The disclosure relates to a process to perform an endothermic steam reforming of hydrocarbons, said process comprising the steps of providing a fluidized bed reactor comprising at least two electrodes and a bed comprising particles, wherein the particles are put in a fluidized state to obtain a fluidized bed; heating the fluidized bed to a temperature ranging from 500? C. to 1200? C. by passing an electric current through the fluidized bed to conduct the endothermic reaction. The process is remarkable in that the particles of the bed comprise electrically conductive particles and particles of a catalytic composition, wherein at least 10 wt. % of the particles are electrically conductive particles and have a resistivity ranging from 0.001 to 500 Ohm.Math.cm at 800? C. and in that the step of heating the fluidized bed is performed by passing an electric current through the fluidized bed.

A hydrocarbon reforming catalyst for producing a synthesis gas containing hydrogen and carbon monoxide from a hydrocarbon-based gas, the hydrocarbon reforming catalyst containing a complex oxide having a perovskite structure including at least Ba, Zr, and Ru; and a hydrocarbon reforming apparatus that includes the hydrocarbon-reforming catalyst.

Systems and methods are provided for improving the flow distribution in the high temperature zone of a cyclic flow reactor, such as a reverse flow reactor. The systems can include a plurality of mixing plates that can facilitate mixing of flows that have been maintained separately until a mixing location. Based in part on the use of a plurality of mixing plates, methods are provided for operating a reverse flow reactor with a temperature profile that has improved uniformity across the cross-section of the reactor. In some aspects, a flame diffuser can be included downstream from the plurality of mixing plates to further improve the uniformity of the temperature distribution.

The present invention discloses a catalytic process for the manufacture of hydrogen and hydrocarbons simultaneously in the same reactor from renewable source, i.e. lipids, glycerides and fatty acids from plant, animal or algae oil, where in the multiple unsaturations in the renewable feedstock and the catalytic intermediates produced in the process from renewable feedstock is converted catalytically using simultaneous combination of in-situ occurring reactions. These in-situ occurring reactions are simultaneous combination of hydroconversion, reforming and water gas shift reactions wherein the reaction is performed in the presence of one or more metal sulfides form of metals of Group VI and/or Group IX and/or Group X elements, specifically comprises of one or more active metal combinations such as Co, W, Mo, Ni, P, with Pt, Pd encapsulated inside sodalite cages for prevention against poisoning from sulfur based compounds. The hydroconversion comprises of reactions in presence of hydrogen such as hydrocracking, dehydrogenation, dehydrocyclization, hydrodeoxygenation, hydrodesulfurization, hydrodenitrogenation, decarboxylation, decarbonylation, cyclization and aromatization reactions. The catalyst along with the active metals also includes porous silica-alumina, zeolite, silica, alumina, silicoaluminophosphates or a combination of two or more thereof used as support for the above said process. These catalysts are loaded in a graded beds (two or more beds of different catalyst mixtures) or simultaneously (mixture of different catalyst systems) and reacted specifically at lower temperatures than the steam reforming conditions i.e. at pressure from 10 to 150 atmosphere, average temperature of the catalytic bed from 250 C. to 500 C., space-velocity of from 0.5 h.sup.1 to 8 h.sup.1, and hydrogen to feed ratio of from 300 NL of hydrogen/L of feed to 3500 NL hydrogen/L of feed. Initially hydrogen gas is supplied for conversion of the renewable feed stocks, as the reaction process the hydrogen consumed during the conversion of plant, animal or algae oil into hydrocarbons is balanced from the in-situ reactions such as reforming, dehydrogenation, water gas shift etc occurring during the same process. This production of hydrogen makes the entire process refinery independent and more economical and sustainable. Along with hydrogen the renewable feed stock is also converted into hydrocarbons ranging between C1-C24 carbon number, comprising of n-paraffins, isoparaffins, cyclo paraffins, naphthenes, and aromatics and polynuclear aromatics.

The invention relates to a mixture, which is liquid at room temperature and which is composed of two or more compounds, which are constructed exclusively of the elements carbon and hydrogen and, in individual known compositions, form a synthetic substance mix that can be used as a heat-transfer liquid. The mixture is characterized in that the mixture contains at least one compound having at least two non-condensed, non-pi-conjugated aromatic units and is used in catalytic methods to bind hydrogen to or release hydrogen from the mixture.

A method for producing hydrocarbons and hydrogen from methane. The method includes packing a catalyst comprising platinum, bismuth and a support material into a reactor; introducing a reactant mixture containing methane into the reactor such that the reactant mixture containing methane is in close contact with the reactant mixture; and heating the reactant mixture containing methane to a temperature for a period of time.

Disclosed are methods and systems of producing acetic acid and hydrogen from a two carbon (C.sub.2) alcohol source, the method comprising (a) obtaining a homogeneous aqueous solution comprising a C.sub.2 alcohol source and an organoruthenium (II) halide catalyst; and (b) subjecting the homogeneous aqueous solution to conditions suitable to produce a product stream comprising acetic acid and hydrogen.

Provided is a liquid hydrogen storage material including 1,1-biphenyl and 1,1-methylenedibenzene, the liquid hydrogen storage material including the corresponding 1,1-biphenyl and 1,1-methylenedibenzene at a weight ratio of 1:1 to 1:2.5. The corresponding liquid hydrogen storage material has excellent hydrogen storage capacity value by including materials having high hydrogen storage capacity, and is supplied in a liquid state, and as a result, it is possible to minimize initial investment costs and the like required when the corresponding liquid hydrogen storage material is used as a hydrogen storage material in a variety of industries.

Sulfur-tolerant reforming catalysts that include bulk alumina in the catalyst support are provided. The sulfur-tolerant reforming catalysts can include a sulfur-tolerant catalytic metal to facilitate reforming. The catalyst can further include a support material that includes at least some alumina as bulk alumina and/or octahedrally coordinated alumina. The sulfur-tolerant reforming catalysts can be regenerated, such as periodically regenerated, under relatively mild conditions that allow the catalysts to maintain reforming activity in the presence of 1 vppm to 1000 vppm of sulfur in the feed for reforming.

The invention concerns a process and apparatus for cracking ammonia in which heated ammonia gas at super-atmospheric pressure is partially cracked catalytically in an adiabatic reaction unit to produce partially cracked ammonia gas which is heated and fed to catalyst-containing reactor tubes in a furnace to cause cracking of further ammonia and produce a cracked gas comprising hydrogen gas, nitrogen gas and residual ammonia gas. At least some, preferably all, of the duty required to heat the partially cracked ammonia gas is provided by heat exchange with the cracked gas, enabling more efficient heat integration within the process.