The present invention relates to improved hydrogen storage materials and improved processes for their preparation. The hydrogen storage materials prepared by the processes described herein exhibit enhanced hydrogen storage capacity when used as hydrogen storage systems. The processes described herein may be undertaken on a commercial scale.

The present invention relates to a process for producing and for regenerating siloxane hydrogen carrier compounds.

The present invention provides a hydrogen storage and release material including a two-dimensional hydrogen boride-containing sheet including a two-dimensional network containing n(H.sub.xB.sub.y) (n≥4, 0.001≤x/y≤0.999) having a molar ratio of boron to hydrogen from 1:0.999 to 1:0.001, the molar ratio being determined by thermal desorption spectroscopy, and mass measurement before and after a temperature rise, wherein the hydrogen storage and release material has: peaks derived from B1s of boron at 187.5±1.0 eV and 191.2±1.0 eV to 193±1.0 eV in X-ray photoelectron spectroscopy, and a peak derived from a B—H stretching vibration at from 2400 cm.sup.−1 to 2600 cm.sup.−1 and also a peak derived from a B—H—B stretching vibration at from 1200 cm.sup.−1 to 1800 cm.sup.−1 in infrared spectroscopy.

The present invention relates to siloxane hydrogen carrier compounds and to a method for producing hydrogen from said siloxane hydrogen carrier compounds.

The present disclosure relates to improved processes for the preparation of metal hydrides. The present disclosure also relates to metal hydrides, e.g., metal hydrides prepared by the processes described herein, that exhibit enhanced hydrogen storage capacity when used as hydrogen storage systems.

A hydrogen release and storage system (100) of the present invention includes a first hydrogen release and storage unit (100A) composed of a first hydrogen compound member (101A), a first container (102A) that accommodates the first hydrogen compound member (101A), a first heating apparatus (103A) configured to heat an inside of the first container (102A), a first cooling apparatus (104A) configured to cool the inside of the first container (102A), a first water supply apparatus (105A) configured to supply water to the first container (102A), a second hydrogen release and storage unit (100B) composed of a second hydrogen compound member (101B), a second container (102B) that accommodates the second hydrogen compound member (101B), a second heating apparatus (103B) configured to heat an inside of the second container (102B), a second cooling apparatus (104B) configured to cool the inside of the second container (102B) and a second water supply apparatus (105B) configured to supply water to the second container (102B).

Apparatuses and methods of measuring a hydrogen diffusivity of a metal structure including during operation of the metal structure, are provided. A hydrogen charging surface is provided at a first location on an external surface of the structure. In addition, a hydrogen oxidation surface is provided at a second location adjacent to the first location on the external surface of the structure. Hydrogen flux is generated and directed into the metal surface at the charging surface. At least a portion of the hydrogen flux generated by the charging surface is diverted back toward the surface. A transient of the diverted hydrogen fluxes measured, and this measurement is used to determine the hydrogen diffusivity of the metal structure in service.

A novel hydrogen absorption material is provided comprising a mixture of a lithium hydride with a fullerene. The subsequent reaction product provides for a hydrogen storage material which reversibly stores and releases hydrogen at temperatures of about 270° C.

A storage medium and an inert material, either integrated into the storage medium or existing as a separate phase in the storage medium, form a storage structure. The inert material at least partially contains or is formed by a polymorphous inert material. The polymorphous inert material has at least one polymorphous phase transition in the range between ambient temperature and maximum operating temperature of the solid electrolyte battery. The polymorphous phase transition induces a distortion of the lattice structure of the inert material, thus causing a change in the specific volume and acting on the surrounding grains of the storage medium. A mechanical coupling of the stresses triggered by the phase transition of the inert material causes the neighboring grains of the storage medium to break apart, such that new reactive zones become available in the storage medium, thereby regenerating the solid electrolyte battery.

The present disclosure relates to improved processes for the preparation of metal hydrides. The present disclosure also relates to metal hydrides, e.g., metal hydrides prepared by the processes described herein, that exhibit enhanced hydrogen storage capacity when used as hydrogen storage systems.