US20090008598A1 - Method and apparatus for on-site mixing of liquid deicer - Google Patents
Method and apparatus for on-site mixing of liquid deicer Download PDFInfo
- Publication number
- US20090008598A1 US20090008598A1 US12/233,037 US23303708A US2009008598A1 US 20090008598 A1 US20090008598 A1 US 20090008598A1 US 23303708 A US23303708 A US 23303708A US 2009008598 A1 US2009008598 A1 US 2009008598A1
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- US
- United States
- Prior art keywords
- deicer
- precursor
- mixture
- liquid
- vessel
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 238000000034 method Methods 0.000 title claims abstract description 34
- 239000007788 liquid Substances 0.000 title abstract description 104
- 239000002243 precursor Substances 0.000 claims abstract description 41
- 238000006243 chemical reaction Methods 0.000 claims abstract description 23
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 claims abstract description 13
- 235000011056 potassium acetate Nutrition 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims description 30
- 238000005260 corrosion Methods 0.000 claims description 10
- 230000007797 corrosion Effects 0.000 claims description 10
- 239000003112 inhibitor Substances 0.000 claims description 9
- 238000003756 stirring Methods 0.000 claims description 5
- 239000003929 acidic solution Substances 0.000 claims 2
- 239000012670 alkaline solution Substances 0.000 claims 2
- 239000000243 solution Substances 0.000 claims 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract description 21
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract description 21
- 239000004615 ingredient Substances 0.000 abstract description 6
- 230000002378 acidificating effect Effects 0.000 description 27
- 238000012546 transfer Methods 0.000 description 16
- 230000007246 mechanism Effects 0.000 description 15
- 239000002253 acid Substances 0.000 description 11
- 239000007795 chemical reaction product Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- 235000011054 acetic acid Nutrition 0.000 description 6
- 239000003513 alkali Substances 0.000 description 4
- 230000003068 static effect Effects 0.000 description 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000004891 communication Methods 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 230000008014 freezing Effects 0.000 description 2
- 238000007710 freezing Methods 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 239000004280 Sodium formate Substances 0.000 description 1
- 238000010669 acid-base reaction Methods 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- VZTDIZULWFCMLS-UHFFFAOYSA-N ammonium formate Chemical compound [NH4+].[O-]C=O VZTDIZULWFCMLS-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000002238 attenuated effect Effects 0.000 description 1
- XJMWHXZUIGHOBA-UHFFFAOYSA-N azane;propanoic acid Chemical compound N.CCC(O)=O XJMWHXZUIGHOBA-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 235000011167 hydrochloric acid Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000013072 incoming material Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000012705 liquid precursor Substances 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000001508 potassium citrate Substances 0.000 description 1
- 229960002635 potassium citrate Drugs 0.000 description 1
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 description 1
- 235000011082 potassium citrates Nutrition 0.000 description 1
- WFIZEGIEIOHZCP-UHFFFAOYSA-M potassium formate Chemical compound [K+].[O-]C=O WFIZEGIEIOHZCP-UHFFFAOYSA-M 0.000 description 1
- BWILYWWHXDGKQA-UHFFFAOYSA-M potassium propanoate Chemical compound [K+].CCC([O-])=O BWILYWWHXDGKQA-UHFFFAOYSA-M 0.000 description 1
- 239000004331 potassium propionate Substances 0.000 description 1
- 235000010332 potassium propionate Nutrition 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 description 1
- 235000019254 sodium formate Nutrition 0.000 description 1
- JXKPEJDQGNYQSM-UHFFFAOYSA-M sodium propionate Chemical compound [Na+].CCC([O-])=O JXKPEJDQGNYQSM-UHFFFAOYSA-M 0.000 description 1
- 239000004324 sodium propionate Substances 0.000 description 1
- 235000010334 sodium propionate Nutrition 0.000 description 1
- 229960003212 sodium propionate Drugs 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000013022 venting Methods 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F35/00—Accessories for mixers; Auxiliary operations or auxiliary devices; Parts or details of general application
- B01F35/80—Forming a predetermined ratio of the substances to be mixed
- B01F35/83—Forming a predetermined ratio of the substances to be mixed by controlling the ratio of two or more flows, e.g. using flow sensing or flow controlling devices
- B01F35/831—Forming a predetermined ratio of the substances to be mixed by controlling the ratio of two or more flows, e.g. using flow sensing or flow controlling devices using one or more pump or other dispensing mechanisms for feeding the flows in predetermined proportion, e.g. one of the pumps being driven by one of the flows
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/18—Materials not provided for elsewhere for application to surfaces to minimize adherence of ice, mist or water thereto; Thawing or antifreeze materials for application to surfaces
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F25/00—Flow mixers; Mixers for falling materials, e.g. solid particles
- B01F25/40—Static mixers
- B01F25/42—Static mixers in which the mixing is affected by moving the components jointly in changing directions, e.g. in tubes provided with baffles or obstructions
- B01F25/43—Mixing tubes, e.g. wherein the material is moved in a radial or partly reversed direction
- B01F25/431—Straight mixing tubes with baffles or obstructions that do not cause substantial pressure drop; Baffles therefor
- B01F25/4316—Straight mixing tubes with baffles or obstructions that do not cause substantial pressure drop; Baffles therefor the baffles being flat pieces of material, e.g. intermeshing, fixed to the wall or fixed on a central rod
- B01F25/43161—Straight mixing tubes with baffles or obstructions that do not cause substantial pressure drop; Baffles therefor the baffles being flat pieces of material, e.g. intermeshing, fixed to the wall or fixed on a central rod composed of consecutive sections of flat pieces of material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F27/00—Mixers with rotary stirring devices in fixed receptacles; Kneaders
- B01F27/50—Pipe mixers, i.e. mixers wherein the materials to be mixed flow continuously through pipes, e.g. column mixers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F33/00—Other mixers; Mixing plants; Combinations of mixers
- B01F33/50—Movable or transportable mixing devices or plants
- B01F33/502—Vehicle-mounted mixing devices
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/18—Materials not provided for elsewhere for application to surfaces to minimize adherence of ice, mist or water thereto; Thawing or antifreeze materials for application to surfaces
- C09K3/185—Thawing materials
Definitions
- the present invention is directed to apparatuses and methods for making deicing compositions, as well as to deicer compositions made use the apparatuses or methods.
- the invention is directed to apparatuses and methods for making heated deicing compositions on-site at locations where the deicer will be applied, and to such heated deicing compositions.
- Liquid deicer compositions are used for many applications, such as deicing roadways, bridges, machinery, airport runways, and aircraft.
- deicing systems are in place at most modem airports, a need remains for improved deicing equipment and deicers. In particular, a need remains for deicing equipment and methods that improves on existing equipment and methods.
- the present invention is directed to an apparatus and method for forming a heated liquid deicer.
- the apparatus includes two vessels configured and arranged for retaining deicer precursors: one vessel with an acidic liquid and one with an alkaline liquid. These liquids, when combined, undergo an exotherrnic reaction to produce a heated liquid deicer.
- deicer precursors For example, acetic acid and potassium hydroxide can be mixed to produce heated potassium acetate, which is an effective liquid deicer.
- the apparatus generally includes a mixing vessel configured and arranged for the mixing and exothermic reacting of the acidic liquid and the alkaline liquid.
- the mixing vessel has an input for the acidic liquid, an input for the alkaline liquid, and an output for the heated reaction product of the acidic liquid and alkaline liquid.
- This heated reaction product is a heated liquid deicer.
- a liquid transfer mechanism in communication with the first and second vessels is also provided, and this mechanism is configured for the controlled transfer of the acidic liquid and the alkaline liquid into the mixing vessel.
- deicer composition The material formed using the apparatus and method is referred to herein as a deicer composition.
- deicer compositions are used to remove ice from a surface.
- the composition made in accordance with the invention is also suitable for use as an anti-icer that is applied to a surface before ice forms on it.
- the apparatus and method of the invention can also be used to make a composition that is applied before or after ice has formed.
- a “deicer” both such uses of the composition are referred to herein as a “deicer”, unless otherwise noted.
- deicers referred to within this description can be used both to deice a surface or as an anti-icer for preventing ice formation.
- the composition can function as both a deicer and an anti-icer because it can be applied initially as a deicer, but remaining material then functions as an anti-icer after existing ice has been removed.
- FIG. 1 is a simplified drawing of a vehicle on which a system constructed and arranged in accordance with the invention has been installed.
- FIG. 2A is a general schematic diagram of a system constructed and arranged in accordance with a first implementation of the invention.
- FIG. 2B is a general schematic diagram of a system constructed and arranged in accordance with a second implementation of the invention.
- FIG. 3A is a simplified drawing of a first mixing vessel constructed and arranged in accordance with the invention.
- FIG. 3B is a simplified drawing of a second mixing vessel constructed and arranged in accordance with the invention.
- FIG. 3C is a simplified drawing of a Third mixing vessel constructed and arranged in accordance with the invention.
- FIG. 4A is a simplified drawing of a first mixing vessel constructed and arranged in accordance with the invention.
- FIG. 4B is a simplified drawing of a second mixing vessel constructed and arranged in accordance with the invention.
- FIG. 4C is a simplified drawing of a third mixing vessel constructed and arranged in accordance with the invention.
- the present invention is directed to an apparatus and method for preparing and dispensing a liquid deicer.
- the apparatus and method allow deicer ingredients (also referred to as deicer precursors) to be combined in an exothermic reaction to produce a heated deicer. This mixing reaction typically occurs at the location where the deicer will be used.
- deicer ingredients also referred to as deicer precursors
- This mixing reaction typically occurs at the location where the deicer will be used.
- potassium hydroxide and acetic acid can be combined using the apparatus and method to make hot potassium acetate for use as a deicer, such as to deice runways at airports.
- the hot potassium acetate functions primarily as a chemical deicer that depresses the freezing point of water, thereby causing ice to melt at temperatures below 0° C.
- the elevated temperature of the deicer provides additional deicing effect.
- the present invention includes a first vessel configured and arranged for retaining and dispensing an acidic liquid and a second vessel configured and arranged for holding and dispensing an alkaline liquid.
- a third vessel is configured and arranged for the mixing and exothermic reacting of the acidic liquid and the alkaline liquid.
- This mixing vessel has an input for the acidic liquid, an input for the alkaline liquid, and an output for the heated reaction product of the acidic liquid and the alkaline liquid, this reaction product being a liquid deicer.
- the invention includes a liquid transfer mechanism, such as one or more pumps, in communication with the first and second vessels. This liquid transfer mechanism is configured for the controlled transfer of the acidic liquid and the alkaline liquid into the mixing vessel.
- FIG. 1 This system is shown generally in FIG. 1 and more specifically in FIG. 2A .
- the system 10 is shown with a tank 12 containing a deicer precursor (such as potassium hydroxide or acetic acid).
- This tank 12 connects to a mixing vessel 14 .
- Another tank, not shown, containing a different precursor would also connect to mixing vessel 14 .
- the two precursors mix in chamber 14 and then travel on to an optional dispenser 16 that generally includes at least one nozzle 18 used to spray the deicer onto a surface or object that is to be deiced.
- the nozzle is at the end of a hose contained on a spool 19 , which provides greater flexibility in applying deicer to large objects or surfaces.
- the heated deicer formed using the system is pumped up a boom in order to be sprayed on elevated objects.
- First vessel 20 is configured and arranged for retaining and dispensing an acidic liquid and second vessel 22 is configured and arranged for holding and dispensing an alkaline liquid.
- a third vessel 24 is configured and arranged for the mixing and exothermic reacting of the acidic liquid and the alkaline liquid.
- This mixing vessel 24 is connected by a liquid carrying line 26 (such as a hose or pipe) to the first vessel 20 and by liquid carrying line 28 (also a hose or pipe, for example) to second vessel 22 .
- a liquid transfer mechanism consisting of pumps 30 and 32 is used to controllably move liquid deicer precursors from the two vessels 20 , 22 into the mixing vessel 24 .
- This liquid transfer mechanism is configured for the controlled transfer of the acidic liquid and the alkaline liquid into the mixing vessel 24 .
- liquid deicer flows out of the mixing vessel and out a nozzle 31 as spray 33 .
- this liquid moves through a hose 34 , but it will be appreciated that this hose is optional and other ways of dispensing the liquid deicer are appropriate.
- FIG. 2B shows an alternative embodiment of a system for creating a heated deicer.
- This system is similar to the one depicted in FIG. 2A , but contains one pump 27 rather than the two pumps 30 , 32 . Although this system has just one pump, the pump simultaneously pumps the two liquids without mixing them together. Not until the liquids reach the mixing vessel 24 do they come together to react and form the liquid deicer
- FIG, 2 B also shows an additional tank 36 .
- This tank 36 contains a corrosion inhibitor that can be added to the deicer so that the deicer is less corrosive to surfaces and objects on which it is applied.
- FIGS. 2A and 2B represent two acceptable implementations of how an apparatus can be constructed in accordance with the invention.
- various changes, additions, and subtractions can be made from the two depicted apparatuses.
- various nozzle configurations are possible, and some implementations do not even use a nozzle.
- various pressure release mechanisms may be added to the mixing vessels, as well as control systems for regulating the mixing of the two deicer precursors.
- FIGS. 2A and 2B show examples of how the present invention may be practiced, but are not limiting in that regard.
- the mixing vessel can be, and typically is, smaller than the primary chambers containing the unmixed acidic and alkaline liquids.
- the purpose of the mixing vessel is not to retain large volumes of mixed deicer, but rather to provide a temporary location in which the exothermic reaction between the two ingredients can occur, after which the resultant liquid deicer is applied to a surface.
- the mixing vessel or chamber is constructed to allow the highly exothermic acid-base reaction to progress to completion or nearly to completion. It is important that this reaction proceed to completion or near completion before the deicer is dispensed because it is normally not desirable to have non-reacted precursors discharged from the apparatus due to their corrosive natures.
- the mixing vessel is generally constructed in a fashion that allows it to withstand the high temperatures, and also to withstand steam generated during the exothermic reaction. Certain implementations require the mixing vessel to withstand pressures developed by the exothermic reaction, while other implementations provide one or more vents or pressure release valves to release this pressure.
- One way of handling steam generated within the mixing vessel is to permit it to escape or venting through a release valve.
- Another way of handling the steam is to use it to force the mixed deicer through an exit in the mixing vessel. In this manner the steam and vapors can be used to generate pressure. Alternatively, the steam can be partially vented and partially used to force the mixed deicer through the exit.
- the mixing vessel should have a configuration that allows for the acidic and alkaline liquids to be rapidly and safely mixed together.
- Numerous configurations are within the scope of the present invention, including elongate chambers, some of which can be formed of a long, relatively narrow pipe.
- the mixing vessel contains one or more static mixing vanes.
- a stirring means can be used, such as a rotating prop or blade.
- the invention covers numerous implementations in which different vessel configurations are used.
- the vessel can be as simple as the convergence of two pipes carrying deicer precursors into a third pipe that will discharge the deicer onto a surface, or can be relatively complex.
- the vessel comprises a substantially enclosed chamber 40 that has inputs 42 , 44 and an outlet 46 .
- a release vent 48 is also depicted, the release vent configured to permit the escape of excess pressure. When such pressure is released, it typically includes the release of steam along with incidental amounts of liquids. However, in certain circumstances it is possible that larger amounts of liquids will be released, in which case it is desirable that the liquids comprise mixed deicer as opposed to precursor ingredients.
- the vented gas or liquids be discharged away from where persons are likely to be positioned.
- the optional release vent is often positioned at the end of the chamber most distant from the input streams, thereby promoting the thorough reaction of any incidentally discharged materials.
- FIG. 3B An alternative embodiment is shown in FIG. 3B , where a plurality of static fins 48 is positioned within chamber 40 .
- the static fins 50 promote the thorough mixing of the deicer precursors by stirring the procurers together as they pass through the chamber.
- the heat (and sometimes steam) generated by the exothermic reaction of the precursors also helps to promote movement and stirring of the ingredients.
- the acid liquid and alkaline liquid are rapidly mixed together at one junction.
- the reaction is attenuated by slowly mixing the two liquids together.
- FIG. 3C which has a chamber with a single entrance for one liquid (either the acid or the alkaline liquid) plus multiple entrances 54 for the other liquid.
- the apparatus includes a mixing vessel having multiple inputs for the. alkaline liquid.
- the mixing vessel has multiple inputs for acid liquid. This gradual mixing approach is suitable for various implementations, particularly when one of the ingredients is highly concentrated.
- FIGS. 4A , 4 B, and 4 C depict long, narrow mixing chambers.
- Such chambers can be constructed, for example, from segments of stainless steel pipe.
- the chamber of FIG. 4A is long and narrow, but without internal mixing vanes.
- Such implementations are suitable for circumstances where the length of the chamber is long enough to have thorough mixing merely by the turbulence generated within the chamber by movement of the liquids and by the warming of the liquids as a result of the exothermic reaction.
- FIG. 4B a similar chamber 62 is depicted, but this chamber 62 also contains a rotating stirrer 66 to promote mixing.
- FIG. 4C shows yet another implementation with a chamber 64 having multiple mixing vanes 68 . These mixing vanes 68 are constructed so as to stir the liquid as it passes through the chamber, thereby promoting reaction.
- An alternative means for mixing the acid and alkali deicer precursors is by an impingement mechanism that directs streams of the precursors together so that that they adequately react.
- an impingement mechanism that directs streams of the precursors together so that that they adequately react.
- two nozzles can be placed adjacent to one another, one nozzle with an acid and one with an alkali, and the streams from each nozzle are directed toward each other to cause mixing of the precursors to form a heated deicer.
- a vessel or chamber is not necessarily used to mix them, although it is possible to impinge the two liquids within a chamber to promote mixing.
- the invention typically includes a transfer mechanism for moving the acid and alkaline liquids from their storage containers into the mixing vessel or chamber.
- a transfer mechanism for moving the acid and alkaline liquids from their storage containers into the mixing vessel or chamber.
- such transfer mechanism will include one or more pumps.
- gravity fed systems can also be used, as can other systems that can move a regular, metered amount of liquid from one tank into the other.
- the liquid transfer mechanism can comprise a first pump connected to the first vessel and a second pump connected to the second vessel.
- Various acidic liquids are useful with the invention, including, but not limited to, hydrochloric acid, formic acid, adipic acid, sulfuric acid, maleic acid, acetic anhydride, maleic anhydride, propionic acid, lactic acid and acetic acid.
- One particularly desirable acidic liquid is acetic acid.
- various alkaline liquids are useful with the invention, and include but are not limited to sodium hydroxide, calcium hydroxide, magnesium hydroxide, potassium hydroxide, ammonia, calcium oxide, magnesium oxide, calcium hydroxide, and annnonium hydroxide.
- One particularly desirable alkaline liquid comprises potassium hydroxide. Normally from 25 to 75 percent concentrations of each reactant can be used, but concentrations of 100% such as glacial acid in some embodiments are contemplated.
- the deicer produced using the present invention is typically a potassium acetate solution made from the mixing of potassium hydroxide and acetic acid.
- Other deicers that can be produced include, but are not limited to, ammonium acetate, ammonium formate, ammonium propionate, sodium acetate, sodium formate, sodium propionate, potassium formate, potassium propionate, and potassium citrate.
- the acidic and alkaline materials be combined in acid/base equivalents, which is typically equimolar quantities, to promote a complete reaction of both materials.
- An excess of either composition can result in an undesirably corrosive deicer composition.
- the apparatus and method typically include one or more aspects that promotes and ensures that proper amounts of each precursor liquid (the acid and alkali) are added in proper quantities.
- the primary manner in which such control is maintained is typically by having a transfer mechanism that accurately transfers the two (or more) precursors. Thus, when one or more pumps are used they should be accurate and reliable.
- Another aspect of the invention can include a controller for regulating the transfer mechanism, the controller configured to regulate the relative flows of acidic liquid and basic liquid such that the reaction product leaving the mixing vessel has a substantially neutral pH.
- the controller can be configured to regulate the relative flows of acidic liquid and basic liquid such that the reaction product leaving the mixing vessel has a pH substantially equal to the pH of a solution having the complete neutralization of the acidic and basic liquids.
- the controller is configured to regulate the relative flows of acidic liquid and basic liquid such that the reaction product leaving the mixing vessel has a pH from about 4 to about 11.
- the apparatus includes a sensor 70 for determining the concentration of the alkaline liquid, the acidic liquid, or both. Also, in some implementations the apparatus includes a sensor and feed-back loop that shuts the system down when the mixing of the acid and alkali are not complete. For example, a pH feed-back loop may be incorporated into certain implementations of the system. This pH feedback loop measures the pH of the deicer as it exits the apparatus, and the system shuts down when the pH moves outside of desired parameters.
- the apparatus of the invention normally also contains at least one nozzle in liquid communication with the mixing vessel, the nozzle configured to discharge the heated reaction product of the acidic liquid and alkaline liquid.
- the nozzle may include just one hole, or can include a plurality of holes.
- the reaction product is discharged under pressure through this nozzle or nozzles, and the pressure is developed at least in part by the reaction of the acidic liquid and alkaline liquid.
- the deicer is formed from a combination of precursors plus premixed deicer.
- the deicer can include the precursors that are mixed together and then added to pre-mixed deicer. This implementation has the advantage of warming the premixed deicer to a higher temperature, although typically not to the temperature reached by using just the deicer precursor materials.
- corrosion inhibitors are added to the deicer in order to prevent corrosion of objects that are being deiced (such as airport runways) and surrounding objects in the environment (such as iron reinforcements in the concrete).
- suitable corrosion inhibitors are appropriate for use with the present invention, and include phosphates, amines, nitrates, and silicates. These corrosion inhibitors can be used individually or in combination with one another.
- the inhibitors can be pre-added to the vessel containing the acidic liquid, pre-added to the vessel containing the alkaline liquid, or both.
- the corrosion inhibitor may be added to the acid/base mixture from a tank containing the corrosion inhibitor by means of a metering pump.
- Such controls can be accomplished by having a static system that mixes preset amounts of the liquids together based upon their original concentration.
- sensors can be placed in the input flow streams, the output stream, or both to measure the concentration of incoming materials and outgoing materials to assure that a proper mixture is obtained.
- Sensors providing feedback with regard to the mechanical, electrical, thermal, pH, conductivity or other properties of the liquid precursors or the mixed deicer can be included. These sensors function with the control system to ensure that adequate amounts of precursors are safely mixed together properly and fully to make a suitable deicer.
- This deicing system can also be used on bridges or any paved surface that requires deicing. Typically this deicing system is used on a mobile basis, but can also be a stationary system.
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Abstract
An apparatus and method for preparing and dispensing a liquid deicer. The apparatus and method allow deicer ingredients or precursors to be combined in an exothermic reaction to produce a heated deicer at the location where it will be used. In one implementation, potassium hydroxide and acetic acid are combined using the apparatus and method to make hot potassium acetate for use in numerous deicer applications, including deicing of airport runways.
Description
- This application is a divisional of U.S. patent application Ser. No. 11/614,755 filed Dec. 21, 2006, entitled “Method and Apparatus for On-Site Mixing of a Liquid Deicer”, which is a divisional of U.S. patent application Ser. No. 10/302,759 filed Nov. 22, 2002, entitled “Method and Apparatus for On-Site Mixing of Liquid Deicer,” which is incorporated herein by reference.
- The present invention is directed to apparatuses and methods for making deicing compositions, as well as to deicer compositions made use the apparatuses or methods. In particular, the invention is directed to apparatuses and methods for making heated deicing compositions on-site at locations where the deicer will be applied, and to such heated deicing compositions.
- Liquid deicer compositions are used for many applications, such as deicing roadways, bridges, machinery, airport runways, and aircraft. One of the most important criteria for some deicers, in particular those used in airport applications, is that they be non-corrosive because they are used near corrosion sensitive equipment. Today, modem airports in temperate climates usually have deicing programs in place that carefully deice runways. These deicing programs use liquid deicers applied at ambient temperatures, often at or below the freezing temperature of water. Although these deicing systems are in place at most modem airports, a need remains for improved deicing equipment and deicers. In particular, a need remains for deicing equipment and methods that improves on existing equipment and methods.
- The present invention is directed to an apparatus and method for forming a heated liquid deicer. In one implementation of the invention the apparatus includes two vessels configured and arranged for retaining deicer precursors: one vessel with an acidic liquid and one with an alkaline liquid. These liquids, when combined, undergo an exotherrnic reaction to produce a heated liquid deicer. For example, acetic acid and potassium hydroxide can be mixed to produce heated potassium acetate, which is an effective liquid deicer.
- The apparatus generally includes a mixing vessel configured and arranged for the mixing and exothermic reacting of the acidic liquid and the alkaline liquid. The mixing vessel has an input for the acidic liquid, an input for the alkaline liquid, and an output for the heated reaction product of the acidic liquid and alkaline liquid. This heated reaction product is a heated liquid deicer. A liquid transfer mechanism in communication with the first and second vessels is also provided, and this mechanism is configured for the controlled transfer of the acidic liquid and the alkaline liquid into the mixing vessel.
- The material formed using the apparatus and method is referred to herein as a deicer composition. Generally, deicer compositions are used to remove ice from a surface. However, the composition made in accordance with the invention is also suitable for use as an anti-icer that is applied to a surface before ice forms on it. The apparatus and method of the invention can also be used to make a composition that is applied before or after ice has formed. For the sake of simplicity, both such uses of the composition are referred to herein as a “deicer”, unless otherwise noted. Thus, deicers referred to within this description can be used both to deice a surface or as an anti-icer for preventing ice formation. In addition, the composition can function as both a deicer and an anti-icer because it can be applied initially as a deicer, but remaining material then functions as an anti-icer after existing ice has been removed.
- The above summary of the present invention is not intended to describe each 5 discussed embodiment of the present invention. This is the purpose of the detailed description that follows.
- The invention will be more fully explained with reference to the following drawings.
-
FIG. 1 is a simplified drawing of a vehicle on which a system constructed and arranged in accordance with the invention has been installed. -
FIG. 2A is a general schematic diagram of a system constructed and arranged in accordance with a first implementation of the invention. -
FIG. 2B is a general schematic diagram of a system constructed and arranged in accordance with a second implementation of the invention. -
FIG. 3A is a simplified drawing of a first mixing vessel constructed and arranged in accordance with the invention. -
FIG. 3B is a simplified drawing of a second mixing vessel constructed and arranged in accordance with the invention. -
FIG. 3C is a simplified drawing of a Third mixing vessel constructed and arranged in accordance with the invention. -
FIG. 4A is a simplified drawing of a first mixing vessel constructed and arranged in accordance with the invention. -
FIG. 4B is a simplified drawing of a second mixing vessel constructed and arranged in accordance with the invention. -
FIG. 4C is a simplified drawing of a third mixing vessel constructed and arranged in accordance with the invention. - While principles of the invention are amenable to various modifications and alternative forms, specifics thereof have been shown by way of example in the drawings and will be described in detail. It should be understood, however, that the intention is not to limit the invention to the particular embodiments described. On the contrary, the intention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the disclosure and claims.
- The present invention is directed to an apparatus and method for preparing and dispensing a liquid deicer. The apparatus and method allow deicer ingredients (also referred to as deicer precursors) to be combined in an exothermic reaction to produce a heated deicer. This mixing reaction typically occurs at the location where the deicer will be used. For example, potassium hydroxide and acetic acid can be combined using the apparatus and method to make hot potassium acetate for use as a deicer, such as to deice runways at airports. The hot potassium acetate functions primarily as a chemical deicer that depresses the freezing point of water, thereby causing ice to melt at temperatures below 0° C. However, the elevated temperature of the deicer provides additional deicing effect.
- In one implementation, the present invention includes a first vessel configured and arranged for retaining and dispensing an acidic liquid and a second vessel configured and arranged for holding and dispensing an alkaline liquid. A third vessel is configured and arranged for the mixing and exothermic reacting of the acidic liquid and the alkaline liquid. This mixing vessel has an input for the acidic liquid, an input for the alkaline liquid, and an output for the heated reaction product of the acidic liquid and the alkaline liquid, this reaction product being a liquid deicer. In addition, the invention includes a liquid transfer mechanism, such as one or more pumps, in communication with the first and second vessels. This liquid transfer mechanism is configured for the controlled transfer of the acidic liquid and the alkaline liquid into the mixing vessel.
- This system is shown generally in
FIG. 1 and more specifically inFIG. 2A . InFIG. 1 , thesystem 10 is shown with atank 12 containing a deicer precursor (such as potassium hydroxide or acetic acid). Thistank 12 connects to a mixingvessel 14. Another tank, not shown, containing a different precursor would also connect to mixingvessel 14. The two precursors mix inchamber 14 and then travel on to an optional dispenser 16 that generally includes at least onenozzle 18 used to spray the deicer onto a surface or object that is to be deiced. In some implementations the nozzle is at the end of a hose contained on aspool 19, which provides greater flexibility in applying deicer to large objects or surfaces. In certain embodiments the heated deicer formed using the system is pumped up a boom in order to be sprayed on elevated objects. - The various elements of this system are depicted schematically in
FIG. 2A .First vessel 20 is configured and arranged for retaining and dispensing an acidic liquid andsecond vessel 22 is configured and arranged for holding and dispensing an alkaline liquid. Athird vessel 24 is configured and arranged for the mixing and exothermic reacting of the acidic liquid and the alkaline liquid. This mixingvessel 24 is connected by a liquid carrying line 26 (such as a hose or pipe) to thefirst vessel 20 and by liquid carrying line 28 (also a hose or pipe, for example) tosecond vessel 22. A liquid transfer mechanism consisting ofpumps vessels vessel 24. This liquid transfer mechanism is configured for the controlled transfer of the acidic liquid and the alkaline liquid into the mixingvessel 24. After being mixed, liquid deicer flows out of the mixing vessel and out anozzle 31 asspray 33. In the embodiment depicted inFIG. 2A this liquid moves through ahose 34, but it will be appreciated that this hose is optional and other ways of dispensing the liquid deicer are appropriate. -
FIG. 2B shows an alternative embodiment of a system for creating a heated deicer. This system is similar to the one depicted inFIG. 2A , but contains onepump 27 rather than the twopumps vessel 24 do they come together to react and form the liquid deicer FIG, 2B also shows anadditional tank 36. Thistank 36 contains a corrosion inhibitor that can be added to the deicer so that the deicer is less corrosive to surfaces and objects on which it is applied. - The two example apparatuses disclosed in
FIGS. 2A and 2B represent two acceptable implementations of how an apparatus can be constructed in accordance with the invention. However, various changes, additions, and subtractions can be made from the two depicted apparatuses. For example, various nozzle configurations are possible, and some implementations do not even use a nozzle. Also, various pressure release mechanisms may be added to the mixing vessels, as well as control systems for regulating the mixing of the two deicer precursors. Thus,FIGS. 2A and 2B show examples of how the present invention may be practiced, but are not limiting in that regard. - One of the key elements of the present invention is the mixing vessel. The mixing vessel can be, and typically is, smaller than the primary chambers containing the unmixed acidic and alkaline liquids. The purpose of the mixing vessel is not to retain large volumes of mixed deicer, but rather to provide a temporary location in which the exothermic reaction between the two ingredients can occur, after which the resultant liquid deicer is applied to a surface. In most implementations the mixing vessel or chamber is constructed to allow the highly exothermic acid-base reaction to progress to completion or nearly to completion. It is important that this reaction proceed to completion or near completion before the deicer is dispensed because it is normally not desirable to have non-reacted precursors discharged from the apparatus due to their corrosive natures.
- The mixing vessel is generally constructed in a fashion that allows it to withstand the high temperatures, and also to withstand steam generated during the exothermic reaction. Certain implementations require the mixing vessel to withstand pressures developed by the exothermic reaction, while other implementations provide one or more vents or pressure release valves to release this pressure. One way of handling steam generated within the mixing vessel is to permit it to escape or venting through a release valve. Another way of handling the steam is to use it to force the mixed deicer through an exit in the mixing vessel. In this manner the steam and vapors can be used to generate pressure. Alternatively, the steam can be partially vented and partially used to force the mixed deicer through the exit.
- As noted above, the mixing vessel should have a configuration that allows for the acidic and alkaline liquids to be rapidly and safely mixed together. Numerous configurations are within the scope of the present invention, including elongate chambers, some of which can be formed of a long, relatively narrow pipe. In some implementations the mixing vessel contains one or more static mixing vanes. Alternatively, a stirring means can be used, such as a rotating prop or blade.
- The invention covers numerous implementations in which different vessel configurations are used. The vessel can be as simple as the convergence of two pipes carrying deicer precursors into a third pipe that will discharge the deicer onto a surface, or can be relatively complex. In a first embodiment, shown in
FIG. 3A the vessel comprises a substantiallyenclosed chamber 40 that hasinputs outlet 46. Arelease vent 48 is also depicted, the release vent configured to permit the escape of excess pressure. When such pressure is released, it typically includes the release of steam along with incidental amounts of liquids. However, in certain circumstances it is possible that larger amounts of liquids will be released, in which case it is desirable that the liquids comprise mixed deicer as opposed to precursor ingredients. When a release vent is used it is preferable that the vented gas or liquids be discharged away from where persons are likely to be positioned. Thus the optional release vent is often positioned at the end of the chamber most distant from the input streams, thereby promoting the thorough reaction of any incidentally discharged materials. - An alternative embodiment is shown in
FIG. 3B , where a plurality ofstatic fins 48 is positioned withinchamber 40. Thestatic fins 50 promote the thorough mixing of the deicer precursors by stirring the procurers together as they pass through the chamber. The heat (and sometimes steam) generated by the exothermic reaction of the precursors also helps to promote movement and stirring of the ingredients. - In many implementations of the invention the acid liquid and alkaline liquid are rapidly mixed together at one junction. However, in other implementations the reaction is attenuated by slowly mixing the two liquids together. An example of how such gradual mixing can be accomplished is shown in
FIG. 3C , which has a chamber with a single entrance for one liquid (either the acid or the alkaline liquid) plusmultiple entrances 54 for the other liquid. Thus, in some implementations the apparatus includes a mixing vessel having multiple inputs for the. alkaline liquid. In other implementations the mixing vessel has multiple inputs for acid liquid. This gradual mixing approach is suitable for various implementations, particularly when one of the ingredients is highly concentrated. - Additional implementations are shown in
FIGS. 4A , 4B, and 4C, which depict long, narrow mixing chambers. Such chambers can be constructed, for example, from segments of stainless steel pipe. The chamber ofFIG. 4A is long and narrow, but without internal mixing vanes. Such implementations are suitable for circumstances where the length of the chamber is long enough to have thorough mixing merely by the turbulence generated within the chamber by movement of the liquids and by the warming of the liquids as a result of the exothermic reaction. InFIG. 4B asimilar chamber 62 is depicted, but thischamber 62 also contains arotating stirrer 66 to promote mixing.FIG. 4C shows yet another implementation with achamber 64 having multiple mixing vanes 68. These mixing vanes 68 are constructed so as to stir the liquid as it passes through the chamber, thereby promoting reaction. - An alternative means for mixing the acid and alkali deicer precursors is by an impingement mechanism that directs streams of the precursors together so that that they adequately react. For example, two nozzles can be placed adjacent to one another, one nozzle with an acid and one with an alkali, and the streams from each nozzle are directed toward each other to cause mixing of the precursors to form a heated deicer. In such implementations a vessel or chamber is not necessarily used to mix them, although it is possible to impinge the two liquids within a chamber to promote mixing.
- As noted above, the invention typically includes a transfer mechanism for moving the acid and alkaline liquids from their storage containers into the mixing vessel or chamber. In general such transfer mechanism will include one or more pumps. However, gravity fed systems can also be used, as can other systems that can move a regular, metered amount of liquid from one tank into the other. The liquid transfer mechanism can comprise a first pump connected to the first vessel and a second pump connected to the second vessel.
- Various acidic liquids are useful with the invention, including, but not limited to, hydrochloric acid, formic acid, adipic acid, sulfuric acid, maleic acid, acetic anhydride, maleic anhydride, propionic acid, lactic acid and acetic acid. One particularly desirable acidic liquid is acetic acid. Similarly, various alkaline liquids are useful with the invention, and include but are not limited to sodium hydroxide, calcium hydroxide, magnesium hydroxide, potassium hydroxide, ammonia, calcium oxide, magnesium oxide, calcium hydroxide, and annnonium hydroxide. One particularly desirable alkaline liquid comprises potassium hydroxide. Normally from 25 to 75 percent concentrations of each reactant can be used, but concentrations of 100% such as glacial acid in some embodiments are contemplated.
- The deicer produced using the present invention is typically a potassium acetate solution made from the mixing of potassium hydroxide and acetic acid. Other deicers that can be produced include, but are not limited to, ammonium acetate, ammonium formate, ammonium propionate, sodium acetate, sodium formate, sodium propionate, potassium formate, potassium propionate, and potassium citrate.
- In most implementations it is necessary that the acidic and alkaline materials be combined in acid/base equivalents, which is typically equimolar quantities, to promote a complete reaction of both materials. An excess of either composition can result in an undesirably corrosive deicer composition. The apparatus and method typically include one or more aspects that promotes and ensures that proper amounts of each precursor liquid (the acid and alkali) are added in proper quantities. The primary manner in which such control is maintained is typically by having a transfer mechanism that accurately transfers the two (or more) precursors. Thus, when one or more pumps are used they should be accurate and reliable. It is desirable in some implementations to have a single pump mechanism transfer both the acidic liquid and the alkaline liquid, such as by having a single shaft drive two piston pumps, one corresponding to each liquid. Having a single pump mechanism is advantageous because it assures that the two liquids will be pumped simultaneously. This avoids inadvertent transfer of one liquid while the other liquid is not being transferred.
- Another aspect of the invention can include a controller for regulating the transfer mechanism, the controller configured to regulate the relative flows of acidic liquid and basic liquid such that the reaction product leaving the mixing vessel has a substantially neutral pH. Alternatively, the controller can be configured to regulate the relative flows of acidic liquid and basic liquid such that the reaction product leaving the mixing vessel has a pH substantially equal to the pH of a solution having the complete neutralization of the acidic and basic liquids. In yet another implementation the controller is configured to regulate the relative flows of acidic liquid and basic liquid such that the reaction product leaving the mixing vessel has a pH from about 4 to about 11.
- In some such implementations the apparatus includes a
sensor 70 for determining the concentration of the alkaline liquid, the acidic liquid, or both. Also, in some implementations the apparatus includes a sensor and feed-back loop that shuts the system down when the mixing of the acid and alkali are not complete. For example, a pH feed-back loop may be incorporated into certain implementations of the system. This pH feedback loop measures the pH of the deicer as it exits the apparatus, and the system shuts down when the pH moves outside of desired parameters. - The apparatus of the invention normally also contains at least one nozzle in liquid communication with the mixing vessel, the nozzle configured to discharge the heated reaction product of the acidic liquid and alkaline liquid. The nozzle may include just one hole, or can include a plurality of holes. In most implementations the reaction product is discharged under pressure through this nozzle or nozzles, and the pressure is developed at least in part by the reaction of the acidic liquid and alkaline liquid.
- In some implementations of the invention the deicer is formed from a combination of precursors plus premixed deicer. For example, the deicer can include the precursors that are mixed together and then added to pre-mixed deicer. This implementation has the advantage of warming the premixed deicer to a higher temperature, although typically not to the temperature reached by using just the deicer precursor materials.
- In certain implementations corrosion inhibitors are added to the deicer in order to prevent corrosion of objects that are being deiced (such as airport runways) and surrounding objects in the environment (such as iron reinforcements in the concrete). Numerous suitable corrosion inhibitors are appropriate for use with the present invention, and include phosphates, amines, nitrates, and silicates. These corrosion inhibitors can be used individually or in combination with one another. The inhibitors can be pre-added to the vessel containing the acidic liquid, pre-added to the vessel containing the alkaline liquid, or both. Alternatively, the corrosion inhibitor may be added to the acid/base mixture from a tank containing the corrosion inhibitor by means of a metering pump.
- It is typically important to control the amount of each of the liquids being mixed. Such controls can be accomplished by having a static system that mixes preset amounts of the liquids together based upon their original concentration. Alternatively, sensors can be placed in the input flow streams, the output stream, or both to measure the concentration of incoming materials and outgoing materials to assure that a proper mixture is obtained. Sensors providing feedback with regard to the mechanical, electrical, thermal, pH, conductivity or other properties of the liquid precursors or the mixed deicer can be included. These sensors function with the control system to ensure that adequate amounts of precursors are safely mixed together properly and fully to make a suitable deicer.
- This deicing system can also be used on bridges or any paved surface that requires deicing. Typically this deicing system is used on a mobile basis, but can also be a stationary system.
- The present invention may be embodied in other specific forms without departing from its spirit or essential characteristics. The described embodiments are to be considered in all respects only as illustrative and not restrictive. The scope of the invention is, therefore, indicated by the appended claims rather than by the foregoing description.
Claims (16)
1. A method of deicing a surface, comprising:
mixing, in a vessel, a first deicer precursor and a second deicer precursor to create a deicer mixture;
responsive to the mixing of the first and second deicer precursors, permitting an exothermic reaction of the first deicer precursor and the second deicer precursor; and
distributing the deicer mixture on a surface during the exothermic reaction.
2. The method of claim 1 , wherein distributing occurs upon completion of the exothermic reaction.
3. The method of claim 1 , wherein the mixing further includes adding a metered amount of the first deicer precursor to a metered amount of the second deicer precursor.
4. The method of claim 1 , wherein the first deicer precursor is an acidic solution and the second deicer precursor is an alkaline solution.
5. The method of claim 1 , wherein the deicer mixture is a potassium acetate solution.
6. The method of claim 1 , further including transferring the deicer mixture from the vessel to a dispenser prior to distributing the deicer mixture on the surface.
7. The method of claim 1 , further including adding a corrosion inhibitor to the deicer mixture.
8. The method of claim 1 , further including stirring the first deicer precursor and the second deicer precursor in the vessel to promote the exothermic reaction.
9. A method of deicing a surface, comprising:
receiving, at one inlet location of a vessel, a first deicer precursor;
receiving, at a plurality of inlet locations of the vessel, a second deicer precursor;
mixing the first and second deicer precursors resulting in a deicer mixture and causing an exothermic reaction; and
distributing the deicer mixture onto a surface during the exothermic reaction.
10. The method of claim 9 , wherein distributing the deicer mixture occurs upon completion of the exothermic reaction.
11. The method of claim 9 , further comprising transferring the deicer mixture from the vessel to a dispenser prior to distributing the deicer mixture onto the surface.
12. The method of claim 11 , wherein transferring further includes forcing the deicer mixture to exit the vessel using steam generated during the exothermic reaction.
13. The method of claim 9 , wherein the first deicer precursor is an acidic solution and the second deicer precursor is an alkaline solution.
14. The method of claim 9 , wherein the deicer mixture is a potassium acetate solution.
15. The method of claim 9 , further including adding a corrosion inhibitor to the deicer mixture.
16. The method of claim 9 , wherein receiving the first deicer precursor and the second deicer precursor includes controlling the amount of the first and second deicer precursor.
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US12/233,037 US20090008598A1 (en) | 2002-11-22 | 2008-09-18 | Method and apparatus for on-site mixing of liquid deicer |
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US12/233,037 Abandoned US20090008598A1 (en) | 2002-11-22 | 2008-09-18 | Method and apparatus for on-site mixing of liquid deicer |
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US5064551A (en) * | 1988-12-20 | 1991-11-12 | Bp Chemicals Limited | Deicing compositions |
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US5238592A (en) * | 1990-11-02 | 1993-08-24 | Hoechst Aktiengesellschaft | Liquid de-icing agent based on acetates and process for melting snow and ice on traffic surfaces with the aid of this agent |
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2002
- 2002-11-22 US US10/302,759 patent/US7168844B2/en not_active Expired - Lifetime
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- 2003-11-21 EP EP03786956A patent/EP1563031A1/en not_active Withdrawn
- 2003-11-21 JP JP2004555538A patent/JP2006507397A/en not_active Withdrawn
- 2003-11-21 WO PCT/US2003/037261 patent/WO2004048494A1/en active Application Filing
- 2003-11-21 AU AU2003295752A patent/AU2003295752A1/en not_active Abandoned
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2006
- 2006-12-21 US US11/614,660 patent/US7461969B2/en not_active Expired - Lifetime
- 2006-12-21 US US11/614,746 patent/US7461971B2/en not_active Expired - Fee Related
- 2006-12-21 US US11/614,755 patent/US7438827B2/en not_active Expired - Fee Related
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US549682A (en) * | 1895-11-12 | Ignacio panama | ||
US2716068A (en) * | 1952-10-21 | 1955-08-23 | Jacob M Fain | De-icing and freeze depressant composition |
US3502304A (en) * | 1965-11-26 | 1970-03-24 | Otto Pfrengle | Process and apparatus for producing agglomerates |
US3776775A (en) * | 1971-12-14 | 1973-12-04 | Aeroseal Corp | Removal of ice by a self-heating mixture |
US4191348A (en) * | 1977-11-10 | 1980-03-04 | Holwerda-Huizenga Co. | Deicing system |
US4474310A (en) * | 1981-05-02 | 1984-10-02 | Bayer Aktiengesellschaft | Apparatus for producing a reaction mixture |
US4474476A (en) * | 1982-08-05 | 1984-10-02 | Jack Thomsen | Chemical printing liquid method and system |
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US5362150A (en) * | 1992-12-08 | 1994-11-08 | Hughes Aircraft Company | Fluid mixer |
US5387359A (en) * | 1992-12-17 | 1995-02-07 | Hoechst Aktiengesellschaft | Alkaline earth metal potassium acetate, a process for its preparation and its use |
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US6540934B2 (en) * | 2001-07-13 | 2003-04-01 | Metss Corporation | Corrosion inhibited runway deicing fluid |
US6596189B1 (en) * | 2002-02-01 | 2003-07-22 | General Atomics International Services Corporation | Aircraft runway deicing composition |
US6623657B1 (en) * | 2002-04-18 | 2003-09-23 | Board Of Trustees Of Michigan State University | Water-activated, exothermic chemical deicing formulations |
US7168844B2 (en) * | 2002-11-22 | 2007-01-30 | Cargill, Inc. | Method and apparatus for on-site mixing of liquid deicer |
US7438827B2 (en) * | 2002-11-22 | 2008-10-21 | Cargill, Incorporated | Method and apparatus for on-site mixing of liquid deicer |
US7461971B2 (en) * | 2002-11-22 | 2008-12-09 | Cargill, Incorporated | Method and apparatus for on-site mixing of liquid deicer |
US7461969B2 (en) * | 2002-11-22 | 2008-12-09 | Cargill, Incorporated | Method and apparatus for on-site mixing of liquid deicer |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10544340B2 (en) | 2011-10-20 | 2020-01-28 | Henderson Products, Inc. | Brine generation system |
US10766010B2 (en) | 2011-10-20 | 2020-09-08 | Henderson Products, Inc. | High throughput brine generating system |
Also Published As
Publication number | Publication date |
---|---|
WO2004048494A1 (en) | 2004-06-10 |
US7438827B2 (en) | 2008-10-21 |
US20070176138A1 (en) | 2007-08-02 |
AU2003295752A1 (en) | 2004-06-18 |
WO2004048494A9 (en) | 2004-07-15 |
US20070177456A1 (en) | 2007-08-02 |
CA2505187A1 (en) | 2004-06-10 |
US7168844B2 (en) | 2007-01-30 |
US20040129829A1 (en) | 2004-07-08 |
CA2505187C (en) | 2011-04-26 |
US7461969B2 (en) | 2008-12-09 |
EP1563031A1 (en) | 2005-08-17 |
JP2006507397A (en) | 2006-03-02 |
US20070148359A1 (en) | 2007-06-28 |
US7461971B2 (en) | 2008-12-09 |
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Legal Events
Date | Code | Title | Description |
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STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |