WO2009104813A1 - Method of converting solar heat energy - Google Patents
Method of converting solar heat energy Download PDFInfo
- Publication number
- WO2009104813A1 WO2009104813A1 PCT/JP2009/053613 JP2009053613W WO2009104813A1 WO 2009104813 A1 WO2009104813 A1 WO 2009104813A1 JP 2009053613 W JP2009053613 W JP 2009053613W WO 2009104813 A1 WO2009104813 A1 WO 2009104813A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- energy
- ammonia
- solar thermal
- thermal energy
- water
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 117
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims abstract description 266
- 229910021529 ammonia Inorganic materials 0.000 claims abstract description 133
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 99
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 72
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 47
- 230000005855 radiation Effects 0.000 claims abstract description 10
- 238000006243 chemical reaction Methods 0.000 claims description 71
- 239000001257 hydrogen Substances 0.000 claims description 52
- 229910052739 hydrogen Inorganic materials 0.000 claims description 52
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 48
- 238000012546 transfer Methods 0.000 claims description 28
- 238000003786 synthesis reaction Methods 0.000 claims description 25
- 230000015572 biosynthetic process Effects 0.000 claims description 23
- 238000002485 combustion reaction Methods 0.000 claims description 17
- 239000000446 fuel Substances 0.000 claims description 14
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 12
- 239000001301 oxygen Substances 0.000 claims description 12
- 229910052760 oxygen Inorganic materials 0.000 claims description 12
- 230000002194 synthesizing effect Effects 0.000 claims description 10
- 238000000926 separation method Methods 0.000 claims description 6
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 36
- 238000004146 energy storage Methods 0.000 description 20
- 239000000126 substance Substances 0.000 description 20
- 229910002092 carbon dioxide Inorganic materials 0.000 description 18
- 239000001569 carbon dioxide Substances 0.000 description 18
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 16
- 238000003860 storage Methods 0.000 description 12
- 241000196324 Embryophyta Species 0.000 description 10
- 238000010586 diagram Methods 0.000 description 7
- 239000002803 fossil fuel Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 239000003345 natural gas Substances 0.000 description 7
- 239000003245 coal Substances 0.000 description 6
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 5
- 229910002091 carbon monoxide Inorganic materials 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 238000010276 construction Methods 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 238000010792 warming Methods 0.000 description 4
- 239000002028 Biomass Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000002551 biofuel Substances 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 230000005611 electricity Effects 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 239000003502 gasoline Substances 0.000 description 3
- 239000003915 liquefied petroleum gas Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000010248 power generation Methods 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 238000005868 electrolysis reaction Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- SYHGEUNFJIGTRX-UHFFFAOYSA-N methylenedioxypyrovalerone Chemical compound C=1C=C2OCOC2=CC=1C(=O)C(CCC)N1CCCC1 SYHGEUNFJIGTRX-UHFFFAOYSA-N 0.000 description 2
- 239000003507 refrigerant Substances 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- 244000062793 Sorghum vulgare Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- OLBVUFHMDRJKTK-UHFFFAOYSA-N [N].[O] Chemical compound [N].[O] OLBVUFHMDRJKTK-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000005431 greenhouse gas Substances 0.000 description 1
- 238000005338 heat storage Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000002973 irritant agent Substances 0.000 description 1
- 231100000636 lethal dose Toxicity 0.000 description 1
- 229910001416 lithium ion Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- -1 molten metal sodium Chemical class 0.000 description 1
- 239000000618 nitrogen fertilizer Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000005381 potential energy Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000002901 radioactive waste Substances 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 210000002345 respiratory system Anatomy 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical class S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 description 1
- 229910052815 sulfur oxide Inorganic materials 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 239000002918 waste heat Substances 0.000 description 1
- 235000020681 well water Nutrition 0.000 description 1
- 239000002349 well water Substances 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02B—INTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
- F02B43/00—Engines characterised by operating on gaseous fuels; Plants including such engines
- F02B43/10—Engines or plants characterised by use of other specific gases, e.g. acetylene, oxyhydrogen
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
- C01B3/02—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
- C01B3/04—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by decomposition of inorganic compounds, e.g. ammonia
- C01B3/042—Decomposition of water
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B21/00—Nitrogen; Compounds thereof
- C01B21/02—Preparation of nitrogen
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01C—AMMONIA; CYANOGEN; COMPOUNDS THEREOF
- C01C1/00—Ammonia; Compounds thereof
- C01C1/02—Preparation, purification or separation of ammonia
- C01C1/04—Preparation of ammonia by synthesis in the gas phase
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01C—AMMONIA; CYANOGEN; COMPOUNDS THEREOF
- C01C1/00—Ammonia; Compounds thereof
- C01C1/02—Preparation, purification or separation of ammonia
- C01C1/04—Preparation of ammonia by synthesis in the gas phase
- C01C1/0405—Preparation of ammonia by synthesis in the gas phase from N2 and H2 in presence of a catalyst
- C01C1/0488—Processes integrated with preparations of other compounds, e.g. methanol, urea or with processes for power generation
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24S—SOLAR HEAT COLLECTORS; SOLAR HEAT SYSTEMS
- F24S20/00—Solar heat collectors specially adapted for particular uses or environments
- F24S20/20—Solar heat collectors for receiving concentrated solar energy, e.g. receivers for solar power plants
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24S—SOLAR HEAT COLLECTORS; SOLAR HEAT SYSTEMS
- F24S23/00—Arrangements for concentrating solar-rays for solar heat collectors
- F24S23/70—Arrangements for concentrating solar-rays for solar heat collectors with reflectors
- F24S2023/87—Reflectors layout
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24S—SOLAR HEAT COLLECTORS; SOLAR HEAT SYSTEMS
- F24S23/00—Arrangements for concentrating solar-rays for solar heat collectors
- F24S23/70—Arrangements for concentrating solar-rays for solar heat collectors with reflectors
- F24S23/71—Arrangements for concentrating solar-rays for solar heat collectors with reflectors with parabolic reflective surfaces
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24S—SOLAR HEAT COLLECTORS; SOLAR HEAT SYSTEMS
- F24S23/00—Arrangements for concentrating solar-rays for solar heat collectors
- F24S23/70—Arrangements for concentrating solar-rays for solar heat collectors with reflectors
- F24S23/74—Arrangements for concentrating solar-rays for solar heat collectors with reflectors with trough-shaped or cylindro-parabolic reflective surfaces
-
- 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
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/40—Solar thermal energy, e.g. solar towers
- Y02E10/46—Conversion of thermal power into mechanical power, e.g. Rankine, Stirling or solar thermal engines
-
- 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
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/36—Hydrogen production from non-carbon containing sources, e.g. by water electrolysis
-
- 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
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
-
- 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
- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T10/00—Road transport of goods or passengers
- Y02T10/10—Internal combustion engine [ICE] based vehicles
- Y02T10/30—Use of alternative fuels, e.g. biofuels
Definitions
- coal energy, biomass energy, nuclear energy, and natural energy such as wind energy and solar energy are being considered as alternative energy alternatives to fossil fuel energy such as oil and natural gas.
- JP2009 / 053613 When using coal energy as an alternative energy, JP2009 / 053613 It is considered that a large amount of carbon dioxide is released by firing. For this, it has been proposed to capture carbon dioxide during combustion and store it underground, and many studies have been carried out, but there is still uncertainty about long-term stable storage. There are also uneven locations suitable for storage. In addition, it may be a problem that a lot of cost is required to collect, transport, and throw carbon dioxide into the ground. Furthermore, the combustion of coal, sulfur oxides (so x), also considered to be a problem that is likely to cause environmental problems due to occurrence of such smoke.
- enormous energy is required for the production and concentration of ethanol from plants, which may be disadvantageous in terms of energy efficiency.
- corn, soybeans, sugar millet, etc. are used as raw materials for biofuels, these will naturally also be used as food and feed, which will increase the price of food and feed. . Therefore, biomass energy cannot be considered as a substantial energy source outside of special regions such as Brazil.
- nuclear energy as an alternative energy has not been found to be a sufficient solution for the treatment of radioactive waste from nuclear power plants, and there are also many dissents based on fear of proliferation. From that, we can not expect great progress globally. Rather, the use of nuclear energy as an alternative energy is expected to decrease over the long term due to an increase in the number of decommissioned nuclear reactors.
- wind energy is a strong alternative energy candidate, but it is not enough.
- Solar energy is considered to be the most stable and abundant natural energy as alternative energy.
- a vast desert spreads out and the solar energy that falls here can be said to be inexhaustible.
- energy of as much as 7,00 GW can be obtained.
- using only a few percent of the Arabian Peninsula and the deserts of North Africa can cover all the energy used by all centuries.
- solar energy is directly generated by solar cells, or 2009/053613 It is converted into electric power as secondary energy indirectly by a steam turbine, etc., and it is made convenient for its use and transportation.
- the energy transfer problem can be solved in principle because electric energy can be transferred through the transmission line.
- a plant that obtains electric energy from solar energy is installed in a desert area rich in solar energy, it is necessary to construct and maintain a new high-capacity transmission line, which is difficult. Many.
- the present invention solves the problems related to the storage and transfer of solar energy, thereby making it possible to use solar energy all over the world, and to solve the problem of the generation of carbon dioxide, a greenhouse gas, and the problem of drought of oil. It is intended to be resolved.
- ammonia is synthesized from air and water using only the acquired solar thermal energy as an energy source
- the ammonia is transferred from the first area to the second area, and the ammonia is generated in the second area so as to generate nitrogen and water.
- 2009/053613 A method characterized by having a process of obtaining driving energy by burning.
- the step of synthesizing the ammonia includes
- step (2) Utilizing another part of the acquired solar thermal energy, causing a reaction to synthesize ammonia from nitrogen and hydrogen obtained in step (1),
- the synthesized ammonia is used as a fuel to obtain at least a part of the electric power, power and Z or heat necessary for carrying out the synthesis step, (A1) to (A6) The method in any one of.
- step (1) The method according to (A 8), wherein at least a part of the lug is obtained by a parabolic dish type concentrator and / or a solar tower type concentrator.
- step (1) The method according to (A 6) or (A 7), wherein in step (1), the electric power is used as a heat source to cause a reaction to generate hydrogen from water.
- step (1) water is electrolyzed with the electric power to cause a reaction to generate hydrogen from water.
- (A 1 2) The method according to any one of (A 1 0) or (A l 1), wherein the solar thermal energy is acquired by a parabolic trough concentrator.
- step (2) ammonia is synthesized from nitrogen and hydrogen using the obtained solar thermal energy directly as a heat source and Z or as a power source, (A 5) to (A 1 2) The method described in any one of the items.
- step (1) the obtained solar thermal energy is directly used as a heat source to cause a reaction to generate hydrogen from water; the solar thermal energy used as a heat source in step (1) is reduced
- part (2) the obtained solar thermal energy is directly used as a heat source and / or as a power source in the step (2).
- ammonia is synthesized from air and water using only the acquired solar thermal energy as an energy source
- a method comprising the step of obtaining driving energy by burning the ammonia so as to generate nitrogen and water in the second region.
- the solar thermal energy acquisition means of the first region collects sunlight and acquires solar thermal energy
- Ammonia synthesis means in the first region synthesizes ammonia from air and water using only the acquired solar heat energy as an energy source
- the ammonia is liquefied
- An ammonia transfer means for transferring the liquefied ammonia from the first region to the second region
- the driving energy generating means in the second region comprises the step of obtaining the driving energy by burning the ammonia so as to generate nitrogen and water.
- step (c) using another part of the acquired solar thermal energy to cause a reaction to synthesize ammonia from nitrogen and hydrogen obtained in step (b);
- step (B 2) Using the solar thermal energy acquired in step (a), obtain at least a part of the electric power and / or power necessary for the implementation of this method.
- (B 3) Use the synthesized ammonia as fuel to obtain at least part of the power, power and / or heat required to perform this method. 3 The method according to (B 1) or (B 2).
- step (b) the solar heat energy obtained in the step (a) is directly used as a heat source to carry out a reaction for generating hydrogen from water (B 1) to (B 4 The method according to any one of the paragraphs).
- At least a part of the solar heat energy used as a heat source in the step (b) is obtained by a parapoly dish type concentrator and Z or a solar evening type concentrator. 5) The method described in the paragraph.
- step (B 7) The method according to (B 2) or (B 3), wherein in step (b), a reaction for generating hydrogen from water is performed using the electric power as a heat source.
- step (B 8) The method according to (B 2) or (B 3), wherein in step (b), water is electrolyzed with the electric power to cause a reaction to generate hydrogen from water.
- step (B 9) The method according to any one of (B 7) or (B 8), wherein, in step (a), the solar thermal energy is acquired by a parapoly trough-type concentrator.
- step (c) ammonia is synthesized from nitrogen and hydrogen using the solar heat energy obtained in step (a) directly as a heat source and Z or as a power source.
- step (B 9) ammonia is synthesized from nitrogen and hydrogen using the solar heat energy obtained in step (a) directly as a heat source and Z or as a power source.
- step (B 1 2) the solar heat energy obtained in step (a) is directly used as a heat source to cause a reaction to generate hydrogen from water; used as a heat source in step (b) At least a part of the solar heat energy is obtained with a parapoly dish type concentrator and a Z or solar tower type concentrator; in step (c), the solar thermal energy obtained in step (a) is directly obtained. And a reaction to synthesize ammonia from nitrogen and hydrogen as a heat source and / or as a power source; and the solar heat energy used as a heat source in step (c) The method according to any one of (B1) to (B4), which is obtained by an apparatus.
- FIG. 1 is a diagram for explaining an example of the conversion system 1.
- FIG. 2 is a diagram for explaining an example of the conversion system 2.
- FIG. 3 is a diagram for explaining the energy flow of the conversion system 1.
- FIG. 4 is a diagram showing an outline of a parapoly dish type condensing device.
- FIG. 5 is a diagram showing an outline of a solar tower type condensing device.
- FIG. 6 is a diagram showing an outline of a parapoly trough-type concentrating device.
- FIG. 7 is a diagram showing an example of equipment for implementing a solar thermal energy storage method. BEST MODE FOR CARRYING OUT THE INVENTION
- ammonia is considered to be a useful candidate.
- Ammonia is a strongly irritating gas, and it is a deleterious substance that damages the respiratory system when inhaling high-concentration gas, but due to its strong odor, the lethal dose is less than 1/1, 0 0 0 or less Humans can detect leaks from around 5 ppm, and there are very few accidents in the actual market.
- ammonia is used as a refrigerant for refrigeration equipment such as fish boats along with chlorofluorocarbons.
- a fatal accident at the time of leakage of ammonia is 1/1 0 Degree. Explosive disasters during the transfer of ammonia are less than 1/5 of gasoline and liquefied petroleum gas (LPG).
- ammonia is considered to be sufficiently socially acceptable.
- T / JP2009 / 053613 The physical properties of ammonia are close to those of LPG, easily liquefy at about 8 atmospheres at room temperature, and have a sufficient track record for storage and transfer, and are not a particular problem.
- ammonia is defined as a non-flammable substance, and it is difficult to ignite, and even if ignited, the burning rate is slow and the flammable range is narrow, so its handling is not considered to be a particular problem.
- the energy density of ammonia is about half that of gasoline and almost the same as methanol, but the calorific value in theoretical mixing is higher than that of gasoline, and it can be applied to a moving body as a fuel. Furthermore, it can be sent to a thermal power plant in a remote area by a tanker or the like and burned instead of natural gas or coal. In this case, the efficiency is theoretically considered to exceed that of natural gas or coal.
- the conversion system 1 condenses sunlight 20 0 to produce solar thermal energy, solar thermal energy acquisition means 10, and ammonia synthesis means 20 0 to synthesize ammonia from water and air using solar thermal energy For details, see Solar Energy Storage Method below.
- the solar heat acquisition means 10 and the ammonia synthesis means 20 are arranged in the first area 3, and the drive energy generation means 40 is arranged in the second area 5 that is geographically different from the first area 3. .
- the ammonia synthesis means 20 uses solar heat energy as reaction heat and converts ammonia (NH 3 ) and oxygen ( ⁇ 2 ) from nitrogen (N 2 ) and water (H 2 0) contained in the air. Generate.
- the produced ammonia is optionally liquefied and transferred from the first region 3 to the second region 5 as fuel by the ammonia transfer means 30.
- ammonia is burned by the driving energy generation means 4 0 so as to generate nitrogen and water, and driving energy 1 2 40 and thermal energy 2 5 0 are generated.
- Nitrogen and water are non-polluting substances that are abundant in the atmosphere. Therefore, nitrogen and water generated by combustion are released into the atmosphere and circulate according to convection existing in nature, and can be used again as raw materials for ammonia synthesis means 20 in the first region 3. become.
- the conversion system 1 has an energy balance of driving energy 2 4 0 and thermal energy 2 5 0 with sunlight 2 0 0 as input, while nitrogen + water-ammonia + oxygen (ammonia synthesis), It has a material balance of the circulation loop of ammonia + oxygen-nitrogen + water (ammonia combustion). And all the processes of the conversion system 1 do not require chemical substances containing carbon atoms, and therefore do not emit any carbon dioxide (C 0 2 ).
- the conversion system 1 uses the ammonia generated using air and water as a solar thermal energy transfer material. Solar thermal energy acquired in Region 3 in 1 can be used as driving energy in Region 5 in the second. In addition, since the conversion system 1 converts energy by circulating chemical substances that do not contain carbon atoms (water, nitrogen in the air, ammonia), it does not emit carbon dioxide at any step in the system.
- the solar heat acquisition means 10 is preferably located in an area with a large amount of sunlight, so the first area should have a higher solar radiation than the second area that uses drive energy. .
- the ammonia synthesizing means 20 also discharges oxygen. Oxygen is a valuable substance for the manufacture of chemical products, so oxygen utilization facilities may be established in the first area.
- the ammonia synthesis means 20 is composed of an ammonia synthesis brand 22, an ammonia liquefaction device 24 that liquefies compressed ammonia with cooling water, and lowers the temperature of the liquefied ammonia by the expanded self-refrigerant.
- Power generation plant that generates power from steam turbines that use steam generated or gas turbines that use ammonia combustion (including those combined with steam turbines) 25, liquefied ammonia shipping facilities 26, cooling not shown Includes water cooling towers, water treatment equipment that purifies water from well water, seawater, etc.
- the ammonia transfer means 30 is carried out by a liquefied ammonia ship 3 2 for on-board transfer, or tank lorry 3 4 or pipeline 3 6 for land transfer.
- ammonia is received by the ammonia receiving facility 42, or ammonia is directly transferred to the drive energy generating means 40.
- Drive energy generating means 4 0 gas turbine, Automobiles, etc.
- the conversion system 2 uses the ammonia generated using air and water as a solar thermal energy transfer material, so that the solar thermal energy acquired in the first region 3 can be driven in the second region 5. It can be used as energy.
- the conversion system 2 converts energy by circulation of chemical substances without carbon atoms (water, nitrogen in the air, ammonia), the solar heat acquisition means 10 and ammonia synthesis means 20 in the first region, Carbon dioxide is not emitted in the driving energy generation means 40 in the second region.
- Sunlight 20 0 is converted into solar heat energy 2 10 through solar heat acquisition means 10.
- Solar thermal energy 2 1 0 is converted to chemical energy 2 2 0 as potential energy of ammonia by ammonia synthesis means 2 0.
- a part 2 15 of the solar thermal energy 2 10 is used for the ammonia synthesizing means 2 0 as a heat source, a power source and / or a power source.
- the chemical energy 220 is transferred from the first region 3 to the second region 5 by the ammonia transfer means 30.
- the ammonia transfer means 30 is combusted by the internal combustion engine of the ammonia transfer means 30 with a part of chemical energy (that is, a part of the ammonia to be transferred). Power and Z or at least part of power).
- the chemical energy 2 2 0 is partially consumed by the ammonia transfer means 30, and becomes chemical energy 2 3 0 after being transferred to the second area 5.
- the chemical energy 2 3 0 is obtained by combusting ammonia so that the driving energy generating means 40 generates nitrogen and water, and the driving energy 1 2 4 0
- the thermal energy 2 50 is output (not shown in the figure, the ammonia synthesizing means 20 and the ammonia transfer means 30 can generate waste heat energy).
- the conversion system 1 does not need to use an energy source other than the sunlight 20 0. Therefore, the conversion system 1 enables conversion of solar thermal energy 2 10 to driving energy 2 40 without emitting carbon dioxide at any step in the system.
- Methods for storing solar thermal energy include: (a) acquiring solar thermal energy; (b) utilizing a portion of the acquired solar thermal energy, for example, as a heat source, power source and / or power source, particularly directly (C) using other part of the acquired solar thermal energy, for example as a heat source, power source and / or power Use as a source, in particular as a heat source and / or power source, to carry out a reaction to synthesize ammonia from nitrogen and hydrogen obtained in step (b).
- solar heat energy can be stored in the form of chemical energy of ammonia by synthesizing ammonia using solar heat energy.
- the solar heat energy obtained in step (a) is used to obtain at least a portion of the power and Z or power required to perform this method.
- the synthesized ammonia is used as a fuel to obtain at least a portion of the power, dynamics and / or heat required to perform this method. Also other preferred this way In a new embodiment, only the solar thermal energy acquired in step (a) is used as a source of energy.
- examples of the electric power required for carrying out this method include electric power for driving a pump / compressor that flows and compresses a fluid such as a raw material, electric power for further heating of a heat source, and the like. it can.
- the power necessary for carrying out this method may include power for driving a pump / compressor that causes a fluid such as a raw material to flow and is Z or compressed.
- heat necessary for carrying out this method can include heat for further heating of the heat source.
- supplying a part of the heat energy for the heat source by electric power may be preferable in order to make the temperature of the heat source higher than the temperature obtained directly by the solar heat energy.
- the method can be implemented with reduced, and preferably no, use of conventional fossil fuels such as petroleum.
- step (a) solar energy is acquired in step (a).
- T / JP2009 / 053613 any solar concentrator can be used to obtain solar thermal energy.
- the following solar collectors (1) to (3) are used. be able to :
- the parapoly dish type condensing device shown in FIG. 4 has a dish-shaped reflecting portion 1 4 1 that reflects and collects sunlight 20 0 and a light receiving portion 1 4 2 that receives the collected light.
- the solar receiver 1 4 2 acquires solar thermal energy.
- Solar thermal energy obtained from the light-receiving unit 1 4 2 can be transferred to the required location using a heat carrier such as a molten alkali metal such as molten metal sodium, molten salt, oil, or water vapor. .
- This type of concentrator is suitable for a relatively small plant, and is preferably used as solar heat energy of about 10 1 to several 10 O kw.
- this type of condensing device has a high condensing degree, which can provide a high-temperature heat source of 2,00 ° C. or higher, but the cost is relatively high.
- the solar tower type concentrator shown in Fig. 5 has a plurality of heliostats (reflectors) 1 5 1 that reflect sunlight 2 0 0 and collects light and a light receiver 1 5 3 that receives the collected light. And the solar light energy is acquired at the light receiving section 15 2.
- the light receiving portion 1 5 3 is disposed on the upper portion of the light receiving tower 1 5 2.
- the solar thermal energy obtained by the light-receiving unit 15 3 can be moved to a required location using a heat medium as required.
- This type of concentrator is suitable for large plants ranging from 10 MW to several 100 MW.
- this type of concentrator has a high condensing degree and can provide a high-temperature heat source of several 1,00 0 ° C. 053613 is high, and advanced technology is also required for control of the reflector.
- the parapoly trough-type concentrator shown in Fig. 6 has a trough-type reflector 1 6 1 that reflects sunlight 2 0 0 to collect light and a light receiver 1 6 2 that receives the collected light.
- the solar thermal energy is acquired in this light receiving unit 1 4 2.
- the solar thermal energy obtained by the light receiving section 16 2 can be moved to a necessary location by optionally circulating the heat medium via the heat medium flow path 16 3.
- This type of concentrator is simple in structure and low in cost, and is suitable for large-scale plants. In general, it is suitable for a number of 100 MW, but has a low concentration, and the obtained heat source is a low-temperature heat source of 400 to 500 ° C.
- each concentrator has advantages and disadvantages. Therefore, any of these or a combination of them can be used in the energy storage method.
- solar thermal energy for a high-temperature heat source is obtained by a concentrator with a high degree of concentration (for example, a parapoly dish type concentrator and / or a solar evening-type concentrator), and other solar heat Solar energy for generating energy, for example, a low-temperature heat source, power and / or energy, can be obtained with a concentrator with a low concentration (eg, a parapoly trough concentrator).
- solar thermal energy obtained by a concentrating device with a high degree of concentration is less than 1/2 of the total solar thermal energy obtained by a concentrating device with a high degree of condensing and a concentrating device with a low degree of concentrating, It can be in the range of 1 Z 2.
- limiting the proportion of light concentrators that are generally high cost and have a high degree of light condensing may be desirable with respect to the cost of the overall light concentrating equipment.
- step (b) Production of hydrogen> 3613
- step (b) a part of the acquired solar thermal energy is used, and in particular, only the acquired solar thermal energy is used as an energy source to cause a reaction to generate hydrogen from water. .
- any method can be used to obtain hydrogen from water.
- water electrolysis for example, the following (1) to (3) water splitting methods are known.
- water decomposition is known. The focus is on reducing the reaction temperature required for the reaction: (1) Direct method
- Equation 1 Equation 1
- Equation 1 originally reaction, requires a temperature thousands 1 C, can be achieved with 2, 0 0 0 ° C before and after the temperature by utilizing a catalyst.
- This method requires two types of heat sources: a high-temperature heat source (approximately 1500 ° C) and a low-temperature heat source (4200 ° C).
- This method requires two types of heat sources: a high-temperature heat source (950 ° C) and a low-temperature heat source (400 ° C).
- This relatively high temperature heat source can be provided by directly using the solar heat energy acquired in step (a) as a heat source, in which case at least a portion of the required solar heat energy is collected. It can be obtained with a concentrator with a high luminous intensity, such as a parapoly dish type concentrator and a Z or solar tower type concentrator.
- this relatively high temperature heat source uses electric power, particularly electric power obtained using solar thermal energy acquired in step (a), or electric power obtained using synthesized ammonia as fuel. be able to.
- JP2009 / 053613 Acquisition of solar thermal energy can be performed by a light collecting device having a low light collecting degree, for example, a parapoly trough type light collecting device. This may be preferable with respect to the overall cost of the light collection equipment.
- step (C) a part of the obtained solar thermal energy was used, and in particular, only the obtained solar thermal energy was used as an energy source, and was obtained in nitrogen and step (b). A reaction for synthesizing ammonia from hydrogen is performed.
- the synthesis of ammonia from nitrogen and hydrogen can be achieved by any method.
- the relatively low temperature heat source for this reaction and / or the power for this reaction can be provided using the solar thermal energy obtained in step (a), in which case the necessary solar heat Collecting energy PT / JP2009 / 053613 It can be obtained with a condensing device with a low luminous intensity, for example, a parabolic trough concentrating device.
- the electric power and Z or power obtained by using the solar thermal energy obtained in the step (a), or the electric power obtained by using the synthesized ammonia as the fuel and Power can be used.
- the production of carbon dioxide due to the use of the fossil fuel can be suppressed and preferably eliminated.
- Equation 7 the combustion product is only water, and the combustion product is not generated as carbon monoxide and carbon dioxide. This reduces or even eliminates the need for carbon monoxide and carbon dioxide removal. Since this reaction is an exothermic reaction, it is possible to use the heat energy generated at this time as necessary to produce the electric power required for the energy storage method.
- One example of a solar thermal energy storage method can be implemented using equipment as shown in Figure 7.
- solar heat energy is acquired by a solar tower type condensing device 15 0 having a relatively high light concentration, and the solar heat energy obtained here is used to distribute a heat medium that is a molten salt 1 7 8 to transfer to reactor 1 7 1.
- the parabolic trough-type concentrator with a relatively low concentration is used to obtain solar thermal energy, and the solar thermal energy obtained here is used to circulate a heat medium that is water vapor. Transfer to reactor 1 7 1 by 9.
- a solar collector type concentrator 1 50 having a relatively high concentration is used as a high-temperature heat source, and a parapoly trough type collector having a relatively low concentration is used.
- Hydrogen is obtained by performing a reaction for generating hydrogen from water using the thermal energy supplied from the optical device 160 as a low-temperature heat source and / or a power source.
- Solar thermal energy is acquired by a parabolic trough concentrator 1 60 having a relatively low concentration, and transferred to a reactor 1 7 3 by a pipe 1 7 9 through which a heat medium that is water vapor flows.
- a reactor 1 7 3 solar thermal energy is converted into heat source and Z or power source.
- JP2009 / 053613 is used to synthesize ammonia from nitrogen and hydrogen to obtain ammonia.
- the nitrogen supplied to the reactor 1 7 3 is obtained by cryogenic separation of air by the air cryogenic separator 1 7 2, and the hydrogen supplied to the reactor 1 7 3 Is obtained with the reaction device 1 7 1.
- the supply to the system of the facility 700 that performs solar thermal energy is only solar energy 20 0, water (H 2 0) and air (A ir), and from these Ammonia (NH 3) is obtained. Therefore, in this example, it does not involve the generation of oxygen dioxide to store solar thermal energy in the form of ammonia chemical energy.
- the ammonia obtained in reactor 1 7 3 is optionally liquefied in liquefier 1 7 4 and then stored in storage tank 1 7 5 until shipping.
- solar energy can also be used as a power source for the liquefaction device.
- a condensing device having a relatively high condensing degree for example, a parapoly dish type condensing device can be used.
- a solar tower type concentrator 150 and a parapoly trough concentrator 1660 instead of using two types of concentrators, only one type of concentrator can be used.
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Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
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ES201090056A ES2383184B1 (en) | 2008-02-22 | 2009-02-20 | METHOD FOR CONVERTING THERMAL SOLAR ENERGY |
CN2009801053268A CN101946070B (en) | 2008-02-22 | 2009-02-20 | Method of converting solar heat energy |
AU2009216073A AU2009216073B2 (en) | 2008-02-22 | 2009-02-20 | Method of converting solar heat energy |
ZA2010/05525A ZA201005525B (en) | 2008-02-22 | 2010-08-03 | Method of converting solar heat energy |
IL207473A IL207473A0 (en) | 2008-02-22 | 2010-08-08 | Method of converting solar heat energy |
MA33171A MA32189B1 (en) | 2008-02-22 | 2010-09-13 | Method of converting solar energy |
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JP2008042012A JP2009197734A (en) | 2008-02-22 | 2008-02-22 | Method of converting solar heat energy |
JP2008-042012 | 2008-02-22 |
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JP (1) | JP2009197734A (en) |
CN (1) | CN101946070B (en) |
AU (1) | AU2009216073B2 (en) |
ES (1) | ES2383184B1 (en) |
IL (1) | IL207473A0 (en) |
MA (1) | MA32189B1 (en) |
WO (1) | WO2009104813A1 (en) |
ZA (1) | ZA201005525B (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2010128682A1 (en) * | 2009-05-05 | 2010-11-11 | Nakamura Norihiko | Combined plant |
US8272216B2 (en) | 2008-02-22 | 2012-09-25 | Toyota Jidosha Kabushiki Kaisha | Method for converting solar thermal energy |
US9506400B2 (en) | 2008-03-18 | 2016-11-29 | Toyota Jidosha Kabushiki Kaisha | Hydrogen generator, ammonia-burning internal combustion engine, and fuel cell |
Families Citing this family (7)
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JP4877373B2 (en) | 2009-08-28 | 2012-02-15 | 日産自動車株式会社 | Assembled battery and manufacturing method of assembled battery |
JP5755905B2 (en) * | 2011-02-10 | 2015-07-29 | 健 秋元 | Global environment improvement |
JP2013242070A (en) * | 2012-05-18 | 2013-12-05 | Toshiba Corp | Steam generation system |
JP5327686B1 (en) * | 2012-06-13 | 2013-10-30 | 武史 畑中 | Next-generation carbon-free boiler, operation method thereof, method for producing hydrogen-rich ammonia in next-generation carbon-free boiler, next-generation carbon-free boiler, operation method, and urea water used for production method of hydrogen-rich ammonia in next-generation carbon-free boiler |
CN105697250A (en) * | 2016-03-16 | 2016-06-22 | 绍兴文理学院 | Tower type solar synthetic ammonia system |
CN106082270B (en) * | 2016-06-08 | 2018-02-06 | 南京科技职业学院 | A kind of method of photocatalytic synthesis ammonification |
US11380830B2 (en) * | 2017-12-20 | 2022-07-05 | The Boeing Company | Thermal energy apparatus and related methods |
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- 2009-02-20 WO PCT/JP2009/053613 patent/WO2009104813A1/en active Application Filing
- 2009-02-20 ES ES201090056A patent/ES2383184B1/en not_active Withdrawn - After Issue
- 2009-02-20 CN CN2009801053268A patent/CN101946070B/en not_active Expired - Fee Related
- 2009-02-20 AU AU2009216073A patent/AU2009216073B2/en not_active Ceased
-
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JPS50114625A (en) * | 1974-01-31 | 1975-09-08 | ||
JPH05332152A (en) * | 1991-06-25 | 1993-12-14 | Koji Korematsu | Ammonia combustion engine |
JPH1146460A (en) * | 1997-03-14 | 1999-02-16 | Toshiba Corp | Power storage system |
JP2004035383A (en) * | 2002-06-28 | 2004-02-05 | Masaya Nagai | Method for fixing and regenerating hydrogen |
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Publication number | Publication date |
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CN101946070B (en) | 2013-01-09 |
ES2383184A1 (en) | 2012-06-19 |
JP2009197734A (en) | 2009-09-03 |
AU2009216073A1 (en) | 2009-08-27 |
AU2009216073B2 (en) | 2011-10-27 |
ES2383184B1 (en) | 2013-05-07 |
MA32189B1 (en) | 2011-04-01 |
IL207473A0 (en) | 2010-12-30 |
CN101946070A (en) | 2011-01-12 |
ZA201005525B (en) | 2011-04-28 |
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