US20220177304A1 - Desalination methods and devices using geothermal energy - Google Patents
Desalination methods and devices using geothermal energy Download PDFInfo
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- US20220177304A1 US20220177304A1 US17/555,279 US202117555279A US2022177304A1 US 20220177304 A1 US20220177304 A1 US 20220177304A1 US 202117555279 A US202117555279 A US 202117555279A US 2022177304 A1 US2022177304 A1 US 2022177304A1
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- oxygen
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- water
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- 238000000034 method Methods 0.000 title claims abstract description 56
- 238000010612 desalination reaction Methods 0.000 title claims description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 102
- 239000001257 hydrogen Substances 0.000 claims abstract description 77
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 77
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 43
- 239000003054 catalyst Substances 0.000 claims abstract description 33
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 30
- 239000001301 oxygen Substances 0.000 claims abstract description 30
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 30
- 230000005611 electricity Effects 0.000 claims abstract description 18
- 239000007789 gas Substances 0.000 claims abstract description 18
- 239000013535 sea water Substances 0.000 claims abstract description 12
- 238000006243 chemical reaction Methods 0.000 claims description 32
- 239000000243 solution Substances 0.000 claims description 24
- 239000010949 copper Substances 0.000 claims description 17
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 16
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 14
- 229910052782 aluminium Inorganic materials 0.000 claims description 14
- 229910052802 copper Inorganic materials 0.000 claims description 14
- 229910052709 silver Inorganic materials 0.000 claims description 14
- 239000004332 silver Substances 0.000 claims description 14
- 235000002639 sodium chloride Nutrition 0.000 claims description 14
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 13
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 7
- 238000002485 combustion reaction Methods 0.000 claims description 7
- 239000003929 acidic solution Substances 0.000 claims description 5
- 239000011780 sodium chloride Substances 0.000 claims description 5
- 230000003197 catalytic effect Effects 0.000 claims description 3
- 150000002431 hydrogen Chemical class 0.000 claims description 3
- 238000003860 storage Methods 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 230000003647 oxidation Effects 0.000 claims 6
- 238000007254 oxidation reaction Methods 0.000 claims 6
- 238000005868 electrolysis reaction Methods 0.000 claims 4
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 claims 2
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 claims 1
- 239000005751 Copper oxide Substances 0.000 claims 1
- 229910000431 copper oxide Inorganic materials 0.000 claims 1
- 229910001923 silver oxide Inorganic materials 0.000 claims 1
- 150000003839 salts Chemical class 0.000 abstract description 10
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 23
- 229910052751 metal Inorganic materials 0.000 description 19
- 239000002184 metal Substances 0.000 description 19
- 229910001882 dioxygen Inorganic materials 0.000 description 16
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
- 229910002804 graphite Inorganic materials 0.000 description 7
- 239000010439 graphite Substances 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 150000002739 metals Chemical class 0.000 description 5
- 230000008929 regeneration Effects 0.000 description 5
- 238000011069 regeneration method Methods 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 4
- 150000004699 copper complex Chemical class 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 238000004146 energy storage Methods 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- -1 silver metals Chemical class 0.000 description 2
- 239000002918 waste heat Substances 0.000 description 2
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 description 1
- 239000005750 Copper hydroxide Substances 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910001956 copper hydroxide Inorganic materials 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000010892 electric spark Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000003014 ion exchange membrane Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 238000006303 photolysis reaction Methods 0.000 description 1
- 238000005381 potential energy Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- UKHWJBVVWVYFEY-UHFFFAOYSA-M silver;hydroxide Chemical compound [OH-].[Ag+] UKHWJBVVWVYFEY-UHFFFAOYSA-M 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
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- 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
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- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
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- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/48—Silver or gold
- B01J23/50—Silver
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/72—Copper
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- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/89—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals
- B01J23/8926—Copper and noble metals
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B01J38/00—Regeneration or reactivation of catalysts, in general
- B01J38/48—Liquid treating or treating in liquid phase, e.g. dissolved or suspended
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B01J7/02—Apparatus for generating gases by wet methods
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- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
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- 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
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- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
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- C25B1/04—Hydrogen or oxygen by electrolysis of water
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B11/00—Electrodes; Manufacture thereof not otherwise provided for
- C25B11/04—Electrodes; Manufacture thereof not otherwise provided for characterised by the material
- C25B11/051—Electrodes formed of electrocatalysts on a substrate or carrier
- C25B11/073—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalyst material
- C25B11/075—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalyst material consisting of a single catalytic element or catalytic compound
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- C25B15/00—Operating or servicing cells
- C25B15/08—Supplying or removing reactants or electrolytes; Regeneration of electrolytes
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F03—MACHINES OR ENGINES FOR LIQUIDS; WIND, SPRING, OR WEIGHT MOTORS; PRODUCING MECHANICAL POWER OR A REACTIVE PROPULSIVE THRUST, NOT OTHERWISE PROVIDED FOR
- F03G—SPRING, WEIGHT, INERTIA OR LIKE MOTORS; MECHANICAL-POWER PRODUCING DEVICES OR MECHANISMS, NOT OTHERWISE PROVIDED FOR OR USING ENERGY SOURCES NOT OTHERWISE PROVIDED FOR
- F03G4/00—Devices for producing mechanical power from geothermal energy
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- B01J2219/00049—Controlling or regulating processes
- B01J2219/00051—Controlling the temperature
- B01J2219/00139—Controlling the temperature using electromagnetic heating
- B01J2219/00144—Sunlight; Visible light
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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Definitions
- the present invention relates to hydrogen and oxygen production. More specifically, the present invention relates to hydrogen and oxygen production using geothermal heat, water, and an environmentally safe catalyst.
- Typical methods and devices for desalinating sea/salt water require much energy to push the salt water through an ion exchange membrane. Distillation of salt water is inefficient in terms of its energy use. More energy efficient methods and device for desalination are needed.
- the apparatus comprises a main reactor, a gas turbine, and a source of geothermal heat.
- a method of desalination comprising applying a voltage to a solution containing sodium chloride and a hydrogen producing catalyst, generating an amount of hydrogen with the hydrogen producing catalyst, and generating an amount of pure water by combusting the amount of hydrogen and oxygen.
- the method further comprises providing geothermal heat.
- the voltage is equal or less than 1V.
- the solution comprises water having salt.
- the solution comprises sea water.
- the hydrogen producing catalyst contains aluminum, silver, and copper.
- the oxygen is generated by the hydrogen producing catalyst.
- the method further comprises driving an electricity generating turbine using the hydrogen generated.
- a hydrogen producing system comprises a non-acidic solution containing a hydrogen generating catalyst, wherein the hydrogen generating catalyst contains a charge-treated aluminum metal, a charge-treated copper metal, and a charged-treated silver metal, wherein the charge-treated aluminum, copper, and silver metals are treated by a voltage not less than 1V, and wherein the hydrogen generating catalyst is capable of generating hydrogen gas in a catalytic manner with an applied voltage no greater than 1V, an electric energy providing device, and a geothermal heating device providing heat to the non-acidic solution.
- the system comprises a light source.
- the light source comprises LED.
- the light source provides lights having wavelengths approximately in the visible light region.
- the geothermal heating device receives a amount of geothermal heat from the earth.
- the hydrogen generating catalyst comprises aluminum hydroxide.
- the hydrogen generating catalyst comprises copper hydroxide.
- the hydrogen generating catalyst comprises silver hydroxide.
- the system further comprises a computer automating a transportation of the non-acidic solution.
- a method of generating electricity comprises applying a voltage less than 1V to a solution having a catalyst, wherein the catalysts containing aluminum complex, copper complex, and silver complex, and providing heat from a geothermal heat source to the solution.
- the solution is a non-acidic solution.
- the solution has a pH value equal or great than 7.
- the method further comprises turning a turbine to generate electricity by using one or more gases that are generated at the solution.
- the method further comprises using the electricity generated as an energy source to be applied to the solution.
- the one or more gases comprise hydrogen, oxygen, or a combination thereof.
- the method further comprises combusting the hydrogen and oxygen to generate heat and water.
- the method further comprises transporting the heat and the water to add to the solution.
- a hydrogen generating method comprises generating hydrogen gas and oxygen gas by applying a pulsed voltage less than 1V to a solution, wherein the solution containing a catalyst having aluminum, copper, and silver, and heating the solution by a geothermal heat and a heat generated by combusting the hydrogen gas and the oxygen gas.
- the method further comprises regenerating the catalyst by providing an amount of light.
- the light comprises LED.
- FIG. 1 illustrates a hydrogen producing system in accordance with some embodiments.
- FIG. 2 illustrates another hydrogen producing system in accordance with some embodiments.
- FIG. 3 is a flow chart illustrating a hydrogen producing process using geothermal as a heat source in accordance with some embodiments.
- FIG. 1 illustrates a hydrogen producing system 100 in accordance with some embodiments.
- the hydrogen producing system 100 is able to use geothermal heat as the heat source for chemical reactions.
- the hydrogen producing system 100 comprises a reactor 102 .
- the reactor 102 allows an active ion displacement reaction to occur.
- the chemical reactions in the reactor 102 generate hydrogen gas and oxygen gas. Details of the compositions, starting materials, and catalysts that are used in the reactor 102 are described in the following.
- the hydrogen gas producing reaction occurs in the reactor 102 .
- a heat source 106 such as a geothermal source, having heat to be provided to the reactor 102 .
- the geothermal source is able to provide/supply heat to the reactor 102 .
- the geothermal heat is able to be pre-stored before providing heat to the reactor 102 .
- the water source of the reaction is able to be from the water tank 101 .
- the hydrogen producing reaction in the reactor 102 generates hydrogen gas 108 and oxygen gas 110 .
- the hydrogen gas 108 and oxygen gas 110 are sent to drive a expansion turbine 104 to generate electricity by using the gas pressure/gas flow generated at the hydrogen producing reaction.
- the hydrogen gas 108 and the oxygen gas 110 after passing through the expansion turbine 104 , are triggered to be combusted/reacted at a combustion chamber 112 .
- the hydrogen gas is able to react with the oxygen gas by using electric sparks.
- Heat that is generated through reacting hydrogen gas 108 and the oxygen gas 110 is able to be transferred to a heat exchanger 114 , which is able to be applied back to the reactor 102 for recycling and reusing the heat.
- the combustion reaction of the oxygen gas 110 and the hydrogen gas 108 produces pure water, which is able to be condensed and collected at the condenser 116 , such that the system 100 is able to be used as a desalination device to produce pure water.
- the water is able to be recycled back to the reactor 102 , so no new water or external water is needed for continuously running the hydrogen producing reaction.
- FIG. 2 illustrates a hydrogen producing system 200 in accordance with some embodiments.
- the system 200 comprises a preparation reactor 203 and a main reactor 214 .
- the main reactor 214 comprises a photochemical/oxidizer reacting device 232 , and a thermal source 230 , which is able to be a geothermal source.
- a hydrogen producing reaction is able to begin from preparing a solution 201 containing Al metal 202 (250 mg), Cu metal 204 (250 mg), Ag metal 206 (250 mg), a graphite electrode 212 and 1 liter of water 208 having 1.5% NaCl 210 by weight.
- a negative voltage ⁇ 2.5V is applied to the graphite electrode 212 and a first positive voltage 1.7V is applied to the Al metal 202 for 15 minutes.
- the first positive voltage applied to the Al metal 202 is removed, and a second positive voltage of 1.4V is applied to the Cu metal 204 for 10 minutes while the negative voltage of ⁇ 2.5V is applied to the graphite electrode 212 .
- the second positive voltage is removed from the Cu metal 204 , and a third positive voltage of 1.0V is applied to the Ag metal 206 for 5 minutes with the negative voltage still applied to the graphite electrode 212 .
- the temperature of the solution is maintained at 88° F. by controlling the heat source 230 .
- the solution 201 is transferred to the main reaction vessel 214 , so that the main reaction vessel 214 contains aluminum complex 215 , copper complex 217 , silver complex 220 , sodium ions 222 , and chloride ions 224 from the preparation vessel 203 .
- Water is able to be input from a water tank 251 .
- the term “complex” comprises all ligand states of a metal.
- an aluminum complex includes Al 3+ or Al(OH) x , where the x represents the coordinated ligand numbers of the aluminum ion.
- a voltage between 0.4V and 0.9V is applied to the cathode of the electrodes.
- a voltage of 0.85V is applied to the cathode of the electrodes.
- a voltage not exceeding 0.9V is applied to the cathode of the electrodes. Some experiments indicate that hydrogen production is reduced when a voltage exceeding 0.9V is applied.
- the applied voltage of the anode is at 0V compared with a voltage on the standard hydrogen electrode.
- the voltage is applied in a way that a negative charge is applied to the stainless steel electrode 216 and a positive charge is applied to the graphite electrode 218 .
- a hydrolysis reaction begins to occur when sufficient voltage is applied, and hydrogen gas 236 is generated at the stainless steel electrode 216 when the voltage is applied to the stainless steel electrode 216 and the graphite electrode 218 . While the hydrogen producing reaction is going, heat is provided through the heat source 230 and lightings 232 (such as, LED lights) are applied to the main reactor 214 for assisting a photolysis reaction.
- Oxygen gas 240 and hydrogen gas 236 are output to the expansion turbine 244 to generate electricity.
- the oxygen gas 240 and the hydrogen gas 236 are able to react at the combustion chamber 246 to generate electricity through a combustion reaction.
- the heat generated at the combustion chamber 246 is able to be collected at the heat exchanger 248 and the water generated is able to be collected at the condenser 250 .
- the water collected at the condenser 250 is able to be used as pure water or recycled back to the main reactor 214 .
- the whole reaction is able to be automatically controlled by a computer system to maintain a continuous operation of the reaction, including maintaining an optimized reaction condition for the hydrogen producing reaction.
- FIG. 3 is a flow chart illustrating a hydrogen producing process 300 using geothermal as a heat source.
- the process 300 is able to begin from preparing a reaction solution at Step 302 .
- the solution preparation is able to be performed at the preparation reactor 203 ( FIG. 2 ) with the procedures described above.
- Step 304 voltage is applied to the solution to generate hydrogen gas and oxygen gas.
- Step 306 the hydrogen gas and the oxygen gas are sent to a gas turbine to generate electricity.
- Step 308 the hydrogen gas and the oxygen gas are combusted to generate heat and pure water.
- Step 310 the heat and water is recycled back to the main reactor for running the reaction. All the steps that are contained in the methods/procedures described above are some embodiments of the present application. All the steps are optional and all the steps when applicable are able to be performed in any sequences or orders. Additional steps are also able to be added when a person skilled in the art deems proper.
- the systems and methods use the hydrogen and/or oxygen as an intermediate energy storage device.
- it can be used as a device or method for storing heat from a geothermal source.
- Heat in general is a type of energy that is more difficult to store than storing energy in a form of gases, which are more stable and storable when compared with heat.
- the hydrogen and oxygen gases are able to be generated using thermal energy, which are used to drive one or more gas turbines via gas flow or pressure difference to generate electricity.
- the hydrogen and oxygen are combusted to release their potential energy and make water. Since hydrogen and oxygen are generated and consumed without additional gases generated or consumed, the hydrogen and oxygen are able to be used as a form of energy storage.
- the systems and devices are used as a desalination device or method, wherein a geothermal heat is used to perform the process.
- a low temperature e.g., below 40° C.
- the low temperature e.g., below 40° C.
- 31° C. is the temperature that is used for generating the hydrogen gas.
- an amount of sea water is used as a source of the water supply.
- salts that are contained in the sea water are left at the main reactor and pure water is generated by combining and combusting the hydrogen and oxygen gases generated.
- a regular cleaning or removal of the salts at the reactor where the salts are left is performed (e.g, once a day, once a week, or any other predetermined duration).
- the methods and devices disclosed herein are configured to generate hydrogen/oxygen gases, serve as a desalination device, and/or a geothermal storage using an amount of the geothermal heat, sea water, or a combination thereof.
- a main reactor 214 is coupled with or located at or near a source of the geothermal heat 230 .
- the main reactor 214 is a geothermal power plant.
- An amount of the geothermal heat 230 is conducted via one or more thermal paths, such as by direct contact, to be transferred to the main reactor 214 , such as a wall or a bottom surface of a reactor.
- a continuous supply of the geothermal heat 230 is provided to the main reactor 214 .
- one or more of the light sources 232 are in the main reactor 214 , so that a regeneration reaction of the hydrogen generating catalysts can be performed inside the main reactor 214 .
- the light sources 232 are included in a separate chamber, reactor, or container, so that the regeneration of the hydrogen generating reaction can be performed in a regeneration reactor that is separated or independent from the solution of the main reactor 214 .
- an additional heat source such as a heating coil heater, is used to provide heat needed for the regeneration reaction of the hydrogen generating catalysts.
- the preparation of the hydrogen generating catalysts is able to be followed by the description in the FIG. 2 and its accompanying text.
- the preparation of the hydrogen generating catalysts including applying a first voltage to a graphite electrode (e.g., a voltage greater than ⁇ 2.0V, such as ⁇ 2.0 to ⁇ 2.5V) and one or more voltages to the metal catalysts (e.g., aluminum metal, copper metal, and silver metal respectively).
- the voltage that is applied to the metals is greater than 1V.
- the voltage that is applied to the metals is 0.9V or greater (e.g., 0.9V-1.9V).
- a voltage of 1.1V-1.9V, 1.7V, or 1.5-2.0V is applied to the aluminum metal.
- a voltage of 1.1V-1.9V, 1.4V, or 1.2-2.0V is applied to the copper metal.
- a voltage of 1.1V-1.9V, 1.4V, or 1.2-2.0V is applied to the silver metal.
- a voltage for generating hydrogen gas, oxygen gas, or both is applied to the electrodes/solution containing the hydrogen generating catalysts.
- the voltage for generating the above mentioned gases is configured to or limited to a voltage that is equal or below 0.9V. For example, a voltage between 0.4V to 0.9V is applied to the electrodes and solutions for generating a continuous stream of hydrogen gas and oxygen gas.
- a voltage of 0.85V is configured to be applied to the electrodes for driving the catalysts to produce the gases mentioned above.
- the systems and procedures are able to be utilized to produce electricity, hydrogen, oxygen, pure water on-demand using a geothermal heat.
- a low voltage such as less than 0.9V
- a prepared solution having active catalysts hydrogen generating substances
- the hydrogen and oxygen are used to move a gas turbine to generate electricity.
- the oxygen and hydrogen are combusted to generate heat and pure water. This process is advantageous in many aspects including desalinating salt/sea water using a geothermal heat.
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Abstract
A method of and apparatus for desalinating sea water using geothermal energy. A low voltage (such as less than 0.9V) is applied to a hydrogen generating catalysts to generate hydrogen and oxygen, wherein geothermal heat is used as a heat source. The hydrogen and oxygen are used to drive a gas turbine to generate electricity. The oxygen and hydrogen are transported away and combusted to generate heat and pure water, as such salt are separated from the pure water.
Description
- This application is a continuation patent application of the co-pending U.S. patent application Ser. No. 16/162,562, published as U.S. Patent Application Publication No. 2019/0047854, filed Oct. 17, 2018, and entitled “DESALINATION METHODS AND DEVICES USING GEOTHERMAL ENERGY,” which is a continuation-in-part of U.S. patent application Ser. No. 14/095,765, filed Dec. 3, 2013, and entitled “Hydrogen Generating System and Method Using Geothermal Energy,” which claims priority of U.S. Provisional Application Ser. No. 61/733,868, filed Dec. 5, 2012 and titled, “Hydrogen Generating System and Method Using Geothermal Energy,” which are hereby incorporated by reference in their entirety for all purposes.
- Additionally, the co-pending U.S. patent application Ser. No. 16/162,562, published as U.S. Patent Application Publication No. 2019/0047854, filed Oct. 17, 2018, and entitled “DESALINATION METHODS AND DEVICES USING GEOTHERMAL ENERGY,” is a continuation-in-part of U.S. patent application Ser. No. 15/204,609, filed Jul. 7, 2016, and entitled “METHOD AND APPARATUS FOR EFFICIENT ON-DEMAND PRODUCTION OF H2 AND O2 FROM WATER USING WASTE HEAT AND ENVIRONMENTALLY SAFE METALS,” which is a divisional application of U.S. patent application Ser. No. 12/706,639, filed Feb. 16, 2010, issued as U.S. Pat. No. 9,415,363, and entitled “METHOD AND APPARATUS FOR EFFICIENT ON-DEMAND PRODUCTION OF H2 AND O2 FROM WATER USING WASTE HEAT AND ENVIRONMENTALLY SAFE METALS,” which claims priority of U.S. Provisional Application Ser. No. 61/154,282, filed Feb. 20, 2009 and titled, “METHOD AND APPARATUS FOR EFFICIENT ON-DEMAND PRODUCTION OF H2 AND O2 FROM WATER USING ENVIRONMENTALLY SAFE METALS,” which are hereby incorporated by reference in their entirety for all purposes.
- The present invention relates to hydrogen and oxygen production. More specifically, the present invention relates to hydrogen and oxygen production using geothermal heat, water, and an environmentally safe catalyst.
- Typical methods and devices for desalinating sea/salt water require much energy to push the salt water through an ion exchange membrane. Distillation of salt water is inefficient in terms of its energy use. More energy efficient methods and device for desalination are needed.
- Methods of and apparatuses for producing H2 and O2 from salt water using geothermal heat are disclosed. In one aspect, the apparatus comprises a main reactor, a gas turbine, and a source of geothermal heat.
- In one aspect, a method of desalination comprising applying a voltage to a solution containing sodium chloride and a hydrogen producing catalyst, generating an amount of hydrogen with the hydrogen producing catalyst, and generating an amount of pure water by combusting the amount of hydrogen and oxygen. In some embodiments, the method further comprises providing geothermal heat. In other embodiments, the voltage is equal or less than 1V. In some other embodiments, the solution comprises water having salt. In some embodiments, the solution comprises sea water. In some other embodiments, the hydrogen producing catalyst contains aluminum, silver, and copper. In some embodiments, the oxygen is generated by the hydrogen producing catalyst. In other embodiments, the method further comprises driving an electricity generating turbine using the hydrogen generated.
- In another aspect, a hydrogen producing system comprises a non-acidic solution containing a hydrogen generating catalyst, wherein the hydrogen generating catalyst contains a charge-treated aluminum metal, a charge-treated copper metal, and a charged-treated silver metal, wherein the charge-treated aluminum, copper, and silver metals are treated by a voltage not less than 1V, and wherein the hydrogen generating catalyst is capable of generating hydrogen gas in a catalytic manner with an applied voltage no greater than 1V, an electric energy providing device, and a geothermal heating device providing heat to the non-acidic solution.
- In some embodiments, the system comprises a light source. In other embodiments, the light source comprises LED. In some other embodiments, the light source provides lights having wavelengths approximately in the visible light region. In some embodiments, the geothermal heating device receives a amount of geothermal heat from the earth. In other embodiments, the hydrogen generating catalyst comprises aluminum hydroxide. In some other embodiments, the hydrogen generating catalyst comprises copper hydroxide. In some embodiments, the hydrogen generating catalyst comprises silver hydroxide. In other embodiments, the system further comprises a computer automating a transportation of the non-acidic solution.
- In another aspect, a method of generating electricity comprises applying a voltage less than 1V to a solution having a catalyst, wherein the catalysts containing aluminum complex, copper complex, and silver complex, and providing heat from a geothermal heat source to the solution. In some embodiments, the solution is a non-acidic solution. In other embodiments, the solution has a pH value equal or great than 7. In some other embodiments, the method further comprises turning a turbine to generate electricity by using one or more gases that are generated at the solution. In some embodiments, the method further comprises using the electricity generated as an energy source to be applied to the solution. In other embodiments, the one or more gases comprise hydrogen, oxygen, or a combination thereof. In some other embodiments, the method further comprises combusting the hydrogen and oxygen to generate heat and water. In some embodiments, the method further comprises transporting the heat and the water to add to the solution.
- In another aspect, a hydrogen generating method comprises generating hydrogen gas and oxygen gas by applying a pulsed voltage less than 1V to a solution, wherein the solution containing a catalyst having aluminum, copper, and silver, and heating the solution by a geothermal heat and a heat generated by combusting the hydrogen gas and the oxygen gas.
- In some embodiments, the method further comprises regenerating the catalyst by providing an amount of light. In other embodiments, the light comprises LED.
-
FIG. 1 illustrates a hydrogen producing system in accordance with some embodiments. -
FIG. 2 illustrates another hydrogen producing system in accordance with some embodiments. -
FIG. 3 is a flow chart illustrating a hydrogen producing process using geothermal as a heat source in accordance with some embodiments. -
FIG. 1 illustrates ahydrogen producing system 100 in accordance with some embodiments. Thehydrogen producing system 100 is able to use geothermal heat as the heat source for chemical reactions. In some embodiments, thehydrogen producing system 100 comprises areactor 102. Thereactor 102 allows an active ion displacement reaction to occur. In some embodiments, the chemical reactions in thereactor 102 generate hydrogen gas and oxygen gas. Details of the compositions, starting materials, and catalysts that are used in thereactor 102 are described in the following. In some embodiments, the hydrogen gas producing reaction occurs in thereactor 102. Aheat source 106, such as a geothermal source, having heat to be provided to thereactor 102. The geothermal source is able to provide/supply heat to thereactor 102. The geothermal heat is able to be pre-stored before providing heat to thereactor 102. A person of ordinary skill in the art appreciates that any other sources of heat from nature are within the scope of the present invention. The water source of the reaction is able to be from thewater tank 101. The hydrogen producing reaction in thereactor 102 generateshydrogen gas 108 andoxygen gas 110. Thehydrogen gas 108 andoxygen gas 110 are sent to drive aexpansion turbine 104 to generate electricity by using the gas pressure/gas flow generated at the hydrogen producing reaction. Thehydrogen gas 108 and theoxygen gas 110, after passing through theexpansion turbine 104, are triggered to be combusted/reacted at a combustion chamber 112. The hydrogen gas is able to react with the oxygen gas by using electric sparks. Heat that is generated through reactinghydrogen gas 108 and theoxygen gas 110 is able to be transferred to aheat exchanger 114, which is able to be applied back to thereactor 102 for recycling and reusing the heat. The combustion reaction of theoxygen gas 110 and thehydrogen gas 108 produces pure water, which is able to be condensed and collected at thecondenser 116, such that thesystem 100 is able to be used as a desalination device to produce pure water. In some embodiments, the water is able to be recycled back to thereactor 102, so no new water or external water is needed for continuously running the hydrogen producing reaction. -
FIG. 2 illustrates ahydrogen producing system 200 in accordance with some embodiments. In some embodiments, thesystem 200 comprises apreparation reactor 203 and amain reactor 214. Themain reactor 214 comprises a photochemical/oxidizer reacting device 232, and athermal source 230, which is able to be a geothermal source. A hydrogen producing reaction is able to begin from preparing asolution 201 containing Al metal 202 (250 mg), Cu metal 204 (250 mg), Ag metal 206 (250 mg), agraphite electrode 212 and 1 liter ofwater 208 having 1.5% NaCl 210 by weight. A negative voltage −2.5V is applied to thegraphite electrode 212 and a first positive voltage 1.7V is applied to theAl metal 202 for 15 minutes. - Next, the first positive voltage applied to the
Al metal 202 is removed, and a second positive voltage of 1.4V is applied to theCu metal 204 for 10 minutes while the negative voltage of −2.5V is applied to thegraphite electrode 212. Next, the second positive voltage is removed from theCu metal 204, and a third positive voltage of 1.0V is applied to theAg metal 206 for 5 minutes with the negative voltage still applied to thegraphite electrode 212. The temperature of the solution is maintained at 88° F. by controlling theheat source 230. - Next, the
solution 201 is transferred to themain reaction vessel 214, so that themain reaction vessel 214 containsaluminum complex 215,copper complex 217,silver complex 220,sodium ions 222, andchloride ions 224 from thepreparation vessel 203. Water is able to be input from awater tank 251. The term “complex” comprises all ligand states of a metal. For example, an aluminum complex includes Al3+ or Al(OH)x, where the x represents the coordinated ligand numbers of the aluminum ion. In some embodiments, a voltage between 0.4V and 0.9V is applied to the cathode of the electrodes. In alternative embodiments, a voltage of 0.85V is applied to the cathode of the electrodes. In other embodiments, a voltage not exceeding 0.9V is applied to the cathode of the electrodes. Some experiments indicate that hydrogen production is reduced when a voltage exceeding 0.9V is applied. In some embodiments, the applied voltage of the anode is at 0V compared with a voltage on the standard hydrogen electrode. In some embodiments, the voltage is applied in a way that a negative charge is applied to thestainless steel electrode 216 and a positive charge is applied to thegraphite electrode 218. A hydrolysis reaction begins to occur when sufficient voltage is applied, andhydrogen gas 236 is generated at thestainless steel electrode 216 when the voltage is applied to thestainless steel electrode 216 and thegraphite electrode 218. While the hydrogen producing reaction is going, heat is provided through theheat source 230 and lightings 232 (such as, LED lights) are applied to themain reactor 214 for assisting a photolysis reaction. -
Oxygen gas 240 andhydrogen gas 236 are output to theexpansion turbine 244 to generate electricity. Theoxygen gas 240 and thehydrogen gas 236 are able to react at the combustion chamber 246 to generate electricity through a combustion reaction. The heat generated at the combustion chamber 246 is able to be collected at theheat exchanger 248 and the water generated is able to be collected at thecondenser 250. The water collected at thecondenser 250 is able to be used as pure water or recycled back to themain reactor 214. The whole reaction is able to be automatically controlled by a computer system to maintain a continuous operation of the reaction, including maintaining an optimized reaction condition for the hydrogen producing reaction. -
FIG. 3 is a flow chart illustrating ahydrogen producing process 300 using geothermal as a heat source. Theprocess 300 is able to begin from preparing a reaction solution atStep 302. - The solution preparation is able to be performed at the preparation reactor 203 (
FIG. 2 ) with the procedures described above. AtStep 304, voltage is applied to the solution to generate hydrogen gas and oxygen gas. AtStep 306, the hydrogen gas and the oxygen gas are sent to a gas turbine to generate electricity. AtStep 308, the hydrogen gas and the oxygen gas are combusted to generate heat and pure water. AtStep 310, the heat and water is recycled back to the main reactor for running the reaction. All the steps that are contained in the methods/procedures described above are some embodiments of the present application. All the steps are optional and all the steps when applicable are able to be performed in any sequences or orders. Additional steps are also able to be added when a person skilled in the art deems proper. - Geothermal Heat Storing and/or Desalination Devices and Systems
- In some embodiments, the systems and methods use the hydrogen and/or oxygen as an intermediate energy storage device. In other words, it can be used as a device or method for storing heat from a geothermal source. Heat in general is a type of energy that is more difficult to store than storing energy in a form of gases, which are more stable and storable when compared with heat. Here, the hydrogen and oxygen gases are able to be generated using thermal energy, which are used to drive one or more gas turbines via gas flow or pressure difference to generate electricity. Next, the hydrogen and oxygen are combusted to release their potential energy and make water. Since hydrogen and oxygen are generated and consumed without additional gases generated or consumed, the hydrogen and oxygen are able to be used as a form of energy storage.
- Additionally, the systems and devices are used as a desalination device or method, wherein a geothermal heat is used to perform the process. Since the unique property of the hydrogen generating catalysts (e.g., an aluminum complex, a copper complex, and a silver complex), a low temperature (e.g., below 40° C.) is used to perform the hydrogen generating reaction. In some embodiments, the low temperature (e.g., below 40° C.) is used for the entire reaction, including the catalysts preparation and hydrogen generating catalysts regeneration reaction. In some embodiments, 31° C. is the temperature that is used for generating the hydrogen gas. In some embodiments, an amount of sea water is used as a source of the water supply. By using the desalination methods and devices described herein, salts that are contained in the sea water are left at the main reactor and pure water is generated by combining and combusting the hydrogen and oxygen gases generated. A regular cleaning or removal of the salts at the reactor where the salts are left is performed (e.g, once a day, once a week, or any other predetermined duration). As described above, the methods and devices disclosed herein are configured to generate hydrogen/oxygen gases, serve as a desalination device, and/or a geothermal storage using an amount of the geothermal heat, sea water, or a combination thereof.
- In one of the exemplary cases as illustrated by the
FIG. 2 , amain reactor 214 is coupled with or located at or near a source of thegeothermal heat 230. In some embodiments, themain reactor 214 is a geothermal power plant. An amount of thegeothermal heat 230 is conducted via one or more thermal paths, such as by direct contact, to be transferred to themain reactor 214, such as a wall or a bottom surface of a reactor. In some embodiments, a continuous supply of thegeothermal heat 230 is provided to themain reactor 214. - In the reactor, one or more of the light sources 232 (e.g., LED light) are in the
main reactor 214, so that a regeneration reaction of the hydrogen generating catalysts can be performed inside themain reactor 214. In some embodiments, thelight sources 232 are included in a separate chamber, reactor, or container, so that the regeneration of the hydrogen generating reaction can be performed in a regeneration reactor that is separated or independent from the solution of themain reactor 214. In some embodiments, an additional heat source, such as a heating coil heater, is used to provide heat needed for the regeneration reaction of the hydrogen generating catalysts. - In some embodiments, the preparation of the hydrogen generating catalysts is able to be followed by the description in the
FIG. 2 and its accompanying text. In some embodiments, the preparation of the hydrogen generating catalysts including applying a first voltage to a graphite electrode (e.g., a voltage greater than −2.0V, such as −2.0 to −2.5V) and one or more voltages to the metal catalysts (e.g., aluminum metal, copper metal, and silver metal respectively). In some embodiments, the voltage that is applied to the metals is greater than 1V. In some embodiments, the voltage that is applied to the metals is 0.9V or greater (e.g., 0.9V-1.9V). For example, a voltage of 1.1V-1.9V, 1.7V, or 1.5-2.0V is applied to the aluminum metal. A voltage of 1.1V-1.9V, 1.4V, or 1.2-2.0V is applied to the copper metal. A voltage of 1.1V-1.9V, 1.4V, or 1.2-2.0V is applied to the silver metal. - In some embodiments, a voltage for generating hydrogen gas, oxygen gas, or both is applied to the electrodes/solution containing the hydrogen generating catalysts. In some embodiments, the voltage for generating the above mentioned gases is configured to or limited to a voltage that is equal or below 0.9V. For example, a voltage between 0.4V to 0.9V is applied to the electrodes and solutions for generating a continuous stream of hydrogen gas and oxygen gas.
- In some embodiments, a voltage of 0.85V is configured to be applied to the electrodes for driving the catalysts to produce the gases mentioned above.
- The systems and procedures are able to be utilized to produce electricity, hydrogen, oxygen, pure water on-demand using a geothermal heat. In operation, a low voltage (such as less than 0.9V) is applied to a prepared solution having active catalysts (hydrogen generating substances) to generate hydrogen and oxygen. The hydrogen and oxygen are used to move a gas turbine to generate electricity. The oxygen and hydrogen are combusted to generate heat and pure water. This process is advantageous in many aspects including desalinating salt/sea water using a geothermal heat.
- The present invention has been described in terms of specific embodiments incorporating details to facilitate the understanding of principles of construction and operation of the invention. Such reference herein to specific embodiments and details thereof is not intended to limit the scope of the claims appended hereto. It will be readily apparent to one skilled in the art that other various modifications may be made in the embodiment chosen for illustration without departing from the spirit and scope of the invention as defined by the claims.
Claims (21)
1-20. (canceled)
21. A method of desalination of sea water using geothermal heat comprising:
a. providing an amount of sea water with sea salt and an amount of geothermal heat as a heat source to a reaction vessel;
b. generating an amount of oxygen and an amount of hydrogen by performing a catalytic electrolysis reaction by applying an electric voltage between 0.4V to 0.9V to a hydrogen generating catalyst having aluminum, copper, and silver in the sea water in the reaction vessel;
c. driving a turbine to generate an amount of generated electricity by using a gas pressure generated by the amount of hydrogen, the amount of oxygen, or both;
d. combusting the amount of hydrogen and the amount of oxygen generating an amount of desalinated water and generated heat; and
e. providing the amount of generated electricity or the amount of generated heat in assisting the catalytic electrolysis reaction in the reaction vessel.
22. The method of claim 21 , further comprising leaving the sea salt in the reaction vessel.
23. The method of claim 21 , wherein the electric voltage is 0.85V.
24. The method of claim 21 , further comprising separating the desalinated water and the amount of generated heat.
25. The method of claim 24 , further comprising collecting the generated heat using a heat exchanger.
26. The method of claim 21 , further comprising condensing the desalinated water using a condenser.
27. The method of claim 21 , wherein the solution is a non-acidic solution.
28. A sea water desalination method comprising:
a. providing an amount of sea water and geothermal heat in a reaction vessel, wherein the amount of sea water contains water and sea salt;
b. converting the water into hydrogen and oxygen by performing an electrolysis reaction using a hydrogen generating catalyst containing aluminum, copper, and silver in the reaction vessel with a voltage between 0.4V to 0.9V applied;
c. generating electricity by driving an electricity generating device using a pressure generated by the hydrogen and oxygen;
d. combusting the hydrogen and oxygen in a combustion vessel generating desalinated water and heat; and
e. collecting the desalinated water.
29. The method of claim 28 , wherein the electricity generating device comprises an expansion turbine fluidically connected between the reaction vessel and the combustion vessel.
30. The method of claim 28 , further comprising utilizing a light source configured to regenerate the hydrogen generating catalyst.
31. The method of claim 28 , further comprising utilizing a light source configured to generate a wavelength that reduces an oxidation state of silver oxide, copper oxide, or both generated from the silver, the copper, or both.
32. A method of storing an amount of energy comprising:
a. providing an amount of water and geothermal heat in a reaction vessel;
b. converting the water and geothermal heat into hydrogen and oxygen by performing an electrolysis reaction using a hydrogen generating catalyst containing aluminum, copper, and silver in the reaction vessel with a voltage between 0.4V to 0.9V applied;
c. storing the hydrogen and oxygen as an energy source in a storage vessel;
d. generating electricity by releasing the hydrogen and oxygen stored at a predetermined event to drive an expansion turbine; and
e. combusting the hydrogen and oxygen release to generate an amount of stored chemical energy.
33. The method of claim 32 , further comprising using a light source to generate a light energy to regenerate the hydrogen generating catalyst.
34. The method of claim 32 , wherein the light source comprises a LED.
35. The method of claim 34 , further comprising reducing an oxidation state of the aluminum, copper, and silver using the LED.
36. The method of claim 32 , further comprising reducing an oxidation state of the aluminum, copper, and silver.
37. The method of claim 32 , further comprising reducing an oxidation state of the aluminum by using the copper.
38. The method of claim 32 , further comprising reducing an oxidation state of the copper by using the silver.
39. The method of claim 32 , further comprising reducing an oxidation state of the silver by using a light source.
40. The method of claim 39 , wherein the light source comprises a LED.
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