The disclosure relates to a process to perform an endothermic dehydrogenation and/or aromatization reaction of hydrocarbons, said process comprising the steps of providing at least one fluidized bed reactor comprising at least two electrodes and a bed comprising particles; putting the particles in a fluidized state to obtain a fluidized bed; heating the fluidized bed to a temperature ranging from 480° C. to 700° C. to conduct the reaction; and obtaining a reactor effluent containing hydrogen, unconverted hydrocarbons, and olefins and/or aromatics; wherein 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 Ohm.Math.cm to 500 Ohm.Math.cm at 500° C. and wherein the step of heating the fluidized bed is performed by passing an electric current of through the fluidized bed.

The invention relates to a process for removing dienes from a material stream comprising C.sub.3 to C.sub.5 hydrocarbons by selective hydrogenation at a specified reaction pressure and a specified reaction temperature in the presence of a hydrogenation catalyst, wherein the reaction pressure and the reaction temperature at the reactor inlet are regulated such that the reaction pressure at the reactor inlet does not deviate by more than 0.01 bar from the specified reaction pressure and the reaction temperature at the reactor inlet does not deviate by more than 0.1° C. from the specified reaction temperature and the proportion of hydrogen supplied to the selective hydrogenation is in the range from 2 to 20 moles per mole of diene present in the material stream comprising C.sub.3 to C.sub.5 hydrocarbons.

Simple and economical conversion of aqueous ethanol feed streams into butenes by a single step method using transition metal oxides on a silica supports under preselected processing conditions. By directly producing a C4-rich olefin mixture from an ethanol containing stream various advantages are presented including, but not limited to, significant cost reduction in capital expenses and operational expenses.

Simple and economical conversion of aqueous ethanol feed streams into butenes by a single step method using transition metal oxides on a silica supports under preselected processing conditions. By directly producing a C4-rich olefin mixture from an ethanol containing stream various advantages are presented including, but not limited to, significant cost reduction in capital expenses and operational expenses.

A catalyst support comprising at least 95% silicon carbide, having surface areas of 10 m.sup.2/g and pore volumes of 1 cc/g. A method of producing a catalyst support, the method including mixing SiC particles of 0.1-20 microns, SiO.sub.2 and carbonaceous materials to form an extrusion, under inert atmospheres, heating the extrusion at temperatures of greater than 1400 C., and removing residual carbon from the heated support under temperatures below 1000 C. A catalyst on a carrier, comprising a carrier support having at least about 95% SiC, with a silver solution impregnated thereon comprising silver oxide, ethylenediamine, oxalic acid, monoethanolamine and cesium hydroxide. A process for oxidation reactions (e.g., for the production of ethylene oxide, or oxidation reactions using propane or methane), or for endothermic reactions (e.g., dehydrogenation of paraffins, of ethyl benzene, or cracking and hydrocracking hydrocarbons).

The purpose of the invention is to provide a supported bimetallic core-shell structure catalyst and its preparation method. Supporter, metal salt and reducing agent solution are mixed to synthesize the catalyst M@PdM/ZT by using a one-step synthesis method, wherein the active metal particle M@PdM as core-shell structure, M Is the core representing one of the Ag, Pt, Au and Ir. ZT is the supporter, representing one of hydrotalcite (Mg.sub.2Al-LDH), alumina (Al.sub.2O.sub.3) and silica (SiO.sub.2). By changing the temperature and the reaction time to control the kinetic behavior of the reduction of two kinds of metal ions to realize the construction of core-shell structure. Active metal particle composition and shell thickness are regulated by controlling metal ion concentration. The bimetallic core-shell catalyst prepared by this method showed excellent selectivity and stability in acetylene selective hydrogenation and anthraquinone hydrogenation.

The present disclosure relates to methods for selectively hydrogenating acetylene, to methods for starting up a selective hydrogenation reactor, and to hydrogenation catalysts useful in such methods. In one aspect, the disclosure provides a variety of methods for starting up reactors for use in methods for selectively hydrogenating acetylene using a catalyst composition comprises a porous support, palladium, and one or more ionic liquids.

The purpose of the invention is to provide a supported bimetallic core-shell structure catalyst and its preparation method. Supporter, metal salt and reducing agent solution are mixed to synthesize the catalyst M@PdM/ZT by using a one-step synthesis method, wherein the active metal particle M@PdM as core-shell structure, M Is the core representing one of the Ag, Pt, Au and Ir. ZT is the supporter, representing one of hydrotalcite (Mg.sub.2Al-LDH), alumina (Al.sub.2O.sub.3) and silica (SiO.sub.2). By changing the temperature and the reaction time to control the kinetic behavior of the reduction of two kinds of metal ions to realize the construction of core-shell structure. Active metal particle composition and shell thickness are regulated by controlling metal ion concentration. The bimetallic core-shell catalyst prepared by this method showed excellent selectivity and stability in acetylene selective hydrogenation and anthraquinone hydrogenation.

The invention relates to a catalyst composition, suitable for producing ethylene and other commercially high value C.sub.2+ hydrocarbons from methane. The composition contains a silver promoted mixed metal catalyst composition comprising at least two rare earth elements and an alkaline rare earth metal element. The catalyst composition has high catalyst activity and enables oxidative coupling of methane reactions to be conducted at a low reactor temperature while retaining sufficient catalyst selectivity. The invention further provides a method for preparing such a catalyst composition and a process for producing C.sub.2+ hydrocarbons, using such a catalyst composition.

The present invention relates to a palladium-based supported hydrogenation catalyst and a preparation method and application thereof. The catalyst is prepared by the following method: impregnating an Al.sub.2O.sub.3-containing carrier with an organic solution containing a bipyridine derivative having hydroxy group, optionally drying followed by impregnating with a mixed solution containing the main active component palladium ions and the auxiliary active component M.sup.n+ ions, where M is one selected from Ag, Au, Ni, Pb and Cu; and then optionally drying, and calcining to obtain the catalyst. The preparation method provided by the present invention allows Pd atoms and M atoms to be highly uniformly dispersed on the carrier, which overcomes the adverse impact of the surface tension of the impregnation solution and the solvation effect on the dispersibility of active components. The palladium-based supported hydrogenation catalyst provided by the present invention has excellent hydrogenation activity, ethylene selectivity and anti-coking performance, and can be used in a selective hydrogenation process of C2 fraction.