Provided is a method for synthesizing cobalt-incorporated carbon nanotubes (Co/MWCNTs). The method includes a step of mixing cobalt acetate, cobalt nitrate, cobalt chloride, or cobalt sulfate with multi-wall carbon nanotubes in a solvent. A method for generating hydrogen by using the Co/MWCNTs as a catalyst component is also provided herein.

A method for ammonia decomposition to produce hydrogen, the method comprising the steps of introducing an ammonia stream to a reactor, wherein the ammonia stream comprises ammonia, wherein the reactor comprises a cobalt-based catalyst, the cobalt-based catalyst comprising 15 wt % and 70 wt % of cobalt, 5 wt % and 45 wt % of cerium, and 0.4 wt % and 0.5 wt % barium, wherein a remainder of weight of the cobalt-based catalyst is oxygen; contacting the ammonia in the ammonia stream with the cobalt-based catalyst, wherein the cobalt-based catalyst is operable to catalyze an ammonia decomposition reaction; catalyzing the ammonia decomposition reaction to cause the ammonia decomposition in the presence of the cobalt-based catalyst to produce hydrogen; and withdrawing a product stream from the reactor, the product stream comprising hydrogen.

A method for ammonia decomposition to produce hydrogen, the method comprising the steps of introducing an ammonia stream to a reactor, wherein the ammonia stream comprises ammonia, wherein the reactor comprises a cobalt-based catalyst, the cobalt-based catalyst comprising 15 wt % and 70 wt % of cobalt, 5 wt % and 45 wt % of cerium, and 0.4 wt % and 0.5 wt % barium, wherein a remainder of weight of the cobalt-based catalyst is oxygen; contacting the ammonia in the ammonia stream with the cobalt-based catalyst, wherein the cobalt-based catalyst is operable to catalyze an ammonia decomposition reaction; catalyzing the ammonia decomposition reaction to cause the ammonia decomposition in the presence of the cobalt-based catalyst to produce hydrogen; and withdrawing a product stream from the reactor, the product stream comprising hydrogen.

Disclosed is a reaction system including: a reforming device including a reaction tube, and a reforming catalyst that is provided inside the reaction tube and generates carbon monoxide from a raw material gas containing hydrocarbon; a solid carbon capturing device including a reaction tube, and a solid carbon capturing catalyst provided inside the reaction tube; and a flow path through which a gas flows from the reforming device to the solid carbon capturing device. The solid carbon capturing catalyst includes a base material, and a coating layer formed on a surface of the base material. The coating layer contains at least one kind of metal-containing component selected from iron oxide, cobalt oxide, and the like.

The present invention refers to a method for cracking ammonia, producing hydrogen and generating electrical power including electrolysis of water in feed ammonia, evaporation, pre-heating and cracking of ammonia, using ammonia synthesis catalysts at low temperatures. A method for cracking ammonia including a) electrolysis of water in feed ammonia, wherein feed ammonia includes make-up ammonia; b) evaporation; c) cracking; wherein cracking of ammonia takes place between 300-700° C., using ammonia synthesis catalysts.

It is provided solid, heterogeneous catalysts and a method for producing H.sub.2 by steam reforming. More particularly, the catalyst comprises at least one metal element of Cu, Ni, Fe, Co, Mo, Mn, Mg, Zr, La, Ce, Ti, Zn and W, having a formula Cu.sub.aNi.sub.bFe.sub.c-Co.sub.dMO.sub.eMn.sub.fMg.sub.gZr.sub.hLa.sub.iCe.sub.jTi.sub.kZn.sub.lW.sub.mO.sub.x, wherein a, b, c, d, e, f, g, h, i, j, k, I and m are molar ratios for the respective elements, wherein a, b, c, d, e, f, g and m are >0, h, I, j, k and I are >0 or a, b, c, d, e, f, g, i, and j are ≥0, h, k, I and m are >0 and x is such that the catalyst is electrically neutral. The produced H.sub.2 can be used to powered vehicle as described herein.

A process of catalytic partial oxidation of hydrocarbons, particularly methane and/or natural gas to form a product containing hydrogen and carbon monoxide where the first catalyst comprises Co—Ni—Cr—W alloy.

A porous carbon-based metal catalyst, a preparation method and application thereof are provided. The preparation method includes: successively performing activation, surface corrosion, nitrogen-doping treatment and graphitization treatment on washed micro-grade porous carbon, then performing sensitization treatment, and subsequently carrying out loading, reduction and other treatments of catalytic metal, so as to finally obtain the porous carbon-based metal catalyst. The porous carbon-based metal catalyst provided by the present application has excellent catalytic performance, is especially suitable for producing hydrogen by efficiently catalytically decomposing ammonia borane, is not prone to inactivation, and is easy to regenerate after inactivation. Meanwhile, the preparation method is environmental-friendly, is suitable for large-scale production and has a wide application prospect in the fields such as hydrogen fuel batteries.

The present invention relates to processes for the preparation of biofuel from biomass by fast hydropyrolysis or fast pyrolysis, using hydrogen generated by sorption enhanced steam reforming. The present invention also relates to fixed bed tandem catalytic-upgrading processes, and reactors and hydrodeoxygenation (HDO) catalysts useful in those processes.

Apparatus and associated methods relate to cooling hot biochar based on applying cool gas directly to the hot biochar. The gas may be steam comprising water vapor. Biochar may be cooled in a cooling chamber by cool steam injected into a steam loop configured to cool the steam. The biochar cooled with steam may be dried in a drying chamber by dry gas injected from a gas loop. The gas may be hydrocarbon gas. Biochar may be heated in a processing chamber. Heated biochar may be cooled in a cooling chamber by cool hydrocarbon gas injected to the cooling chamber. Biochar in the processing chamber may be heated with heat recovered from cooling. Filtered byproducts and tail gas may be recovered from the cooling chamber. Tail gas may be recycled. Various direct biochar cooling implementations may produce biochar having enhanced carbon content, increased surface area, and a hydrogen stream byproduct.