The present invention concerns a hydrogen store comprising a hydrogenable material, and a method for producing a hydrogen store.

A carbon material that is compact and exhibits an excellent hydrogen storage capacity. A carbon material has a specific surface area of 200 m.sup.2/g or less and exhibits a hydrogen storage capacity of 1.5×10.sup.−5 g/m.sup.2 or more at a hydrogen pressure of 10 MPa.

The present application is generally directed to gas storage materials such as activated carbon comprising enhanced gas adsorption properties. The gas storage materials find utility in any number of gas storage applications. Methods for making the gas storage materials are also disclosed.

A method of separating combustible gasses from the pores of carbon black. A method of making carbon black in a reactor is described that results in a high concentration of combustible gasses contained in the pores of the carbon black produced. The combustible gasses contained in the pores are replaced with inert gas to render the carbon black safer to process in downstream equipment.

A carbon nanomaterial for gas storage and a method for manufacturing the same are provided. The specific surface area of the carbon nanomaterial for gas storage is greater than 2000 m2/g. The mesopore volume of the carbon nanomaterial for gas storage is greater than the micropore volume of the carbon nanomaterial for gas storage, and the carbon nanomaterial for gas storage has a peak intensity ratio (ID/IG) between G band and D band, as determined from the Raman spectrum, between 1.1 and 2. In the carbon nanomaterial for gas storage, the pore volume of pores with a pore width of 6 nm or less is bigger than that of pores with a pore width greater than 6 nm.

The present relates to a carbon material having a 3D structure and made of graphene oxide and carbon nanotubes, characterized in that the 3D structure consists in that the carbon nanotubes are located with some agglomeration between the graphene oxide layers so as to extend the spacing between the graphene oxide layers.

The present application is generally directed to gas storage materials such as activated carbon comprising enhanced gas adsorption properties. The gas storage materials find utility in any number of gas storage applications. Methods for making the gas storage materials are also disclosed.

The objective of the present invention is to provide a carbon-based hydrogen storage material having an autocatalytic capability and an atomic vacancy, wherein the hydrogen storage is a hydrocarbon compound which produces a non-endothermic release or an exothermic release of hydrogen adsorbed in the compound. In addition, the present invention provides a method of manufacturing the material comprising: preparing a hydrocarbon compound as the raw material of the carbon-based hydrogen storage material; setting the raw material in a container having a predetermined gas partial pressure; producing the hydrocarbon compound by ion beam irradiation of the raw material; performing annealing treatment under the predetermined conditions; and exposing the product to the hydrogen under the predetermined conditions, wherein the product is a hydrogen storage hydrocarbon compound producing a non-endothermic or an exothermic release of hydrogen adsorbed thereto with autocatalysis activity.

The hydrogen storage product comprises one or more reduced-graphene oxide layers functionalized with a boron species and decorated with an alkali or alkaline earth metal. Each layer of the structure further comprises boron-oxygen functional groups comprising oxygen atoms bonded to boron atoms. The hydrogen storage product has a composition suitable for physisorption of hydrogen molecule, and operates to reversibly store hydrogen under operating conditions of low pressure and ambient temperature.

The present relates to a carbon material having a 3D structure and made of graphene oxide and carbon nanotubes, characterized in that the 3D structure consists in that the carbon nanotubes are located with some agglomeration between the graphene oxide layers so as to extend the spacing between the graphene oxide layers