Abstract: The invention discloses nano magnesium hydride and an in-situ preparation method thereof, including disposing and stirring magnesium chloride and lithium hydride in an organic solvent under a protection of an inert atmosphere, so as to obtain an organic suspension of a mixture; performing an ultrasonic treatment to the organic suspension, so as to promote a chemical reaction of the mixture. After the reaction is completed, the suspension is filtered; the solid reaction product is washed, centrifuged and dried to remove residual organic matter, so as to obtain nano-magnesium hydride.

Abstract: An energy harvesting apparatus may include a thermoelectric device, a heat exchanger coupled to the thermoelectric device, a thermal capacitor container, and a thermal capacitor generation device. The thermal capacitor generation device may be configured to generate a thermal capacitor fluid, to be contained in the thermal capacitor container. An electrical energy storage device may be electrically connected to the thermoelectric device, to store electricity generated by the thermoelectric device.

Abstract: A method for making a metal-hydride slurry includes adding metal to a liquid carrier to create a metal slurry and hydriding the metal in the metal slurry to create a metal-hydride slurry. In some embodiments, a metal hydride is added to the liquid carrier of the metal slurry prior to hydriding the metal. The metal can be magnesium and the metal hydride can be magnesium hydride.

Abstract: This disclosure relates to novel metal hydrides, processes for their preparation, and their use in hydrogen storage applications.

Abstract: Provided is an electrode alloy powder that is useful to obtain a nickel-metal hydride storage battery having a high battery capacity and a reduced self-discharge. The alloy powder is: a mixture including particles of a first hydrogen storage alloy having an AB5-type crystal structure, and particles of at least one second hydrogen storage alloy selected from the group consisting of a hydrogen storage alloy a having an AB2-type crystal structure and a hydrogen storage alloy b having an AB3-type crystal structure, wherein an amount of the first hydrogen storage alloy included in the mixture is greater than 50 mass %.

Abstract: An ambient-heat engine has a substantially thermally-conductive housing whose interior is divided into a high-pressure chamber and a low-pressure chamber by a substantially gas-impermeable barrier. An ionically-conductive, electrical-energy-generating mechanism forms at least a portion of the barrier. First hydrogen-storage medium is disposed within the high-pressure chamber and second hydrogen-storage medium is disposed within the low-pressure chamber. An electrical-energy storage device connected to the ionically-conductive, electrical-energy-generating mechanism is operable between a charge condition and a discharge condition. In a charge condition, hydrogen atoms within the high-pressure chamber are converted to hydrogen ions and conducted through the electrical-energy-generating mechanism to the low-pressure chamber causing electrical-energy to be generated to the electrical-energy storage device.

Abstract: A transition metal composite hydroxide can be used as a precursor to allow a lithium transition metal composite oxide having a small and highly uniform particle diameter to be obtained. A method also is provided for producing a transition metal composite hydroxide represented by a general formula (1) MxWsAt(OH)2+?, coated with a compound containing the additive element, and serving as a precursor of a positive electrode active material for nonaqueous electrolyte secondary batteries. The method includes producing a composite hydroxide particle, forming nuclei, growing a formed nucleus; and forming a coating material containing a metal oxide or hydroxide on the surfaces of composite hydroxide particles obtained through the upstream step.

Abstract: Hydrogen storage alloy powder, an anode, and a nickel-hydrogen rechargeable battery are provided, which are excellent in low-temperature characteristics and both in initial activity and cycle life at the same time, which properties are trading-off in conventional nickel-hydrogen rechargeable batteries. The alloy powder has a composition represented by formula (1) R1-aMgaNibAlcMd (R: rare earth elements including Sc and Y, or the like; 0.005?a?0.40, 3.00?b?4.50, 0?c?0.50, 0?d?1.00, 3.00?b+c+d?4.50), and has an arithmetical mean roughness (Ra) of the powder particle outer surface of not less than 2 ?m, or a crushing strength of not higher than 35,000 gf/mm2.

Abstract: Disclosed are an apparatus and method for continuously producing carbon nanotubes, the apparatus includes i) a reactor to synthesize carbon nanotubes, ii) a separator to separate a mixed gas from the carbon nanotubes transferred from the reactor, iii) a filter to remove all or part of one or more component gases from the separated mixed gas, and iv) a recirculation pipe to recirculate the filtered mixed gas to the reactor for carbon nanotubes.

Abstract: The invention provides a thermal energy storage system comprising a metal-containing first material with a thermal energy storage density of about 1300 kJ/kg to about 2200 kJ/kg based on hydrogenation; a metal-containing second material with a thermal energy storage density of about 200 kJ/kg to about 1000 kJ/kg based on hydrogenation; and a hydrogen conduit for reversibly transporting hydrogen between the first material and the second material. At a temperature of 20° C. and in 1 hour, at least 90% of the metal is converted to the hydride. At a temperature of 0° C. and in 1 hour, at least 90% of the metal hydride is converted to the metal and hydrogen. The disclosed metal hydride materials have a combination of thermodynamic energy storage densities and kinetic power capabilities that previously have not been demonstrated. This performance enables practical use of thermal energy storage systems for electric vehicle heating and cooling.

Abstract: Disclosed are an apparatus and method for continuously producing carbon nanotubes. More specifically, disclosed are an apparatus for continuously producing carbon nanotubes including i) a reactor to synthesize carbon nanotubes, ii) a separator to separate a mixed gas from the carbon nanotubes transferred from the reactor, iii) a filter to remove all or part of one or more component gases from the separated mixed gas, and iv) a recirculation pipe to recirculate the filtered mixed gas to the reactor for carbon nanotubes.

Abstract: To provide a conductive agent for a nonaqueous electrolyte secondary battery and the like, in which oxidative decomposition reaction of an electrolyte is sufficiently suppressed during charging and discharging under high-temperature, high-voltage conditions and thus the cycle characteristics under these conditions are improved. A conductive agent main body composed of carbon and a compound attached to a surface of the conductive agent main body are contained. The average particle size of primary particles or secondary particles of the conductive agent main body is larger than the average particle size of the compound and the compound contains at least one metal element selected from the group consisting of aluminum, zirconium, magnesium, and a rare earth element.

Abstract: A device includes a chemical hydride fuel pellet having a plurality of holes extending from a first end to a second end. A plurality of tubes formed of water vapor permeable and hydrogen impermeable material extend from the first end to the second end through the tubes. A container has an inlet for water vapor containing gas coupled to the first end of the tubes and an outlet coupled to the second end of the tubes. A hydrogen outlet is coupled to the fuel pellet.

Abstract: Complex hydrides based on Al(BH4)3 are stabilized by the presence of one or more additional metal elements or organic adducts to provide high capacity hydrogen storage material.

Abstract: A crystalline AlH3 is ball-milled in a hydrogen atmosphere while applying a force of 10 G to 30 G (in which G is gravitational acceleration). The milling time is more than 10 minutes and less than 60 minutes. The hydrogen storage material thus produced has a structure containing a plurality of matrix phases and a grain boundary phase disposed between the matrix phases. The matrix phases comprise Al and have a side length of 1 to 200 nm, and the grain boundary phase comprises an amorphous phase and contains hydrogen in the state of a solid solution.

Abstract: A hydrogen storage material is formed by mixing and combining particles of a metal A selected from Mg and Al, particles of a metal B selected from Ni and Cu, and particles of an intermetallic compound A-B of the metal A and the metal B, together. A method of producing the hydrogen storage material includes a step of mixing the particles of the intermetallic compound A-B with the particles of the metal B, a step of adding particles of a hydride A-H of the metal A to the mixture and mixing them together, and a step of dehydrogenating the hydride A-H to convert it to the metal A.

Abstract: Hydrogen energy systems for obtaining hydrogen gas from a solid storage medium using controlled laser beams. Also disclosed are systems for charging/recharging magnesium with hydrogen to obtain magnesium hydride. Other relatively safe systems assisting storage, transport and use (as in vehicles) of such solid storage mediums are disclosed.

Abstract: Disclosed are a negative active material for a secondary lithium battery and a secondary lithium battery including the same. The negative active material for a secondary lithium battery includes an amorphous silicon-based compound represented by the following Chemical Formula 1. SiAxHy??Chemical Formula 1 In Chemical Formula 1, A is at least one element selected from C, N, or a combination thereof, 0<x, 0<y, and 0.1?x+y?1.5.

Abstract: A hydrogen storage alloy is provided which has an extremely low Co content, and can maintain the drain (power) performance (especially pulse discharge characteristics), activity (degree of activity), and life performance at high levels. The hydrogen storage alloy is manufactured by weighing and mixing every material for the hydrogen storage alloy so as to provide an alloy composition represented by the general formula MmNiaMnbAlcCod or MmNiaMnbAlcCodFee, and controlling the manufacturing method and manufacturing conditions so that both the a-axis length and the c-axis length of the crystal lattice are in a predetermined range. Although it is sufficient if the a-axis length of the crystal lattice is 499 pm or more and the c-axis length is 405 pm or more, by further specifying the a-axis length and c-axis length depending on the values of ABx, a hydrogen storage alloy having high durability can be provided.

Abstract: A hydrogen storage alloy comprises a hydrogen storage base formed of a mixture of magnesium and an alloy, such as a magnesium-nickel alloy, a magnesium-titanium alloy, a magnesium-niobium alloy, a magnesium-manganese alloy, or a magnesium-cobalt alloy, and a catalytic layer covering a surface of the base. A hydrogen storage alloy unit includes the hydrogen storage base and a porous body including an assembly of nanofibers. The alloy may be vapor-deposited onto the assembly of nanofibers. The nanofibers may be tangled to provide spaces between the fibers for the passage of hydrogen molecules. The nanofibers in one example are also porous. A catalytic layer of platinum may cover a surface of the hydrogen storage base.

Abstract: A doped hydrogen storage material according to the general formula: MgxByMzHn wherein: (i) the ratio of x/y is in the range of from 0.15 to 1.5; (ii) z is in the range of from 0.005 to 0.35; (iii) x+y+z equals 1; (iv) M=is one or more metals selected from the group of selected Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu and Zn; (v) n is no more than 4y; and wherein x/y does not equal 0.5 and at least part of the doped hydrogen storage material is amorphous. The doped hydrogen storage materials are used for storing hydrogen, and also disclosed is a method for reversibly desorbing and/or absorbing hydrogen.

Abstract: A ternary hydrogen storage system having a constant stoichiometric molar ratio of LiNH2:MgH2:LiBH4 of 2:1:1. It was found that the incorporation of MgH2 particles of approximately 10 nm to 20 nm exhibit a lower initial hydrogen release temperature of 150° C. Furthermore, it is observed that the particle size of LiBNH quaternary hydride has a significant effect on the hydrogen sorption concentration with an optimum size of 28 nm. The as-synthesized hydrides exhibit two main hydrogen release temperatures, one around 160° C. and the other around 300° C., with the main hydrogen release temperature reduced from 310° C. to 270° C., while hydrogen is first reversibly released at temperatures as low as 150° C. with a total hydrogen capacity of 6 wt. % to 8 wt. %. Detailed thermal, capacity, structural and microstructural properties have been demonstrated and correlated with the activation energies of these materials.

Abstract: A mixed powder of AlH3 and MgH2 is ball-milled in a hydrogen atmosphere while applying force of 5 G through 30 G (in which G is gravitational acceleration), and the thus-obtained milled product is dehydrogenated to produce a hydrogen storage material. The hydrogen storage material comprises an amorphous phase containing an Al—Mg alloy as a mother phase, and a crystalline Al phase having a maximum length of 100 nm or less, the crystalline Al phase being distributed as a dispersed phase in the mother phase.

Abstract: A crystalline Al phase and a crystalline TiH2 phase each having a maximum length of 200 nm or less are dispersed in an amorphous phase containing an Al—Mg alloy to obtain a hydrogen storage material capable of reversibly storing and releasing hydrogen.

Abstract: The present invention relates to a doped hydrogen storage material according to the general formula: MgxByMzHn wherein: (i) the ratio of x/y is in the range of from 0.15 to 1.5; (ii) z is in the range of from 0.005 to 0.35; (iii) x+y+z equals 1; (iv) M=is one or more metals selected from the group of selected Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu and Zn; (v) n is no more than 4y; and wherein x/y does not equal 0.5 and at least part of the doped hydrogen storage material is amorphous. The present invention further relates to the use of doped hydrogen storage materials according to the invention for storing hydrogen and a method for reversibly desorbing and/or absorbing hydrogen.

Abstract: In a method of synthesizing magnesium-cobalt pentahydride, a MgCo2 alloy is synthesized by completely reacting cobalt (Co) metal and excess magnesium (Mg) metal, followed by an isothermal evaporation casting process (IECP) for removing the residual magnesium metal. Then, the magnesium-cobalt alloy and another magnesium metal are ball-milled and hydrogenated to synthesize the magnesium-cobalt pentahydride (Mg2CoH5).

Abstract: A ternary hydrogen storage system having a constant stoichiometric molar ratio of LiNH2:MgH2:LiBH4 of 2:1:1. It was found that the incorporation of MgH2 particles of approximately 10 nm to 20 nm exhibit a lower initial hydrogen release temperature of 150° C. Furthermore, it is observed that the particle size of LiBNH quaternary hydride has a significant effect on the hydrogen sorption concentration with an optimum size of 28 nm. The as-synthesized hydrides exhibit two main hydrogen release temperatures, one around 160° C. and the other around 300° C., with the main hydrogen release temperature reduced from 310° C. to 270° C., while hydrogen is first reversibly released at temperatures as low as 150° C. with a total hydrogen capacity of 6 wt. % to 8 wt. %. Detailed thermal, capacity, structural and microstructural properties have been demonstrated and correlated with the activation energies of these materials.

Abstract: In accordance with the present disclosure, a process for synthesis of a complex hydride material for hydrogen storage is provided. The process includes mixing a borohydride with at least one additive agent and at least one catalyst and heating the mixture at a temperature of less than about 600° C. and a pressure of H2 gas to form a complex hydride material. The complex hydride material comprises MAlxByHz, wherein M is an alkali metal or group IIA metal, Al is the element aluminum, x is any number from 0 to 1, B is the element boron, y is a number from 0 to 13, and z is a number from 4 to 57 with the additive agent and catalyst still being present. The complex hydride material is capable of cyclic dehydrogenation and rehydrogenation and has a hydrogen capacity of at least about 4 weight percent.

Abstract: In one embodiment, a hydrogen storage system includes a core of hydrogen sorbent material and a shell of crystalline metal hydride material enclosing at least a portion of the core of hydrogen sorbent material. In another embodiment, the hydrogen storage system further includes an intermediate layer of amorphous metal hydride material, at least a portion of which being positioned between the core of hydrogen sorbent material and the shell of crystalline metal hydride material.

Abstract: State-of-the-art electronic structure calculations yield results consistent with the observed compound SiLi2Mg and provide likelihood of the availability of IrLi2Mg and RhLi2Mg. Similar calculations provide likelihood of the availability of YLi2MgHn, ZrLi2MgHn, NbLi2MgHn, MoLi2MgHn, TcLi2MgHn, RuLi2MgHn, RhLi2MgHn, LaLi2MgHn, Ce4+Li2MgHn, Ce3+Li2MgHn, PrLi2MgHn, NdLi2MgHn, PmLi2MgHn, SmLi2MgHn, EuLi2MgHn, GdLi2MgHn, TbLi2MgHn, DyLi2MgHn, HoLi2MgHn, ErLi2MgHn, TmLi2MgHn, YbLi2MgHn, LuLi2MgHn, HfLi2MgHn, TaLi2MgHn, ReLi2MgHn, OsLi2MgHn, and IrLi2MgHn (here n is an integer having a value in a particular compound of 4-7) as solid hydrides for the storage and release of hydrogen. Different hydrogen contents may be obtained in compounds having the same XLi2Mg crystal structures. These materials offer utility for hydrogen storage systems.

Abstract: Hydrogen is stored by adsorbing the hydrogen to a carbon nanomaterial that includes carbon nanospheres. The carbon nanospheres are multi-walled, hollow carbon nanostructures with a maximum diameter in a range from about 10 nm to about 200 nm. The nanospheres have an irregular outer surface with graphitic defects and an aspect ratio of less than 3:1. The carbon nanospheres can store hydrogen in quantities of at least 1.0% by weight.

Abstract: A hydrogen storage alloy containing a phase of a chemical composition defined by a general formula A5·xB1+xC24: wherein in the general formula A5·xB1+xC24, A denotes one or more element(s) selected from rare earth elements; B denotes one or more element(s) selected from a group consisting of Mg, Ca, Sr, and Ba; C denotes one or more element(s) selected from a group consisting of Ni, Co, Mn, Al, Cr, Fe, Cu, Zn, Si, Sn, V, Nb, Ta, Ti, Zr, and Hf; and x denotes a numeral in a range from ?0.1 to 0.8: and the phase has a crystal structure belonging to a space group of R-3m and having a length ratio of the c-axis to the a-axis of the lattice constant in a range of 11.5 to 12.5.

Abstract: The invention relates to a method for preparation of a material adapted to reversible storage of hydrogen, including steps consisting of providing a first powder of a magnesium-based material, hydrogenating the first powder to convert at least part of the first powder into metal hydrides, mixing the first hydrogenating powder with a second powder additive, the proportion by mass of the second powder in the mix obtained being between 1% and 20% by mass, wherein the additive is formed from an alloy with a centred cubic structure based on titatnium, vanadium and at least one other metal chosen from chromium or manganese, and grinding the mix of first and second powders.

Abstract: In order to accurately and efficiently alloy a Mg-REM-Ni based hydrogen-absorbing alloy in accordance with a target composition, which was difficult in the industrial production by the conventional technique, a rare earth element starting material and a nickel starting material are firstly melted in a melting furnace to form a melt of REM-Ni alloy, and then a magnesium starting material is added to the alloy melt and an interior of the melting furnace is kept at a given pressure to form a melt of Mg-REM-Ni alloy, and thereafter the alloy melt is cooled and solidified at a given cooling rate to produce a Mg-REM-Ni based hydrogen-absorbing alloy.

Abstract: State-of-the-art electronic structure calculations provide the likelihood of the availability of AlLi2MgHn, ScLi2MgHn, TiLi2MgHn, VLi2MgHn, CrLi2MgHn, MnLi2MgHn, FeLi2MgHn, CoLi2MgHn, NiLi2MgHn, CuLi2MgHn, ZnLi2MgHn, GaLi2MgHn, GeLi2MgHn, PdLi2MgHn, AgLi2MgHn, CdLi2MgHn, InLi2MgHn, SnLi2MgHn, SbLi2MgHn, PtLi2MgHn, AuLi2MgHn, HgLi2MgHn, TlLi2MgHn, PbLi2MgHn, and BiLi2MgHn (here n is an integer having a value in a particular compound of 4-7) as solid hydrides for the storage and release of hydrogen. Different hydrogen contents may be obtained in compounds having the same XLi2Mg crystal structures. These materials offer utility for hydrogen storage systems.

Abstract: A method of manufacturing a hydrogen-absorption alloy electrode which comprises particles of a hydrogen-absorption alloy that comprises a rare earth element, Ni, Co and Al. The method comprises subjecting the hydrogen-absorption alloy particles to an alkaline treatment in a 10 to 50 weight % NaOH solution at 60 to 140° C. for 0.5 to 5 hours such that on the surface of the particles (amount of Al on surface/amount of Al in alloy)<(amount of Co on surface/amount of Co in alloy).

Abstract: The present invention relates to hydrogen storage alloys, methods for producing the same, and anodes produced with such alloys for nickel-hydrogen rechargeable batteries. The alloys are useful as electrode materials for nickel-hydrogen rechargeable batteries, excellent, when used as anode materials, in corrosion resistance or activity such as initial activity and high rate discharge performance, of low cost compared to the conventional alloys with a higher Co content, and recyclable. The alloys are of a composition represented by the formula (1), and has a substantially single phase structure, and the crystals thereof have an average long axis diameter of 30 to 160 ?m, or not smaller than 5 ?m and smaller than 30 ?m. The present anodes for rechargeable batteries contain at least one of these hydrogen storage alloys: RNixCoyMz??(1) (R: rare earth elements etc., M: Mg, Al, etc., 3.7?x?5.3, 0.1?y?5.0, 0.1?z?1.0, 5.1?x+y+z?5.5).

Abstract: A process for encapsulating a metal hydride within a hollow glass sphere is provided. The process includes providing a hollow glass sphere, the hollow glass sphere having a shell enclosing an inner volume. The hollow glass sphere is placed within an enclosed chamber and the chamber is evacuated such that a negative pressure is present therewithin. The hollow glass sphere within the evacuated enclosed chamber is subjected to an external element such that the shell affords for molecules to diffuse therethrough. In some instances, the external element is heat, infrared light and combinations thereof. Thereafter, a metal hydride is provided in the form of a vapor and the evacuated enclosed chamber with the hollow glass sphere is exposed to metal hydride vapor and molecules of the metal hydride diffuse through the shell into the inner volume.

Abstract: A method for fabricating a magnesium-based hydrogen storage material according to the present invention comprises a) forming a mixture of a magnesium hydride powder and a transition metal halide powder, b) adding the mixture and balls into a vessel, c) filling the vessel with an inert gas or hydrogen, and d) subjecting the mixture to high energy ball milling.

Abstract: The invention relates to a metal-containing, hydrogen-storing material which contains a catalyst for the purpose of hydration or dehydration, said catalyst being a metal carbonate. The method for producing such a metal-containing, hydrogen-storing material is characterized by subjecting the metal-containing material and/or the catalyst in the form of a metal carbonate to a mechanical milling process.

Abstract: An active material composition for an alkaline storage battery comprises a) an alloy capable of forming a hydride, of formula R1-yMgyNit-zMz in which R is La, optionally substituted by Nd and/or Pr, M is at least one element chosen from the group comprising Mn, Fe, Al, Co, Cu, Zr and Sn, in which 0.1?y?0.4, 3.2?t?3.5, and z?0.5, and of which the equilibrium hydrogen pressure with the alloy, for a hydrogen insertion into the alloy of 0.5 H/Metal at 40°, is less than 0.7 bar, and b) a yttrium-based compound in a mixture with alloy a).

Abstract: A hydrogen storage alloy includes a composition defined by the following formula (Ca1-XLX)(Li1-Y-ZMYNiZ)m, wherein the L denotes one or more elements selected from the group consisting of Na, K, Rb, Cs, Mg, Sr, Ba, Sc, Ti, Zr, Hf, V, Nb, Ta, La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu, the M denotes one or more elements selected from the group consisting of Cr, Mo, W, Mn, Fe, Ru, Co, Ir, Ni, Pd, Pt, Cu, Ag, Au, Zn, Cd, B, Al, Ga, In, Si, Ge, Sn, Pb, Sb, Bi, and S, and the mole ratios X, Y, Z, and m respectively satisfy the following 0<X?0.4, 0?Y?0.4, 0.1?Z?0.4, and 1.8?m?2.2.

Abstract: A hydrogen occlusive alloy has a cubic structure and a composition represented by the following general formula (1): (Mg1-XLX)(Ni1-Y-ZMYLiZ)m??(1) where the element L is at least one element selected from the group consisting of Na, Cs, Ca, Sr, Ba, Sc, Ti, Zr, Hf, V, Nb, Ta, Y, La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu, the element M is at least one element selected from the group consisting of Cr, Mo, W, Mn, Fe, Co, Pd, Pt, Cu, Ag, Zn, Cd, B, Al, Ga, In, Si, Ge, Sn, Pb, Sb and Bi, and mole ratios X, Y, Z and m are 0<X?0.5, 0<Y?0.5, 0.1?Z?0.9, and 1.8?m?2.2, respectively.

Abstract: Embodiments of the invention relate to a composite hydrogen storage material comprising active material particles and a binder, wherein the binder immobilizes the active material particles sufficient to maintain relative spatial relationships between the active material particles.

Abstract: The composition of hydrogen storage alloy particles used in a negative plate of an alkaline secondary battery is expressed by a general formula: (Laa Prb Ndc Zd)1-w Mgw Niz-x-y Alx Ty. In the formula, Z is an element selected from the group consisting of Ce and others, and T is an element selected from the group consisting of V and others. Subscripts a, b, c and d fall in ranges of 0?a?0.25, 0<b, 0<c, and 0?d?0.20, respectively, and satisfy the relationship expressed by a+b+c+d=1, where 0.20?b/c?0.35. Subscripts x, y, z and w fall in ranges of 0.15?x ?0.30, 0?y?0.5, 3.3?z?3.8, and 0.05?w?0.15, respectively.

Abstract: A melt of a hydrogen storage alloy having an arbitrary composition is cooled gradually at a cooling rate of 5° C./min or less and solidified. Alternatively an alloy having an arbitrary composition, after heating to a temperature equal to or more than a melting point thereof, is cooled gradually at a cooling rate of 5° C./min or less and solidified. Thereby a homogeneous alloy reduced in segregation, precipitates, or inclusions is obtained. The homogeneous alloy is excellent in the hydrogen storage amount, in the plateau property and in durability.

Abstract: An alkaline storage cell has a positive electrode, a negative electrode containing a hydrogen storage alloy, and an alkaline electrolyte. The hydrogen storage alloy has a composition expressed by a general expression: ((PrNd)?Ln1-?)1-?Mg?Ni?-?-?Al?T?, where Ln represents at least one element chosen from a group consisting of La, Ce, etc., T represents at least one element chosen from a group consisting of V, Nb, etc., and subscripts ?, ?, ?, ? and ? represent numerical values which satisfy 0.7<?, 0.05<?<0.15, 3.0???4.2, 0.15???0.30 and 0???0.20.

Abstract: Hydrogen gas at a hydrogen refueling site is cooled below liquid nitrogen temperature (e.g., about 80K) for more efficient adsorption of hydrogen on hydrogen adsorbent particles in the fuel storage of a hydrogen powered vehicle. When compressed hydrogen gas is available it may be cooled with liquid nitrogen and then sub-cooled below about 70K by a Joule-Thompson expansion. When liquid hydrogen provides hydrogen gas it may be cooled below liquid nitrogen temperatures by mixing with liquid hydrogen or by heat exchange with liquid hydrogen.

Abstract: Hydrogen is stored by adsorbing the hydrogen to a carbon nanomaterial that includes carbon nanospheres. The carbon nanospheres are multi-walled, hollow carbon nanostructures with a maximum diameter in a range from about 10 nm to about 200 nm. The nanospheres have an irregular outer surface and an aspect ratio of less than 3:1. The carbon nanospheres can store hydrogen in quantities of at least 1.0% by weight.

Abstract: The present invention provides a method for manufacturing high-purity hydrogen storage alloy Mg2Ni applicable to industry and capable of manufacturing continuously. First, raw materials of magnesium-nickel with weight percentage of nickel between 23.5 and 50.2 are heated, melt, and mixed uniformly. Cool the magnesium-nickel liquid and control the temperature to be above the solidification temperature and below the liquification temperature in the phase diagram of magnesium-nickel. By making advantage of segregation principle in phase diagrams, solid-state high-purity ?-phase Mg2Ni hydrogen storage alloy is given. Then high-purity ?-phase Mg2Ni hydrogen storage alloy with atomic ratio of 2:1, no other phases, and with excellent hydrogen absorption-desorption dynamics is given.