Abstract: Disclosed are compositions, methods, and devices that generally relate to silanes and silicides and to uses thereof for hydrogen generation. Methods and devices for generating hydrogen for fuel cells and for other applications such as fuel or a supplementary fuel for internal combustion engines and reducing agents to improve catalyst efficiency are also disclosed.

Abstract: Systems and processes for adjusting hydrogen content of a synthesis gas are provided. At least a portion of carbon monoxide in a syngas can be converted to carbon dioxide to provide a shifted syngas and condensed water. The syngas can have a first hydrogen to carbon monoxide ratio and a first temperature, and the shifted syngas can have a second hydrogen to carbon monoxide ratio and a second temperature, both greater than the first. Heat from the shifted syngas can be at least partially transferred from the shifted syngas to the condensed water to at least partially vaporize the condensed water. The syngas can be at least partially saturated with the at least partially vaporized condensed water. A ratio of the water vapor to syngas can be about 1.0 or less.

Abstract: A chemical hydride liquid reactant distribution mixture is provided. The mixture includes a fuel mixture having at least one hydride and at least one activating agent. The invention further includes a liquid-distributing agent (LDA), a form-stabilizing agent, and at least one anti-caking agent. The liquid reactant distribution mixture reduces caking and precipitation while promoting liquid reactant distribution, where the chemical hydride liquid reactant distribution mixture generates hydrogen via hydrolysis.

Abstract: There is disclosed a surprising reaction of an alkane thiol with a catalyst and heat to become dehydrogenated and form a thiophene rather than an expected desulfurization reaction to form the corresponding alkane or alkene. Moreover, there are disclosed surprising results regarding the form of a catalyst to allow a reaction of an alkane thiol to form the dehydrogenated thiophene at lower temperatures and at higher conversion percentages to allow for more efficient recovery of thiophenes to allow for recycling and reuse of thiophenes to hydrogenate to form alkane thiols. Further still, there is disclosed a set of reaction conditions and catalyst presentation that allows for recovery of usable diatomic hydrogen gas from a dehydrogenation reaction of substituted or unsubstituted cyclic thioethers to substituted or unsubstituted thiophene.

Abstract: Disclosed are a method and a corresponding apparatus for converting a biomass reactant into synthesis gas. The method includes the steps of (1) heating biomass in a first molten liquid bath at a first temperature, wherein the first temperature is at least about 100° C., but less than the decomposition temperature of the biomass, wherein gas comprising water is evaporated and air is pressed from the biomass, thereby yielding dried biomass with minimal air content. (2) Recapturing the moisture evaporated from the biomass in step 1 for use in the process gas. (3) Heating the dried biomass in a second molten liquid bath at a second temperature, wherein the second temperature is sufficiently high to cause flash pyrolysis of the dried biomass, thereby yielding product gases, tar, and char. (4) Inserting recaptured steam into the process gas, which may optionally include external natural gas or hydrogen gas or recycled syngas for mixing and reforming with tar and non-condensable gases.

Abstract: A method of shutting down a hydrogen generation apparatus for limiting degradation in a catalyst due to dew condensation at the time of shutdown is provided. The method of shutting down the hydrogen generation apparatus comprising, a combustor which supplies heat necessary to a reforming device, a first air supplier which supplies air to the combustor, a combustion exhaust gas path formed such that the combustion exhaust gas produced in the combustor makes heat exchange with the reforming device and then with a CO reducing device, and a controller which operates the first air supplier so that the temperature of the gas in the CO reducing device does not become equal to or lower than a dew point after shutdown of the combustion operation of the combustor and before a start of a purging operation to purge the interiors of the reforming device and the CO reducing device with a replacement gas.

Abstract: Provided is a gas storage method of a gas storage medium having a multilayer structure in which crystalline structures are stacked to be spaced from each other, including selectively storing gas by relatively controlling a space between the crystalline structures or a lattice distance between crystals of each crystalline structure with respect to the van der Waals diameter of gas which is to be stored. According to the gas storage method, it is possible to selectively store gas.

Abstract: A hydrogen generating apparatus contains a hydrogen generating device containing a reforming device; a desulfurizing device; a hydrocarbon removing device; a first raw material supplying path that passes the raw material through only the desulfurizing device among the desulfurizing device and the hydrocarbon removing device, and flows the raw material into the hydrogen generating device; a second raw material supplying path that passes the raw material through the desulfurizing device and the hydrocarbon removing device, and flows the raw material into the hydrogen generating device; and a controlling device that switches the flow path of the raw material to the second raw material supplying path in an operating step of supplying only the raw material to the hydrogen generating device.

Abstract: In a hydrogen generation device according to the invention, PSR reformers have a heat capacity smaller than that of the other PSR reformers. Therefore, the temperature of the catalyst reaches to a reforming-start temperature more quickly in the PSR reformers than in the other PSR reformers. When the hydrogen generation device is started and the reforming reaction is carried out, the mixture of gasoline vapor and water vapor is selectively and preferentially supplied to the PSR reformers so that the reforming reaction is carried out in the PSR reformers.

Abstract: A method of manufacturing a hydrogen separation membrane comprises the steps of forming an intermediate layer suitable for controlling oxidation of a hydrogen permeable metal layer on the surface of the hydrogen permeable metal layer on the surface of the hydrogen permeable metal used as a substrate; and attaching a catalytic metal in a granular form on the surface of the intermediate layer. This method can be used to manufacture a hydrogen separation membrane in which the quantity of catalytic metal used is controlled.

Abstract: Disclosed is a multi-burner gasification reactor for gasification of slurry or pulverized hydrocarbon feed materials and industry applications thereof. Burners are disposed on the periphery or top of a gasification reactor vessel, wherein the side burners are at a small downward angle relative to the horizontal plane, which can prolong the life of refractory bricks. The operating pressure of the gasification reactor is 0.1˜12 MPa, and the operating temperature thereof is 1350° C.˜1700° C. The gasification reactor is applicable to a hot-wall lining as well as a cold-wall lining. The notable advantages of the gasification reactor are carbon conversion is high and can reach 99%, and the effective gas content is high; specific coal consumption and specific oxygen consumption are low; and it is applicable to a large coal gasification plant that processes above 3000 tons of coal per day.

Abstract: In one aspect, the invention provides a hydrogen storage material that is formed by reacting solid precursors (a) and (b). The (a) precursor is a compound containing X—H and Y—H bonds, where X is a Group 13 and Y is a Group 15 element. Preferably X is boron (B—H) and Y is nitrogen (N—H). Most preferably, the precursor (a) is borazane. The (b) precursor is preferably a hydride, such as LiH or LiAlH4. Another feature of the present invention is a novel hydrogen storage composition material that is formed as an intermediate (INT) in the reaction of the (a) with the (b) precursors. The INT hydrogen storage material can be a quaternary B—H—Li—N composition. Other aspects of hydrogen storage materials are provided herein.

Abstract: There is disclosed a hydrogen storage material which may comprise an optionally substituted M-amino-borane complex or a composite comprising: (i) at least one of a M-nitrogen compound; and (ii) a compound comprising (Y—Z)—R bonds. M is a metal or metalloid; Y is an element selected from Group 13 of the Periodic Table of Elements; Z is an element selected from Group 15 of the Periodic Table of Elements; and R is hydrogen (H) or a hydrocarbyl.

Abstract: A hydrogen production method includes: a first process in which nitrogen compounds of metal and water are reacted to produce ammonia and hydroxide of the metal; a second process in which hydrogen compounds of a metal and the ammonia produced in the first process are reacted; and a third process in which hydrogen compounds of a metal and the hydroxide of the metal produced in the first process are reacted.

Abstract: A preferred embodiment of the present invention is a hydrogen gas storage and supply method, comprising (a) providing a dry, solid-state hydrogen fuel source comprising a solid metal hydride or chemical hydride and a reaction-controlling agent in a solid state, wherein the hydride and the reaction-controlling agent are mixed at a desired proportion; and (b) delivering a desired amount of a liquid reactant to contact and react with a desired amount of the solid-state fuel source to produce hydrogen gas continuously or intermittently on demand, responsive to the needs of a fuel cell.

Abstract: The inventive method of gaseous hydrogen purification from a gaseous mixture comprises purifying hydrogen from a permeate gas enriched with compressed hydrogen by pressure modulation (PSA) in which one or more adsorbers are used that each follow a cycle at intervals with an adsorption phase at a high cycle pressure and a regeneration phase, producing two regeneration flows; a first recycled regeneration flow and a second non-recycled regeneration flow, characterized by the fact that the recycled regeneration flow exiting the adsorber(s) is recycled, directly or indirectly, by a sole compressor, without intermediate compression so that the sole compressor ensures both the compression of the hydrogen-enriched permeate and compression of the recycled regeneration gas.

Abstract: Embodiments are described that generally relate to the storage and release of a gas using piezoelectric materials.

Abstract: The invention relates to the use of biomethanol from the pulp industry in the production of biohydrogen. The preferred biomethanol comprises purified biomethanol derived from black liquor. The invention also relates to a process for the production of biohydrogen from crude biomethanol recovered from black liquor and to a process for producing hydrocarbon biofuel using such biohydrogen as a hydrogen source. The invention further relates to a biofuel production facility for producing fuel from biohydrogen and biohydrocarbon, and to biofuel so produced. The invention makes it possible to produce a biofuel, wherein 100% of the raw material stems from non-fossil sources.

Abstract: An apparatus and method including storage and dispensing vessels to safely store and dispense gaseous hydrides, where the storage and dispensing vessels contain a solid-phase physical sorbent medium having a physically sorptive affinity for gaseous hydrides, and wherein the gaseous hydride is decomposed in the apparatus to generate hydrogen gas. The gaseous hydrides include, but are not limited to, silane, germane, stibine and diborane. The gaseous hydrides decompose spontaneously and/or decomposition is enhanced using surface modified adsorbents. The hydrogen generated by the apparatus may be used in a fuel cell or other hydrogen gas consuming unit.

Abstract: A hydrogen generator comprises a reformer configured to generate a hydrogen-containing gas through a reforming reaction in an internal space thereof using a material gas and steam; a material gas supply passage through which the material gas is supplied to the reformer; a material gas supplier which is provided at the material gas supply passage to supply the material gas to the reformer; a first valve configured to open and close the material gas supply passage; an evaporator configured to generate a steam supplied to the reformer; a water supplier configured to supply water to the evaporator; a communicating passage for allowing the reformer to communicate with atmosphere; a second valve configured to open and close the communicating passage; and a controller configured to stop the material gas supplier and the water supplier and close the first valve and the second valve at shutdown of the hydrogen generator; and open the second valve prior to opening the first valve when the material gas supplier resumes

Abstract: Organic pigments are capable of catalyzing the decomposition reaction of hydrogen-rich, stabilized, borohydride solutions to generate hydrogen gas on-board an operable hydrogen-consuming device such as a motor vehicle or other combustion engine. The organic pigments are used in hydrogen generating systems and in methods for controlling the generation of hydrogen gas from metal hydride solutions.

Abstract: Provided is a reaction vessel for a fuel cell, and more particularly to a reaction vessel exhibiting improved thermal efficiency, and a reaction device for a steam reforming reaction for a fuel cell. The reaction device includes a cylindrical reaction catalyst chamber on which a target reaction catalyst for a predetermined target reaction is disposed; and a tubular oxidation catalyst chamber surrounding the reaction catalyst chamber, comprising an oxidation reaction catalyst therein. The reaction device according features an increased contact area between catalyst and gas, and rapidly heating of the gas in contact with the catalyst to a desired reaction temperature.

Abstract: A control system and method for a fuel processing system. The control system automates the operation of a fuel processing system by monitoring operating parameters and automatically controlling the operation of the system responsive to the monitored parameters, predefined subroutines and/or user inputs.

Abstract: A method for production of hydrogen from organic matter, includes: pyrolysis of a feed of organic matter by passing a gaseous treatment stream essentially having carbon dioxide through the organic matter, the pyrolysis producing, on the one hand, a pyrolysis gas stream having the gaseous treatment stream, steam and volatile organic compounds originating from the organic matter, and on the other hand pyrolysis chars having carbon components; oxycombustion of at least a proportion of the volatile organic compounds present in the pyrolysis gas stream, by injection of oxygen, upstream of a layer of redox filtering matter comprising high-temperature carbon components; and after the oxycombustion, passing the oxidized pyrolysis gas stream through the redox layer, the passage producing a synthesis gas stream comprising hydrogen obtained by deoxidation of steam by the high-temperature carbon components.

Abstract: A process for producing hydrogen, comprising the steps of: (a) gasifying a fuel into a raw synthesis gas comprising CO, hydrogen, steam and sulfur and halide contaminants in the form of H2S, COS and HX, where X is a halide; (b) passing the raw synthesis gas through a water gas shift reactor (WGSR) into which CaO and steam are injected, the CaO reacting with the shifted gas to remove CO2, sulfur and halides in a solid-phase calcium-containing product comprising CaCO3, CaS and CaX2; (c) separating the solid-phase calcium-containing product from an enriched gaseous hydrogen product; and (d) regenerating the CaO by calcining the solid-phase calcium-containing product at a condition selected from the group consisting of: in the presence of steam, in the presence of CO2, in the presence of synthesis gas, in the presence of H2 and O2, under partial vacuum, and combinations thereof. The CaO may have a surface area of at least 12.0 m2/g and a pore volume of at least 0.

Abstract: In one aspect, the invention relates to activated aluminum hydride hydrogen storage compositions containing aluminum hydride in the presence of, or absence of, hydrogen desorption stimulants. The invention particularly relates to such compositions having one or more hydrogen desorption stimulants selected from metal hydrides and metal aluminum hydrides. In another aspect, the invention relates to methods for generating hydrogen from such hydrogen storage compositions.

Abstract: A hot solids process operable selectively for combustion purposes and gasification purposes wherein a pre-identified product is selected from a group of products to be generated through the use of the hot solids process. Based on the nature of the pre-identified product, which is to be generated through the use of the hot solids process, a specific fuel from which the pre-identified product is capable of being derived is selected from a group of fuels. Then, from a group of reactors there is selected a first reactor, which is operable for generating in the first reactor the pre-identified product as an output from the first reactor. Thereafter, from a group of reactors, there is selected a second reactor, which is operable for effecting in the second reactor the conversion of air and of a predetermined carrier selected from a group of carriers to produce a predefined output from the second reactor.

Abstract: A process to efficiently remove sulfur compounds from a hydrocarbon stream in a refinery operation includes the production and recycle of hydrogen from the sulfur compounds. The sulfur compounds present in the hydrocarbon cut are converted to hydrogen sulphide which is split to hydrogen and sulfur in a non-thermal plasma reactor.

Abstract: A process is provided for producing a porous substance, which is lightweight, and has a highly developed pore structure and an excellent gas absorbability, by dehydrogenating a compound having two or more amine-borane adduct structures per molecule.

Abstract: In a gas generator for gasifying solid granular fuels to obtain combustible gaseous compounds for producing synthesis gas or H2-suitable raw gas, a fluidized bed formed of the fuels moves through a closed reaction vessel with a sluice mounted at the top for continuously introducing the fuels and with a closure mounted below the funnel-shaped constriction of the bottom for discharging the ash formed into an ash sluice, wherein above the funnel-shaped constriction of the bottom a revolving grate is arranged, through which the gasifying medium can be introduced from below into the fluidized bed, and through which the ash formed can be discharged into the ash sluice via the funnel-shaped constriction and an adjoining tubular portion. To achieve a continuous operation of the revolving grate, a bulk-material slide valve is mounted in the tubular portion.

Abstract: The electronic structure of nanowires, nanotubes and thin films deposited on a substrate is varied by doping with electrons or holes. The electronic structure can then be tuned by varying the support material or by applying a gate voltage. The electronic structure can be controlled to absorb a gas, store a gas, or release a gas, such as hydrogen, oxygen, ammonia, carbon dioxide, and the like.

Abstract: A torpedo-shaped, flexible wing-equipped, hydrogen generator is disclosed, comprising a case filled with magnesium and other natural mineral grains which produces hydrogen-abundant water without electrolysis. The generation of hydrogen is effected by a simple, natural chemical reaction between water and magnesium. The hallmark of this invention is the flexible wing component, which solves two major problems of current hydrogen generators: slippage and water flow obstruction. By nature of its design, the wings act as a stopper to prevent the hydrogen generator from slipping out of an inverted PET water bottle.

Abstract: Methods for the reduction of gaseous carbon dioxide emissions from combustion or oxidation reactions are provided. The various methods involve the formation of carbon suboxides and/or polymerized carbon suboxides (PCS), preferentially over gaseous carbon oxides to thereby reduce gaseous carbon dioxide emissions. The various methods can be employed for efficient generation of energy and/or hydrogen. In addition, various methods for the use of polymerized carbon suboxide are disclosed.

Abstract: A process for initiating a reaction between methanol and a peroxide to produce a gas, which comprises contacting methanol and peroxide in the liquid phase and at a pressure equal to, below or above atmospheric pressure in the presence of a catalyst comprising at least one group 7, 8, 9, 10 or 11 transition metal.

Abstract: A method and an arrangement for reforming a hydrocarbon fuel such as dimethyl ether (DME), methanol, ethanol, propanol, or any variants or other oxidized fuels is disclosed for generating hydrogen especially for supplying a fuel cell. Furthermore, a fuel cell system is disclosed which includes such an arrangement, especially for providing power to a stationary or mobile power consuming unit like especially an auxiliary power unit (APU) for application in aircraft, ships and vehicles, or as a part of a hybrid drive or as a sole driving unit for, e.g., a ship or a vehicle.

Abstract: The present invention relates to a new process for removal of carbon dioxide from a feed gas, wherein the feed gas is fed to and concentrated in a stripper column (A) before condensation of the gaseous carbon dioxide. The present invention also relates to different uses of the removed carbon dioxide and to a plant for removal of carbon dioxide from the feed gas.

Abstract: Systems and methods are provided for storing and releasing hydrogen using packed-bed hydrogen storage elements in conjunction with elements such as optical or thermal energy for stimulating the release of stored hydrogen. The hydrogen storage system may include valves, piping, and other fixtures for ease of filling and emptying the unit. The system may also serve as a portable self-contained means of safe hydrogen storage that may be transported between the filling or generation site and the site of hydrogen release or use.

Abstract: Method and apparatus for generating hydrogen from a fuel comprising an endothermically decomposable compound, preferably methanol, and optionally comprising water. A catalyst is preferably used to decompose the methanol into hydrogen and CO. The catalyst preferably has low selectivity for reacting the CO and water to form CO2 and hydrogen. A permselective membrane, preferably cleaned by the water, is used to separate the hydrogen. The retentate has fuel value and is reacted or otherwise burned in order to provide heat for the decomposition reaction.

Abstract: Processes are disclosure which comprise alternately contacting an oxygen-carrying catalyst with a reducing substance, or a lower partial pressure of an oxidizing gas, and then with the oxidizing gas or a higher partial pressure of the oxidizing gas, whereby the catalyst is alternately reduced and then regenerated to an oxygenated state. In certain embodiments, the oxygen-carrying catalyst comprises at least one metal oxide-containing material containing a composition having one of the following formulas: (a) CexByB?zB?O?, wherein B=Ba, Sr, Ca, or Zr; B?=Mn, Co, or Fe; B?=Cu; 0.01<x<0.99; 0<y<0.6; 0<z<0.5; and 1<?<2.2; (b) SrvLawBxB?yB?zO?, wherein B=Co or Fe; B?=Al or Ga; B?=Cu; 0.01<v<1.4; 0.1<w<1.6; 0.1<x<1.9; 0.1<y<0.9; 0<z<2.2; and 3<?<5.5).

Abstract: The present invention provides technology for controlling, or tuning, the catalytic activity of gold provided upon nanoporous supports such as those derived from nanoparticulate titania. It has been discovered that the nature of the surfaces of the nanoparticles used to support a nano-metal catalyst, such as catalytically active gold, has a profound effect upon the catalytic properties of the supported catalyst. The support surface may be altered as desired to control the activity of the gold. The present invention teaches how thermal treatment of nanoparticulate media incorporated into a nanoporous support prior to deposition of catalytically active gold dramatically suppresses the ability of a resultant catalyst system to oxidize hydrogen. Yet, the system still readily oxidizes CO.

Abstract: A method for producing an alcohol of the present invention provides an alcohol having the total sulfur content of 10 ppm by weight or less, by subjecting an alcohol having the total sulfur content of 30 ppm by weight or more and the propanols content of 200 ppm to at least one desulfurization treatment selected from at least one of a desulfurization treatment by a reaction process, a desulfurization treatment with a physical adsorbent, and a desulfurization treatment with a chemical adsorbent.

Abstract: The present invention provides several variations for converting biomass, and other carbon-containing feedstocks, into syngas. Some variations include pyrolyzing or torrefying biomass in a devolatilization unit to form a gas stream and char, and gasifying the char. Other variations include introducing biomass into a fluid-bed gasifier to generate a solid stream and a gas stream, followed by a partial-oxidation or reforming reactor to generate additional syngas from either, or both, of the solid or gas stream from the fluid-bed gasifier. Hot syngas is preferably subjected to heat recovery. The syngas produced by the disclosed methods may be used in any desired manner, such as conversion to liquid fuels (e.g., ethanol).

Abstract: The invention relates to a process for preparing Cu/Zn/Al catalysts. In this process, the metals are used in the form of their formates and are precipitated in a suitable form. Suitable precipitants are, for example, alkali metal carbonates. The invention further relates to a catalyst as can be obtained by the process according to the invention and to its use.

Abstract: A method for the thermo-neutral reforming of liquid hydrocarbon fuels which employs a Ni—Ce2O—Pt—Rh catalyst having dual functionalities to achieve both combustion and steam reforming.

Abstract: A compacted material includes magnesium hydride and expanded natural graphite and a method for preparing such a material including the steps which consist in: (i) mixing a magnesium hydride or powdered magnesium with a powdered graphite; and (ii) shaping the mixture by compaction. It also proposes the use of the material for hydrogen storage and a method for hydrogen storage and release from storage including the steps which consist in: (a) introducing the material into a suitable hydrogen tank; (b) placing the material under hydrogen pressure in pressure and temperature conditions that enable the hydrogen to be absorbed by the material; and (c) desorbing the hydrogen from the material in pressure and temperature conditions permitting the desorption of the material.

Abstract: The invention provides a method for generating power with a gas turbine which utilizes pressure swing reforming under conditions that facilitate CO2 capture. First a synthesis gas stream at a first pressure is produced in a pressure swing reformer. Next the synthesis gas stream is subjected to a high temperature water gas shift process to produce a CO2 containing hydrogen enriched stream from which hydrogen and CO2 each are separated. The separated hydrogen in turn is combusted with air to produce a gas turbine and the separated CO2 is easily sequestered.

Abstract: A hydrogen manufacturing apparatus for manufacturing hydrogen by utilizing heat generated in a nuclear plant. The apparatus has a heat exchanger or steam reformer to be brought into contact with cooling water containing tritium produced from the nuclear plant and a tritium permeation suppressing ceramic coating at least either the outer surface or the inner surface of the heat exchanger or steam reformer for suppressing permeation of tritium. Instead of coating with a tritium permeation suppressing ceramic, a structure prepared by combining at least two types of materials having different crystal structures may be used.

Abstract: A system is described for storing and generating hydrogen and, in particular, a system for storing and generating hydrogen for use in an H2/O2 fuel cell. The hydrogen storage system uses beta particles from a beta particle emitting material to degrade an organic polymer material to release substantially pure hydrogen. In a preferred embodiment of the invention, beta particles from 63Ni are used to release hydrogen from linear polyethylene.

Abstract: A compact hydrogen generator for use with fuel cells and other applications includes a hydrogen membrane reactor having a combustion chamber and a reaction chamber. The two chambers are have a fluid connection and a heat exchange relationship with one another. The hydrogen generation apparatus also includes a fuel supply, a fuel supply line for transporting fuel from the fuel supply to the reaction chamber, an oxygen supply, an oxygen supply line for transporting oxygen form the oxygen supply to the combustion chamber, as well as a tail gas supply line for transporting tail gas supply line for transporting tail gases form the reaction chamber, a combustion by-product line for transporting combustion by-products for the combustion chamber, and a reaction product line for transporting hydrogen from the reaction chamber.

Abstract: Compositions are described for catalyzing or facilitating hydrogen transfer kinetics in various kinds of chemical reactions that depend on the efficiency of hydrogen relocation or exchange. One such composition has the formula M-H-E, where M is a metal, metalloid, alloy of a metal, alloy of a metalloid, compound of a metal or compound of a metalloid, H is hydrogen and E is an electronegative element. Another such composition is a hydrogen storage composition that includes the catalytic composition having the formula M-H-E and a hydride or a material capable of absorbing hydrogen to form a hydride.