric field device of the invention.
- the method of reducing the electric field coupling includes the following steps: selecting the ratio of the dust collecting area of the intake dust removal electric field anode to the discharge area of the intake dust removal electric field cathode to make Coupling times ⁇ 3.
- the ratio of the dust collecting area of the intake air dedusting electric field anode to the discharge area of the intake air dedusting electric field cathode can be: 1.667: 1-1680: 1; 3.334: 1-113.34: 1; 6.67: 1- 56.67: 1; 13.34: 1-28.33: 1.
- This embodiment selects a relatively large area of the intake area of the intake air dust removal electric field anode and a relatively small intake air discharge electric field cathode discharge area.
- the above area ratio can reduce the discharge area of the intake air dust removal electric field cathode.
- the dust collection area refers to the area of the anode working surface of the air intake dust removal electric field.
- the dust collection area is the inner surface area of the hollow regular hexagonal tube, and the dust collection area is also This is called the dust accumulation area.
- the discharge area refers to the area of the cathode working surface of the intake dust removal electric field. For example, if the cathode of the intake dust removal electric field is rod-shaped, the discharge area is the rod-shaped outer surface area.
- the length of the anode of the air intake dust removal electric field may be 10 to 180 mm, 10 to 20 mm, 20 to 30 mm, 60 to 180 mm, 30 to 40 mm, 40 to 50 mm, 50 to 60 mm, 60 to 70 mm, 70 to 80mm, 80-90mm, 90-100mm, 100-110mm, 110-120mm, 120-130mm, 130-140mm, 140-150mm, 150-160mm, 160-170mm, 170-180mm, 60mm, 180mm, 10mm or 30mm.
- the length of the anode of the intake air dedusting electric field refers to the minimum length from one end to the other end of the working surface of the anode of the intake air dedusting electric field. Selecting this length for the anode of the electric field for air intake dust removal can effectively reduce the electric field coupling.
- the length of the anode of the air intake dust removal electric field may be 10 to 90 mm, 15 to 20 mm, 20 to 25 mm, 25 to 30 mm, 30 to 35 mm, 35 to 40 mm, 40 to 45 mm, 45 to 50 mm, 50 to 55mm, 55-60mm, 60-65mm, 65-70mm, 70-75mm, 75-80mm, 80-85mm or 85-90mm, the design of this length can make the intake air dedusting anode and intake electric field device have high temperature resistance Characteristics, and makes the intake electric field device have high efficiency dust collection capacity under high temperature impact.
- the length of the cathode of the air intake dust removal electric field may be 30 to 180 mm, 54 to 176 mm, 30 to 40 mm, 40 to 50 mm, 50 to 54 mm, 54 to 60 mm, 60 to 70 mm, 70 to 80 mm, 80 to 90mm, 90-100mm, 100-110mm, 110-120mm, 120-130mm, 130-140mm, 140-150mm, 150-160mm, 160-170mm, 170-176mm, 170-180mm, 54mm, 180mm, or 30mm.
- the length of the cathode of the air intake dust removal electric field refers to the minimum length from one end to the other end of the working surface of the dust removal electric field cathode. Choosing this length for the cathode of the air intake dust removal electric field can effectively reduce the electric field coupling.
- the length of the cathode of the air intake dust removal electric field may be 10 to 90 mm, 15 to 20 mm, 20 to 25 mm, 25 to 30 mm, 30 to 35 mm, 35 to 40 mm, 40 to 45 mm, 45 to 50 mm, 50 to 55mm, 55-60mm, 60-65mm, 65-70mm, 70-75mm, 75-80mm, 80-85mm or 85-90mm, the design of this length can make the air intake dust removal electric field cathode and the air intake electric field device have high temperature resistance Characteristics, and makes the intake electric field device have high efficiency dust collection capacity under high temperature impact.
- the distance between the anode of the intake air dust removal electric field and the cathode of the intake air dust removal electric field may be 5-30 mm, 2.5-139.9 mm, 9.9-139.9 mm, 2.5-9.9 mm, 9.9-20 mm, 20-30 mm , 30-40mm, 40-50mm, 50-60mm, 60-70mm, 70-80mm, 80-90mm, 90-100mm, 100-110mm, 110-120mm, 120-130mm, 130-139.9mm, 9.9mm, 139.9 mm, or 2.5mm.
- the distance between the anode of the intake air dedusting electric field and the cathode of the intake air dedusting electric field is also called the pole spacing.
- the pole spacing specifically refers to the minimum vertical distance between the anode of the intake air dedusting electric field and the cathode of the intake air dedusting electric field. This choice of pole spacing can effectively reduce the electric field coupling and make the intake electric field device have high temperature resistance characteristics.
- the diameter of the cathode of the intake air dedusting electric field is 1-3 mm, and the pole spacing between the anode of the intake air dedusting electric field and the cathode of the intake air dedusting electric field is 2.5-139.9 mm;
- the ratio of the dust accumulation area of the anode of the dust removal electric field to the discharge area of the cathode of the intake dust removal electric field is 1.667: 1-1680: 1.
- ionization dust removal can be applied to remove particulate matter in the gas.
- the existing electric field dust removal device can only remove about 70% of the particulate matter, which cannot meet the needs of many industries.
- the volume of the electric field dust removal device in the prior art is too large.
- the inventor of the present invention has found that the disadvantages of the electric field dust removal device in the prior art are caused by electric field coupling.
- the present invention can significantly reduce the size (ie, volume) of the electric field dust removal device by reducing the number of electric field couplings.
- the size of the ionization and dust removal device provided by the present invention is about one fifth of the size of the existing ionization and dust removal device.
- the current ionization dust removal device sets the gas flow rate to about 1 m / s, and the present invention can still obtain a higher gas flow rate when the gas flow rate is increased to 6 m / s. Particle removal rate.
- the size of the electric field dust collector can be reduced.
- the present invention can significantly improve the particle removal efficiency. For example, when the gas flow rate is about 1m / s, the prior art electric field dust removal device can remove about 70% of the particulate matter in the engine exhaust, but the present invention can remove about 99% of the particulate matter, even when the gas flow rate is 6m / s .
- the present invention achieves the above unexpected results.
- the ionization and dust removal electric field between the anode of the intake dust removal electric field and the cathode of the intake dust removal electric field is also called a first electric field.
- a second electric field that is not parallel to the first electric field is formed between the anode of the intake air dust removal electric field and the cathode of the intake air dust removal electric field.
- the second electric field is not perpendicular to the flow path of the ionization and dedusting electric field.
- the second electric field is also called an auxiliary electric field and can be formed by one or two first auxiliary electrodes.
- the first auxiliary electrode When the second electric field is formed by a first auxiliary electrode, the first auxiliary electrode may be placed at the inlet or outlet of the ionization and dust removal electric field, and the first auxiliary electrode may have a negative potential or a positive potential.
- the second electric field is formed by two first auxiliary electrodes, one of the first auxiliary electrodes can have a negative potential and the other first auxiliary electrode can have a positive potential; one first auxiliary electrode can be placed at the entrance of the ionization electric field, and the other A first auxiliary electrode is placed at the exit of the ionization electric field.
- the first auxiliary electrode may be part of the cathode of the intake air dedusting electric field or the anode of the intake air dedusting electric field, that is, the first auxiliary electrode may be composed of an extension of the cathode of the intake air dedusting electric field or the anode of the intake air dedusting electric field.
- the length of the cathode of the dust removal electric field and the anode of the intake dust removal electric field are different.
- the first auxiliary electrode may also be a separate electrode, which means that the first auxiliary electrode may not be part of the cathode of the intake air dedusting electric field or the anode of the intake air dedusting electric field. In this case, the voltage of the second electric field and the voltage of the first electric field are not Similarly, it can be controlled individually according to the working conditions.
- the second electric field can exert a force toward the outlet of the ionized electric field between the negatively charged oxygen ion flow between the anode of the intake air dedusting electric field and the cathode of the intake air dedusting electric field, so that the anode between the anode of the air dedusting electric field and the cathode of the air dedusting electric field
- the flow of charged oxygen ions has a moving speed toward the outlet.
- the negatively charged oxygen ions When the gas flows into the ionization electric field and flows toward the outlet of the ionization electric field, the negatively charged oxygen ions also move toward the anode of the intake dust removal electric field and toward the outlet of the ionization electric field, and the negatively charged oxygen ions are The anode of the gas dedusting electric field will be combined with the particulate matter in the gas during the movement to the outlet of the ionization electric field. Because the oxygen ions have a moving speed to the outlet, when the oxygen ions are combined with the particulate matter, the two will not be strong.
- the intake electric field device's collection rate of particulate matter entering the electric field in the direction of ion flow is nearly double that of particulate matter entering the electric field in the direction of counter ion flow, thereby increasing the dust collection efficiency of the electric field and reducing the electric power consumption of the electric field.
- the main reason for the low dust removal efficiency of the dust collection electric field in the prior art is that the direction of the dust entering the electric field is opposite to or perpendicular to the direction of the ion flow in the electric field, which causes the dust and ion flow to collide violently with each other and produce greater energy consumption. It also affects the charging efficiency, thereby reducing the electric field dust collection efficiency and increasing energy consumption in the prior art.
- the air intake electric field device collects the dust in the gas, the gas and dust enter the electric field along the ion flow direction, the dust is fully charged, and the electric field consumption is small; the unipolar electric field dust collection efficiency will reach 99.99%.
- the ion flow formed by the air intake electric field device is beneficial to fluid delivery of unpowered fans, air intake oxygenation, or heat exchange.
- the air intake electric field device detects the electric field current and cleans the dust in any of the following ways:
- the intake electric field device detects that the electric field current increases to a given value, the electric field reverse corona discharge phenomenon is used to increase the electric field voltage, limit the injection current, and complete the dust cleaning.
- the electric field reverse corona discharge phenomenon is used to increase the electric field voltage and limit the injection current, so that the rapid discharge occurring at the position of the anode carbon deposit generates plasma
- the plasma oxidizes the organic components of the dust deeply, breaks the polymer bonds, and forms small molecules of carbon dioxide and water to complete the dust cleaning.
- the anode of the intake air dust removal electric field and the cathode of the intake air dust removal electric field are electrically connected to the two electrodes of the power supply, respectively.
- the voltage loaded on the anode of the intake air dedusting electric field and the cathode of the intake air dedusting electric field needs to select an appropriate voltage level, and the specific voltage level to be selected depends on the volume, temperature resistance and dust holding rate of the air intake electric field device.
- the voltage is from 1kv to 50kv; the temperature resistance conditions are first considered in the design, the parameters of the pole spacing and temperature: 1MM ⁇ 30 degrees, the dust accumulation area is greater than 0.1 square / thousand cubic meters / hour, and the electric field length is greater than 5 Times, control the electric field air flow velocity to be less than 9 meters per second.
- the anode of the air intake dust removal electric field is composed of a first hollow anode tube and has a honeycomb shape.
- the shape of the first hollow anode tube port may be circular or polygonal.
- the value of the inscribed circle of the first hollow anode tube ranges from 5-400mm, the corresponding voltage is between 0.1-120kv, and the corresponding current of the first hollow anode tube is between 0.1-30A;
- the tangent circle corresponds to different corona voltage, about 1KV / 1MM.
- the intake electric field device includes a first electric field stage.
- the first electric field stage includes a plurality of first electric field generating units, and there may be one or more first electric field generating units.
- the first electric field generating unit is also called a first dust collecting unit.
- the first dust collecting unit includes the anode of the intake air dust removal electric field and the cathode of the intake air dust removal electric field. There are one or more first dust collecting units.
- the dust collection efficiency of the intake electric field device can be effectively improved.
- the anodes of each intake dust removal electric field have the same polarity
- the cathodes of each intake dust removal electric field have the same polarity.
- the intake electric field device further includes a plurality of connecting housings, and the first electric field stages connected in series are connected through the connecting housings; the distance between the first electric field stages of two adjacent stages is greater than 1.4 times the pole spacing.
- the electret material is charged with an electric field.
- the electret material will be used to remove dust.
- the intake electric field device includes an intake electret element.
- the air intake electret element is provided in the anode of the air intake dust removal electric field.
- the air intake electret element when the anode of the intake air dedusting electric field and the cathode of the intake air dedusting electric field are turned on, the air intake electret element is in the intake ionization dedusting electric field.
- the intake electret element is close to the outlet of the intake electric field device, or the intake electret element is provided at the outlet of the intake electric field device.
- the anode of the intake air dust removal electric field and the cathode of the intake air dust removal electric field form an intake air flow channel, and the intake air electret element is provided in the intake air flow channel.
- the intake runner includes an intake runner outlet, the intake electret element is close to the intake runner outlet, or the intake electret element is provided at the inlet Air outlet.
- the cross section of the intake electret element in the intake flow channel occupies 5% to 100% of the cross section of the intake flow channel.
- the cross section of the intake electret element in the intake flow passage accounts for 10% -90%, 20% -80%, or 40% -60% of the cross section of the intake flow passage.
- the intake ionization and dedusting electric field charges the intake electret element.
- the intake electret element has a porous structure.
- the air intake electret element is a fabric.
- the anode of the intake air dedusting electric field is tubular, the outside of the air intake electret element is tubular, and the outside of the air intake electret element is sleeved on the anode of the intake air dedusting electric field internal.
- the intake electret element and the anode of the intake dust removal electric field are detachably connected.
- the material of the intake electret element includes an inorganic compound having electret properties.
- the electret performance refers to that the intake electret element is charged after being charged by an external power source, and still retains a certain charge when completely disconnected from the power source, thereby acting as an electrode as an electric field electrode.
- the inorganic compound is selected from one or more combinations of oxygen-containing compounds, nitrogen-containing compounds, or glass fibers.
- the oxygen-containing compound is selected from one or more combinations of metal-based oxides, oxygen-containing composites, and oxygen-containing inorganic heteropoly acid salts.
- the metal-based oxide is selected from one or more combinations of aluminum oxide, zinc oxide, zirconium oxide, titanium oxide, barium oxide, tantalum oxide, silicon oxide, lead oxide, and tin oxide .
- the metal-based oxide is alumina.
- the oxygen-containing composite is selected from one or more combinations of titanium-zirconium composite oxide or titanium-barium composite oxide.
- the oxygen-containing inorganic heteropoly acid salt is selected from one or more combinations of zirconium titanate, lead zirconate titanate, or barium titanate.
- the nitrogen-containing compound is silicon nitride.
- the material of the intake electret element includes an organic compound having electret properties.
- the electret performance refers to that the intake electret element is charged after being charged by an external power source, and still retains a certain charge when completely disconnected from the power source, thereby acting as an electrode as an electric field electrode.
- the organic compound is selected from one or more combinations of fluoropolymer, polycarbonate, PP, PE, PVC, natural wax, resin, and rosin.
- the fluoropolymer is selected from polytetrafluoroethylene (PTFE), polyperfluoroethylene propylene (Teflon-FEP), soluble polytetrafluoroethylene (PFA), and polyvinylidene fluoride (PVDF) One or more combinations.
- PTFE polytetrafluoroethylene
- Teflon-FEP polyperfluoroethylene propylene
- PFA soluble polytetrafluoroethylene
- PVDF polyvinylidene fluoride
- the fluoropolymer is polytetrafluoroethylene.
- the air intake ionization and dust removal electric field is generated under the condition of power-on driving voltage.
- the intake air ionization and dust removal electric field is used to ionize part of the to-be-processed objects and adsorb the particulate matter in the intake air, while charging the intake air electret element.
- the charged intake electret element When there is no power-on driving voltage, the charged intake electret element generates an electric field, and the electric field generated by the charged intake electret element absorbs particulate matter in the intake, that is, the intake ionization dust removal electric field fails Particulate matter can still be adsorbed.
- the intake dust removal system further includes an ozone removal device for removing or reducing ozone generated by the intake electric field device.
- the ozone removal device is located at the outlet of the intake electric field device and the intake dust removal Between system exits.
- the ozone removing device includes an ozone digester.
- the ozone digester is selected from at least one of an ultraviolet ozone digester and a catalytic ozone digester.
- the air intake dust removing system of the present invention further includes an ozone removing device, which is used to remove or reduce the ozone generated by the air intake electric field device. Ozone in the air participates in ionization to form ozone, which affects the performance of subsequent devices.
- the intake air dedusting also includes an ozone removal device to avoid or reduce the subsequent performance degradation of the device, such as avoiding or reducing the performance degradation of the lubricating oil in the engine.
- the present invention provides an air intake electric field dust removal method, including the following steps:
- the dust-containing gas passes through the intake ionization dust removal electric field anode of the intake air dust removal electric field anode and the intake air dust removal electric field cathode;
- the dust removal process is performed.
- the dust is cleaned in any of the following ways:
- the dust is carbon black.
- the cathode of the air intake dust removal electric field includes a plurality of cathode wires.
- the diameter of the cathode wire can be 0.1mm-20mm, and the size parameter can be adjusted according to the application and dust accumulation requirements. In an embodiment of the invention, the diameter of the cathode wire is not greater than 3 mm.
- the cathode wire uses a metal wire or an alloy wire that is easy to discharge, is temperature resistant, can support its own weight, and is electrochemically stable.
- the material of the cathode wire is titanium. The specific shape of the cathode wire is adjusted according to the shape of the anode of the dust removal electric field.
- the cross section of the cathode wire is circular; Face, the cathode wire needs to be designed to be polyhedral. The length of the cathode wire is adjusted according to the anode of the dust removal electric field.
- the cathode of the air intake dust removal electric field includes a plurality of cathode rods.
- the diameter of the cathode rod is not greater than 3 mm.
- a metal rod or an alloy rod that is easy to discharge is used as the cathode rod.
- the shape of the cathode rod may be needle-shaped, polygonal, burr-shaped, threaded rod-shaped, columnar or the like. The shape of the cathode rod can be adjusted according to the shape of the anode of the intake dust removal electric field.
- the cross section of the cathode rod needs to be designed to be circular; if the dust collection surface of the anode of the intake dust removal electric field If it is a circular arc surface, the cathode rod needs to be designed into a polyhedron shape.
- the cathode of the intake air dedusting electric field passes through the anode of the intake air dedusting electric field.
- the anode of the air intake dust removal electric field includes one or more hollow anode tubes arranged in parallel. When there are a plurality of hollow anode tubes, all the hollow anode tubes constitute a honeycomb-shaped anode for the electric field of air intake dust removal.
- the hollow anode tube may have a circular or polygonal cross section. If the cross section of the hollow anode tube is circular, a uniform electric field can be formed between the anode of the air intake dust removal electric field and the cathode of the air intake dust removal electric field, and the inner wall of the hollow anode tube is not easy to accumulate dust.
- the cross section of the hollow anode tube is a triangular shape, three dust accumulation surfaces and three distant dust holding angles can be formed on the inner wall of the hollow anode tube.
- This structure of the hollow anode tube has the highest dust holding rate. If the cross section of the hollow anode tube is quadrangular, 4 dust-collecting surfaces and 4 dust-holding angles can be obtained, but the grouping structure is unstable. If the cross section of the hollow anode tube is hexagonal, 6 dust accumulation surfaces and 6 dust accumulation angles can be formed, and the dust accumulation surface and the dust accumulation rate are balanced. If the cross section of the hollow anode tube is more polygonal, more dust accumulation edges can be obtained, but the dust holding rate is lost.
- the diameter of the inscribed circle diameter of the hollow anode tube ranges from 5 mm to 400 mm.
- the present invention provides a method for accelerating gas, including the following steps:
- An electric field is generated in the flow channel, the electric field is not perpendicular to the flow channel, and the electric field includes an inlet and an outlet.
- the electric field includes a first anode and a first cathode, the first anode and the first cathode form the flow channel, and the flow channel connects the inlet and the outlet.
- the first anode and the first cathode ionize the gas in the flow channel.
- the electric field includes a second electrode, and the second electrode is disposed at or near the inlet.
- the second electrode is a cathode and serves as an extension of the first cathode.
- the second electrode is provided independently of the first anode and the first cathode.
- the electric field includes a third electrode, and the third electrode is disposed at or near the outlet.
- the third electrode is an anode, and the third electrode is an extension of the first anode.
- the third electrode is provided independently of the first anode and the first cathode.
- the first cathode includes a plurality of cathode wires.
- the diameter of the cathode wire can be 0.1mm-20mm, and the size parameter can be adjusted according to the application and dust accumulation requirements. In an embodiment of the invention, the diameter of the cathode wire is not greater than 3 mm.
- the cathode wire uses a metal wire or an alloy wire that is easy to discharge, is temperature resistant, can support its own weight, and is electrochemically stable.
- the material of the cathode wire is titanium. The specific shape of the cathode wire is adjusted according to the shape of the first anode.
- the cross section of the cathode wire is circular; if the dust collecting surface of the first anode is an arc surface, the cathode wire Need to be designed as a polyhedron. The length of the cathode wire is adjusted according to the first anode.
- the first cathode includes a number of cathode rods.
- the diameter of the cathode rod is not greater than 3 mm.
- a metal rod or an alloy rod that is easy to discharge is used as the cathode rod.
- the shape of the cathode rod may be needle-shaped, polygonal, burr-shaped, threaded rod-shaped, columnar or the like. The shape of the cathode rod can be adjusted according to the shape of the first anode.
- the cross section of the cathode rod needs to be designed to be circular; if the dust collecting surface of the first anode is an arc surface , The cathode rod needs to be designed into a polyhedron shape.
- the first cathode is disposed in the first anode.
- the first anode includes one or more hollow anode tubes arranged in parallel. When there are multiple hollow anode tubes, all the hollow anode tubes constitute a honeycomb first anode.
- the hollow anode tube may have a circular or polygonal cross section. If the cross section of the hollow anode tube is circular, a uniform electric field can be formed between the first anode and the first cathode, and the inner wall of the hollow anode tube is not prone to dust accumulation. If the cross section of the hollow anode tube is a triangular shape, three dust accumulation surfaces and three distant dust holding angles can be formed on the inner wall of the hollow anode tube.
- This structure of the hollow anode tube has the highest dust holding rate. If the cross section of the hollow anode tube is quadrangular, 4 dust-collecting surfaces and 4 dust-holding angles can be obtained, but the grouping structure is unstable. If the cross section of the hollow anode tube is hexagonal, 6 dust accumulation surfaces and 6 dust accumulation angles can be formed, and the dust accumulation surface and the dust accumulation rate are balanced. If the cross section of the hollow anode tube is more polygonal, more dust accumulation edges can be obtained, but the dust holding rate is lost. In an embodiment of the present invention, the diameter of the inscribed circle diameter of the hollow anode tube ranges from 5 mm to 400 mm.
- the present invention provides a method for reducing electric field coupling of intake dust removal, including the following steps:
- the anode of the intake dust removal electric field or / and the cathode of the intake dust removal electric field is selected.
- the size of the anode of the intake dust removal electric field or / and the cathode of the intake dust removal electric field is selected such that the number of electric field couplings is ⁇ 3.
- the ratio of the dust collecting area of the anode of the intake air dust removal electric field to the discharge area of the cathode of the intake air dust removal electric field is selected.
- the ratio of the dust accumulation area of the anode of the intake air dust removal electric field to the discharge area of the cathode of the intake air dust removal electric field is 1.667: 1-1680: 1.
- the ratio of the dust accumulation area of the intake dust removal electric field anode to the discharge area of the intake dust removal electric field cathode is selected to be 6.67: 1-56.67: 1.
- the diameter of the cathode of the intake air dedusting electric field is 1-3 mm, and the pole spacing between the anode of the intake air dedusting electric field and the cathode of the intake air dedusting electric field is 2.5-139.9 mm;
- the ratio of the dust accumulation area of the anode of the dust removal electric field to the discharge area of the cathode of the intake dust removal electric field is 1.667: 1-1680: 1.
- the distance between the anode of the intake air dust removal electric field and the cathode of the intake air dust removal electric field is selected to be less than 150 mm.
- the pole distance between the intake air dust removal electric field anode and the intake air electric field cathode is selected to be 2.5-139.9 mm. More preferably, the pole spacing between the anode of the intake air dust removal electric field and the cathode of the intake air dust removal electric field is selected to be 5.0-100 mm.
- the length of the anode of the air intake dust removal electric field is selected to be 10-180 mm. More preferably, the length of the anode of the intake dust removal electric field is selected to be 60-180 mm.
- the cathode length of the air intake dust removal electric field is selected to be 30-180 mm. More preferably, the cathode length of the intake dust removal electric field is selected to be 54-176 mm.
- the cathode of the air intake dust removal electric field includes a plurality of cathode wires.
- the diameter of the cathode wire can be 0.1mm-20mm, and the size parameter can be adjusted according to the application and dust accumulation requirements. In an embodiment of the invention, the diameter of the cathode wire is not greater than 3 mm.
- the cathode wire uses a metal wire or an alloy wire that is easy to discharge, is temperature resistant, can support its own weight, and is electrochemically stable.
- the material of the cathode wire is titanium. The specific shape of the cathode wire is adjusted according to the shape of the anode of the intake dust removal electric field.
- the cross section of the cathode wire is circular;
- the cathode wire needs to be designed into a polyhedron shape. The length of the cathode wire is adjusted according to the anode of the intake dust removal electric field.
- the cathode of the air intake dust removal electric field includes a plurality of cathode rods.
- the diameter of the cathode rod is not greater than 3 mm.
- a metal rod or an alloy rod that is easy to discharge is used as the cathode rod.
- the shape of the cathode rod may be needle-shaped, polygonal, burr-shaped, threaded rod-shaped, columnar or the like. The shape of the cathode rod can be adjusted according to the shape of the anode of the intake air dedusting electric field.
- the cross section of the cathode rod needs to be designed to be circular;
- the dust surface is a circular arc surface, and the cathode rod needs to be designed into a polyhedron shape.
- the cathode of the intake air dedusting electric field passes through the anode of the intake air dedusting electric field.
- the anode of the air intake dust removal electric field includes one or more hollow anode tubes arranged in parallel. When there are a plurality of hollow anode tubes, all the hollow anode tubes constitute a honeycomb-shaped anode for the electric field of air intake dust removal.
- the hollow anode tube may have a circular or polygonal cross section. If the cross section of the hollow anode tube is circular, a uniform electric field can be formed between the anode of the air intake dust removal electric field and the cathode of the air intake dust removal electric field, and the inner wall of the hollow anode tube is not easy to accumulate dust.
- the cross section of the hollow anode tube is a triangular shape, three dust accumulation surfaces and three distant dust holding angles can be formed on the inner wall of the hollow anode tube.
- This structure of the hollow anode tube has the highest dust holding rate. If the cross section of the hollow anode tube is quadrangular, 4 dust-collecting surfaces and 4 dust-holding angles can be obtained, but the grouping structure is unstable. If the cross section of the hollow anode tube is hexagonal, 6 dust accumulation surfaces and 6 dust accumulation angles can be formed, and the dust accumulation surface and the dust accumulation rate are balanced. If the cross section of the hollow anode tube is more polygonal, more dust accumulation edges can be obtained, but the dust holding rate is lost.
- the diameter of the inscribed circle diameter of the hollow anode tube ranges from 5 mm to 400 mm.
- An air intake dust removal method includes the following steps:
- the intake electret element is close to the outlet of the intake electric field device, or the intake electret element is provided at the outlet of the intake electric field device.
- the anode of the intake air dust removal electric field and the cathode of the intake air dust removal electric field form an intake air flow channel, and the intake air electret element is provided in the intake air flow channel.
- the intake runner includes an intake runner outlet, the intake electret element is close to the intake runner outlet, or the intake electret element is provided at the inlet Air outlet.
- the charged intake electret element when the intake ionization and dust removal electric field has no electrified driving voltage, the charged intake electret element is used to adsorb particulate matter in the intake air.
- the charged intake electret element adsorbs certain particulate matter in the intake, it is replaced with a new intake electret element.
- the intake ionization and dedusting electric field is restarted to adsorb particulate matter in the intake and charge the new intake electret element.
- the material of the intake electret element includes an inorganic compound having electret properties.
- the electret performance refers to that the intake electret element is charged after being charged by an external power supply, and still retains a certain charge when completely disconnected from the power supply, thereby acting as an electrode as an electric field electrode.
- the inorganic compound is selected from one or more combinations of oxygen-containing compounds, nitrogen-containing compounds, or glass fibers.
- the oxygen-containing compound is selected from one or more combinations of metal-based oxides, oxygen-containing composites, and oxygen-containing inorganic heteropoly acid salts.
- the metal-based oxide is selected from one or more combinations of aluminum oxide, zinc oxide, zirconium oxide, titanium oxide, barium oxide, tantalum oxide, silicon oxide, lead oxide, and tin oxide .
- the metal-based oxide is alumina.
- the oxygen-containing composite is selected from one or more combinations of titanium-zirconium composite oxide or titanium-barium composite oxide.
- the oxygen-containing inorganic heteropoly acid salt is selected from one or more combinations of zirconium titanate, lead zirconate titanate, or barium titanate.
- the nitrogen-containing compound is silicon nitride.
- the material of the intake electret element includes an organic compound having electret properties.
- the electret performance refers to that the intake electret element is charged after being charged by an external power source, and still retains a certain charge when completely disconnected from the power source, thereby acting as an electrode as an electric field electrode.
- the organic compound is selected from one or more combinations of fluoropolymer, polycarbonate, PP, PE, PVC, natural wax, resin, and rosin.
- the fluoropolymer is selected from polytetrafluoroethylene (PTFE), polyperfluoroethylene propylene (Teflon-FEP), soluble polytetrafluoroethylene (PFA), and polyvinylidene fluoride (PVDF) One or more combinations.
- PTFE polytetrafluoroethylene
- Teflon-FEP polyperfluoroethylene propylene
- PFA soluble polytetrafluoroethylene
- PVDF polyvinylidene fluoride
- the fluoropolymer is polytetrafluoroethylene.
- An intake air dust removal method includes the following steps: the intake air is subjected to intake air ionization and dust removal to remove or reduce ozone generated by the intake air ionization and dust removal.
- ozone generated by the ionization and dust removal of the intake air is subjected to ozone digestion.
- the ozone digestion is selected from at least one of ultraviolet digestion and catalytic digestion.
- the engine emission treatment system includes an exhaust gas dedusting system.
- the exhaust gas dedusting system is connected to the outlet of the engine. The exhaust gas discharged by the engine will flow through the exhaust dust removal system.
- the exhaust gas dust removal system further includes a water removal device for removing liquid water before the entrance of the exhaust gas electric field device.
- the engine exhaust gas when the exhaust gas temperature or the engine temperature is lower than a certain temperature, the engine exhaust gas may contain liquid water, and the water removal device removes the liquid water in the exhaust gas.
- the certain temperature is above 90 ° C and below 100 ° C.
- the certain temperature is above 80 ° C and below 90 ° C.
- the certain temperature is below 80 ° C.
- the water removal device is an electrocoagulation device.
- the water removal device When the engine is cold-started, the water removal device removes the water droplets or liquid water in the exhaust gas before the exhaust gas enters the exhaust gas electric field device inlet, thereby reducing the water droplets or liquid water in the exhaust gas, and reducing the uneven discharge of the exhaust gas ionization and dust removal electric field and The cathode of the exhaust gas dedusting electric field and the anode of the exhaust gas dedusting electric field break down, thereby improving the efficiency of ionization dust removal and achieving unexpected technical effects.
- the water removal device is not particularly limited, and the present invention can be applied to remove liquid water from exhaust gas in the prior art.
- the exhaust gas dedusting system further includes an oxygen supplement device for adding a gas including oxygen, such as air, before the exhaust gas ionizes the dedusting electric field.
- an oxygen supplement device for adding a gas including oxygen, such as air, before the exhaust gas ionizes the dedusting electric field.
- the oxygen supplementing device adds oxygen by simply adding oxygen, passing in outside air, passing in compressed air, and / or passing in ozone.
- the amount of oxygen supplementation is determined based at least on the content of exhaust gas particles.
- the exhaust gas dedusting system of the present invention including an oxygen supplement device, which can be simply oxygenated, vented to outside air, vented to compressed air and / or vented to ozone Oxygen is added to increase the oxygen content of the exhaust gas entering the exhaust ionization and dust removal electric field, so that when the exhaust gas passes through the exhaust ionization and dust removal electric field between the cathode and the anode of the exhaust gas removal electric field, the ionized oxygen is increased to make more dust in the exhaust gas Charged, and then collect more charged dust under the action of the anode of the exhaust gas dedusting electric field, making the exhaust gas field device's dust removal efficiency higher, which is
- the exhaust gas dedusting system may include an exhaust gas equalizing device.
- the exhaust gas equalization device is installed before the exhaust gas electric field device, which can make the air flow entering the ionization dust removal device pass evenly
- the anode of the exhaust gas dedusting electric field device of the exhaust gas electric field device may be a cube
- the exhaust air equalization device may include an air inlet pipe located on one side of the cathode support plate, and an air outlet pipe located on the other side of the cathode support plate.
- the supporting plate is located at the intake end of the anode of the exhaust gas dedusting electric field; wherein, the side where the intake pipe is installed is opposite to the side where the outlet pipe is installed.
- the tail gas equalizing device can make the tail gas entering the tail gas electric field device evenly pass through the electrostatic field.
- the anode of the exhaust gas dedusting electric field may be a cylinder
- the exhaust air equalization device is between the inlet of the exhaust gas dedusting system and the exhaust gas ionization dedusting field formed by the anode of the exhaust gas dedusting electric field and the cathode of the exhaust gas dedusting electric field.
- the exhaust air equalization device includes several air equalization blades rotating around the inlet center of the exhaust gas electric field device.
- the exhaust air equalization device can make various changes of the intake air evenly pass through the electric field generated by the anode of the exhaust gas dedusting electric field. At the same time, it can keep the internal temperature of the anode of the exhaust gas dedusting electric field constant and the oxygen is sufficient.
- the tail gas equalizing device can make the tail gas entering the tail gas electric field device evenly pass through the electrostatic field.
- the exhaust air equalization device includes an air inlet plate provided at the inlet end of the anode of the exhaust gas dedusting electric field and an air outlet plate provided at the outlet end of the anode of the exhaust gas dedusting electric field.
- the board is provided with air outlet holes, the air inlet holes and the air outlet holes are arranged in a staggered arrangement, and the front air inlet and the side air outlet form a cyclone structure.
- the tail gas equalizing device can make the tail gas entering the tail gas electric field device evenly pass through the electrostatic field.
- the exhaust gas dedusting system may include an exhaust gas dedusting system inlet, an exhaust gas dedusting system outlet, and an exhaust gas electric field device.
- the exhaust electric field device may include an exhaust electric field device inlet, an exhaust electric field device outlet, and an exhaust gas front electrode between the exhaust electric field device inlet and the exhaust electric field device outlet.
- the tail gas electric field device includes a tail gas front electrode between the inlet of the tail gas electric field device and the tail gas ionization and dust removal electric field formed by the tail gas electric field anode and the tail gas electric field cathode.
- the shape of the exhaust gas pre-electrode may be dot-shaped, wire-shaped, mesh-shaped, orifice-shaped, plate-shaped, needle-rod-shaped, ball cage-shaped, box-shaped, tubular, natural form of material, or material processing form.
- the exhaust gas pre-electrode has a hole structure
- the exhaust gas pre-electrode is provided with one or more exhaust gas through holes.
- the shape of the exhaust gas through hole may be a polygon, a circle, an ellipse, a square, a rectangle, a trapezoid, or a rhombus.
- the outline size of the exhaust gas through hole may be 0.1 to 3 mm, 0.1 to 0.2 mm, 0.2 to 0.5 mm, 0.5 to 1 mm, 1 to 1.2 mm, 1.2 to 1.5 mm, 1.5 to 2 mm, 2 to 2.5 mm, 2.5 ⁇ 2.8mm, or 2.8 ⁇ 3mm.
- the shape of the tail gas front electrode may be one of solid, liquid, gas molecular group, plasma, conductive mixed state substance, biological natural mixed conductive substance, or an object artificially processed to form a conductive substance or Combination of various forms.
- the exhaust front electrode is solid, solid metal, such as 304 steel, or other solid conductors, such as graphite, can be used.
- the tail gas front electrode is a liquid, it may be an ion-conducting liquid.
- the tail gas pre-electrode causes pollution Things are charged.
- the anode of the tail gas dedusting electric field exerts an attractive force on the charged pollutants, so that the pollutants move toward the anode of the tail gas dedusting electric field until the pollutants adhere to the anode of the tail gas dedusting electric field.
- the tail gas pre-electrode introduces electrons into the pollutants, and the electrons are transferred between the pollutants located between the tail gas pre-electrode and the tail gas dedusting electric field anode, so that more pollutants are charged.
- the front electrode of the exhaust gas and the anode of the exhaust gas dedusting electric field conduct electrons through pollutants and form an electric current.
- the exhaust gas front electrode charges the pollutants by contacting the pollutants. In an embodiment of the present invention, the exhaust gas front electrode charges pollutants by means of energy fluctuation. In an embodiment of the invention, the exhaust gas front electrode transfers electrons to the pollutant by contacting the pollutant, and charges the pollutant. In an embodiment of the present invention, the exhaust gas front electrode transfers electrons to the pollutants by means of energy fluctuations, and charges the pollutants.
- the tail gas pre-electrode is linear, and the tail gas dedusting electric field anode is planar.
- the exhaust gas front electrode is perpendicular to the anode of the exhaust gas dedusting electric field.
- the tail gas pre-electrode is parallel to the anode of the tail gas dedusting electric field.
- the exhaust gas pre-electrode is curved or arc-shaped.
- the exhaust gas pre-electrode uses a metal wire mesh.
- the voltage between the exhaust gas front electrode and the exhaust gas dedusting electric field anode is different from the voltage between the exhaust gas dedusting electric field cathode and the exhaust gas dedusting electric field anode. In an embodiment of the invention, the voltage between the exhaust gas front electrode and the exhaust gas dedusting electric field anode is less than the initial halo voltage.
- the initial halo voltage is the minimum voltage between the cathode of the exhaust gas dedusting electric field and the anode of the exhaust gas dedusting electric field. In an embodiment of the invention, the voltage between the exhaust gas front electrode and the exhaust gas dedusting electric field anode may be 0.1-2 kV / mm.
- the tail gas electric field device includes a tail gas flow channel, and the tail gas front electrode is located in the tail gas flow channel.
- the ratio of the cross-sectional area of the tail gas pre-electrode to the cross-sectional area of the tail gas channel is 99% -10%, or 90-10%, or 80-20%, or 70-30%, or 60- 40%, or 50%.
- the cross-sectional area of the exhaust gas front electrode refers to the sum of the areas of the exhaust gas front electrode along the solid part of the cross section.
- the exhaust gas pre-electrode has a negative potential.
- pollutants such as highly conductive metal dust, mist droplets, or aerosol in the exhaust gas are in contact with the exhaust gas front electrode, or When the distance of the tail gas front electrode reaches a certain range, it will be directly negatively charged. Then, all pollutants will enter the tail gas ionization and dust removal electric field with the air flow. The anode of the tail gas removal electric field exerts attractive force on the negatively charged metal dust, mist droplets, or aerosol. To move the negatively charged pollutants toward the anode of the exhaust gas dedusting electric field until the part of the pollutants adheres to the anode of the exhaust gas dedusting electric field, so that the pollutants can be collected.
- the anode of the exhaust gas dedusting electric field and the cathode of the exhaust gas dedusting electric field obtains oxygen ions from the oxygen in the ionized gas, and after the negatively charged oxygen ions are combined with the common dust, the common dust is negatively charged, and the anode of the tail gas removal electric field gives the negatively charged dust to this part
- the pollutants exert an attractive force, so that dust and other pollutants move toward the anode of the exhaust gas dedusting electric field until the
- the pollutants are attached to the anode of the exhaust gas dedusting electric field, so that some common dust and other pollutants are also collected, thereby collecting the pollutants with strong conductivity and weak conductivity in the exhaust gas, and making the exhaust gas dedusting electric field anode
- the types of pollutants in the exhaust gas can be collected more widely, and the collection ability is stronger and the collection efficiency is higher.
- the inlet of the exhaust gas electric field device communicates with the outlet of the engine.
- the exhaust gas electric field device may include an exhaust gas dedusting electric field cathode and an exhaust gas dedusting electric field anode, and an ionization dedusting electric field is formed between the exhaust gas dedusting electric field cathode and the exhaust gas dedusting electric field anode.
- the oxygen ions in the exhaust gas will be ionized and form a large number of charged oxygen ions.
- the oxygen ions are combined with the dust and other particles in the exhaust gas to charge the particles.
- the anode of the exhaust gas removal electric field gives negatively charged particles
- the adsorption force is applied so that the particulate matter is adsorbed on the anode of the exhaust gas dedusting electric field to remove the particulate matter in the exhaust gas.
- the exhaust gas dedusting electric field cathode includes a plurality of cathode wires.
- the diameter of the cathode wire can be 0.1mm-20mm, and the size parameter can be adjusted according to the application and dust accumulation requirements. In an embodiment of the invention, the diameter of the cathode wire is not greater than 3 mm.
- the cathode wire uses a metal wire or an alloy wire that is easy to discharge, is temperature resistant, can support its own weight, and is electrochemically stable.
- the material of the cathode wire is titanium. The specific shape of the cathode wire is adjusted according to the shape of the anode of the exhaust gas dedusting electric field.
- the cross section of the cathode wire is circular; if the dust collecting surface of the anode of the exhaust gas dedusting electric field is an arc surface
- the cathode wire needs to be designed into a polyhedron shape. The length of the cathode wire is adjusted according to the anode of the exhaust gas dedusting electric field.
- the exhaust gas dedusting electric field cathode includes a plurality of cathode rods.
- the diameter of the cathode rod is not greater than 3 mm.
- a metal rod or an alloy rod that is easy to discharge is used as the cathode rod.
- the shape of the cathode rod may be needle-shaped, polygonal, burr-shaped, threaded rod-shaped, columnar or the like. The shape of the cathode rod can be adjusted according to the shape of the anode of the exhaust gas dedusting electric field.
- the cross section of the cathode rod needs to be designed to be circular; if the dust collecting surface of the anode of the exhaust gas dedusting electric field is For the arc surface, the cathode rod needs to be designed as a polyhedron.
- the cathode of the exhaust gas dedusting electric field is disposed in the anode of the exhaust gas dedusting electric field.
- the exhaust gas dedusting electric field anode includes one or more hollow anode tubes arranged in parallel. When there are multiple hollow anode tubes, all the hollow anode tubes constitute a honeycomb-shaped exhaust gas dedusting electric field anode.
- the hollow anode tube may have a circular or polygonal cross section. If the cross section of the hollow anode tube is circular, a uniform electric field can be formed between the anode of the exhaust gas dedusting electric field and the cathode of the exhaust gas dedusting electric field, and the inner wall of the hollow anode tube is not easy to accumulate dust.
- the cross section of the hollow anode tube is a triangle, three dust accumulation surfaces and three far angle dust holding angles can be formed on the inner wall of the hollow anode tube.
- the hollow tube of this structure has the highest dust holding rate. If the cross section of the hollow anode tube is quadrangular, 4 dust-collecting surfaces and 4 dust-holding angles can be obtained, but the grouping structure is unstable. If the cross section of the hollow anode tube is hexagonal, 6 dust accumulation surfaces and 6 dust accumulation angles can be formed, and the dust accumulation surface and the dust accumulation rate are balanced. If the cross section of the hollow anode tube is more polygonal, more dust accumulation edges can be obtained, but the dust holding rate is lost. In an embodiment of the invention, the diameter of the inscribed circle diameter of the hollow anode tube ranges from 5 mm to 400 mm.
- the cathode of the exhaust gas dedusting electric field is installed on a cathode support plate, and the cathode support plate and the anode of the exhaust gas dedusting electric field are connected by an exhaust gas insulation mechanism.
- the exhaust gas dedusting electric field anode includes a third anode part and a fourth anode part, that is, the third anode part is close to the exhaust gas electric field device inlet, and the fourth anode part is close to the exhaust gas electric field device outlet.
- the cathode support plate and the exhaust gas insulation mechanism are located between the third anode part and the fourth anode part, that is, the exhaust gas insulation mechanism is installed in the middle of the exhaust gas ionization dust removal electric field or the exhaust gas dust removal electric field cathode, which can play a good support for the exhaust gas dust removal electric field cathode It plays a role in fixing the cathode of the exhaust gas dedusting electric field relative to the anode of the exhaust gas dedusting electric field, so as to maintain a set distance between the exhaust gas dedusting electric field cathode and the exhaust gas dedusting electric field anode.
- the support point of the cathode is at the end of the cathode, and it is difficult to maintain the distance between the cathode and the anode.
- the exhaust gas insulation mechanism is provided outside the dust removal flow path, that is, outside the second-stage flow path, to prevent or reduce the accumulation of dust and the like in the exhaust gas on the exhaust gas insulation mechanism, causing the exhaust gas insulation mechanism to break down or conduct electricity.
- the exhaust gas insulation mechanism uses a high-pressure-resistant ceramic insulator to insulate the cathode of the exhaust gas dedusting electric field and the anode of the exhaust gas dedusting electric field.
- the anode of the exhaust gas dedusting electric field is also called a kind of shell.
- the third anode portion is located in front of the cathode support plate and the exhaust gas insulation mechanism in the gas flow direction.
- the third anode portion can remove water in the exhaust gas and prevent water from entering the exhaust gas insulation mechanism, resulting in a short circuit of the exhaust gas insulation mechanism. Light a fire.
- the third positive stage can remove a considerable part of the dust in the exhaust gas. When the exhaust gas passes through the exhaust gas insulation mechanism, a considerable part of the dust has been eliminated, reducing the possibility of dust short-circuiting the exhaust gas insulation mechanism.
- the exhaust gas insulation mechanism includes an insulating ceramic pillar.
- the design of the third anode part is mainly to protect the insulating ceramic column from being contaminated by particulate matter in the gas. Once the gas pollutes the insulating ceramic column, the anode of the exhaust gas dedusting electric field and the cathode of the exhaust gas dedusting electric field will be conducted, so that the anode of the exhaust gas dedusting electric field The dust accumulation function is invalid, so the design of the third anode part can effectively reduce the pollution of the insulating ceramic column and improve the service time of the product.
- the third anode part and the cathode of the exhaust gas dedusting electric field first contact with the polluting gas, and the exhaust gas insulation mechanism contacts the gas afterwards, so as to achieve the purpose of removing the dust first and then passing through the exhaust gas insulation mechanism, reducing the exhaust gas
- the pollution caused by the insulation mechanism prolongs the cleaning and maintenance cycle, and the insulation support after the corresponding electrode is used.
- the length of the third anode portion is long enough to remove part of dust, reduce dust accumulated on the exhaust gas insulation mechanism and the cathode support plate, and reduce electric shock caused by dust wear.
- the length of the third anode portion accounts for 1/10 to 1/4, 1/4 to 1/3, 1/3 to 1/2, 1/2 to 2/2 of the total length of the anode of the exhaust gas dedusting electric field 3. 2/3 to 3/4, or 3/4 to 9/10.
- the fourth anode portion is located behind the cathode support plate and the exhaust gas insulation mechanism in the exhaust gas flow direction.
- the fourth anode part includes a dust accumulation section and a reserved dust accumulation section.
- the dust accumulation section uses static electricity to adsorb the particulate matter in the exhaust gas.
- the dust accumulation section is to increase the dust accumulation area and prolong the use time of the exhaust gas electric field device.
- the reserved dust accumulation section can provide failure protection for the dust accumulation section.
- the dust accumulation section is reserved to further increase the dust accumulation area on the premise of meeting the design dust removal requirements.
- the dust accumulation section is reserved for supplementing the dust accumulation in the previous section.
- different power sources can be used for the reserved dust accumulation section and the third anode portion.
- the exhaust gas insulation mechanism is provided at the cathode of the exhaust gas dedusting electric field and the exhaust gas Except for the second-stage flow channel between the anodes of the dust electric field. Therefore, the exhaust gas insulation mechanism is hung outside the anode of the exhaust gas dedusting electric field.
- the exhaust gas insulation mechanism may use non-conductor temperature-resistant materials, such as ceramics and glass.
- completely sealed air-free material insulation requires an insulation isolation thickness> 0.3 mm / kv; air insulation requirements> 1.4 mm / kv.
- the insulation distance can be set according to 1.4 times the pole spacing between the cathode of the exhaust gas dedusting electric field and the anode of the exhaust gas dedusting electric field.
- the exhaust gas insulation mechanism uses ceramics with a glazed surface; it cannot be filled with glue or organic materials, and the temperature resistance is greater than 350 degrees Celsius.
- the exhaust gas insulation mechanism includes an insulation portion and a heat insulation portion.
- the material of the insulation part is ceramic material or glass material.
- the insulating portion may be an umbrella-shaped string ceramic column or a glass column, and the umbrella is glazed inside and outside.
- the distance between the outer edge of the umbrella-shaped string ceramic column or glass column and the anode of the exhaust gas dedusting electric field is greater than 1.4 times the electric field distance, that is, greater than 1.4 times the pole spacing.
- the sum of the umbrella flange spacing of the umbrella-shaped string ceramic column or glass column is greater than 1.4 times the insulation spacing of the umbrella-shaped string ceramic column.
- the total length of the inner depth of the umbrella-shaped string ceramic column or glass column is 1.4 times greater than the insulation distance of the umbrella-shaped string ceramic column.
- the insulating part can also be a columnar string ceramic column or a glass column with glaze inside and outside. In an embodiment of the present invention, the insulating portion may also have a tower shape.
- a heating rod is provided in the insulating portion.
- the heating rod is activated and heated. Due to the temperature difference between the inside and outside of the insulating part during use, condensation is likely to occur inside and outside of the insulating part and outside.
- the outer surface of the insulation may spontaneously or be heated by gas to generate high temperature, which requires necessary isolation and protection to prevent burns.
- the heat insulation part includes a protective baffle located outside the second insulation part and a denitration purification reaction chamber.
- the tail portion of the insulating portion needs to be insulated at the same location to prevent the environment and heat dissipation from heating the condensation component.
- the lead wire of the power supply of the exhaust gas electric field device uses an umbrella-shaped string ceramic column or a glass column to pass through the wall connection, an elastic bumper is used in the wall to connect the cathode support plate, and a sealed insulating protective wiring cap is used to plug in and out the wall
- the insulation distance between the lead-through conductor and the wall is greater than that of the umbrella-shaped string ceramic column or glass column.
- the high-voltage part is eliminated from the lead, and directly installed on the end to ensure safety.
- the overall outer insulation of the high-voltage module is protected by ip68, and the medium is used for heat dissipation.
- an asymmetric structure is adopted between the cathode of the exhaust gas dedusting electric field and the anode of the exhaust gas dedusting electric field.
- polar particles are subjected to a force of the same size but in opposite directions, and polar particles reciprocate in the electric field; in an asymmetric electric field, polar particles are subjected to two forces of different sizes, and polar particles act Moving in the direction of high force can avoid coupling.
- an ionization and dust removal electric field is formed between the cathode of the exhaust gas electric field and the anode of the exhaust gas electric field.
- the method of reducing electric field coupling includes the following steps: selecting the ratio of the area of the exhaust gas anode of the exhaust gas dedusting electric field to the discharge area of the cathode of the exhaust gas dedusting electric field, so that the electric field Coupling times ⁇ 3.
- the ratio of the dust collecting area of the anode of the exhaust gas dedusting electric field to the discharge area of the cathode of the exhaust gas dedusting electric field may be: 1.667: 1-1680: 1; 3.334: 1-113.34: 1; 6.67: 1-56.67: 1; 13.34: 1-28.33: 1.
- the relatively large area of the anode dust collection area of the exhaust gas dedusting electric field anode and the relatively extremely small exhaust gas discharge electric field cathode discharge area can reduce the exhaust gas dedusting electric field cathode discharge area, reduce suction, and expand
- the dust collection area of the anode of the exhaust gas dedusting electric field expands the suction, that is, the asymmetric electrode suction between the cathode of the exhaust gas dedusting electric field and the anode of the exhaust gas dedusting electric field causes the charged dust to fall into the dust collecting surface of the anode of the exhaust gas dedusting electric field, although the polarity changes However, it can no longer be sucked away by the cathode of the exhaust gas dedusting electric field, reducing the electric field coupling, and realizing the number of electric field couplings ⁇ 3.
- the dust collecting area refers to the area of the anode working surface of the exhaust gas dedusting electric field.
- the dust collecting area is the inner surface area of the hollow regular hexagonal tube.
- the dust collecting area is also called Dust area.
- the discharge area refers to the area of the cathode working surface of the exhaust gas dedusting electric field. For example, if the cathode of the exhaust gas dedusting electric field is rod-shaped, the discharge area is the rod-shaped outer surface area.
- the length of the anode of the exhaust gas dedusting electric field may be 10 to 180 mm, 10 to 20 mm, 20 to 30 mm, 60 to 180 mm, 30 to 40 mm, 40 to 50 mm, 50 to 60 mm, 60 to 70 mm, 70 to 80 mm, 80 ⁇ 90mm, 90 ⁇ 100mm, 100 ⁇ 110mm, 110 ⁇ 120mm, 120 ⁇ 130mm, 130 ⁇ 140mm, 140 ⁇ 150mm, 150 ⁇ 160mm, 160 ⁇ 170mm, 170 ⁇ 180mm, 60mm, 180mm, 10mm or 30mm.
- the length of the anode of the exhaust gas dedusting electric field refers to the minimum length from one end to the other end of the anode working surface of the exhaust gas dedusting electric field. Selecting this length for the anode of the exhaust gas dedusting electric field can effectively reduce the electric field coupling.
- the length of the anode of the exhaust gas dedusting electric field may be 10 to 90 mm, 15 to 20 mm, 20 to 25 mm, 25 to 30 mm, 30 to 35 mm, 35 to 40 mm, 40 to 45 mm, 45 to 50 mm, 50 to 55 mm , 55 ⁇ 60mm, 60 ⁇ 65mm, 65 ⁇ 70mm, 70 ⁇ 75mm, 75 ⁇ 80mm, 80 ⁇ 85mm or 85 ⁇ 90mm, the design of this length can make the exhaust gas dedusting electric field anode and exhaust gas electric field device have high temperature resistance, and The exhaust gas electric field device has high efficiency dust collection ability under high temperature impact.
- the length of the exhaust gas dedusting electric field cathode may be 30 to 180 mm, 54 to 176 mm, 30 to 40 mm, 40 to 50 mm, 50 to 54 mm, 54 to 60 mm, 60 to 70 mm, 70 to 80 mm, 80 to 90 mm , 90-100mm, 100-110mm, 110-120mm, 120-130mm, 130-140mm, 140-150mm, 150-160mm, 160-170mm, 170-176mm, 170-180mm, 54mm, 180mm, or 30mm.
- the length of the cathode of the exhaust gas dedusting electric field refers to the minimum length from one end to the other end of the cathode working surface of the exhaust gas dedusting electric field. Choosing this length for the cathode of the exhaust gas dedusting electric field can effectively reduce the electric field coupling.
- the length of the exhaust gas dedusting electric field cathode can be 10 to 90 mm, 15 to 20 mm, 20 to 25 mm, 25 to 30 mm, 30 to 35 mm, 35 to 40 mm, 40 to 45 mm, 45 to 50 mm, 50 to 55 mm , 55 ⁇ 60mm, 60 ⁇ 65mm, 65 ⁇ 70mm, 70 ⁇ 75mm, 75 ⁇ 80mm, 80 ⁇ 85mm or 85 ⁇ 90mm, the design of this length can make the exhaust gas dedusting electric field cathode and exhaust gas electric field device have high temperature resistance, and The exhaust gas electric field device has high efficiency dust collection ability under high temperature impact.
- the corresponding dust collection efficiency is 99.9%; when the electric field temperature is 400 °C, the corresponding dust collection efficiency is 90%; when the electric field temperature is 500 °C, the corresponding dust collection efficiency is 50 %.
- the distance between the anode of the exhaust gas dedusting electric field and the cathode of the exhaust gas dedusting electric field may be 5-30 mm, 2.5-139.9 mm, 9.9-139.9 mm, 2.5-9.9 mm, 9.9-20 mm, 20-30 mm, 30 ⁇ 40mm, 40 ⁇ 50mm, 50 ⁇ 60mm, 60 ⁇ 70mm, 70 ⁇ 80mm, 80 ⁇ 90mm, 90 ⁇ 100mm, 100 ⁇ 110mm, 110 ⁇ 120mm, 120 ⁇ 130mm, 130 ⁇ 139.9mm, 9.9mm, 139.9mm, Or 2.5mm.
- the distance between the anode of the exhaust gas dedusting electric field and the cathode of the exhaust gas dedusting electric field is also called the pole spacing.
- the pole spacing specifically refers to the minimum vertical distance between the anode of the exhaust gas dedusting electric field and the cathode working surface of the exhaust gas dedusting electric field. This choice of pole spacing can effectively reduce electric field coupling and make the exhaust gas electric field device have high temperature resistance characteristics.
- the diameter of the cathode of the exhaust gas dedusting electric field is 1-3 mm, the pole spacing between the anode of the exhaust gas dedusting electric field and the cathode of the exhaust gas dedusting electric field is 2.5-139.9 mm;
- the ratio of the dust accumulation area to the discharge area of the cathode of the exhaust gas dedusting electric field is 1.667: 1-1680: 1
- ionization dust removal can be applied to remove particulate matter in the gas, for example, can be used to remove particulate matter in engine exhaust.
- the existing electric field dust removal device is still not suitable for use in vehicles.
- the electric field dedusting device in the prior art is too large to be installed in a vehicle.
- it is important that the electric field dust removal device in the prior art can only remove about 70% of the particulate matter, and cannot meet the emission standards of many countries.
- the inventor of the present invention has found that the disadvantages of the electric field dust removal device in the prior art are caused by electric field coupling.
- the present invention can significantly reduce the size (ie, volume) of the electric field dust removal device by reducing the number of electric field couplings.
- the size of the ionization and dust removal device provided by the present invention is about one fifth of the size of the existing ionization and dust removal device.
- the current ionization dust removal device sets the gas flow rate to about 1 m / s, and the present invention can still obtain a higher gas flow rate when the gas flow rate is increased to 6 m / s. Particle removal rate.
- the size of the electric field dust collector can be reduced.
- the present invention can significantly improve the particle removal efficiency. For example, when the gas flow rate is about 1m / s, the prior art electric field dust removal device can remove about 70% of the particulate matter in the engine exhaust, but the present invention can remove about 99% of the particulate matter, even when the gas flow rate is 6m / s . Therefore, the present invention can meet the latest emission standards.
- the present invention can be used to manufacture electric field dust collectors suitable for vehicles.
- the ionization and dedusting electric field between the anode of the exhaust gas dedusting electric field and the cathode of the exhaust gas dedusting electric field is also called the third electric field.
- a fourth electric field that is not parallel to the third electric field is formed between the anode of the exhaust gas dedusting electric field and the cathode of the exhaust gas dedusting electric field.
- the fourth electric field is not perpendicular to the flow channel of the ionization and dust removal electric field.
- the fourth electric field is also called an auxiliary electric field and can be formed by one or two second auxiliary electrodes.
- the second auxiliary electrode When the fourth electric field is formed by a second auxiliary electrode, the second auxiliary electrode may be placed at the inlet or the outlet of the ionization electric field, and the second auxiliary electrode may have a negative potential or a positive potential.
- the fourth electric field is formed by two second auxiliary electrodes, one of the second auxiliary electrodes can have a negative potential and the other second auxiliary electrode can have a positive potential; one second auxiliary electrode can be placed at the entrance of the ionization dust removal electric field, Another second auxiliary electrode is placed at the outlet of the ionization dust removal electric field.
- the second auxiliary electrode may be a cathode of the exhaust gas dedusting electric field or a part of the anode of the exhaust gas dedusting electric field, that is, the second auxiliary electrode may be composed of an extension of the exhaust gas dedusting electric field cathode or the exhaust gas dedusting electric field anode, and the exhaust gas dedusting electric field cathode and exhaust gas The length of the anode of the dust removal electric field is different.
- the second auxiliary electrode may also be a separate electrode, which means that the second auxiliary electrode may not be part of the cathode of the exhaust gas dedusting electric field or the anode of the exhaust gas dedusting electric field. In this case, the voltage of the fourth electric field is different from the voltage of the third electric field. Can be individually controlled according to the working conditions.
- the fourth electric field can exert a force toward the outlet of the ionizing electric field between the anode of the exhaust gas dedusting electric field anode and the cathode of the exhaust gas dedusting electric field toward the outlet of the ionization electric field, so that the anode ion of the exhaust gas dedusting electric field and the cathode of the exhaust gas dedusting electric field have negatively charged oxygen ions
- the flow has a moving speed towards the outlet.
- the anode of the electric field will be combined with the particulate matter in the exhaust gas during the movement to the outlet of the ionizing electric field. Due to the moving speed of the oxygen ions to the outlet, when the oxygen ions are combined with the particulate matter, there will be no strong collision between the two , So as to avoid greater energy consumption caused by strong collision, ensure that oxygen ions are easily combined with particulate matter, and make the particulate matter in the gas more efficient in charging, and then under the action of the anode of the exhaust gas dedusting electric field, The collection of more particulate matter ensures that the exhaust gas electric field device has a higher dust removal efficiency.
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Abstract
一种发动机排放处理系统,包括进气除尘系统(101)、尾气除尘系统(102)、尾气臭氧净化系统中。所述尾气除尘系统(102)包括尾气除尘系统入口、尾气除尘系统出口、尾气电场装置(1021)。所述尾气臭氧净化系统包括反应场(202),用于将臭氧流股与尾气流股混合反应。该发动机排放处理系统能有效地处理发动机排放,使得发动机的排放更加清洁。
Description
本发明属于环保领域,涉及一种发动机排放处理系统和方法。
现有技术中,通常通过柴油颗粒物过滤器(DPF)来进行颗粒物过滤。其中,DPF以燃烧方式工作,即利用积碳在多孔结构中充分堵塞后升温达到燃点后通过自然或者助燃的方式燃烧。具体地,DPF的工作原理如下:带有颗粒物的进气进入DPF的蜂窝状载体,颗粒物在蜂窝装载体中被拦截,当进气流出DPF时大部分的颗粒物已经被过滤掉。DPF的载体材料主要为堇青石、碳化硅、钛酸铝等,具体可根据实际情况进行选择使用。然而,上述方式存储以下缺陷:
(1)当DPF捕集到一定程度的颗粒物后就需要再生,否则发动机排气背压上升,工作状态恶化,严重影响性能及油耗,更有甚者为堵死DPF导致发动机无法工作。因此,DPF需要定期维护和添加催化剂。即使有定期维护,颗粒物的积聚限制了排气流,因此增加了背压,这会影响发动机性能和燃油消耗。
(2)DPF的除尘效果不稳定,无法满足发动机进气处理的最新过滤要求。
静电除尘是一种气体除尘方法,通常在冶金、化学等工业领域中用以净化气体或回收有用尘粒。现有技术中,由于占用空间较大、系统结构复杂、除尘效果差等问题,无法基于静电除尘对发动机进气颗粒物进行处理。
发动机对环境的污染主要来自发动机的排气产物即发动机尾气,目前对于柴油机尾气净化,常规的技术路线是采用氧化催化剂DOC除去碳氢化合物THC和CO,同时把低价态NO氧化成高价态的NO
2;在DOC之后采用柴油机微粒捕集器DPF对颗粒物PM进行过滤;在柴油机微粒捕集器DPF之后喷射尿素,尿素在排气中分解成氨气NH
3,NH
3在其后的选择性催化剂SCR上和NO
2发生选择性催化还原反应,生成氮气N
2和水。在最后在氨气氧化催化剂ASC上将过量的NH
3氧化成N
2和水,现有技术对发动机尾气的净化需添加大量尿素,且净化效果一般。
发明内容
鉴于以上所述现有技术的缺点,本发明的目的在于提供一种发动机排放处理系统和方法,用于解决现有技术除尘系统需要定期维护以及效果不稳定和需添加大量尿素处理尾气且净化 尾气效果一般中至少一个问题。同时,本发明通过研究发现现有电离除尘技术中存在的新问题,并通过一系列技术手段来解决,例如,当尾气温度或发动机温度低于一定温度时,发动机尾气中可能含有液体水,本发明在尾气电场装置前安装除水装置,脱除尾气中的液体水,提高电离除尘效果;在高温条件下,通过控制尾气电场装置阳极的集尘面积与阴极的放电面积比、阴极/阳极的长度、极间距以及设置辅助电场等,有效减少电场耦合,并使得尾气电场装置在高温冲击下仍具有高效率的集尘能力。对于进气系统,本发明在进气电离除尘电场的阳极和阴极之间还设有与电离电场不平行的辅助电场,辅助电场能给阳离子施加朝向电离电场的出口的力,使得氧离子流向出口的流速大于空气流速,起到增氧作用,进入发动机的进气中氧气含量增多,进而大大提高发动机的功率。因此,本发明适合在苛刻条件下作业,并保证除尘效率,故从商业角度出发,本发明完全可适用于发动机。
本发明提供一种发动机排放处理系统,包括进气除尘系统、尾气除尘系统、尾气臭氧净化系统中的至少一个。所述进气除尘系统包括进气除尘系统入口、进气除尘系统出口、进气电场装置。所述尾气除尘系统包括尾气除尘系统入口、尾气除尘系统出口、尾气电场装置。所述尾气臭氧净化系统包括反应场,用于将臭氧流股与尾气流股混合反应。该发动机排放处理系统能有效地处理发动机排放,使得发动机的排放更加清洁。
为实现上述目的及其他相关目的,本发明提供以下示例:
1.本发明提供的示例1:一种发动机排放处理系统。
2.本发明提供的示例2:上述示例1包括进气除尘系统,所述进气除尘系统包括进气除尘系统入口、进气除尘系统出口、进气电场装置。
3.本发明提供的示例3:包括上述示例2,其中,所述进气电场装置包括进气电场装置入口、进气电场装置出口、进气除尘电场阴极和进气除尘电场阳极,所述进气除尘电场阴极和所述进气除尘电场阳极用于产生进气电离除尘电场。
4.本发明提供的示例4:包括上述示例3,其中,所述进气除尘电场阳极包括第一阳极部和第二阳极部,所述第一阳极部靠近所述进气电场装置入口,第二阳极部靠近所述进气电场装置出口,所述第一阳极部和所述第二阳极部之间设置有至少一个阴极支撑板。
5.本发明提供的示例5:包括上述示例4,其中,所述进气电场装置还包括进气绝缘机构,用于实现所述阴极支撑板和所述进气除尘电场阳极之间的绝缘。
6.本发明提供的示例6:包括上述示例4,其中,所述进气除尘电场阳极和所述进气除尘电场阴极之间形成电场流道,所述进气绝缘机构设置在所述电场流道外。
7.本发明提供的示例7:包括上述示例5或6,其中,所述进气绝缘机构包括绝缘部和隔 热部;所述绝缘部的材料采用陶瓷材料或玻璃材料。
8.本发明提供的示例8:包括上述示例7,其中,所述绝缘部为伞状串陶瓷柱、伞状串玻璃柱、柱状串陶瓷柱或柱状玻璃柱,伞内外或柱内外挂釉。
9.本发明提供的示例9:包括上述示例8,其中,伞状串陶瓷柱或伞状串玻璃柱的外缘与所述进气除尘电场阳极的距离大于电场距离1.4倍,伞状串陶瓷柱或伞状串玻璃柱的伞突边间距总和大于伞状串陶瓷柱或伞状串玻璃柱的绝缘间距1.4倍,伞状串陶瓷柱或伞状串玻璃柱的伞边内深总长大于伞状串陶瓷柱或伞状串玻璃柱的绝缘距离1.4倍。
10.本发明提供的示例10:包括上述示例4至9中的任一项,其中,所述第一阳极部的长度是所述进气除尘电场阳极长度的1/10至1/4、1/4至1/3、1/3至1/2、1/2至2/3、2/3至3/4,或3/4至9/10。
11.本发明提供的示例11:包括上述示例4至10中的任一项,其中,所述第一阳极部的长度是足够的长,以清除部分灰尘,减少积累在所述进气绝缘机构和所述阴极支撑板上的灰尘,减少灰尘造成的电击穿。
12.本发明提供的示例12:包括上述示例4至11中的任一项,其中,所述第二阳极部包括积尘段和预留积尘段。
13.本发明提供的示例13:包括上述示例3至12中的任一项,其中,所述进气除尘电场阴极包括至少一根电极棒。
14.本发明提供的示例14:包括上述示例13,其中,所述电极棒的直径不大于3mm。
15.本发明提供的示例15:包括上述示例13或14,其中,所述电极棒的形状呈针状、多角状、毛刺状、螺纹杆状或柱状。
16.本发明提供的示例16:包括上述示例3至15中的任一项,其中,所述进气除尘电场阳极由中空的管束组成。
17.本发明提供的示例17:包括上述示例16,其中,所述进气除尘电场阳极管束的中空的截面采用圆形或多边形。
18.本发明提供的示例18:包括上述示例17,其中,所述多边形为六边形。
19.本发明提供的示例19:包括上述示例15至18中的任一项,其中,所述进气除尘电场阳极的管束呈蜂窝状。
20.本发明提供的示例20:包括上述示例3至19中的任一项,其中,所述进气除尘电场阴极穿射于所述进气除尘电场阳极内。
21.本发明提供的示例21:包括上述示例3至20中的任一项,其中,当电场积尘到一定 程度时,所述进气电场装置进行除尘处理。
22.本发明提供的示例22:包括上述示例21,其中,所述进气电场装置检测电场电流来确定是否积尘到一定程度,需要进行除尘处理。
23.本发明提供的示例23:包括上述示例21或22,其中,所述进气电场装置增高电场电压来进行除尘处理。
24.本发明提供的示例24:包括上述示例21或22,其中,所述进气电场装置利用电场反电晕放电现象来进行除尘处理。
25.本发明提供的示例25:包括上述示例21或22,其中,所述进气电场装置利用电场反电晕放电现象,增高电场电压,限制入注电流,使发生在阳极积碳位置的急剧放电产生等离子,所述等离子使灰尘有机成分深度氧化,高分子键断裂,形成小分子二氧化碳和水,来进行除尘处理。
26.本发明提供的示例26:包括上述示例3至25中的任一项,其中,所述进气电场装置还包括辅助电场单元,用于产生与所述进气电离除尘电场不平行的辅助电场。
27.本发明提供的示例27:包括上述示例3至25中的任一项,其中,所述进气电场装置还包括辅助电场单元,所述进气电离除尘电场包括流道,所述辅助电场单元用于产生与所述流道不垂直的辅助电场。
28.本发明提供的示例28:包括上述示例26或27,其中,所述辅助电场单元包括第一电极,所述辅助电场单元的第一电极设置在或靠近所述进气电离除尘电场的进口。
29.本发明提供的示例29:包括上述示例28,其中,所述第一电极为阴极。
30.本发明提供的示例30:包括上述示例28或29,其中,所述辅助电场单元的第一电极是所述进气除尘电场阴极的延伸。
31.本发明提供的示例31:包括上述示例30,其中,所述辅助电场单元的第一电极与所述进气除尘电场阳极具有夹角α,且0°<α≤125°、或45°≤α≤125°、或60°≤α≤100°、或α=90°。
32.本发明提供的示例32:包括上述示例26至31中的任一项,其中,所述辅助电场单元包括第二电极,所述辅助电场单元的第二电极设置在或靠近所述进气电离除尘电场的出口。
33.本发明提供的示例33:包括上述示例32,其中,所述第二电极为阳极。
34.本发明提供的示例34:包括上述示例32或33,其中,所述辅助电场单元的第二电极是所述进气除尘电场阳极的延伸。
35.本发明提供的示例35:包括上述示例34,其中,所述辅助电场单元的第二电极与所述进气除尘电场阴极具有夹角α,且0°<α≤125°、或45°≤α≤125°、或60°≤α≤100°、或α=90°。
36.本发明提供的示例36:包括上述示例26至29、32和33中的任一项,其中,所述辅助电场的电极与所述进气电离除尘电场的电极独立设置。
37.本发明提供的示例37:包括上述示例3至36中的任一项,其中,所述进气除尘电场阳极的积尘面积与所述进气除尘电场阴极的放电面积的比为1.667:1-1680:1。
38.本发明提供的示例38:包括上述示例3至36中的任一项,其中,所述进气除尘电场阳极的积尘面积与所述进气除尘电场阴极的放电面积的比为6.67:1-56.67:1。
39.本发明提供的示例39:包括上述示例3至38中的任一项,其中,所述进气除尘电场阴极直径为1-3毫米,所述进气除尘电场阳极与所述进气除尘电场阴极的极间距为2.5-139.9毫米;所述进气除尘电场阳极的积尘面积与所述进气除尘电场阴极的放电面积的比为1.667:1-1680:1。
40.本发明提供的示例40:包括上述示例3至38中的任一项,其中,所述进气除尘电场阳极和所述进气除尘电场阴极的极间距小于150mm。
41.本发明提供的示例41:包括上述示例3至38中的任一项,其中,所述进气除尘电场阳极与所述进气除尘电场阴极的极间距为2.5-139.9mm。
42.本发明提供的示例42:包括上述示例3至38中的任一项,其中,所述进气除尘电场阳极与所述进气除尘电场阴极的极间距为5-100mm。
43.本发明提供的示例43:包括上述示例3至42中的任一项,其中,所述进气除尘电场阳极长度为10-180mm。
44.本发明提供的示例44:包括上述示例3至42中的任一项,其中,所述进气除尘电场阳极长度为60-180mm。
45.本发明提供的示例45:包括上述示例3至44中的任一项,其中,所述进气除尘电场阴极长度为30-180mm。
46.本发明提供的示例46:包括上述示例3至44中的任一项,其中,所述进气除尘电场阴极长度为54-176mm。
47.本发明提供的示例47:包括上述示例37至46中的任一项,其中,当运行时,所述进气电离除尘电场的耦合次数≤3。
48.本发明提供的示例48:包括上述示例26至46中的任一项,其中,当运行时,所述进气电离除尘电场的耦合次数≤3。
49.本发明提供的示例49:包括上述示例3至48中的任一项,其中,所述进气电离除尘电场电压的取值范围为1kv-50kv。
50.本发明提供的示例50:包括上述示例3至49中的任一项,其中,所述进气电场装置还包括若干连接壳体,串联电场级通过所述连接壳体连接。
51.本发明提供的示例51:包括上述示例50,其中,相邻的电场级的距离大于所述极间距的1.4倍。
52.本发明提供的示例52:包括上述示例3至51中的任一项,其中,所述进气电场装置还包括进气前置电极,所述进气前置电极在所述进气电场装置入口与所述进气除尘电场阳极和所述进气除尘电场阴极形成的进气电离除尘电场之间。
53.本发明提供的示例53:包括上述示例52,其中,所述进气前置电极呈点状、线状、网状、孔板状、板状、针棒状、球笼状、盒状、管状、物质自然形态、或物质加工形态。
54.本发明提供的示例54:包括上述示例52或53,其中,所述进气前置电极上设有进气通孔。
55.本发明提供的示例55:包括上述示例54,其中,所述进气通孔呈多角形、圆形、椭圆形、正方形、长方形、梯形、或菱形。
56.本发明提供的示例56:包括上述示例54或55,其中,所述进气通孔的大小为0.1-3毫米。
57.本发明提供的示例57:包括上述示例52至56中的任一项,其中,所述进气前置电极为固体、液体、气体分子团、或等离子体中的一种或多种形态的组合。
58.本发明提供的示例58:包括上述示例52至57中的任一项,其中,所述进气前置电极为导电混合态物质、生物体自然混合导电物质、或物体人工加工形成导电物质。
59.本发明提供的示例59:包括上述示例52至58中的任一项,其中,所述进气前置电极为304钢或石墨。
60.本发明提供的示例60:包括上述示例52至58中的任一项,其中,所述进气前置电极为含离子导电液体。
61.本发明提供的示例61:包括上述示例52至60中的任一项,其中,在工作时,在带污染物的气体进入所述进气除尘电场阴极、进气除尘电场阳极形成的进气电离除尘电场之前,且带污染物的气体通过所述进气前置电极时,所述进气前置电极使气体中的污染物带电。
62.本发明提供的示例62:包括上述示例61,其中,当带污染物的气体进入所述进气电离除尘电场时,所述进气除尘电场阳极给带电的污染物施加吸引力,使污染物向所述进气除尘电场阳极移动,直至污染物附着在所述进气除尘电场阳极上。
63.本发明提供的示例63:包括上述示例61或62,其中,所述进气前置电极将电子导入 污染物,电子在位于所述进气前置电极和所述进气除尘电场阳极之间的污染物之间进行传递,使更多污染物带电。
64.本发明提供的示例64:包括上述示例61至63中的任一项,其中,所述进气前置电极和所述进气除尘电场阳极之间通过污染物传导电子、并形成电流。
65.本发明提供的示例65:包括上述示例61至64中的任一项,其中,所述进气前置电极通过与污染物接触的方式使污染物带电。
66.本发明提供的示例66:包括上述示例61至65中的任一项,其中,所述进气前置电极通过能量波动的方式使污染物带电。
67.本发明提供的示例67:包括上述示例61至66中的任一项,其中,所述进气前置电极上设有进气通孔。
68.本发明提供的示例68:包括上述示例52至67中的任一项,其中,所述进气前置电极呈线状,所述进气除尘电场阳极呈面状。
69.本发明提供的示例69:包括上述示例52至68中的任一项,其中,所述进气前置电极垂直于所述进气除尘电场阳极。
70.本发明提供的示例70:包括上述示例52至69中的任一项,其中,所述进气前置电极与所述进气除尘电场阳极相平行。
71.本发明提供的示例71:包括上述示例51至69中的任一项,其中,所述进气前置电极呈曲线状或圆弧状。
72.本发明提供的示例72:包括上述示例52至71中的任一项,其中,所述进气前置电极采用金属丝网。
73.本发明提供的示例73:包括上述示例52至72中的任一项,其中,所述进气前置电极与所述进气除尘电场阳极之间的电压不同于所述进气除尘电场阴极与所述进气除尘电场阳极之间的电压。
74.本发明提供的示例74:包括上述示例52至73中的任一项,其中,所述进气前置电极与所述进气除尘电场阳极之间的电压小于起始起晕电压。
75.本发明提供的示例75:包括上述示例52至74中的任一项,其中,所述进气前置电极与所述进气除尘电场阳极之间的电压为0.1kv/mm-2kv/mm。
76.本发明提供的示例76:包括上述示例52至75中的任一项,其中,所述进气电场装置包括进气流道,所述进气前置电极位于所述进气流道中;所述进气前置电极的截面面积与进气流道的截面面积比为99%-10%、或90-10%、或80-20%、或70-30%、或60-40%、或50%。
77.本发明提供的示例77:包括上述示例3至76中的任一项,其中,所述进气电场装置包括进气驻极体元件。
78.本发明提供的示例78:包括上述示例77,其中,所述进气除尘电场阳极和所述进气除尘电场阴极接通电源时,所述进气驻极体元件在所述进气电离除尘电场中。
79.本发明提供的示例79:包括上述示例77或78,其中,所述进气驻极体元件靠近所述进气电场装置出口,或者,所述进气驻极体元件设于所述进气电场装置出口。
80.本发明提供的示例80:包括上述示例78至79中的任一项,其中,所述进气除尘电场阳极和所述进气除尘电场阴极形成进气流道,所述进气驻极体元件设于所述进气流道中。
81.本发明提供的示例81:包括上述示例80,其中,所述进气流道包括进气流道出口,所述进气驻极体元件靠近所述进气流道出口,或者,所述进气驻极体元件设于所述进气流道出口。
82.本发明提供的示例82:包括上述示例80或81,其中,所述进气驻极体元件于所述进气流道中的横截面占进气流道横截面5%-100%。
83.本发明提供的示例83:包括上述示例82,其中,所述进气驻极体元件于所述进气流道中的横截面占进气流道横截面10%-90%、20%-80%、或40%-60%。
84.本发明提供的示例84:包括上述示例77至83中的任一项,其中,所述进气电离除尘电场给所述进气驻极体元件充电。
85.本发明提供的示例85:包括上述示例77至84中的任一项,其中,所述进气驻极体元件具有多孔结构。
86.本发明提供的示例86:包括上述示例77至85中的任一项,其中,所述进气驻极体元件为织品。
87.本发明提供的示例87:包括上述示例77至86中的任一项,其中,所述进气除尘电场阳极内部为管状,所述进气驻极体元件外部为管状,所述进气驻极体元件外部套设于所述进气除尘电场阳极内部。
88.本发明提供的示例88:包括上述示例77至87中的任一项,其中,所述进气驻极体元件与所述进气除尘电场阳极为可拆卸式连接。
89.本发明提供的示例89:包括上述示例77至88中的任一项,其中,所述进气驻极体元件的材料包括具有驻极性能的无机化合物。
90.本发明提供的示例90:包括上述示例89,其中,所述无机化合物选自含氧化合物、含氮化合物或玻璃纤维中的一种或多种组合。
91.本发明提供的示例91:包括上述示例90,其中,所述含氧化合物选自金属基氧化物、含氧复合物、含氧的无机杂多酸盐中的一种或多种组合。
92.本发明提供的示例92:包括上述示例91,其中,所述金属基氧化物选自氧化铝、氧化锌、氧化锆、氧化钛、氧化钡、氧化钽、氧化硅、氧化铅、氧化锡中的一种或多种组合。
93.本发明提供的示例93:包括上述示例91,其中,所述金属基氧化物为氧化铝。
94.本发明提供的示例94:包括上述示例91,其中,所述含氧复合物选自钛锆复合氧化物或钛钡复合氧化物中的一种或多种组合。
95.本发明提供的示例95:包括上述示例91,其中,所述含氧的无机杂多酸盐选自钛酸锆、锆钛酸铅或钛酸钡中的一种或多种组合。
96.本发明提供的示例96:包括上述示例90,其中,所述含氮化合物为氮化硅。
97.本发明提供的示例97:包括上述示例77至96中的任一项,其中,所述进气驻极体元件的材料包括具有驻极性能的有机化合物。
98.本发明提供的示例98:包括上述示例97,其中,所述有机化合物选自氟聚合物、聚碳酸酯、PP、PE、PVC、天然蜡、树脂、松香中的一种或多种组合。
99.本发明提供的示例99:包括上述示例98,其中,所述氟聚合物选自聚四氟乙烯、聚全氟乙丙烯、可溶性聚四氟乙烯、聚偏氟乙烯中的一种或多种组合。
100.本发明提供的示例100:包括上述示例98,其中,所述氟聚合物为聚四氟乙烯。
101.本发明提供的示例101:包括上述示例2至100中的任一项,其中,还包括进气均风装置。
102.本发明提供的示例102:包括上述示例101,其中,所述进气均风装置在所述进气除尘系统入口与所述进气除尘电场阳极和所述进气除尘电场阴极形成的进气电离除尘电场之间,当所述进气除尘电场阳极为四方体时,所述进气均风装置包括:设置于所述进气除尘电场阳极一侧边的进气管和设置于另一侧边的出气管;其中,所述进气管与所述出气管相对立。
103.本发明提供的示例103:包括上述示例101,其中,所述进气均风装置在所述进气除尘系统入口与所述进气除尘电场阳极和所述进气除尘电场阴极形成的进气电离除尘电场之间,当所述进气除尘电场阳极为圆柱体时,所述进气均风装置由若干可旋转的均风叶片组成。
104.本发明提供的示例104:包括上述示例101,其中,所述进气均风装置第一文氏板均风机构和设置于所述进气除尘电场阳极的出气端的第二文氏板均风机构,所述第一文氏板均风机构上开设有进气孔,所述第二文氏板均风机构上开设有出气孔,所述进气孔与所述出气孔错位排布,且正面进气侧面出气,形成旋风结构。
105.本发明提供的示例105:包括上述示例2至104中的任一项,其中,还包括除臭氧装置,用于去除去或减少所述进气电场装置产生的臭氧,所述除臭氧装置在所述进气电场装置出口与所述进气除尘系统出口之间。
106.本发明提供的示例106:包括上述示例105,其中,所述除臭氧装置还包括臭氧消解器。
107.本发明提供的示例107:包括上述示例106,其中,所述臭氧消解器选自紫外线臭氧消解器和催化臭氧消解器中的至少一种。
108.本发明提供的示例108:包括上述示例2至107中的任一项,其中,还包括离心分离机构。
109.本发明提供的示例109:包括上述示例108,其中,所述离心分离机构包括气流转向通道,且气流转向通道能改变气流的流动方向。
110.本发明提供的示例110:包括上述示例109,其中,所述气流转向通道能引导气体沿圆周方向流动。
111.本发明提供的示例111:包括上述示例108或109,其中,所述气流转向通道呈螺旋形或圆锥形。
112.本发明提供的示例112:包括上述示例108至111中的任一项,其中,所述离心分离机构包括分离筒。
113.本发明提供的示例113:包括上述示例112,其中,所述分离筒中设有所述气流转向通道,所述分离筒的底部设有出尘口。
114.本发明提供的示例114:包括上述示例112或113,其中,所述分离筒侧壁上设有与所述气流转向通道的第一端相连通的进气口。
115.本发明提供的示例115:包括上述示例112至114中的任一项,其中,所述分离筒的顶部设有与所述气流转向通道的第二端相连通的出气口。
116.本发明提供的示例116:包括上述示例1-115中的任一项,还包括尾气除尘系统,所述尾气除尘系统包括尾气除尘系统入口、尾气除尘系统出口、尾气电场装置。
117.本发明提供的示例117:包括上述示例116,其中,所述尾气电场装置包括尾气电场装置入口、尾气电场装置出口、尾气除尘电场阴极和尾气除尘电场阳极,所述尾气除尘电场阴极和所述尾气除尘电场阳极用于产生尾气电离除尘电场。
118.本发明提供的示例118:包括上述示例117,其中,所述尾气除尘电场阳极包括第一阳极部和第二阳极部,所述第一阳极部靠近尾气电场装置入口,第二阳极部靠近尾气电场装 置出口,所述第一阳极部和所述第二阳极部之间设置有至少一个阴极支撑板。
119.本发明提供的示例119:包括上述示例118,其中,所述尾气电场装置还包括尾气绝缘机构,用于实现所述阴极支撑板和所述尾气除尘电场阳极之间的绝缘。
120.本发明提供的示例120:包括上述示例119,其中,所述尾气除尘电场阳极和所述尾气除尘电场阴极之间形成电场流道,所述尾气绝缘机构设置在所述电场流道外。
121.本发明提供的示例121:包括上述示例119或120,其中,所述尾气绝缘机构包括绝缘部和隔热部;所述绝缘部的材料采用陶瓷材料或玻璃材料。
122.本发明提供的示例122:包括上述示例121,其中,所述绝缘部为伞状串陶瓷柱、伞状串玻璃柱、柱状串陶瓷柱或柱状玻璃柱,伞内外或柱内外挂釉。
123.本发明提供的示例123:包括上述示例122,其中,伞状串陶瓷柱或伞状串玻璃柱的外缘与所述尾气除尘电场阳极的距离大于电场距离1.4倍,伞状串陶瓷柱或伞状串玻璃柱的伞突边间距总和大于伞状串陶瓷柱或伞状串玻璃柱的绝缘间距1.4倍,伞状串陶瓷柱或伞状串玻璃柱的伞边内深总长大于伞状串陶瓷柱或伞状串玻璃柱的绝缘距离1.4倍。
124.本发明提供的示例124:包括上述示例118至123中的任一项,其中,所述第一阳极部的长度是所述尾气除尘电场阳极长度的1/10至1/4、1/4至1/3、1/3至1/2、1/2至2/3、2/3至3/4,或3/4至9/10。
125.本发明提供的示例125:包括上述示例118至124中的任一项,其中,所述第一阳极部的长度是足够的长,以清除部分灰尘,减少积累在所述尾气绝缘机构和所述阴极支撑板上的灰尘,减少灰尘造成的电击穿。
126.本发明提供的示例126:包括上述示例118至125中的任一项,其中,所述第二阳极部包括积尘段和预留积尘段。
127.本发明提供的示例127:包括上述示例117至126中的任一项,其中,所述尾气除尘电场阴极包括至少一根电极棒。
128.本发明提供的示例128:包括上述示例127,其中,所述电极棒的直径不大于3mm。
129.本发明提供的示例129:包括上述示例127或128,其中,所述电极棒的形状呈针状、多角状、毛刺状、螺纹杆状或柱状。
130.本发明提供的示例130:包括上述示例117至129中的任一项,其中,所述尾气除尘电场阳极由中空的管束组成。
131.本发明提供的示例131:包括上述示例130,其中,所述尾气除尘电场阳极管束的中空的截面采用圆形或多边形。
132.本发明提供的示例132:包括上述示例131,其中,所述多边形为六边形。
133.本发明提供的示例133:包括上述示例130至132中的任一项,其中,所述尾气除尘电场阳极的管束呈蜂窝状。
134.本发明提供的示例134:包括上述示例117至133中的任一项,其中,所述尾气除尘电场阴极穿射于所述尾气除尘电场阳极内。
135.本发明提供的示例135:包括上述示例117至134中的任一项,其中,当电场积尘到一定程度时,所述尾气电场装置进行除碳黑处理。
136.本发明提供的示例136:包括上述示例135,其中,所述尾气电场装置检测电场电流来确定是否积尘到一定程度,需要进行除碳黑处理。
137.本发明提供的示例137:包括上述示例135或136,其中,所述尾气电场装置增高电场电压来进行除碳黑处理。
138.本发明提供的示例138:包括上述示例135或136,其中,所述尾气电场装置利用电场反电晕放电现象来进行除碳黑处理。
139.本发明提供的示例139:包括上述示例135或136,其中,所述尾气电场装置利用电场反电晕放电现象,增高电压,限制入注电流,使发生在阳极积碳位置的急剧放电产生等离子,所述等离子使碳黑有机成分深度氧化,高分子键断裂,形成小分子二氧化碳和水,来进行除碳黑处理。
140.本发明提供的示例140:包括上述示例117至139中的任一项,其中,所述尾气除尘电场阳极长度为10-90mm,所述尾气除尘电场阴极长度为10-90mm。
141.本发明提供的示例141:包括上述示例140,其中,当电场温度为200℃时,对应的集尘效率为99.9%。
142.本发明提供的示例142:包括上述示例140或141,其中,当电场温度为400℃时,对应的集尘效率为90%。
143.本发明提供的示例143:包括上述示例140至142中的任一项,其中,当电场温度为500℃时,对应的集尘效率为50%。
144.本发明提供的示例144:包括上述示例117至143中的任一项,其中,所述尾气电场装置还包括辅助电场单元,用于产生与所述尾气电离除尘电场不平行的辅助电场。
145.本发明提供的示例145:包括上述示例117至143中的任一项,其中,所述尾气电场装置还包括辅助电场单元,所述尾气电离除尘电场包括流道,所述辅助电场单元用于产生与所述流道不垂直的辅助电场。
146.本发明提供的示例146:包括上述示例144或145,其中,所述辅助电场单元包括第一电极,所述辅助电场单元的第一电极设置在或靠近所述尾气电离除尘电场的进口。
147.本发明提供的示例147:包括上述示例146,其中,所述第一电极为阴极。
148.本发明提供的示例148:包括上述示例146或147,其中,所述辅助电场单元的第一电极是所述尾气除尘电场阴极的延伸。
149.本发明提供的示例149:包括上述示例148,其中,所述辅助电场单元的第一电极与所述尾气除尘电场阳极具有夹角α,且0°<α≤125°、或45°≤α≤125°、或60°≤α≤100°、或α=90°。
150.本发明提供的示例150:包括上述示例144至149中的任一项,其中,所述辅助电场单元包括第二电极,所述辅助电场单元的第二电极设置在或靠近所述尾气电离除尘电场的出口。
151.本发明提供的示例151:包括上述示例150,其中,所述第二电极为阳极。
152.本发明提供的示例152:包括上述示例150或151,其中,所述辅助电场单元的第二电极是所述尾气除尘电场阳极的延伸。
153.本发明提供的示例153:包括上述示例152,其中,所述辅助电场单元的第二电极与所述尾气除尘电场阴极具有夹角α,且0°<α≤125°、或45°≤α≤125°、或60°≤α≤100°、或α=90°。
154.本发明提供的示例154:包括上述示例144至147、150和151中的任一项,其中,所述辅助电场的电极与所述尾气电离除尘电场的电极独立设置。
155.本发明提供的示例155:包括上述示例117至154中的任一项,其中,所述尾气除尘电场阳极的积尘面积与所述尾气除尘电场阴极的放电面积的比为1.667:1-1680:1。
156.本发明提供的示例156:包括上述示例117至154中的任一项,其中,所述尾气除尘电场阳极的积尘面积与所述尾气除尘电场阴极的放电面积的比为6.67:1-56.67:1。
157.本发明提供的示例157:包括上述示例117至156中的任一项,其中,所述尾气除尘电场阴极直径为1-3毫米,所述尾气除尘电场阳极与所述尾气除尘电场阴极的极间距为2.5-139.9毫米;所述尾气除尘电场阳极的积尘面积与所述尾气除尘电场阴极的放电面积的比为1.667:1-1680:1。
158.本发明提供的示例158:包括上述示例117至156中的任一项,其中,所述尾气除尘电场阳极和所述尾气除尘电场阴极的极间距小于150mm。
159.本发明提供的示例159:包括上述示例117至156中的任一项,其中,所述尾气除尘 电场阳极与所述尾气除尘电场阴极的极间距为2.5-139.9mm。
160.本发明提供的示例160:包括上述示例117至156中的任一项,其中,所述尾气除尘电场阳极与所述尾气除尘电场阴极的极间距为5-100mm。
161.本发明提供的示例161:包括上述示例117至160中的任一项,其中,所述尾气除尘电场阳极长度为10-180mm。
162.本发明提供的示例162:包括上述示例117至160中的任一项,其中,所述尾气除尘电场阳极长度为60-180mm。
163.本发明提供的示例163:包括上述示例117至162中的任一项,其中,所述尾气除尘电场阴极长度为30-180mm。
164.本发明提供的示例164:包括上述示例117至162中的任一项,其中,所述尾气除尘电场阴极长度为54-176mm。
165.本发明提供的示例165:包括上述示例155至164中的任一项,其中,当运行时,所述尾气电离除尘电场的耦合次数≤3。
166.本发明提供的示例166:包括上述示例144至164中的任一项,其中,当运行时,所述尾气电离除尘电场的耦合次数≤3。
167.本发明提供的示例167:包括上述示例117至166中的任一项,其中,所述尾气电离除尘电场电压的取值范围为1kv-50kv。
168.本发明提供的示例168:包括上述示例117至167中的任一项,其中,所述尾气电场装置还包括若干连接壳体,串联电场级通过所述连接壳体连接。
169.本发明提供的示例169:包括上述示例168,其中,相邻的电场级的距离大于所述极间距的1.4倍。
170.本发明提供的示例170:包括上述示例117至169中的任一项,其中,所述尾气电场装置还包括尾气前置电极,所述尾气前置电极在所述尾气电场装置入口与所述尾气除尘电场阳极和所述尾气除尘电场阴极形成的尾气电离除尘电场之间。
171.本发明提供的示例171:包括上述示例170,其中,所述尾气前置电极呈点状、线状、网状、孔板状、板状、针棒状、球笼状、盒状、管状、物质自然形态、或物质加工形态。
172.本发明提供的示例172:包括上述示例170或171,其中,所述尾气前置电极上设有尾气通孔。
173.本发明提供的示例173:包括上述示例172,其中,所述尾气通孔呈多角形、圆形、椭圆形、正方形、长方形、梯形、或菱形。
174.本发明提供的示例174:包括上述示例172或173,其中,所述尾气通孔的大小为0.1-3毫米。
175.本发明提供的示例175:包括上述示例170至174中的任一项,其中,所述尾气前置电极为固体、液体、气体分子团、或等离子体中的一种或多种形态的组合。
176.本发明提供的示例176:包括上述示例170至175中的任一项,其中,所述尾气前置电极为导电混合态物质、生物体自然混合导电物质、或物体人工加工形成导电物质。
177.本发明提供的示例177:包括上述示例170至176中的任一项,其中,所述尾气前置电极为304钢或石墨。
178.本发明提供的示例178:包括上述示例170至176中的任一项,其中,所述尾气前置电极为含离子导电液体。
179.本发明提供的示例179:包括上述示例170至178中的任一项,其中,在工作时,在带污染物的气体进入所述尾气除尘电场阴极、尾气除尘电场阳极形成的尾气电离除尘电场之前,且带污染物的气体通过所述尾气前置电极时,所述尾气前置电极使气体中的污染物带电。
180.本发明提供的示例180:包括上述示例179,其中,当带污染物的气体进入所述尾气电离除尘电场时,所述尾气除尘电场阳极给带电的污染物施加吸引力,使污染物向所述尾气除尘电场阳极移动,直至污染物附着在所述尾气除尘电场阳极上。
181.本发明提供的示例181:包括上述示例179或180,其中,所述尾气前置电极将电子导入污染物,电子在位于所述尾气前置电极和所述尾气除尘电场阳极之间的污染物之间进行传递,使更多污染物带电。
182.本发明提供的示例182:包括上述示例178至180中的任一项,其中,所述尾气前置电极和所述尾气除尘电场阳极之间通过污染物传导电子、并形成电流。
183.本发明提供的示例183:包括上述示例179至182中的任一项,其中,所述尾气前置电极通过与污染物接触的方式使污染物带电。
184.本发明提供的示例184:包括上述示例179至183中的任一项,其中,所述尾气前置电极通过能量波动的方式使污染物带电。
185.本发明提供的示例185:包括上述示例179至184中的任一项,其中,所述尾气前置电极上设有尾气通孔。
186.本发明提供的示例186:包括上述示例170至185中的任一项,其中,所述尾气前置电极呈线状,所述尾气除尘电场阳极呈面状。
187.本发明提供的示例187:包括上述示例170至186中的任一项,其中,所述尾气前置 电极垂直于所述尾气除尘电场阳极。
188.本发明提供的示例188:包括上述示例170至187中的任一项,其中,所述尾气前置电极与所述尾气除尘电场阳极相平行。
189.本发明提供的示例189:包括上述示例170至188中的任一项,其中,所述尾气前置电极呈曲线状或圆弧状。
190.本发明提供的示例190:包括上述示例170至189中的任一项,其中,所述尾气前置电极采用金属丝网。
191.本发明提供的示例191:包括上述示例170至190中的任一项,其中,所述尾气前置电极与所述尾气除尘电场阳极之间的电压不同于所述尾气除尘电场阴极与所述尾气除尘电场阳极之间的电压。
192.本发明提供的示例192:包括上述示例170至191中的任一项,其中,所述尾气前置电极与所述尾气除尘电场阳极之间的电压小于起始起晕电压。
193.本发明提供的示例193:包括上述示例170至192中的任一项,其中,所述尾气前置电极与所述尾气除尘电场阳极之间的电压为0.1kv/mm-2kv/mm。
194.本发明提供的示例194:包括上述示例170至193中的任一项,其中,所述尾气电场装置包括尾气流道,所述尾气前置电极位于所述尾气流道中;所述尾气前置电极的截面面积与尾气流道的截面面积比为99%-10%、或90-10%、或80-20%、或70-30%、或60-40%、或50%。
195.本发明提供的示例195:包括上述示例117至194中的任一项,其中,所述尾气电场装置包括尾气驻极体元件。
196.本发明提供的示例196:包括上述示例195,其中,所述尾气除尘电场阳极和所述尾气除尘电场阴极接通电源时,所述尾气驻极体元件在所述尾气电离除尘电场中。
197.本发明提供的示例197:包括上述示例195或196,其中,所述尾气驻极体元件靠近所述尾气电场装置出口,或者,所述尾气驻极体元件设于所述尾气电场装置出口。
198.本发明提供的示例198:包括上述示例195至197中的任一项,其中,所述尾气除尘电场阳极和所述尾气除尘电场阴极形成尾气流道,所述尾气驻极体元件设于所述尾气流道中。
199.本发明提供的示例199:包括上述示例198,其中,所述尾气流道包括尾气流道出口,所述尾气驻极体元件靠近所述尾气流道出口,或者,所述尾气驻极体元件设于所述尾气流道出口。
200.本发明提供的示例200:包括上述示例198或199,其中,所述尾气驻极体元件于所 述尾气流道中的横截面占尾气流道横截面5%-100%。
201.本发明提供的示例201:包括上述示例200,其中,所述尾气驻极体元件于所述尾气流道中的横截面占尾气流道横截面10%-90%、20%-80%、或40%-60%。
202.本发明提供的示例202:包括上述示例195至201中的任一项,其中,所述尾气电离除尘电场给所述尾气驻极体元件充电。
203.本发明提供的示例203:包括上述示例195至202中的任一项,其中,所述尾气驻极体元件具有多孔结构。
204.本发明提供的示例204:包括上述示例195至203中的任一项,其中,所述尾气驻极体元件为织品。
205.本发明提供的示例205:包括上述示例195至204中的任一项,其中,所述尾气除尘电场阳极内部为管状,所述尾气驻极体元件外部为管状,所述尾气驻极体元件外部套设于所述尾气除尘电场阳极内部。
206.本发明提供的示例206:包括上述示例195至205中的任一项,其中,所述尾气驻极体元件与所述尾气除尘电场阳极为可拆卸式连接。
207.本发明提供的示例207:包括上述示例195至206中的任一项,其中,所述尾气驻极体元件的材料包括具有驻极性能的无机化合物。
208.本发明提供的示例208:包括上述示例207,其中,所述无机化合物选自含氧化合物、含氮化合物或玻璃纤维中的一种或多种组合。
209.本发明提供的示例209:包括上述示例208,其中,所述含氧化合物选自金属基氧化物、含氧复合物、含氧的无机杂多酸盐中的一种或多种组合。
210.本发明提供的示例210:包括上述示例209,其中,所述金属基氧化物选自氧化铝、氧化锌、氧化锆、氧化钛、氧化钡、氧化钽、氧化硅、氧化铅、氧化锡中的一种或多种组合。
211.本发明提供的示例211:包括上述示例209,其中,所述金属基氧化物为氧化铝。
212.本发明提供的示例212:包括上述示例209,其中,所述含氧复合物选自钛锆复合氧化物或钛钡复合氧化物中的一种或多种组合。
213.本发明提供的示例213:包括上述示例209,其中,所述含氧的无机杂多酸盐选自钛酸锆、锆钛酸铅或钛酸钡中的一种或多种组合。
214.本发明提供的示例214:包括上述示例208,其中,所述含氮化合物为氮化硅。
215.本发明提供的示例215:包括上述示例195至214中的任一项,其中,所述尾气驻极体元件的材料包括具有驻极性能的有机化合物。
216.本发明提供的示例216:包括上述示例215,其中,所述有机化合物选自氟聚合物、聚碳酸酯、PP、PE、PVC、天然蜡、树脂、松香中的一种或多种组合。
217.本发明提供的示例217:包括上述示例216,其中,所述氟聚合物选自聚四氟乙烯、聚全氟乙丙烯、可溶性聚四氟乙烯、聚偏氟乙烯中的一种或多种组合。
218.本发明提供的示例218:包括上述示例216,其中,所述氟聚合物为聚四氟乙烯。
219.本发明提供的示例219:包括上述示例116至218中的任一项,其中,还包括尾气均风装置。
220.本发明提供的示例220:包括上述示例219,其中,所述尾气均风装置在所述尾气除尘系统入口与所述尾气除尘电场阳极和所述尾气除尘电场阴极形成的尾气电离除尘电场之间,当所述尾气除尘电场阳极为四方体时,所述尾气均风装置包括:设置于所述尾气除尘电场阳极一侧边的进气管和设置于另一侧边的出气管;其中,所述进气管与所述出气管相对立。
221.本发明提供的示例221:包括上述示例219,其中,所述尾气均风装置在所述尾气除尘系统入口与所述尾气除尘电场阳极和所述尾气除尘电场阴极形成的尾气电离除尘电场之间,当所述尾气除尘电场阳极为圆柱体时,所述尾气均风装置由若干可旋转的均风叶片组成。
222.本发明提供的示例222:包括上述示例219,其中,所述尾气均风装置第一文氏板均风机构和设置于所述尾气除尘电场阳极的出气端的第二文氏板均风机构,所述第一文氏板均风机构上开设有进气孔,所述第二文氏板均风机构上开设有出气孔,所述进气孔与所述出气孔错位排布,且正面进气侧面出气,形成旋风结构.
223.本发明提供的示例223:包括上述示例116至222中的任一项,其中,还包括补氧装置,用于在所述尾气电离除尘电场之前添加包括氧气的气体。
224.本发明提供的示例224:包括上述示例223,其中,所述补氧装置通过单纯增氧、通入外界空气、通入压缩空气和/或通入臭氧的方式添加氧气。
225.本发明提供的示例225:包括上述示例223或224,其中,至少根据尾气颗粒含量决定补氧量。
226.本发明提供的示例226:包括上述示例116至225中的任一项,其中,还包括除水装置,用于在所述尾气电场装置入口之前去除液体水。
227.本发明提供的示例227:包括上述示例226,其中,当尾气温度或发动机温度低于一定温度时,所述除水装置脱除尾气中的液体水。
228.本发明提供的示例228:包括上述示例227,其中,所述一定温度在90℃以上、100℃以下。
229.本发明提供的示例229:包括上述示例227,其中,所述一定温度在80℃以上、90℃以下。
230.本发明提供的示例230:包括上述示例227,其中,所述一定温度为80℃以下。
231.本发明提供的示例231:包括上述示例226至230,其中,所述除水装置为电凝装置。
232.本发明提供的示例232:包括上述示例116至231中的任一项,其中,还包括尾气降温装置,用于在所述尾气电场装置入口之前降低尾气温度。
233.本发明提供的示例233:包括上述示例232,其中,所述尾气降温装置包括换热单元,用于与发动机的尾气进行热交换,以将换热单元中液态的换热介质加热成气态的换热介质。
234.本发明提供的示例234:包括上述示例233,其中,所述换热单元包括:
尾气通过腔,与发动机的排气管路相连通,所述尾气通过腔用于供发动机的尾气通过;
介质气化腔,所述介质气化腔用于将液态换热介质与尾气发生热交换后转化成气态。
235.本发明提供的示例235:包括上述示例233或234,其中,还包括动力产生单元,所述动力产生单元用于将换热介质的热能和/或尾气的热能转换为机械能。
236.本发明提供的示例236:包括上述示例235,其中,所述动力产生单元包括涡扇。
237.本发明提供的示例237:包括上述示例236,其中,所述涡扇包括:
涡扇轴;
介质腔涡扇组件,安装在涡扇轴上,且所述介质腔涡扇组件位于介质气化腔中。
238.本发明提供的示例238:包括上述示例237,其中,所述介质腔涡扇组件包括介质腔导流扇和介质腔动力扇。
239.本发明提供的示例239:包括上述示例236至238中的任一项,其中,所述涡扇包括:
尾气腔涡扇组件,安装在涡扇轴上,且所述尾气腔涡扇组件位于尾气通过腔中。
240.本发明提供的示例240:包括上述示例239,其中,所述尾气腔涡扇组件包括尾气腔导流扇和尾气腔动力扇。
241.本发明提供的示例241:包括上述示例235至240中的任一项,其中,所述尾气降温装置还包括发电单元,所述发电单元用于将动力产生单元产生的机械能转换为电能。
242.本发明提供的示例242:包括上述示例241,其中,所述发电单元包括发电机定子和发电机转子,所述发电机转子与动力产生单元的涡扇轴相连接。
243.本发明提供的示例:包括上述示例241或242,其中,所述发电单元包括电池组件。
244.本发明提供的示例244:包括上述示例241至243中的任一项,其中,所述发电单元包括发电机调控组件,所述发电机调控组件用于调节发电机的电动转矩。
245.本发明提供的示例245:包括上述示例235至244中的任一项,其中,所述尾气降温装置还包括介质传输单元,所述介质传输单元连接于换热单元和动力产生单元之间。
246.本发明提供的示例246:包括上述示例245,其中,所述介质传输单元包括反推涵道。
247.本发明提供的示例247:包括上述示例245,其中,所述介质传输单元包括承压管路。
248.本发明提供的示例248:包括上述示例241至247中的任一项,其中,所述尾气降温装置还包括耦合单元,所述耦合单元电性连接于动力产生单元和发电单元之间。
249.本发明提供的示例249:包括上述示例248,其中,所述耦合单元包括电磁耦合器。
250.本发明提供的示例250:包括上述示例233至249中的任一项,其中,所述尾气降温装置还包括保温管路,所述保温管路连接于发动机的尾气管路和换热单元之间。
251.本发明提供的示例251:包括上述示例232至250中的任一项,其中,所述尾气降温装置包括风机,所述风机将空气通入所述尾气电场装置入口之前,对尾气起到降温的作用。
252.本发明提供的示例252:包括上述示例251,其中,通入的空气是尾气的50%至300%。
253.本发明提供的示例253:包括上述示例251,其中,通入的空气是尾气的100%至180%。
254.本发明提供的示例254:包括上述示例251,其中,通入的空气是尾气的120%至150%。
255.本发明提供的示例255:包括上述示例234,其中,所述补氧装置包括风机,所述风机将空气通入所述尾气电场装置入口之前,对尾气起到降温的作用。
256.本发明提供的示例256:包括上述示例255,其中,通入的空气是尾气的50%至300%。
257.本发明提供的示例257:包括上述示例255,其中,通入的空气是尾气的100%至180%。
258.本发明提供的示例258:包括上述示例255,其中,通入的空气是尾气的120%至150%。
259.本发明提供的示例259:包括上述示例1-258中的任一项,还包括尾气臭氧净化系统,所述尾气臭氧净化系统包括反应场,用于将臭氧流股与尾气流股混合反应。
260.本发明提供的示例260:包括上述示例259,其中,所述反应场包括管道和/或反应器。
261.本发明提供的示例261:包括上述示例260,其中,还包括如下技术特征中的至少一项:
1)管道的管段通径为100-200毫米;
2)管道的长度大于管径0.1倍;
3)所述反应器选自如下至少一种:
反应器一:所述反应器具有反应腔室,尾气与臭氧在所述反应腔室混合并反应;
反应器二:所述反应器包括若干蜂窝状腔体,用于提供尾气与臭氧混合并反应的空间;所述蜂窝状腔体内之间设有间隙,用于通入冷态介质,控制尾气与臭氧的反应温度;
反应器三:所述反应器包括若干载体单元,所述载体单元提供反应场地;
反应器四:所述反应器包括催化剂单元,所述催化剂单元用于促进尾气的氧化反应;
4)所述反应场设有臭氧进口,所述臭氧进口选自喷口、喷格栅、喷嘴、旋流喷嘴、设有文丘里管的喷口中的至少一种;
5)所述反应场设有臭氧进口,所述臭氧通过所述臭氧进口进入反应场与尾气进行接触,臭氧进口的设置形成如下方向中至少一种:与尾气流动的方向相反、与尾气流动的方向垂直、与尾气流动的方向相切、插入尾气流动方向、多个方向与尾气进行接触。
262.本发明提供的示例262:包括上述示例259至261中的中的任一项,其中,所述反应场包括排气管、蓄热体装置或催化器。
263.本发明提供的示例263:包括上述示例259至262中的中的任一项,其中,所述反应场的温度为-50-200℃。
264.本发明提供的示例264:包括上述示例263,其中,所述反应场的温度为60-70℃。
265.本发明提供的示例265:包括上述示例259至264中的中的任一项,其中,所述尾气臭氧净化系统还包括臭氧源,用于提供臭氧流股。
266.本发明提供的示例266:包括上述示例265,其中,所述臭氧源包括存储臭氧单元和/或臭氧发生器。
267.本发明提供的示例267:包括上述示例266,其中,所述臭氧发生器包括延面放电臭氧发生器、工频电弧臭氧发生器、高频感应臭氧发生器、低气压臭氧发生器、紫外线臭氧发生器、电解液臭氧发生器、化学药剂臭氧发生器和射线辐照粒子发生器中的一种或多种的组合。
268.本发明提供的示例268:包括上述示例266,其中,所述臭氧发生器包括电极,所述电极上设有催化剂层,所述催化剂层包括氧化催化键裂解选择性催化剂层。
269.本发明提供的示例269:包括上述示例268,其中,所述电极包括高压电极或设有阻挡介质层的高压电极,当所述电极包括高压电极时,所述氧化催化键裂解选择性催化剂层设于所述高压电极表面上,当所述电极包括阻挡介质层的高压电极时,所述氧化催化键裂解选择性催化剂层设于阻挡介质层的表面上。
270.本发明提供的示例270:包括上述示例269,其中,所述阻挡介质层选自陶瓷板、陶瓷管、石英玻璃板、石英板和石英管中的至少一种。
271.本发明提供的示例271:包括上述示例269,其中,当所述电极包括高压电极时,所述氧化催化键裂解选择性催化剂层的厚度为1-3mm;当所述电极包括阻挡介质层的高压电极时,所述氧化催化键裂解选择性催化剂层的负载量包括阻挡介质层的1-12wt%。
272.本发明提供的示例272:包括上述示例268至271中的中的任一项,其中,所述氧化催化键裂解选择性催化剂层包括如下重量百分比的各组分:
活性组分5-15%;
涂层85-95%;
其中,所述活性组分选自金属M和金属元素M的化合物中的至少一种,金属元素M选自碱土金属元素、过渡金属元素、第四主族金属元素、贵金属元素和镧系稀土元素中的至少一种;
所述涂层选自氧化铝、氧化铈、氧化锆、氧化锰、金属复合氧化物、多孔材料和层状材料中的至少一种,所述金属复合氧化物包括铝、铈、锆和锰中一种或多种金属的复合氧化物。
273.本发明提供的示例273:包括上述示例272,其中,所述碱土金属元素选自镁、锶和钙中的至少一种。
274.本发明提供的示例274:包括上述示例272,其中,所述过渡金属元素选自钛、锰、锌、铜、铁、镍、钴、钇和锆中的至少一种。
275.本发明提供的示例275:包括上述示例272,其中,所述第四主族金属元素为锡。
276.本发明提供的示例276:包括上述示例272,其中,所述贵金属元素选自铂、铑、钯、金、银和铱中的至少一种。
277.本发明提供的示例277:包括上述示例272,其中,所述镧系稀土元素选自镧、铈、镨和钐中的至少一种。
278.本发明提供的示例278:包括上述示例272,其中,所述金属元素M的化合物选自氧化物、硫化物、硫酸盐、磷酸盐、碳酸盐,以及钙钛矿中的至少一种。
279.本发明提供的示例279:包括上述示例272,其中,所述多孔材料选自分子筛、硅藻土、沸石和纳米碳管中的至少一种。
280.本发明提供的示例280:包括上述示例272,其中,所述层状材料选自石墨烯和石墨中的至少一种。
281.本发明提供的示例281:包括上述示例259至280中的任一项,其中,所述尾气臭氧净化系统还包括臭氧量控制装置,用于控制臭氧量以致有效氧化尾气中待处理的气体组分,所述臭氧量控制装置包括控制单元。
282.本发明提供的示例282:包括上述示例281,其中,所述臭氧量控制装置还包括臭氧处理前尾气组分检测单元,用于检测臭氧处理前尾气组分含量。
283.本发明提供的示例283:包括上述示例281至282中的任一项,其中,所述控制单元根据所述臭氧处理前尾气组分含量控制混合反应所需臭氧量。
284.本发明提供的示例284:包括上述示例282或283,其中,所述臭氧处理前尾气组分检测单元选自以下检测单元中至少一个:
第一挥发性有机化合物检测单元,用于检测臭氧处理前尾气中挥发性有机化合物含量;
第一CO检测单元,用于检测臭氧处理前尾气中CO含量;
第一氮氧化物检测单元,用于检测臭氧处理前尾气中氮氧化物含量。
285.本发明提供的示例285:包括上述示例284,其中,所述控制单元根据至少一个所述臭氧处理前尾气组分检测单元的输出值控制混合反应所需臭氧量。
286.本发明提供的示例286:包括上述示例281至285中的任一项,其中,所述控制单元用于按照预设的数学模型控制混合反应所需臭氧量。
287.本发明提供的示例287:包括上述示例281至286中的任一项,其中,所述控制单元用于按照理论估计值控制混合反应所需臭氧量。
288.本发明提供的示例288:包括上述示例287中的任一项,其中,所述理论估计值为:臭氧通入量与尾气中待处理物的摩尔比为2-10。
289.本发明提供的示例289:包括上述示例281至288中的任一项,其中,所述臭氧量控制装置包括臭氧处理后尾气组分检测单元,用于检测臭氧处理后尾气组分含量。
290.本发明提供的示例290:包括上述示例281至289中的任一项,其中,所述控制单元根据所述臭氧处理后尾气组分含量控制混合反应所需臭氧量。
291.本发明提供的示例291:包括上述示例289或290,其中,所述臭氧处理后尾气组分检测单元选自以下检测单元中至少一个:
第一臭氧检测单元,用于检测臭氧处理后尾气中臭氧含量;
第二挥发性有机化合物检测单元,用于检测臭氧处理后尾气中挥发性有机化合物含量;
第二CO检测单元,用于检测臭氧处理后尾气中CO含量;
第二氮氧化物检测单元,用于检测臭氧处理后尾气中氮氧化物含量。
292.本发明提供的示例292:包括上述示例291,其中,所述控制单元根据至少一个所述臭氧处理后尾气组分检测单元的输出值控制臭氧量。
293.本发明提供的示例293:包括上述示例259至292中的任一项,其中,所述尾气臭氧 净化系统还包括脱硝装置,用于脱除臭氧流股与尾气流股混合反应产物中的硝酸。
294.本发明提供的示例294:包括上述示例293,其中,所述脱硝装置包括电凝装置,所述电凝装置包括:
电凝流道;
第一电极,所述第一电极位于电凝流道中;
第二电极。
295.本发明提供的示例295:包括上述示例294,其中,所述第一电极为固体、液体、气体分子团、等离子体、导电混合态物质、生物体自然混合导电物质、或物体人工加工形成导电物质中的一种或多种形态的组合。
296.本发明提供的示例296:包括上述示例294或295,其中,所述第一电极为固态金属、石墨、或304钢。
297.本发明提供的示例297:包括上述示例294至296中的任一项,其中,所述第一电极呈点状、线状、网状、孔板状、板状、针棒状、球笼状、盒状、管状、自然形态物质、或加工形态物质。
298.本发明提供的示例298:包括上述示例294至297中的任一项,其中,所述第一电极上设有前通孔。
299.本发明提供的示例299:包括上述示例298,其中,所述前通孔的形状为多角形、圆形、椭圆形、正方形、长方形、梯形、或菱形。
300.本发明提供的示例300:包括上述示例298或299,其中,所述前通孔的孔径为0.1-3毫米。
301.本发明提供的示例301:包括上述示例294至300中的任一项,其中,所述第二电极呈多层网状、网状、孔板状、管状、桶状、球笼状、盒状、板状、颗粒堆积层状、折弯板状、或面板状。
302.本发明提供的示例302:包括上述示例294至301中的任一项,其中,所述第二电极上设有后通孔。
303.本发明提供的示例303:包括上述示例302,其中,所述后通孔呈多角形、圆形、椭圆形、正方形、长方形、梯形、或菱形。
304.本发明提供的示例304:包括上述示例302或303,其中,所述后通孔的孔径为0.1-3毫米。
305.本发明提供的示例305:包括上述示例294至304中的任一项,其中,所述第二电极 由导电物质制成。
306.本发明提供的示例306:包括上述示例294至305中的任一项,其中,所述第二电极的表面具有导电物质。
307.本发明提供的示例307:包括上述示例294至306中的任一项,其中,所述第一电极和第二电极之间具有电凝电场,所述电凝电场为点面电场、线面电场、网面电场、点桶电场、线桶电场、或网桶电场中的一种或多种电场的组合。
308.本发明提供的示例308:包括上述示例294至307中的任一项,其中,所述第一电极呈线状,所述第二电极呈面状。
309.本发明提供的示例309:包括上述示例294至308中的任一项,其中,所述第一电极垂直于第二电极。
310.本发明提供的示例310:包括上述示例294至309中的任一项,其中,所述第一电极与第二电极相平行。
311.本发明提供的示例311:包括上述示例294至310中的任一项,其中,所述第一电极呈曲线状或圆弧状。
312.本发明提供的示例312:包括上述示例294至311中的任一项,其中,所述第一电极和第二电极均呈面状,且所述第一电极与第二电极相平行。
313.本发明提供的示例313:包括上述示例294至312中的任一项,其中,所述第一电极采用金属丝网。
314.本发明提供的示例314:包括上述示例294至313中的任一项,其中,所述第一电极呈平面状或球面状。
315.本发明提供的示例315:包括上述示例294至314中的任一项,其中,所述第二电极呈曲面状或球面状。
316.本发明提供的示例316:包括上述示例294至315中的任一项,其中,所述第一电极呈点状、线状、或网状,所述第二电极呈桶状,所述第一电极位于第二电极的内部,且所述第一电极位于第二电极的中心对称轴上。
317.本发明提供的示例317:包括上述示例294至316中的任一项,其中,所述第一电极与电源的一个电极电性连接,所述第二电极与电源的另一个电极电性连接。
318.本发明提供的示例318:包括上述示例294至317中的任一项,其中,所述第一电极与电源的阴极电性连接,所述第二电极与电源的阳极电性连接
319.本发明提供的示例319:包括上述示例317或318,其中,所述电源的电压为5-50KV。
320.本发明提供的示例320:包括上述示例317至319中的任一项,其中,所述电源的电压小于起始起晕电压。
321.本发明提供的示例321:包括上述示例317至320中的任一项,其中,所述电源的电压为0.1kv/mm-2kv/mm。
322.本发明提供的示例322:包括上述示例317至321中的任一项,其中,所述电源的电压波形为直流波形、正弦波、或调制波形。
323.本发明提供的示例323:包括上述示例317至322中的任一项,其中,所述电源为交流电源,所述电源的变频脉冲范围为0.1Hz-5GHz。
324.本发明提供的示例324:包括上述示例294至323中的任一项,其中,所述第一电极和第二电极均沿左右方向延伸,所述第一电极的左端位于第二电极的左端的左方。
325.本发明提供的示例325:包括上述示例294至324中的任一项,其中,所述第二电极有两个,所述第一电极位于两个第二电极之间。
326.本发明提供的示例326:包括上述示例294至325中的任一项,其中,所述第一电极和第二电极之间的距离为5-50毫米。
327.本发明提供的示例327:包括上述示例294至326中的任一项,其中,所述第一电极和第二电极构成吸附单元,且所述吸附单元有多个。
328.本发明提供的示例328:包括上述示例327,其中,全部吸附单元沿左右方向、前后方向、斜向、或螺旋方向中的一个方向或多个方向上进行分布。
329.本发明提供的示例329:包括上述示例294至328中的任一项,其中,还包括电凝壳体,所述电凝壳体包括电凝进口、电凝出口、及所述电凝流道,所述电凝流道的两端分别与电凝进口和电凝出口相连通。
330.本发明提供的示例330:包括上述示例329,其中,所述电凝进口呈圆形,且所述电凝进口的直径为300-1000mm、或500mm。
331.本发明提供的示例331:包括上述示例329或330,其中,所述电凝出口呈圆形,且所述电凝出口的直径为300-1000mm、或500mm。
332.本发明提供的示例332:包括上述示例329至331中的任一项,其中,所述电凝壳体包括由电凝进口至电凝出口方向依次分布的第一壳体部、第二壳体部、及第三壳体部,所述电凝进口位于第一壳体部的一端,所述电凝出口位于第三壳体部的一端。
333.本发明提供的示例333:包括上述示例332,其中,所述第一壳体部的轮廓大小由电凝进口至电凝出口方向逐渐增大。
334.本发明提供的示例334:包括上述示例332或333,其中,所述第一壳体部呈直管状。
335.本发明提供的示例335:包括上述示例332至334中的任一项,其中,所述第二壳体部呈直管状,且所述第一电极和第二电极安装在第二壳体部中。
336.本发明提供的示例336:包括上述示例332至335中的任一项,其中,所述第三壳体部的轮廓大小由电凝进口至电凝出口方向逐渐减小。
337.本发明提供的示例337:包括上述示例332至336中的任一项,其中,所述第一壳体部、第二壳体部、及第三壳体部的截面均呈矩形。
338.本发明提供的示例338:包括上述示例329至337中的任一项,其中,所述电凝壳体的材质为不锈钢、铝合金、铁合金、布、海绵、分子筛、活性炭、泡沫铁、或泡沫碳化硅。
339.本发明提供的示例339:包括上述示例294至338中的任一项,其中,所述第一电极通过电凝绝缘件与电凝壳体相连接。
340.本发明提供的示例340:包括上述示例339,其中,所述电凝绝缘件的材质为绝缘云母。
341.本发明提供的示例341:包括上述示例339或340,其中,所述电凝绝缘件呈柱状、或塔状。
342.本发明提供的示例342:包括上述示例294至341中的任一项,其中,所述第一电极上设有呈圆柱形的前连接部,且所述前连接部与电凝绝缘件固接。
343.本发明提供的示例343:包括上述示例294至342中的任一项,其中,所述第二电极上设有呈圆柱形的后连接部,且所述后连接部与电凝绝缘件固接。
344.本发明提供的示例344:包括上述示例294至343中的任一项,其中,所述第一电极的截面面积与电凝流道的截面面积比为99%-10%、或90-10%、或80-20%、或70-30%、或60-40%、或50%。
345.本发明提供的示例345:包括上述示例293至344中的任一项,其中,所述脱硝装置包括冷凝单元,用于将臭氧处理后的尾气进行冷凝,实现气液分离。
346.本发明提供的示例346:包括上述示例293至345中的任一项,其中,所述脱硝装置包括淋洗单元,用于将臭氧处理后的尾气进行淋洗。
347.本发明提供的示例347:包括上述示例346,其中,所述脱硝装置还包括淋洗液单元,用于向所述淋洗单元提供淋洗液。
348.本发明提供的示例348:包括上述示例347,其中,所述淋洗液单元中淋洗液包括水和/或碱。
349.本发明提供的示例349:包括上述示例293至348中的任一项,其中,所述脱硝装置还包括脱硝液收集单元,用于存储尾气中脱除的硝酸水溶液和/或硝酸盐水溶液。
350.本发明提供的示例350:包括上述示例349,其中,当所述脱硝液收集单元中存储有硝酸水溶液时,所述脱硝液收集单元设有碱液加入单元,用于与硝酸形成硝酸盐。
351.本发明提供的示例351:包括上述示例259至350中的任一项,其中,所述尾气臭氧净化系统还包括臭氧消解器,用于消解经反应场处理后的尾气中的臭氧。
352.本发明提供的示例352:包括上述示例351,其中,所述臭氧消解器选自紫外线臭氧消解器和催化臭氧消解器中的至少一种。
353.本发明提供的示例353:包括上述示例259至352中的任一项,其中,所述尾气臭氧净化系统还包括第一脱硝装置,用于脱除尾气中氮氧化物;所述反应场用于将经所述第一脱硝装置处理后的尾气与臭氧流股混合反应,或者,用于将尾气在经所述第一脱硝装置处理前先与臭氧流股混合反应。
354.本发明提供的示例354:包括上述示例353,其中,所述第一脱硝装置选自非催化还原装置、选择性催化还原装置、非选择性催化还原装置和电子束脱硝装置中的至少一种。
355.本发明提供的示例355:包括上述示例1至354中的任一项,其中,还包括发动机。
356.本发明提供的示例356:一种发动机进气电场除尘方法,包括以下步骤:
使含尘气体通过进气除尘电场阳极和进气除尘电场阴极产生的电离除尘电场;
进气电场积尘时,进行清尘处理。
357.本发明提供的示例357:包括示例356的发动机进气电场除尘方法,其中,利用电场反电晕放电现象完成清尘处理。
358.本发明提供的示例358:包括示例356的发动机进气电场除尘方法,其中,利用电场反电晕放电现象,增高电压,限制入注电流,完成清尘处理。
359.本发明提供的示例359:包括示例356的发动机进气电场除尘方法,其中,利用电场反电晕放电现象,增高电压,限制入注电流,使发生在阳极积尘位置的急剧放电产生等离子,所述等离子使灰尘有机成分深度氧化,高分子键断裂,形成小分子二氧化碳和水,完成清尘处理。
360.本发明提供的示例360:包括示例356至359任一项的发动机进气电场除尘方法,其中,当所述电场装置检测到电场电流增加到一个给定值,所述电场装置进行清尘处理。
361.本发明提供的示例361:包括示例356至360任一项的发动机进气电场除尘方法,其中,所述除尘电场阴极包括至少一根电极棒。
362.本发明提供的示例362:包括示例361的发动机进气电场除尘方法,其中,所述电极棒的直径不大于3mm。
363.本发明提供的示例363:包括示例361或362的发动机进气电场除尘方法,其中,所述电极棒的形状呈针状、多角状、毛刺状、螺纹杆状或柱状。
364.本发明提供的示例364:包括示例356至363任一项的发动机进气电场除尘方法,其中,所述除尘电场阳极由中空的管束组成。
365.本发明提供的示例365:包括示例364的发动机进气电场除尘方法,其中,所述阳极管束的中空的截面采用圆形或多边形。
366.本发明提供的示例366:包括示例365的发动机进气电场除尘方法,其中,所述多边形为六边形。
367.本发明提供的示例367:包括示例364至366任一项的发动机进气电场除尘方法,其中,所述除尘电场阳极的管束呈蜂窝状。
368.本发明提供的示例368:包括示例356至367任一项的发动机进气电场除尘方法,其中,所述除尘电场阴极穿射于所述除尘电场阳极内。
369.本发明提供的示例369:包括示例356至368任一项的发动机进气电场除尘方法,其中,当检测到的电场电流增加到一个给定值时,进行清尘处理。
370.本发明提供的示例370:一种发动机尾气电场除炭黑方法,包括以下步骤:
使含尘气体通过尾气除尘电场阳极和尾气除尘电场阴极产生的电离除尘电场;
电场积尘时,进行清理炭黑处理。
371.本发明提供的示例371:包括示例370的发动机尾气电场除炭黑方法,其中,利用电场反电晕放电现象完成清理炭黑处理。
372.本发明提供的示例372:包括示例370的发动机尾气电场除炭黑方法,其中,利用电场反电晕放电现象,增高电压,限制入注电流,完成清理炭黑处理。
373.本发明提供的示例373:包括示例370的发动机尾气电场除炭黑方法,其中,利用电场反电晕放电现象,增高电压,限制入注电流,使发生在阳极积尘位置的急剧放电产生等离子,所述等离子使清理炭黑有机成分深度氧化,高分子键断裂,形成小分子二氧化碳和水,完成清理炭黑处理。
374.本发明提供的示例374:包括示例370至373任一项的发动机尾气电场除炭黑方法,其中,当所述电场装置检测到电场电流增加到一个给定值,所述电场装置进行清尘处理。
375.本发明提供的示例375:包括示例370至374任一项的发动机尾气电场除炭黑方法, 其中,所述除尘电场阴极包括至少一根电极棒。
376.本发明提供的示例376:包括示例375的发动机尾气电场除炭黑方法,其中,所述电极棒的直径不大于3mm。
377.本发明提供的示例377:包括示例375或376的发动机尾气电场除炭黑方法,其中,所述电极棒的形状呈针状、多角状、毛刺状、螺纹杆状或柱状。
378.本发明提供的示例378:包括示例370至377任一项的发动机尾气电场除炭黑方法,其中,所述除尘电场阳极由中空的管束组成。
379.本发明提供的示例379:包括示例378的发动机尾气电场除炭黑方法,其中,所述阳极管束的中空的截面采用圆形或多边形。
380.本发明提供的示例380:包括示例379的发动机尾气电场除炭黑方法,其中,所述多边形为六边形。
381.本发明提供的示例381:包括示例378至380任一项的发动机尾气电场除炭黑方法,其中,所述除尘电场阳极的管束呈蜂窝状。
382.本发明提供的示例382:包括示例370至381任一项的发动机尾气电场除炭黑方法,其中,所述除尘电场阴极穿射于所述除尘电场阳极内。
383.本发明提供的示例383:包括示例370至382任一项的发动机尾气电场除炭黑方法,其中,当检测到的电场电流增加到一个给定值时,进行清理炭黑处理。
384.本发明提供的示例384:一种给发动机进气增氧的方法,包括以下步骤:
使进气通过一个流道;
在流道中产生电场,所述电场不与所述流道垂直,所述电场包括进口和出口。
385.本发明提供的示例385:包括示例384的给发动机进气增氧的方法,其中,所述电场包括第一阳极和第一阴极,所述第一阳极和第一阴极形成所述流道,所述流道接通所述进口和出口。
386.本发明提供的示例386:包括示例384至385任一项的给发动机进气增氧的方法,其中,所述第一阳极和第一阴极电离所述进气中的氧气。
387.本发明提供的示例387:包括示例384至386任一项的给发动机进气增氧的方法,其中,所述电场包括第二电极,所述第二电极设置在或靠近所述进口。
388.本发明提供的示例388:包括示例387的给发动机进气增氧的方法,其中,所述第二电极为阴极。
389.本发明提供的示例389:包括示例387或388的给发动机进气增氧的方法,其中,所 述第二电极是所述第一阴极的延伸。
390.本发明提供的示例390:包括示例389的给发动机进气增氧的方法,其中,所述第二电极与所述第一阳极具有夹角α,且0°<α≤125°、或45°≤α≤125°、或60°≤α≤100°、或α=90°。
391.本发明提供的示例391:包括示例384至390任一项的给发动机进气增氧的方法,其中,所述电场包括第三电极,所述第三电极设置在或靠近所述出口。
392.本发明提供的示例392:包括示例391的给发动机进气增氧的方法,其中,所述第三电极为阳极。
393.本发明提供的示例393:包括示例391或392的给发动机进气增氧的方法,其中,所述第三电极是所述第一阳极的延伸。
394.本发明提供的示例394:包括示例393的给发动机进气增氧的方法,其中,所述第三电极与所述第一阴极具有夹角α,且0°<α≤125°、或45°≤α≤125°、或60°≤α≤100°、或α=90°。
395.本发明提供的示例395:包括示例389至394任一项的给发动机进气增氧的方法,其中,所述第三电极与所述第一阳极和第一阴极独立设置。
396.本发明提供的示例396:包括示例387至395任一项的给发动机进气增氧的方法,其中,所述第二电极与所述第一阳极和第一阴极独立设置。
397.本发明提供的示例397:包括示例385至396任一项的给发动机进气增氧的方法,其中,所述第一阴极包括至少一根电极棒。
398.本发明提供的示例398:包括示例385至397任一项的给发动机进气增氧的方法,其中,所述第一阳极由中空的管束组成。
399.本发明提供的示例399:包括示例398的给发动机进气增氧的方法,其中,所述阳极管束的中空的截面采用圆形或多边形。
400.本发明提供的示例400:包括示例399的给发动机进气增氧的方法,其中,所述多边形为六边形。
401.本发明提供的示例401:包括示例398至400任一项的给发动机进气增氧的方法,其中,所述第一阳极的管束呈蜂窝状。
402.本发明提供的示例402:包括示例385至401任一项的给发动机进气增氧的方法,其中,所述第一阴极穿射于所述第一阳极内。
403.本发明提供的示例403:包括示例385至402任一项的给发动机进气增氧的方法,其中,所述电场作用于所述流道中的氧气离子,增加氧气离子流量,增加所述出口进气含氧量。
404.本发明提供的示例404:一种减少发动机进气除尘电场耦合的方法,包括以下步骤:
选择进气除尘电场阳极参数或/和进气除尘电场阴极参数以减少电场耦合次数。
405.本发明提供的示例405:包括示例404的减少发动机进气除尘电场耦合的方法,其中,包括选择所述进气除尘电场阳极的集尘面积与进气除尘电场阴极的放电面积的比。
406.本发明提供的示例406:包括示例405的减少发动机进气除尘电场耦合的方法,其中,包括选择所述进气除尘电场阳极的积尘面积与所述进气除尘电场阴极的放电面积的比为1.667:1-1680:1。
407.本发明提供的示例407:包括示例405的减少发动机进气除尘电场耦合的方法,其中,包括选择所述进气除尘电场阳极的积尘面积与所述进气除尘电场阴极的放电面积的比为6.67:1-56.67:1。
408.本发明提供的示例408:包括示例404至407任一项的减少发动机进气除尘电场耦合的方法,其中,所述进气除尘电场阴极直径为1-3毫米,所述进气除尘电场阳极与所述进气除尘电场阴极的极间距为2.5-139.9毫米;所述进气除尘电场阳极的积尘面积与所述进气除尘电场阴极的放电面积的比为1.667:1-1680:1。
409.本发明提供的示例409:包括示例404至408任一项的减少发动机进气除尘电场耦合的方法,其中,包括选择所述进气除尘电场阳极和所述进气除尘电场阴极的极间距小于150mm。
410.本发明提供的示例410:包括示例404至408任一项的减少发动机进气除尘电场耦合的方法,其中,包括选择所述进气除尘电场阳极与所述进气除尘电场阴极的极间距为2.5-139.9mm。
411.本发明提供的示例411:包括示例404至408任一项的减少发动机进气除尘电场耦合的方法,其中,包括选择所述进气除尘电场阳极与所述进气除尘电场阴极的极间距为5-100mm。
412.本发明提供的示例412:包括示例404至411任一项的减少发动机进气除尘电场耦合的方法,其中,包括选择所述进气除尘电场阳极长度为10-180mm。
413.本发明提供的示例413:包括示例404至411任一项的减少发动机进气除尘电场耦合的方法,其中,包括选择所述进气除尘电场阳极长度为60-180mm。
414.本发明提供的示例414:包括示例404至413任一项的减少发动机进气除尘电场耦合的方法,其中,包括选择所述进气除尘电场阴极长度为30-180mm。
415.本发明提供的示例415:包括示例404至413任一项的减少发动机进气除尘电场耦合的方法,其中,包括选择所述进气除尘电场阴极长度为54-176mm。
416.本发明提供的示例416:包括示例404至415任一项的减少发动机进气除尘电场耦合 的方法,其中,包括选择所述进气除尘电场阴极包括至少一根电极棒。
417.本发明提供的示例417:包括示例416的减少发动机进气除尘电场耦合的方法,其中,包括选择所述电极棒的直径不大于3mm。
418.本发明提供的示例418:包括示例416或417的减少发动机进气除尘电场耦合的方法,其中,包括选择所述电极棒的形状呈针状、多角状、毛刺状、螺纹杆状或柱状。
419.本发明提供的示例419:包括示例404至418任一项的减少发动机进气除尘电场耦合的方法,其中,包括选择所述进气除尘电场阳极由中空的管束组成。
420.本发明提供的示例420:包括示例419的减少发动机进气除尘电场耦合的方法,其中,包括选择所述阳极管束的中空的截面采用圆形或多边形。
421.本发明提供的示例421:包括示例420的减少发动机进气除尘电场耦合的方法,其中,包括选择所述多边形为六边形。
422.本发明提供的示例422:包括示例419至421任一项的减少发动机进气除尘电场耦合的方法,其中,包括选择所述进气除尘电场阳极的管束呈蜂窝状。
423.本发明提供的示例423:包括示例404至422任一项的减少发动机进气除尘电场耦合的方法,其中,包括选择所述进气除尘电场阴极穿射于所述进气除尘电场阳极内。
424.本发明提供的示例424:包括示例404至423任一项的减少发动机进气除尘电场耦合的方法,其中,包括选择的所述进气除尘电场阳极或/和进气除尘电场阴极尺寸使电场耦合次数≤3。
425.本发明提供的示例425:一种减少发动机尾气除尘电场耦合的方法,包括以下步骤:
选择尾气除尘电场阳极参数或/和尾气除尘电场阴极参数以减少电场耦合次数。
426.本发明提供的示例426:包括示例425的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述尾气除尘电场阳极的集尘面积与尾气除尘电场阴极的放电面积的比。
427.本发明提供的示例427:包括示例426的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述尾气除尘电场阳极的积尘面积与所述尾气除尘电场阴极的放电面积的比为1.667:1-1680:1。
428.本发明提供的示例428:包括示例426的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述尾气除尘电场阳极的积尘面积与所述尾气除尘电场阴极的放电面积的比为6.67:1-56.67:1。
429.本发明提供的示例429:包括示例425至428任一项的减少发动机尾气除尘电场耦合的方法,其中,所述尾气除尘电场阴极直径为1-3毫米,所述尾气除尘电场阳极与所述尾气 除尘电场阴极的极间距为2.5-139.9毫米;所述尾气除尘电场阳极的积尘面积与所述尾气除尘电场阴极的放电面积的比为1.667:1-1680:1。
430.本发明提供的示例430:包括示例425至429任一项的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述尾气除尘电场阳极和所述尾气除尘电场阴极的极间距小于150mm。
431.本发明提供的示例431:包括示例425至429任一项的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述尾气除尘电场阳极与所述尾气除尘电场阴极的极间距为2.5-139.9mm。
432.本发明提供的示例432:包括示例425至429任一项的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述尾气除尘电场阳极与所述尾气除尘电场阴极的极间距为5-100mm。
433.本发明提供的示例433:包括示例425至432任一项的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述尾气除尘电场阳极长度为10-180mm。
434.本发明提供的示例434:包括示例425至432任一项的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述尾气除尘电场阳极长度为60-180mm。
435.本发明提供的示例435:包括示例425至434任一项的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述尾气除尘电场阴极长度为30-180mm。
436.本发明提供的示例436:包括示例425至434任一项的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述尾气除尘电场阴极长度为54-176mm。
437.本发明提供的示例437:包括示例425至436任一项的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述尾气除尘电场阴极包括至少一根电极棒。
438.本发明提供的示例438:包括示例437的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述电极棒的直径不大于3mm。
439.本发明提供的示例439:包括示例437或438的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述电极棒的形状呈针状、多角状、毛刺状、螺纹杆状或柱状。
440.本发明提供的示例440:包括示例425至439任一项的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述尾气除尘电场阳极由中空的管束组成。
441.本发明提供的示例441:包括示例440的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述阳极管束的中空的截面采用圆形或多边形。
442.本发明提供的示例442:包括示例441的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述多边形为六边形。
443.本发明提供的示例443:包括示例440至442任一项的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述尾气除尘电场阳极的管束呈蜂窝状。
444.本发明提供的示例444:包括示例425至443任一项的减少发动机尾气除尘电场耦合的方法,其中,包括选择所述尾气除尘电场阴极穿射于所述尾气除尘电场阳极内。
445.本发明提供的示例445:包括示例425至444任一项的减少发动机尾气除尘电场耦合的方法,其中,包括选择的所述尾气除尘电场阳极或/和尾气除尘电场阴极尺寸使电场耦合次数≤3。
446.本发明提供的示例446:一种发动机尾气除尘方法,包括以下步骤:尾气温度低于100℃时,脱除尾气中的液体水,然后电离除尘。
447.本发明提供的示例447:包括示例446的发动机尾气除尘方法,其中,尾气温度≥100℃时,对尾气进行电离除尘。
448.本发明提供的示例448:包括示例446或447的发动机尾气除尘方法,其中,尾气温度≤90℃时,脱除尾气中的液体水,然后电离除尘。
449.本发明提供的示例449:包括示例446或447的发动机尾气除尘方法,其中,尾气温度≤80℃时,脱除尾气中的液体水,然后电离除尘。
450.本发明提供的示例450:包括示例446或447的发动机尾气除尘方法,其中,尾气温度≤70℃时,脱除尾气中的液体水,然后电离除尘。
451.本发明提供的示例451:包括示例446或447的发动机尾气除尘方法,其中,采用电凝除雾方法脱除尾气中的液体水,然后电离除尘。
452.本发明提供的示例452:一种发动机尾气除尘方法,包括以下步骤:在尾气电离除尘电场之前添加包括氧气的气体,进行电离除尘。
453.本发明提供的示例453:包括示例452的发动机尾气除尘方法,其中,通过单纯增氧、通入外界空气、通入压缩空气和/或通入臭氧的方式添加氧气。
454.本发明提供的示例454:包括示例452或453的发动机尾气除尘方法,其中,至少根据尾气颗粒含量决定补氧量。
455.本发明提供的示例455:一种发动机尾气除尘方法,包括如下步骤:
1)利用尾气电离除尘电场吸附尾气中的颗粒物;
2)利用尾气电离除尘电场给尾气驻极体元件充电。
456.本发明提供的示例456:包括示例455的发动机尾气除尘方法,其中,所述尾气驻极体元件靠近尾气电场装置出口,或者,所述尾气驻极体元件设于尾气电场装置出口。
457.本发明提供的示例457:包括示例455的发动机尾气除尘方法,其中,所述尾气除尘电场阳极和所述尾气除尘电场阴极形成尾气流道,所述尾气驻极体元件设于所述尾气流道中。
458.本发明提供的示例458:包括示例457的发动机尾气除尘方法,其中,所述尾气流道包括尾气流道出口,所述尾气驻极体元件靠近所述尾气流道出口,或者,所述尾气驻极体元件设于所述尾气流道出口。
459.本发明提供的示例459:包括示例452至458任一项的发动机尾气除尘方法,其中,当尾气电离除尘电场无上电驱动电压时,利用充电的尾气驻极体元件吸附尾气中的颗粒物。
460.本发明提供的示例460:包括示例458的发动机尾气除尘方法,其中,在充电的尾气驻极体元件吸附一定的尾气中的颗粒物后,将其替换为新的尾气驻极体元件。
461.本发明提供的示例461:包括示例460的发动机尾气除尘方法,其中,替换为新的尾气驻极体元件后重新启动尾气电离除尘电场吸附尾气中的颗粒物,并给新的尾气驻极体元件充电。
462.本发明提供的示例462:包括示例455至461任一项的发动机尾气除尘方法,其中,所述尾气驻极体元件的材料包括具有驻极性能的无机化合物。
463.本发明提供的示例463:包括示例462的发动机尾气除尘方法,其中,所述无机化合物选自含氧化合物、含氮化合物或玻璃纤维中的一种或多种组合。
464.本发明提供的示例464:包括示例463的发动机尾气除尘方法,其中,所述含氧化合物选自金属基氧化物、含氧复合物、含氧的无机杂多酸盐中的一种或多种组合。
465.本发明提供的示例465:包括示例464的发动机尾气除尘方法,其中,所述金属基氧化物选自氧化铝、氧化锌、氧化锆、氧化钛、氧化钡、氧化钽、氧化硅、氧化铅、氧化锡中的一种或多种组合。
466.本发明提供的示例466:包括示例464的发动机尾气除尘方法,其中,所述金属基氧化物为氧化铝。
467.本发明提供的示例467:包括示例464的发动机尾气除尘方法,其中,所述含氧复合物选自钛锆复合氧化物或钛钡复合氧化物中的一种或多种组合。
468.本发明提供的示例468:包括示例464的发动机尾气除尘方法,其中,所述含氧的无机杂多酸盐选自钛酸锆、锆钛酸铅或钛酸钡中的一种或多种组合。
469.本发明提供的示例469:包括示例463的发动机尾气除尘方法,其中,所述含氮化合物为氮化硅。
470.本发明提供的示例470:包括示例455至461任一项的发动机尾气除尘方法,其中, 所述尾气驻极体元件的材料包括具有驻极性能的有机化合物。
471.本发明提供的示例471:包括示例470的发动机尾气除尘方法,其中,所述有机化合物选自氟聚合物、聚碳酸酯、PP、PE、PVC、天然蜡、树脂、松香中的一种或多种组合。
472.本发明提供的示例472:包括示例471的发动机尾气除尘方法,其中,所述氟聚合物选自聚四氟乙烯、聚全氟乙丙烯、可溶性聚四氟乙烯、聚偏氟乙烯中的一种或多种组合。
473.本发明提供的示例473:包括示例471的发动机尾气除尘方法,其中,所述氟聚合物为聚四氟乙烯。
474.本发明提供的示例474:一种发动机进气除尘方法,包括如下步骤:
1)利用进气电离除尘电场吸附进气中的颗粒物;
2)利用进气电离除尘电场给进气驻极体元件充电。
475.本发明提供的示例475:包括示例474的发动机进气除尘方法,其中,所述进气驻极体元件靠近进气电场装置出口,或者,所述进气驻极体元件设于进气电场装置出口。
476.本发明提供的示例476:包括示例474的发动机进气除尘方法,其中,所述进气除尘电场阳极和所述进气除尘电场阴极形成进气流道,所述进气驻极体元件设于所述进气流道中。
477.本发明提供的示例477:包括示例476的发动机进气除尘方法,其中,所述进气流道包括进气流道出口,所述进气驻极体元件靠近所述进气流道出口,或者,所述进气驻极体元件设于所述进气流道出口。
478.本发明提供的示例478:包括示例474至477任一项的发动机进气除尘方法,其中,当进气电离除尘电场无上电驱动电压时,利用充电的进气驻极体元件吸附进气中的颗粒物。
479.本发明提供的示例479:包括示例477的发动机进气除尘方法,其中,在充电的进气驻极体元件吸附一定的进气中的颗粒物后,将其替换为新的进气驻极体元件。
480.本发明提供的示例480:包括示例479的发动机进气除尘方法,其中,替换为新的进气驻极体元件后重新启动进气电离除尘电场吸附进气中的颗粒物,并给新的进气驻极体元件充电。
481.本发明提供的示例481:包括示例474至480任一项的发动机进气除尘方法,其中,所述进气驻极体元件的材料包括具有驻极性能的无机化合物。
482.本发明提供的示例482:包括示例481的发动机进气除尘方法,其中,所述无机化合物选自含氧化合物、含氮化合物或玻璃纤维中的一种或多种组合。
483.本发明提供的示例483:包括示例482的发动机进气除尘方法,其中,所述含氧化合物选自金属基氧化物、含氧复合物、含氧的无机杂多酸盐中的一种或多种组合。
484.本发明提供的示例484:包括示例483的发动机进气除尘方法,其中,所述金属基氧化物选自氧化铝、氧化锌、氧化锆、氧化钛、氧化钡、氧化钽、氧化硅、氧化铅、氧化锡中的一种或多种组合。
485.本发明提供的示例485:包括示例483的发动机进气除尘方法,其中,所述金属基氧化物为氧化铝。
486.本发明提供的示例486:包括示例483的发动机进气除尘方法,其中,所述含氧复合物选自钛锆复合氧化物或钛钡复合氧化物中的一种或多种组合。
487.本发明提供的示例487:包括示例483的发动机进气除尘方法,其中,所述含氧的无机杂多酸盐选自钛酸锆、锆钛酸铅或钛酸钡中的一种或多种组合。
488.本发明提供的示例488:包括示例482的发动机进气除尘方法,其中,所述含氮化合物为氮化硅。
489.本发明提供的示例489:包括示例474至480任一项的发动机进气除尘方法,其中,所述进气驻极体元件的材料包括具有驻极性能的有机化合物。
490.本发明提供的示例490:包括示例489的发动机进气除尘方法,其中,所述有机化合物选自氟聚合物、聚碳酸酯、PP、PE、PVC、天然蜡、树脂、松香中的一种或多种组合。
491.本发明提供的示例491:包括示例490的发动机进气除尘方法,其中,所述氟聚合物选自聚四氟乙烯、聚全氟乙丙烯、可溶性聚四氟乙烯、聚偏氟乙烯中的一种或多种组合。
492.本发明提供的示例492:包括示例490的发动机进气除尘方法,其中,所述氟聚合物为聚四氟乙烯。
493.本发明提供的示例493:一种发动机进气除尘方法,其特征在于,包括以下步骤:所述进气经进气电离除尘后去除或减少进气电离除尘产生的臭氧。
494.本发明提供的示例494:包括示例493的发动机进气除尘方法,其中,对进气电离除尘产生的臭氧进行臭氧消解。
495.本发明提供的示例495:包括示例493的发动机进气除尘方法,其中,所述臭氧消解选自紫外线消解和催化消解中的至少一种。
496.本发明提供的示例496:一种尾气臭氧净化方法,包括如下步骤:将臭氧流股与尾气流股混合反应。
497.本发明提供的示例497:包括示例496所述的尾气臭氧净化方法,其中,所述尾气流股包括氮氧化物和挥发性有机化合物。
498.本发明提供的示例498:包括示例496或497所述的尾气臭氧净化方法,其中,于尾 气的低温段,臭氧流股与尾气流股的混合反应。
499.本发明提供的示例499:包括示例496至498任一项所述的尾气臭氧净化方法,其中,臭氧流股与尾气流股混合反应温度为-50~200℃。
500.本发明提供的示例500:包括示例499所述的尾气臭氧净化方法,其中,臭氧流股与尾气流股混合反应温度为60~70℃。
501.本发明提供的示例501:包括示例496至500任一项所述的尾气臭氧净化方法,其中,臭氧流股与尾气流股的混合方式选自文丘里混合、正压混合、插入混合、动力混合和流体混合中至少一种。
502.本发明提供的示例502:包括示例501所述的尾气臭氧净化方法,其中,当臭氧流股与尾气流股的混合方式为正压混合时,臭氧进气的压力大于尾气的压力。
503.本发明提供的示例503:包括示例496所述的尾气臭氧净化方法,其中,在臭氧流股与尾气流股混合反应前,提高尾气流股流速,采用文丘里原理混入臭氧流股。
504.本发明提供的示例504:包括示例496所述的尾气臭氧净化方法,其中,臭氧流股与尾气流股混合方式选自尾气出口逆流通入、反应场前段混入、除尘器前后插入、脱硝装置前后混入、催化装置前后混入、水洗装置前后通入、过滤装置前后混入、消音装置前后混入、尾气管道内发生混入、吸附装置外置混入和凝露装置前后混入中至少一种。
505.本发明提供的示例505:包括示例496所述的尾气臭氧净化方法,其中,臭氧流股与尾气流股混合反应的反应场包括管道和/或反应器。
506.本发明提供的示例506:包括示例496至505任一项所述的尾气臭氧净化方法,其中,所述反应场包括排气管、蓄热体装置或催化器。
507.本发明提供的示例507:包括示例506所述的尾气臭氧净化方法尾气臭氧净化方法,其中,还包括如下技术特征中的至少一项:
1)管道的管段通径为100-200毫米;
2)管道的长度大于管径0.1倍;
3)所述反应器选自如下至少一种:
反应器一:所述反应器具有反应腔室,尾气与臭氧在所述反应腔室混合并反应;
反应器二:所述反应器包括若干蜂窝状腔体,用于提供尾气与臭氧混合并反应的空间;所述蜂窝状腔体内之间设有间隙,用于通入冷态介质,控制尾气与臭氧的反应温度;
反应器三:所述反应器包括若干载体单元,所述载体单元提供反应场地;
反应器四:所述反应器包括催化剂单元,所述催化剂单元用于促进尾气的氧化反应;
4)所述反应场设有臭氧进口,所述臭氧进口选自喷口、喷格栅、喷嘴、旋流喷嘴、设有文丘里管的喷口中的至少一种;
5)所述反应场设有臭氧进口,所述臭氧通过所述臭氧进口进入反应场与尾气进行接触,臭氧进口的设置形成如下方向中至少一种:与尾气流动的方向相反、与尾气流动的方向垂直、与尾气流动的方向相切、插入尾气流动方向、多个方向与尾气进行接触。
508.本发明提供的示例508:包括示例496至507任一项所述的尾气臭氧净化方法,其中,所述臭氧流股由存储臭氧单元和/或臭氧发生器提供。
509.本发明提供的示例509:包括示例508所述的尾气臭氧净化方法,其中,所述臭氧发生器包括延面放电臭氧发生器、工频电弧臭氧发生器、高频感应臭氧发生器、低气压臭氧发生器、紫外线臭氧发生器、电解液臭氧发生器、化学药剂臭氧发生器和射线辐照粒子发生器中的一种或多种的组合。
510.本发明提供的示例510:包括示例508所述的尾气臭氧净化方法,其中,所述臭氧流股提供方法:在电场和氧化催化键裂解选择性催化剂作用下,含有氧气的气体产生臭氧,其中形成电场的电极上负载氧化催化键裂解选择性催化剂。
511.本发明提供的示例511:包括示例510所述的尾气臭氧净化方法,其中,所述电极包括高压电极或设有阻挡介质层的电极,当所述电极包括高压电极时,所述氧化催化键裂解选择性催化剂负载于所述高压电极表面上,当所述电极包括阻挡介质层的高压电极时,所述氧化催化键裂解选择性催化剂负载于阻挡介质层的表面上。
512.本发明提供的示例512:包括示例510所述的尾气臭氧净化方法,其中,当所述电极包括高压电极时,所述氧化催化键裂解选择性催化剂的厚度为1~3mm;当所述电极包括阻挡介质层的高压电极时,所述氧化催化键裂解选择性催化剂的负载量包括阻挡介质层的1~10wt%。
513.本发明提供的示例513:包括示例510至512任一项所述的尾气臭氧净化方法,其中,所述氧化催化键裂解选择性催化剂包括如下重量百分比的各组分:
活性组分5~15%;
涂层85~95%;
其中,所述活性组分选自金属M和金属元素M的化合物中的至少一种,金属元素M选自碱土金属元素、过渡金属元素、第四主族金属元素、贵金属元素和镧系稀土元素中的至少一种;
所述涂层选自氧化铝、氧化铈、氧化锆、氧化锰、金属复合氧化物、多孔材料和层状材料中的至少一种,所述金属复合氧化物包括铝、铈、锆和锰中一种或多种金属的复合氧化物。
514.本发明提供的示例514:包括示例513所述的尾气臭氧净化方法,其中,所述碱土金属元素选自镁、锶和钙中的至少一种。
515.本发明提供的示例515:包括示例513所述的尾气臭氧净化方法,其中,所述过渡金属元素选自钛、锰、锌、铜、铁、镍、钴、钇和锆中的至少一种。
516.本发明提供的示例516:包括示例513所述的尾气臭氧净化方法,其中,所述第四主族金属元素为锡。
517.本发明提供的示例517:包括示例513所述的尾气臭氧净化方法,其中,所述贵金属元素选自铂、铑、钯、金、银和铱中的至少一种。
518.本发明提供的示例518:包括示例513所述的尾气臭氧净化方法,其中,所述镧系稀土元素选自镧、铈、镨和钐中的至少一种。
519.本发明提供的示例519:包括示例513所述的尾气臭氧净化方法,其中,所述金属元素M的化合物选自氧化物、硫化物、硫酸盐、磷酸盐、碳酸盐,以及钙钛矿中的至少一种。
520.本发明提供的示例520:包括示例513所述的尾气臭氧净化方法,其中,所述多孔材料选自分子筛、硅藻土、沸石和纳米碳管中的至少一种。
521.本发明提供的示例521:包括示例513所述的尾气臭氧净化方法,其中,所述层状材料选自石墨烯和石墨中的至少一种。
522.本发明提供的示例522:包括示例510至512任一项所述的尾气臭氧净化方法,其中,所述电极通过浸渍和/或喷涂的方法负载氧双催化键裂解选择性催化剂。
523.本发明提供的示例523:包括示例522所述的尾气臭氧净化方法,其中,包括如下步骤:
1)按照催化剂组成配比,将涂层原料的浆料负载于高压电极表面上或阻挡介质层的表面上,干燥,煅烧,得到负载涂层的高压电极或阻挡介质层;
2)按照催化剂组成配比,将含金属元素M的原料溶液或浆料负载到步骤1)得到涂层上,干燥,煅烧,当涂层负载于阻挡介质层的表面上时,煅烧后在阻挡介质层相对于负载涂层的另一面设置高压电极,即得所述臭氧发生器用电极;或者,按照催化剂组成配比,将含金属元素M的原料溶液或浆料负载到步骤1)得到涂层上,干燥,煅烧和后处理,当涂层负载于阻挡介质层的表面上时,后处理后在阻挡介质层相对于负载涂层的另一面设置高压电极,即得所述臭氧发生器用电极;
其中,通过对煅烧温度和气氛,以及后处理实现对电极用催化剂中活性组分形态的控制。
524.本发明提供的示例524:包括示例522所述的尾气臭氧净化方法,其中,包括如下步 骤:
1)按照催化剂组成配比,将含金属元素M的原料溶液或浆料负载涂层原料上,干燥,煅烧,得到负载有活性组份的涂层材料;
2)按照催化剂组成配比,将步骤1)得到的负载有活性组份的涂层材料制成浆料,负载在高压电极表面上或阻挡介质层的表面上,干燥,煅烧,当涂层负载在阻挡介质层的表面上时,煅烧后在阻挡介质层相对于负载涂层的另一面设置高压电极,即得所述臭氧发生器用电极;或者,按照催化剂组成配比,将步骤1)得到的负载有活性组份的涂层材料制成浆料,负载在高压电极表面上或阻挡介质层的表面上,干燥,煅烧和后处理,当涂层负载在阻挡介质层的表面上时,后处理后在阻挡介质层相对于负载涂层的另一面设置高压电极,即得所述臭氧发生器用电极;
其中,通过对煅烧温度和气氛,以及后处理实现对电极用催化剂中活性组分形态的控制。
525.本发明提供的示例525:包括示例496至524任一项所述的尾气臭氧净化方法,其中,包括:控制臭氧流股的臭氧量以致有效氧化尾气中待处理的气体组分。
526.本发明提供的示例526:包括示例496至525任一项所述的尾气臭氧净化方法,其中,控制臭氧流股的臭氧量达到如下脱除效率:
氮氧化物脱除效率:60~99.97%;
CO脱除效率:1~50%;
挥发性有机化合物脱除效率:60~99.97%。
527.本发明提供的示例527:包括示例525或526所述的尾气臭氧净化方法,其中,包括:检测臭氧处理前尾气组分含量。
528.本发明提供的示例528:包括示例525至527任一项所述的尾气臭氧净化方法,其中,根据所述臭氧处理前尾气组分含量控制混合反应所需臭氧量。
529.本发明提供的示例529:包括示例527或528所述的尾气臭氧净化方法,其中,检测臭氧处理前尾气组分含量选自以下至少一个:
检测臭氧处理前尾气中挥发性有机化合物含量;
检测臭氧处理前尾气中CO含量;
检测臭氧处理前尾气中氮氧化物含量。
530.本发明提供的示例530:包括示例529所述的尾气臭氧净化方法,其中,根据至少一个检测臭氧处理前尾气组分含量的输出值控制混合反应所需臭氧量。
531.本发明提供的示例531:包括示例525至530任一项所述的尾气臭氧净化方法,其中, 按照预设的数学模型控制混合反应所需臭氧量。
532.本发明提供的示例532:包括示例525至531任一项所述的尾气臭氧净化方法,其中,按照理论估计值控制混合反应所需臭氧量。
533.本发明提供的示例533:包括示例532所述的于尾气臭氧净化方法,其中,所述理论估计值为:臭氧通入量与尾气中待处理物的摩尔比为2~10。
534.本发明提供的示例534:包括示例525至533任一项所述的尾气臭氧净化方法,其中,包括:检测臭氧处理后尾气组分含量。
535.本发明提供的示例535:包括示例525至534任一项所述的尾气臭氧净化方法,其中,根据所述臭氧处理后尾气组分含量控制混合反应所需臭氧量。
536.本发明提供的示例536:包括示例534或535所述的尾气臭氧净化方法,其中,检测臭氧处理后尾气组分含量选自以下至少一个:
检测臭氧处理后尾气中臭氧含量;
检测臭氧处理后尾气中挥发性有机化合物含量;
检测臭氧处理后尾气中CO含量;
检测臭氧处理后尾气中氮氧化物含量。
537.本发明提供的示例537:包括示例536所述的尾气臭氧净化方法,其中,根据至少一个检测臭氧处理后尾气组分含量的输出值控制臭氧量。
538.本发明提供的示例538:包括示例496至537任一项所述的尾气臭氧净化方法,其中,所述尾气臭氧净化方法还包括如下步骤:脱除臭氧流股与尾气流股混合反应产物中的硝酸。
539.本发明提供的示例539:包括示例538所述的尾气臭氧净化方法,其中,使带硝酸雾的气体流经第一电极;
当带硝酸雾的气体流经第一电极时,第一电极使气体中的硝酸雾带电,第二电极给带电的硝酸雾施加吸引力,使硝酸雾向第二电极移动,直至硝酸雾附着在第二电极上。
540.本发明提供的示例540:包括示例539所述尾气臭氧净化方法,其中,第一电极将电子导入硝酸雾,电子在位于第一电极和第二电极之间的雾滴之间进行传递,使更多雾滴带电。
541.本发明提供的示例541:包括示例539或540所述尾气臭氧净化方法,其中,第一电极和第二电极之间通过硝酸雾传导电子、并形成电流。
542.本发明提供的示例542:包括示例539-541任一项所述尾气臭氧净化方法,其中,第一电极通过与硝酸雾接触的方式使硝酸雾带电。
543.本发明提供的示例543:包括示例539-542任一项所述尾气臭氧净化方法,其中,第 一电极通过能量波动的方式使硝酸雾带电。
544.本发明提供的示例544:包括示例539-543任一项所述尾气臭氧净化方法,其中,附着在第二电极上的硝酸雾形成水滴,第二电极上的水滴流入收集槽中。
545.本发明提供的示例545:包括示例544所述尾气臭氧净化方法,其中,第二电极上的水滴在重力作用下流入收集槽。
546.本发明提供的示例546:包括示例544或545所述尾气臭氧净化方法,其中,气体流动时,将吹动水滴流入收集槽中。
547.本发明提供的示例547:包括示例539-546任一项所述尾气臭氧净化方法,其中,所述第一电极为固体、液体、气体分子团、等离子体、导电混合态物质、生物体自然混合导电物质、或物体人工加工形成导电物质中的一种或多种形态的组合。
548.本发明提供的示例548:包括示例539-547任一项所述尾气臭氧净化方法,其中,所述第一电极为固态金属、石墨、或304钢。
549.本发明提供的示例549:包括示例539-548任一项所述尾气臭氧净化方法,其中,所述第一电极呈点状、线状、网状、孔板状、板状、针棒状、球笼状、盒状、管状、自然形态物质、或加工形态物质。
550.本发明提供的示例550:包括示例539-549任一项所述尾气臭氧净化方法,其中,所述第一电极上设有前通孔。
551.本发明提供的示例551:包括示例550所述尾气臭氧净化方法,其中,所述前通孔的形状为多角形、圆形、椭圆形、正方形、长方形、梯形、或菱形。
552.本发明提供的示例552:包括示例550或551所述尾气臭氧净化方法,其中,所述前通孔的孔径为0.1-3毫米。
553.本发明提供的示例553:包括示例539-552中任一项所述尾气臭氧净化方法,其中,所述第二电极呈多层网状、网状、孔板状、管状、桶状、球笼状、盒状、板状、颗粒堆积层状、折弯板状、或面板状。
554.本发明提供的示例554:包括示例539至553任一项所述尾气臭氧净化方法,其中,所述第二电极上设有后通孔。
555.本发明提供的示例555:包括示例554所述尾气臭氧净化方法,其中,所述后通孔呈多角形、圆形、椭圆形、正方形、长方形、梯形、或菱形。
556.本发明提供的示例556:包括示例554或555所述尾气臭氧净化方法,其中,所述后通孔的孔径为0.1-3毫米。
557.本发明提供的示例557:包括示例539至556任一项所述尾气臭氧净化方法,其中,所述第二电极由导电物质制成。
558.本发明提供的示例558:包括示例539至557任一项所述尾气臭氧净化方法,其中,所述第二电极的表面具有导电物质。
559.本发明提供的示例559:包括示例539至558任一项所述尾气臭氧净化方法,其中,所述第一电极和第二电极之间具有电凝电场,所述电凝电场为点面电场、线面电场、网面电场、点桶电场、线桶电场、或网桶电场中的一种或多种电场的组合。
560.本发明提供的示例560:包括示例539至559任一项所述尾气臭氧净化方法,其中,所述第一电极呈线状,所述第二电极呈面状。
561.本发明提供的示例561:包括示例539至560任一项所述尾气臭氧净化方法,其中,所述第一电极垂直于第二电极。
562.本发明提供的示例562:包括示例539至561任一项所述尾气臭氧净化方法,其中,所述第一电极与第二电极相平行。
563.本发明提供的示例563:包括示例539至562任一项所述尾气臭氧净化方法,其中,所述第一电极呈曲线状或圆弧状。
564.本发明提供的示例564:包括示例539至563任一项所述尾气臭氧净化方法,其中,所述第一电极和第二电极均呈面状,且所述第一电极与第二电极相平行。
565.本发明提供的示例565:包括示例539至564任一项所述尾气臭氧净化方法,其中,所述第一电极采用金属丝网。
566.本发明提供的示例566:包括示例539至565任一项所述尾气臭氧净化方法,其中,所述第一电极呈平面状或球面状。
567.本发明提供的示例567:包括示例539至566任一项所述尾气臭氧净化方法,其中,所述第二电极呈曲面状或球面状。
568.本发明提供的示例568:包括示例539至567任一项所述尾气臭氧净化方法,其中,所述第一电极呈点状、线状、或网状,所述第二电极呈桶状,所述第一电极位于第二电极的内部,且所述第一电极位于第二电极的中心对称轴上。
569.本发明提供的示例569:包括示例539至568任一项所述尾气臭氧净化方法,其中,所述第一电极与电源的一个电极电性连接,所述第二电极与电源的另一个电极电性连接。
570.本发明提供的示例570:包括示例539至569任一项所述尾气臭氧净化方法,其中,所述第一电极与电源的阴极电性连接,所述第二电极与电源的阳极电性连接。
571.本发明提供的示例571:包括示例569或570所述尾气臭氧净化方法,其中,所述电源的电压为5-50KV。
572.本发明提供的示例572:包括示例569至571任一项所述尾气臭氧净化方法,其中,所述电源的电压小于起始起晕电压。
573.本发明提供的示例573:包括示例569至572任一顶所述尾气臭氧净化方法,其中,所述电源的电压为0.1kv/mm-2kv/mm。
574.本发明提供的示例574:包括示例569至573任一项所述尾气臭氧净化方法,其中,所述电源的电压波形为直流波形、正弦波、或调制波形。
575.本发明提供的示例575:包括示例569至574任一项所述尾气臭氧净化方法,其中,所述电源为交流电源,所述电源的变频脉冲范围为0.1Hz~5GHz。
576.本发明提供的示例576:包括示例539至575任一项所述尾气臭氧净化方法,其中,所述第一电极和第二电极均沿左右方向延伸,所述第一电极的左端位于第二电极的左端的左方。
577.本发明提供的示例577:包括示例539至576任一项所述尾气臭氧净化方法,其中,所述第二电极有两个,所述第一电极位于两个第二电极之间。
578.本发明提供的示例578:包括示例539至577任一项所述尾气臭氧净化方法,其中,所述第一电极和第二电极之间的距离为5-50毫米。
579.本发明提供的示例579:包括示例539至578任一项所述尾气臭氧净化方法,其中,所述第一电极和第二电极构成吸附单元,且所述吸附单元有多个。
580.本发明提供的示例580:包括示例579所述尾气臭氧净化方法,其中,全部吸附单元沿左右方向、前后方向、斜向、或螺旋方向中的一个方向或多个方向上进行分布。
581.本发明提供的示例581:包括示例539至580任一项所述尾气臭氧净化方法,其中,所述第一电极安装在电凝壳体中,所述电凝壳体具有电凝进口和电凝出口。
582.本发明提供的示例582:包括示例581所述尾气臭氧净化方法,其中,所述电凝进口呈圆形,且所述电凝进口的直径为300~1000mm、或500mm。
583.本发明提供的示例583:包括示例581或582所述尾气臭氧净化方法,其中,所述电凝出口呈圆形,且所述电凝出口的直径为300~1000mm、或500mm。
584.本发明提供的示例584:包括示例581至583任一项所述尾气臭氧净化方法,其中,所述电凝壳体包括由电凝进口至电凝出口方向依次分布的第一壳体部、第二壳体部、及第三壳体部,所述电凝进口位于第一壳体部的一端,所述电凝出口位于第三壳体部的一端。
585.本发明提供的示例585:包括示例584所述尾气臭氧净化方法,其中,所述第一壳体部的轮廓大小由电凝进口至电凝出口方向逐渐增大。
586.本发明提供的示例586:包括示例584或585所述尾气臭氧净化方法,其中,所述第一壳体部呈直管状。
587.本发明提供的示例587:包括示例584至586任一项所述尾气臭氧净化方法,其中,所述第二壳体部呈直管状,且所述第一电极和第二电极安装在第二壳体部中。
588.本发明提供的示例588:包括示例584至587任一项所述尾气臭氧净化方法,其中,所述第三壳体部的轮廓大小由电凝进口至电凝出口方向逐渐减小。
589.本发明提供的示例589:包括示例584至588任一项所述尾气臭氧净化方法,其中,所述第一壳体部、第二壳体部、及第三壳体部的截面均呈矩形。
590.本发明提供的示例590:包括示例581至589任一项所述尾气臭氧净化方法,其中,所述电凝壳体的材质为不锈钢、铝合金、铁合金、布、海绵、分子筛、活性炭、泡沫铁、或泡沫碳化硅。
591.本发明提供的示例591:包括示例539至590任一项所述尾气臭氧净化方法,其中,所述第一电极通过电凝绝缘件与电凝壳体相连接。
592.本发明提供的示例592:包括示例591所述尾气臭氧净化方法,其中,所述电凝绝缘件的材质为绝缘云母。
593.本发明提供的示例593:包括示例591或592所述尾气臭氧净化方法,其中,所述电凝绝缘件呈柱状、或塔状。
594.本发明提供的示例594:包括示例539至593任一项所述尾气臭氧净化方法,其中,所述第一电极上设有呈圆柱形的前连接部,且所述前连接部与电凝绝缘件固接。
595.本发明提供的示例595:包括示例539至594任一项所述尾气臭氧净化方法,其中,所述第二电极上设有呈圆柱形的后连接部,且所述后连接部与电凝绝缘件固接。
596.本发明提供的示例596:包括示例539至595任一项所述尾气臭氧净化方法,其中,所述第一电极位于电凝流道中;带硝酸雾的气体沿电凝流道流动,并流经第一电极;所述第一电极的截面面积与电凝流道的截面面积比为99%~10%、或90~10%、或80~20%、或70~30%、或60~40%、或50%。
597.本发明提供的示例597:包括示例538至596任一项所述的尾气臭氧净化方法,其中,脱除臭氧流股与尾气流股混合反应产物中的硝酸的方法:将臭氧流股与尾气流股混合反应产物进行冷凝。
598.本发明提供的示例598:包括示例538至597任一项所述的尾气臭氧净化方法,其中,脱除臭氧流股与尾气流股混合反应产物中的硝酸的方法:将臭氧流股与尾气流股混合反应产物进行淋洗。
599.本发明提供的示例599:包括示例598所述的尾气臭氧净化方法,其中,脱除臭氧流股与尾气流股混合反应产物中的硝酸的方法还包括:向臭氧流股与尾气流股混合反应产物提供淋洗液。
600.本发明提供的示例600:包括示例599所述的于尾气臭氧净化方法,其中,所述淋洗液为水和/或碱。
601.本发明提供的示例601:包括示例538至600任一项所述的尾气臭氧净化方法,其中,脱除臭氧流股与尾气流股混合反应产物中的硝酸的方法还包括:存储尾气中脱除的硝酸水溶液和/或硝酸盐水溶液。
602.本发明提供的示例602:包括示例601所述的尾气臭氧净化方法,其中,当存储有硝酸水溶液时,加入碱液,与硝酸形成硝酸盐。
603.本发明提供的示例603:包括示例496至602任一项所述的尾气臭氧净化方法,其中,所述尾气臭氧净化方法还包括如下步骤:对脱除硝酸的尾气进行臭氧消解。
604.本发明提供的示例604:包括示例603所述的尾气臭氧净化方法,其中,所述臭氧消解选自紫外线消解和催化消解中的至少一种。
605.本发明提供的示例605:包括示例496至604任一项所述的尾气臭氧净化方法,其中,所述尾气臭氧净化方法还包括如下步骤:第一次脱除尾气中氮氧化物;第一次脱除氮氧化物后的尾气流股与臭氧流股混合反应,或者,在第一次脱除尾气中氮氧化物前先与臭氧流股混合反应。
606.本发明提供的示例606:包括示例605所述的尾气臭氧净化方法,其中,所述第一次脱除尾气中氮氧化物选自非催化还原方法、选择性催化还原方法、非选择性催化还原方法和电子束脱硝方法等中的至少一种。
图1为本发明尾气臭氧净化系统的示意图。
图2为本发明臭氧发生器用电极的示意图一。
图3为本发明臭氧发生器用电极的示意图二。
图4为现有技术中放电式臭氧发生器结构原理图。
图5为本发明基于发动机的气体处理系统中进气除尘系统于一实施例中的结构示意图。
图6为本发明基于发动机的气体处理系统中设置于进气装置内的第一滤水机构的另一实施例结构图。
图7A为本发明基于发动机的气体处理系统中进气装置的进气均风装置的一种实施结构图。
图7B为本发明基于发动机的气体处理系统中进气装置的进气均风装置的另一种实施结构图。
图7C为本发明基于发动机的气体处理系统中进气装置的进气均风装置的又一种实施结构图。
图7D为本发明基于发动机的气体处理系统中进气装置的中第二文氏板均风机构的俯视结构图。
图8为本发明是实施例2进气电场装置的示意图一。
图9为本发明实施例3进气电场装置的示意图二。
图10为本发明图5的进气电场装置的俯视图。
图11为实施例3进气驻极体元件于进气流道中的横截面占进气流道横截面的示意图。
图12为本发明实施例4进气除尘系统的示意图。
图13为本发明实施例5尾气除尘系统的示意图。
图14为本发明实施例6尾气除尘系统的示意图。
图15为本发明基于发动机的气体处理系统中尾气处理装置于一实施例中的立体结构示意图。
图16为本发明基于发动机的气体处理系统中尾气处理装置呈伞状的尾气绝缘机构于一实施例中的结构示意图。
图17A为本发明基于发动机的气体处理系统中尾气处理装置的进气均风装置的一种实施结构图。
图17B为本发明基于发动机的气体处理系统中尾气处理装置的尾气均风装置的另一种实施结构图。
图17C为本发明基于发动机的气体处理系统中尾气处理装置的尾气均风装置的又一种实施结构图。
图18为本发明实施例8尾气臭氧净化系统的示意图。
图19为本发明实施例8尾气臭氧净化系统中反应场的俯视图。
图20为本发明臭氧量控制装置的示意图。
图21为电场发生单元结构示意图。
图22为图21电场发生单元的A-A视图。
图23为标注长度和角度的图21电场发生单元的A-A视图。
图24为两个电场级的电场装置结构示意图。
图25为本发明实施例30中电场装置的结构示意图。
图26为本发明实施例32中电场装置的结构示意图。
图27为本发明实施例33中电场装置的结构示意图。
图28为本发明实施例36中尾气除尘系统的结构示意图。
图29为本发明实施例36中叶轮涵道的结构示意图。
图30为本发明实施例37中电凝装置的结构示意图。
图31为本发明实施例37中电凝装置的左视图。
图32为本发明实施例37中电凝装置的立体图。
图33为本发明实施例38中电凝装置的结构示意图。
图34为本发明实施例38中电凝装置的俯视图。
图35为本发明实施例39中电凝装置的结构示意图。
图36为本发明实施例40中电凝装置的结构示意图。
图37为本发明实施例41中电凝装置的结构示意图。
图38为本发明实施例42中电凝装置的结构示意图。
图39为本发明实施例43中电凝装置的结构示意图。
图40为本发明实施例44中电凝装置的结构示意图。
图41为本发明实施例45中电凝装置的结构示意图。
图42为本发明实施例46中电凝装置的结构示意图。
图43为本发明实施例47中电凝装置的结构示意图。
图44为本发明实施例48中电凝装置的结构示意图。
图45为本发明实施例49中电凝装置的结构示意图。
图46为本发明实施例50中电凝装置的结构示意图。
图47为本发明实施例51中发动机排放处理系统的结构示意图。
图48为本发明实施例52中发动机排放处理系统的结构示意图。
图49为本发明实施例53中发动机排放处理系统的结构示意图。
图50为本发明实施例54中发动机排放处理系统的结构示意图。
图51为本发明实施例55中发动机排放处理系统的结构示意图。
图52为本发明实施例56中发动机排放处理系统的结构示意图。
图53为本发明实施例57中发动机排放处理系统的结构示意图。
图54为本发明实施例58中发动机排放处理系统的结构示意图。
图55为本发明实施例59中发动机排放处理系统的结构示意图。
图56为本发明实施例60中进气电场装置的结构示意图。
图57为本发明实施例61中尾气降温装置的结构示意图。
图58为本发明实施例62中尾气降温装置的结构示意图。
图59为本发明实施例63中尾气降温装置的结构示意图。
图60为本发明实施例63中换热单元的结构示意图。
图61为本发明实施例64中尾气降温装置的结构示意图。
以下由特定的具体实施例说明本发明的实施方式,熟悉此技术的人士可由本说明书所揭露的内容轻易地了解本发明的其他优点及功效。
须知,本说明书所附图式所绘示的结构、比例、大小等,均仅用以配合说明书所揭示的内容,以供熟悉此技术的人士了解与阅读,并非用以限定本发明可实施的限定条件,故不具技术上的实质意义,任何结构的修饰、比例关系的改变或大小的调整,在不影响本发明所能产生的功效及所能达成的目的下,均应仍落在本发明所揭示的技术内容得能涵盖的范围内。同时,本说明书中所引用的如“上”、“下”、“左”、“右”、“中间”及“一”等的用语,亦仅为便于叙述的明了,而非用以限定本发明可实施的范围,其相对关系的改变或调整,在无实质变更技术内容下,当亦视为本发明可实施的范畴。
根据本发明的一个实施例,发动机排放处理系统包括进气除尘系统、尾气除尘系统、尾气臭氧净化系统。本发动机排放处理系统及方法可应用于发动机、发电站、砖窑、炼钢、水泥、化工、炼油等会因碳氢燃料的燃烧而产生尾气的技术领域。
于本发明的一实施例中进气除尘系统包括离心分离机构。于本发明一实施例中离心分离机构包括气流转向通道,该气流转向通道能改变气流的流动方向。当含有颗粒物的气体流经气流转向通道时,气体的流动方向将发生改变;而气体中的颗粒物等将在惯性作用下继续沿原方向移动,直至与气流转向通道的侧壁、即离心分离机构的内壁发生碰撞,颗粒物无法沿原方向继续移动,且在重力作用下向下掉落,这样,颗粒物就从气体中分离出来。
于本发明一实施例中气流转向通道能引导气体沿圆周方向流动。于本发明一实施例中气 流转向通道可以呈螺旋形或圆锥形。于本发明一实施例中离心分离机构包括分离筒。分离筒中设有所述气流转向通道,分离筒的底部可设有出尘口。分离筒侧壁上可设有与气流转向通道的第一端相连通的进气口。分离筒的顶部可设有与气流转向通道的第二端相连通的出气口。出气口也称作排气口,且排气口的大小可根据所需的进气量大小进行设置。气体由进气口流入分离筒的气流转向通道后,气体将由直线运动变为圆周运动,而气体中的颗粒物将在惯性作用下继续沿直线方向运动,直至颗粒物与分离筒的内壁碰撞,颗粒物不能随气体一起继续流动,颗粒物受重力作用下沉,这样,颗粒物就从气体中分离出来,且颗粒物最终由位于底部的出尘口排出,气体最终由位于顶部的排气口排出。于本发明一实施例中进气电场装置入口与离心分离机构的排气口相连通。分离筒的出气口位于分离筒与进气电场装置的连接处。
于本发明一实施例中离心分离机构可呈弯折型结构。离心分离机构的形状可以是环型、回字型、十字型、T字型、L字型、凹字型、或折型中的一种形状或多种形状的组合。离心分离机构的气流转向通道具有至少一个转弯。当气体流经该转弯处时,其流动方向将发生改变,而气体中的颗粒物将在惯性作用下继续沿原方向移动,直至颗粒物与离心分离机构的内壁相碰撞,碰撞后颗粒物将受重力作用下沉,颗粒物从气体中脱离出来,并最终由位于下端的出粉口排出,而气体最终由排气口流出。
于本发明一实施例中离心分离机构的排气口处可设置第一过滤层,第一过滤层可包括金属网片,该金属网片可垂直于气流方向设置。金属网片将对由排气口排出的气体进行过滤,以将气体中仍未分离的颗粒物过滤掉。
于本发明一实施例中进气除尘系统可包括进气均风装置。该进气均风装置设置在进气电场装置之前,能使进入进气电场装置的气流均匀通过。
于本发明一实施例中进气电场装置的进气除尘电场阳极可为立方体,进气均风装置可包括位于阴极支撑板一侧边的进气管、及位于阴极支撑板另一侧边的出气管,阴极支撑板位于进气除尘电场阳极的进气端;其中,安装进气管的侧边与安装出气管的侧边相对立。进气均风装置能使进入进气电场装置的气流均匀通过静电场。
于本发明一实施例中进气除尘电场阳极可为圆柱体,所述进气均风装置在所述进气除尘系统入口与所述进气除尘电场阳极和所述进气除尘电场阴极形成的进气电离除尘电场之间,且进气均风装置包括若干围绕进气电场装置入口中心旋转的均风叶片。进气均风装置能够使各种变化的进气量均匀通过进气除尘电场阳极产生的电场,同时,能够保持进气除尘电场阳极内部温度恒定,氧气充足。进气均风装置能使进入进气电场装置的气流均匀通过静电场。
于本发明一实施例中进气均风装置包括设置于进气除尘电场阳极的进气端的进风板和设 置于进气除尘电场阳极出气端的出风板,进风板上开设有进气孔,出风板上开设有出气孔,进气孔与出气孔错位排布,且正面进气、侧面出气,形成旋风结构。进气均风装置能使进入进气电场装置的气流均匀通过静电场。
于本发明一实施例中进气系统可包括进气除尘入口、进气除尘出口和进气电场装置。且于本发明一实施例中进气电场装置可包括进气电场装置入口、进气电场装置出口、及位于进气电场装置入口和进气电场装置出口之间的进气前置电极,当气体由进气电场装置入口流经进气前置电极时,气体中的颗粒物等将带电。
于本发明一实施例中进气电场装置包括进气前置电极,该进气前置电极在进气电场装置入口与进气除尘电场阳极和进气除尘电场阴极形成的进气电离除尘电场之间。当气体由进气电场装置入口流经进气前置电极时,气体中的颗粒物等将带电。
于本发明一实施例中进气前置电极的形状可以为点状、线状、网状、孔板状、板状、针棒状、球笼状、盒状、管状、物质自然形态、或物质加工形态。当进气前置电极为有孔结构时,进气前置电极上设有一个或多个进气通孔。于本发明一实施例中进气通孔的形状可以为多角形、圆形、椭圆形、正方形、长方形、梯形、或菱形。于本发明一实施例中进气通孔的轮廓大小可以为0.1~3mm、0.1~0.2mm、0.2~0.5mm、0.5~1mm、1~1.2mm、1.2~1.5mm、1.5~2mm、2~2.5mm、2.5~2.8mm、或2.8~3mm。
于本发明一实施例中进气前置电极的形态可以为固体、液体、气体分子团、等离子体、导电混合态物质、生物体自然混合导电物质、或物体人工加工形成导电物质中的一种或多种形态的组合。当进气前置电极为固体时,可采用固态金属,比如304钢,或其它固态的导体、比如石墨等。当进气前置电极为液体时,可以是含离子导电液体。
在工作时,在带污染物的气体进入进气除尘电场阳极和进气除尘电场阴极形成的进气电离除尘电场之前,且带污染物的气体通过进气前置电极时,进气前置电极使气体中的污染物带电。当带污染物的气体进入进气电离除尘电场时,进气除尘电场阳极给带电的污染物施加吸引力,使污染物向进气除尘电场阳极移动,直至污染物附着在进气除尘电场阳极上。
于本发明一实施例中进气前置电极将电子导入污染物,电子在位于进气前置电极和进气除尘电场阳极之间的污染物之间进行传递,使更多污染物带电。进气前置电极和进气除尘电场阳极之间通过污染物传导电子、并形成电流。
于本发明一实施例中进气前置电极通过与污染物接触的方式使污染物带电。于本发明一实施例中进气前置电极通过能量波动的方式使污染物带电。于本发明一实施例中进气前置电极通过与污染物接触的方式将电子转移到污染物上,并使污染物带电。于本发明一实施例中 进气前置电极通过能量波动的方式将电子转移到污染物上,并使污染物带电。
于本发明一实施例中进气前置电极呈线状,进气除尘电场阳极呈面状。于本发明一实施例中进气前置电极垂直于进气除尘电场阳极。于本发明一实施例中进气前置电极与进气除尘电场阳极相平行。于本发明一实施例中进气前置电极呈曲线状或圆弧状。于本发明一实施例中进气前置电极采用金属丝网。于本发明一实施例中进气前置电极与进气除尘电场阳极之间的电压不同于进气除尘电场阴极和进气除尘电场阳极之间的电压。于本发明一实施例中进气前置电极与进气除尘电场阳极之间的电压小于起始起晕电压。起始起晕电压为进气除尘电场阴极和进气除尘电场阳极之间的电压的最小值。于本发明一实施例中进气前置电极与进气除尘电场阳极之间的电压可以为0.1-2kv/mm。
于本发明一实施例中进气电场装置包括进气流道,进气前置电极位于进气流道中。于本发明一实施例中进气前置电极的截面面积与进气流道的截面面积比为99%~10%、或90~10%、或80~20%、或70~30%、或60~40%、或50%。进气前置电极的截面面积是指进气前置电极沿截面上实体部分的面积之和。于本发明一实施例中进气前置电极带负电势。
于本发明一实施例中当气体通过进气电场装置入口流入进气流道中,气体中导电性较强的金属粉尘、雾滴、或气溶胶等污染物在与进气前置电极相接触时,或与进气前置电极的距离达到一定范围时会直接带负电,随后,全部污染物随气流进入进气电离除尘电场,进气除尘电场阳极给已带负电的金属粉尘、雾滴、或气溶胶等施加吸引力,使已带负电的污染物向进气除尘电场阳极移动,直至该部分污染物附着在进气除尘电场阳极上,实现将该部分污染物收集起来,同时,进气除尘电场阳极与进气除尘电场阴极之间形成的进气电离除尘电场通过电离气体中的氧获得氧离子,且带负电荷的氧离子在与普通粉尘结合后,使普通粉尘带负电荷,进气除尘电场阳极给该部分带负电荷的粉尘等污染物施加吸引力,使粉尘等污染物向进气除尘电场阳极移动,直至该部分污染物附着在进气除尘电场阳极上,实现将该部分普通粉尘等污染物也收集起来,从而将气体中导电性较强和导电性较弱的污染物均收集起来,并使得进气除尘电场阳极能收集气体中污染物的种类更广泛,且收集能力更强,收集效率更高。
于本发明一实施例中进气电场装置入口与分离机构的排气口相连通。
于本发明一实施例中进气电场装置可包括进气除尘电场阴极和进气除尘电场阳极,进气除尘电场阴极与进气除尘电场阳极之间形成电离除尘电场。气体进入电离除尘电场,气体中的氧离子将被电离,并形成大量带有电荷的氧离子,氧离子与气体中粉尘等颗粒物结合,使得颗粒物荷电,进气除尘电场阳极给带负电荷的颗粒物施加吸附力,使得颗粒物被吸附在进气除尘电场阳极上,以清除掉气体中的颗粒物。
于本发明一实施例中,所述进气除尘电场阴极包括若干根阴极丝。阴极丝的直径可为0.1mm-20mm,该尺寸参数根据应用场合及积尘要求做调整。于本发明一实施例中阴极丝的直径不大于3mm。于本发明一实施例中阴极丝使用容易放电的金属丝或合金丝,耐温且能支撑自身重量,电化学稳定。于本发明一实施例中阴极丝的材质选用钛。阴极丝的具体形状根据进气除尘电场阳极的形状调整,例如,若进气除尘电场阳极的积尘面是平面,则阴极丝的截面呈圆形;若进气除尘电场阳极的积尘面是圆弧面,阴极丝需要设计成多面形。阴极丝的长度根据进气除尘电场阳极进行调整。
于本发明一实施例中,所述进气除尘电场阴极包括若干阴极棒。于本发明一实施例中,所述阴极棒的直径不大于3mm。于本发明一实施例中阴极棒使用容易放电的金属棒或合金棒。阴极棒的形状可以为针状、多角状、毛刺状、螺纹杆状或柱状等。阴极棒的形状可以根据进气除尘电场阳极的形状进行调整,例如,若进气除尘电场阳极的积尘面是平面,则阴极棒的截面需要设计成圆形;若进气除尘电场阳极的积尘面是圆弧面,则阴极棒需要设计成多面形。
于本发明一实施例中,进气除尘电场阴极穿设于进气除尘电场阳极内。
于本发明一实施例中,进气除尘电场阳极包括一个或多个并行设置的空阳极管。当中空阳极管有多个时,全部中空阳极管构成蜂窝状的进气除尘电场阳极。于本发明一实施例中,中空阳极管的截面可呈圆形或多边形。若中空阳极管的截面呈圆形,进气除尘电场阳极和进气除尘电场阴极之间能形成均匀电场,中空阳极管的内壁不容易积尘。若中空阳极管的截面为三边形时,中空阳极管的内壁上可以形成3个积尘面,3个远角容尘角,此种结构的中空阳极管的容尘率最高。若中空阳极管的截面为四边形,可以获得4个积尘面,4个容尘角,但拼组结构不稳定。若中空阳极管的截面为六边形,可以形成6个积尘面,6个容尘角,积尘面和容尘率达到平衡。若中空阳极管的截面呈更多边形时,可以获得更多的积尘边,但损失容尘率。于本发明一实施例中,中空阳极管的管内切圆直径取值范围为5mm-400mm。
于本发明一实施例中,进气除尘电场阴极安装在阴极支撑板上,阴极支撑板与进气除尘电场阳极通过进气绝缘机构相连接。所述进气绝缘机构用于实现所述阴极支撑板和所述进气除尘电场阳极之间的绝缘。于本发明一实施例中,进气除尘电场阳极包括第一阳极部和第二阳极部,即所述第一阳极部靠近进气除尘装置入口,第二阳极部靠近进气除尘装置出口。阴极支撑板和进气绝缘机构在第一阳极部和第二阳极部之间,即进气绝缘机构安装在电离电场中间、或进气除尘电场阴极中间,可以对进气除尘电场阴极起到良好的支撑作用,并对进气除尘电场阴极起到相对于进气除尘电场阳极的固定作用,使进气除尘电场阴极和进气除尘电场阳极之间保持设定的距离。而现有技术中,阴极的支撑点在阴极的端点,难以保持阴极和 阳极之间的距离。于本发明一实施例中进气绝缘机构设置在除尘流道外、即第二级流道外,以防止或减少气体中的灰尘等聚集在进气绝缘机构上,导致进气绝缘机构击穿或导电。
于本发明一实施例中,进气绝缘机构采用耐高压陶瓷绝缘子,对进气除尘电场阴极和进气除尘电场阳极之间进行绝缘。进气除尘电场阳极也称作一种外壳。
于本发明一实施例中,第一阳极部在气体流动方向上位于阴极支撑板和进气绝缘机构之前,第一阳极部能够除去气体中的水,防止水进入进气绝缘机构,造成进气绝缘机构短路、打火。另外,第一阳级部能够除去气体中相当一部分的灰尘,当气体通过进气绝缘机构时,相当一部分的灰尘已被消除,减少灰尘造成进气绝缘机构短路的可能性。于本发明一实施例中进气绝缘机构包括绝缘瓷柱。第一阳极部的设计,主要是为了保护绝缘瓷柱不被气体中颗粒物等污染,一旦气体污染绝缘瓷柱将会造成进气除尘电场阳极和进气除尘电场阴极导通,从而使进气除尘电场阳极的积尘功能失效,故第一阳极部的设计,能有效减少绝缘瓷柱被污染,提高产品的使用时间。在气体流经第二级流道过程中,第一阳极部和进气除尘电场阴极先接触具有污染性的气体,进气绝缘机构后接触气体,达到先除尘后经过进气绝缘机构的目的,减少对进气绝缘机构造成的污染,延长清洁维护周期,对应电极使用后绝缘支撑。所述第一阳极部的长度是足够的长,以清除部分灰尘,减少积累在所述进气绝缘机构和所述阴极支撑板上的灰尘,减少灰尘造成的电击穿。于本发明一实施例中第一阳极部长度占进气除尘电场阳极总长度的1/10至1/4、1/4至1/3、1/3至1/2、1/2至2/3、2/3至3/4,或3/4至9/10。
于本发明一实施例中,第二阳极部在气体流动方向上位于阴极支撑板和进气绝缘机构之后。第二阳极部包括积尘段和预留积尘段。其中积尘段利用静电吸附气体中的颗粒物,该积尘段是为了增加积尘面积,延长进气电场装置的使用时间。预留积尘段能为积尘段提供失效保护。预留积尘段是为了在满足设计除尘要求的前提下,进一步提高积尘面积,提高除尘效果。预留积尘段作为补充前段积尘使用。于本发明一实施例中,第一阳极部和第二阳极部可使用不同的电源。
于本发明一实施例中,由于进气除尘电场阴极和进气除尘电场阳极之间存在极高电位差,为了防止进气除尘电场阴极和进气除尘电场阳极导通,进气绝缘机构设置在进气除尘电场阴极和进气除尘电场阳极之间的第二级流道之外。因此,进气绝缘机构外悬于进气除尘电场阳极的外侧。于本发明一实施例中进气绝缘机构可采用非导体耐温材料,比如陶瓷、玻璃等。于本发明一实施例中,完全密闭无空气的材料绝缘要求绝缘隔离厚度>0.3mm/kv;空气绝缘要求>1.4mm/kv。可根据进气除尘电场阴极和进气除尘电场阳极之间的极间距的1.4倍设置绝缘距离。于本发明一实施例中进气绝缘机构使用陶瓷,表面上釉;不能使用胶粘或有机材料填 充连接,耐温大于350摄氏度。
于本发明一实施例中,进气绝缘机构包括绝缘部和隔热部。为了使进气绝缘机构具有抗污功能,绝缘部的材料采用陶瓷材料或玻璃材料。于本发明一实施例中,绝缘部可为伞状串陶瓷柱或玻璃柱,伞内外挂釉。伞状串陶瓷柱或玻璃柱的外缘与进气除尘电场阳极的距离大于电场距离的1.4倍、即大于极间距的1.4倍。伞状串陶瓷柱或玻璃柱的伞突边间距总和大于伞状串陶瓷柱的绝缘间距的1.4倍。伞状串陶瓷柱或玻璃柱的伞边内深总长大于伞状串陶瓷柱的绝缘距离1.4倍。绝缘部还可为柱状串陶瓷柱或玻璃柱,柱内外挂釉。于本发明一实施例中绝缘部还可呈塔状。
于本发明一实施例中,绝缘部内设置加热棒,当绝缘部周围温度接近露点时,加热棒启动并进行加热。由于使用中绝缘部的内外存在温差,绝缘部的内外、外部容易产生凝露。绝缘部的外表面可能自发或被气体加热产生高温,需要必要的隔离防护,防烫伤。隔热部包括位于绝缘部外部的防护围挡板、脱硝净化反应腔。于本发明一实施例中绝缘部的尾部需要凝露位置同样需要隔热,防止环境以及散热高温加热凝露组件。
于本发明一实施例中进气电场装置的电源的引出线使用伞状串陶瓷柱或玻璃柱过墙式连接,墙内使用弹性碰头连接阴极支撑板,墙外使用密闭绝缘防护接线帽插拔连接,引出线过墙导体与墙绝缘距离大于伞状串陶瓷柱或玻璃柱的陶瓷绝缘距离。于本发明一实施例中高压部分取消引线,直接安装在端头上,确保安全,高压模块整体外绝缘使用ip68防护,使用介质换热散热。
于本发明一实施例中进气除尘电场阴极和进气除尘电场阳极之间采用非对称结构。在对称电场中极性粒子受到一个相同大小而方向相反的作用力,极性粒子在电场中往复运动;在非对称电场中,极性粒子受到两个大小不同的作用力,极性粒子向作用力大的方向移动,可以避免产生耦合。
本发明的进气电场装置的进气除尘电场阴极和进气除尘电场阳极之间形成电离除尘电场。为了减少电离除尘电场发生电场耦合,于本发明一实施例中,减少电场耦合的方法包括如下步骤:选择进气除尘电场阳极的集尘面积与进气除尘电场阴极的放电面积的比,使电场耦合次数≤3。于本发明一实施例中进气除尘电场阳极的集尘面积与进气除尘电场阴极的放电面积的比可以为:1.667:1-1680:1;3.334:1-113.34:1;6.67:1-56.67:1;13.34:1-28.33:1。该实施例选择相对大面积的进气除尘电场阳极的集尘面积和相对极小的进气除尘电场阴极的放电面积,具体选择上述面积比,可以减少进气除尘电场阴极的放电面积,减小吸力,扩大进气除尘电场阳极的集尘面积,扩大吸力,即进气除尘电场阴极和进气除尘电场阳极间产生不对 称的电极吸力,使荷电后粉尘落入进气除尘电场阳极的集尘表面,虽极性改变但无法再被进气除尘电场阴极吸走,并减少电场耦合,实现电场耦合次数≤3。即在电场极间距小于150mm时电场耦合次数≤3,电场能耗低,能够减少电场对气溶胶、水雾、油雾、松散光滑颗粒物的耦合消耗,节省电场电能30~50%。集尘面积是指进气除尘电场阳极工作面的面积,比如,若进气除尘电场阳极呈中空的正六边形管状,集尘面积即为中空的正六边形管状的内表面积,集尘面积也称作积尘面积。放电面积指进气除尘电场阴极工作面的面积,比如,若进气除尘电场阴极呈棒状,放电面积即为棒状的外表面积。
于本发明一实施例中进气除尘电场阳极的长度可以为10~180mm、10~20mm、20~30mm、60~180mm、30~40mm、40~50mm、50~60mm、60~70mm、70~80mm、80~90mm、90~100mm、100~110mm、110~120mm、120~130mm、130~140mm、140~150mm、150~160mm、160~170mm、170~180mm、60mm、180mm、10mm或30mm。进气除尘电场阳极的长度是指进气除尘电场阳极工作面的一端至另一端的最小长度。进气除尘电场阳极选择此种长度,可以有效减少电场耦合。
于本发明一实施例中进气除尘电场阳极的长度可以为10~90mm、15~20mm、20~25mm、25~30mm、30~35mm、35~40mm、40~45mm、45~50mm、50~55mm、55~60mm、60~65mm、65~70mm、70~75mm、75~80mm、80~85mm或85~90mm,此种长度的设计可以使进气除尘电场阳极及进气电场装置具有耐高温特性,并使得进气电场装置在高温冲击下具有高效率的集尘能力。
于本发明一实施例中进气除尘电场阴极的长度可以为30~180mm、54~176mm、30~40mm、40~50mm、50~54mm、54~60mm、60~70mm、70~80mm、80~90mm、90~100mm、100~110mm、110~120mm、120~130mm、130~140mm、140~150mm、150~160mm、160~170mm、170~176mm、170~180mm、54mm、180mm、或30mm。进气除尘电场阴极的长度是指除尘电场阴极工作面的一端至另一端的最小长度。进气除尘电场阴极选择此种长度,可以有效减少电场耦合。
于本发明一实施例中进气除尘电场阴极的长度可以为10~90mm、15~20mm、20~25mm、25~30mm、30~35mm、35~40mm、40~45mm、45~50mm、50~55mm、55~60mm、60~65mm、65~70mm、70~75mm、75~80mm、80~85mm或85~90mm,此种长度的设计可以使进气除尘电场阴极及进气电场装置具有耐高温特性,并使得进气电场装置在高温冲击下具有高效率的集尘能力。
于本发明一实施例中进气除尘电场阳极和进气除尘电场阴极之间的距离可以为5~30mm、 2.5~139.9mm、9.9~139.9mm、2.5~9.9mm、9.9~20mm、20~30mm、30~40mm、40~50mm、50~60mm、60~70mm、70~80mm、80~90mm、90~100mm、100~110mm、110~120mm、120~130mm、130~139.9mm、9.9mm、139.9mm、或2.5mm。进气除尘电场阳极和进气除尘电场阴极之间的距离也称作极间距。极间距具体是指进气除尘电场阳极、进气除尘电场阴极工作面之间的最小垂直距离。此种极间距的选择可以有效减少电场耦合,并使进气电场装置具有耐高温特性。
于本发明一实施例中,所述进气除尘电场阴极直径为1-3毫米,所述进气除尘电场阳极与所述进气除尘电场阴极的极间距为2.5-139.9毫米;所述进气除尘电场阳极的积尘面积与所述进气除尘电场阴极的放电面积的比为1.667:1-1680:1。
鉴于电离除尘的特有性能,电离除尘可适用去除气体中的颗粒物。但是,经过许多大学、研究机构、企业的多年的研究,现有电场除尘装置只能去除约70%的颗粒物,不能满足许多行业的需要。另外,现有技术中的电场除尘装置体积过于庞大。
本发明的发明人研究发现,现有技术中电场除尘装置的缺点是由电场耦合引起的。本发明通过减小电场耦合次数,可以显著减小电场除尘装置的尺寸(即体积)。比如,本发明提供的电离除尘装置的尺寸约为现有电离除尘装置尺寸的五分之一。原因是,为了获得可接受的颗粒去除率,现有电离除尘装置中将气体流速设为1m/s左右,而本发明在将气体流速提高到6m/s的情况下,仍能获得较高的颗粒去除率。当处理一给定流量的气体时,随着气体速度的提高,电场除尘装置的尺寸可以减小。
另外,本发明可以显著提高颗粒去除效率。例如,在气体流速为1m/s左右时,现有技术电场除尘装置可以去除发动机排气中大约70%的颗粒物,但是本发明可以去除大约99%的颗粒物,即使在气体流速为6m/s时。
由于发明人发现了电场耦合的作用,并且找到了减少电场耦合次数的方法,本发明获得了上述预料不到的结果。
进气除尘电场阳极和进气除尘电场阴极之间的电离除尘电场也称作第一电场。于本发明一实施例中进气除尘电场阳极和进气除尘电场阴极之间还形成有与第一电场不平行的第二电场。于本发明另一实施例中,所述第二电场与所述电离除尘电场的流道不垂直。第二电场也称作辅助电场,可以通过一个或两个第一辅助电极形成。当第二电场由一个第一辅助电极形成时,该第一辅助电极可以放在电离除尘电场的进口或出口,该第一辅助电极可以带负电势、或正电势。其中,当所述第一辅助电极为阴极时,设置在或靠近所述电离除尘电场的进口;所述第一辅助电极与所述进气除尘电场阳极具有夹角α,且0°<α≤125°、或45°≤α≤125°、或60°≤α≤100°、或α=90°。当所述第一辅助电极为阳极时,设置在或靠近所述电离除尘电场的 出口;所述第一辅助电极与所述进气除尘电场阴极具有夹角α,且0°<α≤125°、或45°≤α≤125°、或60°≤α≤100°、或α=90°。当第二电场由两个第一辅助电极形成时,其中一个第一辅助电极可以带负电势,另一个第一辅助电极可以带正电势;一个第一辅助电极可以放在电离电场的进口,另一个第一辅助电极放在电离电场的出口。另外,第一辅助电极可以是进气除尘电场阴极或进气除尘电场阳极的一部分,即第一辅助电极可以是由进气除尘电场阴极或进气除尘电场阳极的延伸段构成,此时进气除尘电场阴极和进气除尘电场阳极的长度不一样。第一辅助电极也可以是一个单独的电极,也就是说第一辅助电极可以不是进气除尘电场阴极或进气除尘电场阳极的一部分,此时,第二电场的电压和第一电场的电压不一样,可以根据工作状况单独地控制。
第二电场能给进气除尘电场阳极和进气除尘电场阴极之间带负电荷的氧离子流施加朝向电离电场的出口的力,使得进气除尘电场阳极和进气除尘电场阴极之间带负电荷的氧离子流具有向出口的移动速度。在气体流入电离电场,并向电离电场的出口方向流动过程中,带负电荷的氧离子也在向进气除尘电场阳极且向电离电场的出口方向移动,且带负电荷的氧离子在向进气除尘电场阳极且向电离电场的出口移动过程中将与气体中的颗粒物等相结合,由于氧离子具有向出口的移动速度,氧离子在与颗粒物相结合时,两者间不会产生较强的碰撞,从而避免因较强碰撞而造成较大的能量消耗,保证氧离子易于与颗粒物相结合,并使得气体中的颗粒物的荷电效率更高,进而在进气除尘电场阳极的作用下,能将更多的颗粒物收集起来,保证进气电场装置的除尘效率更高。进气电场装置对顺离子流方向进入电场的颗粒物的收集率比对逆离子流方向进入电场的颗粒物的收集率提高近一倍,从而提高电场的积尘效率,减少电场电耗。另外,现有技术中集尘电场的除尘效率较低的主要原因也是粉尘进入电场方向与电场内离子流方向相反或垂直交叉,从而导致粉尘与离子流相互冲撞剧烈并产生较大能量消耗,同时也影响荷电效率,进而使现有技术中电场集尘效率下降,且能耗增加。进气电场装置在收集气体中的粉尘时,气体及粉尘顺离子流方向进入电场,粉尘荷电充分,电场消耗小;单极电场集尘效率会达到99.99%。当气体及粉尘逆离子流方向进入电场,粉尘荷电不充分,电场电耗也会增加,集尘效率会在40%-75%。于本发明一实施例中进气电场装置形成的离子流有利于无动力风扇流体输送、进气增氧、或热量交换等。
随着,除尘电场阳极持续收集进气中的颗粒物等,颗粒物等在除尘电场阳极上堆积并形成灰尘,且灰尘厚度不断增加,使极间距减小。于本发明一实施例中,当电场积尘时,所述进气电场装置检测电场电流,并通过以下任一方式进行灰尘清洁:
(1)当所述进气电场装置检测到电场电流增加到一个给定值,增高电场电压。
(2)当所述进气电场装置检测到电场电流增加到一个给定值,利用电场反电晕放电现象完成灰尘清洁。
(3)当所述进气电场装置检测到电场电流增加到一个给定值,利用电场反电晕放电现象,增高电场电压,限制入注电流,完成灰尘清洁。
(4)当所述进气电场装置检测到电场电流增加到一个给定值,利用电场反电晕放电现象,增高电场电压,限制入注电流,使发生在阳极积碳位置的急剧放电产生等离子,所述等离子使灰尘有机成分深度氧化,高分子键断裂,形成小分子二氧化碳和水,完成灰尘清洁。
于本发明一实施例中进气除尘电场阳极和进气除尘电场阴极分别与电源的两个电极电性连接。加载在进气除尘电场阳极和进气除尘电场阴极上的电压需选择适当的电压等级,具体选择何种电压等级取决于进气电场装置的体积、耐温、容尘率等。例如,电压从1kv至50kv;设计时首先考虑耐温条件,极间距与温度的参数:1MM<30度,积尘面积大于0.1平方/千立方米/小时,电场长度大于单管内切圆的5倍,控制电场气流流速小于9米/秒。于本发明一实施例中进气除尘电场阳极由第一中空阳极管构成、并呈蜂窝状。第一中空阳极管端口的形状可以为圆形或多边形。于本发明一实施例中第一中空阳极管的管内切圆取值范围在5-400mm,对应电压在0.1-120kv之间,第一中空阳极管对应电流在0.1-30A之间;不同的内切圆对应不同的电晕电压,约为1KV/1MM。
于本发明一实施例中进气电场装置包括第一电场级,该第一电场级包括若干个第一电场发生单元,第一电场发生单元可以有一个或多个。第一电场发生单元也称作第一集尘单元,第一集尘单元包括上述进气除尘电场阳极和进气除尘电场阴极,第一集尘单元有一个或多个。第一电场级有多个时,能有效提高进气电场装置的集尘效率。同一第一电场级中,各进气除尘电场阳极为相同极性,各进气除尘电场阴极为相同极性。且第一电场级有多个时,各第一电场级之间串联。于本发明一实施例中进气电场装置还包括若干个连接壳体,串联第一电场级通过连接壳体连接;相邻两级的第一电场级的距离大于极间距的1.4倍。
于本发明一实施例中用电场充电驻极体材料。进气电场装置有故障时,充电驻极体材料会用来除尘。
于本发明一实施例中,所述进气电场装置包括进气驻极体元件。
于本发明一实施例中,所述进气驻极体元件设于所述进气除尘电场阳极内。
于本发明一实施例中,所述进气除尘电场阳极和所述进气除尘电场阴极接通电源时,所述进气驻极体元件在所述进气电离除尘电场中。
于本发明一实施例中,所述进气驻极体元件靠近进气电场装置出口,或者,所述进气驻 极体元件设于进气电场装置出口。
于本发明一实施例中,所述进气除尘电场阳极和所述进气除尘电场阴极形成进气流道,所述进气驻极体元件设于所述进气流道中。
于本发明一实施例中,所述进气流道包括进气流道出口,所述进气驻极体元件靠近所述进气流道出口,或者,所述进气驻极体元件设于所述进气流道出口。
于本发明一实施例中,所述进气驻极体元件于所述进气流道中的横截面占进气流道横截面5%~100%。
于本发明一实施例中,所述进气驻极体元件于所述进气流道中的横截面占进气流道横截面10%-90%、20%-80%、或40%-60%。
于本发明一实施例中,所述进气电离除尘电场给所述进气驻极体元件充电。
于本发明一实施例中,所述进气驻极体元件具有多孔结构。
于本发明一实施例中,所述进气驻极体元件为织品。
于本发明一实施例中,所述进气除尘电场阳极内部为管状,所述进气驻极体元件外部为管状,所述进气驻极体元件外部套设于所述进气除尘电场阳极内部。
于本发明一实施例中,所述进气驻极体元件与所述进气除尘电场阳极为可拆卸式连接。
于本发明一实施例中,所述进气驻极体元件的材料包括具有驻极性能的无机化合物。所述驻极性能是指进气驻极体元件在外接电源充电后带有电荷,并在完全脱离电源的条件下,依然保持有一定的电荷,从而作为电极起到电场电极作用的能力。
于本发明一实施例中,所述无机化合物选自含氧化合物、含氮化合物或玻璃纤维中的一种或多种组合。
于本发明一实施例中,所述含氧化合物选自金属基氧化物、含氧复合物、含氧的无机杂多酸盐中的一种或多种组合。
于本发明一实施例中,所述金属基氧化物选自氧化铝、氧化锌、氧化锆、氧化钛、氧化钡、氧化钽、氧化硅、氧化铅、氧化锡中的一种或多种组合。
于本发明一实施例中,所述金属基氧化物为氧化铝。
于本发明一实施例中,所述含氧复合物选自钛锆复合氧化物或钛钡复合氧化物中的一种或多种组合。
于本发明一实施例中,所述含氧的无机杂多酸盐选自钛酸锆、锆钛酸铅或钛酸钡中的一种或多种组合。
于本发明一实施例中,所述含氮化合物为氮化硅。
于本发明一实施例中,所述进气驻极体元件的材料包括具有驻极性能的有机化合物。所述驻极性能是指进气驻极体元件在外接电源充电后带有电荷,并在完全脱离电源的条件下,依然保持有一定的电荷,从而作为电极起到电场电极作用的能力。
于本发明一实施例中,所述有机化合物选自氟聚合物、聚碳酸酯、PP、PE、PVC、天然蜡、树脂、松香中的一种或多种组合。
于本发明一实施例中,所述氟聚合物选自聚四氟乙烯(PTFE)、聚全氟乙丙烯(Teflon-FEP)、可溶性聚四氟乙烯(PFA)、聚偏氟乙烯(PVDF)中的一种或多种组合。
于本发明一实施例中,所述氟聚合物为聚四氟乙烯。
在上电驱动电压条件下产生进气电离除尘电场,利用进气电离除尘电场电离部分待处理物,吸附进气中的颗粒物,同时向进气驻极体元件进行充电,当进气电场装置出现故障时即无上电驱动电压时,充电的进气驻极体元件产生电场,利用充电的进气驻极体元件产生的电场吸附进气中的颗粒物,即在进气电离除尘电场出现故障情况下仍然可以进行颗粒物的吸附。
于本发明一实施例中,所述进气除尘系统还包括除臭氧装置,用于去除或减少所述进气电场装置产生的臭氧,所述除臭氧装置在进气电场装置出口与进气除尘系统出口之间。
于本发明一实施例中,所述除臭氧装置包括臭氧消解器。
于本发明一实施例中,所述臭氧消解器选自紫外线臭氧消解器和催化臭氧消解器中的至少一种。
本发明进气除尘系统还包括除臭氧装置,用于去除或减少所述进气电场装置产生的臭氧,由于空气中的氧气参与电离,形成臭氧,影响后续装置性能,如若臭氧进入发动机后,内部化学成分氧元素增多,分子量增大,由烃类化合物转变成非烃化合物,外现上颜色变深,沉淀增多,腐蚀性增大,使润滑油的使用性能下降,因此,所述进气除尘系统还包括除臭氧装置,避免或减少后续装置性能的下降,如避免或减少发动机中润滑油使用性能的下降。
对于进气系统,于本发明一实施例中,本发明提供一种进气电场除尘方法,包括以下步骤:
使含尘气体通过进气除尘电场阳极和进气除尘电场阴极产生的进气电离除尘电场;
电场积尘时,进行清尘处理。
于本发明一实施例中,当检测到的电场电流增加到一个给定值时,进行清尘处理。
于本发明一实施例中,当电场积尘时,通过以下任一方式进行灰尘清洁:
(1)利用电场反电晕放电现象完成清尘处理。
(2)利用电场反电晕放电现象,增高电压,限制入注电流,完成清尘处理。
(3)利用电场反电晕放电现象,增高电压,限制入注电流,使发生在阳极积尘位置的急剧放电产生等离子,所述等离子使灰尘有机成分深度氧化,高分子键断裂,形成小分子二氧化碳和水,完成清尘处理。
优选地,所述灰尘为炭黑。
于本发明一实施例中,所述进气除尘电场阴极包括若干根阴极丝。阴极丝的直径可为0.1mm-20mm,该尺寸参数根据应用场合及积尘要求做调整。于本发明一实施例中阴极丝的直径不大于3mm。于本发明一实施例中阴极丝使用容易放电的金属丝或合金丝,耐温且能支撑自身重量,电化学稳定。于本发明一实施例中阴极丝的材质选用钛。阴极丝的具体形状根据除尘电场阳极的形状调整,例如,若进气除尘电场阳极的积尘面是平面,则阴极丝的截面呈圆形;若进气除尘电场阳极的积尘面是圆弧面,阴极丝需要设计成多面形。阴极丝的长度根据除尘电场阳极进行调整。
于本发明一实施例中,所述进气除尘电场阴极包括若干阴极棒。于本发明一实施例中,所述阴极棒的直径不大于3mm。于本发明一实施例中阴极棒使用容易放电的金属棒或合金棒。阴极棒的形状可以为针状、多角状、毛刺状、螺纹杆状或柱状等。阴极棒的形状可以根据进气除尘电场阳极的形状进行调整,例如,若除尘电场阳极的积尘面是平面,则阴极棒的截面需要设计成圆形;若进气除尘电场阳极的积尘面是圆弧面,则阴极棒需要设计成多面形。
于本发明一实施例中,进气除尘电场阴极穿设于进气除尘电场阳极内。
于本发明一实施例中,进气除尘电场阳极包括一个或多个并行设置的中空阳极管。当中空阳极管有多个时,全部中空阳极管构成蜂窝状的进气除尘电场阳极。于本发明一实施例中,中空阳极管的截面可呈圆形或多边形。若中空阳极管的截面呈圆形,进气除尘电场阳极和进气除尘电场阴极之间能形成均匀电场,中空阳极管的内壁不容易积尘。若中空阳极管的截面为三边形时,中空阳极管的内壁上可以形成3个积尘面,3个远角容尘角,此种结构的中空阳极管的容尘率最高。若中空阳极管的截面为四边形,可以获得4个积尘面,4个容尘角,但拼组结构不稳定。若中空阳极管的截面为六边形,可以形成6个积尘面,6个容尘角,积尘面和容尘率达到平衡。若中空阳极管的截面呈更多边形时,可以获得更多的积尘边,但损失容尘率。于本发明一实施例中,中空阳极管的管内切圆直径取值范围为5mm-400mm。
对于进气系统,于本发明一实施例中,本发明提供一种给气体加速的方法,包括以下步骤:
使气体通过一个流道;
在流道中产生电场,所述电场不与所述流道垂直,所述电场包括进口和出口。
其中,所述电场电离所述气体。
于本发明一实施例中,所述电场包括第一阳极和第一阴极,所述第一阳极和第一阴极形成所述流道,所述流道接通所述进口和出口。所述第一阳极和第一阴极电离所述流道中的气体。
于本发明一实施例中,所述电场包括第二电极,所述第二电极设置在或靠近所述进口。
其中,所述第二电极为阴极,且作为所述第一阴极的延伸。优选地,所述第二电极与所述第一阳极具有夹角α,且0°<α≤125°、或45°≤α≤125°、或60°≤α≤100°、或α=90°。
于本发明一实施例中,所述第二电极与所述第一阳极和第一阴极独立设置。
于本发明一实施例中,所述电场包括第三电极,所述第三电极设置在或靠近所述出口。
其中,所述第三电极为阳极,所述第三电极是所述第一阳极的延伸。优选地,所述第三电极与所述第一阴极具有夹角α,且0°<α≤125°、或45°≤α≤125°、或60°≤α≤100°、或α=90°。
于本发明一实施例中,所述第三电极与所述第一阳极和第一阴极独立设置。
于本发明一实施例中,所述第一阴极包括若干根阴极丝。阴极丝的直径可为0.1mm-20mm,该尺寸参数根据应用场合及积尘要求做调整。于本发明一实施例中阴极丝的直径不大于3mm。于本发明一实施例中阴极丝使用容易放电的金属丝或合金丝,耐温且能支撑自身重量,电化学稳定。于本发明一实施例中阴极丝的材质选用钛。阴极丝的具体形状根据第一阳极的形状调整,例如,若第一阳极的积尘面是平面,则阴极丝的截面呈圆形;若第一阳极的积尘面是圆弧面,阴极丝需要设计成多面形。阴极丝的长度根据第一阳极进行调整。
于本发明一实施例中,所述第一阴极包括若干阴极棒。于本发明一实施例中,所述阴极棒的直径不大于3mm。于本发明一实施例中阴极棒使用容易放电的金属棒或合金棒。阴极棒的形状可以为针状、多角状、毛刺状、螺纹杆状或柱状等。阴极棒的形状可以根据第一阳极的形状进行调整,例如,若第一阳极的积尘面是平面,则阴极棒的截面需要设计成圆形;若第一阳极的积尘面是圆弧面,则阴极棒需要设计成多面形。
于本发明一实施例中,第一阴极穿设于第一阳极内。
于本发明一实施例中,第一阳极包括一个或多个并行设置的中空阳极管。当中空阳极管有多个时,全部中空阳极管构成蜂窝状的第一阳极。于本发明一实施例中,中空阳极管的截面可呈圆形或多边形。若中空阳极管的截面呈圆形,第一阳极和第一阴极之间能形成均匀电场,中空阳极管的内壁不容易积尘。若中空阳极管的截面为三边形时,中空阳极管的内壁上可以形成3个积尘面,3个远角容尘角,此种结构的中空阳极管的容尘率最高。若中空阳极管的截面为四边形,可以获得4个积尘面,4个容尘角,但拼组结构不稳定。若中空阳极管的截面为六边形,可以形成6个积尘面,6个容尘角,积尘面和容尘率达到平衡。若中空阳极管的截面呈更多边形时,可以获得更多的积尘边,但损失容尘率。于本发明一实施例中,中空 阳极管的管内切圆直径取值范围为5mm-400mm。
对于进气系统,于一实施例中,本发明提供一种减少进气除尘电场耦合的方法,包括以下步骤:
使进气通过进气除尘电场阳极和进气除尘电场阴极产生的进气电离除尘电场;
选择所述进气除尘电场阳极或/和进气除尘电场阴极。
于本发明一实施例中,选择的所述进气除尘电场阳极或/和进气除尘电场阴极尺寸使电场耦合次数≤3。
具体地,选择所述进气除尘电场阳极的集尘面积与进气除尘电场阴极的放电面积的比。优选地,选择所述进气除尘电场阳极的积尘面积与所述进气除尘电场阴极的放电面积的比为1.667:1-1680:1。
更为优选地,选择所述进气除尘电场阳极的积尘面积与所述进气除尘电场阴极的放电面积的比为6.67:1-56.67:1。
于本发明一实施例中,所述进气除尘电场阴极直径为1-3毫米,所述进气除尘电场阳极与所述进气除尘电场阴极的极间距为2.5-139.9毫米;所述进气除尘电场阳极的积尘面积与所述进气除尘电场阴极的放电面积的比为1.667:1-1680:1。
优选地,选择所述进气除尘电场阳极和所述进气除尘电场阴极的极间距小于150mm。
优选地,选择所述进气除尘电场阳极与所述进气电场阴极的极间距为2.5~139.9mm。更为优选地,选择所述进气除尘电场阳极与所述进气除尘电场阴极的极间距为5.0~100mm。
优选地,选择所述进气除尘电场阳极长度为10~180mm。更为优选地,选择所述进气除尘电场阳极长度为60~180mm。
优选地,选择所述进气除尘电场阴极长度为30~180mm。更为优选地,选择所述进气除尘电场阴极长度为54~176mm。
于本发明一实施例中,所述进气除尘电场阴极包括若干根阴极丝。阴极丝的直径可为0.1mm-20mm,该尺寸参数根据应用场合及积尘要求做调整。于本发明一实施例中阴极丝的直径不大于3mm。于本发明一实施例中阴极丝使用容易放电的金属丝或合金丝,耐温且能支撑自身重量,电化学稳定。于本发明一实施例中阴极丝的材质选用钛。阴极丝的具体形状根据进气除尘电场阳极的形状调整,例如,若进气除尘电场阳极的积尘面是平面,则阴极丝的截面呈圆形;若进气除尘电场阳极的积尘面是圆弧面,阴极丝需要设计成多面形。阴极丝的长度根据进气除尘电场阳极进行调整。
于本发明一实施例中,所述进气除尘电场阴极包括若干阴极棒。于本发明一实施例中, 所述阴极棒的直径不大于3mm。于本发明一实施例中阴极棒使用容易放电的金属棒或合金棒。阴极棒的形状可以为针状、多角状、毛刺状、螺纹杆状或柱状等。阴极棒的形状可以根据进气除尘电场阳极的形状进行调整,例如,若进气除尘电场阳极的积尘面是平面,则阴极棒的截面需要设计成圆形;若进气除尘电场阳极的积尘面是圆弧面,则阴极棒需要设计成多面形。
于本发明一实施例中,进气除尘电场阴极穿设于进气除尘电场阳极内。
于本发明一实施例中,进气除尘电场阳极包括一个或多个并行设置的中空阳极管。当中空阳极管有多个时,全部中空阳极管构成蜂窝状的进气除尘电场阳极。于本发明一实施例中,中空阳极管的截面可呈圆形或多边形。若中空阳极管的截面呈圆形,进气除尘电场阳极和进气除尘电场阴极之间能形成均匀电场,中空阳极管的内壁不容易积尘。若中空阳极管的截面为三边形时,中空阳极管的内壁上可以形成3个积尘面,3个远角容尘角,此种结构的中空阳极管的容尘率最高。若中空阳极管的截面为四边形,可以获得4个积尘面,4个容尘角,但拼组结构不稳定。若中空阳极管的截面为六边形,可以形成6个积尘面,6个容尘角,积尘面和容尘率达到平衡。若中空阳极管的截面呈更多边形时,可以获得更多的积尘边,但损失容尘率。于本发明一实施例中,中空阳极管的管内切圆直径取值范围为5mm-400mm。
一种进气除尘方法,包括如下步骤:
1)利用进气电离除尘电场吸附进气中的颗粒物;
2)利用进气电离除尘电场给进气驻极体元件充电。
于本发明一实施例中,所述进气驻极体元件靠近进气电场装置出口,或者,所述进气驻极体元件设于进气电场装置出口。
于本发明一实施例中,所述进气除尘电场阳极和所述进气除尘电场阴极形成进气流道,所述进气驻极体元件设于所述进气流道中。
于本发明一实施例中,所述进气流道包括进气流道出口,所述进气驻极体元件靠近所述进气流道出口,或者,所述进气驻极体元件设于所述进气流道出口。
于本发明一实施例中,当进气电离除尘电场无上电驱动电压时,利用充电的进气驻极体元件吸附进气中的颗粒物。
于本发明一实施例中,在充电的进气驻极体元件吸附一定的进气中的颗粒物后,将其替换为新的进气驻极体元件。
于本发明一实施例中,替换为新的进气驻极体元件后重新启动进气电离除尘电场吸附进气中的颗粒物,并给新的进气驻极体元件充电。
于本发明一实施例中,所述进气驻极体元件的材料包括具有驻极性能的无机化合物。所 述驻极性能是指进气驻极体元件在外接电源充电后带有电荷,并在完全脱离电源的条件下,依然保持有一定的电荷,从而作为电极起到电场电极作用的能力。
于本发明一实施例中,所述无机化合物选自含氧化合物、含氮化合物或玻璃纤维中的一种或多种组合。
于本发明一实施例中,所述含氧化合物选自金属基氧化物、含氧复合物、含氧的无机杂多酸盐中的一种或多种组合。
于本发明一实施例中,所述金属基氧化物选自氧化铝、氧化锌、氧化锆、氧化钛、氧化钡、氧化钽、氧化硅、氧化铅、氧化锡中的一种或多种组合。
于本发明一实施例中,所述金属基氧化物为氧化铝。
于本发明一实施例中,所述含氧复合物选自钛锆复合氧化物或钛钡复合氧化物中的一种或多种组合。
于本发明一实施例中,所述含氧的无机杂多酸盐选自钛酸锆、锆钛酸铅或钛酸钡中的一种或多种组合。
于本发明一实施例中,所述含氮化合物为氮化硅。
于本发明一实施例中,所述进气驻极体元件的材料包括具有驻极性能的有机化合物。所述驻极性能是指进气驻极体元件在外接电源充电后带有电荷,并在完全脱离电源的条件下,依然保持有一定的电荷,从而作为电极起到电场电极作用的能力。
于本发明一实施例中,所述有机化合物选自氟聚合物、聚碳酸酯、PP、PE、PVC、天然蜡、树脂、松香中的一种或多种组合。
于本发明一实施例中,所述氟聚合物选自聚四氟乙烯(PTFE)、聚全氟乙丙烯(Teflon-FEP)、可溶性聚四氟乙烯(PFA)、聚偏氟乙烯(PVDF)中的一种或多种组合。
于本发明一实施例中,所述氟聚合物为聚四氟乙烯。
一种进气除尘方法,包括以下步骤:所述进气经进气电离除尘后去除或减少进气电离除尘产生的臭氧。
于本发明一实施例中,对进气电离除尘产生的臭氧进行臭氧消解。
于本发明一实施例中,所述臭氧消解选自紫外线消解和催化消解中的至少一种。
于本发明一实施例中发动机排放处理系统包括尾气除尘系统。尾气除尘系统与发动机的出口相连通。发动机排放的尾气将流经尾气除尘系统。
于本发明一实施例中,所述尾气除尘系统还包括除水装置,用于在尾气电场装置入口之前去除液体水。
于本发明一实施例中,当尾气温度或发动机温度低于一定温度时,发动机尾气中可能含有液体水,所述除水装置脱除尾气中的液体水。
于本发明一实施例中,所述一定温度在90℃以上、100℃以下。
于本发明一实施例中,所述一定温度在80℃以上、90℃以下。
于本发明一实施例中,所述一定温度为80℃以下。
于本发明一实施例中,所述除水装置为电凝装置。
本领域技术人员没有认识到如下技术问题:在尾气温度低如发动机尾气或发动机温度低时,尾气中会有液体水,吸附在尾气除尘电场阴极和尾气除尘电场阳极上,造成尾气电离除尘电场放电不均匀、打火,而本发明的发明人发现此问题,并提出尾气除尘系统设置除水装置,用于在尾气电场装置入口之前去除液体水,液体水具有导电性,会缩短电离距离,导致尾气电离除尘电场放电不均匀,易导致电极击穿。所述除水装置在发动机冷启动时,在尾气进入尾气电场装置入口之前脱除尾气中的水珠即液体水,从而减少尾气中的水珠即液体水,减少尾气电离除尘电场放电不均匀及尾气除尘电场阴极和尾气除尘电场阳极击穿,从而提高电离除尘效率,取得预料不到的技术效果。所述除水装置没有特别的限制,现有技术中能实现去除尾气中的液体水都适用本发明。
于本发明一实施例中,所述尾气除尘系统还包括补氧装置,用于在尾气电离除尘电场之前添加包括氧气的气体,比如空气。
于本发明一实施例中,所述补氧装置通过单纯增氧、通入外界空气、通入压缩空气和/或通入臭氧的方式添加氧气。
于本发明一实施例中,至少根据尾气颗粒含量决定补氧量。
本领域技术人员没有认识到如下技术问题:在某些情况下,尾气会没有足够的氧气产生足够的氧离子,造成除尘效果不好,即,本领域技术人员没有认识到尾气中的氧气可能不足以支持有效电离,而本发明的发明人发现此问题,并提出本发明尾气除尘系统:包括补氧装置,可以通过单纯增氧、通入外界空气、通入压缩空气和/或通入臭氧的方式添加氧气,提高进入尾气电离除尘电场尾气含氧量,从而当尾气流经尾气除尘电场阴极和尾气除尘电场阳极之间的尾气电离除尘电场时,增加电离的氧气,使得尾气中更多的粉尘荷电,进而在尾气除尘电场阳极的作用下将更多的荷电的粉尘收集起来,使得尾气电场装置的除尘效率更高,有利于尾气电离除尘电场收集尾气颗粒物,取得预料不到的技术效果,同时还取得新的技术效果:能起到降温的作用,增加电力系统效率,而且,补氧也会提高尾气电离除尘电场臭氧含量,有利于提高尾气电离除尘电场对尾气中有机物进行净化、自洁、脱硝等处理的效率。
于本发明一实施例中尾气除尘系统可包括尾气均风装置。该尾气均风装置设置在尾气电场装置之前,能使进入电离除尘装置的气流均匀通过
于本发明一实施例中尾气电场装置的尾气除尘电场阳极可为立方体,尾气均风装置可包括位于阴极支撑板一侧边的进气管、及位于阴极支撑板另一侧边的出气管,阴极支撑板位于尾气除尘电场阳极的进气端;其中,安装进气管的侧边与安装出气管的侧边相对立。尾气均风装置能使进入尾气电场装置的尾气均匀通过静电场。
于本发明一实施例中尾气除尘电场阳极可为圆柱体,尾气均风装置在所述尾气除尘系统入口与所述尾气除尘电场阳极和所述尾气除尘电场阴极形成的尾气电离除尘电场之间,且尾气均风装置包括若干围绕尾气电场装置入口中心旋转的均风叶片。尾气均风装置能够使各种变化的进气量均匀通过尾气除尘电场阳极产生的电场,同时,能够保持尾气除尘电场阳极内部温度恒定,氧气充足。尾气均风装置能使进入尾气电场装置的尾气均匀通过静电场。
于本发明一实施例中尾气均风装置包括设置于尾气除尘电场阳极的进气端的进风板和设置于尾气除尘电场阳极出气端的出风板,进风板上开设有进气孔,出风板上开设有出气孔,进气孔与出气孔错位排布,且正面进气、侧面出气,形成旋风结构。尾气均风装置能使进入尾气电场装置的尾气均匀通过静电场。
于本发明一实施例中尾气除尘系统可包括尾气除尘系统入口、尾气除尘系统出口和尾气电场装置。且于本发明一实施例中尾气电场装置可包括尾气电场装置入口、尾气电场装置出口、及位于尾气电场装置入口和尾气电场装置出口之间的尾气前置电极,当发动机排放的尾气由尾气电场装置入口流经尾气前置电极时,尾气中的颗粒物等将带电。
于本发明一实施例中尾气电场装置包括尾气前置电极,该尾气前置电极在尾气电场装置入口与尾气除尘电场阳极和尾气除尘电场阴极形成的尾气电离除尘电场之间。当气体由尾气电场装置入口流经尾气前置电极时,气体中的颗粒物等将带电。
于本发明一实施例中尾气前置电极的形状可以为点状、线状、网状、孔板状、板状、针棒状、球笼状、盒状、管状、物质自然形态、或物质加工形态。当尾气前置电极为有孔结构时,尾气前置电极上设有一个或多个尾气通孔。于本发明一实施例中尾气通孔的形状可以为多角形、圆形、椭圆形、正方形、长方形、梯形、或菱形。于本发明一实施例中尾气通孔的轮廓大小可以为0.1~3mm、0.1~0.2mm、0.2~0.5mm、0.5~1mm、1~1.2mm、1.2~1.5mm、1.5~2mm、2~2.5mm、2.5~2.8mm、或2.8~3mm。
于本发明一实施例中尾气前置电极的形态可以为固体、液体、气体分子团、等离子体、导电混合态物质、生物体自然混合导电物质、或物体人工加工形成导电物质中的一种或多种 形态的组合。当尾气前置电极为固体时,可采用固态金属,比如304钢,或其它固态的导体、比如石墨等。当尾气前置电极为液体时,可以是含离子导电液体。
在工作时,在带污染物的气体进入尾气除尘电场阳极和尾气除尘电场阴极形成的尾气电离除尘电场之前,且带污染物的气体通过尾气前置电极时,尾气前置电极使气体中的污染物带电。当带污染物的气体进入尾气电离除尘电场时,尾气除尘电场阳极给带电的污染物施加吸引力,使污染物向尾气除尘电场阳极移动,直至污染物附着在尾气除尘电场阳极上。
于本发明一实施例中尾气前置电极将电子导入污染物,电子在位于尾气前置电极和尾气除尘电场阳极之间的污染物之间进行传递,使更多污染物带电。尾气前置电极和尾气除尘电场阳极之间通过污染物传导电子、并形成电流。
于本发明一实施例中尾气前置电极通过与污染物接触的方式使污染物带电。于本发明一实施例中尾气前置电极通过能量波动的方式使污染物带电。于本发明一实施例中尾气前置电极通过与污染物接触的方式将电子转移到污染物上,并使污染物带电。于本发明一实施例中尾气前置电极通过能量波动的方式将电子转移到污染物上,并使污染物带电。
于本发明一实施例中尾气前置电极呈线状,尾气除尘电场阳极呈面状。于本发明一实施例中尾气前置电极垂直于尾气除尘电场阳极。于本发明一实施例中尾气前置电极与尾气除尘电场阳极相平行。于本发明一实施例中尾气前置电极呈曲线状或圆弧状。于本发明一实施例中尾气前置电极采用金属丝网。于本发明一实施例中尾气前置电极与尾气除尘电场阳极之间的电压不同于尾气除尘电场阴极和尾气除尘电场阳极之间的电压。于本发明一实施例中尾气前置电极与尾气除尘电场阳极之间的电压小于起始起晕电压。起始起晕电压为尾气除尘电场阴极和尾气除尘电场阳极之间的电压的最小值。于本发明一实施例中尾气前置电极与尾气除尘电场阳极之间的电压可以为0.1-2kv/mm。
于本发明一实施例中尾气电场装置包括尾气流道,尾气前置电极位于尾气流道中。于本发明一实施例中尾气前置电极的截面面积与尾气流道的截面面积比为99%~10%、或90~10%、或80~20%、或70~30%、或60~40%、或50%。尾气前置电极的截面面积是指尾气前置电极沿截面上实体部分的面积之和。于本发明一实施例中尾气前置电极带负电势。
于本发明一实施例中当尾气通过尾气电场装置入口流入尾气流道中,尾气中导电性较强的金属粉尘、雾滴、或气溶胶等污染物在与尾气前置电极相接触时,或与尾气前置电极的距离达到一定范围时会直接带负电,随后,全部污染物随气流进入尾气电离除尘电场,尾气除尘电场阳极给已带负电的金属粉尘、雾滴、或气溶胶等施加吸引力,使已带负电的污染物向尾气除尘电场阳极移动,直至该部分污染物附着在尾气除尘电场阳极上,实现将该部分污染 物收集起来,同时,尾气除尘电场阳极与尾气除尘电场阴极之间形成的尾气电离除尘电场通过电离气体中的氧获得氧离子,且带负电荷的氧离子在与普通粉尘结合后,使普通粉尘带负电荷,尾气除尘电场阳极给该部分带负电荷的粉尘等污染物施加吸引力,使粉尘等污染物向尾气除尘电场阳极移动,直至该部分污染物附着在尾气除尘电场阳极上,实现将该部分普通粉尘等污染物也收集起来,从而将尾气中导电性较强和导电性较弱的污染物均收集起来,并使得尾气除尘电场阳极能收集尾气中污染物的种类更广泛,且收集能力更强,收集效率更高。
于本发明一实施例中尾气电场装置入口与发动机的出口相连通。
于本发明一实施例中尾气电场装置可包括尾气除尘电场阴极和尾气除尘电场阳极,尾气除尘电场阴极与尾气除尘电场阳极之间形成电离除尘电场。尾气进入电离除尘电场,尾气中的氧离子将被电离,并形成大量带有电荷的氧离子,氧离子与尾气中粉尘等颗粒物结合,使得颗粒物荷电,尾气除尘电场阳极给带负电荷的颗粒物施加吸附力,使得颗粒物被吸附在尾气除尘电场阳极上,以清除掉尾气中的颗粒物。
于本发明一实施例中尾气除尘电场阴极包括若干根阴极丝。阴极丝的直径可为0.1mm-20mm,该尺寸参数根据应用场合及积尘要求做调整。于本发明一实施例中阴极丝的直径不大于3mm。于本发明一实施例中阴极丝使用容易放电的金属丝或合金丝,耐温且能支撑自身重量,电化学稳定。于本发明一实施例中阴极丝的材质选用钛。阴极丝的具体形状根据尾气除尘电场阳极的形状调整,例如,若尾气除尘电场阳极的积尘面是平面,则阴极丝的截面呈圆形;若尾气除尘电场阳极的积尘面是圆弧面,阴极丝需要设计成多面形。阴极丝的长度根据尾气除尘电场阳极进行调整。
于本发明一实施例中尾气除尘电场阴极包括若干阴极棒。于本发明一实施例中阴极棒的直径不大于3mm。于本发明一实施例中阴极棒使用容易放电的金属棒或合金棒。阴极棒的形状可以为针状、多角状、毛刺状、螺纹杆状或柱状等。阴极棒的形状可以根据尾气除尘电场阳极的形状进行调整,例如,若尾气除尘电场阳极的积尘面是平面,则阴极棒的截面需要设计成圆形;若尾气除尘电场阳极的积尘面是圆弧面,则阴极棒需要设计成多面形。
于本发明一实施例中尾气除尘电场阴极穿设于尾气除尘电场阳极内。
于本发明一实施例中尾气除尘电场阳极包括一个或多个并行设置的中空阳极管。当中空阳极管有多个时,全部中空阳极管构成蜂窝状的尾气除尘电场阳极。于本发明一实施例中中空阳极管的截面可呈圆形或多边形。若中空阳极管的截面呈圆形,尾气除尘电场阳极和尾气除尘电场阴极之间能形成均匀电场,中空阳极管的内壁不容易积尘。若中空阳极管的截面为三边形时,中空阳极管的内壁上可以形成3个积尘面,3个远角容尘角,此种结构的中空阳 极管的容尘率最高。若中空阳极管的截面为四边形,可以获得4个积尘面,4个容尘角,但拼组结构不稳定。若中空阳极管的截面为六边形,可以形成6个积尘面,6个容尘角,积尘面和容尘率达到平衡。若中空阳极管的截面呈更多边形时,可以获得更多的积尘边,但损失容尘率。于本发明一实施例中中空阳极管的管内切圆直径取值范围为5mm-400mm。
于本发明一实施例中尾气除尘电场阴极安装在阴极支撑板上,阴极支撑板与尾气除尘电场阳极通过尾气绝缘机构相连接。于本发明一实施例中尾气除尘电场阳极包括第三阳极部和第四阳极部,即所述第三阳极部靠近尾气电场装置入口,第四阳极部靠近尾气电场装置出口。阴极支撑板和尾气绝缘机构在第三阳极部和第四阳极部之间,即尾气绝缘机构安装在尾气电离除尘电场中间、或尾气除尘电场阴极中间,可以对尾气除尘电场阴极起到良好的支撑作用,并对尾气除尘电场阴极起到相对于尾气除尘电场阳极的固定作用,使尾气除尘电场阴极和尾气除尘电场阳极之间保持设定的距离。而现有技术中,阴极的支撑点在阴极的端点,难以保持阴极和阳极之间的距离。于本发明一实施例中尾气绝缘机构设置在除尘流道外、即第二级流道外,以防止或减少尾气中的灰尘等聚集在尾气绝缘机构上,导致尾气绝缘机构击穿或导电。
于本发明一实施例中尾气绝缘机构采用耐高压陶瓷绝缘子,对尾气除尘电场阴极和尾气除尘电场阳极之间进行绝缘。尾气除尘电场阳极也称作一种外壳。
于本发明一实施例中第三阳极部在气体流动方向上位于阴极支撑板和尾气绝缘机构之前,第三阳极部能够除去尾气中的水,防止水进入尾气绝缘机构,造成尾气绝缘机构短路、打火。另外,第三阳级部能够除去尾气中相当一部分的灰尘,当尾气通过尾气绝缘机构时,相当一部分的灰尘已被消除,减少灰尘造成尾气绝缘机构短路的可能性。于本发明一实施例中尾气绝缘机构包括绝缘瓷柱。第三阳极部的设计,主要是为了保护绝缘瓷柱不被气体中颗粒物等污染,一旦气体污染绝缘瓷柱将会造成尾气除尘电场阳极和尾气除尘电场阴极导通,从而使尾气除尘电场阳极的积尘功能失效,故第三阳极部的设计,能有效减少绝缘瓷柱被污染,提高产品的使用时间。在尾气流经第二级流道过程中,第三阳极部和尾气除尘电场阴极先接触具有污染性的气体,尾气绝缘机构后接触气体,达到先除尘后经过尾气绝缘机构的目的,减少对尾气绝缘机构造成的污染,延长清洁维护周期,对应电极使用后绝缘支撑。于本发明一实施例中,所述第三阳极部的长度是足够的长,以清除部分灰尘,减少积累在所述尾气绝缘机构和所述阴极支撑板上的灰尘,减少灰尘造成的电击穿。于本发明一实施例中第三阳极部长度占尾气除尘电场阳极总长度的1/10至1/4、1/4至1/3、1/3至1/2、1/2至2/3、2/3至3/4,或3/4至9/10。
于本发明一实施例中第四阳极部在尾气流动方向上位于阴极支撑板和尾气绝缘机构之后。第四阳极部包括积尘段和预留积尘段。其中,积尘段利用静电吸附尾气中的颗粒物,该积尘段是为了增加积尘面积,延长尾气电场装置的使用时间。预留积尘段能为积尘段提供失效保护。预留积尘段是为了在满足设计除尘要求的前提下,进一步提高积尘面积。预留积尘段作为补充前段积尘使用。于本发明一实施例中预留积尘段和第三阳极部可使用不同的电源。
于本发明一实施例中由于尾气除尘电场阴极和尾气除尘电场阳极之间存在极高电位差,为了防止尾气除尘电场阴极和尾气除尘电场阳极导通,尾气绝缘机构设置在尾气除尘电场阴极和尾气除尘电场阳极之间的第二级流道之外。因此,尾气绝缘机构外悬于尾气除尘电场阳极的外侧。于本发明一实施例中尾气绝缘机构可采用非导体耐温材料,比如陶瓷、玻璃等。于本发明一实施例中,完全密闭无空气的材料绝缘要求绝缘隔离厚度>0.3mm/kv;空气绝缘要求>1.4mm/kv。可根据尾气除尘电场阴极和尾气除尘电场阳极之间的极间距的1.4倍设置绝缘距离。于本发明一实施例中尾气绝缘机构使用陶瓷,表面上釉;不能使用胶粘或有机材料填充连接,耐温大于350摄氏度。
于本发明一实施例中尾气绝缘机构包括绝缘部和隔热部。为了使尾气绝缘机构具有抗污功能,绝缘部的材料采用陶瓷材料或玻璃材料。于本发明一实施例中绝缘部可为伞状串陶瓷柱或玻璃柱,伞内外挂釉。伞状串陶瓷柱或玻璃柱的外缘与尾气除尘电场阳极的距离大于电场距离的1.4倍、即大于极间距的1.4倍。伞状串陶瓷柱或玻璃柱的伞突边间距总和大于伞状串陶瓷柱的绝缘间距的1.4倍。伞状串陶瓷柱或玻璃柱的伞边内深总长大于伞状串陶瓷柱的绝缘距离1.4倍。绝缘部还可为柱状串陶瓷柱或玻璃柱,柱内外挂釉。于本发明一实施例中绝缘部还可呈塔状。
于本发明一实施例中,绝缘部内设置加热棒,当绝缘部周围温度接近露点时,加热棒启动并进行加热。由于使用中绝缘部的内外存在温差,绝缘部的内外、外部容易产生凝露。绝缘部的外表面可能自发或被气体加热产生高温,需要必要的隔离防护,防烫伤。隔热部包括位于第二绝缘部外部的防护围挡板、脱硝净化反应腔。于本发明一实施例中绝缘部的尾部需要凝露位置同样需要隔热,防止环境以及散热高温加热凝露组件。
于本发明一实施例中尾气电场装置的电源的引出线使用伞状串陶瓷柱或玻璃柱过墙式连接,墙内使用弹性碰头连接阴极支撑板,墙外使用密闭绝缘防护接线帽插拔连接,引出线过墙导体与墙绝缘距离大于伞状串陶瓷柱或玻璃柱的陶瓷绝缘距离。于本发明一实施例中高压部分取消引线,直接安装在端头上,确保安全,高压模块整体外绝缘使用ip68防护,使用介质换热散热。
于本发明一实施例中尾气除尘电场阴极和尾气除尘电场阳极之间采用非对称结构。在对称电场中极性粒子受到一个相同大小而方向相反的作用力,极性粒子在电场中往复运动;在非对称电场中,极性粒子受到两个大小不同的作用力,极性粒子向作用力大的方向移动,可以避免产生耦合。
本发明的尾气电场装置的尾气除尘电场阴极和尾气除尘电场阳极之间形成电离除尘电场。为了减少所述电离除尘电场的电场耦合,于本发明一实施例中,减少电场耦合的方法包括如下步骤:选择尾气除尘电场阳极的集尘面积与尾气除尘电场阴极的放电面积的比,使电场耦合次数≤3。于本发明一实施例中尾气除尘电场阳极的集尘面积与尾气除尘电场阴极的放电面积的比可以为:1.667:1-1680:1;3.334:1-113.34:1;6.67:1-56.67:1;13.34:1-28.33:1。该实施例选择相对大面积的尾气除尘电场阳极的集尘面积和相对极小的尾气除尘电场阴极的放电面积,具体选择上述面积比,可以减少尾气除尘电场阴极的放电面积,减小吸力,扩大尾气除尘电场阳极的集尘面积,扩大吸力,即尾气除尘电场阴极和尾气除尘电场阳极间产生不对称的电极吸力,使荷电后粉尘落入尾气除尘电场阳极的集尘表面,虽极性改变但无法再被尾气除尘电场阴极吸走,减少电场耦合,实现电场耦合次数≤3。即在电场极间距小于150mm时电场耦合次数≤3,电场能耗低,能够减少电场对气溶胶、水雾、油雾、松散光滑颗粒物的耦合消耗,节省电场电能30~50%。集尘面积是指尾气除尘电场阳极工作面的面积,比如,若尾气除尘电场阳极呈中空的正六边形管状,集尘面积即为中空的正六边形管状的内表面积,集尘面积也称作积尘面积。放电面积指尾气除尘电场阴极工作面的面积,比如,若尾气除尘电场阴极呈棒状,放电面积即为棒状的外表面积。
于本发明一实施例中尾气除尘电场阳极的长度可以为10~180mm、10~20mm、20~30mm60~180mm、30~40mm、40~50mm、50~60mm、60~70mm、70~80mm、80~90mm、90~100mm、100~110mm、110~120mm、120~130mm、130~140mm、140~150mm、150~160mm、160~170mm、170~180mm、60mm、180mm、10mm或30mm。尾气除尘电场阳极的长度是指尾气除尘电场阳极工作面的一端至另一端的最小长度。尾气除尘电场阳极选择此种长度,可以有效减少电场耦合。
于本发明一实施例中尾气除尘电场阳极的长度可以为10~90mm、15~20mm、20~25mm、25~30mm、30~35mm、35~40mm、40~45mm、45~50mm、50~55mm、55~60mm、60~65mm、65~70mm、70~75mm、75~80mm、80~85mm或85~90mm,此种长度的设计可以使尾气除尘电场阳极及尾气电场装置具有耐高温特性,并使得尾气电场装置在高温冲击下具有高效率的集尘能力。
于本发明一实施例中尾气除尘电场阴极的长度可以为30~180mm、54~176mm、30~40mm、40~50mm、50~54mm、54~60mm、60~70mm、70~80mm、80~90mm、90~100mm、100~110mm、110~120mm、120~130mm、130~140mm、140~150mm、150~160mm、160~170mm、170~176mm、170~180mm、54mm、180mm、或30mm。尾气除尘电场阴极的长度是指尾气除尘电场阴极工作面的一端至另一端的最小长度。尾气除尘电场阴极选择此种长度,可以有效减少电场耦合。
于本发明一实施例中尾气除尘电场阴极的长度可以为10~90mm、15~20mm、20~25mm、25~30mm、30~35mm、35~40mm、40~45mm、45~50mm、50~55mm、55~60mm、60~65mm、65~70mm、70~75mm、75~80mm、80~85mm或85~90mm,此种长度的设计可以使尾气除尘电场阴极及尾气电场装置具有耐高温特性,并使得尾气电场装置在高温冲击下具有高效率的集尘能力。其中,当电场温度为200℃时,对应的集尘效率为99.9%;电场温度为400℃时,对应的集尘效率为90%;当电场温度为500℃时,对应的集尘效率为50%。
于本发明一实施例中尾气除尘电场阳极和尾气除尘电场阴极之间的距离可以为5~30mm、2.5~139.9mm、9.9~139.9mm、2.5~9.9mm、9.9~20mm、20~30mm、30~40mm、40~50mm、50~60mm、60~70mm、70~80mm、80~90mm、90~100mm、100~110mm、110~120mm、120~130mm、130~139.9mm、9.9mm、139.9mm、或2.5mm。尾气除尘电场阳极和尾气除尘电场阴极之间的距离也称作极间距。极间距具体是指尾气除尘电场阳极、尾气除尘电场阴极工作面之间的最小垂直距离。此种极间距的选择可以有效减少电场耦合,并使尾气电场装置具有耐高温特性。
于本发明一实施例中,所述尾气除尘电场阴极直径为1-3毫米,所述尾气除尘电场阳极与所述尾气除尘电场阴极的极间距为2.5-139.9毫米;所述尾气除尘电场阳极的积尘面积与所述尾气除尘电场阴极的放电面积的比为1.667:1-1680:1
鉴于电离除尘的特有性能,电离除尘可适用去除气体中的颗粒物,例如可用于去除发动机排气中的颗粒物。但是,经过许多大学、研究机构、企业的多年的研究,现有电场除尘装置仍然不适合在车辆中使用。首先,现有技术中的电场除尘装置体积过于庞大而较难安装在车辆中。其次,重要的是,现有技术中电场除尘装置只能去除约70%的颗粒物,不能满足许多国家的排放标准。
本发明的发明人研究发现,现有技术中电场除尘装置的缺点是由电场耦合引起的。本发明通过减小电场耦合次数,可以显著减小电场除尘装置的尺寸(即体积)。比如,本发明提供的电离除尘装置的尺寸约为现有电离除尘装置尺寸的五分之一。原因是,为了获得可接受的颗粒去除率,现有电离除尘装置中将气体流速设为1m/s左右,而本发明在将气体流速提高 到6m/s的情况下,仍能获得较高的颗粒去除率。当处理一给定流量的气体时,随着气体速度的提高,电场除尘装置的尺寸可以减小。
另外,本发明可以显著提高颗粒去除效率。例如,在气体流速为1m/s左右时,现有技术电场除尘装置可以去除发动机排气中大约70%的颗粒物,但是本发明可以去除大约99%的颗粒物,即使在气体流速为6m/s时。因此,本发明可以满足最新的排放标准。
由于发明人发现了电场耦合的作用,并且找到了减少电场耦合次数的方法,本发明获得了上述预料不到的结果。所以,本发明可以用来制造适用于车辆的电场除尘装置。
尾气除尘电场阳极和尾气除尘电场阴极之间的电离除尘电场也称作第三电场。于本发明一实施例中尾气除尘电场阳极和尾气除尘电场阴极之间还形成有与第三电场不平行的第四电场。于本发明另一实施例中,所述第四电场与所述电离除尘电场的流道不垂直。第四电场也称作辅助电场,可以通过一个或两个第二辅助电极形成。当第四电场由一个第二辅助电极形成时,该第二辅助电极可以放在电离电场的进口或出口,该第二辅助电极可以带负电势、或正电势。其中,当所述第二辅助电极为阴极时,设置在或靠近所述电离除尘电场的进口;所述第二辅助电极与所述尾气除尘电场阳极具有夹角α,且0°<α≤125°、或45°≤α≤125°、或60°≤α≤100°、或α=90°。当所述第二辅助电极为阳极时,设置在或靠近所述电离除尘电场的出口;所述第二辅助电极与所述尾气除尘电场阴极具有夹角α,且0°<α≤125°、或45°≤α≤125°、或60°≤α≤100°、或α=90°。当第四电场由两个第二辅助电极形成时,其中一个第二辅助电极可以带负电势,另一个第二辅助电极可以带正电势;一个第二辅助电极可以放在电离除尘电场的进口,另一个第二辅助电极放在电离除尘电场的出口。另外,第二辅助电极可以是尾气除尘电场阴极或尾气除尘电场阳极的一部分,即第二辅助电极可以是由尾气除尘电场阴极或尾气除尘电场阳极的延伸段构成,此时尾气除尘电场阴极和尾气除尘电场阳极的长度不一样。第二辅助电极也可以是一个单独的电极,也就是说第二辅助电极可以不是尾气除尘电场阴极或尾气除尘电场阳极的一部分,此时,第四电场的电压和第三电场的电压不一样,可以根据工作状况单独地控制。
第四电场能给尾气除尘电场阳极和尾气除尘电场阴极之间带负电荷的氧离子流施加朝向电离电场的出口的力,使得尾气除尘电场阳极和尾气除尘电场阴极之间带负电荷的氧离子流具有向出口的移动速度。在尾气流入电离电场,并向电离电场的出口方向流动过程中,带负电荷的氧离子也在向尾气除尘电场阳极且向电离电场的出口方向移动,且带负电荷的氧离子在向尾气除尘电场阳极且向电离电场的出口移动过程中将与尾气中的颗粒物等相结合,由于氧离子具有向出口的移动速度,氧离子在与颗粒物相结合时,两者间不会产生较强的碰撞, 从而避免因较强碰撞而造成较大的能量消耗,保证氧离子易于与颗粒物相结合,并使得气体中的颗粒物的荷电效率更高,进而在尾气除尘电场阳极的作用下,能将更多的颗粒物收集起来,保证尾气电场装置的除尘效率更高。尾气电场装置对顺离子流方向进入电场的颗粒物的收集率比对逆离子流方向进入电场的颗粒物的收集率提高近一倍,从而提高电场的积尘效率,减少电场电耗。另外,现有技术中集尘电场的除尘效率较低的主要原因也是粉尘进入电场方向与电场内离子流方向相反或垂直交叉,从而导致粉尘与离子流相互冲撞剧烈并产生较大能量消耗,同时也影响荷电效率,进而使现有技术中电场集尘效率下降,且能耗增加。尾气电场装置在收集气体中的粉尘时,气体及粉尘顺离子流方向进入电场,粉尘荷电充分,电场消耗小;单极电场集尘效率会达到99.99%。当尾气及粉尘逆离子流方向进入电场,粉尘荷电不充分,电场电耗也会增加,集尘效率会在40%-75%。于本发明一实施例中尾气电场装置形成的离子流有利于无动力风扇流体输送、增氧、或热量交换等。
随着,尾气除尘电场阳极持续收集尾气中的颗粒物等,颗粒物等在尾气除尘电场阳极上堆积并形成碳黑,且碳黑厚度不断增加,使极间距减小。于本发明一实施例中,待检测到电场电流增加,利用电场反电晕放电现象,配合增高电压,限制入注电流,使发生在积碳位置急剧放电产生大量等离子,这些低温等离子使碳黑中有机成分深度氧化,高分子键断裂,形成小分子二氧化碳和水,完成碳黑清洁。由于空气中的氧气同时参与电离,形成臭氧,臭氧分子团同时扑捉沉积的油污分子团,加速油污分子中碳氢键断裂,使部分油分子碳化,以达到尾气挥发份净化目的。另外,碳黑清洁是利用等离子体来达到常规清洗方法无法达到的效果。等离子体是物质的一种状态,也叫做物质的第四态,并不属于常见的固、液、气三态。对气体施加足够的能量使之离化便成为等离子状态。等离子体的“活性”组分包括:离子、电子、原子、活性基团、激发态的核素(亚稳态)、光子等。于本发明一实施例中,当电场积尘时,所述尾气电场装置检测电场电流,采用以下任一方式实现碳黑清洁:
(1)当电场电流增加到一个给定值,所述尾气电场装置增高电场电压。
(2)当电场电流增加到一个给定值,所述尾气电场装置利用电场反电晕放电现象完成碳黑清洁。
(3)当电场电流增加到一个给定值,所述尾气电场装置利用电场反电晕放电现象,增高电压,限制入注电流,完成碳黑清洁。
(4)当电场电流增加到一个给定值,所述尾气电场装置利用电场反电晕放电现象,增高电压,限制入注电流,使发生在阳极积碳位置的急剧放电产生等离子,所述等离子使碳黑有机成分深度氧化,高分子键断裂,形成小分子二氧化碳和水,完成碳黑清洁。
于本发明一实施例中尾气除尘电场阳极和尾气除尘电场阴极分别与电源的两个电极电性连接。加载在尾气除尘电场阳极和尾气除尘电场阴极上的电压需选择适当的电压等级,具体选择何种电压等级取决于尾气电场装置的体积、耐温、容尘率等。例如,电压从5kv至50kv;设计时首先考虑耐温条件,极间距与温度的参数:1MM<30度,积尘面积大于0.1平方/千立方米/小时,电场长度大于单管内切圆的5倍,控制电场气流流速小于9米/秒。于本发明一实施例中尾气除尘电场阳极由第二中空阳极管构成、并呈蜂窝状。第二中空阳极管端口的形状可以为圆形或多边形。于本发明一实施例中第二中空阳极管的管内切圆取值范围在5-400mm,对应电压在0.1-120kv之间,第二中空阳极管对应电流在0.1-30A之间;不同的内切圆对应不同的电晕电压,约为1KV/1MM。
于本发明一实施例中尾气电场装置包括第二电场级,该第二电场级包括若干个第二电场发生单元,第二电场发生单元可以有一个或多个。第二电场发生单元也称作第二集尘单元,第二集尘单元包括上述尾气除尘电场阳极和尾气除尘电场阴极,第二集尘单元有一个或多个。第二电场级有多个时,能有效提高尾气电场装置的集尘效率。同一第二电场级中,各尾气除尘电场阳极为相同极性,各尾气除尘电场阴极为相同极性。且第二电场级有多个时,各第二电场级之间串联。于本发明一实施例中尾气电场装置还包括若干个连接壳体,串联第二电场级通过连接壳体连接;相邻两级的第二电场级的距离大于极间距的1.4倍。
于本发明一实施例中用电场充电驻极体材料。尾气电场装置有故障时,充电驻极体材料会用来除尘。
于本发明一实施例中,所述尾气电场装置包括尾气驻极体元件。
于本发明一实施例中,所述尾气驻极体元件设于所述尾气除尘电场阳极内。
于本发明一实施例中,所述尾气除尘电场阳极和所述尾气除尘电场阴极接通电源时,所述尾气驻极体元件在所述尾气电离除尘电场中。
于本发明一实施例中,所述尾气驻极体元件靠近尾气电场装置出口,或者,所述尾气驻极体元件设于尾气电场装置出口。
于本发明一实施例中,所述尾气除尘电场阳极和所述尾气除尘电场阴极形成尾气流道,所述尾气驻极体元件设于所述尾气流道中。
于本发明一实施例中,所述尾气流道包括尾气流道出口,所述尾气驻极体元件靠近所述尾气流道出口,或者,所述尾气驻极体元件设于所述尾气流道出口。
于本发明一实施例中,所述尾气驻极体元件于所述尾气流道中的横截面占尾气流道横截面5%~100%。
于本发明一实施例中,所述尾气驻极体元件于所述尾气流道中的横截面占尾气流道横截面10%-90%、20%-80%、或40%-60%。
于本发明一实施例中,所述尾气电离除尘电场给所述尾气驻极体元件充电。
于本发明一实施例中,所述尾气驻极体元件具有多孔结构。
于本发明一实施例中,所述尾气驻极体元件为织品。
于本发明一实施例中,所述尾气除尘电场阳极内部为管状,所述尾气驻极体元件外部为管状,所述尾气驻极体元件外部套设于所述尾气除尘电场阳极内部。
于本发明一实施例中,所述尾气驻极体元件与所述尾气除尘电场阳极为可拆卸式连接。
于本发明一实施例中,所述尾气驻极体元件的材料包括具有驻极性能的无机化合物。所述驻极性能是指尾气驻极体元件在外接电源充电后带有电荷,并在完全脱离电源的条件下,依然保持有一定的电荷,从而作为电极起到电场电极作用的能力。
于本发明一实施例中,所述无机化合物选自含氧化合物、含氮化合物或玻璃纤维中的一种或多种组合。
于本发明一实施例中,所述含氧化合物选自金属基氧化物、含氧复合物、含氧的无机杂多酸盐中的一种或多种组合。
于本发明一实施例中,所述金属基氧化物选自氧化铝、氧化锌、氧化锆、氧化钛、氧化钡、氧化钽、氧化硅、氧化铅、氧化锡中的一种或多种组合。
于本发明一实施例中,所述金属基氧化物为氧化铝。
于本发明一实施例中,所述含氧复合物选自钛锆复合氧化物或钛钡复合氧化物中的一种或多种组合。
于本发明一实施例中,所述含氧的无机杂多酸盐选自钛酸锆、锆钛酸铅或钛酸钡中的一种或多种组合。
于本发明一实施例中,所述含氮化合物为氮化硅。
于本发明一实施例中,所述尾气驻极体元件的材料包括具有驻极性能的有机化合物。所述驻极性能是指尾气驻极体元件在外接电源充电后带有电荷,并在完全脱离电源的条件下,依然保持有一定的电荷,从而作为电极起到电场电极作用的能力。
于本发明一实施例中,所述有机化合物选自氟聚合物、聚碳酸酯、PP、PE、PVC、天然蜡、树脂、松香中的一种或多种组合。
于本发明一实施例中,所述氟聚合物选自聚四氟乙烯(PTFE)、聚全氟乙丙烯(Teflon-FEP)、可溶性聚四氟乙烯(PFA)、聚偏氟乙烯(PVDF)中的一种或多种组合。
于本发明一实施例中,所述氟聚合物为聚四氟乙烯。
在上电驱动电压条件下产生尾气电离除尘电场,利用尾气电离除尘电场电离部分待处理物,吸附尾气中的颗粒物,同时向尾气驻极体元件进行充电,当尾气电场装置出现故障时即无上电驱动电压时,充电的尾气驻极体元件产生电场,利用充电的尾气驻极体元件产生的电场吸附尾气中的颗粒物,即在尾气电离除尘电场出现故障情况下仍然可以进行颗粒物的吸附。
一种尾气除尘方法,包括以下步骤:尾气温度低于100℃时,脱除尾气中的液体水,然后电离除尘。
于本发明一实施例中,尾气温度≥100℃时,对尾气进行电离除尘。
于本发明一实施例中,尾气温度≤90℃时,脱除尾气中的液体水,然后电离除尘。
于本发明一实施例中,尾气温度≤80℃时,脱除尾气中的液体水,然后电离除尘。
于本发明一实施例中,尾气温度≤70℃时,脱除尾气中的液体水,然后电离除尘。
于本发明一实施例中,采用电凝除雾方法脱除尾气中的液体水,然后电离除尘。
一种尾气除尘方法,包括以下步骤:在尾气电离除尘电场之前添加包括氧气的气体,进行电离除尘。
于本发明一实施例中,通过单纯增氧、通入外界空气、通入压缩空气和/或通入臭氧的方式添加氧气。
于本发明一实施例中,至少根据尾气颗粒含量决定补氧量。
尾气电场除尘方法
对于尾气系统,于本发明一实施例中,本发明提供一种尾气电场除尘方法,包括以下步骤:
使含尘气体通过尾气除尘电场阳极和尾气除尘电场阴极产生的尾气电离除尘电场;
电场积尘时,进行清尘处理。
于本发明一实施例中,当检测到的电场电流增加到一个给定值时,进行清尘处理。
于本发明一实施例中,当电场积尘时,通过以下任一方式进行灰尘清洁:
(1)利用电场反电晕放电现象完成清尘处理。
(2)利用电场反电晕放电现象,增高电压,限制入注电流,完成清尘处理。
(3)利用电场反电晕放电现象,增高电压,限制入注电流,使发生在阳极积尘位置的急剧放电产生等离子,所述等离子使灰尘有机成分深度氧化,高分子键断裂,形成小分子二氧化碳和水,完成清尘处理。
优选地,所述灰尘为炭黑。
于本发明一实施例中,所述尾气除尘电场阴极包括若干根阴极丝。阴极丝的直径可为0.1mm-20mm,该尺寸参数根据应用场合及积尘要求做调整。于本发明一实施例中阴极丝的直径不大于3mm。于本发明一实施例中阴极丝使用容易放电的金属丝或合金丝,耐温且能支撑自身重量,电化学稳定。于本发明一实施例中阴极丝的材质选用钛。阴极丝的具体形状根据除尘电场阳极的形状调整,例如,若除尘电场阳极的积尘面是平面,则阴极丝的截面呈圆形;若除尘电场阳极的积尘面是圆弧面,阴极丝需要设计成多面形。阴极丝的长度根据除尘电场阳极进行调整。
于本发明一实施例中,所述除尘电场阴极包括若干阴极棒。于本发明一实施例中,所述阴极棒的直径不大于3mm。于本发明一实施例中阴极棒使用容易放电的金属棒或合金棒。阴极棒的形状可以为针状、多角状、毛刺状、螺纹杆状或柱状等。阴极棒的形状可以根据尾气除尘电场阳极的形状进行调整,例如,若尾气除尘电场阳极的积尘面是平面,则阴极棒的截面需要设计成圆形;若尾气除尘电场阳极的积尘面是圆弧面,则阴极棒需要设计成多面形。
于本发明一实施例中,尾气除尘电场阴极穿设于尾气除尘电场阳极内。
于本发明一实施例中,尾气除尘电场阳极包括一个或多个并行设置的中空阳极管。当中空阳极管有多个时,全部中空阳极管构成蜂窝状的除尘电场阳极。于本发明一实施例中,中空阳极管的截面可呈圆形或多边形。若中空阳极管的截面呈圆形,尾气除尘电场阳极和尾气除尘电场阴极之间能形成均匀电场,中空阳极管的内壁不容易积尘。若中空阳极管的截面为三边形时,中空阳极管的内壁上可以形成3个积尘面,3个远角容尘角,此种结构的中空阳极管的容尘率最高。若中空阳极管的截面为四边形,可以获得4个积尘面,4个容尘角,但拼组结构不稳定。若中空阳极管的截面为六边形,可以形成6个积尘面,6个容尘角,积尘面和容尘率达到平衡。若中空阳极管的截面呈更多边形时,可以获得更多的积尘边,但损失容尘率。于本发明一实施例中,中空阳极管的管内切圆直径取值范围为5mm-400mm。
对于尾气系统,于一实施例中,本发明提供一种减少尾气除尘电场耦合的方法,包括以下步骤:
使尾气通过尾气除尘电场阳极和尾气除尘电场阴极产生的尾气电离除尘电场;
选择所述尾气除尘电场阳极或/和尾气除尘电场阴极。
于本发明一实施例中,选择的所述尾气除尘电场阳极或/和尾气除尘电场阴极尺寸使电场耦合次数≤3。
具体地,选择所述尾气除尘电场阳极的集尘面积与尾气除尘电场阴极的放电面积的比。优选地,选择所述尾气除尘电场阳极的积尘面积与所述尾气除尘电场阴极的放电面积的比为 1.667:1-1680:1。
更为优选地,选择所述尾气除尘电场阳极的积尘面积与所述尾气除尘电场阴极的放电面积的比为6.67:1-56.67:1。
于本发明一实施例中,所述尾气除尘电场阴极直径为1-3毫米,所述尾气除尘电场阳极与所述尾气除尘电场阴极的极间距为2.5-139.9毫米;所述尾气除尘电场阳极的积尘面积与所述尾气除尘电场阴极的放电面积的比为1.667:1-1680:1。
优选地,选择所述尾气除尘电场阳极和所述尾气除尘电场阴极的极间距小于150mm。
优选地,选择所述尾气除尘电场阳极与所述尾气除尘电场阴极的极间距为2.5~139.9mm。更为优选地,选择所述尾气除尘电场阳极与所述尾气除尘电场阴极的极间距为5.0~100mm。
优选地,选择所述尾气除尘电场阳极长度为10~180mm。更为优选地,选择所述尾气除尘电场阳极长度为60~180mm。
优选地,选择所述尾气除尘电场阴极长度为30~180mm。更为优选地,选择所述尾气除尘电场阴极长度为54~176mm。
于本发明一实施例中,所述尾气除尘电场阴极包括若干根阴极丝。阴极丝的直径可为0.1mm-20mm,该尺寸参数根据应用场合及积尘要求做调整。于本发明一实施例中阴极丝的直径不大于3mm。于本发明一实施例中阴极丝使用容易放电的金属丝或合金丝,耐温且能支撑自身重量,电化学稳定。于本发明一实施例中阴极丝的材质选用钛。阴极丝的具体形状根据除尘电场阳极的形状调整,例如,若尾气除尘电场阳极的积尘面是平面,则阴极丝的截面呈圆形;若尾气除尘电场阳极的积尘面是圆弧面,阴极丝需要设计成多面形。阴极丝的长度根据尾气除尘电场阳极进行调整。
于本发明一实施例中,所述尾气除尘电场阴极包括若干阴极棒。于本发明一实施例中,所述阴极棒的直径不大于3mm。于本发明一实施例中阴极棒使用容易放电的金属棒或合金棒。阴极棒的形状可以为针状、多角状、毛刺状、螺纹杆状或柱状等。阴极棒的形状可以根据除尘电场阳极的形状进行调整,例如,若尾气除尘电场阳极的积尘面是平面,则阴极棒的截面需要设计成圆形;若尾气除尘电场阳极的积尘面是圆弧面,则阴极棒需要设计成多面形。
于本发明一实施例中,尾气除尘电场阴极穿设于尾气除尘电场阳极内。
于本发明一实施例中,尾气除尘电场阳极包括一个或多个并行设置的中空阳极管。当中空阳极管有多个时,全部中空阳极管构成蜂窝状的尾气除尘电场阳极。于本发明一实施例中,中空阳极管的截面可呈圆形或多边形。若中空阳极管的截面呈圆形,尾气除尘电场阳极和尾气除尘电场阴极之间能形成均匀电场,中空阳极管的内壁不容易积尘。若中空阳极管的截面 为三边形时,中空阳极管的内壁上可以形成3个积尘面,3个远角容尘角,此种结构的中空阳极管的容尘率最高。若中空阳极管的截面为四边形,可以获得4个积尘面,4个容尘角,但拼组结构不稳定。若中空阳极管的截面为六边形,可以形成6个积尘面,6个容尘角,积尘面和容尘率达到平衡。若中空阳极管的截面呈更多边形时,可以获得更多的积尘边,但损失容尘率。于本发明一实施例中,中空阳极管的管内切圆直径取值范围为5mm-400mm。
一种尾气除尘方法,包括如下步骤:
1)利用尾气电离除尘电场吸附尾气中的颗粒物;
2)利用尾气电离除尘电场给尾气驻极体元件充电。
于本发明一实施例中,所述尾气驻极体元件靠近尾气电场装置出口,或者,所述尾气驻极体元件设于尾气电场装置出口。
于本发明一实施例中,所述尾气除尘电场阳极和所述尾气除尘电场阴极形成尾气流道,所述尾气驻极体元件设于所述尾气流道中。
于本发明一实施例中,所述尾气流道包括尾气流道出口,所述尾气驻极体元件靠近所述尾气流道出口,或者,所述尾气驻极体元件设于所述尾气流道出口。
于本发明一实施例中,当尾气电离除尘电场无上电驱动电压时,利用充电的尾气驻极体元件吸附尾气中的颗粒物。
于本发明一实施例中,在充电的尾气驻极体元件吸附一定的尾气中的颗粒物后,将其替换为新的尾气驻极体元件。
于本发明一实施例中,替换为新的尾气驻极体元件后重新启动尾气电离除尘电场吸附尾气中的颗粒物,并给新的尾气驻极体元件充电。
于本发明一实施例中,所述尾气驻极体元件的材料包括具有驻极性能的无机化合物。所述驻极性能是指尾气驻极体元件在外接电源充电后带有电荷,并在完全脱离电源的条件下,依然保持有一定的电荷,从而作为电极起到电场电极作用的能力。
于本发明一实施例中,所述无机化合物选自含氧化合物、含氮化合物或玻璃纤维中的一种或多种组合。
于本发明一实施例中,所述含氧化合物选自金属基氧化物、含氧复合物、含氧的无机杂多酸盐中的一种或多种组合。
于本发明一实施例中,所述金属基氧化物选自氧化铝、氧化锌、氧化锆、氧化钛、氧化钡、氧化钽、氧化硅、氧化铅、氧化锡中的一种或多种组合。
于本发明一实施例中,所述金属基氧化物为氧化铝。
于本发明一实施例中,所述含氧复合物选自钛锆复合氧化物或钛钡复合氧化物中的一种或多种组合。
于本发明一实施例中,所述含氧的无机杂多酸盐选自钛酸锆、锆钛酸铅或钛酸钡中的一种或多种组合。
于本发明一实施例中,所述含氮化合物为氮化硅。
于本发明一实施例中,所述尾气驻极体元件的材料包括具有驻极性能的有机化合物。所述驻极性能是指尾气驻极体元件在外接电源充电后带有电荷,并在完全脱离电源的条件下,依然保持有一定的电荷,从而作为电极起到电场电极作用的能力。
于本发明一实施例中,所述有机化合物选自氟聚合物、聚碳酸酯、PP、PE、PVC、天然蜡、树脂、松香中的一种或多种组合。
于本发明一实施例中,所述氟聚合物选自聚四氟乙烯(PTFE)、聚全氟乙丙烯(Teflon-FEP)、可溶性聚四氟乙烯(PFA)、聚偏氟乙烯(PVDF)中的一种或多种组合。
于本发明一实施例中,所述氟聚合物为聚四氟乙烯。
于本发明一实施例中,所述发动机排放处理系统包括尾气臭氧净化系统。
于本发明一实施例中,所述尾气臭氧净化系统包括反应场,用于将臭氧流股与尾气流股混合反应。例如:所述尾气臭氧净化系统可以用于处理汽车发动机210的尾气,利用尾气中的水以及尾气管道220,产生氧化反应,将尾气中的有机挥发份氧化为二氧化碳和水;硫、硝等无害化收集。所述尾气臭氧净化系统还可以包括外置的臭氧发生器230,通过臭氧输送管240给尾气管道220提供臭氧,如图1所示,图中箭头方向为尾气流动方向。
臭氧流股与尾气流股的摩尔比可为2~10,如5~6、5.5~6.5、5~7、4.5~7.5、4~8、3.5~8.5、3~9、2.5~9.5、2~10。
本发明一实施例可以采用不同方式获得臭氧。比如,延面放电产生臭氧为管式、板式放电部件和交流高压电源组成,利用静电吸附粉尘、除水、富氧后的空气进入放电通道,空气氧被电离产生臭氧、高能离子、高能粒子,通过正压或负压通入反应场如尾气通道中。使用管式延面放电结构,放电管内和外层放电管外都通入一冷却液,在管内电极和外管导体间形成电极,电极间通入18kHz、10kV高压交流电,外管内壁和内管外壁面产生高能电离,氧气被电离,产生臭氧。臭氧使用正压送入反应场如尾气通道。臭氧流股与尾气流股的摩尔比为2时,VOCs去除率50%;臭氧流股与尾气流股的摩尔比为5时,VOCs去除率95%以上,然后氮氧化合物气体浓度下降,氮氧化合物去除率90%;臭氧流股与尾气流股的摩尔比大于10时,VOCs去除率99%以上,然后氮氧化合物气体浓度下降,氮氧化合物去除率99%。电耗 增加到30w/克。
紫外线灯管产生臭氧为气体放电产生11-195纳米波长紫外线,直接辐照灯管周围空气,产生生臭氧、高能离子、高能粒子,通过正压或负压通入反应场如尾气通道中。使用172纳米波长和185纳米波长紫外放电管,通过点亮灯管,在灯管外壁的气体中氧气被电离,产生大量氧离子,结合为臭氧。通过正压送入反应场如尾气通道。使用185纳米紫外线臭氧流股与尾气流股的摩尔比为2时,VOCs去除率40%;185纳米紫外线臭氧流股与尾气流股的摩尔比为5时,VOCs去除率85%以上,然后氮氧化合物气体浓度下降,氮氧化合物去除率70%;185纳米紫外线臭氧流股与尾气流股的摩尔比大于10时,VOCs去除率95%以上,然后氮氧化合物气体浓度下降,氮氧化合物去除率95%。电耗25w/克。
使用172纳米紫外线臭氧流股与尾气流股的摩尔比为2时,VOCs去除率45%;172纳米紫外线臭氧流股与尾气流股的的摩尔比为5时,VOCs去除率89%以上,然后氮氧化合物气体浓度下降,氮氧化合物去除率75%;172纳米紫外线臭氧流股与尾气流股的的摩尔比大于10时,VOCs去除率97%以上,然后氮氧化合物气体浓度下降,氮氧化合物去除率95%。电耗22w/克。
于本发明一实施例中,所述反应场包括管道和/或反应器。
于本发明一实施例中,所述反应场还包括如下技术特征中的至少一项:
1)管道直径为100-200毫米;
2)管道长度大于管道直径0.1倍;
3)所述反应器选自如下至少一种:
反应器一:所述反应器具有反应腔室,尾气与臭氧在所述反应腔室混合并反应;
反应器二:所述反应器包括若干蜂窝状腔体,用于提供尾气与臭氧混合并反应的空间;所述蜂窝状腔体内之间设有间隙,用于通入冷态介质,控制尾气与臭氧的反应温度;
反应器三:所述反应器包括若干载体单元,所述载体单元提供反应场地(例如蜂窝结构的介孔陶瓷体载体),没有载体单元时为气相中反应,有载体单元时则为界面反应,加快反应时间;
反应器四:所述反应器包括催化剂单元,所述催化剂单元用于促进尾气的氧化反应;
1)所述反应场设有臭氧进口,所述臭氧进口选自喷口、喷格栅、喷嘴、旋流喷嘴、设有文丘里管的喷口中的至少一种;设有文丘里管的喷口:所述文丘里管设于喷口中,采用文丘里原理混入臭氧;
2)所述反应场设有臭氧进口,所述臭氧通过所述臭氧进口进入反应场与尾气进行接触, 臭氧进口的设置形成如下方向中至少一种:与尾气流动的方向相反、与尾气流动的方向垂直、与尾气流动的方向相切、插入尾气流动方向、多个方向与尾气进行接触;所述与尾气流动的方向相反即为反方向进入,增加反应时间,减少体积;所述与尾气流动的方向垂直,使用文氏效应;与尾气流动的方向相切,便于混合;插入尾气流动方向,克服漩涡流;多个方向,克服重力。
于本发明一实施例中,所述反应场包括排气管、蓄热体装置或催化器,臭氧可对蓄热体、催化剂、陶瓷体清洁再生。
于本发明一实施例中,所述反应场的温度为-50~200℃,可以为60~70℃,50~80℃、40~90℃、30~100℃、20~110℃、10~120℃、0~130℃、-10~140℃、-20~150℃、-30~160℃、-40~170℃、-50~180℃、-180~190℃或190~200℃。
于本发明一实施例中,所述反应场的温度为60~70℃。
于本发明一实施例中,所述尾气臭氧净化系统还包括臭氧源,用于提供臭氧流股。所述臭氧流股可以为臭氧发生器即时生成也可以为存储的臭氧。所述反应场可以与臭氧源流体连通,臭氧源所提供的臭氧流股可以被引入反应场中,从而可以与尾气流股混合,使尾气流股经受氧化处理。
于本发明一实施例中,所述臭氧源包括存储臭氧单元和/或臭氧发生器。所述臭氧源可以包括臭氧引入管道,还可以包括臭氧发生器,所述臭氧发生器可以是包括但不限于电弧臭氧发生器即延面放电臭氧发生器、工频电弧臭氧发生器、高频感应臭氧发生器、低气压臭氧发生器、紫外线臭氧发生器、电解液臭氧发生器、化学药剂臭氧发生器、射线辐照粒子发生器等中的一种或多种的组合。
于本发明一实施例中,所述臭氧发生器包括延面放电臭氧发生器、工频电弧臭氧发生器、高频感应臭氧发生器、低气压臭氧发生器、紫外线臭氧发生器、电解液臭氧发生器、化学药剂臭氧发生器和射线辐照粒子发生器中的一种或多种的组合。
于本发明一实施例中,所述臭氧发生器包括电极,所述电极上设有催化剂层,所述催化剂层包括氧化催化键裂解选择性催化剂层。
于本发明一实施例中,所述电极包括高压电极或设有阻挡介质层的高压电极,当所述电极包括高压电极时,所述氧化催化键裂解选择性催化剂层250设于所述高压电极260表面上(如图2所示),当所述电极包括阻挡介质层270的高压电极260时,所述氧化催化键裂解选择性催化剂层250设于阻挡介质层270的表面上(如图3所示)。
高压电极是指电压高于500V的直流或交流电极。电极是指用做导电介质(固体、气体、 真空或电解质溶液)中输入或导出电流的极板。输入电流的一极叫阳极或正极,放出电流的一极叫阴极或负极。
放电式臭氧产生机理主要为物理(电学)方法。放电式臭氧发器也有很多类型,但其基本原理就是利用高电压产生电场,再利用电场的电能削弱乃至打断氧气的双键,生成臭氧。现有的放电式臭氧发生器结构原理图如图4所示,该放电式臭氧发生器包括高压交流电源280、高压电极260、阻挡介质层270、气隙290、地极291。在高压电场作用下,气隙290中的氧气分子的双氧键被电能打断,产生臭氧。但利用电场能量产生臭氧是有极限的,目前行业标准要求每kg臭氧的电耗不超过8kWh,行业平均水平7.5kWh左右。
于本发明一实施例中,所述阻挡介质层选自陶瓷板、陶瓷管、石英玻璃板、石英板和石英管中的至少一种。所述陶瓷板、陶瓷管可以为氧化铝、氧化锆、氧化硅等氧化物或其复合氧化物的陶瓷板、陶瓷管。
于本发明一实施例中,当所述电极包括高压电极时,所述氧化催化键裂解选择性催化剂层的厚度为1~3mm,该氧化催化键裂解选择性催化剂层兼作阻挡介质,如1~1.5mm或1.5~3mm;当所述电极包括阻挡介质层的高压电极时,所述氧化催化键裂解选择性催化剂层的负载量包括阻挡介质层的1~12wt%,如1~5wt%或5~12wt%。
于本发明一实施例中,所述氧化催化键裂解选择性催化剂层包括如下重量百分比的各组分:
活性组分5~15%,如5~8%、8~10%、10~12%、12~14%或14~15%;
涂层85~95%,如85~86%、86~88%、88~90%、90~92%或92~95%;
其中,所述活性组分选自金属M和金属元素M的化合物中的至少一种,金属元素M选自碱土金属元素、过渡金属元素、第四主族金属元素、贵金属元素和镧系稀土元素中的至少一种;
所述涂层选自氧化铝、氧化铈、氧化锆、氧化锰、金属复合氧化物、多孔材料和层状材料中的至少一种,所述金属复合氧化物包括铝、铈、锆和锰中一种或多种金属的复合氧化物。
于本发明一实施例中,所述碱土金属元素选自镁、锶和钙中的至少一种。
于本发明一实施例中,所述过渡金属元素选自钛、锰、锌、铜、铁、镍、钴、钇和锆中的至少一种。
于本发明一实施例中,所述第四主族金属元素为锡。
于本发明一实施例中,所述贵金属元素选自铂、铑、钯、金、银和铱中的至少一种。
于本发明一实施例中,所述镧系稀土元素选自镧、铈、镨和钐中的至少一种。
于本发明一实施例中,所述金属元素M的化合物选自氧化物、硫化物、硫酸盐、磷酸盐、碳酸盐,以及钙钛矿中的至少一种。
于本发明一实施例中,所述多孔材料选自分子筛、硅藻土、沸石和纳米碳管中的至少一种。多孔材料孔隙率为60%以上,如60~80%,比表面积为300-500平方米/克,平均孔径为10-100纳米。
于本发明一实施例中,所述层状材料选自石墨烯和石墨中的至少一种。
所述氧化催化键裂解选择性催化剂层将化学和物理方法相结合,降低、削弱甚至直接打断双氧键,充分发挥和利用电场和催化的协同作用,达到大幅度提高臭氧产生速率和产生量的目的,以本发明的臭氧发生器与现有的放电式臭氧发生器相比,同样条件臭氧产生量提高10~30%、产生速率提高10~20%。
于本发明一实施例中,所述尾气臭氧净化系统还包括臭氧量控制装置,用于控制臭氧量以致有效氧化尾气中待处理的气体组分,所述臭氧量控制装置包括控制单元。
于本发明一实施例中,所述臭氧量控制装置还包括臭氧处理前尾气组分检测单元,用于检测臭氧处理前尾气组分含量。
于本发明一实施例中,所述控制单元根据所述臭氧处理前尾气组分含量控制混合反应所需臭氧量。
于本发明一实施例中,所述臭氧处理前尾气组分检测单元选自以下检测单元中至少一个:
第一挥发性有机化合物检测单元,用于检测臭氧处理前尾气中挥发性有机化合物含量,如挥发性有机化合物传感器等;
第一CO检测单元,用于检测臭氧处理前尾气中CO含量,如CO传感器等;
第一氮氧化物检测单元,用于检测臭氧处理前尾气中氮氧化物含量,如氮氧化物(NO
x)传感器等。
于本发明一实施例中,所述控制单元根据至少一个所述臭氧处理前尾气组分检测单元的输出值控制混合反应所需臭氧量。
于本发明一实施例中,所述控制单元用于按照预设的数学模型控制混合反应所需臭氧量。所述预设的数学模型与臭氧处理前尾气组分含量相关,通过上述含量及尾气组分与臭氧的反应摩尔比来确定混合反应所需臭氧量,确定混合反应所需臭氧量时可增加臭氧量,使臭氧过量。
于本发明一实施例中,所述控制单元用于按照理论估计值控制混合反应所需臭氧量。
于本发明一实施例中,所述理论估计值为:臭氧通入量与尾气中待处理物的摩尔比为 2~10。例如:13L柴油发动机可控制臭氧通入量为300~500g;2L汽油发动机可控制臭氧通入量为5~20g。
于本发明一实施例中,所述臭氧量控制装置包括臭氧处理后尾气组分检测单元,用于检测臭氧处理后尾气组分含量。
于本发明一实施例中,所述控制单元根据所述臭氧处理后尾气组分含量控制混合反应所需臭氧量。
于本发明一实施例中,所述臭氧处理后尾气组分检测单元选自以下检测单元中至少一个:
第一臭氧检测单元,用于检测臭氧处理后尾气中臭氧含量;
第二挥发性有机化合物检测单元,用于检测臭氧处理后尾气中挥发性有机化合物含量;
第二CO检测单元,用于检测臭氧处理后尾气中CO含量;
第二氮氧化物检测单元,用于检测臭氧处理后尾气中氮氧化物含量。
于本发明一实施例中,所述控制单元根据至少一个所述臭氧处理后尾气组分检测单元的输出值控制臭氧量。
于本发明一实施例中,所述尾气臭氧净化系统还包括脱硝装置,用于脱除臭氧流股与尾气流股混合反应产物中的硝酸。
于本发明一实施例中,所述脱硝装置包括电凝装置,所述电凝装置包括:电凝流道、位于电凝流道中的第一电极、及第二电极。
于本发明一实施例中,所述脱硝装置包括冷凝单元,用于将臭氧处理后的尾气进行冷凝,实现气液分离。
于本发明一实施例中,所述脱硝装置包括淋洗单元,用于将臭氧处理后的尾气进行淋洗,例如:水和/或碱进行淋洗。
于本发明一实施例中,所述脱硝装置还包括淋洗液单元,用于向所述淋洗单元提供淋洗液。
于本发明一实施例中,所述淋洗液单元中淋洗液包括水和/或碱。
于本发明一实施例中,所述脱硝装置还包括脱硝液收集单元,用于存储尾气中脱除的硝酸水溶液和/或硝酸盐水溶液。
于本发明一实施例中,当所述脱硝液收集单元中存储有硝酸水溶液时,所述脱硝液收集单元设有碱液加入单元,用于与硝酸形成硝酸盐。
于本发明一实施例中,所述尾气臭氧净化系统还包括臭氧消解器,用于消解经反应场处理后的尾气中的臭氧。所述臭氧消解器可以通过紫外线,催化等方式进行臭氧消解。
于本发明一实施例中,所述臭氧消解器选自紫外线臭氧消解器和催化臭氧消解器中的至少一种。
于本发明一实施例中,所述尾气臭氧净化系统还包括第一脱硝装置,用于脱除尾气中氮氧化物;所述反应场用于将经所述第一脱硝装置处理后的尾气与臭氧流股混合反应,或者,用于将尾气在经所述第一脱硝装置处理前先与臭氧流股混合反应。
所述第一脱硝装置可以为现有技术中实现脱硝的装置,例如:非催化还原装置(如氨气脱硝)、选择性催化还原装置(SCR:氨气加催化剂脱硝)、非选择性催化还原装置(SNCR)和电子束脱硝装置等中的至少一种。所述第一脱硝装置处理后发动机尾气中氮氧化物(NO
x)含量不达标,在所述第一脱硝装置处理后或者处理前的尾气与臭氧流股混合反应可达到最新标准。
于本发明一实施例中,所述第一脱硝装置选自非催化还原装置、选择性催化还原装置、非选择性催化还原装置和电子束脱硝装置中的至少一种。
本领域技术人员基于现有技术认为:臭氧处理尾气中氮氧化物NO
X时,氮氧化物NO
X被臭氧氧化成高价态氮氧化物如NO
2、N
2O
5和NO
3等,所述高价态氮氧化物还是气体,仍然不能从尾气中脱除,即臭氧处理尾气中氮氧化物NO
X无效,但是,本申请人却发现臭氧和尾气中氮氧化物反应产生的高价态氮氧化物并不是最后的产物,高价态氮氧化物会和水反应产生硝酸,硝酸则更容易从尾气中脱除,比如使用电凝和冷凝,该效果对所属技术领域的技术人员来说是预料不到的。该预料不到的技术效果是因为本领域技术人员没有认识到臭氧还会和尾气中的VOC反应产生足够水和高价氮氧化物反应产生硝酸。
用臭氧来处理尾气时,臭氧最优先与挥发性有机化合物VOC反应,被氧化成CO
2和水,然后再与氮氧化合物NO
X,被氧化成高价态氮氧化物如NO
2、N
2O
5和NO
3等,最后再与一氧化碳CO反应,被氧化成CO
2,即反应优先顺序为挥发性有机化合物VOC>氮氧化合物NO
X>一氧化碳CO,而且尾气中有足够的挥发性有机化合物VOC产生足够的水可以充分与高价态氮氧化物反应生成硝酸,因此,用臭氧来处理尾气使得臭氧除NO
X效果更好,该效果对所属技术领域的技术人员来说是预料不到的技术效果。
臭氧处理尾气可达到如下脱除效果:氮氧化物NO
X脱除效率:60~99.97%;一氧化碳CO脱除效率:1~50%;挥发性有机化合物VOC脱除效率:60~99.97%,对所属技术领域的技术人员来说是预料不到的技术效果。
所述高价态氮氧化物与挥发性有机化合物VOC被氧化得到的水反应得到的硝酸更易脱除且脱除得到的硝酸可回收利用,例如可以通过本发明的电凝装置脱除硝酸、也可以通过现 有技术中脱除硝酸的方法例如碱洗脱除硝酸。本发明电凝装置包括第一电极和第二电极,含硝酸水雾流经第一电极时,含硝酸水雾将带电,第二电极给带电的含硝酸水雾施加吸引力,含硝酸水雾向第二电极移动,直至含硝酸水雾附着在第二电极上,然后再进行收集,本发明电凝装置对含硝酸水雾的收集能力更强、收集效率更高。
尾气电离除尘时空气中的氧气参与电离,形成臭氧,尾气电离除尘系统与尾气臭氧净化系统结合后,电离形成的臭氧可用于氧化尾气中的污染物,如氮氧化合物NO
X、挥发性有机化合物VOC、一氧化碳CO,即电离形成的臭氧可被臭氧处理NO
X用来处理污染物,氧化氮氧化合物NO
X的同时还会氧化挥发性有机化合物VOC、一氧化碳CO,节省臭氧处理NO
X的臭氧消耗量,而且也不需要再增加除臭氧机构对电离形成的臭氧进行消解,不会造成温室效应,破坏大气中的紫外线,可见,尾气电离除尘系统与尾气臭氧净化系统结合后,在功能上彼此支持,并取得了新的技术效果:电离形成的臭氧被尾气臭氧净化系统用来处理污染物,节省臭氧处理污染物的臭氧消耗量,而且也不需要再增加除臭氧机构对电离形成的臭氧进行消解,不会造成温室效应,破坏大气中的紫外线,具有突出的实质性特点和显著的进步。
一种尾气臭氧净化方法,包括如下步骤:将臭氧流股与尾气流股混合反应。
于本发明一实施例中,所述尾气流股包括氮氧化物和挥发性有机化合物。所述尾气流股可以是发动机尾气,所述发动机通常是将燃料的化学能转化为机械能的装置,具体可以是内燃机等,更具体可以是如柴油发动机尾气等。所述尾气流股中氮氧化物(NO
x)与臭氧流股混合反应,被氧化成高价态的氮氧化物如NO
2、N
2O
5和NO
3等。所述尾气流股中挥发性有机化合物(VOC)与臭氧流股混合反应,被氧化成CO
2和水。所述高价态的氮氧化物与挥发性有机化合物(VOC)被氧化得到的水反应得到硝酸。经过上述反应,尾气流股中的氮氧化物(NO
x)得以脱除,以硝酸的形态存在于废气中。
于本发明一实施例中,于尾气的低温段,臭氧流股与尾气流股的混合反应。
于本发明一实施例中,臭氧流股与尾气流股混合反应温度为-50~200℃,可以为60~70℃,50~80℃、40~90℃、30~100℃、20~110℃、10~120℃、0~130℃、-10~140℃、-20~150℃、-30~160℃、-40~170℃、-50~180℃、-180~190℃或190~200℃。
于本发明一实施例中,臭氧流股与尾气流股混合反应温度为60~70℃。
于本发明一实施例中,臭氧流股与尾气流股的混合方式选自文丘里混合、正压混合、插入混合、动力混合和流体混合中至少一种。
于本发明一实施例中,当臭氧流股与尾气流股的混合方式为正压混合时,臭氧进气的压力大于尾气的压力。当臭氧流股进气的压力小于尾气流股的排压时,可同时使用文丘里混合 方式。
于本发明一实施例中,在臭氧流股与尾气流股混合反应前,提高尾气流股流速,采用文丘里原理混入臭氧流股。
于本发明一实施例中,臭氧流股与尾气流股混合方式选自尾气出口逆流通入、反应场前段混入、除尘器前后插入、脱硝装置前后混入、催化装置前后混入、水洗装置前后通入、过滤装置前后混入、消音装置前后混入、尾气管道内发生混入、吸附装置外置混入和凝露装置前后混入中至少一种。可设于尾气的低温段,避免臭氧的消解。
于本发明一实施例中,臭氧流股与尾气流股混合反应的反应场包括管道和/或反应器。
于本发明一实施例中,所述反应场包括排气管、蓄热体装置或催化器。
于本发明一实施例中,还包括如下技术特征中的至少一项:
1)管道直径为100~200毫米;
2)管道长度大于管道直径0.1倍;
3)所述反应器选自如下至少一种:
反应器一:所述反应器具有反应腔室,尾气与臭氧在所述反应腔室混合并反应;
反应器二:所述反应器包括若干蜂窝状腔体,用于提供尾气与臭氧混合并反应的空间;所述蜂窝状腔体内之间设有间隙,用于通入冷态介质,控制尾气与臭氧的反应温度;
反应器三:所述反应器包括若干载体单元,所述载体单元提供反应场地(例如蜂窝结构的介孔陶瓷体载体),没有载体单元时为气相中反应,有载体单元时则为界面反应,加快反应时间;
反应器四:所述反应器包括催化剂单元,所述催化剂单元用于促进尾气的氧化反应;
4)所述反应场设有臭氧进口,所述臭氧进口选自喷口、喷格栅、喷嘴、旋流喷嘴、设有文丘里管的喷口中的至少一种;设有文丘里管的喷口:所述文丘里管设于喷口中,采用文丘里原理混入臭氧;
5)所述反应场设有臭氧进口,所述臭氧通过所述臭氧进口进入反应场与尾气进行接触,臭氧进口的设置形成如下方向中至少一种:与尾气流动的方向相反、与尾气流动的方向垂直、与尾气流动的方向相切、插入尾气流动方向、多个方向与尾气进行接触;所述与尾气流动的方向相反即为反方向进入,增加反应时间,减少体积;所述与尾气流动的方向垂直,使用文氏效应;与尾气流动的方向相切,便于混合;插入尾气流动方向,克服漩涡流;多个方向,克服重力。
于本发明一实施例中,所述臭氧流股由存储臭氧单元和/或臭氧发生器提供。
于本发明一实施例中,所述臭氧发生器包括延面放电臭氧发生器、工频电弧臭氧发生器、高频感应臭氧发生器、低气压臭氧发生器、紫外线臭氧发生器、电解液臭氧发生器、化学药剂臭氧发生器和射线辐照粒子发生器中的一种或多种的组合。
于本发明一实施例中,所述臭氧流股提供方法:在电场和氧化催化键裂解选择性催化剂层作用下,含有氧气的气体产生臭氧,其中形成电场的电极上负载氧化催化键裂解选择性催化剂层。
于本发明一实施例中,所述电极包括高压电极或设有阻挡介质层的电极,当所述电极包括高压电极时,所述氧化催化键裂解选择性催化剂层负载于所述高压电极表面上,当所述电极包括阻挡介质层的高压电极时,所述氧化催化键裂解选择性催化剂层负载于阻挡介质层的表面上。
于本发明一实施例中,当所述电极包括高压电极时,所述氧化催化键裂解选择性催化剂层的厚度为1~3mm,该氧化催化键裂解选择性催化剂层兼作阻挡介质,如1~1.5mm或1.5~3mm;当所述电极包括阻挡介质层的高压电极时,所述氧化催化键裂解选择性催化剂层的负载量包括阻挡介质层的1~12wt%,如1~5wt%或5~12wt%。
于本发明一实施例中,所述氧化催化键裂解选择性催化剂层包括如下重量百分比的各组分:
活性组分5~15%,如5~8%、8~10%、10~12%、12~14%或14~15%;
涂层85~95%,如85~86%、86~88%、88~90%、90~92%或92~95%;
其中,所述活性组分选自金属M和金属元素M的化合物中的至少一种,金属元素M选自碱土金属元素、过渡金属元素、第四主族金属元素、贵金属元素和镧系稀土元素中的至少一种;
所述涂层选自氧化铝、氧化铈、氧化锆、氧化锰、金属复合氧化物、多孔材料和层状材料中的至少一种,所述金属复合氧化物包括铝、铈、锆和锰中一种或多种金属的复合氧化物。
于本发明一实施例中,所述碱土金属元素选自镁、锶和钙中的至少一种。
于本发明一实施例中,所述过渡金属元素选自钛、锰、锌、铜、铁、镍、钴、钇和锆中的至少一种。
于本发明一实施例中,所述第四主族金属元素为锡。
于本发明一实施例中,所述贵金属元素选自铂、铑、钯、金、银和铱中的至少一种。
于本发明一实施例中,所述镧系稀土元素选自镧、铈、镨和钐中的至少一种。
于本发明一实施例中,所述金属元素M的化合物选自氧化物、硫化物、硫酸盐、磷酸盐、 碳酸盐,以及钙钛矿中的至少一种。
于本发明一实施例中,所述多孔材料选自分子筛、硅藻土、沸石和纳米碳管中的至少一种。多孔材料孔隙率为60%以上,如60~80%,比表面积为300-500平方米/克,平均孔径为10-100纳米。
于本发明一实施例中,所述层状材料选自石墨烯和石墨中的至少一种。
于本发明一实施例中,所述电极通过浸渍和/或喷涂的方法负载氧双催化键裂解选择性催化剂。
于本发明一实施例中,包括如下步骤:
1)按照催化剂组成配比,将涂层原料的浆料负载于高压电极表面上或阻挡介质层的表面上,干燥,煅烧,得到负载涂层的高压电极或阻挡介质层;
2)按照催化剂组成配比,将含金属元素M的原料溶液或浆料负载到步骤1)得到涂层上,干燥,煅烧,当涂层负载于阻挡介质层的表面上时,煅烧后在阻挡介质层相对于负载涂层的另一面设置高压电极,即得所述臭氧发生器用电极;或者,按照催化剂组成配比,将含金属元素M的原料溶液或浆料负载到步骤1)得到涂层上,干燥,煅烧和后处理,当涂层负载于阻挡介质层的表面上时,后处理后在阻挡介质层相对于负载涂层的另一面设置高压电极,即得所述臭氧发生器用电极;
其中,通过对煅烧温度和气氛,以及后处理实现对电极用催化剂中活性组分形态的控制。
于本发明一实施例中,包括如下步骤:
1)按照催化剂组成配比,将含金属元素M的原料溶液或浆料负载涂层原料上,干燥,煅烧,得到负载有活性组份的涂层材料;
2)按照催化剂组成配比,将步骤1)得到的负载有活性组份的涂层材料制成浆料,负载在高压电极表面上或阻挡介质层的表面上,干燥,煅烧,当涂层负载在阻挡介质层的表面上时,煅烧后在阻挡介质层相对于负载涂层的另一面设置高压电极,即得所述臭氧发生器用电极;或者,按照催化剂组成配比,将步骤1)得到的负载有活性组份的涂层材料制成浆料,负载在高压电极表面上或阻挡介质层的表面上,干燥,煅烧和后处理,当涂层负载在阻挡介质层的表面上时,后处理后在阻挡介质层相对于负载涂层的另一面设置高压电极,即得所述臭氧发生器用电极;
其中,通过对煅烧温度和气氛,以及后处理实现对电极用催化剂中活性组分形态的控制。
上述负载方式可以为浸渍、喷涂、涂刷等等,能实现负载即可。
活性组分包括金属元素M的硫酸盐、磷酸盐、碳酸盐中的至少一种时,含金属元素M的 硫酸盐、磷酸盐、碳酸盐中的至少一种的溶液或浆料负载涂层原料上,干燥,煅烧,煅烧温度不能超过活性组分的分解温度,例如:要获得金属元素M的硫酸盐则煅烧温度不能超过硫酸盐的分解温度(分解温度一般在600℃以上)。
通过对煅烧温度和气氛,以及后处理实现对电极用催化剂中活性组分形态的控制,例如:活性组分包括金属M时,煅烧后可再进行还原气还原(后处理)获得,煅烧温度可为200~550℃;活性组分包括金属元素M的硫化物时,煅烧后可再与硫化氢反应(后处理)获得,煅烧温度可为200~550℃。
于本发明一实施例中,包括:控制臭氧流股的臭氧量以致有效氧化尾气中待处理的气体组分。
于本发明一实施例中,控制臭氧流股的臭氧量达到如下脱除效率:
氮氧化物脱除效率:60~99.97%;
CO脱除效率:1~50%;
挥发性有机化合物脱除效率:60~99.97%。
于本发明一实施例中,包括:检测臭氧处理前尾气组分含量。
于本发明一实施例中,根据所述臭氧处理前尾气组分含量控制混合反应所需臭氧量。
于本发明一实施例中,检测臭氧处理前尾气组分含量选自以下至少一个:
检测臭氧处理前尾气中挥发性有机化合物含量;
检测臭氧处理前尾气中CO含量;
检测臭氧处理前尾气中氮氧化物含量。
于本发明一实施例中,根据至少一个检测臭氧处理前尾气组分含量的输出值控制混合反应所需臭氧量。
于本发明一实施例中,按照预设的数学模型控制混合反应所需臭氧量。所述预设的数学模型与臭氧处理前尾气组分含量相关,通过上述含量及尾气组分与臭氧的反应摩尔比来确定混合反应所需臭氧量,确定混合反应所需臭氧量时可增加臭氧量,使臭氧过量。
于本发明一实施例中,按照理论估计值控制混合反应所需臭氧量。
于本发明一实施例中,所述理论估计值为:臭氧通入量与尾气中待处理物的摩尔比为2~10,如5~6、5.5~6.5、5~7、4.5~7.5、4~8、3.5~8.5、3~9、2.5~9.5、2~10。例如:13L柴油发动机可控制臭氧通入量为300~500g;2L汽油发动机可控制臭氧通入量为5~20g。
于本发明一实施例中,包括:检测臭氧处理后尾气组分含量。
于本发明一实施例中,根据所述臭氧处理后尾气组分含量控制混合反应所需臭氧量。
于本发明一实施例中,检测臭氧处理后尾气组分含量选自以下至少一个:
检测臭氧处理后尾气中臭氧含量;
检测臭氧处理后尾气中挥发性有机化合物含量;
检测臭氧处理后尾气中CO含量;
检测臭氧处理后尾气中氮氧化物含量。
于本发明一实施例中,根据至少一个检测臭氧处理后尾气组分含量的输出值控制臭氧量。
于本发明一实施例中,所述尾气臭氧净化方法还包括如下步骤:脱除臭氧流股与尾气流股混合反应产物中的硝酸。
于本发明一实施例中,使带硝酸雾的气体流经第一电极;当带硝酸雾的气体流经第一电极时,第一电极使气体中的硝酸雾带电,第二电极给带电的硝酸雾施加吸引力,使硝酸雾向第二电极移动,直至硝酸雾附着在第二电极上。
于本发明一实施例中,脱除臭氧流股与尾气流股混合反应产物中的硝酸的方法:将臭氧流股与尾气流股混合反应产物进行冷凝。
于本发明一实施例中,脱除臭氧流股与尾气流股混合反应产物中的硝酸的方法:将臭氧流股与尾气流股混合反应产物进行淋洗。
于本发明一实施例中,脱除臭氧流股与尾气流股混合反应产物中的硝酸的方法还包括:向臭氧流股与尾气流股混合反应产物提供淋洗液。
于本发明一实施例中,所述淋洗液为水和/或碱。
于本发明一实施例中,脱除臭氧流股与尾气流股混合反应产物中的硝酸的方法还包括:存储尾气中脱除的硝酸水溶液和/或硝酸盐水溶液。
于本发明一实施例中,当存储有硝酸水溶液时,加入碱液,与硝酸形成硝酸盐。
于本发明一实施例中,所述尾气臭氧净化方法还包括如下步骤:对脱除硝酸的尾气进行臭氧消解,例如:可以通过紫外线,催化等方式进行消解。
于本发明一实施例中,所述臭氧消解选自紫外线消解和催化消解中的至少一种。
于本发明一实施例中,所述尾气臭氧净化方法还包括如下步骤:第一次脱除尾气中氮氧化物;第一次脱除氮氧化物后的尾气流股与臭氧流股混合反应,或者,在第一次脱除尾气中氮氧化物前先与臭氧流股混合反应。
第一次脱除尾气中氮氧化物可以为现有技术中实现脱硝的方法,例如:非催化还原方法(如氨气脱硝)、选择性催化还原方法(SCR:氨气加催化剂脱硝)、非选择性催化还原方法(SNCR)和电子束脱硝方法等中的至少一种。第一次脱除尾气中氮氧化物后的尾气中氮氧化 物(NO
x)含量不达标,在第一次脱除尾气中氮氧化物后或前经与臭氧混合反应后可达到最新标准。于本发明一实施例中,所述第一次脱除尾气中氮氧化物选自非催化还原方法、选择性催化还原方法、非选择性催化还原方法和电子束脱硝方法等中的至少一种。
于本发明一实施例中提供一种电凝装置,包括:电凝流道、位于电凝流道中的第一电极、及第二电极。当尾气流经电凝流道中的第一电极时,尾气中含硝酸的水雾、即硝酸液将带电,第二电极给带电的硝酸液施加吸引力,含硝酸的水雾向第二电极移动,直至含硝酸的水雾附着在第二电极上,从而实现对尾气中硝酸液的去除。该电凝装置也称作电凝除雾装置。
于本发明一实施例中电凝装置的第一电极可为固体、液体、气体分子团、等离子体、导电混合态物质、生物体自然混合导电物质、或物体人工加工形成导电物质中的一种或多种形态的组合。当第一电极为固体时,第一电极可采用固态金属、比如304钢,或其它固态的导体、比如石墨等;当第一电极为液体时,第一电极可以是含离子导电液体。
于本发明一实施例中电凝装置的第一电极的形状可以呈点状、线状、网状、孔板状、板状、针棒状、球笼状、盒状、管状、自然形态物质、或加工形态物质等。当第一电极呈板状、球笼状、盒状或管状时,第一电极可以是无孔结构,也可以是有孔结构。当第一电极为有孔结构时,第一电极上可以设有一个或多个前通孔。于本发明一实施例中前通孔的形状可以是多角形、圆形、椭圆形、正方形、长方形、梯形、或菱形等。于本发明一实施例中前通孔的孔径大小可以为10~100mm、10~20mm、20~30mm、30~40mm、40~50mm、50~60mm、60~70mm、70~80mm、80~90mm、或90~100mm。另外,在其它实施例中第一电极还可以是其它形状。
于本发明一实施例中电凝装置的第二电极的形状可以呈多层网状、网状、孔板状、管状、桶状、球笼状、盒状、板状、颗粒堆积层状、折弯板状、或面板状。当第二电极呈板状、球笼状、盒状或管状时,第二电极也可以是无孔结构,或有孔结构。当第二电极为有孔结构时,第二电极上可以设有一个或多个后通孔。于本发明一实施例中后通孔的形状可以是多角形、圆形、椭圆形、正方形、长方形、梯形、或菱形等。后通孔的孔径大小可以为10~100mm、10~20mm、20~30mm、30~40mm、40~50mm、50~60mm、60~70mm、70~80mm、80~90mm、或90~100mm。
于本发明一实施例中电凝装置的第二电极由导电物质制成。于本发明一实施例中第二电极的表面具有导电物质。
于本发明一实施例中电凝装置的第一电极与第二电极之间具有电凝电场,该电凝电场可以是点面电场、线面电场、网面电场、点桶电场、线桶电场、或网桶电场中的一种或多种电场的组合。比如:第一电极呈针状或线状,第二电极呈面状,且第一电极垂直或平行于第二 电极,从而形成线面电场;或第一电极呈网状,第二电极呈面状,第一电极平行于第二电极,从而形成网面电场;或第一电极呈点状,并通过金属丝或金属针进行固定,第二电极呈桶状,第一电极位于第二电极的几何对称中心处,从而形成点桶电场;或第一电极呈线状,并通过金属丝或金属针进行固定,第二电极呈桶状,第一电极位于第二电极的几何对称轴上,从而形成线桶电场;或第一电极呈网状,并通过金属丝或金属针进行固定,第二电极呈桶状,第一电极位于第二电极的几何对称中心处,从而形成网桶电场。当第二电极呈面状时,具体可以是平面状、曲面状、或球面状。当第一电极呈线状时,具体可以是直线状、曲线状、或圆圈状。第一电极还可以是圆弧状。当第一电极呈网状时,具体可以是平面的、球面的或其它几何面状,也可以是矩形,或不规则形状。第一电极也可以呈点状,且可以是直径很小的真实点,也可以是一个小球,还可以是一个网状球。当第二电极呈桶状时,第二电极还可以进一步演化成各种盒状。第一电极也可作相应变化,形成电极和电凝电场层套。
于本发明一实施例中电凝装置的第一电极呈线状,第二电极呈面状。于本发明一实施例中第一电极垂直于第二电极。于本发明一实施例中第一电极和第二电极相平行。于本发明一实施例中第一电极和第二电极均呈面状,且第一电极和第二电极相平行。于本发明一实施例中第一电极采用金属丝网。于本发明一实施例中第一电极呈平面状或球面状。于本发明一实施例中第二电极呈曲面状或球面状。于本发明一实施例中第一电极呈点状、线状、或网状,第二电极呈桶状,第一电极位于第二电极的内部,且第一电极位于第二电极的中心对称轴上。
于本发明一实施例中电凝装置的第一电极与电源的一个电极电性连接;第二电极与电源的另一个电极电性连接。于本发明一实施例中第一电极具体与电源的阴极电性连接,第二电极具体与电源的阳极电性连接。
同时,于本发明一些实施例中电凝装置的第一电极可以具有正电势或负电势;当第一电极具有正电势时,第二电极具有负电势;当第一电极具有负电势时,第二电极具有正电势,第一电极和第二电极均与电源电性连接,具体地第一电极和第二电极可分别与电源的正负极电性连接。该电源的电压称作上电驱动电压,上电驱动电压大小的选择与环境温度、介质温度等有关。例如,电源的上电驱动电压范围可以为5~50KV、5~50KV、10~50KV、5~10KV、10~20KV、20~30KV、30~40KV、或40~50KV,从生物电至空间雾霾治理用电。电源可以是直流电源或交流电源,其上电驱动电压的波形可以是直流波形、正弦波、或调制波形。直流电源作为吸附的基本应用;正弦波作为移动使用,如正弦波的上电驱动电压作用于第一电极和第二电极之间,所产生的电凝电场将驱动电凝电场中带电的粒子、如雾滴等向第二电极移动;斜波作为拉动使用,根据拉动力度需要调制波形,如非对称电凝电场的两端边缘处,对 其中的介质所产生的拉力具有明显的方向性,以驱动电凝电场中的介质沿该方向移动。当电源采用交流电源时,其变频脉冲的范围可以为0.1Hz~5GHz、0.1Hz~1Hz、0.5Hz~10Hz、5Hz~100Hz、50Hz~1KHz、1KHz~100KHz、50KHz~1MHz、1MHz~100MHz、50MHz~1GHz、500MHz~2GHz、或1GHz~5GHz,适用生物体至污染物颗粒的吸附。第一电极可作为导线,在与含硝酸的水雾接触时,直接将正负电子导入含硝酸的水雾,此时含硝酸的水雾本身可作为电极。第一电极可通过能量波动的方法使电子转移到含硝酸的水雾或电极上,这样第一电极就可以不接触含硝酸的水雾。含硝酸的水雾在由第一电极向第二电极移动过程中,将重复得到电子和失去电子;与此同时,大量电子在位于第一电极和第二电极之间的多个含硝酸的水雾之间进行传递,使更多雾滴带电,并最终到达第二电极,从而形成电流,该电流也称作上电驱动电流。上电驱动电流的大小与环境温度、介质温度、电子量、被吸附物质量、逃逸量有关。比如,随电子量增加,可移动的粒子、如雾滴增加,由移动的带电粒子形成的电流会随之增加。单位时间内被吸附的带电物质、如雾滴越多,电流越大。逃逸的雾滴只是带了电,但并未到达第二电极,也就是说未形成有效的电中和,从而在相同的条件下,逃逸的雾滴越多,电流越小。相同的条件下,环境温度越高,气体粒子和雾滴速度越快,其自身的动能也就越高,其自身与第一电极和第二电极碰撞机率就会越大,也越不易被第二电极吸附住,从而产生逃逸,但由于其逃逸是发生在电中和之后,且可能是发生了反复多次的电中和之后,从而相应的增加了电子传导速度,电流也就相应增加。同时,由于环境温度越高,气体分子、雾滴等的动量越高,且越不易被第二电极吸附,即使第二电极吸附后,再次从第二电极逃逸、即电中和之后逃逸的机率也越大,因此在第一电极与第二电极的间距不变的情况下,需要增加上述上电驱动电压,该上电驱动电压的极限为达到空气击穿的效果。另外,介质温度的影响基本与环境温度的影响相当。介质温度越低,需激发介质、如雾滴带电的能量小,且其自身所具有的动能也越小,在同样的电凝电场力作用下,越容易被吸附到第二电极上,从而形成的电流较大。电凝装置对冷态的含硝酸的水雾吸附效果更好。而随介质、如雾滴的浓度增加,带电的介质在与第二电极碰撞之前已与其它介质产生电子传递的机率越大,从而形成有效电中和的机会也会越大,形成的电流也相应地会越大;所以当介质浓度越高时,形成的电流越大。上电驱动电压与介质温度的关系与上电驱动电压与环境温度的关系基本相同。
于本发明一实施例中与第一电极和第二电极相连接的电源的上电驱动电压可小于起始起晕电压。该起始起晕电压为能使第一电极和第二电极之间产生放电并电离气体的最小电压值。对于不同的气体、及不同的工作环境等,起始起晕电压的大小可能会不相同。但对于本领域技术人员来说,针对确定的气体、及工作环境,所对应的起始起晕电压是确定的。于本发明 一实施例中电源的上电驱动电压具体可为0.1-2kv/mm。电源的上电驱动电压小于空气电晕起晕电压。
于本发明一实施例中第一电极和第二电极均沿左右方向延伸,第一电极的左端位于第二电极的左端的左方。
于本发明一实施例中第二电极有两个,第一电极位于两个第二电极之间。
第一电极与第二电极之间的距离可根据两者间的上电驱动电压大小、水雾的流速、以及含硝酸的水雾的带电能力等进行设置。比如,第一电极和第二电极的间距可以为5~50mm、5~10mm、10~20mm、20~30mm、30~40mm、或40~50mm。第一电极和第二电极的间距越大,需要的上电驱动电压越高,以形成足够强大的电凝电场,用于驱动带电的介质快速移向第二电极,以免介质逃逸。同样的条件下,第一电极和第二电极的间距越大,顺着气流方向,越靠近中心位置,物质流速越快;越靠近第二电极的物质的流速越慢;而垂直于气流方向,带电介质粒子、如雾粒,随第一电极和第二电极的间距增加,在没有发生碰撞的情况下,被电凝电场加速的时间越长,因此,物质在接近第二电极之前沿垂直方向的移动速度越大。在同样的条件下,如果上电驱动电压不变,随距离增加,电凝电场强度不断减小,电凝电场中介质带电的能力也就越弱。
第一电极和第二电极构成吸附单元。吸附单元可以有一个或多个,具体数量依据实际需要来确定。在一种实施例中,吸附单元有一个。在另一种实施例中吸附单元有多个,以利用多个吸附单元吸附更多的硝酸液,从而提高收集硝酸液的效率。当吸附单元有多个时,全部吸附单元的分布形式可以根据需要灵活进行调整;全部吸附单元可以是相同的,也可以是不同的。比如,全部吸附单元可沿左右方向、前后方向、斜向或螺旋方向中的一个方向或多个方向进行分布,以满足不同风量的要求。全部吸附单元可以呈矩形阵列分布,也可以呈金字塔状分布。上述各种形状的第一电极和第二电极可以自由组合形成吸附单元。例如,线状的第一电极插入管状的第二电极形成吸附单元,再与线状的第一电极组合,形成新的吸附单元,此时两个线状的第一电极可电连接;新的吸附单元再在左右方向、上下方向、斜向或螺旋方向中的一个方向或多个方向进行分布。再例如,线状的第一电极插入管状的第二电极形成吸附单元,此吸附单元在左右方向、上下方向、斜向或螺旋方向中的一个方向或多个方向进行分布,形成新的吸附单元,该新的吸附单元再与上述各种形状的第一电极进行组合,以形成新的吸附单元。吸附单元中的第一电极和第二电极之间的距离可以任意调整,以适应不同的工作电压和吸附对象的要求。不同的吸附单元之间可以进行组合。不同的吸附单元可以使用同一电源,也可以使用不同的电源。当使用不同的电源时,各电源的上电驱动电压可以是相 同的,也可以是不同的。另外,本电凝装置也可以有多个,且全部电凝装置可以沿左右方向、上下方向、螺旋方向或斜向中的一个方向或多个方向进行分布。
于本发明一实施例中电凝装置还包括电凝壳体,该电凝壳体包括电凝进口、电凝出口及电凝流道,电凝流道的两端分别与电凝进口和电凝出口相连通。于本发明一实施例中电凝进口呈圆形,且电凝进口的直径为300~1000mm、或500mm。于本发明一实施例中电凝出口呈圆形,且电凝出口的直径为300~1000mm、或500mm。于本发明一实施例中电凝壳体包括由电凝进口至电凝出口方向依次分布的第一壳体部、第二壳体部、及第三壳体部,电凝进口位于第一壳体部的一端,电凝出口位于第三壳体部的一端。于本发明一实施例中第一壳体部的轮廓大小由电凝进口至电凝出口方向逐渐增大。于本发明一实施例中第一壳体部呈直管状。于本发明一实施例中第二壳体部呈直管状,且第一电极和第二电极安装在第二壳体部中。于本发明一实施例中第三壳体部的轮廓大小由电凝进口至电凝出口方向逐渐减小。于本发明一实施例中第一壳体部、第二壳体部、及第三壳体部的截面均呈矩形。于本发明一实施例中电凝壳体的材质为不锈钢、铝合金、铁合金、布、海绵、分子筛、活性炭、泡沫铁、或泡沫碳化硅。于本发明一实施例中第一电极通过电凝绝缘件与电凝壳体相连接。于本发明一实施例中电凝绝缘件的材质为绝缘云母。于本发明一实施例中电凝绝缘件呈柱状、或塔状。于本发明一实施例中第一电极上设有呈圆柱形的前连接部,且前连接部与电凝绝缘件固接。于本发明一实施例中第二电极上设有呈圆柱形的后连接部,且后连接部与电凝绝缘件固接。
于本发明一实施例中第一电极位于电凝流道中。于本发明一实施例中第一电极的截面面积与电凝流道的截面面积比为99%~10%、或90~10%、或80~20%、或70~30%、或60~40%、或50%。第一电极的截面面积是指第一电极沿截面上实体部分的面积之和。
在收集含硝酸的水雾过程中,含硝酸的水雾由电凝进口进入电凝壳体,并朝向电凝出口处移动;在含硝酸的水雾朝向电凝出口移动过程中,含硝酸的水雾将经过第一电极,并带电;第二电极将带电的含硝酸的水雾吸附住,以将含硝酸的水雾收集在第二电极上。本发明利用电凝壳体引导尾气及含硝酸的水雾流经第一电极,以利用第一电极使硝酸的水雾带电,并利用第二电极收集硝酸的水雾,从而有效降低由电凝出口处流出的硝酸的水雾。于本发明一些实施例中电凝壳体的材质可以是金属、非金属、导体、非导体、水、各类导电液体、各类多孔材料、或各类泡沫材料等。当电凝壳体的材质为金属时,其材质具体可以是不锈钢、或铝合金等。当电凝壳体的材质是非金属时,其材质具体可以是布、或海绵等。当电凝壳体的材质是导体时,其材质具体可以是铁合金等。当电凝壳体的材质是非导体时,其表面形成水层水即成为电极,如吸水后的沙层。当电凝壳体的材质为水和各类导电液体时,电凝壳体是静 止或流动的。当电凝壳体的材质为各类多孔材料时,其材质具体可以是分子筛或活性炭。当电凝壳体的材质为各类泡沫材料时,其材质具体可以是泡沫铁、泡沫碳化硅等。在一种实施例中第一电极通过电凝绝缘件与电凝壳体固接,电凝绝缘件的材质可以为绝缘云母。同时,在一种实施例中第二电极直接与电凝壳体电连接,此种连接方式使得电凝壳体可以与第二电极具有相同的电势,这样电凝壳体也能吸附带电的含硝酸的水雾,电凝壳体也构成一种第二电极。电凝壳体中设有上述电凝流道,第一电极安装在电凝流道中。
当含硝酸的水雾附着在第二电极后,将形成凝露。于本发明一些实施例中第二电极可沿上下方向延伸,这样堆积在第二电极上的凝露达到一定重量时,将在重力的作用下沿第二电极向下流动,并最终汇集在设定位置或装置中,从而实现对附着在第二电极上的硝酸液的回收。本电凝装置可用于制冷除雾。另外,也可以采用外加电凝电场的方式对附着在第二电极上的物质进行收集。对第二电极上的物质收集方向既可以同气流相同,也可以与气流方向不同。在具体实施时,因为是要充分利用重力作用,使第二电极上的水滴或水层尽快流入收集槽中的;同时会尽量利用气流方向及其作用力,来加速第二电极上水流的速度。因此会根据不同的安装条件,以及绝缘的方便性、经济性和可行性等,尽量达到上述目的,不拘束于特定的方向。
另外,当前已有的静电场荷电理论是利用电晕放电,电离氧气,产生大量的负氧离子,负氧离子和粉尘接触,粉尘荷电,荷电后的粉尘被异极吸附。但当遇到含硝酸的水雾等低比电阻物质时,现有的电场吸附作用几乎没有。因低比电阻物质在得电后容易失电,当移动中的负氧离子使低比电阻物质荷电后,低比电阻物质又将很快失电,而负氧离子只移动一次,导致如含硝酸的水雾等低比电阻物质失电后难以再带电,或此种带电方式大大降低了低比电阻物质带电的几率,使得低比电阻物质整体处于不带电状态,这样异极就难以对低比电阻物质持续施加吸附力,最终导致现有的电场对含硝酸的水雾等低比电阻物质的吸附效率极低。上述电凝装置及电凝方法,不是采用荷电方式让水雾带电,而是直接将电子传递给含硝酸的水雾使其带电,在某个雾滴带电又失电后,新的电子将快速由第一电极、并通过其它雾滴传递到该失电的雾滴上,使得雾滴失电后又能快速得电,大大增加了雾滴带电几率,如次重复,使得雾滴整体处于得电状态,并使得第二电极能持续给雾滴施加吸引力,直至吸附住雾滴,从而保证本电凝装置对含硝酸的水雾的收集效率更高。本发明采用的上述使雾滴带电的方法,不需要使用电晕线、电晕极、或电晕板等,简化了本电凝装置的整体结构,降低了本电凝装置的制造成本。同时,本发明采用上述上电方式,也使得第一电极上的大量电子,将通过雾滴传递给第二电极,并形成电流。当流经本电凝装置的水雾的浓度越大时,第一电极上的电 子更容易通过含硝酸的水雾传递给第二电极,更多的电子将在雾滴间传递,使得第一电极和第二电极之间形成的电流更大,并使得雾滴的带电几率更高,且使本电凝装置对水雾的收集效率更高。
于本发明一实施例中提供一种电凝除雾方法,包括如下步骤:
使带水雾的气体流经第一电极;
当带水雾的气体流经第一电极时,第一电极使气体中的水雾带电,第二电极给带电的水雾施加吸引力,使水雾向第二电极移动,直至水雾附着在第二电极上。
于本发明一实施例中第一电极将电子导入水雾,电子在位于第一电极和第二电极之间的雾滴之间进行传递,使更多雾滴带电。
于本发明一实施例中第一电极和第二电极之间通过水雾传导电子、并形成电流。
于本发明一实施例中第一电极通过与水雾接触的方式使水雾带电。
于本发明一实施例中第一电极通过能量波动的方式使水雾带电。
于本发明一实施例中附着在第二电极上的水雾形成水滴,第二电极上的水滴流入收集槽中。
于本发明一实施例中第二电极上的水滴在重力作用下流入收集槽。
于本发明一实施例中气体流动时,将吹动水滴流入收集槽中。
于本发明一实施例中使带硝酸雾的气体流经第一电极;当带硝酸雾的气体流经第一电极时,第一电极使气体中的硝酸雾带电,第二电极给带电的硝酸雾施加吸引力,使硝酸雾向第二电极移动,直至硝酸雾附着在第二电极上。
于本发明一实施例中第一电极将电子导入硝酸雾,电子在位于第一电极和第二电极之间的雾滴之间进行传递,使更多雾滴带电。
于本发明一实施例中第一电极和第二电极之间通过硝酸雾传导电子、并形成电流。
于本发明一实施例中第一电极通过与硝酸雾接触的方式使硝酸雾带电。
于本发明一实施例中第一电极通过能量波动的方式使硝酸雾带电。
于本发明一实施例中附着在第二电极上的硝酸雾形成水滴,第二电极上的水滴流入收集槽中。
于本发明一实施例中第二电极上的水滴在重力作用下流入收集槽。
于本发明一实施例中气体流动时,将吹动水滴流入收集槽中。
实施例1
请参阅图5,显示为进气除尘系统于一实施例中的结构示意图。所述进气除尘系统101包 括进气除尘系统入口1011、离心分离机构1012、第一滤水机构1013、进气电场装置1014、进气绝缘机构1015、进气均风装置、第二滤水机构1017和/或进气臭氧机构1018。本发明中第一滤水机构1013和/或第二滤水机构1017是可选的,即本发明提供的进气除尘系统中可包括第一滤水机构1013和/或第二滤水机构1017,也可不包括第一滤水机构1013和/或第二滤水机构1017。
如图5所示,所述进气除尘系统入口1011设置于所述离心分离机构1012的进气壁上,以接收带有颗粒物的气体。
设置于所述进气除尘系统101下端的离心分离机构1012采用圆锥形筒。圆锥形筒与进气电场装置1014的衔接处为一排气口,所述排气口上设置有用于过滤颗粒物的第一过滤层。所述圆锥形筒的筒底设置有接收颗粒物的出粉口。
具体地,含颗粒物的气体一般以12—30m/s速度由进气除尘系统入口1011进入离心分离机构1012时,气体将由直线运动变为圆周运动。旋转气流的绝大部分,沿器壁自圆筒体呈螺旋形向下朝锥体流动。此外,颗粒物在离心力的作用下,被甩向分离机构的内壁,颗粒物一旦与内壁接触,靠内壁附近的向下轴向速度的动量沿壁面下落,由出粉口排出。旋转下降的外旋气流,在下降过程中不断向分离机构的中心部分流入,形成向心的径向气流,这部分气流就构成了旋转向上的内旋流。内、外旋流的旋转方向是相同的。最后净化气经排气口及第一过滤网(未予图示)排入所述进气电场装置1014,一部分未被分离下来的较细尘粒也未能逃逸。
设置于所述离心分离机构1012内的第一滤水机构1013包括设置于所述进气除尘系统入口1011的第一电极为一导电网板,所述导电网板用于在上电后,将电子传导给水(低比电阻物质)。用于吸附带电的水的第二电极于本实施例中为所述进气电场装置1014的阳极积尘部,即除尘电场阳极10141。
请参阅图6,显示为设置于所述进气装置内的第一滤水机构的另一实施例结构图。所述第一滤水机构的第一电极10131设置于所述进气口,所述第一电极10131为一带有负电势导电网板。同时,本实施例的第二电极10132设置于所述进气装置内呈面网状,且第二电极10132带有正电势,该第二电极10132也称作收集极。本实施例中第二电极10132具体呈平面网状,且第一电极10131平行于第二电极10132。本实施例中第一电极10131和第二电极10132之间形成网面电场。另外,第一电极10131由金属丝制成的网状结构,该第一电极10131由金属丝网构成。本实施例中第二电极10132的面积大于第一电极10131的面积。所述进气电场装置1014包括进气除尘电场阳极10141和设置于进气除尘电场阳极10141内的进气除尘电 场阴极10142,进气除尘电场阳极10141与进气除尘电场阴极10142之间形成非对称静电场,其中,待含有颗粒物的气体通过所述排气口进入所述进气电场装置1014后,由于所述进气除尘电场阴极10142放电,电离所述气体,以使所述颗粒物获得负电荷,向所述进气除尘电场阳极10141移动,并沉积在所述进气除尘电场阳极10141上。
具体地,所述进气除尘电场阳极10141的内部由呈蜂窝状(如图19中所示的蜂窝状)、且中空的阳极管束组组成,阳极管束的端口的形状为六边形。
所述进气除尘电场阴极10142包括若干根电极棒,其一一对应地穿设所述阳极管束组中的每一阳极管束,其中,所述电极棒的形状呈针状、多角状、毛刺状、螺纹杆状或柱状。
在本实施例中,所述进气除尘电场阴极10142的出气端低于所述进气除尘电场阳极10141的出气端,且所述进气除尘电场阴极10142的出气端与所述进气除尘电场阳极10141的进气端齐平,以使所述进气电场装置1014内部形成加速电场。
所述进气绝缘机构1015包括绝缘部和隔热部。所述绝缘部的材料采用陶瓷材料或玻璃材料。所述绝缘部为伞状串陶瓷柱或玻璃柱,或柱状串陶瓷柱或玻璃柱,伞内外或柱内外挂釉。
如图5所示,于本发明一实施例中,进气除尘电场阴极10142安装在进气阴极支撑板10143上,进气阴极支撑板10143与进气除尘电场阳极10141通过进气绝缘机构1015相连接。所述进气绝缘机构1015用于实现所述进气阴极支撑板10143和所述进气除尘电场阳极10141之间的绝缘。于本发明一实施例中,进气除尘电场阳极10141包括第一阳极部101412和第二阳极部101411,即所述第一阳极部101412靠近进气除尘装置入口,第二阳极部101411靠近进气除尘装置出口。进气阴极支撑板和进气绝缘机构在第一阳极部101412和第二阳极部101411之间,即进气绝缘机构1015安装在进气电离电场中间、或进气除尘电场阴极10142中间,可以对进气除尘电场阴极10142起到良好的支撑作用,并对进气除尘电场阴极10142起到相对于进气除尘电场阳极10141的固定作用,使进气除尘电场阴极10142和进气除尘电场阳极10141之间保持设定的距离。
请参阅图7A、图7B及图7C,显示为进气均风装置的三种实施结构图。
如图7A所示,进气均风装置1016当所述进气除尘电场阳极的外型呈圆柱体时,所述进气均风装置1016位于所述进气除尘系统入口1011与所述进气除尘电场阳极10141和所述进气除尘电场阴极10142形成的进气电离除尘电场之间,且由若干围绕所述进气除尘系统入口1011中心旋转的均风叶片10161组成。所述均风装置能够使发动机在各种转速下变化的进气量均匀通过所述进气除尘电场阳极产生的电场。同时能够保持所述进气除尘电场阳极内部温度恒定,氧气充足。
如图7B所示,当所述进气除尘电场阳极的外型呈立方体时,所述进气均风装置1020包括:
设置于位于所述进气除尘电场阳极一侧边的进气管10201;及
设置于所述进气除尘电场阳极另一侧边的出气管10202;其中,安装进气管10201的侧边与安装出气管10202的另一侧边相对立。
如图7C所示,所述进气均风装置1026还可以包括设置于所述进气除尘电场阳极的进气端的第一文氏板均风机构1028和设置于所述进气除尘电场阳极的出气端的第二文氏板均风机构1030(第二文氏板均风机构1030如图7D所示的第二文氏板均风机构俯视图可以看出其呈折型),所述第一文氏板均风机构上开设与进气孔,所述第二文氏板均风机构上开设有出气孔,所述进气孔与所述出气孔错位排布,且正面进气侧面出气,形成旋风结构。
在本实施例中,所述进气电场装置1014与所述第二滤水机构1017的衔接处设置第二过滤网用于过滤未经所述进气电场装置1014处理过的粒径较小的细颗粒。
设置于所述出气端处的第二滤水机构1017包括:第三过滤网、转轴及阻水球。
所述第三过滤网通过转轴倾斜式安装于所述出气端处,其中,所述第三过滤网与所述出气口对应的位置处安装有阻水球。待进入的气体推动所述第三过滤网绕转轴旋转,所述第三过滤网上形成水膜,所述阻水球堵住所述出气端,以防止水份冲出。
设置于所述进气装置出气端的所述进气臭氧机构1018采用除臭氧灯管。
实施例2
如图8所示的进气电场装置,包括进气除尘电场阳极10141、进气除尘电场阴极10142和进气驻极体元件205,所述进气除尘电场阳极10141和所述进气除尘电场阴极10142接通电源时形成进气电离除尘电场,所述进气驻极体元件205设于所述进气电离除尘电场中,图8中箭头方向为待处理物流动方向。所述进气驻极体元件205设于进气电场装置出口。所述进气电离除尘电场给所述进气驻极体元件充电。所述进气驻极体元件具有多孔结构,所述进气驻极体元件的材料为氧化铝。所述进气除尘电场阳极内部为管状,所述进气驻极体元件外部为管状,所述进气驻极体元件外部套设于所述进气除尘电场阳极内部。所述进气驻极体元件与所述进气除尘电场阳极为可拆卸式连接。
一种进气除尘方法,包括如下步骤:
a)利用进气电离除尘电场吸附进气中的颗粒物;
b)利用进气电离除尘电场给进气驻极体元件充电。
其中,所述进气驻极体元件设于进气电场装置出口;所述进气驻极体元件的材料为氧化 铝;当进气电离除尘电场无上电驱动电压时,利用充电的进气驻极体元件吸附进气中的颗粒物;在充电的进气驻极体元件吸附一定的进气中的颗粒物后,将其替换为新的进气驻极体元件;替换为新的进气驻极体元件后重新启动进气电离除尘电场吸附进气中的颗粒物,并给新的进气驻极体元件充电。
将上述进气电场装置和静电除尘的方法用于处理机动车启动后的尾气,利用进气电离除尘电场吸附机动车启动后的尾气中的颗粒物,同时利用该进气电离除尘电场给进气驻极体元件充电。当进气电离除尘电场无上电驱动电压(即故障)时,利用充电的进气驻极体元件吸附进气中的颗粒物,可达到50%以上的净化效率。
上述电场装置的结构也可作为尾气电场装置,上述除尘方法也可作为尾气除尘方法。
实施例3
如图9和图10所示的进气电场装置,包括进气除尘电场阳极10141、进气除尘电场阴极10142和进气驻极体元件205,所述进气除尘电场阳极10141和所述进气除尘电场阴极10142形成进气流道292,所述进气驻极体元件205设于所述进气流道292中,图9中箭头方向为待处理物流动方向。所述进气流道292包括进气流道出口,所述进气驻极体元件205靠近所述进气流道出口。所述进气驻极体元件205于所述进气流道中的横截面占进气流道横截面10%,如图11所示,即为S2/(S1+S2)*100%,其中S2第一横截面面积为所述进气驻极体元件于所述进气流道中的横截面面积,S1第一横截面面积和S2第二横截面面积的和为进气流道横截面面积,S1第一横截面面积不包括进气除尘电场阴极10142的横截面面积。所述进气除尘电场阳极和所述进气除尘电场阴极接通电源时形成进气电离除尘电场。所述进气电离除尘电场给所述进气驻极体元件充电。所述进气驻极体元件具有多孔结构,所述进气驻极体元件的材料为聚四氟乙烯。所述进气除尘电场阳极内部为管状,所述进气驻极体元件外部为管状,所述进气驻极体元件外部套设于所述进气除尘电场阳极内部。所述进气驻极体元件与所述进气除尘电场阳极为可拆卸式连接。
一种进气除尘方法,包括如下步骤:
1)利用进气电离除尘电场吸附进气中的颗粒物;
2)利用进气电离除尘电场给进气驻极体元件充电。
其中,所述进气驻极体元件靠近所述进气流道出口;所述进气驻极体元件的材料为聚四氟乙烯;当进气电离除尘电场无上电驱动电压时,利用充电的进气驻极体元件吸附进气中的颗粒物;在充电的进气驻极体元件吸附一定的进气中的颗粒物后,将其替换为新的进气驻极体元件;替换为新的进气驻极体元件后重新启动进气电离除尘电场吸附进气中的颗粒物,并 给新的进气驻极体元件充电。
将上述进气电场装置和静电除尘的方法用于处理机动车启动后的尾气,利用进气电离除尘电场吸附机动车启动后的尾气中的颗粒物,同时利用该进气电离除尘电场给进气驻极体元件充电。当进气电离除尘电场无上电驱动电压(即故障)时,利用充电的进气驻极体元件吸附进气中的颗粒物,可达到30%以上的净化效率。
上述电场装置的结构也可作为尾气电场装置,上述除尘方法也可作为尾气除尘方法。
实施例4
如图12所示,所述进气除尘系统包括进气电场装置和除臭氧装置206,所述进气电场装置包括括进气除尘电场阳极10141和进气除尘电场阴极10142,所述除臭氧装置用于去除或减少所述进气电场装置产生的臭氧,所述除臭氧装置206在进气电场装置出口与进气除尘系统出口之间。所述进气除尘电场阳极10141和所述进气除尘电场阴极10142用于产生进气电离除尘电场。所述除臭氧装置206包括臭氧消解器,用于消解所述进气电场装置产生的臭氧,所述臭氧消解器为紫外线臭氧消解器,图中箭头方向为进气流动方向。
一种进气除尘方法,包括以下步骤:所述进气经进气电离除尘,然后对进气电离除尘产生的臭氧进行臭氧消解,所述臭氧消解为紫外线消解。
所述除臭氧装置用于去除或减少所述进气电场装置产生的臭氧,由于空气中的氧气参与电离,形成臭氧,影响后续装置性能,如若臭氧进入发动机后,内部化学成分氧元素增多,分子量增大,由烃类化合物转变成非烃化合物,外现上颜色变深,沉淀增多,腐蚀性增大,使润滑油的使用性能下降,因此,本发明进气除尘系统还包括除臭氧装置,避免或减少后续装置性能的下降,如避免或减少发动机中润滑油使用性能的下降。
实施例5
如图13所示,所述尾气除尘系统包括除水装置207和尾气电场装置。所述尾气电场装置包括尾气除尘电场阳极10211和尾气除尘电场阴极10212,所述尾气除尘电场阳极10211和所述尾气除尘电场阴极10212用于产生尾气电离除尘电场。所述除水装置207用于在尾气电场装置入口之前去除液体水,当尾气温度低于100℃时,所述除水装置207脱除尾气中的液体水,所述除水装置207为电凝装置,图中箭头方向为尾气流动方向。
一种尾气除尘方法,包括以下步骤:尾气温度低于100℃时,脱除尾气中的液体水,然后电离除尘,其中采用电凝除雾方法脱除尾气中的液体水,所述尾气为汽油发动机冷启动时的尾气,减少尾气中的水珠即液体水,减少尾气电离除尘电场放电不均匀及尾气除尘电场阴极 和尾气除尘电场阳极击穿,提高电离除尘效率,电离除尘效率为99.9%以上,未脱除尾气中的液体水的除尘方法的电离除尘效率为70%以下。因此,尾气温度低于100℃时,脱除尾气中的液体水,然后电离除尘,减少尾气中的水珠即液体水,减少尾气电离除尘电场放电不均匀及尾气除尘电场阴极和尾气除尘电场阳极击穿,提高电离除尘效率。
实施例6
如图14所示,所述尾气除尘系统包括补氧装置208和尾气电场装置。所述尾气电场装置包括尾气除尘电场阳极10211和尾气除尘电场阴极10212,所述尾气除尘电场阳极10211和所述尾气除尘电场阴极10212用于产生尾气电离除尘电场。所述补氧装置208用于在尾气电离除尘电场之前添加包括氧气的气体,所述补氧装置208通过通入外界空气的方式添加氧气,根据尾气颗粒含量决定补氧量。图中箭头方向为补氧装置208添加包括氧气的气体流动方向。
一种尾气除尘方法,包括以下步骤:在尾气电离除尘电场之前添加包括氧气的气体,进行电离除尘,通过通入外界空气方式添加氧气,根据尾气颗粒含量决定补氧量。
本发明尾气除尘系统:包括补氧装置,可以通过单纯增氧、通入外界空气、通入压缩空气和/或通入臭氧的方式添加氧气,提高进入尾气电离除尘电场尾气含氧量,从而当尾气流经尾气除尘电场阴极和尾气除尘电场阳极之间的尾气电离除尘电场时,增加电离的氧气,使得尾气中更多的粉尘荷电,进而在尾气除尘电场阳极的作用下将更多的荷电的粉尘收集起来,使得尾气电场装置的除尘效率更高,有利于尾气电离除尘电场收集尾气颗粒物,同时还能起到降温的作用,增加电力系统效率,而且,补氧也会提高尾气电离除尘电场臭氧含量,有利于提高尾气电离除尘电场对尾气中有机物进行净化、自洁、脱硝等处理的效率。
实施例7
本实施例所述基于发动机的气体处理系统还包括尾气除尘系统,所述尾气除尘系统用于处理欲排入大气中的废气。
请参阅图15,显示为尾气处理装置于一实施例中的结构示意图。如图15所示,所述尾气除尘系统102包括尾气电场装置1021、尾气绝缘机构1022、尾气均风装置、尾气滤水机构及尾气臭氧机构。
本发明中尾气滤水机构是可选的,即本发明提供的尾气除尘系统中可包括尾气滤水机构,也可不包括尾气滤水机构。
所述尾气电场装置1021包括尾气除尘电场阳极10211和设置于尾气除尘电场阳极10211内的尾气除尘电场阴极10212,尾气除尘电场阳极10211与尾气除尘电场阴极10212之间形 成非对称静电场,其中,待含有颗粒物的气体通过所述尾气均风装置的排气口进入所述尾气电场装置1021后,由于所述尾气除尘电场阴极10212放电,电离所述气体,以使所述颗粒物获得负电荷,向所述尾气除尘电场阳极10211移动,并沉积在所述尾气除尘电场阴极10212上。
具体地,所述尾气除尘电场阴极10212的内部由呈蜂窝状、且中空的阳极管束组组成,阳极管束的端口的形状为六边形。
所述尾气除尘电场阴极10212包括若干根电极棒,其一一对应地穿设所述阳极管束组中的每一阳极管束,其中,所述电极棒的形状呈针状、多角状、毛刺状、螺纹杆状或柱状。
在本实施例中,所述尾气除尘电场阴极10212的进气端低于所述尾气除尘电场阳极10211的进气端,且所述尾气除尘电场阴极10212的出气端与所述尾气除尘电场阳极10211的出气端齐平,以使所述尾气电场装置1021内部形成加速电场。
气道外悬的所述尾气绝缘机构1022包括绝缘部和隔热部。所述绝缘部的材料采用陶瓷材料或玻璃材料。所述绝缘部为伞状串陶瓷柱,伞内外挂釉。请参阅图16,显示为呈伞状的尾气绝缘机构于一实施例中的结构示意图。
如图15所示,于本发明一实施例中尾气除尘电场阴极10212安装在尾气阴极支撑板10213上,尾气阴极支撑板10213与尾气除尘电场阳极10211通过尾气绝缘机构1022相连接。于本发明一实施例中尾气除尘电场阳极10211包括第三阳极部102112和第四阳极部102111,即所述第三阳极部102112靠近尾气除尘装置入口,第四阳极部102111靠近尾气除尘装置出口。尾气阴极支撑板10213和尾气绝缘机构1022在第三阳极部102112和第四阳极部102111之间,即尾气绝缘机构1022安装在尾气电离电场中间、或尾气除尘电场阴极10212中间,可以对尾气除尘电场阴极10212起到良好的支撑作用,并对尾气除尘电场阴极10212起到相对于尾气除尘电场阳极10211的固定作用,使尾气除尘电场阴极10212和尾气除尘电场阳极10211之间保持设定的距离。
所述尾气均风装置1023设置于所述尾气电场装置1021的进气端处的。请参阅图17A、图17B及图17C,显示为尾气均风装置的三种实施结构图。
如图17A所示,当所述尾气除尘电场阳极10211的外型呈圆柱体时,所述尾气均风装置1023为位于尾气除尘系统入口与所述尾气除尘电场阳极10211和所述尾气除尘电场阴极10212形成的尾气电离除尘电场之间、且由若干围绕所述尾气除尘系统入口中心旋转的均风叶片10231组成。所述尾气均风装置1023能够使发动机在各种转速下变化的进气量均匀通过所述尾气除尘电场阳极产生的电场。同时能够保持所述尾气除尘电场阳极内部温度恒定,氧 气充足。
如图17B所示,当所述尾气除尘电场阳极10211的外型呈立方体时,所述尾气均风装置包括:
设置于位于所述尾气除尘电场阳极一侧边的进气管10232;及
设置于所述除尘电场阳极另一侧边的出气管10233;其中,安装进气管10232的侧边与安装出气管10233的另一侧边相对立。
如图17C所示,所述尾气均风装置还可以包括设置于所述尾气除尘电场阳极的进气端的第二文氏板均风机构10234和设置于所述尾气除尘电场阳极的出气端的第三文氏板均风机构10235(第三文氏板均风机构俯视时呈折型),所述第三文氏板均风机构上开设与进气孔,所述第三文氏板均风机构上开设有出气孔,所述进气孔与所述出气孔错位排布,且正面进气侧面出气,形成旋风结构。
设置于所述尾气电场装置1021内的尾气滤水机构包括作为第一电极的导电网板,所述导电网板用于在上电后,将电子传导给水(低比电阻物质)。用于吸附带电的水的第二电极于本实施例中为所述尾气电场装置的尾气除尘电场阳极10211。
所述尾气滤水机构的第一电极设置于所述进气口,所述第一电极为一带有负电势导电网板。同时,本实施例的第二电极设置于所述进气装置内呈面网状,且第二电极带有正电势,该第二电极也称作收集极。本实施例中第二电极具体呈平面网状,且第一电极平行于第二电极。本实施例中第一电极和第二电极之间形成网面电场。另外,第一电极由金属丝制成的网状结构,该第一电极由金属丝网构成。本实施例中第二电极的面积大于第一电极的面积。
实施例8
一种尾气臭氧净化系统,如图18所示,包括:
臭氧源201,用于提供臭氧流股,所述臭氧流股为臭氧发生器即时生成。
反应场202,用于将臭氧流股与尾气流股混合反应。
脱硝装置203,用于脱除臭氧流股与尾气流股混合反应产物中的硝酸;所述脱硝装置203包括电凝装置2031,用于将臭氧处理后的发动机尾气进行电凝,含硝酸的水雾堆积在电凝装置2031中的第二电极上。所述脱硝装置203还包括脱硝液收集单元2032,用于存储废气中脱除的硝酸水溶液和/或硝酸盐水溶液;当所述脱硝液收集单元中存储有硝酸水溶液时,所述脱硝液收集单元2032设有碱液加入单元,用于与硝酸形成硝酸盐。
臭氧消解器204,用于消解经反应场处理后的尾气中的臭氧。臭氧消解器可以通过紫外线,催化等方式进行臭氧消解。
所述反应场202为反应器二,如图19所示,内设有若干蜂窝状腔体2021,用于提供尾气与臭氧混合并反应的空间;所述蜂窝状腔体内之间设有间隙2022,用于通入冷态介质,控制尾气与臭氧的反应温度,图中右侧箭头为冷媒进口,左侧箭头为冷媒出口。
所述电凝装置包括:
第一电极301,能将电子传导给含硝酸的水雾(低比电阻物质);当电子被传导给含硝酸的水雾时,含硝酸的水雾带电;
第二电极302,能给带电的含硝酸的水雾施加吸引力。
本实施例中第一电极301有两个,两个第一电极301均呈网状且呈球笼状。本实施例中第二电极302有一个,该第二电极302呈网状且呈球笼状。第二电极302位于两个第一电极301之间。同时,如图33所示,本实施例中电凝装置还包括具有进口3031和出口3032的外壳303,第一电极301和第二电极302均安装在外壳303中。且第一电极301通过绝缘件304与外壳303的内壁固接,第二电极302直接与外壳303固接。本实施例中绝缘件304呈柱状,又称作绝缘柱。本实施例中第一电极301具有负电势,第二电极302具有正电势。同时,本实施例中外壳303与第二电极302具有相同的电势,该外壳303同样对带电的物质具有吸附作用。
本实施例中电凝装置用于处理含有酸雾的工业尾气。本实施例中进口3031与排放工业尾气的口相连通。本实施例中电凝装置的工作原理如下:工业尾气由进口3031流入外壳303,并经出口3032流出;在此过程中,工业尾气将先流经其中一个第一电极301,当工业尾气中的酸雾与该第一电极301接触时,或与该第一电极301的距离达到一定值时,第一电极301将电子传递给酸雾,部分酸雾带电,第二电极302给带电的酸雾施加吸引力,酸雾向第二电极302移动,并附着在第二电极302上;另有一部分酸雾未被吸附在第二电极302上,该部分酸雾继续向出口3032方向流动,当该部分酸雾与另一个第一电极301接触时,或与另一个第一电极301的距离达到一定值时,该部分酸雾将带电,外壳303给该部分带电的酸雾施加吸附力,使得该部分带电的酸雾附着在外壳303的内壁上,从而大大减少了工业尾气中酸雾的排放量,且本实施例中处理装置能去除工业尾气中90%的酸雾,去除酸雾的效果非常显著。另外,本实施例中进口3031和出口3032均呈圆形,进口3031也可称作进气口,出口3032也可称作出气口。
实施例9
如图20所示,实施例8中尾气臭氧净化系统还包括臭氧量控制装置209,用于控制臭氧量以致有效氧化尾气中待处理的气体组分,所述臭氧量控制装置209包括控制单元2091。所 述臭氧量控制装置209还包括臭氧处理前尾气组分检测单元2092,用于检测臭氧处理前尾气组分含量。所述控制单元根据所述臭氧处理前尾气组分含量控制混合反应所需臭氧量。
所述臭氧处理前尾气组分检测单元2092选自以下检测单元中至少一个:
第一挥发性有机化合物检测单元20921,用于检测臭氧处理前尾气中挥发性有机化合物含量,如挥发性有机化合物传感器等;
第一CO检测单元20922,用于检测臭氧处理前尾气中CO含量,如CO传感器等;
第一氮氧化物检测单元20923,用于检测臭氧处理前尾气中氮氧化物含量,如氮氧化物(NO
x)传感器等。
所述控制单元2091根据至少一个所述臭氧处理前尾气组分检测单元2092的输出值控制混合反应所需臭氧量。
所述控制单元用于按照理论估计值控制混合反应所需臭氧量。所述理论估计值为:臭氧通入量与尾气中待处理物的摩尔比为2~10。
所述臭氧量控制装置209包括臭氧处理后尾气组分检测单元2093,用于检测臭氧处理后尾气组分含量。所述控制单元2091根据所述臭氧处理后尾气组分含量控制混合反应所需臭氧量。
所述臭氧处理后尾气组分检测单元2093选自以下检测单元中至少一个:
第一臭氧检测单元20931,用于检测臭氧处理后尾气中臭氧含量;
第二挥发性有机化合物检测单元20932,用于检测臭氧处理后尾气中挥发性有机化合物含量;
第二CO检测单元20933,用于检测臭氧处理后尾气中CO含量;
第二氮氧化物检测单元20934,用于检测臭氧处理后尾气中氮氧化物含量。
所述控制单元2091根据至少一个所述臭氧处理后尾气组分检测单元2093的输出值控制臭氧量。
实施例10
制备臭氧发生器用电极:
取长300mm,宽30mm,厚1.5mm的α-氧化铝板材作为阻挡介质层;
催化剂(含涂层和活性组份)涂覆在阻挡介质层的一面,涂覆催化剂之后,所述催化剂为所述阻挡介质层质量的12%,所述催化剂包括如下重量百分比的各组分:活性组分为12wt%,涂层为88wt%,其中,所述活性组分为氧化铈和氧化锆(依次物质的量比为1:1.3),所述涂层为gama氧化铝;
在涂覆好催化剂的阻挡介质层另一面贴铜箔,制成电极。
其中,催化剂涂覆方法如下:
(1)取200g 800目的gama氧化铝粉、5g硝酸铈、4g硝酸锆、4g草酸、5g拟薄水铝石、1g硝酸铝、0.5g EDTA(分解用),倒入玛瑙磨中。再加入1300g去离子水。200rpm/min下研磨10个小时。制成浆料;
(2)把上述阻挡介质层放入烘箱中于150℃下烘干2小时,烘干时打开烘箱风扇。然后保持烘箱门关闭的条件下冷却到室温;
(3)把上述催化剂浆料装入通过高压喷枪,均匀喷涂到烘干后的阻挡介质层表面。放入真空干燥器中阴干2小时;
(4)阴干后放入马弗中加热至550℃,加热升温速度为每分钟5℃。恒温两小时,保持炉门关闭条件下,自然冷却到室温。涂覆过程完成。
以同样的方法,制备4块电极。取河南迪诺环保科技股份有限公司XF-B-3-100型臭氧发生器,把其中的4块电极全换成上述制成的电极。进行比对试验,试验条件为:纯氧气气源,进气压力为0.6MPa,进气风量为每小时1.5立方米,交流电压,5000V、2万赫兹的正弦波。通过出气风量和质量浓度检测结果计算得每小时臭氧产生量。
实验结果如下:
XF-B-3-100型原臭氧产生量为120g/小时;更换电极后,同样的试验条件下,臭氧产生量为160g/小时。实验条件下,功率损耗均为830W。
实施例11
制备臭氧发生器用电极:
取长300mm,宽30mm,厚1.5mm的α-氧化铝板材作为阻挡介质层;
催化剂(含涂层和活性组份)涂覆在阻挡介质层的一面,涂覆催化剂之后,所述催化剂为所述阻挡介质层质量的5%,所述催化剂包括如下重量百分比的各组分:活性组分占催化剂总重15wt%,涂层85%,其中,所述活性组分为MnO和CuO,所述涂层为gama氧化铝;
在涂覆好催化剂的阻挡介质层另一面贴铜箔,制成电极。
其中,催化剂涂覆方法如下:
(1)取200g 800目的gama氧化铝粉、4g草酸、5g拟薄水铝石、1g硝酸铝、0.5g表面活性剂(分解用),倒入玛瑙磨中。再加入1300g去离子水。200rpm/min下研磨10个小时。制成浆料;
(2)把上述阻挡介质层放入烘箱中于150℃下烘干2小时,烘干时打开烘箱风扇。然后保持烘箱门关闭的条件下冷却到室温。通过测量烘干前后的质量变化,测出阻挡介质层的吸水量(A);
(3)把上述浆料装入通过高压喷枪,均匀喷涂到烘干后的阻挡介质层表面。放入真空干燥器中阴干2小时;
(4)阴干后放入马弗中加热至550℃,加热升温速度为每分钟5℃。恒温两小时,保持炉门关闭条件下,自然冷却到室温。称重。
(5)将上述负载有涂层的阻挡介质层浸入水中1分钟后取出,吹净表面浮水,称重。计算得到其吸水量(B);
(6)计算得到涂层的净吸水量C(C=B–A)。根据活性组份目标负载量,涂层净吸水量C,计算得活性组份水溶液的浓度。以此配制活性组份溶液;(活性组份目标负载量CuO0.1g;MnO0.2g)
(7)将负载有涂层的阻挡介质层150℃烘干2小时,保持烘箱门关闭条件下冷却至室温。不需负载活组份的面进行防水保护。
(8)取(6)配制好的活性组份溶液(硝酸铜和硝酸锰),以浸渍法负载到涂层中去,吹去表面浮液。150℃烘干2小时。转入马弗炉中焙烧。以每分钟15℃加热到550℃,恒温3小时。微开炉门,冷却到室温。涂覆过程完成。
同样的方法,制备4块电极。取河南迪诺环保科技股份有限公司XF-B-3-100型臭氧发生器,把其中的4块电极全换成上述制成的电极。进行比对试验,试验条件为:纯氧气气源,进气压力为0.6MPa,进气风量为每小时1.5立方米,交流电压,5000V、2万赫兹的正弦波。通过出气风量和质量浓度检测结果计算得每小时臭氧产生量。
实验结果如下:
XF-B-3-100型原臭氧产生量为120g/小时;更换电极后,同样的试验条件下,臭氧产生量为168g/小时。实验条件下,功率损耗均为830W。
实施例12
制备臭氧发生器用电极:
取长300mm,宽30mm,厚1.5mm的石英玻璃板作为阻挡介质层;
催化剂(含涂层和活性组份)涂覆在阻挡介质层的一面,涂覆催化剂之后,所述催化剂为所述阻挡介质层质量的1%,所述催化剂包括如下重量百分比的各组分:活性组分为5wt%, 涂层为95wt%,其中,所述活性组分为银、铑、铂、钴和镧(依次物质的量比为1:1:1:2:1.5),所述涂层为氧化锆;
在涂覆好催化剂的阻挡介质层另一面贴铜箔,制成电极。
其中,催化剂涂覆方法如下:
(1)取400g氧化锆、1.7g硝酸银、2.89g硝酸铑、3.19g硝酸铂、4.37g硝酸钴、8.66g硝酸镧、15g草酸、25g EDTA(分解用),倒入玛瑙磨中。再加入1500g去离子水。200rpm/min下研磨10个小时。制成浆料;
(2)把上述阻挡介质层放入烘箱中于150℃下烘干2小时,烘干时打开烘箱风扇。然后保持烘箱门关闭的条件下冷却到室温;
(3)把上述催化剂浆料装入通过高压喷枪,均匀喷涂到烘干后的阻挡介质层表面。放入真空干燥器中阴干2小时;
(4)阴干后放入马弗中加热至550℃,加热升温速度为每分钟5℃。恒温两小时,保持炉门关闭条件下,自然冷却到室温;然后于220℃在氢气还原气氛下进行还原1.5小时。涂覆过程完成。
以同样的方法,制备4块电极。取河南迪诺环保科技股份有限公司XF-B-3-100型臭氧发生器,把其中的4块电极全换成上述制成的电极。进行比对试验,试验条件为:纯氧气气源,进气压力为0.6MPa,进气风量为每小时1.5立方米,交流电压,5000V、2万赫兹的正弦波。通过出气风量和质量浓度检测结果计算得每小时臭氧产生量。
实验结果如下:
XF-B-3-100型原臭氧产生量为120g/小时;更换电极后,同样的试验条件下,臭氧产生量为140g/小时。实验条件下,功率损耗均为830W。
实施例13
制备臭氧发生器用电极:
催化剂(含涂层和活性组份)涂覆在铜箔(电极)的一面,涂覆催化剂之后,所述催化剂的厚度为1.5mm,所述催化剂包括如下重量百分比的各组分:活性组分为8wt%,涂层为92wt%,其中,所述活性组分为硫酸锌、硫酸钙、硫酸钛和硫酸镁(依次物质的量比为1:2:1:1),所述涂层为石墨烯。
其中,催化剂涂覆方法如下:
(1)取100g石墨烯、1.61g硫酸锌、3.44g硫酸钙、2.39g硫酸钛、1.20g硫酸镁、25g草酸、15g EDTA(分解用),倒入玛瑙磨中。再加入800g去离子水。200rpm/min下研磨10 个小时。制成浆料;
(2)把上述催化剂浆料装入通过高压喷枪,均匀喷涂到铜箔(电极)的表面上。放入真空干燥器中阴干2小时;
(3)阴干后放入马弗中加热至350℃,加热升温速度为每分钟5℃。恒温两小时,保持炉门关闭条件下,自然冷却到室温。
以同样的方法,制备4块电极。取河南迪诺环保科技股份有限公司XF-B-3-100型臭氧发生器,把其中的4块电极全换成上述制成的电极。进行比对试验,试验条件为:纯氧气气源,进气压力为0.6MPa,进气风量为每小时1.5立方米,交流电压,5000V、2万赫兹的正弦波。通过出气风量和质量浓度检测结果计算得每小时臭氧产生量。
实验结果如下:
XF-B-3-100型原臭氧产生量为120g/小时;更换电极后,同样的试验条件下,臭氧产生量为165g/小时。实验条件下,功率损耗均为830W。
实施例14
制备臭氧发生器用电极:
催化剂(含涂层和活性组份)涂覆在铜箔(电极)的一面,涂覆催化剂之后,所述催化剂的厚度为3mm,所述催化剂包括如下重量百分比的各组分:活性组分为10wt%,涂层为90wt%,其中,所述活性组分为氧化镨、氧化钐和氧化钇(依次物质的量比为1:1:1),所述涂层为氧化铈和氧化锰(依次物质的量比为1:1)。
其中,催化剂涂覆方法如下:
(1)取62.54g氧化铈、31.59g氧化锰、3.27g硝酸镨、3.36g硝酸钐、3.83g硝酸钇、12g草酸、20g EDTA(分解用),倒入玛瑙磨中。再加入800g去离子水。200rpm/min下研磨10个小时。制成浆料;
(2)把上述催化剂浆料装入通过高压喷枪,均匀喷涂到铜箔(电极)的表面上。放入真空干燥器中阴干2小时;
(3)阴干后放入马弗中加热至500℃,加热升温速度为每分钟5℃。恒温两小时,保持炉门关闭条件下,自然冷却到室温。
以同样的方法,制备4块电极。取河南迪诺环保科技股份有限公司XF-B-3-100型臭氧发生器,把其中的4块电极全换成上述制成的电极。进行比对试验,试验条件为:纯氧气气源,进气压力为0.6MPa,进气风量为每小时1.5立方米,交流电压,5000V、2万赫兹的正弦波。通过出气风量和质量浓度检测结果计算得每小时臭氧产生量。
实验结果如下:
XF-B-3-100型原臭氧产生量为120g/小时;更换电极后,同样的试验条件下,臭氧产生量为155g/小时。实验条件下,功率损耗均为830W。
实施例15
制备臭氧发生器用电极:
催化剂(含涂层和活性组份)涂覆在铜箔(电极)的一面,涂覆催化剂之后,所述催化剂的厚度为1mm,所述催化剂包括如下重量百分比的各组分:活性组分为14wt%,涂层为86wt%,其中,所述活性组分为硫化锶、硫化镍、硫化锡和硫化铁(依次物质的量比为2:1:1:1),所述涂层为硅藻土,孔隙率为80%,比表面积为350平方米/克,平均孔径为30纳米。
其中,催化剂涂覆方法如下:
(1)取58g硅藻土、3.66g硫酸锶、2.63g硫酸镍、2.18g硫酸亚锡、2.78g硫酸亚铁、3g草酸、5g EDTA(分解用),倒入玛瑙磨中。再加入400g去离子水。200rpm/min下研磨10个小时。制成浆料;
(2)把上述催化剂浆料装入通过高压喷枪,均匀喷涂到铜箔(电极)的表面上。放入真空干燥器中阴干2小时;
(3)阴干后放入马弗中加热至500℃,加热升温速度为每分钟5℃。恒温两小时,保持炉门关闭条件下,自然冷却到室温;然后再通入CO进行硫化反应,涂敷过程完成。
以同样的方法,制备4块电极。取河南迪诺环保科技股份有限公司XF-B-3-100型臭氧发生器,把其中的4块电极全换成上述制成的电极。进行比对试验,试验条件为:纯氧气气源,进气压力为0.6MPa,进气风量为每小时1.5立方米,交流电压,5000V、2万赫兹的正弦波。通过出气风量和质量浓度检测结果计算得每小时臭氧产生量。
实验结果如下:
XF-B-3-100型原臭氧产生量为120g/小时;更换电极后,同样的试验条件下,臭氧产生量为155g/小时。实验条件下,功率损耗均为830W。
实施例16
本实施例中电场发生单元可应用于进气电场装置,也可应用于尾气电场装置,如图21所示,包括用于发生电场的除尘电场阳极4051和除尘电场阴极4052,所述除尘电场阳极4051和除尘电场阴极4052分别与电源的两个电极电性连接,所述电源为直流电源,所述除尘电场 阳极4051和除尘电场阴极4052分别与直流电源的阳极和阴极电性连接。本实施例中除尘电场阳极4051具有正电势,除尘电场阴极4052具有负电势。
本实施例中直流电源具体可为直流高压电源。上述除尘电场阳极4051和除尘电场阴极4052之间形成放电电场,该放电电场是一种静电场。
如图21、图22和图23所示,本实施例中除尘电场阳极4051呈中空的正六边形管状,除尘电场阴极4052呈棒状,除尘电场阴极4052穿设在除尘电场阳极4051中。
减少电场耦合的方法,包括如下步骤:选择除尘电场阳极4051的集尘面积与除尘电场阴极4052的放电面积的比为6.67:1,除尘电场阳极4051和除尘电场阴极4052的极间距为9.9mm,除尘电场阳极4051长度为60mm,除尘电场阴极4052长度为54mm,所述除尘电场阳极4051包括流体通道,所述流体通道包括进口端与出口端,所述除尘电场阴极4052置于所述流体通道中,所述除尘电场阴极4052沿集尘极流体通道的方向延伸,除尘电场阳极4051的进口端与除尘电场阴极4052的近进口端齐平,除尘电场阳极4051的出口端与除尘电场阴极4052的近出口端之间具有夹角α,且α=118°,进而在除尘电场阳极4051和除尘电场阴极4052的作用下,能将更多的待处理物质收集起来,实现电场耦合次数≤3,能够减少电场对气溶胶、水雾、油雾、松散光滑颗粒物的耦合消耗,节省电场电能30~50%。
本实施例中进气电场装置或尾气电场装置包括由多个上述电场发生单元构成的电场级,所述电场级有多个,以利用多个集尘单元有效提高本电场装置的集尘效率。同一电场级中,各除尘电场阳极为相同极性,各除尘电场阴极为相同极性。
多个电场级中各电场级之间串联,串联电场级通过连接壳体连接,相邻两级的电场级的距离大于极间距的1.4倍。如图24所示,所述电场级为两级即第一级电场和第二级电场,第一级电场和第二级电场通过连接壳体串联连接。
本实施例中上述待处理物质可以是呈颗粒状的粉尘,也可以是其它需处理的杂质,如气溶胶、水雾、油雾等。
本实施例中上述气体可以是欲进入发动机的气体,或发动机排出的气体。
实施例17
本实施例中电场发生单元可应用于进气电场装置,也可应用于尾气电场装置,如图21所示,包括用于发生电场的除尘电场阳极4051和除尘电场阴极4052,所述除尘电场阳极4051和除尘电场阴极4052分别与电源的两个电极电性连接,所述电源为直流电源,所述除尘电场阳极4051和除尘电场阴极4052分别与直流电源的阳极和阴极电性连接。本实施例中除尘电场阳极4051具有正电势,除尘电场阴极4052具有负电势。
本实施例中直流电源具体可为直流高压电源。上述除尘电场阳极4051和除尘电场阴极4052之间形成放电电场,该放电电场是一种静电场。
本实施例中除尘电场阳极4051呈中空的正六边形管状,除尘电场阴极4052呈棒状,除尘电场阴极4052穿设在除尘电场阳极4051中。
减少电场耦合的方法,包括如下步骤:选择除尘电场阳极4051的集尘面积与除尘电场阴极4052的放电面积的比为1680:1,除尘电场阳极4051和除尘电场阴极4052的极间距为139.9mm,除尘电场阳极4051长度为180mm,除尘电场阴极4052长度为180mm,所述除尘电场阳极4051包括流体通道,所述流体通道包括进口端与出口端,所述除尘电场阴极4052置于所述流体通道中,所述除尘电场阴极4052沿集尘极流体通道的方向延伸,除尘电场阳极4051的进口端与除尘电场阴极4052的近进口端齐平,除尘电场阳极4051的出口端与除尘电场阴极4052的近出口端齐平,进而在除尘电场阳极4051和除尘电场阴极4052的作用下,能将更多的待处理物质收集起来,实现电场耦合次数≤3,能够减少电场对气溶胶、水雾、油雾、松散光滑颗粒物的耦合消耗,节省电场电能20~40%。
本实施例中上述待处理物质可以是呈颗粒状的粉尘,也可以是其它需处理的杂质,如气溶胶、水雾、油雾等。
本实施例中上述气体可以是欲进入发动机的气体,或发动机排出的气体。
实施例18
本实施例中电场发生单元可应用于进气电场装置,也可应用于尾气电场装置,如图21所示,包括用于发生电场的除尘电场阳极4051和除尘电场阴极4052,所述除尘电场阳极4051和除尘电场阴极4052分别与电源的两个电极电性连接,所述电源为直流电源,所述除尘电场阳极4051和除尘电场阴极4052分别与直流电源的阳极和阴极电性连接。本实施例中除尘电场阳极4051具有正电势,除尘电场阴极4052具有负电势。
本实施例中直流电源具体可为直流高压电源。上述除尘电场阳极4051和除尘电场阴极4052之间形成放电电场,该放电电场是一种静电场。
本实施例中除尘电场阳极4051呈中空的正六边形管状,除尘电场阴极4052呈棒状,除尘电场阴极4052穿设在除尘电场阳极4051中。
减少电场耦合的方法,包括如下步骤:选择除尘电场阳极4051的集尘面积与除尘电场阴极4052的放电面积的比为1.667:1,除尘电场阳极4051和除尘电场阴极4052的极间距为2.4mm,除尘电场阳极4051长度为30mm,除尘电场阴极4052长度为30mm,所述除尘电场阳极4051包括流体通道,所述流体通道包括进口端与出口端,所述除尘电场阴极4052置于 所述流体通道中,所述除尘电场阴极4052沿集尘极流体通道的方向延伸,除尘电场阳极4051的进口端与除尘电场阴极4052的近进口端齐平,除尘电场阳极4051的出口端与除尘电场阴极4052的近出口端齐平,进而在除尘电场阳极4051和除尘电场阴极4052的作用下,能将更多的待处理物质收集起来,实现电场耦合次数≤3,能够减少电场对气溶胶、水雾、油雾、松散光滑颗粒物的耦合消耗,节省电场电能10~30%。
本实施例中上述待处理物质可以是呈颗粒状的粉尘,也可以是其它需处理的杂质,如气溶胶、水雾、油雾等。
本实施例中上述气体可以是欲进入发动机的气体,或发动机排出的气体。
实施例19
本实施例中电场发生单元可应用于进气电场装置,也可应用于尾气电场装置,如图21所示,包括用于发生电场的除尘电场阳极4051和除尘电场阴极4052,所述除尘电场阳极4051和除尘电场阴极4052分别与电源的两个电极电性连接,所述电源为直流电源,所述除尘电场阳极4051和除尘电场阴极4052分别与直流电源的阳极和阴极电性连接。本实施例中除尘电场阳极4051具有正电势,除尘电场阴极4052具有负电势。
本实施例中直流电源具体可为直流高压电源。上述除尘电场阳极4051和除尘电场阴极4052之间形成放电电场,该放电电场是一种静电场。
如图21、图22和图23所示,本实施例中除尘电场阳极4051呈中空的正六边形管状,除尘电场阴极4052呈棒状,除尘电场阴极4052穿设在除尘电场阳极4051中,除尘电场阳极4051的集尘面积与除尘电场阴极4052的放电面积的比为6.67:1,所述除尘电场阳极4051和除尘电场阴极4052的极间距为9.9mm,除尘电场阳极4051长度为60mm,除尘电场阴极4052长度为54mm,所述除尘电场阳极4051包括流体通道,所述流体通道包括进口端与出口端,所述除尘电场阴极4052置于所述流体通道中,所述除尘电场阴极4052沿集尘极流体通道的方向延伸,除尘电场阳极4051的进口端与除尘电场阴极4052的近进口端齐平,除尘电场阳极4051的出口端与除尘电场阴极4052的近出口端之间具有夹角α,且α=118°,进而在除尘电场阳极4051和除尘电场阴极4052的作用下,能将更多的待处理物质收集起来,保证本电场发生单元的集尘效率更高,典型尾气颗粒pm0.23集尘效率为99.99%。
本实施例中进气电场装置或尾气电场装置包括由多个上述电场发生单元构成的电场级,所述电场级有多个,以利用多个集尘单元有效提高本电场装置的集尘效率。同一电场级中,各除尘电场阳极为相同极性,各除尘电场阴极为相同极性。
多个电场级中各电场级之间串联,串联电场级通过连接壳体连接,相邻两级的电场级的 距离大于极间距的1.4倍。如图24所示,所述电场级为两级即第一级电场4053和第二级电场4054,第一级电场4053和第二级电场4054通过连接壳体4055串联连接。
本实施例中上述待处理物质可以是呈颗粒状的粉尘,也可以是其它需处理的杂质,如气溶胶、水雾、油雾等。
本实施例中上述气体可以是欲进入发动机的气体,或发动机排出的气体。
实施例20
本实施例中电场发生单元可应用于进气电场装置,也可应用于尾气电场装置,如图21所示,包括用于发生电场的除尘电场阳极4051和除尘电场阴极4052,所述除尘电场阳极4051和除尘电场阴极4052分别与电源的两个电极电性连接,所述电源为直流电源,所述除尘电场阳极4051和除尘电场阴极4052分别与直流电源的阳极和阴极电性连接。本实施例中除尘电场阳极4051具有正电势,除尘电场阴极4052具有负电势。
本实施例中直流电源具体可为直流高压电源。上述除尘电场阳极4051和除尘电场阴极4052之间形成放电电场,该放电电场是一种静电场。
本实施例中除尘电场阳极4051呈中空的正六边形管状,除尘电场阴极4052呈棒状,除尘电场阴极4052穿设在除尘电场阳极4051中,除尘电场阳极4051的集尘面积与除尘电场阴极4052的放电面积的比为1680:1,所述除尘电场阳极4051和除尘电场阴极4052的极间距为139.9mm,除尘电场阳极4051长度为180mm,除尘电场阴极4052长度为180mm,所述除尘电场阳极4051包括流体通道,所述流体通道包括进口端与出口端,所述除尘电场阴极4052置于所述流体通道中,所述除尘电场阴极4052沿集尘极流体通道的方向延伸,除尘电场阳极4051的进口端与除尘电场阴极4052的近进口端齐平,除尘电场阳极4051的出口端与除尘电场阴极4052的近出口端齐平,进而在除尘电场阳极4051和除尘电场阴极4052的作用下,能将更多的待处理物质收集起来,保证本电场装置的集尘效率更高,典型尾气颗粒pm0.23集尘效率为99.99%。
本实施例中进气电场装置或尾气电场装置包括由多个上述电场发生单元构成的电场级,所述电场级有多个,以利用多个集尘单元有效提高本电场装置的集尘效率。同一电场级中,各除尘电场阳极为相同极性,各除尘电场阴极为相同极性。
本实施例中上述待处理物质可以是呈颗粒状的粉尘,也可以是其它需处理的杂质,如气溶胶、水雾、油雾等。
本实施例中上述气体可以是欲进入发动机的气体,或发动机排出的气体。
实施例21
本实施例中电场发生单元可应用于进气电场装置,也可应用于尾气电场装置,如图21所示,包括用于发生电场的除尘电场阳极4051和除尘电场阴极4052,所述除尘电场阳极4051和除尘电场阴极4052分别与电源的两个电极电性连接,所述电源为直流电源,所述除尘电场阳极4051和除尘电场阴极4052分别与直流电源的阳极和阴极电性连接。本实施例中除尘电场阳极4051具有正电势,除尘电场阴极4052具有负电势。
本实施例中直流电源具体可为直流高压电源。上述除尘电场阳极4051和除尘电场阴极4052之间形成放电电场,该放电电场是一种静电场。
本实施例中除尘电场阳极4051呈中空的正六边形管状,除尘电场阴极4052呈棒状,除尘电场阴极4052穿设在除尘电场阳极4051中,除尘电场阳极4051的集尘面积与除尘电场阴极4052的放电面积的比为1.667:1,所述除尘电场阳极4051和除尘电场阴极4052的极间距为2.4mm。除尘电场阳极4051长度为30mm,除尘电场阴极4052长度为30mm,所述除尘电场阳极4051包括流体通道,所述流体通道包括进口端与出口端,所述除尘电场阴极4052置于所述流体通道中,所述除尘电场阴极4052沿集尘极流体通道的方向延伸,除尘电场阳极4051的进口端与除尘电场阴极4052的近进口端齐平,除尘电场阳极4051的出口端与除尘电场阴极4052的近出口端齐平,进而在除尘电场阳极4051和除尘电场阴极4052的作用下,能将更多的待处理物质收集起来,保证本电场装置的集尘效率更高,典型尾气颗粒pm0.23集尘效率为99.99%。
本实施例中除尘电场阳极4051及除尘电场阴极4052构成集尘单元,且该集尘单元有多个,以利用多个集尘单元有效提高本电场装置的集尘效率。
本实施例中上述待处理物质可以是呈颗粒状的粉尘,也可以是其它需处理的杂质,如气溶胶、水雾、油雾等。
本实施例中上述气体可以是欲进入发动机的气体,或发动机排出的气体。
实施例22
本实施例中发动机进气系统,包括上述实施例19、实施例20或实施例21中的电场装置。欲进入发动机的气体需先流经该电场装置,以利用该电场装置有效地将气体中的粉尘等待处理物质清除掉;随后,经处理后的气体再进入发动机,以保证进入发动机的气体更加干净,所含粉尘等杂质较少;进而保证发动机的工作效率更高,且发动机排放气体中所含污染物更少。该发动机进气系统也称作进气装置。
实施例23
本实施例中发动机排气系统,包括上述实施例19、实施例20或实施例21中的电场装置。由发动机排出的气体需先流经该电场装置,以利用该电场装置有效地将气体中的粉尘等污染物清除掉;随后,经处理后的气体再排放至大气,以降低发动机尾气对大气造成的影响。该发动机排气系统也称作尾气处理装置。
实施例24
本实施例中电场发生单元可应用于进气电场装置,也可应用于尾气电场装置,如图21所示,包括用于发生电场的除尘电场阳极4051和除尘电场阴极4052,所述除尘电场阳极4051和除尘电场阴极4052分别与电源的两个电极电性连接,所述电源为直流电源,所述除尘电场阳极4051和除尘电场阴极4052分别与直流电源的阳极和阴极电性连接。本实施例中除尘电场阳极4051具有正电势,除尘电场阴极4052具有负电势。
本实施例中直流电源具体可为直流高压电源。上述除尘电场阳极4051和除尘电场阴极4052之间形成放电电场,该放电电场是一种静电场。
本实施例中除尘电场阳极4051呈中空的正六边形管状,除尘电场阴极4052呈棒状,除尘电场阴极4052穿设在除尘电场阳极4051中,除尘电场阳极4051长度为5cm,除尘电场阴极4052长度为5cm,所述除尘电场阳极4051包括流体通道,所述流体通道包括进口端与出口端,所述除尘电场阴极4052置于所述流体通道中,所述除尘电场阴极4052沿集尘极流体通道的方向延伸,除尘电场阳极4051的进口端与除尘电场阴极4052的近进口端齐平,除尘电场阳极4051的出口端与除尘电场阴极4052的近出口端齐平,所述除尘电场阳极4051和除尘电场阴极4052的极间距为9.9mm,进而在除尘电场阳极4051和除尘电场阴极4052的作用下,使得其耐高温冲击,而且能将更多的待处理物质收集起来,保证本电场发生单元的集尘效率更高。电场温度为200℃对应的集尘效率为99.9%;电场温度为400℃对应的集尘效率为90%;电场温度为500℃对应的集尘效率为50%。
本实施例中进气电场装置或尾气电场装置包括由多个上述电场发生单元构成的电场级,所述电场级有多个,以利用多个集尘单元有效提高本电场装置的集尘效率。同一电场级中,各除尘电场阳极为相同极性,各除尘电场阴极为相同极性。
本实施例中上述待处理物质可以是呈颗粒状的粉尘。
本实施例中上述气体可以是欲进入发动机的气体,或发动机排出的气体。
实施例25
本实施例中电场发生单元可应用于进气电场装置,也可应用于尾气电场装置,如图21所示,包括用于发生电场的除尘电场阳极4051和除尘电场阴极4052,所述除尘电场阳极4051和除尘电场阴极4052分别与电源的两个电极电性连接,所述电源为直流电源,所述除尘电场阳极4051和除尘电场阴极4052分别与直流电源的阳极和阴极电性连接。本实施例中除尘电场阳极4051具有正电势,除尘电场阴极4052具有负电势。
本实施例中直流电源具体可为直流高压电源。上述除尘电场阳极4051和除尘电场阴极4052之间形成放电电场,该放电电场是一种静电场。
本实施例中除尘电场阳极4051呈中空的正六边形管状,除尘电场阴极4052呈棒状,除尘电场阴极4052穿设在除尘电场阳极4051中,除尘电场阳极4051长度为9cm,除尘电场阴极4052长度为9cm,所述除尘电场阳极4051包括流体通道,所述流体通道包括进口端与出口端,所述除尘电场阴极4052置于所述流体通道中,所述除尘电场阴极4052沿集尘极流体通道的方向延伸,除尘电场阳极4051的进口端与除尘电场阴极4052的近进口端齐平,除尘电场阳极4051的出口端与除尘电场阴极4052的近出口端齐平,所述除尘电场阳极4051和除尘电场阴极4052的极间距为139.9mm,进而在除尘电场阳极4051和除尘电场阴极4052的作用下,使得其耐高温冲击,而且能将更多的待处理物质收集起来,保证本电场发生单元的集尘效率更高。电场温度为200℃对应的集尘效率为99.9%;电场温度为400℃对应的集尘效率为90%;电场温度为500℃对应的集尘效率为50%。
本实施例中进气电场装置或尾气电场装置包括由多个上述电场发生单元构成的电场级,所述电场级有多个,以利用多个集尘单元有效提高本电场装置的集尘效率。同一电场级中,各存储电场阳极为相同极性,各除尘电场阴极为相同极性。
本实施例中上述待处理物质可以是呈颗粒状的粉尘。
本实施例中上述气体可以是欲进入发动机的气体,或发动机排出的气体。
实施例26
本实施例中电场发生单元可应用于进气电场装置,也可应用于尾气电场装置,如图21所示,包括用于发生电场的除尘电场阳极4051和除尘电场阴极4052,所述除尘电场阳极4051和除尘电场阴极4052分别与电源的两个电极电性连接,所述电源为直流电源,所述除尘电场阳极4051和除尘电场阴极4052分别与直流电源的阳极和阴极电性连接。本实施例中除尘电场阳极4051具有正电势,除尘电场阴极4052具有负电势。
本实施例中直流电源具体可为直流高压电源。上述除尘电场阳极4051和除尘电场阴极4052之间形成放电电场,该放电电场是一种静电场。
本实施例中除尘电场阳极4051呈中空的正六边形管状,除尘电场阴极4052呈棒状,除尘电场阴极4052穿设在除尘电场阳极4051中,除尘电场阳极4051长度为1cm,除尘电场阴极4052长度为1cm,所述除尘电场阳极4051包括流体通道,所述流体通道包括进口端与出口端,所述除尘电场阴极4052置于所述流体通道中,所述除尘电场阴极4052沿集尘极流体通道的方向延伸,除尘电场阳极4051的进口端与除尘电场阴极4052的近进口端齐平,除尘电场阳极4051的出口端与除尘电场阴极4052的近出口端齐平,所述除尘电场阳极4051和除尘电场阴极4052的极间距为2.4mm,进而在除尘电场阳极4051和除尘电场阴极4052的作用下,使得其耐高温冲击,而且能将更多的待处理物质收集起来,保证本电场发生单元的集尘效率更高。电场温度为200℃对应的集尘效率为99.9%;电场温度为400℃对应的集尘效率为90%;电场温度为500℃对应的集尘效率为50%。
本实施例中进气电场装置或尾气电场装置包括由多个上述电场发生单元构成的电场级,所述电场级有多个,以利用多个集尘单元有效提高本电场装置的集尘效率。同一电场级中,各除尘电场阳极为相同极性,各除尘电场阴极为相同极性。
多个电场级中各电场级之间串联,串联电场级通过连接壳体连接,相邻两级的电场级的距离大于极间距的1.4倍。所述电场级为两级即第一级电场和第二级电场,第一级电场和第二级电场通过连接壳体串联连接。
本实施例中上述待处理物质可以是呈颗粒状的粉尘。
本实施例中上述气体可以是欲进入发动机的气体,或发动机排出的气体。
实施例27
本实施例中电场发生单元可应用于进气电场装置,也可应用于尾气电场装置,如图21所示,包括用于发生电场的除尘电场阳极4051和除尘电场阴极4052,所述除尘电场阳极4051和除尘电场阴极4052分别与电源的两个电极电性连接,所述电源为直流电源,所述除尘电场阳极4051和除尘电场阴极4052分别与直流电源的阳极和阴极电性连接。本实施例中除尘电场阳极4051具有正电势,除尘电场阴极4052具有负电势。
本实施例中直流电源具体可为直流高压电源。上述除尘电场阳极4051和除尘电场阴极4052之间形成放电电场,该放电电场是一种静电场。
如图21和图22所示,本实施例中除尘电场阳极4051呈中空的正六边形管状,除尘电场阴极4052呈棒状,除尘电场阴极4052穿设在除尘电场阳极4051中,除尘电场阳极4051长度为3cm,除尘电场阴极4052长度为2cm,所述除尘电场阳极4051包括流体通道,所述流体通道包括进口端与出口端,所述除尘电场阴极4052置于所述流体通道中,所述除尘电场阴 极4052沿集尘极流体通道的方向延伸,除尘电场阳极4051的进口端与除尘电场阴极4052的近进口端齐平,除尘电场阳极4051的出口端与除尘电场阴极4052的近出口端之间具有夹角α,且α=90°,所述除尘电场阳极4051和除尘电场阴极4052的极间距为20mm,进而在除尘电场阳极4051和除尘电场阴极4052的作用下,使得其耐高温冲击,而且能将更多的待处理物质收集起来,保证本电场发生单元的集尘效率更高。电场温度为200℃对应的集尘效率为99.9%;电场温度为400℃对应的集尘效率为90%;电场温度为500℃对应的集尘效率为50%。
本实施例中进气电场装置或尾气电场装置包括由多个上述电场发生单元构成的电场级,所述电场级有多个,以利用多个集尘单元有效提高本电场装置的集尘效率。同一电场级中,各集尘极为相同极性,各放电极为相同极性。
多个电场级中各电场级之间串联,串联电场级通过连接壳体连接,相邻两级的电场级的距离大于极间距的1.4倍。如图24所示,所述电场级为两级即第一级电场和第二级电场,第一级电场和第二级电场通过连接壳体串联连接。
本实施例中上述待处理物质可以是呈颗粒状的粉尘。
本实施例中上述气体可以是欲进入发动机的气体,或发动机排出的气体。
实施例28
本实施例中发动机进气系统,包括上述实施例24、实施例25、实施例26或实施例27中的电场装置。欲进入发动机的气体需先流经该电场装置,以利用该电场装置有效地将气体中的粉尘等待处理物质清除掉;随后,经处理后的气体再进入发动机,以保证进入发动机的气体更加干净,所含粉尘等杂质较少;进而保证发动机的工作效率更高,且发动机排放气体中所含污染物更少。该发动机进气系统也称作进气装置。
实施例29
本实施例中发动机排气系统,包括上述实施例24、实施例25、实施例26或实施例27中的电场装置。由发动机排出的气体需先流经该电场装置,以利用该电场装置有效地将气体中的粉尘等污染物清除掉;随后,经处理后的气体再排放至大气,以降低发动机尾气对大气造成的影响。该发动机排气系统也称作尾气处理装置。
实施例30
本实施例中电场装置可应用于进气系统,也可应用于尾气系统,包括除尘电场阴极5081和除尘电场阳极5082分别与直流电源的阴极和阳极电性连接,辅助电极5083与直流电源的 阳极电性连接。本实施例中除尘电场阴极5081具有负电势,除尘电场阳极5082和辅助电极5083均具有正电势。
同时,如图25所示,本实施例中辅助电极5083与除尘电场阳极5082固接。在除尘电场阳极5082与直流电源的阳极电性连接后,也实现了辅助电极5083与直流电源的阳极电性连接,且辅助电极5083与除尘电场阳极5082具有相同的正电势。
如图25所示,本实施例中辅助电极5083可沿前后方向延伸,即辅助电极5083的长度方向可与除尘电场阳极5082的长度方向相同。
如图25所示,本实施例中除尘电场阳极5082呈管状,除尘电场阴极5081呈棒状,除尘电场阴极5081穿设在除尘电场阳极5082中。同时本实施例中上述辅助电极5083也呈管状,辅助电极5083与除尘电场阳极5082构成阳极管5084。阳极管5084的前端与除尘电场阴极5081齐平,阳极管5084的后端向后超出了除尘电场阴极5081的后端,该阳极管5084相比于除尘电场阴极5081向后超出的部分为上述辅助电极5083。即本实施例中除尘电场阳极5082和除尘电场阴极5081的长度相同,除尘电场阳极5082和除尘电场阴极5081在前后方向上位置相对;辅助电极5083位于除尘电场阳极5082和除尘电场阴极5081的后方。这样,辅助电极5083与除尘电场阴极5081之间形成辅助电场,该辅助电场给除尘电场阳极5082和除尘电场阴极5081之间带负电荷的氧离子流施加向后的力,使得除尘电场阳极5082和除尘电场阴极5081间带负电荷的氧离子流具有向后的移动速度。当含有待处理物质的气体由前向后流入阳极管5084,带负电荷的氧离子在向除尘电场阳极5082且向后移动过程中将与待处理物质相结合,由于氧离子具有向后的移动速度,氧离子在与待处理物质相结合时,两者间不会产生较强的碰撞,从而避免因较强碰撞而造成较大的能量消耗,使得氧离子易于与待处理物质相结合,并使得气体中待处理物质的荷电效率更高,进而在除尘电场阳极5082及阳极管5084的作用下,能将更多的待处理物质收集起来,保证本电场装置的除尘效率更高。
另外,如图17所示,本实施例中阳极管5084的后端与除尘电场阴极5081的后端之间具有夹角α,且0°<α≤125°、或45°≤α≤125°、或60°≤α≤100°、或α=90°。
本实施例中除尘电场阳极5082、辅助电极5083、及除尘电场阴极5081构成除尘单元,且该除尘单元有多个,以利用多个除尘单元有效提高本电场装置的除尘效率。
本实施例中上述待处理物质可以是呈颗粒状的粉尘,也可以是其它需处理的杂质。
本实施例中上述气体可以是欲进入发动机的气体,或发动机排出的气体。
本实施例中直流电源具体可为直流高压电源。上述除尘电场阴极5081和除尘电场阳极5082之间形成放电电场,该放电电场是一种静电场。在无上述辅助电极5083的情况下,除尘 电场阴极5081和除尘电场阳极5082之间电场中离子流沿垂直于电极方向,且在两电极间折返流动,并导致离子在电极间来回折返消耗。为此,本实施例利用辅助电极5083使电极相对位置错开,形成除尘电场阳极5082和除尘电场阴极5081间相对不平衡,这个不平衡会使电场中离子流发生偏转。本电场装置利用辅助电极5083形成能使离子流具有方向性的电场。本实施例中上述电场装置也称作一种有加速方向电场装置。本电场装置对顺离子流方向进入电场的颗粒物的收集率比对逆离子流方向进入电场的颗粒物的收集率提高近一倍,从而提高电场积尘效率,减少电场电耗。另外,现有技术中集尘电场的除尘效率较低的主要原因也是粉尘进入电场方向与电场内离子流方向相反或垂直交叉,从而导致粉尘与离子流相互冲撞剧烈并产生较大能量消耗,同时也影响荷电效率,进而使现有技术中电场集尘效率下降,且能耗增加。
本实施例中电场装置在用于收集气体中的粉尘时,气体及粉尘顺离子流方向进入电场,粉尘荷电充分,电场消耗小;单极电场集尘效率会达到99.99%。当气体及粉尘逆离子流方向进入电场,粉尘荷电不充分,电场电耗也会增加,集尘效率会在40%-75%。另外,本实施例中电场装置形成的离子流有利于无动力风扇流体输送、增氧、热量交换等。
实施例31
本实施例中电场装置可应用于进气系统,也可应用于尾气系统,包括除尘电场阴极和除尘电场阳极分别与直流电源的阴极和阳极电性连接,辅助电极与直流电源的阴极电性连接。本实施例中辅助电极和除尘电场阴极均具有负电势,除尘电场阳极具有正电势。
本实施例中辅助电极可与除尘电场阴极固接。这样,在实现除尘电场阴极与直流电源的阴极电性连接后,也实现了辅助电极与直流电源的阴极电性连接。同时,本实施例中辅助电极沿前后方向延伸。
本实施例中除尘电场阳极呈管状,除尘电场阴极呈棒状,除尘电场阴极穿设在除尘电场阳极中。同时本实施例中上述辅助电极也棒状,且辅助电极和除尘电场阴极构成阴极棒。该阴极棒的前端向前超出除尘电场阳极的前端,该阴极棒与除尘电场阳极相比向前超出的部分为上述辅助电极。即本实施例中除尘电场阳极和除尘电场阴极的长度相同,除尘电场阳极和除尘电场阴极在前后方向上位置相对;辅助电极位于除尘电场阳极和除尘电场阴极的前方。这样,辅助电极与除尘电场阳极之间形成辅助电场,该辅助电场给除尘电场阳极和除尘电场阴极之间带负电荷的氧离子流施加向后的力,使得除尘电场阳极和除尘电场阴极间带负电荷的氧离子流具有向后的移动速度。当含有待处理物质的气体由前向后流入管状的除尘电场阳极,带负电荷的氧离子在向除尘电场阳极且向后移动过程中将与待处理物质相结合,由于氧 离子具有向后的移动速度,氧离子在与待处理物质相结合时,两者间不会产生较强的碰撞,从而避免因较强碰撞而造成较大的能量消耗,使得氧离子易于与待处理物质相结合,并使得气体中待处理物质的荷电效率更高,进而在除尘电场阳极作用下,能将更多的待处理物质收集起来,保证本电场装置的除尘效率更高。
本实施例中除尘电场阳极、辅助电极、及除尘电场阴极构成除尘单元,且该除尘单元有多个,以利用多个除尘单元有效提高本电场装置的除尘效率。
本实施例中上述待处理物质可以是呈颗粒状的粉尘,也可以是其它需处理的杂质。
实施例32
如图26所示,本实施例中电场装置可应用于进气系统,也可应用于尾气系统,辅助电极5083沿左右方向延伸。本实施例中辅助电极5083的长度方向与除尘电场阳极5082和除尘电场阴极5081的长度方向不同。且辅助电极5083具体可与除尘电场阳极5082相垂直。
本实施例中除尘电场阴极5081和除尘电场阳极5082分别与直流电源的阴极和阳极电性连接,辅助电极5083与直流电源的阳极电性连接。本实施例中除尘电场阴极5081具有负电势,除尘电场阳极5082和辅助电极5083均具有正电势。
如图26所示,本实施例中除尘电场阴极5081和除尘电场阳极5082在前后方向上位置相对,辅助电极5083位于除尘电场阳极5082和除尘电场阴极5081的后方。这样,辅助电极5083与除尘电场阴极5081之间形成辅助电场,该辅助电场给除尘电场阳极5082和除尘电场阴极5081之间带负电荷的氧离子流施加向后的力,使得除尘电场阳极5082和除尘电场阴极5081间带负电荷的氧离子流具有向后的移动速度。当含有待处理物质的气体由前向后流入除尘电场阳极5082和除尘电场阴极5081之间的电场,带负电荷的氧离子在向除尘电场阳极5082且向后移动过程中将与待处理物质相结合,由于氧离子具有向后的移动速度,氧离子在与待处理物质相结合时,两者间不会产生较强的碰撞,从而避免因较强碰撞而造成较大的能量消耗,使得氧离子易于与待处理物质相结合,并使得气体中待处理物质的荷电效率更高,进而在除尘电场阳极5082的作用下,能将更多的待处理物质收集起来,保证本电场装置的除尘效率更高。
实施例33
如图27所示,本实施例中电场装置可应用于进气系统,也可应用于尾气系统,辅助电极5083沿左右方向延伸。本实施例中辅助电极5083的长度方向与除尘电场阳极5082和除尘电场阴极5081的长度方向不同。且辅助电极5083具体可与除尘电场阴极5081相垂直。
本实施例中除尘电场阴极5081和除尘电场阳极5082分别与直流电源的阴极和阳极电性 连接,辅助电极5083与直流电源的阴极电性连接。本实施例中除尘电场阴极5081和辅助电极5083均具有负电势,除尘电场阳极5082具有正电势。
如图27所示,本实施例中除尘电场阴极5081和除尘电场阳极5082在前后方向上位置相对,辅助电极5083位于除尘电场阳极5082和除尘电场阴极5081的前方。这样,辅助电极5083与除尘电场阳极5082之间形成辅助电场,该辅助电场给除尘电场阳极5082和除尘电场阴极5081之间带负电荷的氧离子流施加向后的力,使得除尘电场阳极5082和除尘电场阴极5081间带负电荷的氧离子流具有向后的移动速度。当含有待处理物质的气体由前向后流入除尘电场阳极5082和除尘电场阴极5081之间的电场,带负电荷的氧离子在向除尘电场阳极5082且向后移动过程中将与待处理物质相结合,由于氧离子具有向后的移动速度,氧离子在与待处理物质相结合时,两者间不会产生较强的碰撞,从而避免因较强碰撞而造成较大的能量消耗,使得氧离子易于与待处理物质相结合,并使得气体中待处理物质的荷电效率更高,进而在除尘电场阳极5082的作用下,能将更多的待处理物质收集起来,保证本电场装置的除尘效率更高。
实施例34
本实施例中发动机进气装置,包括上述实施例30、31、32、或33中的电场装置。欲进入发动机的气体需先流经该电场装置,以利用该电场装置有效地将气体中的粉尘等待处理物质清除掉;随后,经处理后的气体再进入发动机,以保证进入发动机的气体更加干净,所含粉尘等杂质较少;进而保证发动机的工作效率更高,且发动机排放气体中所含污染物更少。本实施例中发动机进气装置也简称进气装置,电场装置也称作进气电场装置,除尘电场阴极5081也称作进气除尘电场阴极,除尘电场阳极5082也称作进气除尘电场阳极。
实施例35
本实施例中发动机排气装置,包括上述实施例30、31、32、或33中的电场装置。由发动机排出的气体需先流经该电场装置,以利用该电场装置有效地将气体中的粉尘等污染物清除掉;随后,经处理后的气体再排放至大气,以降低发动机尾气对大气造成的影响。本实施例中发动机排气装置也称作尾气处理装置,尾气除尘机构也称作尾气电场装置,除尘电场阴极5081也称作尾气除尘电场阴极,除尘电场阳极5082也称作尾气除尘电场阳极。
实施例36(补氧装置)
本实施例提供一种尾气电场装置,包括尾气除尘电场阴极和尾气除尘电场阳极。尾气除尘电场阴极和尾气除尘电场阳极分别与直流电源的两个电极电性连接,尾气除尘电场阴极和尾气除尘电场阳极之间具有尾气电离除尘电场,尾气电场装置还包括补氧装置。补氧装置用 于在所述尾气电离除尘电场之前向尾气中添加包括氧气的气体。补氧装置可通过单纯增氧、通入外界空气、通入压缩空气和/或通入臭氧的方式添加氧气。本实施例中尾气电场装置,利用补氧装置向尾气中补充氧气,以提高气体含氧量,从而当尾气流经尾气电离除尘电场时,使得气体中更多的粉尘荷电,进而在尾气除尘电场阳极的作用下将更多的荷电的粉尘收集起来,使得本尾气电场装置的除尘效率更高。
本实施例中至少根据尾气颗粒含量决定补氧量。
本实施例中尾气除尘电场阴极和尾气除尘电场阳极分别与直流电源的阴极和阳极电性连接,使得尾气除尘电场阳极具有正电势、尾气除尘电场阴极具有负电势。同时,本实施例中直流电源具体可为高压直流电源。本实施例中尾气除尘电场阴极和尾气除尘电场阳极之间形成的电场具体可称作一种静电场。
本实施例中尾气电场装置适用于低氧环境中,该尾气电场装置也称作一种适用于低氧环境的电场装置。本实施例中补氧装置包括风机,以利用风机将外界的空气及氧气补入尾气中,让进入电场的尾气中氧的浓度得以提高,从而提高尾气中粉尘等颗粒物的荷电几率,进而提高电场及本尾气电场装置对氧浓度较低的尾气中粉尘等物质的收集效率。另外,风机向尾气中补入的空气也能作为冷却风,对尾气起到降温的作用。本实施例中风机将空气通入尾气中,并在尾气电场装置入口之前,对尾气起到降温的作用。通入的空气可以是尾气的50%至300%、或100%至180%、或120%至150%。
本实施例中尾气电离除尘电场及尾气电场装置具体可用于收集燃油发动机尾气或燃烧炉尾气中的粉尘等颗粒物,即上述气体具体可为燃油发动机尾气或燃烧炉尾气。本实施例利用补氧装置向尾气中补入新风或单纯增氧,以提高尾气的含氧量,就能提升尾气电离除尘电场收集尾气中颗粒物以及气溶胶态物质的效率。同时,还能对尾气起到降温的作用,从而更有利于电场收集尾气中的颗粒物。
本实施例也可通过补氧装置向尾气中通入压缩空气、或臭氧等方式实现尾气增氧;同时调整前级发动机或锅炉等设备的燃烧情况,使产生的尾气含氧量稳定,从而满足电场荷电及集尘需要。
本实施例中补氧装置具体可包括正压风机和管道。尾气除尘电场阴极和尾气除尘电场阳极构成电场组件,且上述尾气除尘电场阴极也称作一种电晕极。高压直流电源和电源线构成电源组件。本实施例利用补氧装置将空气中的氧气补充到尾气中,使粉尘充荷电,避免尾气因氧含量波动引发电场效率波动。同时,补氧也会提高电场臭氧含量,有利于提高电场对尾气中有机物进行净化、自洁、脱硝等处理的效率。
本实施例中尾气电场装置也称作一种除尘器。上述尾气除尘电场阴极和尾气除尘电场阳极之间具有除尘通道,该除尘通道中形成上述尾气电离除尘电场。如图28和图29所示,本尾气电场装置还包括与除尘通道相通的叶轮涵道3091、与叶轮涵道3091相通的尾气通道3092、及与叶轮涵道3091相通的增氧涵道3093。叶轮涵道3091中安装有叶轮3094,该叶轮3094构成上述风机,即上述补氧装置包括叶轮3094。增氧涵道3093位于尾气通道3092的外围,增氧涵道3093也称作外涵道。增氧涵道3093的一端设有空气进口30931,尾气通道3092的一端设有尾气进口30921,且该尾气进口30921与燃油发动机或燃烧炉的排气口相通。这样,发动机或燃烧炉等排放的尾气将通过尾气进口30921及尾气通道3092进入叶轮涵道3091,并推动叶轮涵道3091中的叶轮3094旋转,同时起到对尾气降温的作用,且叶轮3094旋转时将外界的空气由空气进口30931吸入增氧涵道3093及叶轮涵道3091,从而使空气混入尾气中,达到对尾气增氧降温的目的;补入氧气的尾气再经叶轮涵道3091流经除尘通道,进而利用电场对增氧后的尾气进行除尘,且使得除尘效率更高。本实施例中上述叶轮涵道3091及叶轮3094构成涡扇。
实施例37
如图30至图32所示,本实施例提供一种电凝装置,包括:
第一电极301,能将电子传导给含硝酸的水雾;当电子被传导给硝酸的水雾时,硝酸的水雾带电;
第二电极302,能给带电的水雾施加吸引力。
同时,如图30所示,本实施例中电凝装置还包括具有电凝进口3031和电凝出口3032的电凝壳体303,第一电极301和第二电极302均安装在电凝壳体303中。且第一电极301通过电凝绝缘件304与电凝壳体303的内壁固接,第二电极302直接与电凝壳体303固接。本实施例中电凝绝缘件304呈柱状,又称作绝缘柱。在另一种实施例中电凝绝缘件304还可以呈塔状等。本电凝绝缘件304主要是防污染防漏电。本实施例中第一电极301和第二电极302均呈网状,且两者均于电凝进口3031和电凝出口3032之间。第一电极301具有负电势,第二电极302具有正电势。同时,本实施例中电凝壳体303与第二电极302具有相同的电势,该电凝壳体303同样对带电的物质具有吸附作用。本实施例中电凝壳体中设有电凝流道3036,第一电极301和第二电极302均安装在电凝流道3036中,且第一电极301的截面面积与电凝流道3036的截面面积比为99%~10%、或90~10%、或80~20%、或70~30%、或60~40%、或50%。
本实施例中电凝装置还可以用于处理含有酸雾的工业尾气。当电凝装置用于处理含有酸 雾的工业尾气时,本实施例中电凝进口3031与排放工业尾气的口相连通。如图30所示,本实施例中电凝装置的工作原理如下:工业尾气由电凝进口3031流入电凝壳体303,并经电凝出口3032流出;在此过程中,工业尾气将流经第一电极301,当工业尾气中的酸雾与第一电极301接触时,或与第一电极301的距离达到一定值时,第一电极301将电子传递给酸雾,酸雾带电,第二电极302给带电的酸雾施加吸引力,酸雾向第二电极302移动,并附着在第二电极302上;由于酸雾具有易带且易失电特性,某个带电的雾滴在向第二电极302移动过程中又将失电,此时其它带电的雾滴又将快速将电子传递给该失电的雾滴,如此重复,雾滴处于持续带电状态,第二电极302就能持续给雾滴施加吸附力,并使得雾滴附着在第二电极302,从而实现对工业尾气中酸雾的去除,避免酸雾直接排放至大气中,并对大气造成污染。本实施例中上述第一电极301和第二电极302构成吸附单元。且在吸附单元仅有一个的情况下,本实施例中电凝装置能除去工业尾气中80%的酸雾,大大降低了酸雾的排放量,具有显著的环保效果。
如图32所示,本实施例中第一电极301上设有3个前连接部3011,3个前连接部3011分别通过3个电凝绝缘件304与电凝壳体303的内壁上的3个连接部固接,此种连接形式能有效增强第一电极301与电凝壳体303间的连接强度。本实施例中前连接部3011呈圆柱形,在其它实施例中前连接部3011还可以呈塔状等。本实施例中电凝绝缘件304呈圆柱状,在其它实施例中电凝绝缘件304还可以呈塔状等。本实施例中后连接部呈圆柱状,在其它实施例中电凝绝缘件304还可以呈塔状等。如图30所示,本实施例中电凝壳体303包括由电凝进口3031至电凝出口3032方向依次分布的第一壳体部3033、第二壳体部3034、及第三壳体部3035。电凝进口3031位于第一壳体部3033的一端,电凝出口3032位于第三壳体部3035的一端。第一壳体部3033的轮廓大小由电凝进口3031至电凝出口3032方向逐渐增大,第三壳体部3035的轮廓大小由电凝进口3031至电凝出口3032方向逐渐减小。本实施例中第二壳体部3034的截面呈矩形。本实施例中电凝壳体303采用上述结构设计,使尾气在电凝进口3031处达到一定的入口流速,更主要能使气流分布更加均匀,进而使尾气中的介质、如雾滴更容易在第一电极301的激发作用下带电。同时本电凝壳体303封装更加方便,减少材料用量,并节省空间,可以用管道连接,且还有利用于绝缘的考虑。任何可达到上述效果的电凝壳体303均可以接受。
本实施例中电凝进口3031和电凝出口3032均呈圆形,电凝进口3031也可称作进气口,电凝出口3032也可称作出气口。本实施例中电凝进口3031的直径为300mm~1000mm,具体为500mm。同时,本实施例中电凝进口3031的直径为300mm~1000mm,具体为500mm。
实施例38
如图33和图34所示,本实施例提供一种电凝装置,包括:
第一电极301,能将电子传导给含硝酸的水雾;当电子被传导给含硝酸的水雾时,含硝酸的水雾带电;
第二电极302,能给带电的水雾施加吸引力。
如图33和图34所示,本实施例中第一电极301有两个,两个第一电极301均呈网状且呈球笼状。本实施例中第二电极302有一个,该第二电极302呈网状且呈球笼状。第二电极302位于两个第一电极301之间。同时,如图33所示,本实施例中电凝装置还包括具有电凝进口3031和电凝出口3032的电凝壳体303,第一电极301和第二电极302均安装在电凝壳体303中。且第一电极301通过电凝绝缘件304与电凝壳体303的内壁固接,第二电极302直接与电凝壳体303固接。本实施例中电凝绝缘件304呈柱状,又称作绝缘柱。本实施例中第一电极301具有负电势,第二电极302具有正电势。同时,本实施例中电凝壳体303与第二电极302具有相同的电势,该电凝壳体303同样对带电的物质具有吸附作用。
本实施例中电凝装置还可用于处理含有酸雾的工业尾气。本实施例中电凝进口3031可与排放工业尾气的口相连通。如图33所示,本实施例中电凝装置的工作原理如下:工业尾气由电凝进口3031流入电凝壳体303,并经电凝出口3032流出;在此过程中,工业尾气将先流经其中一个第一电极301,当工业尾气中的酸雾与该第一电极301接触时,或与该第一电极301的距离达到一定值时,第一电极301将电子传递给酸雾,部分酸雾带电,第二电极302给带电的酸雾施加吸引力,酸雾向第二电极302移动,并附着在第二电极302上;另有一部分酸雾未被吸附在第二电极302上,该部分酸雾继续向电凝出口3032方向流动,当该部分酸雾与另一个第一电极301接触时,或与另一个第一电极301的距离达到一定值时,该部分酸雾将带电,电凝壳体303给该部分带电的酸雾施加吸附力,使得该部分带电的酸雾附着在电凝壳体303的内壁上,从而大大减少了工业尾气中酸雾的排放量,且本实施例中处理装置能去除工业尾气中90%的酸雾,去除酸雾的效果非常显著。另外,本实施例中电凝进口3031和电凝出口3032均呈圆形,电凝进口3031也可称作进气口,电凝出口3032也可称作出气口。
实施例39
如图35所示,本实施例提供一种电凝装置,包括:
第一电极301,能将电子传导给水雾;当电子被传导给水雾时,水雾带电;
第二电极302,能给带电的水雾施加吸引力。
本实施例中第一电极301呈针状,且第一电极301带有负电势。同时,本实施例中第二 电极302呈面状,且第二电极302带有正电势,该第二电极302也称作收集极。本实施例中第二电极302具体呈平面状,且第一电极301垂直于第二电极302。本实施例中第一电极301和第二电极302之间形成线面电场。
实施例40
如图36所示,本实施例提供一种电凝装置,包括:
第一电极301,能将电子传导给水雾;当电子被传导给水雾时,水雾带电;
第二电极302,能给带电的水雾施加吸引力。
本实施例中第一电极301呈线状,且第一电极301带有负电势。同时,本实施例中第二电极302呈面状,且第二电极302带有正电势,该第二电极302也称作收集极。本实施例中第二电极302具体呈平面状,且第一电极301平行于第二电极302。本实施例中第一电极301和第二电极302之间形成线面电场。
实施例41
如图37所示,本实施例提供一种电凝装置,包括:
第一电极301,能将电子传导给水雾;当电子被传导给水雾时,水雾带电;
第二电极302,能给带电的水雾施加吸引力。
本实施例中第一电极301呈网状,且第一电极301带有负电势。同时,本实施例中第二电极302呈面状,且第二电极302带有正电势,该第二电极302也称作收集极。本实施例中第二电极302具体呈平面状,且第一电极301平行于第二电极302。本实施例中第一电极301和第二电极302之间形成网面电场。另外,本实施例中第一电极301由金属丝制成的网状结构,该第一电极301由金属丝网构成。本实施例中第二电极302的面积大于第一电极301的面积。
实施例42
如图38所示,本实施例提供一种电凝装置,包括:
第一电极301,能将电子传导给水雾;当电子被传导给水雾时,水雾带电;
第二电极302,能给带电的水雾施加吸引力。
本实施例中第一电极301呈点状,且第一电极301带有负电势。同时,本实施例中第二电极302呈桶状,且第二电极302带有正电势,该第二电极302也称作收集极。本实施例中第一电极301通过金属线或金属针进行固定。且本实施例中第一电极301位于桶状的第二电极302的几何对称中心处。本实施例中第一电极301和第二电极302之间形成点桶电场。
实施例43
如图39所示,本实施例提供一种电凝装置,包括:
第一电极301,能将电子传导给水雾;当电子被传导给水雾时,水雾带电;
第二电极302,能给带电的水雾施加吸引力。
本实施例中第一电极301呈线状,且第一电极301带有负电势。同时,本实施例中第二电极302呈桶状,且第二电极302带有正电势,该第二电极302也称作收集极。本实施例中第一电极301通过金属线或金属针进行固定。且本实施例中第一电极301位于桶状的第二电极302的几何对称轴上。本实施例中第一电极301和第二电极302之间形成线桶电场。
实施例44
如图40所示,本实施例提供一种电凝装置,包括:
第一电极301,能将电子传导给水雾;当电子被传导给水雾时,水雾带电;
第二电极302,能给带电的水雾施加吸引力。
本实施例中第一电极301呈网状,且第一电极301带有负电势。同时,本实施例中第二电极302呈桶状,且第二电极302带有正电势,该第二电极302也称作收集极。本实施例中第一电极301通过金属线或金属针进行固定。且本实施例中第一电极301位于桶状的第二电极302的几何对称中心处。本实施例中第一电极301和第二电极302之间形成网桶电凝电场。
实施例45
如图41所示,本实施例提供一种电凝装置,包括:
第一电极301,能将电子传导给水雾;当电子被传导给水雾时,水雾带电;
第二电极302,能给带电的水雾施加吸引力。
本实施例中第二电极302有两个,且第一电极301位于两个第二电极302之间,第一电极301沿左右方向方向上的长度大于第二电极302沿左右方向上的长度,有第一电极301的左端位于第二电极302的左方。第一电极301的左端与第二电极302的左端形成沿斜向延伸的电力线。本实施例中第一电极301与第二电极302之间形成非对称电凝电场。在使用时,水雾(低比电阻物质)、如雾滴由左进入两个第二电极302之间。部分雾滴带电后,由第一电极301的左端沿斜向向第二电极302的左端移动,从而对雾滴形成拉动作用。
实施例46
如图42所示,本实施例提供一种电凝装置,包括:
第一电极,能将电子传导给水雾;当电子被传导给水雾时,水雾带电;
第二电极,能给带电的水雾施加吸引力。
本实施例中第一电极和第二电极构成吸附单元3010。本实施例中吸附单元3010有多个, 且全部吸附单元3010沿水平方向分布。本实施例中全部吸附单元3010具体沿左右方向分布。
实施例47
如图43所示,本实施例提供一种电凝装置,包括:
第一电极,能将电子传导给水雾;当电子被传导给水雾时,水雾带电;
第二电极,能给带电的水雾施加吸引力。
本实施例中第一电极和第二电极构成吸附单元3010。本实施例中吸附单元3010有多个,且全部吸附单元3010沿上下方向分布。
实施例48
如图44所示,本实施例提供一种电凝装置,包括:
第一电极,能将电子传导给水雾;当电子被传导给水雾时,水雾带电;
第二电极,能给带电的水雾施加吸引力。
本实施例中第一电极和第二电极构成吸附单元3010。本实施例中吸附单元3010有多个,且全部吸附单元3010沿斜向分布。
实施例49
如图45所示,本实施例提供一种电凝装置,包括:
第一电极,能将电子传导给水雾;当电子被传导给水雾时,水雾带电;
第二电极,能给带电的水雾施加吸引力。
本实施例中第一电极和第二电极构成吸附单元3010。本实施例中吸附单元3010有多个,且全部吸附单元3010沿螺旋方向分布。
实施例50
如图46所示,本实施例提供一种电凝装置,包括:
第一电极,能将电子传导给水雾;当电子被传导给水雾时,水雾带电;
第二电极,能给带电的水雾施加吸引力。
本实施例中第一电极和第二电极构成吸附单元3010。本实施例中吸附单元3010有多个,且全部吸附单元3010沿左右方向、上下方向和斜向分布。
实施例51
如图47所示,本实施例提供一种发动机排放处理系统,包括上述电凝装置30100和文氏板3051。本实施例中电凝装置30100与文氏板3051组合使用。
实施例52
如图48所示,本实施例提供一种发动机排放处理系统,包括上述电凝装置30100、文氏 板3051、NO
x氧化催化装置3052、及臭氧消解装置3053。本实施例中电凝装置30100和文氏板3051位于NO
x氧化催化装置3052和臭氧消解装置3053之间。且NO
x氧化催化装置3052中具有NO
x氧化催化剂,臭氧消解装置3053中具有臭氧消解催化剂。
实施例53
如图49所示,本实施例提供一种发动机排放处理系统,包括上述电凝装置30100、电晕装置3054和文氏板3051,其中电凝装置30100位于电晕装置3054和文氏板3051之间。
实施例54
如图50所示,本实施例提供一种发动机排放处理系统,包括上述电凝装置30100、加热装置3055和臭氧消解装置3053,其中加热装置3055位于电凝装置30100和臭氧消解装置3053之间。
实施例55
如图51所示,本实施例提供一种发动机排放处理系统,包括上述电凝装置30100、离心装置3056和文氏板3051,其中电凝装置30100位于离心装置3056和文氏板3051之间。
实施例56
如图52所示,本实施例提供一种发动机排放处理系统,包括上述电凝装置30100、电晕装置3054、文氏板3051、及分子筛3057,其中文氏板3051和电凝装置30100位于电晕装置3054和分子筛3057之间。
实施例57
如图53所示,本实施例提供一种发动机排放处理系统,包括上述电凝装置30100、电晕装置3054和电磁装置3058,其中电凝装置30100位于电晕装置3054和电磁装置3058之间。
实施例58
如图54所示,本实施例提供一种发动机排放处理系统,包括上述电凝装置30100、电晕装置3054和辐照装置3059,其中辐照装置3059位于电晕装置3054和电凝装置30100之间。
实施例59
如图55所示,本实施例提供一种发动机排放处理系统,包括上述电凝装置30100、电晕装置3054和湿电除尘装置3061,其中湿电除尘装置3061位于电晕装置3054和电凝装置30100之间。
实施例60
如图56所示,本实施例提供一种电场装置,包括依次相通的电场装置入口3085、流道3086、电场流道3087、及电场装置出口3088,流道3086中安装有前置电极3083,前置电极 3083的截面面积与流道3086的截面面积比为99%~10%,电场装置还包括除尘电场阴极3081和除尘电场阳极3082,电场流道3087位于除尘电场阴极3081和除尘电场阳极3082之间。本实施例中电场装置的工作原理为:含污染物的气体通过电场装置入口3085进入流道3086,安装在流道3086中的前置电极3083将电子传导给部分污染物,部分污染物带电,当污染物由流道3086进入电场流道3087后,除尘电场阳极3082给已带电的污染物施加吸引力,带电的污染物向除尘电场阳极3082移动,直至该部分污染物附着在除尘电场阳极3082上,同时,电场流道3087中除尘电场阴极3081和除尘电场阳极3082之间形成电离除尘电场,该电离除尘电场将使另一部分未带电的污染物带电,这样另一部分污染物在带电后同样会受到除尘电场阳极3082施加的吸引力,并最终附着在除尘电场阳极3082上,从而利用上述电场装置使污染物带电效率更高,带电更充分,进而保证除尘电场阳极3082能收集更多的污染物,并保证本电场装置对污染物的收集效率更高。
前置电极3083的截面面积是指前置电极3083沿截面上实体部分的面积之和。另外,前置电极3083的截面面积与流道3086的截面面积比可以为99%~10%、或90~10%、或80~20%、或70~30%、或60~40%、或50%。
如图56所示,本实施例中前置电极3083和除尘电场阴极3081均与直流电源的阴极电性连接,除尘电场阳极3082与直流电源的阳极电性连接。本实施例中前置电极3083和除尘电场阴极3081均具有负电势,除尘电场阳极3082具有正电势。
如图56所示,本实施例中前置电极3083具体可呈网状。这样,当气体流经流道3086时,利用前置电极3083呈网状的结构特点,便于气体及污染物流过前置电极3083,并使气体中污染物与前置电极3083接触更加充分,从而使前置电极3083能将电子传导给更多的污染物,并使污染物的带电效率更高。
如图56所示,本实施例中除尘电场阳极3082呈管状,除尘电场阴极3081呈棒状,除尘电场阴极3081穿设在除尘电场阳极3082中。本实施例中除尘电场阳极3082和除尘电场阴极3081呈非对称结构。当气体流入除尘电场阴极3081和除尘电场阳极3082之间形的电离电场将使污染物带电,且在除尘电场阳极3082施加的吸引力作用下,将带电的污染物收集在除尘电场阳极3082的内壁上。
另外,如图56所示,本实施例中除尘电场阳极3082和除尘电场阴极3081均沿前后方向延伸,除尘电场阳极3082的前端沿前后方向上位于除尘电场阴极3081的前端的前方。且如图56所示,除尘电场阳极3082的后端沿前后方向上位于除尘电场阴极3081的后端的后方。本实施例中除尘电场阳极3082沿前后方向上的长度更长,使得位于除尘电场阳极3082内壁 上的吸附面面积更大,从而对带有负电势的污染物的吸引力更大,并能收集更多的污染物。
如图56所示,本实施例中除尘电场阴极3081和除尘电场阳极3082构成电离单元,电离单元有多个,以利用多个电离单元收集更多的污染物,并使得本电场装置对污染物的收集能力更强,且收集效率更高。
本实施例中上述污染物包括导电性较弱的普通粉尘等、及导电性较强的金属粉尘、雾滴、气溶胶等。本实施例中电场装置,对气体中导电性较弱的普通粉尘,及导电性较强的污染物的收集过程为:当气体通过电场装置入口3085流入流道3086中,气体中导电性较强的金属粉尘、雾滴、或气溶胶等污染物在与前置电极3083相接触时,或与前置电极3083的距离达到一定范围时会直接带负电,随后,全部污染物随气流进入电场流道3087,除尘电场阳极3082给已带负电的金属粉尘、雾滴、或气溶胶等施加吸引力,并将该部分污染物收集起来,同时,除尘电场阳极3082与除尘电场阴极3081形成电离电场,该电离电场通过电离气体中的氧获得氧离子,且带负电荷的氧离子在与普通粉尘结合后,使普通粉尘带负电荷,除尘电场阳极3082给该部分带负电荷的粉尘施加吸引力,并将该部分污染物收集起来,从而将气体中导电性较强和导电性较弱的污染物均收集起来,并使得本电场装置所能收集物质的种类更广泛,且收集能力更强。
本实施例中上述除尘电场阴极3081也称作电晕荷电电极。上述直流电源具体为直流高压电源。前置电极3083和除尘电场阳极3082之间通入直流高压,形成导电回路;除尘电场阴极3081和除尘电场阳极3082之间通入直流高压,形成电离放电电晕电场。本实施例中前置电极3083为密集分布的导体。当容易带电的粉尘经过前置电极3083时,前置电极3083直接将电子给粉尘,粉尘带电,随后被异极的除尘电场阳极3082吸附;同时未带电的粉尘经过除尘电场阴极3081和除尘电场阳极3082形成的电离区,电离区形成的电离氧会把电子荷电给粉尘,这样粉尘继续带电,并被异极的除尘电场阳极3082吸附。
本实施例中电场装置能形成两种及两种以上的上电方式。比如,在气体中氧气充足情况下,可利用除尘电场阴极3081和除尘电场阳极3082之间形成的电离放电电晕电场,电离氧,来使污染物荷电,再利用除尘电场阳极3082收集污染物;而在气体中氧气含量过低、或无氧状态、或污染物为导电尘雾等时,利用前置电极3083直接使污染物上电,让污染物充分带电后被除尘电场阳极3082吸附。本电场装置让电场可以收集各类粉尘同时,也可以应用在各种含氧量尾气环境中,扩大了集尘电场治理粉尘应用范围,提高了集尘效率。本实施例采用上述两种带电方式的电场,可以同时收集容易荷电的高阻值粉尘以及容易上电的低阻值金属粉尘、气溶胶、液雾等。两种上电方式同时使用,电场适用范围扩大。
本实施例中电场装置可应用于进气除尘系统和尾气除尘系统中。当本实施例中电场装置应用于进气除尘系统中时,该电场装置也称作进气电场装置,前置电极3083也称作进气前置电极,除尘电场阳极3082也称作进气除尘电场阳极,除尘电场阴极3081也称作进气除尘电场阴极,流道3086也称作进气流道。当本实施例中电场装置应用于尾气除尘系统中时,该电场装置也称作尾气电场装置,前置电极3083也称作尾气前置电极,除尘电场阳极3082也称作尾气除尘电场阳极,除尘电场阴极3081也称作尾气除尘电场阴极,流道3086也称作尾气流道。
实施例61
本实施例中尾气除尘系统包括尾气降温装置,用于在尾气电场装置入口之前降低尾气温度。本实施例中尾气降温装置可与尾气电场装置入口相连通。
如图57所示,本实施例提供一种尾气降温装置,包括:
换热单元3071,用于与发动机的尾气进行热交换,以将换热单元3071中液态的换热介质加热成气态的换热介质。
本实施例中换热单元3071可以包括:
尾气通过腔,与发动机的排气管路相连通,该尾气通过腔用于供发动机的尾气通过;
介质气化腔,介质气化腔用于将液态换热介质与尾气发生热交换后转化成气态的换热介质。
本实施例中介质气化腔中具有液态的换热介质,液态的换热介质与尾气通过腔中的尾气发生热交换后会转化成气态的换热介质。尾气通过腔实现对汽车尾气的收集。本实施例中介质气化腔和尾气通过腔的长度方向可以相同,即介质气化腔的轴线与尾气通过腔的轴线相重合。本实施例中介质气化腔可以位于尾气通过腔内,或位于尾气通过腔外部。这样,当汽车尾气流过尾气通过腔时,汽车尾气携带的热量将传递给对介质气化腔内的液体,将液体加热到沸点以上,液体汽化为高温高压的蒸气等气态介质,该蒸气将在介质气化腔中流动。本实施例中介质气化腔具体可全包覆或除其前端外的部分包覆在尾气通过腔的内外侧。
本实施例中尾气降温装置还包括动力产生单元3072,该动力产生单元3072用于将换热介质的热能和/或尾气的热能转换为机械能。
本实施例中尾气降温装置还包括发电单元3073,该发电单元3073用于将动力产生单元3072产生的机械能转换为电能。
本实施例中尾气降温装置的工作原理为:换热单元3071与发动机的尾气进行热交换,以将换热单元3071中的液态的换热介质加热成气态的换热介质;动力产生单元3072将换热介 质的热能或尾气的热能转换机械能;发电单元3073将动力产生单元3072产生的机械能转换为电能,从而实现利用发动机的尾气进行发电,避免尾气携带的热量及压力被浪费掉;且换热单元3071在与尾气进行热交换时,还能起到对尾气散热、降温的作用,以便于能采用其它尾气净化装置等对尾气进行处理,并提高后续对尾气处理的效率。
本实施例中换热介质可以为水、甲醇、乙醇、油、或烷等。上述换热介质为能因温度而相变的物质,同时在相变过程其体积及压力也产生相应的变化。
本实施例中换热单元3071也称作换热器。本实施例中换热单元3071可采用管式换热设备。换热单元3071的设计考虑因素包括承压、减少体积、及增加换热面积等。
如图57所示,本实施例中尾气降温装置还可以包括连接于换热单元3071与动力产生单元3072之间的介质传输单元3074。介质气化腔中形成的蒸气等气态介质通过介质传输单元3074作用于动力产生单元3072。介质传输单元3074包括承压管路。
本实施例中动力产生单元3072包括涡扇。该涡扇能将蒸气或尾气等气态介质产生的压力转换成动能。且涡扇包括涡扇轴、及至少一组固定在涡扇轴上的涡扇组件。涡扇组件包括导流扇和动力扇。当蒸气的压力作用于涡扇组件时,涡扇轴将随涡扇组件一起转动,从而将蒸气的压力转换成动能。当动力产生单元3072包括涡扇时,发动机尾气的压力也可作用于涡扇上,以带动涡扇转动。这样,蒸气的压力和尾气产生的压力可交替地、无缝切换作用于涡扇上。当涡扇以第一方向转动时,发电单元3073将动能转换为电能,实现余热发电;当产生的电能反过来带动涡扇转动,且涡扇以第二方向转动时,发电单元3073将电能转换为排气阻力,为发动机提供排气阻力,当安装于发动机上的排气制动装置起作用,产生发动机制动高温高压尾气时,涡扇将这种制动能转换为电能,实现发动机排气制动和制动发电。本实施例可通过高速涡扇抽气产生恒定排气负压,减少了发动机的排气阻力,实现发动机助动。且当动力产生单元3072包括涡扇时,动力产生单元3072还包括涡扇调节模块,该涡扇调节模块利用发动机排气压力峰值推动涡扇产生转动惯量,进一步延时产生尾气负压,推动发动机吸气、降低使发动机排气阻力,提升发动机功率。
本实施例中尾气降温装置可应用于燃油发动机,如柴油发动机、或汽油发动机。本实施例中尾气降温装置还可应用于燃气发动机。具体地,本尾气降温装置用于车辆的柴油发动机上,即上述尾气通过腔与柴油发动机的排气口相连通。
发电单元3073包括发电机定子和发电机转子,发电机转子与动力产生单元3072的涡扇轴相连接。这样,发电机转子将随涡扇轴的转动而转动,从而与发电机定子共同作用实现发电。本实施例中发电单元3073可采用可变负荷发电机,或使用直流发电机将转矩变换为电能。 同时,本发电单元3073可通过调整励磁绕组电流,调整发电量匹配尾气热量的变化;以适应车辆上坡、下坡、重载、轻载等尾气温度变化。本实施例中发电单元3073还可以包括电池组件,以利用该电池组件储存电能,即实现对发出的电暂时缓存。本实施例中电池组件中储存的电可供换热器动力扇、水泵、制冷压缩机以及车辆中其它电器使用。
如图57所示,本实施例中尾气降温装置还可以包括耦合单元3075,该耦合单元3075电性连接于动力产生单元3072和发电单元3073之间,发电单元3073通过该耦合单元3075与动力产生单元3072同轴耦合。本实施例中耦合单元3075包括电磁耦合器。
本实施例中发电单元3073还可以包括发电机调控组件,该发电机调控组件用于调节发电机的电动转矩,产生排气负压以改变发动机强制制动力大小,产生排气背压以提高余热转换效率。具体地,发电机调控组件通过调节发电励磁或发电电流,能够改变发电功输出,从而调节汽车尾气排放阻力,实现发动机做功、排气背压、排气负压平衡,提高发电机效率。
本实施例中尾气降温装置还可以包括保温管路,该保温管路连接于发动机的排气管路和换热单元3071之间。具体地,保温管路的两端分别与发动机系统的排气口和尾气通过腔相连通,以利用该保温管路来维持尾气的高温,并将尾气引入尾气通过腔中。
本实施例中尾气降温装置还可以包括风机,该风机将空气通入尾气中,并在尾气电场装置入口之前,对尾气起到降温的作用。通入的空气可以是尾气的50%至300%、或100%至180%、或120%至150%。
本实施例中尾气降温装置可以协助发动机系统实现发动机排气余热的回收再利用,有助于减少发动机排放温室气体,也助于减少燃油发动机排放有害气体,减少了污染物的排放,并使燃油发动机排放更环保。
实施例62
如图58所示,本实施例在上述实施例61的基础上,其换热单元3071还可以包括介质循环回路3076;该介质循环回路3076的两端分别与介质气化腔的前后两端相连通,并形成封闭式的气液循环回路;介质循环回路3076上安装有冷凝器30761,冷凝器30761用于将气态的换热介质冷凝为液态的换热介质。介质循环回路3076通过动力产生单元3072与介质气化腔相连通。本实施例中介质循环回路3076的一端用于收集蒸气等气态换热介质,并将蒸气冷凝为液态的换热介质、即液体,另一端用于将液态的换热介质注入到介质气化腔中,以重新生成蒸气,从而实现了换热介质的循环回收利用。本实施例中介质循环回路3076包括蒸气回路30762,该蒸气回路30762与介质气化腔的后端相连通。另外,本实施例中上述冷凝器30761还通过介质传输单元3074与动力产生单元3072相连通。本实施例中气液循环回路与尾气通 过腔不相通。
本实施例中冷凝器30761可采用风冷散热器等散热设备,具体可采用承压翘片风冷散热器。当车辆行驶时,冷凝器30761通过自然风强行散热,无自然风时,可使用电扇对冷凝器30761进行散热。具体地,介质气化腔中形成的蒸气等气态介质在作用于动力产生单元3072后将进行泄压,并流入介质循环回路3076及风冷散热器,蒸气的温度随着散热器的散热而降低,并继续冷凝为液体。
如图58所示,本实施例中介质循环回路3076的一端可以设有增压模块30763,该增压模块30763用于将冷凝后的换热介质进行加压,以推动冷凝后的换热介质流入介质气化腔。本实施例中增压模块30763包括循环水泵或高压泵,液态的换热介质在循环水泵的叶轮推动下实现增压,并通过补水管道被挤压、进入介质气化腔中,以在介质气化腔中继续进行加热、并汽化。另外,涡扇转动时可替代循环水泵或高压泵,此时液体在涡扇余压的推动下,通过补水管道被挤压进介质气化腔中,继续被加热汽化。
如图58所示,本实施例中介质循环回路3076还可以包括设置在冷凝器30761和增压模块30763之间的储液模块30764,该储液模块30764用于存储经过冷凝器30761冷凝后液态的换热介质。上述增压模块30763位于储液模块30764和介质气化腔之间的一输送管路上,储液模块30764中的液体经增压模块30763增压后注入介质气化腔。本实施例中介质循环回路3076还包括液体调节模块30765,该液体调节模块30765设置于储液模块30764与介质气化腔之间,具体设置在位于储液模块30764与介质气化腔之间的另一输送管路上。上述液体调节模块30765用于调节向介质气化腔回流液体的量。当汽车尾气的温度持续高于液态换热介质的沸点温度时,液体调节模块30765将储液模块30764中的液体注入介质气化腔。本实施例中介质循环回路3076还包括设置于储液模块30764与介质气化腔之间的加注模块30766,该加注模块30766具体与上述增压模块30763和液体调节模块30765相通。本实施例中加注模块30766可包括喷嘴307661。喷嘴307661位于介质循环回路3076的一端,且喷嘴307661设置在介质气化腔的前端内,以通过该喷嘴307661向介质气化腔内注入液体。上述增压模块30763将储液模块30764中的液体加压后,经加注模块30766的喷嘴307661注入介质气化腔中。上述储液模块30764中的液体也可经液体调节模块30765注入加注模块30766,并经加注模块30766的喷嘴307661注入介质气化腔中。上述输送管路也称作热介质管道。
本实施例中尾气降温装置具体应于一台13升柴油发动机上,上述尾气通过腔具体与该柴油发动机的排气口相连通,发动机排放的尾气温度为650摄氏度,流量约4000立方米/小时,尾气热量约80千瓦左右。本实施例具体采用水作为介质气化腔中的换热介质,并采用涡扇为 动力产生单元3072。本尾气降温装置可以回收15千瓦电能,可以用于驱动车载电器;同时,加上循环水泵的直接效能回收利用,可回收40千瓦尾气热能。本实施例中尾气降温装置既可以提高燃油经济性,还可以把尾气温度降低到露点以下,以有利于需要低温环境的湿电除尘和臭氧脱硝尾气净化工艺的进行。
综上所述,本尾气降温装置可应用于柴油、汽油、燃气发动机节能减排领域,是发动机效率提升、节省燃料技术、提高发动机经济性的创新技术。本尾气降温装置能够帮助汽车省油、提高燃油经济性;也能使发动机废热得到回收利用,实现能源高效利用。
实施例63
如图59和图60所示,本实施例中上述实施例62的基础上,其动力产生单元3072具体采用涡扇。同时,本实施例中涡扇包括涡扇轴30721和介质腔涡扇组件30722,介质腔涡扇组件30722安装在涡扇轴30721上,且介质腔涡扇组件30722位于介质气化腔30711中,具体可位于介质气化腔30711中的后端处。
本实施例中介质腔涡扇组件30722包括介质腔导流扇307221和介质腔动力扇307222。
本实施例中涡扇包括尾气腔涡扇组件30723,安装在涡扇轴30721上,且尾气腔涡扇组件30723位于尾气通过腔30712中。
本实施例中尾气腔涡扇组件30723包括尾气腔导流扇307231和尾气腔动力扇307232。
本实施例中尾气通过腔30712位于介质气化腔30711中,即介质气化腔30711套设在尾气通过腔30712的外侧。本实施例中介质气化腔30711具体可全包覆或除其前端外的部分包覆在尾气通过腔30712的外侧。介质气化腔30711中形成的蒸气等气态介质流过介质腔涡扇组件30722,在蒸气压力的作用下推动介质腔涡扇组件30722及涡扇轴30721运转。介质腔导流扇307221具体设置在介质气化腔30711的后端处,蒸气等气态介质流经介质腔导流扇307221时,推动介质腔导流扇307221运转,并在该介质腔导流扇307221的作用下,蒸气按设定的路径流动至介质腔动力扇307222;介质腔动力扇307222设置在介质气化腔30711的后端处,具体位于介质腔导流扇307221的后方,流过介质腔导流扇307221的蒸气流动至介质腔动力扇307222,并推动介质腔动力扇307222及涡扇轴30721运转。本实施例中介质腔动力扇307222又称作第一级动力扇。尾气腔涡扇组件30723设置在介质腔涡扇组件30722的后方或前方,与介质腔涡扇组件30722同轴运转。尾气腔导流扇307231设置在尾气通过腔30712中,尾气流经尾气通过腔30712时,推动尾气腔导流扇307231运转,并在该尾气腔导流扇307231的作用下,尾气按设定的路径流动至尾气腔动力扇307232。尾气腔动力扇307232设置在尾气通过腔30712中,具体位于尾气腔导流扇307231的后方,流过尾气腔导流扇307231 的尾气流动至尾气腔动力扇307232,且在尾气压力作用下推动尾气腔动力扇307232及涡扇轴30721运转,最后尾气经尾气腔动力扇307232及尾气通过腔30712排出。本实施例中尾气腔动力扇307232又称作第二级动力扇。
如图59所示,本实施例中发电单元3073包括发电机定子30731和发电机转子30732。另外,本实施例中上述发电单元3073也设置在尾气通过腔30712外部,并与涡扇同轴连接,即发电机转子30732与涡扇轴30721相连接,这样发电机转子30732将随涡扇轴30721的转动而转动。
本实施例中动力产生单元3072正是采用涡扇,使得蒸气和尾气能够快速移动,节省了体积和重量,满足汽车尾气能量转换的需求。当本实施例中涡扇以第一方向转动时,发电单元3073将涡扇轴30721的动能转换为电能,从而实现余热发电;当涡扇以第二方向转动时,发电单元3073将电能转换为排气阻力,为发动机提供排气阻力,当安装于发动机上的排气制动装置起作用,产生发动机制动高温高压尾气时,涡扇将这种制动能转换为电能,实现发动机排气制动和制动发电。具体地,涡扇产生的动能可以用于发电,从而实现汽车余热发电;所产生的电能反过来带动涡扇转动,为发动机提供排气负压,从而就实现发动机排气制动和制动发电,极大地提升了发动机的效率。
如图59和图60所示,本实施例中尾气通过腔30712全部设置在介质气化腔30711内,从而实现汽车尾气收集。本实施例中介质气化腔30711与尾气通过腔30712的横向轴向相重合。
本实施例中动力产生单元3072还包括涡扇转动负压调节模块,该涡扇转动负压调节模块利用发动机排气压力峰值推动涡扇产生转动惯量,进一步延时产生尾气负压,推动发动机吸气、降低使发动机排气阻力,提升发动机功率。
如图59所示,本实施例中发电单元3073包括电池组件30733,以利用该电池组件30733储存电能,即实现对发出的电暂时缓存。本实施例中电池组件30733中储存的电可供换热器动力扇、水泵、制冷压缩机以及车辆中其它电器使用。
本实施例中尾气降温装置能够利用汽车尾气的余热进行发电,同时兼顾了体积和重量的要求,且热能转换效率高,换热介质可循环利用,极大地提升了能源利用率,绿色环保,实用性强。
在初始状态下,发动机排放的尾气推动尾气腔动力扇307232旋转,实现尾气压力直接换能;由尾气腔动力扇307232和涡扇轴30721的转动惯量,实现尾气排气瞬时负压;发电机调控组件3078通过调节发电励磁或发电电流,能够改变发电功输出,从而调节汽车尾气排放阻 力,适应发动机做功工况。
当采用汽车尾气余热发电时,且汽车尾气温度连续高于200摄氏度时,向介质气化腔30711注入水,水吸收尾气的热量形成高温高压的蒸气,同时产生蒸气动力,继续加速推动介质腔动力扇307222,使介质腔动力扇307222和尾气腔动力扇307232转动更快,力矩更大。通过调节发动电流或励磁电流平衡发动机做功和排气背压平衡;通过调节向介质气化腔30711注入的水量,适应排气温度变化,从而恒定排气温度。
当汽车制动发电时,发动机压气通过尾气腔动力扇307232,并推动尾气腔动力扇307232转动,从而将压力转变为发电机旋转动力,通过调节发电电流或励磁电流,改变阻力大小,实现发动机制动和制动力缓释。
当汽车电动制动时,发动机压气通过尾气腔动力扇307232,推动尾气腔动力扇307232正向转动,开启电动机,输出反向转动力矩,通过涡扇轴30721传递到介质腔动力扇307222和尾气腔动力扇307232上,形成强烈反推阻力,将能耗转变为腔体热量,同时使发动机制动力增加,强制制动。
介质传输单元3074包括反推涵道。当蒸气制动时,连续压气制动蓄积热量通过蒸气,产生更大推力,并通过反推涵道,将蒸气输出到介质腔动力扇307222上,强制介质腔动力扇307222和尾气腔动力扇307232反转,实现制动发动同时进行。
实施例64
如图61所示,本实施例在上述实施例63的基础上,其介质气化腔30711位于尾气通过腔30712中;且介质腔涡扇组件30722位于介质气化腔30711中,并具体位于介质气化腔30711的后端处;尾气腔涡扇组件30723位于尾气通过腔30712中,并具体位于尾气通过腔30712的后端处。介质腔涡扇组件30722和尾气腔涡扇组件30723均安装在涡扇轴30721上。本实施例中尾气腔涡扇组件30723位于介质腔涡扇组件30722的后方。这样,流经尾气通过腔30712的汽车尾气将直接作用于尾气腔涡扇组件30723,以带动尾气腔涡扇组件30723及涡扇轴30721转动;同时,当汽车尾气流经尾气通过腔30712时,将与介质气化腔30711中的液体进行换热,并使介质气化腔30711中的液体形成蒸气,该蒸气的压力作用于介质腔涡扇组件30722,以带动介质腔涡扇组件30722及涡扇轴30721转动,从而进一步加快推动涡扇轴30721转动;涡扇轴30721转动时将带动与其相连接的发电机转子30732一起转动,进而利用发电单元3073实现发电。另外,介质气化腔30711中的蒸气在向后流经介质腔涡扇组件30722后,将流入介质循环回路3076,并经介质循环回路3076中的冷凝器30761冷凝为液体后,再重新注入介质气化腔30711,以实现换热介质的循环回收利用。尾气通过腔30712 中的汽车尾气在流经尾气腔涡扇组件30723后排放至大气。
另外,本实施例中介质气化腔30711的侧壁上设有弯折段307111,该弯折段307111能有效增加介质气化腔30711与尾气通过腔30712的接触面积,即换热面积。本实施例中弯折段307111的截面呈锯齿状。
实施例65
为提高发动机热效率,需要把发动机尾气热能和背压回收换能,达到高效率,特别是混动车辆,既要燃油直接带动发电机,也要尾热高效转换为电能,这样燃油热效率可以提高15%-20%。对于混动车辆来说,在节省燃油同时可以为电池组件充更多的电,燃油转换为电能的效率可以达到70%以上。
具体地,在混动车辆燃油发动机的排气口,安装上述实施例63或实施例64中尾气降温装置,开启燃油发动机,发动机尾气进入尾气通过腔30712,在尾气背压作用下,经尾气腔导流扇307231调整方向,直接推动尾气腔动力扇307232旋转,从而在涡扇轴30721上产生旋转扭矩。由于存在转动惯量介质腔动力扇307222和尾气腔动力扇307232继续旋转时,将产生抽气,使发动机排气处于瞬时负压,这样,发动机排气阻力极低,有利于发动机继续排气并做功。同样燃油供给和输出负载情况下,提升发动机转速3%-5%左右。
发动机排气温度会因为翘片导热集聚在介质气化腔30711,当集聚温度大于水的沸点温度时,将水注入介质气化腔30711,水瞬间汽化,体积急剧膨胀,通过介质腔导流扇导向,推动介质腔动力扇307222及涡扇轴30721进一步加速旋转,产生更大的转动惯量和转矩。继续提升发动机转速,而燃油并没有增加,负载也没有减轻,获得的额外转速提升10%-15%。在转速因回收背压和温度提升同时,发动机动力输出将增加,根据排气温度差异,提高功率输出13%-20%左右,对于提高燃油经济性、减少发动机体积来说,非常有帮助。
实施例66
本实施例将实施例63或实施例64中的尾气降温装置应用于一台13升柴油发动机上,该柴油发动机尾气温度为650摄氏度,流量约4000立方米/小时,尾气热量约80千瓦左右。同时,本实施例使用水为换热介质,本尾气降温装置可以回收20千瓦电能,可以用于驱动车载电器。因此,本实施例中尾气降温装置既可以提高燃油经济性,还可以把尾气温度降低到露点以下,有利于需要低温环境的静电除尘、湿电除尘及臭氧脱硝尾气净化工艺的实施;同时实现了发动机变扭连续高效制动和强制连续制动。
具体地,本实施例的尾气降温装置直接连接在一台13升柴油发动机的排气口,并通过在本尾气降温装置的出口、即上述尾气通过腔30712的出口连接尾气电场装置、尾气湿电除尘 和臭氧脱硝系统,就能够实现尾热发电、尾气降温、发动机制动、除尘、脱硝等。本实施例中尾气降温装置安装在尾气电场装置的前方。
其中,本实施例使用3寸的介质腔动力扇307222和尾气腔动力扇307232,并使用10kw高速直流发电电动机,电池组件采用48v300ah动力电池组,使用发电电动手动切换开关。初始状态时,发动机怠速运转,转速小于750转,发动机输出功率10%左右,通过发动机排气推动尾气腔动力扇307232旋转,转速在2000转左右,实现尾气压力直接换能;尾气腔动力扇307232以及涡扇轴30721的转动惯量使尾气排气瞬时负压;由于尾气腔动力扇307232转动,在排气管道内产生瞬时负压-80kp左右,通过调节发电电流,改变发电功输出,从而调节尾气排放阻力,适应发动机做功工况,获得发电功率0.1-1.2kw。
当带负载30%时,发动机转速上升到1300转,尾气温度连续高于300摄氏度,向介质气化腔30711注入水,尾气温度下降到200摄氏度,产生大量高温高压蒸气,吸收尾气温度同时产生蒸气动力,由于介质腔导流扇和喷口限制,喷到介质腔动力扇上的蒸气压力继续加速推动介质腔动力扇转动,使介质腔动力扇及涡扇轴转动更快,力矩更大,带动发电机高速大扭矩旋转,通过调节发动电流或励磁电流平衡发动做功和排气背压平衡,获得发电量1kw-3kw,通过调节注入水量,适应排气温度变化,达到恒定排气温度目的,从而获得连续排气温度150摄氏度。低温排气有利于后续尾气电场装置回收颗粒物和臭氧脱硝,达到环保目的。
当发动机停止供油时,通过涡扇轴30721拖动发动机压气,发动机压气通过排气管路到达尾气腔动力扇307232,推动尾气腔动力扇307232,将压力转变为涡扇轴30721旋转动力,在涡扇轴30721上同时安装的发电机,通过调节发电电流,改变通过涡扇的排气量,从而改变排气阻力大小,实现发动机制动和制动力缓释,可以获得3-10kw左右的制动力,同时回收1-5kw的发电量。
当发电机切换到电动制动模式时,发电机瞬间变成电动机,等于驾驶员快速踏下制动踏板。这时发动机压气通过尾气腔动力扇307232,推动尾气腔动力扇307232正向转动。开启电动机,输出反向转动力矩,通过涡扇轴30721传递到介质腔动力扇307222和尾气腔动力扇307232上,形成强烈反推阻力,进一步增加制动效果。大量压气做功将能耗转变为高温气体,使腔体热量蓄积,同时使发动机制动力增加,强制制动。强制制动功率15-30kw。这种制动可以间歇发电,发电功率3-5kw左右。
当使用电动反推制动同时间歇发电时,突然需要紧急制动,可以停止发电,将制动热量产生蒸气用于制动,连续压气制动蓄积热量传递给介质气化腔中的水,介质气化腔中产生的蒸气通过反推涵道,输出到介质腔动力扇307222上,且蒸气反推介质腔动力扇307222,强制 介质腔动力扇307222和尾气腔动力扇307232反转,实现强制制动,可产生制动功率30kw以上。
综上所述,本发明的尾气降温装置能够基于汽车尾气实现余热发电,且热能转换效率高,换热介质可循环利用;能够应用于柴油发动机、汽油发动机和燃气发动机等的节能减排领域,使发动机废热得到回收利用,从而提高发动机的经济性;通过高速涡扇抽气产生恒定排气负压,减少了发动机的排气阻力,提了高发动机效率。所以,本发明有效克服了现有技术中的种种缺点而具高度产业利用价值。
综上所述,本发明有效克服了现有技术中的种种缺点而具高度产业利用价值。
上述实施例仅例示性说明本发明的原理及其功效,而非用于限制本发明。任何熟悉此技术的人士皆可在不违背本发明的精神及范畴下,对上述实施例进行修饰或改变。因此,举凡所属技术领域中具有通常知识者在未脱离本发明所揭示的精神与技术思想下所完成的一切等效修饰或改变,仍应由本发明的权利要求所涵盖。
Claims (8)
- 一种发动机排放处理系统,其特征在于,包括进气电离除尘系统、尾气电离除尘系统、尾气臭氧净化系统;所述尾气电离除尘系统包括尾气除尘系统入口、尾气除尘系统出口、尾气电场装置;所述尾气电场装置包括尾气电场装置入口、尾气电场装置出口、尾气除尘电场阴极和尾气除尘电场阳极,所述尾气除尘电场阴极和所述尾气除尘电场阳极用于产生尾气电离除尘电场;所述尾气电离除尘系统包括尾气降温装置;所述尾气臭氧净化系统包括反应场,用于将臭氧流股与尾气流股混合反应。
- 根据权利要求1所述的发动机排放处理系统,其特征在于,所述尾气降温装置包括换热单元,用于与发动机的尾气进行热交换,以将换热单元中液态的换热介质加热成气态的换热介质。
- 根据权利要求1或2所述的发动机排放处理系统,其特征在于,所述尾气降温装置将空气通入所述尾气电场装置入口之前,对尾气起到降温的作用。
- 根据权利要求1至3任一项所述发动机排放处理系统,其特征在于,所述尾气电离除尘系统还包括除水装置,用于在所述尾气电场装置入口之前去除液体水。
- 根据权利要求1至4任一项所述的发动机排放处理系统,其特征在于,所述尾气臭氧净化系统包括臭氧量控制装置,用于控制臭氧量以致有效氧化尾气中待处理的气体组分,所述臭氧量控制装置包括控制单元。
- 根据权利要求1至5任一项所述的发动机排放处理系统,其特征在于,所述尾气臭氧净化系统包括臭氧处理前尾气组分检测单元,用于检测臭氧处理前尾气组分含量。
- 根据权利要求1至6任一项所述的发动机排放处理系统,其特征在于,所述臭氧量控制装置包括臭氧处理后尾气组分检测单元,用于检测臭氧处理后尾气组分含量。
- 根据权利要求1至7任一项所述的发动机排放处理系统,其特征在于,还包括发动机。
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Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
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PCT/CN2019/112300 WO2020083226A1 (zh) | 2018-10-22 | 2019-10-21 | 排气处理系统及方法 |
PCT/CN2019/112306 WO2020083230A1 (zh) | 2018-10-22 | 2019-10-21 | 发动机尾气处理系统和方法 |
PCT/CN2019/112310 WO2020083234A1 (zh) | 2018-10-22 | 2019-10-21 | 发动机尾气处理系统和方法 |
PCT/CN2019/112256 WO2020083198A1 (zh) | 2018-10-22 | 2019-10-21 | 排气处理系统及方法 |
PCT/CN2019/112289 WO2020083217A1 (zh) | 2018-10-22 | 2019-10-21 | 发动机尾气处理系统和方法 |
PCT/CN2019/112295 WO2020083222A1 (zh) | 2018-10-22 | 2019-10-21 | 发动机尾气处理系统和方法 |
PCT/CN2019/112262 WO2020083203A1 (zh) | 2018-10-22 | 2019-10-21 | 排气处理系统及方法 |
PCT/CN2019/112292 WO2020083219A1 (zh) | 2018-10-22 | 2019-10-21 | 发动机尾气处理系统和方法 |
PCT/CN2019/112303 WO2020083228A1 (zh) | 2018-10-22 | 2019-10-21 | 发动机尾气处理系统和方法 |
PCT/CN2019/112299 WO2020083225A1 (zh) | 2018-10-22 | 2019-10-21 | 发动机尾气处理系统和方法 |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11441464B2 (en) | 2021-02-02 | 2022-09-13 | Saudi Arabian Oil Company | Use of ozone with LNT and MnO2 catalyst for the treatment of residual pollutant for the exhaust gas of an internal engine combustion |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20220250087A1 (en) * | 2018-10-22 | 2022-08-11 | Shanghai Bixiufu Enterprise Management Co., Ltd. | Engine exhaust dust removing system and method |
WO2020083141A1 (zh) * | 2018-10-22 | 2020-04-30 | 上海必修福企业管理有限公司 | 一种发动机进气除尘系统及方法 |
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IL298651A (en) * | 2022-11-28 | 2024-06-01 | Tadiran Consumer And Tech Products Ltd | Air disinfection device for use in air conditioning systems |
WO2024127071A1 (en) * | 2022-12-15 | 2024-06-20 | Kuregyan Kamo | Method for neutralizing exhaust gases of internal combustion engines and a device for its implementation |
GB2627532A (en) * | 2023-02-27 | 2024-08-28 | Dyson Technology Ltd | Microplasma catalytic reactor |
CN116983807B (zh) * | 2023-08-04 | 2024-02-02 | 浙江佳环电子有限公司 | 一种脉冲等离子体烟气净化装置 |
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CN118341249A (zh) * | 2024-03-12 | 2024-07-16 | 上海羿清环保科技有限公司 | 锂电子电池正极材料回收过程中浸出工艺废气的处理方法及其应用 |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010234195A (ja) * | 2009-03-30 | 2010-10-21 | Kyocera Corp | 放電装置および放電装置に用いられるプラズマ発生体、並びに放電装置を用いた反応装置 |
CN102588050A (zh) * | 2012-02-23 | 2012-07-18 | 庄建中 | 汽车尾气净化器 |
CN103993934A (zh) * | 2014-03-25 | 2014-08-20 | 张子生 | 柴油机动车尾气净化装置 |
CN203925685U (zh) * | 2014-02-19 | 2014-11-05 | 吕英 | 一种汽车尾气处理系统 |
CN204380852U (zh) * | 2014-10-11 | 2015-06-10 | 国家电网公司 | 一种除尘装置 |
CN104888576A (zh) * | 2015-05-12 | 2015-09-09 | 北京建筑大学 | 一种尾气处理系统及方法 |
CN107433092A (zh) * | 2016-05-27 | 2017-12-05 | 深圳市汇清科技有限公司 | 风口式电子除尘净化装置 |
CN206903785U (zh) * | 2017-06-09 | 2018-01-19 | 北汽福田汽车股份有限公司 | 空气滤清器以及车辆 |
CN207178071U (zh) * | 2017-06-30 | 2018-04-03 | 中国大唐集团科学技术研究院有限公司华东分公司 | 一种燃气轮机进气过滤装置 |
Family Cites Families (170)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2563297A (en) * | 1947-11-24 | 1951-08-07 | Research Corp | Electrical precipitator, including an electrode washing device |
US3745751A (en) * | 1970-10-26 | 1973-07-17 | American Standard Inc | Sulfur dioxide collection system |
CS178566B1 (en) * | 1974-11-14 | 1979-05-15 | Jan Skalny | Method and device for continuous concentration lowering of polycyclic aromatic hydrocarbons in gas-flow |
JPS5317566A (en) * | 1976-07-31 | 1978-02-17 | Kobe Steel Ltd | Denitration method for of exhaust gas |
US5003774A (en) * | 1987-10-09 | 1991-04-02 | Kerr-Mcgee Chemical Corporation | Apparatus for soot removal from exhaust gas |
DE3820067A1 (de) * | 1988-06-13 | 1989-12-14 | Kramb Mothermik Gmbh & Co Kg | Verfahren und vorrichtung zur entfernung von russ und kondensierbaren bestandteilen aus dieselabgasen |
EP0379760A1 (en) * | 1989-01-26 | 1990-08-01 | Univerzita Komenskeho | Device for continuously reducing concentration of carbon monoxide and other harmful types of emission |
KR910002599Y1 (ko) * | 1989-06-15 | 1991-04-22 | 삼성전자 주식회사 | 공기청정기 이온회선의 전열발생 구조 |
GB8919440D0 (en) * | 1989-08-25 | 1989-10-11 | Advanced Energy Systems Limite | Methods and apparatus to filter gas and air streams |
US5229077A (en) * | 1991-08-16 | 1993-07-20 | Environmental Elements Corp. | Sulfur rate control system |
US5236672A (en) * | 1991-12-18 | 1993-08-17 | The United States Of America As Represented By The United States Environmental Protection Agency | Corona destruction of volatile organic compounds and toxics |
JPH05317639A (ja) * | 1992-05-18 | 1993-12-03 | Daikin Ind Ltd | 空気清浄装置 |
CN1027828C (zh) * | 1992-11-11 | 1995-03-08 | 申进忠 | 臭氧-催化剂法汽车尾气净化器 |
CN2205248Y (zh) * | 1994-09-13 | 1995-08-16 | 郑天安 | 高效静电除尘器 |
KR0148563B1 (ko) * | 1995-12-28 | 1998-10-01 | 전경호 | 내연기관 및 외연기관에 있어서 매연처리 저감방법 및 그 장치 |
GB9605574D0 (en) * | 1996-03-16 | 1996-05-15 | Mountain Breeze Ltd | Treatment of particulate pollutants |
JP3108649B2 (ja) * | 1997-04-18 | 2000-11-13 | 株式会社ヤマダコーポレーション | 車両排ガス浄化装置 |
JP3530368B2 (ja) * | 1997-12-16 | 2004-05-24 | 三菱重工業株式会社 | 乾式電気集塵器 |
JPH11290719A (ja) * | 1998-04-14 | 1999-10-26 | Sumitomo Heavy Ind Ltd | 電気集塵装置 |
CN2336869Y (zh) * | 1998-07-22 | 1999-09-08 | 淄博永恒环保技术有限公司 | 高压电脉冲烟尘荷电器 |
DE19846320C1 (de) * | 1998-10-08 | 2000-06-29 | Dickels Karl | Vorrichtung zur Abscheidung von Stickoxiden und Partikeln aus einem Gasstrom |
CN1256354A (zh) * | 1998-12-04 | 2000-06-14 | 杜成林 | 一种机动车消烟消声防火除尘净化器 |
JP2001182975A (ja) * | 1999-12-24 | 2001-07-06 | Masaya Nagashima | 家屋室内加圧装置、および、その方法 |
US6212883B1 (en) * | 2000-03-03 | 2001-04-10 | Moon-Ki Cho | Method and apparatus for treating exhaust gas from vehicles |
JP2002045643A (ja) * | 2000-08-03 | 2002-02-12 | Hitachi Plant Eng & Constr Co Ltd | 排ガス処理方法 |
JP4040833B2 (ja) * | 2000-10-24 | 2008-01-30 | 日産ディーゼル工業株式会社 | ディーゼルエンジンの排気浄化装置 |
US6969494B2 (en) * | 2001-05-11 | 2005-11-29 | Continental Research & Engineering, Llc | Plasma based trace metal removal apparatus and method |
CN1332341A (zh) * | 2001-07-06 | 2002-01-23 | 俞其进 | 空气净化机 |
JP2004027949A (ja) * | 2002-06-25 | 2004-01-29 | Yukio Kinoshita | 高効率排気ガス処理システム |
FR2841484B1 (fr) * | 2002-06-26 | 2004-09-10 | Boucq De Beaudignies Ghisla Le | Dispositif et procede de filtration de l'air et des gaz avec regeneration des particules captees |
DE10231620A1 (de) * | 2002-07-12 | 2004-01-29 | Robert Bosch Gmbh | Vorrichtung und Verfahren zur Abgasreinigung einer Brennkraftmaschine |
JP2004122301A (ja) * | 2002-10-03 | 2004-04-22 | Okuma Corp | 噴霧潤滑排気用濾過装置 |
US7514047B2 (en) * | 2003-01-15 | 2009-04-07 | Toyota Jidosha Kabushiki Kaisha | Exhaust gas purifying apparatus |
US20040188238A1 (en) * | 2003-03-28 | 2004-09-30 | Hemingway Mark David | System and method for concurrent particulate and NOx control |
JP2004360512A (ja) * | 2003-06-03 | 2004-12-24 | Hino Motors Ltd | 排気浄化装置 |
JP4327506B2 (ja) * | 2003-06-03 | 2009-09-09 | 日野自動車株式会社 | 排気浄化装置 |
CN1513753A (zh) * | 2003-06-13 | 2004-07-21 | 大连海事大学 | 一种羟基氧化二氧化硫生成硫酸的方法 |
CN2770786Y (zh) * | 2004-03-04 | 2006-04-12 | 何保海 | 电除尘器辅助电极 |
CN100418637C (zh) * | 2004-06-10 | 2008-09-17 | 中钢集团天澄环保科技股份有限公司 | 泛比电阻电除尘器及除尘方法 |
CN2767671Y (zh) * | 2004-11-03 | 2006-03-29 | 高永祥 | 汽车尾气电子净化器 |
CN2761244Y (zh) * | 2005-01-06 | 2006-03-01 | 合肥水泥研究设计院 | 低压长袋双侧脉冲袋式除尘器 |
JP4239992B2 (ja) * | 2005-03-16 | 2009-03-18 | トヨタ自動車株式会社 | ガス浄化装置 |
JP4254751B2 (ja) * | 2005-06-17 | 2009-04-15 | トヨタ自動車株式会社 | 排気ガス浄化装置 |
CN2811818Y (zh) * | 2005-06-22 | 2006-08-30 | 孙一聪 | 微型空气净化器 |
JP4263711B2 (ja) * | 2005-09-16 | 2009-05-13 | トヨタ自動車株式会社 | 内燃機関の排気浄化装置 |
JP2007113497A (ja) * | 2005-10-20 | 2007-05-10 | Toyota Motor Corp | 内燃機関の排気浄化装置 |
EP1985371A4 (en) * | 2006-02-14 | 2013-05-22 | Kagome Kk | FUNIGZID PROCESSES ABOUT CONIDIUM ADSORPTION USING DIELECTRIC POLARIZATION DEVICE FOR ELIMINATING FLYING ORGANISMS AND DEVICE FOR PROTECTING PLANTS |
CN2898683Y (zh) * | 2006-03-31 | 2007-05-09 | 北京禹辉水处理技术有限公司 | 全自动空气净化装置 |
ZA200703388B (en) * | 2006-05-01 | 2009-08-26 | Boc Group Inc | Ozone production process and its use in industrial processes |
CN200951364Y (zh) * | 2006-09-12 | 2007-09-26 | 党小朋 | 在线清灰脉喷袋除尘器 |
JP4453700B2 (ja) * | 2006-12-28 | 2010-04-21 | トヨタ自動車株式会社 | 内燃機関の排気ガス浄化装置 |
JP4497158B2 (ja) * | 2006-12-28 | 2010-07-07 | トヨタ自動車株式会社 | 内燃機関の排気ガス浄化装置 |
JP5119690B2 (ja) * | 2007-03-12 | 2013-01-16 | トヨタ自動車株式会社 | 内燃機関の排気ガス浄化装置 |
CN201064735Y (zh) * | 2007-07-18 | 2008-05-28 | 尤今 | 静电式烟雾净化设备 |
JP2009052440A (ja) * | 2007-08-24 | 2009-03-12 | Hitachi Plant Technologies Ltd | 舶用排ガス処理装置 |
CN201141320Y (zh) * | 2008-01-14 | 2008-10-29 | 关哲夫 | 一种发动机尾气净化装置 |
CN201168531Y (zh) * | 2008-03-17 | 2008-12-24 | 江苏科宝机械制造有限公司 | 电袋组合式收尘器 |
CN101337152A (zh) * | 2008-08-07 | 2009-01-07 | 大连海事大学 | 资源化同时脱除烟气中二氧化硫、氮氧化物的臭氧氧化干法 |
NL2002005C (nl) * | 2008-09-22 | 2010-03-23 | Stichting Energie | Werkwijze en inrichting voor het behandelen van een uitlaatgas, systeem omvattende een verbrandingsmotor en een dergelijke inrichting, alsmede schip. |
US7790127B1 (en) * | 2009-03-02 | 2010-09-07 | Gm Global Technology Operations, Inc. | NOx emission control system for hydrocarbon fueled power source |
CN201394503Y (zh) * | 2009-03-12 | 2010-02-03 | 河北大学 | 一种工业窑炉用高压静电除尘器 |
CN101524668B (zh) * | 2009-03-12 | 2011-04-13 | 河北大学 | 一种工业窑炉用高压静电除尘器 |
DE102009041091A1 (de) * | 2009-09-14 | 2011-03-24 | Emitec Gesellschaft Für Emissionstechnologie Mbh | Vorrichtung zur Behandlung von Rußpartikel enthaltendem Abgas |
WO2011046187A1 (ja) * | 2009-10-14 | 2011-04-21 | 臼井国際産業株式会社 | 電気式排気ガス処理方法および電気式排気ガス処理装置 |
KR101655452B1 (ko) * | 2010-01-29 | 2016-09-08 | 삼성전자주식회사 | 전기집진장치 및 그 전극판 |
CN101798944A (zh) * | 2010-02-09 | 2010-08-11 | 尤今 | 柴油发电机黑烟净化设备 |
JP2011179461A (ja) * | 2010-03-03 | 2011-09-15 | Toyota Industries Corp | 排ガス浄化装置 |
CN101757842B (zh) * | 2010-03-16 | 2012-01-25 | 仲立军 | 低温等离子废气净化装置 |
CN201644221U (zh) * | 2010-05-17 | 2010-11-24 | 山东电力研究院 | 干湿混合电除尘器 |
CN101961596A (zh) * | 2010-07-19 | 2011-02-02 | 大连海事大学 | 氧活性粒子注入烟道中的羟基自由基氧化脱硫脱硝方法 |
CN201943784U (zh) * | 2010-10-14 | 2011-08-24 | 中国石油化工股份有限公司 | 一种机动车排放尾气的脱水装置 |
CN102151609A (zh) * | 2010-12-03 | 2011-08-17 | 江苏中科节能环保技术有限公司 | 电除尘器电场收尘机构 |
JP6041418B2 (ja) * | 2010-12-16 | 2016-12-07 | 臼井国際産業株式会社 | 重油以下の低質燃料を使用する大排気量船舶用ディーゼルエンジンの排気ガス浄化装置 |
US8784762B2 (en) * | 2011-02-15 | 2014-07-22 | Ati Properties, Inc. | Treatment of NOx-containing gas streams |
US9145805B2 (en) * | 2011-09-05 | 2015-09-29 | Hino Motors, Ltd. | Exhaust gas purifier |
CN202207630U (zh) * | 2011-09-07 | 2012-05-02 | 苏州巨联科技有限公司 | 蜂巢电场 |
CN102671763A (zh) * | 2012-04-30 | 2012-09-19 | 莱芜钢铁集团有限公司 | 管道式高风速双荷电区电凝聚装置 |
JP5957284B2 (ja) * | 2012-05-09 | 2016-07-27 | 株式会社Kri | 排ガス浄化装置 |
JP6062660B2 (ja) * | 2012-05-15 | 2017-01-18 | 臼井国際産業株式会社 | 重油より低質な燃料を使用する大排気量船舶用ディーゼルエンジン排ガス処理装置 |
JP2014047670A (ja) * | 2012-08-30 | 2014-03-17 | Denso Corp | オゾン生成手段を含むエンジン用NOx後処理装置の制御方法および制御装置 |
CN102958264B (zh) * | 2012-11-20 | 2015-04-22 | 浙江大学 | 一种基于催化剂反电晕沿面击穿的等离子体发生装置及方法和应用 |
CN103055675B (zh) * | 2013-01-18 | 2015-04-15 | 大恩(天津)环境技术研发有限公司 | 一种基于高级氧化作用的工业烟气综合治理系统及方法 |
CN203469745U (zh) * | 2013-09-09 | 2014-03-12 | 深圳市汇清科技有限公司 | 风口式电子除尘净化装置 |
CN204275723U (zh) * | 2013-11-15 | 2015-04-22 | 北京科之建环保工程有限公司 | 一种用于烟气综合处理装置的静电除尘器 |
CN103768942A (zh) * | 2014-02-19 | 2014-05-07 | 大连海事大学 | 一种等离子体净化柴油机尾气方法 |
CN103817003A (zh) * | 2014-02-28 | 2014-05-28 | 天津机科环保科技有限公司 | 立管式高压湿式静电精除尘器 |
CN203791052U (zh) * | 2014-02-28 | 2014-08-27 | 天津机科环保科技有限公司 | 立管式高压湿式静电精除尘器 |
CN104941802A (zh) * | 2014-03-26 | 2015-09-30 | 王彤 | 空气净化器及用于空气净化器的高压电源控制方法 |
CN105268555A (zh) * | 2014-06-05 | 2016-01-27 | 东北师范大学 | 除尘量控制装置 |
JP6107748B2 (ja) * | 2014-06-20 | 2017-04-05 | 株式会社デンソー | 還元剤添加装置 |
CN204099004U (zh) * | 2014-09-25 | 2015-01-14 | 刘国强 | 汽车尾气综合处理系统 |
CN204170851U (zh) * | 2014-10-15 | 2015-02-25 | 厦门锐传科技有限公司 | 电除尘器 |
CN204219982U (zh) * | 2014-11-17 | 2015-03-25 | 安吉润风空气净化科技有限公司 | 一种介质阻挡放电的气体净化装置 |
CN104587813B (zh) * | 2015-02-03 | 2017-12-19 | 山东派力迪环保工程有限公司 | 一种中小型锅炉废气的等离子体脱硝方法 |
CN104791051A (zh) * | 2015-03-17 | 2015-07-22 | 上海唐亨能源科技有限公司 | 一种柴油机废气综合处理装置 |
CN104841557B (zh) * | 2015-03-23 | 2017-01-11 | 常州大学 | 一种柴油发动机尾气处理和检测系统 |
CN104847452B (zh) * | 2015-05-14 | 2017-11-03 | 哈尔滨工业大学 | 等离子体与静电吸附耦合的汽车尾气净化器及净化方法 |
CN104984626B (zh) * | 2015-07-14 | 2018-03-30 | 河北中清环保科技有限公司 | 一种木炭窑烟气治理系统 |
CN204768126U (zh) * | 2015-07-14 | 2015-11-18 | 河北中清环保科技有限公司 | 一种木炭窑烟气治理系统 |
CN204996568U (zh) * | 2015-08-07 | 2016-01-27 | 浙江大学 | 一种采用颗粒冲刷清灰的线管式高温静电除尘装置 |
CN105080715B (zh) * | 2015-08-07 | 2017-04-19 | 浙江大学 | 采用颗粒冲刷清灰的线管式高温静电除尘装置及清灰方法 |
JP6384429B2 (ja) * | 2015-08-27 | 2018-09-05 | 株式会社デンソー | オゾン供給装置の故障診断システム |
CN204911793U (zh) * | 2015-08-27 | 2015-12-30 | 东方电气集团东方锅炉股份有限公司 | 一种湿式静电除尘器设备 |
CN105149092B (zh) * | 2015-09-02 | 2017-08-29 | 中国科学院过程工程研究所 | 一种用于导电粉尘的除尘方法 |
CN204911132U (zh) * | 2015-09-12 | 2015-12-30 | 王伟珍 | 一种烟气高效除尘装置 |
JP6413998B2 (ja) * | 2015-09-29 | 2018-10-31 | 株式会社デンソー | オゾン供給装置の制御システム |
JP6409731B2 (ja) * | 2015-10-05 | 2018-10-24 | 株式会社デンソー | 燃焼システムの制御装置 |
CN205055799U (zh) * | 2015-10-27 | 2016-03-02 | 李继凤 | 一体化湿法烟气脱硫除尘的装置 |
CN205182953U (zh) * | 2015-10-27 | 2016-04-27 | 大唐宝鸡热电厂 | 一种改进型电除尘器 |
CN105214465A (zh) * | 2015-10-27 | 2016-01-06 | 李继凤 | 一体化湿法烟气脱硫除尘的装置和方法 |
CN205199730U (zh) * | 2015-12-07 | 2016-05-04 | 福建龙净环保股份有限公司 | 一种湿式电除尘器 |
CN105464767A (zh) * | 2015-12-10 | 2016-04-06 | 成都德善能科技有限公司 | 一种基于汽车尾气发电的汽车尾气处理装置及其控制系统 |
JP6447486B2 (ja) * | 2015-12-22 | 2019-01-09 | 株式会社デンソー | 放電制御装置、ガス供給装置及び放電制御方法 |
CN105642080A (zh) * | 2015-12-31 | 2016-06-08 | 神华集团有限责任公司 | 一种烟气净化的装置和方法 |
WO2017114049A1 (zh) * | 2015-12-31 | 2017-07-06 | 靳瑞廷 | 气体介质悬浮颗粒物净化系统 |
CN105562207A (zh) * | 2016-02-02 | 2016-05-11 | 北京清新环境技术股份有限公司 | 一种管束式除尘除雾装置 |
CN205518212U (zh) * | 2016-02-02 | 2016-08-31 | 北京清新环境技术股份有限公司 | 一种管束式除尘除雾装置 |
JP2017155643A (ja) * | 2016-03-01 | 2017-09-07 | 株式会社Soken | NOx浄化装置、およびNOx浄化装置の製造方法 |
CN105749679B (zh) * | 2016-03-23 | 2018-08-28 | 航天凯天环保科技股份有限公司 | 一种高温烟气除尘方法及系统 |
CN205627552U (zh) * | 2016-04-09 | 2016-10-12 | 嘉兴天盾环保科技有限公司 | 一种高通量紧凑型电晕离子发生器 |
CN105781701B (zh) * | 2016-04-13 | 2018-07-10 | 赵会东 | 一种减少雾霾的汽油车尾气排气管及汽油车 |
CN105697110A (zh) * | 2016-04-25 | 2016-06-22 | 安徽理工大学 | 汽车尾气净化及余热回收一体化装置 |
CN205638640U (zh) * | 2016-04-29 | 2016-10-12 | 陈聪 | 一种利用汽车尾气热量发电的尾气处理装置 |
CN107433091A (zh) * | 2016-05-27 | 2017-12-05 | 深圳市汇清科技有限公司 | 风口式电子除尘净化装置 |
CN105952509B (zh) * | 2016-06-24 | 2018-06-15 | 王增荣 | 组合式汽车发动机尾气处理系统 |
CN206111281U (zh) * | 2016-06-29 | 2017-04-19 | 浙江中通检测科技有限公司 | 一种柴油发动机废气冷却净化装置 |
CN205995620U (zh) * | 2016-06-30 | 2017-03-08 | 河北安维环境工程有限公司 | 湿式电除雾装置 |
CN105944838B (zh) * | 2016-06-30 | 2018-07-06 | 广东佳德环保科技有限公司 | 湿式电除尘器用钛电极电离管 |
CN105921275A (zh) * | 2016-06-30 | 2016-09-07 | 河北安维环境工程有限公司 | 湿式电除雾装置 |
CN106247522A (zh) * | 2016-07-07 | 2016-12-21 | 格林韦尔(北京)科技发展有限公司 | 新风空气净化方法及系统 |
CN106269256A (zh) * | 2016-08-10 | 2017-01-04 | 福建龙净环保股份有限公司 | 一种用于烟气净化的电除雾器 |
CN205966185U (zh) * | 2016-08-10 | 2017-02-22 | 福建龙净环保股份有限公司 | 一种用于烟气净化的电除雾器 |
CN206329373U (zh) * | 2016-08-22 | 2017-07-14 | 张济飞 | 一种汽车尾气净化处理装置 |
CN206256947U (zh) * | 2016-08-31 | 2017-06-16 | 重庆市吉德环保工程有限公司 | 一种汽车尾气扬尘收集装置 |
CN107780994A (zh) * | 2016-08-31 | 2018-03-09 | 重庆市吉德环保工程有限公司 | 一种汽车尾气扬尘收集装置 |
CN108070398A (zh) * | 2016-11-07 | 2018-05-25 | 简阳市龙兴炭素有限公司 | 炭素焙烧炉沥青烟气净化回收利用方法 |
CN206276238U (zh) * | 2016-11-17 | 2017-06-27 | 武汉大学 | 一种等离子体催化反应器及其空气净化器 |
CN108211698A (zh) * | 2016-12-14 | 2018-06-29 | 李平 | 燃煤烟气所有污染物四级净化系统及方法 |
CN106492988A (zh) * | 2016-12-23 | 2017-03-15 | 福建省沃特宝环保科技有限公司 | 一种微通道阳极除水雾装置 |
CN206509115U (zh) * | 2016-12-29 | 2017-09-22 | 天津钢铁集团有限公司 | 一种电除尘系统改进结构 |
CN106593580B (zh) * | 2016-12-30 | 2022-07-08 | 三河市科达科技有限公司 | 一种发动机废气循环净化消声系统 |
CN106907215A (zh) * | 2017-02-27 | 2017-06-30 | 上海必修福企业管理有限公司 | 一种处理发动机排放尾气的装置和方法 |
CN206661444U (zh) * | 2017-03-16 | 2017-11-24 | 淄博卓意玻纤材料有限公司 | 单丝涂塑防虫网生产用静电除尘系统 |
CN106861909A (zh) * | 2017-03-16 | 2017-06-20 | 淄博卓意玻纤材料有限公司 | 单丝涂塑防虫网生产用静电除尘工艺方法及其设备系统 |
CN206625882U (zh) * | 2017-03-30 | 2017-11-10 | 武汉大学 | 一种汽车尾气净化装置 |
CN106733194B (zh) * | 2017-03-31 | 2018-10-16 | 广东美的厨房电器制造有限公司 | 静电装置和油烟机 |
CN206716211U (zh) * | 2017-05-16 | 2017-12-08 | 孟金来 | 去除金属或石墨或炭黑粉尘用电除尘器电极 |
GB201710147D0 (en) * | 2017-06-24 | 2017-08-09 | Wynford Peter Holloway | Exhaust treatment device |
CN206911574U (zh) * | 2017-07-06 | 2018-01-23 | 辽宁国泰众欣环保科技有限公司 | 一种带清洁阴阳极的静电除尘单元 |
CN206911575U (zh) * | 2017-07-06 | 2018-01-23 | 辽宁国泰众欣环保科技有限公司 | 一种带清洁阴阳极的静电除尘组件 |
CN207056790U (zh) * | 2017-08-02 | 2018-03-02 | 南京德力通通风设备有限公司 | 一种用于餐饮油烟净化器的高低压静电场 |
CN107387203A (zh) * | 2017-08-17 | 2017-11-24 | 南京汉尔斯生物科技有限公司 | 一种汽车尾气净化装置 |
CN107605579A (zh) * | 2017-08-24 | 2018-01-19 | 南京理工大学 | 一种利用汽车尾气废热温差发电的尾气净化器 |
CN207013155U (zh) * | 2017-09-01 | 2018-02-16 | 无锡幸运环保设备有限公司 | 带有拉瓦尔喷嘴的新型静电除尘器 |
CN207102904U (zh) * | 2017-09-26 | 2018-03-16 | 江苏菲特滤料有限公司 | 一种工业除尘设备 |
CN207385713U (zh) * | 2017-09-29 | 2018-05-22 | 广西博世科环保科技股份有限公司 | 一种高风速耐高温高效静电除尘器 |
CN107497265B (zh) * | 2017-09-30 | 2019-12-31 | 江苏大学 | 臭氧协同微波激发飞灰诱导自由基的一体化烟气净化系统及方法 |
CN107476865A (zh) * | 2017-10-09 | 2017-12-15 | 张延艳 | 一种环保型汽车尾气净化器 |
CN108096969B (zh) * | 2017-12-05 | 2024-03-22 | 青岛科技大学 | 一种基于挥发油气净化技术的尾气光氧裂解处理方法 |
CN207342893U (zh) * | 2017-12-13 | 2018-05-11 | 平顶山市博翔碳素有限公司 | 一种冷风式电捕焦油器 |
CN207446500U (zh) * | 2017-12-13 | 2018-06-05 | 浙江深澜环境工程有限公司 | 一种高压静电除尘器 |
CN108561208A (zh) * | 2018-04-28 | 2018-09-21 | 中国计量大学 | 一种汽车尾气净化装置 |
CN209155539U (zh) * | 2018-06-11 | 2019-07-26 | 河北冀研能源科学技术研究院有限公司 | 一种电站内臭氧氧化协同scr的全负荷脱硝系统 |
CN108672089A (zh) * | 2018-06-28 | 2018-10-19 | 西安交通大学 | 一种基于石墨烯的湿式电除尘器极板 |
CN108939916A (zh) * | 2018-09-29 | 2018-12-07 | 国电环境保护研究院 | 一种利用臭氧进行scr高效脱硝的系统 |
WO2020083165A1 (zh) * | 2018-10-22 | 2020-04-30 | 上海必修福企业管理有限公司 | 一种发动机尾气臭氧净化系统和方法 |
CN109772136A (zh) * | 2019-02-13 | 2019-05-21 | 大唐绥化热电有限公司 | 低温除尘脱硫脱硝一体化系统及脱硫脱硝工艺 |
CN109876615A (zh) * | 2019-04-09 | 2019-06-14 | 江苏科行环保股份有限公司 | 利用脉冲电晕放电进行臭氧脱硝提效的装置和方法 |
CN113522023A (zh) * | 2020-04-15 | 2021-10-22 | 上海必修福企业管理有限公司 | 一种发动机尾气中VOCs气体处理系统和方法 |
CN215784106U (zh) * | 2021-09-17 | 2022-02-11 | 北京中新国能环保科技有限公司 | 一种带自冲洗功能的湿式电除尘电极结构 |
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- 2019-10-18 MX MX2021004573A patent/MX2021004573A/es unknown
- 2019-10-18 EP EP19876543.0A patent/EP3872312A4/en not_active Withdrawn
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- 2019-10-18 WO PCT/CN2019/111813 patent/WO2020083096A1/zh active Application Filing
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- 2019-10-21 WO PCT/CN2019/112280 patent/WO2020083211A1/zh active Application Filing
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- 2019-10-21 WO PCT/CN2019/112250 patent/WO2020083194A1/zh unknown
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- 2019-10-21 WO PCT/CN2019/112307 patent/WO2020083231A1/zh active Application Filing
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- 2019-10-21 WO PCT/CN2019/112287 patent/WO2020083215A1/zh active Application Filing
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- 2019-10-21 JP JP2021546432A patent/JP2022508866A/ja active Pending
- 2019-10-21 CA CA3117397A patent/CA3117397A1/en not_active Abandoned
- 2019-10-21 US US17/287,700 patent/US20210379599A1/en not_active Abandoned
- 2019-10-21 JP JP2021547628A patent/JP2022509335A/ja active Pending
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- 2019-10-21 JP JP2021547629A patent/JP2022509336A/ja active Pending
- 2019-10-21 WO PCT/CN2019/112260 patent/WO2020083202A1/zh active Application Filing
- 2019-10-21 EP EP19876827.7A patent/EP3871756A4/en not_active Withdrawn
- 2019-10-21 WO PCT/CN2019/112266 patent/WO2020083206A1/zh active Application Filing
- 2019-10-21 WO PCT/CN2019/112252 patent/WO2020083196A1/zh active Application Filing
- 2019-10-21 WO PCT/CN2019/112259 patent/WO2020083201A1/zh active Application Filing
- 2019-10-21 EP EP19876816.0A patent/EP3872321A1/en not_active Withdrawn
- 2019-10-21 WO PCT/CN2019/112281 patent/WO2020083212A1/zh active Application Filing
- 2019-10-21 AU AU2019364463A patent/AU2019364463A1/en not_active Abandoned
- 2019-10-21 WO PCT/CN2019/112288 patent/WO2020083216A1/zh active Application Filing
- 2019-10-21 WO PCT/CN2019/112300 patent/WO2020083226A1/zh unknown
- 2019-10-21 WO PCT/CN2019/112306 patent/WO2020083230A1/zh active Application Filing
- 2019-10-21 WO PCT/CN2019/112310 patent/WO2020083234A1/zh active Application Filing
- 2019-10-21 WO PCT/CN2019/112256 patent/WO2020083198A1/zh unknown
- 2019-10-21 US US17/287,714 patent/US20220275739A1/en not_active Abandoned
- 2019-10-21 WO PCT/CN2019/112289 patent/WO2020083217A1/zh active Application Filing
- 2019-10-21 WO PCT/CN2019/112295 patent/WO2020083222A1/zh active Application Filing
- 2019-10-21 EP EP19876825.1A patent/EP3872314A1/en not_active Withdrawn
- 2019-10-21 US US17/287,783 patent/US20220251993A1/en not_active Abandoned
- 2019-10-21 US US17/287,682 patent/US20210404355A1/en not_active Abandoned
- 2019-10-21 WO PCT/CN2019/112262 patent/WO2020083203A1/zh unknown
- 2019-10-21 JP JP2021523042A patent/JP2022505951A/ja active Pending
- 2019-10-21 WO PCT/CN2019/112292 patent/WO2020083219A1/zh active Application Filing
- 2019-10-21 BR BR112021007618-2A patent/BR112021007618A2/pt not_active Application Discontinuation
- 2019-10-21 US US17/309,082 patent/US20220054974A1/en not_active Abandoned
- 2019-10-21 WO PCT/CN2019/112303 patent/WO2020083228A1/zh active Application Filing
- 2019-10-21 JP JP2021546433A patent/JP2022508867A/ja active Pending
- 2019-10-21 WO PCT/CN2019/112299 patent/WO2020083225A1/zh active Application Filing
-
2021
- 2021-04-21 IL IL282550A patent/IL282550A/en unknown
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010234195A (ja) * | 2009-03-30 | 2010-10-21 | Kyocera Corp | 放電装置および放電装置に用いられるプラズマ発生体、並びに放電装置を用いた反応装置 |
CN102588050A (zh) * | 2012-02-23 | 2012-07-18 | 庄建中 | 汽车尾气净化器 |
CN203925685U (zh) * | 2014-02-19 | 2014-11-05 | 吕英 | 一种汽车尾气处理系统 |
CN103993934A (zh) * | 2014-03-25 | 2014-08-20 | 张子生 | 柴油机动车尾气净化装置 |
CN204380852U (zh) * | 2014-10-11 | 2015-06-10 | 国家电网公司 | 一种除尘装置 |
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