US20050175868A1 - Storage, generation, and use of hydrogen - Google Patents
Storage, generation, and use of hydrogen Download PDFInfo
- Publication number
- US20050175868A1 US20050175868A1 US11/074,360 US7436005A US2005175868A1 US 20050175868 A1 US20050175868 A1 US 20050175868A1 US 7436005 A US7436005 A US 7436005A US 2005175868 A1 US2005175868 A1 US 2005175868A1
- Authority
- US
- United States
- Prior art keywords
- hydride
- hydrogen
- water
- slurry
- reservoir
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 title claims abstract description 95
- 239000001257 hydrogen Substances 0.000 title claims abstract description 94
- 229910052739 hydrogen Inorganic materials 0.000 title claims abstract description 94
- 238000003860 storage Methods 0.000 title description 8
- 150000004678 hydrides Chemical class 0.000 claims abstract description 88
- 239000000126 substance Substances 0.000 claims abstract description 36
- 239000007788 liquid Substances 0.000 claims abstract description 34
- 239000002270 dispersing agent Substances 0.000 claims abstract description 29
- 239000000203 mixture Substances 0.000 claims abstract description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 102
- 238000006243 chemical reaction Methods 0.000 claims description 30
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 19
- 229910000103 lithium hydride Inorganic materials 0.000 claims description 15
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 14
- -1 lithium aluminum hydride Chemical compound 0.000 claims description 13
- 229910052987 metal hydride Inorganic materials 0.000 claims description 10
- 150000004681 metal hydrides Chemical class 0.000 claims description 10
- 229910012375 magnesium hydride Inorganic materials 0.000 claims description 9
- 230000007246 mechanism Effects 0.000 claims description 9
- 239000000376 reactant Substances 0.000 claims description 9
- CSDQQAQKBAQLLE-UHFFFAOYSA-N 4-(4-chlorophenyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine Chemical compound C1=CC(Cl)=CC=C1C1C(C=CS2)=C2CCN1 CSDQQAQKBAQLLE-UHFFFAOYSA-N 0.000 claims description 8
- 230000000694 effects Effects 0.000 claims description 6
- 239000012280 lithium aluminium hydride Substances 0.000 claims description 6
- 239000012448 Lithium borohydride Substances 0.000 claims description 5
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims description 4
- 239000012279 sodium borohydride Substances 0.000 claims description 4
- 229910000033 sodium borohydride Inorganic materials 0.000 claims description 4
- 239000012312 sodium hydride Substances 0.000 claims description 4
- 229910000104 sodium hydride Inorganic materials 0.000 claims description 4
- RSHAOIXHUHAZPM-UHFFFAOYSA-N magnesium hydride Chemical compound [MgH2] RSHAOIXHUHAZPM-UHFFFAOYSA-N 0.000 claims 2
- 239000002184 metal Substances 0.000 abstract description 36
- 229910052751 metal Inorganic materials 0.000 abstract description 35
- 239000000446 fuel Substances 0.000 abstract description 22
- 238000000034 method Methods 0.000 abstract description 16
- 239000006227 byproduct Substances 0.000 abstract description 10
- 230000008569 process Effects 0.000 abstract description 5
- 239000002002 slurry Substances 0.000 description 81
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 24
- 229910052799 carbon Inorganic materials 0.000 description 23
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 18
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 17
- 229910002091 carbon monoxide Inorganic materials 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 17
- 239000002245 particle Substances 0.000 description 17
- 238000002156 mixing Methods 0.000 description 11
- 229910052744 lithium Inorganic materials 0.000 description 10
- 229910044991 metal oxide Inorganic materials 0.000 description 9
- 150000004706 metal oxides Chemical class 0.000 description 9
- 239000002480 mineral oil Substances 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 235000010446 mineral oil Nutrition 0.000 description 8
- 229910000000 metal hydroxide Inorganic materials 0.000 description 7
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 6
- 238000002485 combustion reaction Methods 0.000 description 6
- 150000002431 hydrogen Chemical class 0.000 description 6
- 229940059904 light mineral oil Drugs 0.000 description 6
- 150000002739 metals Chemical class 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
- 239000007789 gas Substances 0.000 description 5
- 239000011261 inert gas Substances 0.000 description 5
- SIAPCJWMELPYOE-UHFFFAOYSA-N lithium hydride Chemical compound [LiH] SIAPCJWMELPYOE-UHFFFAOYSA-N 0.000 description 5
- 150000004692 metal hydroxides Chemical class 0.000 description 5
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- BAECOWNUKCLBPZ-HIUWNOOHSA-N Triolein Natural products O([C@H](OCC(=O)CCCCCCC/C=C\CCCCCCCC)COC(=O)CCCCCCC/C=C\CCCCCCCC)C(=O)CCCCCCC/C=C\CCCCCCCC BAECOWNUKCLBPZ-HIUWNOOHSA-N 0.000 description 3
- PHYFQTYBJUILEZ-UHFFFAOYSA-N Trioleoylglycerol Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(OC(=O)CCCCCCCC=CCCCCCCCC)COC(=O)CCCCCCCC=CCCCCCCCC PHYFQTYBJUILEZ-UHFFFAOYSA-N 0.000 description 3
- 150000001335 aliphatic alkanes Chemical class 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 238000004891 communication Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 230000008929 regeneration Effects 0.000 description 3
- 238000011069 regeneration method Methods 0.000 description 3
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 3
- 229940117972 triolein Drugs 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- XUCJHNOBJLKZNU-UHFFFAOYSA-M dilithium;hydroxide Chemical compound [Li+].[Li+].[OH-] XUCJHNOBJLKZNU-UHFFFAOYSA-M 0.000 description 2
- 238000007599 discharging Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 150000004679 hydroxides Chemical class 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000002028 Biomass Substances 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- 229910015136 FeMn Inorganic materials 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
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 229910002090 carbon oxide Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- DALUDRGQOYMVLD-UHFFFAOYSA-N iron manganese Chemical compound [Mn].[Fe] DALUDRGQOYMVLD-UHFFFAOYSA-N 0.000 description 1
- FUJCRWPEOMXPAD-UHFFFAOYSA-N lithium oxide Chemical compound [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 description 1
- 229910001947 lithium oxide Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 125000005457 triglyceride group Chemical group 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Images
Classifications
-
- 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
- C01B3/06—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of inorganic compounds containing electro-positively bound hydrogen, e.g. water, acids, bases, ammonia, with inorganic reducing agents
- C01B3/065—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of inorganic compounds containing electro-positively bound hydrogen, e.g. water, acids, bases, ammonia, with inorganic reducing agents from a hydride
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/04—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
- H01M8/04082—Arrangements for control of reactant parameters, e.g. pressure or concentration
- H01M8/04201—Reactant storage and supply, e.g. means for feeding, pipes
- H01M8/04208—Cartridges, cryogenic media or cryogenic reservoirs
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/04—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
- H01M8/04082—Arrangements for control of reactant parameters, e.g. pressure or concentration
- H01M8/04201—Reactant storage and supply, e.g. means for feeding, pipes
- H01M8/04216—Reactant storage and supply, e.g. means for feeding, pipes characterised by the choice for a specific material, e.g. carbon, hydride, absorbent
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/06—Combination of fuel cells with means for production of reactants or for treatment of residues
- H01M8/0606—Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants
- H01M8/065—Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants by dissolution of metals or alloys; by dehydriding metallic substances
-
- 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
- Y02E60/32—Hydrogen storage
-
- 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
- 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
- Y02E60/50—Fuel cells
Definitions
- This invention relates to the storage, generation, and use of hydrogen.
- Hydrogen also has been incorporated into metal hydrides from which the hydrogen can be released by the application of water.
- U.S. Pat. No. 4,155,712, issued May 22, 1979, to Walter G. Taschek discloses a hydrogen generator in which water vapor is combined with a metal hydride, preferably calcium hydride (CaH 2 ) or lithium aluminum hydride (LiAlH 4 ) to release hydrogen (H 2 ) stored in the hydride.
- a metal hydride preferably calcium hydride (CaH 2 ) or lithium aluminum hydride (LiAlH 4 ) to release hydrogen (H 2 ) stored in the hydride.
- U.S. Pat. No. 4,261,955, issued Apr. 14, 1981, to Cornelius E. Bailey, Jr., et al describes subjecting a metal hydride, such as calcium hydride, to water vapor to generate essentially pure hydrogen.
- Known hydrogen-fueled power devices include fuel cells, internal combustion engines, and other devices.
- a light metal hydride such as lithium hydride and a reactant, such as water to produce hydrogen also produces, as a byproduct, a hydroxide of the elemental metal, lithium hydroxide.
- a reactant such as water
- the byproduct i.e., the lithium hydroxide, accumulates until removed.
- the invention features a composition comprising a carrier liquid; a dispersant; and a chemical hydride.
- Implementations of the invention may include one or more of the following features.
- the chemical hydride has a concentration of at least 40% by weight of the composition. In some examples, the chemical hydride has a concentration of less than 75% by weight of the composition, for example, about 61%. In other examples, the chemical hydride has a concentration of more than 90%.
- the carrier liquid includes an organic liquid.
- the organic liquid includes mineral oil, e.g., a light mineral oil.
- the carrier liquid includes a hydrocarbon.
- the hydrocarbon includes an alkane. The alkane is selected from a group consisting of pentane and hexane.
- the composition is in the form of a slurry.
- the carrier liquid has a viscosity in the range of about 32 Saybolt Universal seconds (S.U.s.) at standard temperature and pressure (STP) to about 100 S.U.s but preferably about 42 S.U.s. to about 59 S.U.s.
- STP standard temperature and pressure
- the carrier liquid exhibits a flash point in the range of about 100° C. to about 350° C. and preferably about 154° C. to about 177° C.
- the chemical hydride includes a light metal hydride.
- the light metal hydride is selected from the group consisting of lithium hydride, lithium borohydride, lithium aluminum hydride, sodium hydride, sodium borohydride, sodium aluminum hydride, magnesium hydride, and calcium hydride.
- the chemical hydride includes lithium hydride.
- the dispersant comprises a triglyceride.
- the triglyceride includes a triglyceride of oleic acid.
- the triglyceride includes triolein.
- the chemical hydride includes magnesium hydride.
- the invention features a method that includes mixing chemical hydride particles and an oil to form a slurry.
- the invention in general, in another aspect, includes a composition comprising a mass of chemical hydride particles in a concentration of about 90-95% by weight of the composition, and an oil coating the chemical hydride particles, the oil comprising 5-10% by weight of the composition.
- the invention features apparatus comprising: a reservoir containing a chemical hydride, and a mechanism configured to introduce a reactant to selected different portions of the chemical hydride to effect hydrogen generating reactions at different locations within the reservoir.
- the reservoir includes a canister.
- the reservoir includes chambers that contain chemical hydride.
- the mechanism includes conduits that have open delivery ends arranged to introduce the reactant to respective selected portions of the chemical hydride.
- the conduits are arranged in parallel. The ends are located at different distances along an axis of the reservoir.
- the mechanism is configured to be movable relative to the chemical hydride contained in the reservoir.
- the conduits comprise needles.
- the mechanism includes a valving system that controls the introduction of the reactant to the different portions.
- the reservoir includes an exit for hydrogen generated in the reaction.
- the invention features a hydrogen fuel generation assembly that includes: (a) a reservoir for a slurry comprising a carrier liquid, a triglyceride dispersant, and a chemical hydride; (b) a reservoir for water; (c) a hydride reactor in communication with said slurry reservoir and said water reservoir and adapted to receive the slurry and water from the reservoirs, respectively, and to mix the slurry and water to effect release of hydrogen from the slurry; (d) a tank for receiving the hydrogen from said reactor and for receiving hydroxide byproduct from said reactor, and for facilitating separation of the hydrogen and the hydroxide byproduct; (e) a heat exchanger for receiving the hydrogen from said tank and adapted to condense water from the hydrogen; (f) a gas-liquid separator for receiving hydrogen and water from said heat exchanger and adapted to separate the water from the hydrogen and to dispense dried hydrogen; (g) a conduit for conveying the water from said separator to said water reservoir; and (h
- the reactor includes a tubular housing and a mixer for mixing the slurry and the water.
- the tank is provided with an outlet for flowing hydrogen gas from the tank, and a bottom portion for the receiving of the hydroxide byproduct.
- the power-producing device includes a selected one of a fuel cell, an internal combustion engine, and an external combustion engine. There are also conduit means for conveying condensed water from said fuel cell to said water reservoir.
- the power-producing device includes a selected one of the internal combustion engine and the external combustion engine and the assembly further includes a condenser for condensing water from water vapor from said engine, said condenser being in communication with means for conveying water from said condenser to said water reservoir.
- the invention includes a method for generating hydrogen fuel for a power-producing hydrogen-fueled device, the method includes the steps of: (a) providing a slurry comprising an organic carrier liquid, a triglyceride dispersant, and a chemical hydride; (b) mixing said slurry with water to effect release of hydrogen from the slurry; (c) removing water vapor from the hydrogen released from the slurry, to provide dried hydrogen; and (d) conveying the dried hydrogen to the hydrogen-fueled device for the production of power.
- Implementations of the invention may include one or more of the following features.
- the organic carrier liquid includes a light mineral oil.
- the mixing of said slurry and said water is undertaken with an auger.
- the water removed from the hydrogen is returned back to a source of the water for mixing with the slurry.
- Water condensed from a fuel cell is returned to a source of the water for mixing with the slurry.
- the invention features a regeneration assembly for converting metal oxides and hydroxides to elemental metals, the assembly comprising: (a) a reactor adapted to receive the metal hydroxide and carbon, and adapted to retain a molten carbon-dissolving metal in the reactor; (b) means for flowing gases comprising the elemental metal in gaseous form, carbon monoxide, and hydrogen from said reactor; (c) a condenser adapted to receive the gases flowed from said reactor and adapted to discharge carbon monoxide and hydrogen from a first outlet and the elemental metal, metal oxide, and carbon from a second outlet; (d) a separator adapted to receive the elemental metal, oxide thereof, and carbon from said condenser and to discharge the elemental metal in gaseous form; (e) means for flowing the elemental metal and the carbon dissolving metal in liquid form from said reactor to said separator; and (f) means for flowing the metal oxide and the carbon dissolving metal from said separator to said reactor.
- Implementations of the invention may include one or more of the following features.
- a second separator receives the carbon monoxide and hydrogen from said condenser, said second separator having a first outlet for discharging carbon monoxide and a second outlet for discharging hydrogen.
- the invention features a method for converting metal oxides and metal hydroxides to elemental metals thereof, the method comprising the steps of: (a) admitting the metal hydroxide and carbon into a reactor having molten carbon-dissolving metal therein; (b) flowing gases comprising the elemental metal in gaseous form, carbon monoxide and hydrogen from the reactor to a condenser; (c) condensing out the elemental metal and oxide thereof, and carbon, and flowing same to a separator; (d) flowing carbon monoxide and hydrogen from the condenser; (e) flowing the elemental metal and the carbon dissolving metal from the reactor to the separator; (f) flowing elemental metal oxide and the carbon dissolving metal from the separator to the reactor; and (g) flowing the elemental metal from the separator.
- an inert gas is flowed into the reactor.
- FIGS. 1, 2 , 3 , and 6 show hydride containers with water feed tubes.
- FIG. 4 is a block diagram of a hydrogen generator.
- FIG. 5 is a block diagram of a hydrogen generator and a metal regenerator.
- FIGS. 7 and 8 are side sectional and top views of a hydrogen generation canister.
- Hydrogen fuel can be stored in a medium that takes the form of a slurry.
- the slurry includes a carrier liquid, such as an organic carrier, a dispersant, such as a triglyceride, for stabilizing the slurry, and a chemical hydride dispersed in the carrier liquid at a concentration of at least 40 and typically less than 75%, except for a dry, non-pumpable slurry described later, in which the concentration may be higher.
- the best range can be determined experimentally. Higher percentages yield higher energy densities. Lower percentages are less viscous.
- a good tradeoff for a slurry of LiH with light mineral oil and a triglyceride dispersant is about 61% of LiH. Above this percentage, the slurry became too thick to pump. Higher concentrations may be achievable by replacing LiH with MgH 2 .
- Typical slurries will be in the 50-70% range depending on the hydride used. LiH slurries will likely be in the 50-61% range. A thinner slurry, with as little as 40% hydride by weight of the slurry may be useful for certain applications.
- the slurry may be safely stored and transported and the hydrogen may be easily extracted for use as a fuel.
- the slurry is not highly flammable or combustible and may be safely handled, stored, and transported.
- the slurry is stable at normal environmental temperatures and pressures and, because it is a liquid, can easily be pumped through conduits. The reaction rate with the slurry is easily controlled.
- the carrier liquid may be an organic carrier liquid, such as mineral oil or a low molecular weight hydrocarbon, such as an alkane, preferably pentane or hexane.
- a preferable mineral oil is a non-toxic light mineral oil which exhibits a high flash point, in the range of about 154 degrees C. to about 177 degrees C. and a viscosity in the range of about 42 Saybolt Universal seconds (S.U.s.) to about 59 S.U.s.
- the mineral oil is not chemically reactive with metal hydrides, produces relatively low vapor pressure, and remains liquid through a temperature range of about ⁇ 40 to 200 degrees C.
- the carrier liquid renders the slurry pumpable and, as a safe liquid, simple to store or transport.
- the carrier slows the reaction rate when water is introduced into the hydride.
- Other carriers may work well, including carriers that are without water bonds and preferably are without OH bonds.
- Silicone-based carriers may also work for slurries. Light mineral oils have been tested successfully at percentages of 37 to 50% by weight of the slurry.
- the dispersant in the slurry may be, for example, a triglyceride dispersant, which sterically stabilizes the slurry.
- the triglyceride dispersant preferably is triglyceride of oleic acid, or triolein.
- Triolein is not normally considered to have the properties of a dispersant.
- Other dispersants that could be used include Hypermer LP1, a polymeric dispersant.
- One function of the dispersant is to attach to the particles of chemical hydride, increasing the drag of the particle in the carrier fluid thus helping to prevent settling.
- the dispersant also helps to keep the particles from agglomerating. The dispersant promotes the formation of the slurry and the stabilization of the hydride into the mineral oil.
- dispersant concentrations range from 0.68% to 1.88% in tests. A particularly good percentage is 0.75%. A broader range of percentages, from about 0.5 to about 2% of the slurry could be used.
- the dispersants could be polymeric dispersants. A combination of triglyceride and polymeric dispersants may also be used, and may be particularly useful if the hydride is magnesium hydride.
- Dispersants sometimes have surfactant properties that may also be useful in the formation of the slurry.
- the chemical hydride in the slurry may be a light metal hydride, such as lithium hydride, lithium borohydride, lithium aluminum hydride, magnesium hydride, calcium hydride, sodium hydride, sodium borohydride, and sodium aluminum hydride, all of which react with water to produce high purity hydrogen.
- a light metal hydride such as lithium hydride, lithium borohydride, lithium aluminum hydride, magnesium hydride, calcium hydride, sodium hydride, sodium borohydride, and sodium aluminum hydride, all of which react with water to produce high purity hydrogen.
- reaction LiH+H 2 O ⁇ LiOH+H 2 LiBH 4 +4H 2 O ⁇ LiOH+H 3 BO 3 +4H 2 MgH 2 +2H 2 O ⁇ Mg(OH) 2 +2H 2 CaH 2 +2H 2 O ⁇ Ca(OH) 2 +2H 2 NaBH 4 +4H 2 O ⁇ NaOH+H 3 BO 3 +4H 2
- the hydrides are finely ground before being mixed with the other components of the slurry.
- the particles of the slurry are between 5 and 10 microns in diameter.
- a powder form of hydride This powder is first combined with a mixture of the mineral oil and dispersant. Then the mixture is ground in a grinder to further reduce the size of the particles. The final particles were measured to be primarily between 5 and 10 microns in diameter.
- the hydrogen generation capability of the above hydrides when reacted with water is outstanding.
- the volume of H 2 produced by complete hydrolysis of 1 kg. (2.2 lb.) of lithium hydride is 2800 liters (99 ft 3 ), and by complete hydrolysis of 1 kg of lithium borohydride is 4100 liters (145 ft 3 ).
- pumpable mixtures can usefully have proportions of components that are 40-75% hydride (but see the later discussion concerning dry slurries having greater concentrations), 28-59.5% carrier, and 0.5 to 2% dispersant.
- a particularly good mixture is 60% lithium hydride, 0.75% triglyceride, and 39.25% light mineral oil.
- Slurries of the kind described here have a liquid-like flow characteristic and may be used in generation processes that involve continuous formation and extraction of hydrogen.
- the slurry can be continuously introduced into a tank, while a portion of the slurry is continuously drawn off and subjected to water to release hydrogen.
- the reaction may be stopped and started quickly and repeatedly without sacrificing control of the reaction or safety.
- the oil in the slurry protects the hydride from unintentional contact with moisture in the air and renders the hydride pumpable:
- the slurry when in the form of a continuing stream, provides a path for dissipating heat generated from the hydride/water reaction. That, in conjunction with control of surface chemistry of the carrier liquid, permits easy control of the hydride reaction rate. In a continuous process, the hydrogen production rate is controlled by the injection rate of water and hydride.
- the dispersant maintains the hydride particles in suspension.
- the dispersant attaches to the particles and fends off adjacent particles to prevent agglomeration of the particles.
- the mineral oil protects the particles from unintentional reaction with water.
- the amount of the dispersant and the size of the hydride particles control the viscosity of the slurry.
- the slurry burns only if high heat is applied, as by a blow torch, and maintained. Upon removal of heat, the burning of the slurry ceases and flames die out.
- An alternative hydrogen storage medium would be in the form of a dry slurry comprising 90%-95% hydride.
- a drop of water is injected into a mass of dry slurry in a test tube, a volume of about 1 cubic centimeter of the hydride around the droplet reacts with the water, releasing hydrogen.
- Some of the water flashes to steam and the steam reacts with hydride as it escapes the tube with the released hydrogen.
- this effect can be exploited by packing dry hydride slurry 102 into a tube 100 and pulling a needle 104 (which had been placed in the tube when it was packed) out of the tube while intermittently passing water droplets through the needle. Each water droplet would then strike fresh hydride until the needle is fully withdrawn.
- an alternate configuration would be to locate needles 106 strategically throughout (e.g., along the length of) a large mass of dry hydride or in tubes 108 of hydride (only one tube is shown in FIG. 2 ).
- a valve 110 would then be controlled to selectively put water droplets into different parts of the mass or into different parts of the tube to produce hydrogen as required.
- This arrangement would have the advantage of requiring only one moving part, the valve, and would provide the opportunity to control where the heat is being generated and how the heat of reaction is dissipated.
- another configuration would use several parallel needles 120 with ends 122 located at different distances along the length of a tube of hydride 124 .
- hydride would be reacted along the tube at several locations.
- the set of needles would be moved outward 125 along the centerline 126 of the tube so that the ends 122 are in contact with new hydride slurry.
- This configuration reduces the distance that must be traversed by any one needle. Because reacted hydride 128 will exist downstream of the lower needles, a path of egress 132 must be provided for the generated hydrogen and steam.
- the path could be provided by non-reacting porous material 130 positioned along the wall of the hydride tube far enough away from the centerline of the tube so that all the water vapor is consumed in reaction with hydride before the gases reach the porous wall. Then only hydrogen would be conducted along the porous material to an outlet end 134 .
- the oil in the dry slurry coats the hydride particles and reduces the rates of reactions with the slurry.
- a wet slurry can be used to generate hydrogen in a hydrogen fuel generation assembly 8 that includes a reservoir 10 for the slurry, a reservoir 14 for water, and a hydride reactor 18 .
- the water and slurry are delivered by pumps 16 , 12 to the reactor 18 , which mixes the slurry and water to release hydrogen.
- a tank 26 receives the hydrogen and hydroxide waste from the reactor, and separates the hydrogen from the hydroxide byproduct.
- a heat exchanger 32 receives the hydrogen (and associated water vapor) carried in conduit 30 from the tank and condenses the water.
- a gas-liquid separator 40 receives hydrogen and water carried in line 34 from the heat exchanger, separates the water from the hydrogen, and dispenses dried hydrogen and water in discrete streams 44 , 42 .
- the water that is carried in conduit 34 is partly in droplet form, and partly in liquid stream form.
- the water from the separator is conveyed to the water reservoir 14 (or to water flowing from the reservoir to the reactor) through conduits 42 , 36 , and the dried hydrogen is conveyed to a hydrogen-fueled power-producing device 38 , such as a fuel cell.
- the hydride reactor 18 includes a tubular member 20 housing a mixing device, such as an auger 22 , rotatable in the housing.
- a mixing device such as an auger 22
- Other mixing devices could also be used including ultrasonic mixers or vibratory mixers.
- the amount of water pumped to the reactor 18 is more than is needed to complete the release of hydrogen from the slurry.
- the excess water is converted to steam and carries heat produced in the reaction out of the reaction chamber, thus controlling the temperature of the reaction.
- the tubular member 20 may be fixed to, or otherwise in communication with an inlet 24 of the tank 26 .
- tank 26 the hydroxide solid material falls to the bottom 28 for removal by way of an outlet 29 .
- the hydrogen-fueled power-providing device is a fuel cell 38
- water condensed from the exhaust of the fuel cell is also returned to the water reservoir 14 , or to the water flowing from the reservoir to the reactor.
- the assembly also includes a condenser 46 that accepts water vapor from the device 38 through a conduit 48 and condenses water.
- the condensed water passes through conduit 50 into the conduit 38 for return to the water reservoir 14 (or water flowing from the reservoir into the reactor 18 ).
- hydrogen suitable for use with fuel cells or engines is generated by providing a slurry including an organic carrier liquid, such as a light mineral oil, a triglyceride dispersant, and a chemical hydride, such as lithium hydride, mixing the slurry with water to release hydrogen from the slurry, controlling the reaction temperature by vaporization of water, condensing water from the hydrogen released from the slurry, and conveying the dried hydrogen to the hydrogen-fueled power-producing device.
- organic carrier liquid such as a light mineral oil, a triglyceride dispersant, and a chemical hydride, such as lithium hydride
- the slurry may be prepared at centralized plants, where it is readily pumpable into tank trucks or through pipes to distribution centers where the slurry can be pumped into tanks of vehicles powered by hydrogen fuel cells, or into slurry reservoirs of homes or business and industrial facilities.
- the hydroxide byproduct of the hydrogen production reaction may be picked up upon the next delivery of slurry is made and transported back to a regeneration plant, where the hydroxide will be separated from the mineral oil and will be regenerated to hydride, as explained below.
- Another method of distributing water to the hydride in a chamber is through needles placed in hydride tubes in locations that permit water droplets that pass through needles to react with enough of the hydride to release more than 90% of the potential hydrogen.
- Several needles could be placed along the length of each tube. Water would be delivered first to the needle 154 that is farthest from the exit of the tube 156 . This water would react with the hydride around it. Some of the water would be evaporated and would travel through unreacted hydride causing further reaction along the tube.
- a valving system 158 would be incorporated with the tubes of hydride to deliver water to the needles selectively.
- a computer control system 160 would record which needles had already delivered water and would select needles that had not delivered water for future hydrogen release.
- the system of FIG. 6 overcomes the blockage of water and hydrogen flow to all portions of hydride by the metal hydroxide byproduct that is formed during the reaction. By selecting the sequence of tubes and needles for water injection, water is delivered only to fresh hydride.
- the arrangement of FIG. 6 also allows the heat released from the reaction in one tube to be dissipated from the tube while another tube in the system is reacting with water to deliver hydrogen. By causing the reactions to occur in different tubes, the heat of reaction on one tube can dissipate to the environment while slurry and water are reacting in another tube to continue to produce hydrogen.
- the system may be designed so that the heat in one tube is dissipated before another reaction must take place in that tube. This will control the temperature of the tube and the materials within the tube.
- the needles could be retractable from the tubes in a manner similar to that shown in FIG. 3 .
- the water supply tubes 170 are buried in a bed 172 of chemical-hydride slurry in such a manner that each supply tube will provide enough water to react with the chemical hydride near the outlet 174 of the tube.
- Water is stored in chambers 176 located around the perimeter of a canister 180 that holds the lithium hydrid tubes 182 .
- a valve 177 sequentially directs charges of water to each successive region of chemical hydride.
- the valving mechanism could be based on inkjet technology. Water charges would be supplied when the pressure in the canister drops below a set value. In this manner, the pressure in the canister will be cycled between a high value of about 200 psi and a low value of about 50 psi.
- the generated hydrogen exits the canister through conduit 183 after passing through a carbon filter 184 .
- the hydrogen produced could be consumed by an attached fuel cell as fast as it is generated and the electricity produced by the fuel cell may be stored in a battery or capacitor.
- the reaction within the canister 176 can be controlled so that there is never a surplus of water.
- the chemical hydride reacts with water, its volume increases. This increased volume occupies the storage volume of the water that is consumed, to achieve a minimum system volume.
- Flexible walls 190 enable the water supply chambers and the hydride tubes to change volume as needed.
- the hydroxide byproduct can be processed to regenerate its elemental metal component.
- the metal can then re-used in the hydride fuel generating process by hydrogenating the elemental metal to produce the hydride fuel.
- the hydrogen generation assembly is similar to the one shown in FIG. 4 and includes a reactor 210 and inlet tubes 212 , 214 which convey slurry and water, respectively, to the reactor 210 .
- the reactor 210 includes a tubular portion 216 housing an auger 218 for mixing the slurry and water to effect release of hydrogen gas (H 2 ) from the slurry.
- a reactor tank portion 219 receives the hydrogen gas and solid matter from the auger 218 .
- the hydrogen gas moves toward a top portion 220 of the reactor tank portion 219 and is carried by a conduit 222 to a separator (not shown) for drying the hydrogen.
- the hydroxide which is a wet solid dust 224 , falls to a bottom portion 226 of the reactor tank portion 219 , from which it is removed and conveyed by transport means 223 to a mixer 228 .
- Mixer 228 receives carbon through a conduit 234 and mixes the carbon with the hydroxide.
- the conduit 234 introduces the carbon, in solid or fluid form, such as coal in pellet or powder form, biomass, or graphite, to the mixer 228 .
- the mixed carbon and hydroxide are transported by transport 229 to a second reactor 230 where there is disposed a molten pool 232 of carbon dissolving metal, such as iron, nickel, manganese, and alloys of those metals.
- the metal because of its high heat capacity and thermal conductivity, provides superior heat transfer characteristics.
- the mixer 228 may be omitted and the carbon and hydroxide fed directly into the reactor 230 .
- the intermixed carbon and hydroxide particles form a layer 238 in the reactor 230 , the layer 238 descending into a layer 236 , and then sinking into the pool of molten carbon dissolving metal 232 .
- layer 236 decomposition of hydroxide into oxide and water vapor occurs.
- layer 232 the reaction between carbon and metal oxide produces elemental metal and carbon monoxide.
- the hydroxide is lithium hydroxide (LiOH) and the carbon-dissolving metal is iron (Fe).
- the lithium hydroxide and carbon introduced into the second reactor 230 forms the upper layer 328 which descends in the reactor 230 and in the area of layer 236 produces lithuim oxide (Li 2 O), water (H 2 O), hydrogen (H 2 ) and carbon monoxide (CO).
- the hydrogen (H 2 ) and carbon monoxide (CO) rise toward the top of the reactor 230 .
- Lithium oxide (Li 2 O) and carbon (C) sink into the molten pool of iron (Fe) where they produce lithium metal (2Li), carbon monoxide (CO) and iron. (Fe).
- lithium gas (Li) is also produced, which rises to the second reactor upper portion 238 .
- Liquid lithium (Li) and iron (Fe) pass from the second reactor metal pool 232 to a separator 240 through a conduit 242 .
- the gaseous lithium (Li) in the upper portion 238 of the reactor 230 along with hydrogen (H 2 ) and carbon monoxide (CO), pass through a conduit 246 to a condenser 244 .
- Condenser 244 separates out carbon, lithium, and lithium oxide, which, in solid/liquid form, pass into the separator 240 through a conduit 248 .
- the condenser 244 discharges carbon monoxide and hydrogen gas through a conduit 250 to another separator 258 , which separates the carbon monoxide from the hydrogen.
- the lithium (Li) is evaporated and released through conduit 252 in vapor form, while the lithium oxide (Li 2 O), in liquid form, is passed through conduit 254 to the molten metal pool 232 in the second reactor 230 .
- the lithium discharged by the separator 240 and the hydrogen discharged by the separator 258 may be recycled for use in the hydride slurry.
- the conduits 242 , 254 may have magneto-hydrodynamic pumps for pumping molten metal.
- the molten metal pool 232 may be maintained at a temperature of at least 1500° Kelvin, somewhat above the melting temperature of carbon saturated iron (1430° K). Alloys can be used to tailor the temperature.
- the operating temperature of the second reactor 230 is maintained lower than would otherwise be required by continuously introducing into the molten pool 232 an inert gas, such as argon, through an inlet 256 .
- the lithium concentration in the lower layer 232 of the reactor 230 is thus maintained at a low level.
- the continuous use of the inert gas tilts the thermodynamic equilibrium in favor of the lithium, allows the operating temperature to be reduced significantly and achieves higher yields at lower temperatures. Without the inert gas, the second reactor 230 would have to be maintained at about 1850° K to obtain the same yield as 1500° K with the inert gas.
- the temperature in the second reactor 230 may also be influenced by using an iron alloy such as iron-manganese (FeMn).
- the carbon components When the carbon components are introduced directly into the reactor 230 , they may include natural gas, which is flowable into the reactor 230 through inlet 256 or a similar inlet.
- the assembly and method provide for a substantially closed-loop conversion, without discharge of harmful elements into the atmosphere.
- elemental metals other than lithium may be recovered, such as sodium and potassium.
- Alkaline-earth metals, such as magnesium and calcium, could also be recovered.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Sustainable Energy (AREA)
- Sustainable Development (AREA)
- Manufacturing & Machinery (AREA)
- Electrochemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Combustion & Propulsion (AREA)
- Inorganic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Fuel Cell (AREA)
- Paints Or Removers (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Hydrogen, Water And Hydrids (AREA)
Abstract
A composition comprising a carrier liquid; a dispersant; and a chemical hydride. The composition can be used in a hydrogen generator to generate hydrogen for use, e.g., as a fuel. A regenerator recovers elemental metal from byproducts of the hydrogen generation process.
Description
- This application claims the benefit of the filing dates of Provisional U.S. Patent Applications Ser. No. 60/261,616, Hydrogen Fuel Storage Slurry, Jonathan L. Rolfe et al.; Ser. No. 60/261,601, Hydrogen Fuel Generation Assembly and Method, Christopher A. Larsen et al.; and Ser. No. 60/261,600, Regeneration Assembly and Method for Converting Metal Oxides and Metal Hydroxides to Elemental Metals, Ravi Konduri et al., all of which were filed on Jan. 12, 2001, and all of which are incorporated here by reference in their entireties.
- This application is a continuation-in-part of U.S. patent application Ser. No. 09/707,105, Disposable Hydrogen Fuel Source, filed Nov. 6, 2000, which is a divisional of U.S. patent application Ser. No. 09/309,198, filed May 10, 1999, now abandoned, and is incorporated by reference here in its entirety.
- This invention was made with Government support under contracts awarded by the U.S. Department of Energy. The Government has certain rights in the invention.
- This invention relates to the storage, generation, and use of hydrogen.
- Traditional storage technologies for hydrogen include bottled compressed hydrogen gas and bottled liquid hydrogen. The use of such technologies has been limited because of dangers in storage and in handling and transporting. Hydrogen gas and cryogenic liquid in storage or transport have evidenced instability and high combustibility.
- Hydrogen also has been incorporated into metal hydrides from which the hydrogen can be released by the application of water. U.S. Pat. No. 4,155,712, issued May 22, 1979, to Walter G. Taschek, discloses a hydrogen generator in which water vapor is combined with a metal hydride, preferably calcium hydride (CaH2) or lithium aluminum hydride (LiAlH4) to release hydrogen (H2) stored in the hydride. U.S. Pat. No. 4,261,955, issued Apr. 14, 1981, to Cornelius E. Bailey, Jr., et al, describes subjecting a metal hydride, such as calcium hydride, to water vapor to generate essentially pure hydrogen.
- Known hydrogen-fueled power devices include fuel cells, internal combustion engines, and other devices.
- Mixing a light metal hydride, such as lithium hydride and a reactant, such as water to produce hydrogen also produces, as a byproduct, a hydroxide of the elemental metal, lithium hydroxide. Although the generation of hydrogen in such a process can occur on a continuing basis, the byproduct, i.e., the lithium hydroxide, accumulates until removed.
- In general, in one aspect, the invention features a composition comprising a carrier liquid; a dispersant; and a chemical hydride. Implementations of the invention may include one or more of the following features. The chemical hydride has a concentration of at least 40% by weight of the composition. In some examples, the chemical hydride has a concentration of less than 75% by weight of the composition, for example, about 61%. In other examples, the chemical hydride has a concentration of more than 90%. The carrier liquid includes an organic liquid. The organic liquid includes mineral oil, e.g., a light mineral oil. The carrier liquid includes a hydrocarbon. The hydrocarbon includes an alkane. The alkane is selected from a group consisting of pentane and hexane. The composition is in the form of a slurry. The carrier liquid has a viscosity in the range of about 32 Saybolt Universal seconds (S.U.s.) at standard temperature and pressure (STP) to about 100 S.U.s but preferably about 42 S.U.s. to about 59 S.U.s. The carrier liquid exhibits a flash point in the range of about 100° C. to about 350° C. and preferably about 154° C. to about 177° C.
- The chemical hydride includes a light metal hydride. The light metal hydride is selected from the group consisting of lithium hydride, lithium borohydride, lithium aluminum hydride, sodium hydride, sodium borohydride, sodium aluminum hydride, magnesium hydride, and calcium hydride. The chemical hydride includes lithium hydride.
- The dispersant comprises a triglyceride. The triglyceride includes a triglyceride of oleic acid. The triglyceride includes triolein. The chemical hydride includes magnesium hydride.
- In general, in another aspect, the invention features a method that includes mixing chemical hydride particles and an oil to form a slurry.
- In general, in another aspect, the invention includes a composition comprising a mass of chemical hydride particles in a concentration of about 90-95% by weight of the composition, and an oil coating the chemical hydride particles, the oil comprising 5-10% by weight of the composition.
- In general, in another aspect, the invention features apparatus comprising: a reservoir containing a chemical hydride, and a mechanism configured to introduce a reactant to selected different portions of the chemical hydride to effect hydrogen generating reactions at different locations within the reservoir.
- Implementations of the invention may include one or more of the following features. The reservoir includes a canister. The reservoir includes chambers that contain chemical hydride. The mechanism includes conduits that have open delivery ends arranged to introduce the reactant to respective selected portions of the chemical hydride. The conduits are arranged in parallel. The ends are located at different distances along an axis of the reservoir. The mechanism is configured to be movable relative to the chemical hydride contained in the reservoir. The conduits comprise needles. The mechanism includes a valving system that controls the introduction of the reactant to the different portions. The reservoir includes an exit for hydrogen generated in the reaction.
- In general, in another aspect, the invention features a hydrogen fuel generation assembly that includes: (a) a reservoir for a slurry comprising a carrier liquid, a triglyceride dispersant, and a chemical hydride; (b) a reservoir for water; (c) a hydride reactor in communication with said slurry reservoir and said water reservoir and adapted to receive the slurry and water from the reservoirs, respectively, and to mix the slurry and water to effect release of hydrogen from the slurry; (d) a tank for receiving the hydrogen from said reactor and for receiving hydroxide byproduct from said reactor, and for facilitating separation of the hydrogen and the hydroxide byproduct; (e) a heat exchanger for receiving the hydrogen from said tank and adapted to condense water from the hydrogen; (f) a gas-liquid separator for receiving hydrogen and water from said heat exchanger and adapted to separate the water from the hydrogen and to dispense dried hydrogen; (g) a conduit for conveying the water from said separator to said water reservoir; and (h) a conduit for conveying the dried hydrogen to a hydrogen-fueled power-producing device.
- Implementations of the invention may include one or more of the following features. The reactor includes a tubular housing and a mixer for mixing the slurry and the water. The tank is provided with an outlet for flowing hydrogen gas from the tank, and a bottom portion for the receiving of the hydroxide byproduct. The power-producing device includes a selected one of a fuel cell, an internal combustion engine, and an external combustion engine. There are also conduit means for conveying condensed water from said fuel cell to said water reservoir. The power-producing device includes a selected one of the internal combustion engine and the external combustion engine and the assembly further includes a condenser for condensing water from water vapor from said engine, said condenser being in communication with means for conveying water from said condenser to said water reservoir.
- In general, in another aspect, the invention includes a method for generating hydrogen fuel for a power-producing hydrogen-fueled device, the method includes the steps of: (a) providing a slurry comprising an organic carrier liquid, a triglyceride dispersant, and a chemical hydride; (b) mixing said slurry with water to effect release of hydrogen from the slurry; (c) removing water vapor from the hydrogen released from the slurry, to provide dried hydrogen; and (d) conveying the dried hydrogen to the hydrogen-fueled device for the production of power.
- Implementations of the invention may include one or more of the following features. The organic carrier liquid includes a light mineral oil. The mixing of said slurry and said water is undertaken with an auger. The water removed from the hydrogen is returned back to a source of the water for mixing with the slurry. Water condensed from a fuel cell is returned to a source of the water for mixing with the slurry.
- In general, in another aspect, the invention features a regeneration assembly for converting metal oxides and hydroxides to elemental metals, the assembly comprising: (a) a reactor adapted to receive the metal hydroxide and carbon, and adapted to retain a molten carbon-dissolving metal in the reactor; (b) means for flowing gases comprising the elemental metal in gaseous form, carbon monoxide, and hydrogen from said reactor; (c) a condenser adapted to receive the gases flowed from said reactor and adapted to discharge carbon monoxide and hydrogen from a first outlet and the elemental metal, metal oxide, and carbon from a second outlet; (d) a separator adapted to receive the elemental metal, oxide thereof, and carbon from said condenser and to discharge the elemental metal in gaseous form; (e) means for flowing the elemental metal and the carbon dissolving metal in liquid form from said reactor to said separator; and (f) means for flowing the metal oxide and the carbon dissolving metal from said separator to said reactor.
- Implementations of the invention may include one or more of the following features. A second separator receives the carbon monoxide and hydrogen from said condenser, said second separator having a first outlet for discharging carbon monoxide and a second outlet for discharging hydrogen.
- In general, in another aspect, the invention features a method for converting metal oxides and metal hydroxides to elemental metals thereof, the method comprising the steps of: (a) admitting the metal hydroxide and carbon into a reactor having molten carbon-dissolving metal therein; (b) flowing gases comprising the elemental metal in gaseous form, carbon monoxide and hydrogen from the reactor to a condenser; (c) condensing out the elemental metal and oxide thereof, and carbon, and flowing same to a separator; (d) flowing carbon monoxide and hydrogen from the condenser; (e) flowing the elemental metal and the carbon dissolving metal from the reactor to the separator; (f) flowing elemental metal oxide and the carbon dissolving metal from the separator to the reactor; and (g) flowing the elemental metal from the separator. In some implementations, an inert gas is flowed into the reactor.
- Other advantages and features will become apparent from the following description and from the claims.
- (
FIGS. 1, 2 , 3, and 6 show hydride containers with water feed tubes. -
FIG. 4 is a block diagram of a hydrogen generator. -
FIG. 5 is a block diagram of a hydrogen generator and a metal regenerator. -
FIGS. 7 and 8 are side sectional and top views of a hydrogen generation canister.) - The Slurry
- Hydrogen fuel can be stored in a medium that takes the form of a slurry. The slurry includes a carrier liquid, such as an organic carrier, a dispersant, such as a triglyceride, for stabilizing the slurry, and a chemical hydride dispersed in the carrier liquid at a concentration of at least 40 and typically less than 75%, except for a dry, non-pumpable slurry described later, in which the concentration may be higher. The best range can be determined experimentally. Higher percentages yield higher energy densities. Lower percentages are less viscous. A good tradeoff for a slurry of LiH with light mineral oil and a triglyceride dispersant is about 61% of LiH. Above this percentage, the slurry became too thick to pump. Higher concentrations may be achievable by replacing LiH with MgH2.
- Typical slurries will be in the 50-70% range depending on the hydride used. LiH slurries will likely be in the 50-61% range. A thinner slurry, with as little as 40% hydride by weight of the slurry may be useful for certain applications.
- The slurry may be safely stored and transported and the hydrogen may be easily extracted for use as a fuel. The slurry is not highly flammable or combustible and may be safely handled, stored, and transported. The slurry is stable at normal environmental temperatures and pressures and, because it is a liquid, can easily be pumped through conduits. The reaction rate with the slurry is easily controlled.
- The Carrier Liquid
- The carrier liquid may be an organic carrier liquid, such as mineral oil or a low molecular weight hydrocarbon, such as an alkane, preferably pentane or hexane. A preferable mineral oil is a non-toxic light mineral oil which exhibits a high flash point, in the range of about 154 degrees C. to about 177 degrees C. and a viscosity in the range of about 42 Saybolt Universal seconds (S.U.s.) to about 59 S.U.s.
- The mineral oil is not chemically reactive with metal hydrides, produces relatively low vapor pressure, and remains liquid through a temperature range of about −40 to 200 degrees C. The carrier liquid renders the slurry pumpable and, as a safe liquid, simple to store or transport. The carrier slows the reaction rate when water is introduced into the hydride. The use of a slurry permits easy refueling, as by simply topping off a tank. Other carriers may work well, including carriers that are without water bonds and preferably are without OH bonds. Silicone-based carriers may also work for slurries. Light mineral oils have been tested successfully at percentages of 37 to 50% by weight of the slurry.
- The Dispersant
- The dispersant in the slurry may be, for example, a triglyceride dispersant, which sterically stabilizes the slurry. The triglyceride dispersant preferably is triglyceride of oleic acid, or triolein.
- Triolein is not normally considered to have the properties of a dispersant. Other dispersants that could be used include Hypermer LP1, a polymeric dispersant. One function of the dispersant is to attach to the particles of chemical hydride, increasing the drag of the particle in the carrier fluid thus helping to prevent settling. The dispersant also helps to keep the particles from agglomerating. The dispersant promotes the formation of the slurry and the stabilization of the hydride into the mineral oil.
- Good dispersant concentrations range from 0.68% to 1.88% in tests. A particularly good percentage is 0.75%. A broader range of percentages, from about 0.5 to about 2% of the slurry could be used. Instead of tryglicerides, the dispersants could be polymeric dispersants. A combination of triglyceride and polymeric dispersants may also be used, and may be particularly useful if the hydride is magnesium hydride.
- Dispersants sometimes have surfactant properties that may also be useful in the formation of the slurry.
- The Chemical Hydride
- U.S. patent application Ser. No. 09/309,198, filed May 10, 1999, and incorporated by reference in its entirety, discloses hydrogen-containing material, such as lithium hydride, lithium aluminum hydride, calcium hydride, sodium hydride, magnesium hydride, and others, for contact with a reactant, such as water, to produce hydrogen.
- The chemical hydride in the slurry may be a light metal hydride, such as lithium hydride, lithium borohydride, lithium aluminum hydride, magnesium hydride, calcium hydride, sodium hydride, sodium borohydride, and sodium aluminum hydride, all of which react with water to produce high purity hydrogen.
- Examples of reactions are:
LiH+H2O→LiOH+H2
LiBH4+4H2O→LiOH+H3BO3+4H2
MgH2+2H2O→Mg(OH)2+2H2
CaH2+2H2O→Ca(OH)2+2H2
NaBH4+4H2O→NaOH+H3BO3+4H2
The hydrides are finely ground before being mixed with the other components of the slurry. The particles of the slurry are between 5 and 10 microns in diameter. - To make the slurry, we start with a powder form of hydride. This powder is first combined with a mixture of the mineral oil and dispersant. Then the mixture is ground in a grinder to further reduce the size of the particles. The final particles were measured to be primarily between 5 and 10 microns in diameter.
- The hydrogen generation capability of the above hydrides when reacted with water is outstanding. For example, the volume of H2 produced by complete hydrolysis of 1 kg. (2.2 lb.) of lithium hydride is 2800 liters (99 ft3), and by complete hydrolysis of 1 kg of lithium borohydride is 4100 liters (145 ft3).
- Characteristics of the Slurry
- In summary, pumpable mixtures (slurries) can usefully have proportions of components that are 40-75% hydride (but see the later discussion concerning dry slurries having greater concentrations), 28-59.5% carrier, and 0.5 to 2% dispersant. A particularly good mixture is 60% lithium hydride, 0.75% triglyceride, and 39.25% light mineral oil.
- Slurries of the kind described here (with hydride concentrations less than about 0.75%) have a liquid-like flow characteristic and may be used in generation processes that involve continuous formation and extraction of hydrogen. In such processes, the slurry can be continuously introduced into a tank, while a portion of the slurry is continuously drawn off and subjected to water to release hydrogen. The reaction may be stopped and started quickly and repeatedly without sacrificing control of the reaction or safety.
- The oil in the slurry protects the hydride from unintentional contact with moisture in the air and renders the hydride pumpable: The slurry, when in the form of a continuing stream, provides a path for dissipating heat generated from the hydride/water reaction. That, in conjunction with control of surface chemistry of the carrier liquid, permits easy control of the hydride reaction rate. In a continuous process, the hydrogen production rate is controlled by the injection rate of water and hydride.
- Because the oil inhibits water access to the hydride, it controls the rate of reaction, which otherwise could be explosive. The dispersant maintains the hydride particles in suspension. The dispersant attaches to the particles and fends off adjacent particles to prevent agglomeration of the particles. The mineral oil protects the particles from unintentional reaction with water. The amount of the dispersant and the size of the hydride particles control the viscosity of the slurry.
- The slurry burns only if high heat is applied, as by a blow torch, and maintained. Upon removal of heat, the burning of the slurry ceases and flames die out.
- Alternative Dry Slurry
- An alternative hydrogen storage medium would be in the form of a dry slurry comprising 90%-95% hydride. When a drop of water is injected into a mass of dry slurry in a test tube, a volume of about 1 cubic centimeter of the hydride around the droplet reacts with the water, releasing hydrogen. Some of the water flashes to steam and the steam reacts with hydride as it escapes the tube with the released hydrogen.
- As shown in
FIG. 1 , this effect can be exploited by packingdry hydride slurry 102 into atube 100 and pulling a needle 104 (which had been placed in the tube when it was packed) out of the tube while intermittently passing water droplets through the needle. Each water droplet would then strike fresh hydride until the needle is fully withdrawn. - As shown in
FIG. 2 , an alternate configuration would be to locateneedles 106 strategically throughout (e.g., along the length of) a large mass of dry hydride or intubes 108 of hydride (only one tube is shown inFIG. 2 ). Avalve 110 would then be controlled to selectively put water droplets into different parts of the mass or into different parts of the tube to produce hydrogen as required. This arrangement would have the advantage of requiring only one moving part, the valve, and would provide the opportunity to control where the heat is being generated and how the heat of reaction is dissipated. - As shown schematically in
FIG. 3 , another configuration would use severalparallel needles 120 withends 122 located at different distances along the length of a tube ofhydride 124. As the water drops are supplied simultaneously to all of the needles of the set, hydride would be reacted along the tube at several locations. Then the set of needles would be moved outward 125 along thecenterline 126 of the tube so that the ends 122 are in contact with new hydride slurry. This configuration reduces the distance that must be traversed by any one needle. Because reactedhydride 128 will exist downstream of the lower needles, a path ofegress 132 must be provided for the generated hydrogen and steam. The path could be provided by non-reactingporous material 130 positioned along the wall of the hydride tube far enough away from the centerline of the tube so that all the water vapor is consumed in reaction with hydride before the gases reach the porous wall. Then only hydrogen would be conducted along the porous material to anoutlet end 134. - The oil in the dry slurry coats the hydride particles and reduces the rates of reactions with the slurry.
- The Hydrogen Generator
- As shown in
FIG. 4 , a wet slurry can be used to generate hydrogen in a hydrogenfuel generation assembly 8 that includes areservoir 10 for the slurry, areservoir 14 for water, and ahydride reactor 18. The water and slurry are delivered bypumps reactor 18, which mixes the slurry and water to release hydrogen. Atank 26 receives the hydrogen and hydroxide waste from the reactor, and separates the hydrogen from the hydroxide byproduct. Aheat exchanger 32 receives the hydrogen (and associated water vapor) carried inconduit 30 from the tank and condenses the water. - A gas-
liquid separator 40 receives hydrogen and water carried inline 34 from the heat exchanger, separates the water from the hydrogen, and dispenses dried hydrogen and water indiscrete streams conduit 34 is partly in droplet form, and partly in liquid stream form.) The water from the separator is conveyed to the water reservoir 14 (or to water flowing from the reservoir to the reactor) throughconduits device 38, such as a fuel cell. - In
FIG. 4 , thehydride reactor 18 includes atubular member 20 housing a mixing device, such as anauger 22, rotatable in the housing. Other mixing devices could also be used including ultrasonic mixers or vibratory mixers. - The amount of water pumped to the
reactor 18 is more than is needed to complete the release of hydrogen from the slurry. The excess water is converted to steam and carries heat produced in the reaction out of the reaction chamber, thus controlling the temperature of the reaction. - The
tubular member 20 may be fixed to, or otherwise in communication with aninlet 24 of thetank 26. Intank 26, the hydroxide solid material falls to the bottom 28 for removal by way of anoutlet 29. - When the hydrogen-fueled power-providing device is a
fuel cell 38, water condensed from the exhaust of the fuel cell is also returned to thewater reservoir 14, or to the water flowing from the reservoir to the reactor. - When the hydrogen-fueled power-providing
device 38 is an internal or external combustion engine, the assembly also includes acondenser 46 that accepts water vapor from thedevice 38 through aconduit 48 and condenses water. The condensed water passes throughconduit 50 into theconduit 38 for return to the water reservoir 14 (or water flowing from the reservoir into the reactor 18). - Thus, hydrogen suitable for use with fuel cells or engines, for example, is generated by providing a slurry including an organic carrier liquid, such as a light mineral oil, a triglyceride dispersant, and a chemical hydride, such as lithium hydride, mixing the slurry with water to release hydrogen from the slurry, controlling the reaction temperature by vaporization of water, condensing water from the hydrogen released from the slurry, and conveying the dried hydrogen to the hydrogen-fueled power-producing device.
- The slurry may be prepared at centralized plants, where it is readily pumpable into tank trucks or through pipes to distribution centers where the slurry can be pumped into tanks of vehicles powered by hydrogen fuel cells, or into slurry reservoirs of homes or business and industrial facilities. The hydroxide byproduct of the hydrogen production reaction may be picked up upon the next delivery of slurry is made and transported back to a regeneration plant, where the hydroxide will be separated from the mineral oil and will be regenerated to hydride, as explained below.
- Other Techniques for Distributing Water to the Hydride
- As shown in
FIG. 6 , another method of distributing water to the hydride in a chamber is through needles placed in hydride tubes in locations that permit water droplets that pass through needles to react with enough of the hydride to release more than 90% of the potential hydrogen. Several needles could be placed along the length of each tube. Water would be delivered first to theneedle 154 that is farthest from the exit of thetube 156. This water would react with the hydride around it. Some of the water would be evaporated and would travel through unreacted hydride causing further reaction along the tube. Avalving system 158 would be incorporated with the tubes of hydride to deliver water to the needles selectively. Acomputer control system 160 would record which needles had already delivered water and would select needles that had not delivered water for future hydrogen release. - The system of
FIG. 6 overcomes the blockage of water and hydrogen flow to all portions of hydride by the metal hydroxide byproduct that is formed during the reaction. By selecting the sequence of tubes and needles for water injection, water is delivered only to fresh hydride. The arrangement ofFIG. 6 also allows the heat released from the reaction in one tube to be dissipated from the tube while another tube in the system is reacting with water to deliver hydrogen. By causing the reactions to occur in different tubes, the heat of reaction on one tube can dissipate to the environment while slurry and water are reacting in another tube to continue to produce hydrogen. The system may be designed so that the heat in one tube is dissipated before another reaction must take place in that tube. This will control the temperature of the tube and the materials within the tube. - Alternatively, the needles could be retractable from the tubes in a manner similar to that shown in
FIG. 3 . - Small Scale Implementation
- In a small scale implementation, shown in
FIGS. 7 and 8 , thewater supply tubes 170 are buried in abed 172 of chemical-hydride slurry in such a manner that each supply tube will provide enough water to react with the chemical hydride near theoutlet 174 of the tube. Water is stored inchambers 176 located around the perimeter of acanister 180 that holds thelithium hydrid tubes 182. Avalve 177 sequentially directs charges of water to each successive region of chemical hydride. The valving mechanism could be based on inkjet technology. Water charges would be supplied when the pressure in the canister drops below a set value. In this manner, the pressure in the canister will be cycled between a high value of about 200 psi and a low value of about 50 psi. The generated hydrogen exits the canister through conduit 183 after passing through acarbon filter 184. - The hydrogen produced could be consumed by an attached fuel cell as fast as it is generated and the electricity produced by the fuel cell may be stored in a battery or capacitor.
- By supplying discrete charges of water sufficient to react with the chemical hydride within a specified diameter of the release location, the reaction within the
canister 176 can be controlled so that there is never a surplus of water. As the chemical hydride reacts with water, its volume increases. This increased volume occupies the storage volume of the water that is consumed, to achieve a minimum system volume. Flexible walls 190 enable the water supply chambers and the hydride tubes to change volume as needed. - The Hydrogen Regenerator
- The hydroxide byproduct can be processed to regenerate its elemental metal component. The metal can then re-used in the hydride fuel generating process by hydrogenating the elemental metal to produce the hydride fuel.
- As shown in
FIG. 5 , the hydrogen generation assembly is similar to the one shown inFIG. 4 and includes areactor 210 andinlet tubes reactor 210. Thereactor 210 includes atubular portion 216 housing anauger 218 for mixing the slurry and water to effect release of hydrogen gas (H2) from the slurry. Areactor tank portion 219 receives the hydrogen gas and solid matter from theauger 218. The hydrogen gas moves toward atop portion 220 of thereactor tank portion 219 and is carried by aconduit 222 to a separator (not shown) for drying the hydrogen. The hydroxide, which is a wetsolid dust 224, falls to abottom portion 226 of thereactor tank portion 219, from which it is removed and conveyed by transport means 223 to amixer 228.Mixer 228 receives carbon through aconduit 234 and mixes the carbon with the hydroxide. - The
conduit 234 introduces the carbon, in solid or fluid form, such as coal in pellet or powder form, biomass, or graphite, to themixer 228. The mixed carbon and hydroxide are transported bytransport 229 to asecond reactor 230 where there is disposed amolten pool 232 of carbon dissolving metal, such as iron, nickel, manganese, and alloys of those metals. The metal, because of its high heat capacity and thermal conductivity, provides superior heat transfer characteristics. - Alternatively, the
mixer 228 may be omitted and the carbon and hydroxide fed directly into thereactor 230. - The intermixed carbon and hydroxide particles form a
layer 238 in thereactor 230, thelayer 238 descending into alayer 236, and then sinking into the pool of moltencarbon dissolving metal 232. Inlayer 236, decomposition of hydroxide into oxide and water vapor occurs. Inlayer 232, the reaction between carbon and metal oxide produces elemental metal and carbon monoxide. - In one example, the hydroxide is lithium hydroxide (LiOH) and the carbon-dissolving metal is iron (Fe). The lithium hydroxide and carbon introduced into the
second reactor 230, forms the upper layer 328 which descends in thereactor 230 and in the area oflayer 236 produces lithuim oxide (Li2O), water (H2O), hydrogen (H2) and carbon monoxide (CO). The hydrogen (H2) and carbon monoxide (CO) rise toward the top of thereactor 230. Lithium oxide (Li2O) and carbon (C) sink into the molten pool of iron (Fe) where they produce lithium metal (2Li), carbon monoxide (CO) and iron. (Fe). - In the
molten layer 232, lithium gas (Li) is also produced, which rises to the second reactorupper portion 238. Liquid lithium (Li) and iron (Fe) pass from the secondreactor metal pool 232 to aseparator 240 through aconduit 242. The gaseous lithium (Li) in theupper portion 238 of thereactor 230, along with hydrogen (H2) and carbon monoxide (CO), pass through aconduit 246 to acondenser 244.Condenser 244 separates out carbon, lithium, and lithium oxide, which, in solid/liquid form, pass into theseparator 240 through aconduit 248. Thecondenser 244 discharges carbon monoxide and hydrogen gas through aconduit 250 to anotherseparator 258, which separates the carbon monoxide from the hydrogen. - In the
separator 240, the lithium (Li) is evaporated and released throughconduit 252 in vapor form, while the lithium oxide (Li2O), in liquid form, is passed throughconduit 254 to themolten metal pool 232 in thesecond reactor 230. The lithium discharged by theseparator 240 and the hydrogen discharged by theseparator 258 may be recycled for use in the hydride slurry. - Pumps may be used in the assembly as needed. For example, the
conduits molten metal pool 232 may be maintained at a temperature of at least 1500° Kelvin, somewhat above the melting temperature of carbon saturated iron (1430° K). Alloys can be used to tailor the temperature. - The operating temperature of the
second reactor 230 is maintained lower than would otherwise be required by continuously introducing into themolten pool 232 an inert gas, such as argon, through aninlet 256. The lithium concentration in thelower layer 232 of thereactor 230 is thus maintained at a low level. The continuous use of the inert gas tilts the thermodynamic equilibrium in favor of the lithium, allows the operating temperature to be reduced significantly and achieves higher yields at lower temperatures. Without the inert gas, thesecond reactor 230 would have to be maintained at about 1850° K to obtain the same yield as 1500° K with the inert gas. The temperature in thesecond reactor 230 may also be influenced by using an iron alloy such as iron-manganese (FeMn). - When the carbon components are introduced directly into the
reactor 230, they may include natural gas, which is flowable into thereactor 230 throughinlet 256 or a similar inlet. - In accordance with a further feature of the invention, there is provided a method for converting metal oxides and hydroxides to the elemental metals thereof.
- The assembly and method provide for a substantially closed-loop conversion, without discharge of harmful elements into the atmosphere.
- Other embodiments are within the scope of the following claims. For example, elemental metals other than lithium may be recovered, such as sodium and potassium. Alkaline-earth metals, such as magnesium and calcium, could also be recovered.
Claims (20)
1-22. (canceled)
23. Apparatus comprising:
a reservoir containing a chemical hydride, and
a mechanism configured to introduce a reactant to selected different portions of the chemical hydride to effect hydrogen generating reactions at different locations within the reservoir.
24. The apparatus of claim 23 in which the reservoir comprises a canister.
25. The apparatus of claim 23 in which the reservoir includes chambers that contain chemical hydride.
26. The apparatus of claim 23 in which the mechanism comprises conduits that have open delivery ends arranged to introduce the reactant to respective selected portions of the chemical hydride.
27. The apparatus of claim 23 in which the conduits are arranged in parallel.
28. The apparatus of claim 27 in which the conduits are located at different distances along an axis of the reservoir.
29. The apparatus of claim 23 in which the mechanism is configured to be movable relative to the chemical hydride contained in the reservoir.
30. The apparatus of claim 16 in which the conduits comprise needles.
31. The apparatus of claim 23 in which the mechanism includes a valving system that controls the introduction of the reactant to the different portions.
32. The apparatus of claim 23 in which the reservoir includes an exit for hydrogen generated in the reaction.
33. The apparatus of claim 23 in which the chemical hydride is dispersed in a carrier liquid at a concentration of about 40-75% by weight of the composition.
34. The apparatus of claim 23 in which the carrier liquid comprises an organic liquid.
35. The apparatus of claim 23 in which the chemical hydride comprises a light metal hydride.
36. The apparatus of claim 35 in which the light metal hydride is selected from the group consisting of lithium hydride, lithium borohydride, lithium aluminum hydride, sodium hydride, sodium borohydride, sodium aluminum hydride, magnesium hydride, and calcium hydride.
37. The apparatus of claim 33 also including a triglyceride acting as a dispersant.
38. The apparatus of claim 23 in which chemical hydride comprises lithium hydride.
39. The apparatus of claim 23 in which chemical hydride comprises magnesium hydride.
40. The apparatus of claim 23 in which the reactant comprises water.
41-62. (canceled)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/074,360 US20050175868A1 (en) | 1999-05-10 | 2005-03-07 | Storage, generation, and use of hydrogen |
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US30919899A | 1999-05-10 | 1999-05-10 | |
US70710500A | 2000-11-06 | 2000-11-06 | |
US26160101P | 2001-01-12 | 2001-01-12 | |
US26161601P | 2001-01-12 | 2001-01-12 | |
US26160001P | 2001-01-12 | 2001-01-12 | |
US10/044,813 US7052671B2 (en) | 1999-05-10 | 2002-01-11 | Storage, generation, and use of hydrogen |
US11/074,360 US20050175868A1 (en) | 1999-05-10 | 2005-03-07 | Storage, generation, and use of hydrogen |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/044,813 Continuation US7052671B2 (en) | 1999-05-10 | 2002-01-11 | Storage, generation, and use of hydrogen |
Publications (1)
Publication Number | Publication Date |
---|---|
US20050175868A1 true US20050175868A1 (en) | 2005-08-11 |
Family
ID=27808585
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/044,813 Expired - Lifetime US7052671B2 (en) | 1999-05-10 | 2002-01-11 | Storage, generation, and use of hydrogen |
US11/074,360 Abandoned US20050175868A1 (en) | 1999-05-10 | 2005-03-07 | Storage, generation, and use of hydrogen |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/044,813 Expired - Lifetime US7052671B2 (en) | 1999-05-10 | 2002-01-11 | Storage, generation, and use of hydrogen |
Country Status (8)
Country | Link |
---|---|
US (2) | US7052671B2 (en) |
EP (1) | EP1355849B1 (en) |
AT (1) | ATE548323T1 (en) |
CA (1) | CA2434650C (en) |
DK (1) | DK1355849T3 (en) |
ES (1) | ES2384442T3 (en) |
TW (1) | TWI260344B (en) |
WO (1) | WO2002066369A1 (en) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060225350A1 (en) * | 2005-01-28 | 2006-10-12 | John Spallone | Systems and methods for controlling hydrogen generation |
US20070020172A1 (en) * | 2005-02-08 | 2007-01-25 | Hyenergy Systems, Inc. | Solid chemical hydride dispenser for generating hydrogen gas |
US20070148508A1 (en) * | 2005-11-10 | 2007-06-28 | Peter Rezac | Reactor purge system and method |
US20080075987A1 (en) * | 2006-05-08 | 2008-03-27 | Andrew Kindler | Method and system for storing and generating hydrogen |
WO2009046471A1 (en) * | 2007-10-08 | 2009-04-16 | Alvatec Alkali Vacuum Technologies Gmbh | Suspension for hydrogen generators |
WO2010035250A1 (en) * | 2008-09-29 | 2010-04-01 | SOCIéTé BIC | Hydrogen generating fuel cell cartridges. |
US20100104481A1 (en) * | 2007-02-02 | 2010-04-29 | Societe Bic | Hydrogen Gas Generators |
US7947094B2 (en) | 2006-06-20 | 2011-05-24 | Lynntech, Inc. | Microcartridge hydrogen generator |
WO2012151582A1 (en) * | 2011-05-05 | 2012-11-08 | Signa Chemistry, Inc. | Water reactive hydrogen generation system and method with separation of waste products from water reactive materials |
US8802769B2 (en) | 2012-01-05 | 2014-08-12 | Toyota Motor Engineering & Manufacturing North America, Inc. | Medium for the stabilization and utility of volatile or liquid hydrides of boron |
US20150125348A1 (en) * | 2012-06-19 | 2015-05-07 | Bio Coke Lab.Co., Ltd. | Hydrogen Generation Apparatus |
US9580308B2 (en) | 2006-03-29 | 2017-02-28 | Safe Hydrogen, Llc | Storing and transporting energy |
CN107922186A (en) * | 2015-08-20 | 2018-04-17 | 通用电气航空系统有限公司 | Solid hydrogen storage system |
US10077190B2 (en) | 2006-03-29 | 2018-09-18 | Safe Hydrogen, Llc | Methods and systems for making metal hydride slurries |
WO2018194442A1 (en) * | 2017-04-22 | 2018-10-25 | Galaxy Fct Sdn. Bhd. | Device for generating hydrogen gas |
Families Citing this family (63)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6946104B2 (en) | 2001-07-09 | 2005-09-20 | Hydrogenics Corporation | Chemical hydride hydrogen generation system and an energy system incorporating the same |
US7045230B2 (en) | 2001-11-09 | 2006-05-16 | Hydrogenics Corporation | Chemical hydride hydrogen generation system and fuel cell stack incorporating a common heat transfer circuit |
US6737184B2 (en) | 2001-11-09 | 2004-05-18 | Hydrogenics Corporation | Chemical hydride hydrogen generation system and an energy system incorporating the same |
US6758981B2 (en) | 2001-12-21 | 2004-07-06 | Hydrogenics Corporation | Method and apparatus for by-product removal in a hydrogen generation system |
US7169489B2 (en) | 2002-03-15 | 2007-01-30 | Fuelsell Technologies, Inc. | Hydrogen storage, distribution, and recovery system |
US7393369B2 (en) | 2002-06-11 | 2008-07-01 | Trulite, Inc. | Apparatus, system, and method for generating hydrogen |
CA2389939A1 (en) * | 2002-06-25 | 2003-12-25 | Alicja Zaluska | New type of catalytic materials based on active metal-hydrogen-electronegative element complexes for reactions involving hydrogen transfer |
US7011768B2 (en) | 2002-07-10 | 2006-03-14 | Fuelsell Technologies, Inc. | Methods for hydrogen storage using doped alanate compositions |
US7083657B2 (en) * | 2002-08-20 | 2006-08-01 | Millennium Cell, Inc. | System for hydrogen generation |
US20040065171A1 (en) | 2002-10-02 | 2004-04-08 | Hearley Andrew K. | Soild-state hydrogen storage systems |
US7094387B2 (en) * | 2002-11-01 | 2006-08-22 | Washington Savannah River Company Llc | Complex hydrides for hydrogen storage |
US7556660B2 (en) | 2003-06-11 | 2009-07-07 | James Kevin Shurtleff | Apparatus and system for promoting a substantially complete reaction of an anhydrous hydride reactant |
US7384574B2 (en) * | 2003-07-17 | 2008-06-10 | Westinghouse Savannah River Co. | Hydrogen storage material and process using graphite additive with metal-doped complex hydrides |
US7601329B2 (en) * | 2004-02-26 | 2009-10-13 | Gm Global Technology Operations, Inc. | Regeneration of hydrogen storage system materials and methods including hydrides and hydroxides |
TWI314918B (en) * | 2004-04-12 | 2009-09-21 | Rohm And Haas Compan | Process for production of a borohydride compound |
CN104118846B (en) | 2004-06-14 | 2018-11-30 | 西格纳化学有限责任公司 | Silicide compositions comprising alkali metal and the method for preparing it |
IL163862A0 (en) | 2004-09-01 | 2005-12-18 | Hyogen Ltd | A system for hydrogen storage and generation |
EP1814653B1 (en) | 2004-11-12 | 2012-07-18 | Trulite, Inc. | Hydrogen generator cartridge |
US7569294B2 (en) * | 2004-12-23 | 2009-08-04 | Air Products And Chemicals, Inc. | Modular portable battery charging system using hydrogen fuel cells |
US7727293B2 (en) | 2005-02-25 | 2010-06-01 | SOCIéTé BIC | Hydrogen generating fuel cell cartridges |
US9079146B2 (en) | 2009-03-30 | 2015-07-14 | Intelligent Energy Limited | Hydrogen generation systems utilizing sodium silicide and sodium silica gel materials |
US7625547B2 (en) | 2005-06-20 | 2009-12-01 | Ford Global Technologies, Llc | High density hydrogen storage material |
US7678362B2 (en) | 2005-06-20 | 2010-03-16 | Uop Llc | High density hydrogen storage material |
KR20080080147A (en) * | 2005-11-30 | 2008-09-02 | 유니버시티 오브 워싱톤 | Carbon-based expanded nanocomposite hydrogen storage materials |
WO2007074220A1 (en) * | 2005-12-29 | 2007-07-05 | Commissariat A L'energie Atomique | Process for producing hydrogen |
US7651542B2 (en) | 2006-07-27 | 2010-01-26 | Thulite, Inc | System for generating hydrogen from a chemical hydride |
US7648786B2 (en) | 2006-07-27 | 2010-01-19 | Trulite, Inc | System for generating electricity from a chemical hydride |
DE102006039869A1 (en) * | 2006-08-03 | 2008-02-21 | Daimler Ag | Method for supplying a fuel cell with hydrogen by means of silanes or polysilanes |
US7858068B2 (en) * | 2007-04-17 | 2010-12-28 | Nanotek Instruments, Inc. | Method of storing and generating hydrogen for fuel cell applications |
JPWO2008136087A1 (en) * | 2007-04-23 | 2010-07-29 | 三菱重工業株式会社 | Energy supply system |
US8357214B2 (en) | 2007-04-26 | 2013-01-22 | Trulite, Inc. | Apparatus, system, and method for generating a gas from solid reactant pouches |
AU2008279082A1 (en) | 2007-07-25 | 2009-01-29 | Trulite, Inc. | Apparatus, system, and method to manage the generation and use of hybrid electric power |
DE102007039478A1 (en) * | 2007-08-21 | 2009-02-26 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Hydrogen generator and method for generating hydrogen |
US20090101520A1 (en) * | 2007-10-18 | 2009-04-23 | Qinglin Zhang | Methods and devices for hydrogen generation |
US20090104481A1 (en) * | 2007-10-18 | 2009-04-23 | Mohring Richard M | Methods and devices for hydrogen generation |
JPWO2009084743A1 (en) * | 2007-12-28 | 2011-05-19 | ミズ株式会社 | External preparation for treatment or prevention |
US7901491B2 (en) * | 2008-03-31 | 2011-03-08 | General Electric Company | Hydrogen storage material and related system |
US20090280367A1 (en) * | 2008-05-12 | 2009-11-12 | Clearedge Power, Inc. | Extraction of Energy From Used Cooking Oil |
FR2933087B1 (en) * | 2008-06-25 | 2012-01-13 | Unither Dev | COLLOIDAL SUSPENSION GENERATING HYDROGEN. |
WO2010027726A1 (en) * | 2008-08-27 | 2010-03-11 | Alliant Techsystems Inc. | Methods and systems of producing hydrogen and oxygen for power generation, and power source |
NL1037461C2 (en) * | 2009-01-27 | 2010-09-03 | Inhaleness B V | Method, device and fuel for hydrogen generation. |
EP3984948A1 (en) * | 2009-01-27 | 2022-04-20 | H2Fuel-Systems B.V. | Method for refuelling a fuel tank, service station and connector line |
NL1036471C2 (en) * | 2009-01-27 | 2010-07-28 | Inhaleness B V | Method, device and fuel for hydrogen generation. |
US9102528B2 (en) | 2009-03-30 | 2015-08-11 | Intelligent Energy Limited | Hydrogen generation systems and methods utilizing sodium silicide and sodium silica gel materials |
US8444846B2 (en) * | 2009-12-07 | 2013-05-21 | Battelle Energy Alliance, Llc | Method and system for producing hydrogen using sodium ion separation membranes |
US20110142754A1 (en) * | 2009-12-10 | 2011-06-16 | Jie-Ren Ku | One-off and adjustment method of hydrogen releasing from chemical hydride |
US20110143240A1 (en) * | 2009-12-10 | 2011-06-16 | Industrial Technology Research Institute | Hydrogen Generation System, Method for Generating Hydrogen Using Solid Hydrogen Fuel and Method for Providing Hydrogen for Fuel Cell Using the Same |
US8895204B2 (en) | 2010-11-08 | 2014-11-25 | Intelligent Energy Limited | Water reactive hydrogen fuel cell power system |
MX2013005185A (en) | 2010-11-08 | 2014-02-17 | Signa Chemistry Inc | Water reactive hydrogen fuel cell power system. |
DK2961683T3 (en) * | 2013-03-01 | 2022-10-03 | Safe Hydrogen Llc | METHODS AND SYSTEMS FOR MANUFACTURE OF METAL HYDRIDE Slurries |
JP5916686B2 (en) * | 2013-11-12 | 2016-05-11 | 株式会社Tkx | Hydrogen gas production method and hydrogen gas production apparatus |
DE102014211422A1 (en) * | 2014-06-13 | 2015-12-17 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Composite material for the hydrolytic production of hydrogen, apparatus for the hydrolytic production of hydrogen, methods for generating hydrogen, apparatus for generating electrical energy and possible uses |
GB201421300D0 (en) * | 2014-12-01 | 2015-01-14 | Cella Acquistion Ltd | Hydrogen generation method |
NL2016374B1 (en) | 2015-11-06 | 2017-05-29 | H2Fuel Cascade B V | Method for Producing Metal borohydride and Molecular Hydrogen. |
DE102016206106A1 (en) | 2016-04-12 | 2017-10-12 | Hydrogenious Technologies Gmbh | Storage device for hydrogen carrier medium, system comprising such a storage device and method for storing hydrogen carrier medium |
CN108238585A (en) * | 2016-12-27 | 2018-07-03 | 天津维金斯环保科技有限公司 | A kind of hydrogen generator for sodium borohydride hydrogen manufacturing |
US10478929B2 (en) | 2017-03-08 | 2019-11-19 | A3 Labs LLC | Energy source supply systems, energy source supply devices, and related methods |
CN108011118B (en) * | 2017-11-14 | 2020-11-20 | 上海柯来浦能源科技有限公司 | Energy system for hydrating magnesium hydride |
CN109956448A (en) * | 2017-12-25 | 2019-07-02 | 正泰集团股份有限公司 | It automatically can continuous hydrogen transmitting apparatus |
JP7178039B2 (en) * | 2018-02-22 | 2022-11-25 | バイオコーク技研株式会社 | Hydrogen generator and hydrogen generation method |
WO2023105532A1 (en) * | 2021-12-08 | 2023-06-15 | Athalye Shrinivas | Autonomous onsite hydrogen generation systems |
EP4245718A1 (en) * | 2022-03-16 | 2023-09-20 | GRÜNLAND Innovations GmbH | Method for the continuous production of hydrogen by means of magnesium-containing base materials |
GB202211758D0 (en) * | 2022-08-11 | 2022-09-28 | Rolls Royce Plc | Fuel precursor |
Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3101592A (en) * | 1961-01-16 | 1963-08-27 | Thompson Ramo Wooldridge Inc | Closed power generating system |
US3346506A (en) * | 1963-10-14 | 1967-10-10 | Foote Mineral Co | Hydrogen-generating composition and use |
US3372996A (en) * | 1963-10-14 | 1968-03-12 | Foote Mineral Co | Underwater gas generator |
US3649360A (en) * | 1970-01-16 | 1972-03-14 | United Aircraft Corp | Combined water removal and hydrogen generation fuel cell powerplant |
US3674702A (en) * | 1970-02-25 | 1972-07-04 | Us Navy | Hydrogen gas generating composition and method for the same |
US3759986A (en) * | 1970-03-30 | 1973-09-18 | Parke Davis & Co | Esters of 2,2-dimethyl-5-(aryloxy)-1-pentanols |
US3975913A (en) * | 1973-12-20 | 1976-08-24 | Erickson Donald C | Gas generator and enhanced energy conversion systems |
US4261955A (en) * | 1978-09-01 | 1981-04-14 | The United States Of America As Represented By The Secretary Of The Army | Vertical type porous membrane hydrogen generator |
US4643166A (en) * | 1984-12-13 | 1987-02-17 | The Garrett Corporation | Steam engine reaction chamber, fuel composition therefore, and method of making and operating same |
US4769255A (en) * | 1987-05-27 | 1988-09-06 | Dairy Research, Inc. | Spreadable butter-like composition and method for production thereof |
US5286462A (en) * | 1992-09-21 | 1994-02-15 | Magnavox Electronic Systems Company | Gas generator system for underwater buoyancy |
US5468880A (en) * | 1992-09-30 | 1995-11-21 | Kabushiki Kaisha Ueno Seiyaku Oyo Kenkyujo | Method of producing α, β-unsaturated ketones |
US5656574A (en) * | 1995-01-13 | 1997-08-12 | University Of Houston | Fabrication of superconducting wires and rods |
US5707499A (en) * | 1995-10-06 | 1998-01-13 | Ceramatec, Inc. | Storage-stable, fluid dispensing device using a hydrogen gas generator |
US5867978A (en) * | 1995-12-04 | 1999-02-09 | The Penn State Research Foundation | System for generating hydrogen |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2626204A (en) * | 1949-01-29 | 1953-01-20 | Universal Oil Prod Co | Apparatus for conducting catalytic endothermic and exothermic reactions |
US3174833A (en) * | 1962-05-15 | 1965-03-23 | Richard H Blackmer | Hydrogen generating canister |
US3456847A (en) * | 1967-02-24 | 1969-07-22 | Westinghouse Electric Corp | Water supply and dispensing apparatus |
US3787186A (en) * | 1972-02-02 | 1974-01-22 | Us Navy | Calcium hydride gas generator |
FR2207885B1 (en) | 1972-11-23 | 1977-04-08 | France Etat | |
JPS56104701A (en) | 1980-01-18 | 1981-08-20 | Masahiro Suzuki | Hydrogen gas generator |
US4769225A (en) * | 1983-12-08 | 1988-09-06 | The United States Of America As Represented By The United States Department Of Energy | System for exchange of hydrogen between liquid and solid phases |
GB8723034D0 (en) * | 1987-10-01 | 1988-03-23 | Dowty Maritime Systems Ltd | Gas generating devices |
JPH06174196A (en) | 1992-12-03 | 1994-06-24 | Mitsui Eng & Shipbuild Co Ltd | Hydrogen storage or release method using metallic hydride slurry |
JPH07172801A (en) | 1993-12-22 | 1995-07-11 | Mitsui Eng & Shipbuild Co Ltd | Hydrogen occluding and discharging device |
US6534033B1 (en) | 2000-01-07 | 2003-03-18 | Millennium Cell, Inc. | System for hydrogen generation |
-
2002
- 2002-01-10 TW TW091100226A patent/TWI260344B/en not_active IP Right Cessation
- 2002-01-11 EP EP02720786A patent/EP1355849B1/en not_active Expired - Lifetime
- 2002-01-11 WO PCT/US2002/000923 patent/WO2002066369A1/en not_active Application Discontinuation
- 2002-01-11 US US10/044,813 patent/US7052671B2/en not_active Expired - Lifetime
- 2002-01-11 ES ES02720786T patent/ES2384442T3/en not_active Expired - Lifetime
- 2002-01-11 CA CA2434650A patent/CA2434650C/en not_active Expired - Fee Related
- 2002-01-11 DK DK02720786.9T patent/DK1355849T3/en active
- 2002-01-11 AT AT02720786T patent/ATE548323T1/en active
-
2005
- 2005-03-07 US US11/074,360 patent/US20050175868A1/en not_active Abandoned
Patent Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3101592A (en) * | 1961-01-16 | 1963-08-27 | Thompson Ramo Wooldridge Inc | Closed power generating system |
US3346506A (en) * | 1963-10-14 | 1967-10-10 | Foote Mineral Co | Hydrogen-generating composition and use |
US3372996A (en) * | 1963-10-14 | 1968-03-12 | Foote Mineral Co | Underwater gas generator |
US3649360A (en) * | 1970-01-16 | 1972-03-14 | United Aircraft Corp | Combined water removal and hydrogen generation fuel cell powerplant |
US3674702A (en) * | 1970-02-25 | 1972-07-04 | Us Navy | Hydrogen gas generating composition and method for the same |
US3759986A (en) * | 1970-03-30 | 1973-09-18 | Parke Davis & Co | Esters of 2,2-dimethyl-5-(aryloxy)-1-pentanols |
US3975913A (en) * | 1973-12-20 | 1976-08-24 | Erickson Donald C | Gas generator and enhanced energy conversion systems |
US4261955A (en) * | 1978-09-01 | 1981-04-14 | The United States Of America As Represented By The Secretary Of The Army | Vertical type porous membrane hydrogen generator |
US4643166A (en) * | 1984-12-13 | 1987-02-17 | The Garrett Corporation | Steam engine reaction chamber, fuel composition therefore, and method of making and operating same |
US4769255A (en) * | 1987-05-27 | 1988-09-06 | Dairy Research, Inc. | Spreadable butter-like composition and method for production thereof |
US5286462A (en) * | 1992-09-21 | 1994-02-15 | Magnavox Electronic Systems Company | Gas generator system for underwater buoyancy |
US5468880A (en) * | 1992-09-30 | 1995-11-21 | Kabushiki Kaisha Ueno Seiyaku Oyo Kenkyujo | Method of producing α, β-unsaturated ketones |
US5656574A (en) * | 1995-01-13 | 1997-08-12 | University Of Houston | Fabrication of superconducting wires and rods |
US5707499A (en) * | 1995-10-06 | 1998-01-13 | Ceramatec, Inc. | Storage-stable, fluid dispensing device using a hydrogen gas generator |
US5867978A (en) * | 1995-12-04 | 1999-02-09 | The Penn State Research Foundation | System for generating hydrogen |
Cited By (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060225350A1 (en) * | 2005-01-28 | 2006-10-12 | John Spallone | Systems and methods for controlling hydrogen generation |
US20070020172A1 (en) * | 2005-02-08 | 2007-01-25 | Hyenergy Systems, Inc. | Solid chemical hydride dispenser for generating hydrogen gas |
US7666386B2 (en) | 2005-02-08 | 2010-02-23 | Lynntech Power Systems, Ltd. | Solid chemical hydride dispenser for generating hydrogen gas |
US20070148508A1 (en) * | 2005-11-10 | 2007-06-28 | Peter Rezac | Reactor purge system and method |
US10077190B2 (en) | 2006-03-29 | 2018-09-18 | Safe Hydrogen, Llc | Methods and systems for making metal hydride slurries |
US10549990B2 (en) | 2006-03-29 | 2020-02-04 | Safe Hydrogen, Llc | Storing and transporting energy |
US10570012B2 (en) | 2006-03-29 | 2020-02-25 | Safe Hydrogen, Llc | Methods and systems for making metal hydride slurries |
US11192784B2 (en) | 2006-03-29 | 2021-12-07 | Safe Hydrogen, Llc | Methods and systems for making metal hydride slurries |
US9580308B2 (en) | 2006-03-29 | 2017-02-28 | Safe Hydrogen, Llc | Storing and transporting energy |
US7951349B2 (en) | 2006-05-08 | 2011-05-31 | The California Institute Of Technology | Method and system for storing and generating hydrogen |
US20080075987A1 (en) * | 2006-05-08 | 2008-03-27 | Andrew Kindler | Method and system for storing and generating hydrogen |
US7947094B2 (en) | 2006-06-20 | 2011-05-24 | Lynntech, Inc. | Microcartridge hydrogen generator |
US8951310B2 (en) * | 2007-02-02 | 2015-02-10 | Societe Bic | Hydrogen gas generators |
US20100104481A1 (en) * | 2007-02-02 | 2010-04-29 | Societe Bic | Hydrogen Gas Generators |
KR101573547B1 (en) * | 2007-02-02 | 2015-12-01 | 인텔리전트 에너지 리미티드 | Hydrogen gas generator |
WO2009046471A1 (en) * | 2007-10-08 | 2009-04-16 | Alvatec Alkali Vacuum Technologies Gmbh | Suspension for hydrogen generators |
US20110176973A1 (en) * | 2008-09-29 | 2011-07-21 | Alain Rosenzweig | Hydrogen Generating Fuel Cell Cartridges |
US8915979B2 (en) | 2008-09-29 | 2014-12-23 | Societe Bic | Hydrogen generating fuel cell cartridges |
WO2010035077A1 (en) * | 2008-09-29 | 2010-04-01 | SOCIéTé BIC | Hydrogen generating fuel cell cartridges |
WO2010035250A1 (en) * | 2008-09-29 | 2010-04-01 | SOCIéTé BIC | Hydrogen generating fuel cell cartridges. |
WO2012151582A1 (en) * | 2011-05-05 | 2012-11-08 | Signa Chemistry, Inc. | Water reactive hydrogen generation system and method with separation of waste products from water reactive materials |
US8802769B2 (en) | 2012-01-05 | 2014-08-12 | Toyota Motor Engineering & Manufacturing North America, Inc. | Medium for the stabilization and utility of volatile or liquid hydrides of boron |
US20150125348A1 (en) * | 2012-06-19 | 2015-05-07 | Bio Coke Lab.Co., Ltd. | Hydrogen Generation Apparatus |
US9884760B2 (en) * | 2012-06-19 | 2018-02-06 | Bio Coke Lab. Co., Ltd. | Hydrogen generation apparatus |
US20180208463A1 (en) * | 2015-08-20 | 2018-07-26 | Ge Aviation Systems Limited | Solid hydrogen storage system |
CN107922186A (en) * | 2015-08-20 | 2018-04-17 | 通用电气航空系统有限公司 | Solid hydrogen storage system |
US10934165B2 (en) * | 2015-08-20 | 2021-03-02 | Ge Aviation Systems Limited | Solid hydrogen storage system |
US11718520B2 (en) | 2015-08-20 | 2023-08-08 | Ge Aviation Systems Limited | Solid hydrogen storage system |
WO2018194442A1 (en) * | 2017-04-22 | 2018-10-25 | Galaxy Fct Sdn. Bhd. | Device for generating hydrogen gas |
KR20190133788A (en) * | 2017-04-22 | 2019-12-03 | 하이드로전 테크 에스디엔. 비에이치디. | Hydrogen gas generating device |
JP2020517577A (en) * | 2017-04-22 | 2020-06-18 | ハイドロジェン テック センディリアン ベルハッド | Hydrogen gas generator |
US11325092B2 (en) | 2017-04-22 | 2022-05-10 | Hydrogen Tech Sdn. Bhd. | Device for generating hydrogen gas |
KR102423167B1 (en) * | 2017-04-22 | 2022-07-20 | 하이드로전 테크 에스디엔. 비에이치디. | Device for generating hydrogen gas |
Also Published As
Publication number | Publication date |
---|---|
WO2002066369A1 (en) | 2002-08-29 |
ES2384442T3 (en) | 2012-07-04 |
EP1355849B1 (en) | 2012-03-07 |
EP1355849A1 (en) | 2003-10-29 |
US7052671B2 (en) | 2006-05-30 |
US20020166286A1 (en) | 2002-11-14 |
CA2434650A1 (en) | 2002-08-29 |
DK1355849T3 (en) | 2012-07-02 |
TWI260344B (en) | 2006-08-21 |
EP1355849A4 (en) | 2006-06-14 |
CA2434650C (en) | 2012-10-02 |
ATE548323T1 (en) | 2012-03-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US7052671B2 (en) | Storage, generation, and use of hydrogen | |
US20200165126A1 (en) | Storing And Transporting Energy | |
US6093501A (en) | Fuel cell using an aqueous hydrogen-generating process | |
US7858068B2 (en) | Method of storing and generating hydrogen for fuel cell applications | |
JP5834069B2 (en) | On-site controllable demand hydrogen generation system using recyclable liquid metal reagent and method used in the system | |
CA2458589C (en) | Powder metal hydride hydrogen generator | |
US11192784B2 (en) | Methods and systems for making metal hydride slurries | |
JP2006520737A (en) | Hydrogen gas generation system | |
US20030198843A1 (en) | Hydrocarbon fueled liquid gallium fuel generator system | |
EP2961683B1 (en) | Methods and systems for making metal hydride slurries | |
AU2011235957B2 (en) | Storing and transporting energy | |
JP2024508988A (en) | Storage and production of dihydrogen by suspension of metal hydride particles in liquid alkali metal alloys |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: SAFE HYDROGEN, LLC, MASSACHUSETTS Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:MCCLAINE, ANDREW W.;ROLFE, JONATHAN L.;LARSEN, CHRISTOPHER A.;AND OTHERS;REEL/FRAME:016376/0171;SIGNING DATES FROM 20020608 TO 20041125 |
|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |