The present disclosure relates to metal oxide catalyst materials useful, for example, in the ammoxidation of propylene or isobutylene, processes for making them, and processes for making acrylonitrile and methacrylonitrile using such catalyst materials. In certain aspects, a catalyst material is a fused composite of a metal oxide catalyst and nanoparticulate silica, the nanoparticulate silica comprising in the range of about 40 wt % to about 80 wt % of silica having a particle size in the range of 10 nm to 35 nm, and in the range of about 20 wt % to about 60 wt % of silica having a particle size in the range of 36 nm to 80 nm. The metal oxide catalyst can be, for example, a molybdenum-containing mixed metal oxide catalyst.

A preparation method of photo catalyst by transition metal halide molten salt and use thereof, wherein low-valence titanium complexes stable in air and water are used as a Ti source, transition metal halide is used as molten salt, mixing the Ti source and the molten salt as per a certain mole ratio and grinding, heating at air atmosphere until no lower than a fusion point of the molten salt, keeping the molten salt in a state of melting, maintaining the temperature, washing with water, and reduced TiO.sub.2−x rich in Ti.sup.3+ and Ov is obtained in one-step melting reaction. Deficiencies that multiple steps are involved for preparing conventional defect titanium dioxide or use of inflammable and explosive reducing gases or other dangerous reducing agents or oxidizing agents have been addressed; and the defect that the Ti source is liable to be dissolved in organic and other solvents is fully avoided.

An acid-resistant alloy catalyst, comprising nickel, one or more rare earth element, tin, aluminum and molybdenum. The catalyst is cheap and stable, does not need a carrier, can be stably applied in industrial continuous production, and can lower the production cost.

The present disclosure relates to a catalyst for direct nonoxidative conversion of methane and a method of preparing the same, and more particularly to a method of preparing a catalyst for direct nonoxidative conversion of methane, in which a catalyst optimized for the direct conversion reaction of methane can be easily prepared without precise control of the reaction conditions for direct conversion of methane, thereby simultaneously maximizing the catalytic reaction rate and minimizing coke formation, and exhibiting stable catalytic performance even after long-term operation, and to a catalyst for direct nonoxidative conversion of methane prepared using the above method.

Provided is a method for preparing a diol. In the method, a saccharide and hydrogen as raw materials are contacted with a catalyst in water to prepare the diol. The employed catalyst is a composite catalyst comprised of a main catalyst and a cocatalyst, wherein the main catalyst is a water-insoluble acid-resistant alloy; and the cocatalyst is a soluble tungstate and/or soluble tungsten compound. The method uses an acid-resistant, inexpensive and stable alloy needless of a support as a main catalyst, and can guarantee a high yield of the diol in the case where the production cost is relatively low.

Electrocatalysts composed of single atoms or metal clusters dispersed over porous carbon support were prepared by a lithium-melt method. The new catalysts demonstrated high selectivity, high Faradic efficiency and low overpotential toward to the electrocatalytic reduction of carbon dioxide to chemicals such as glycerol or isopropanol.

Redox catalysts having surface medication, methods of making redox catalysts with surface modification, and uses of the surface modified redox catalysts are provided. In some aspects, the redox catalysts include a core oxygen carrier region such as CaMnO.sub.3, BaMnO.sub.3−δ, SrMnO.sub.3−δ, Mn.sub.2SiO.sub.4, Mn.sub.2MgO.sub.4−δ, La.sub.0.8Sr.sub.0.2O.sub.3−δ, La.sub.0.8Sr.sub.0.2FeO.sub.3−δ, Ca.sub.9Ti.sub.0.1Mn.sub.0.9O.sub.3−δ, Pr.sub.6O.sub.11−δ, manganese ore, or a combination thereof; and an outer shell having an average thickness of about 1-100 monolayers surrounding the outer surface of the core region. The outer shell can include, for example a salt selected such as Li.sub.2WO.sub.4, Na.sub.2WO.sub.4, K.sub.2WO.sub.4, SrWO.sub.4, Li.sub.2MoO.sub.4, Na.sub.2MoO.sub.4, K.sub.2MoO.sub.4, CsMoO.sub.4, Li.sub.2CO.sub.3, Na.sub.2CO.sub.3, K.sub.2CO.sub.3, or a combination thereof.

Provided are an intermetallic compound having high stability and high activity, and a catalyst using the same. A hydrogen storage/release material containing an intermetallic compound represented by formula (1): RTX . . . (1) wherein R represents a lanthanoid element, T represents a transition metal in period 4 or period 5 in the periodic table, and X represents Si, Al or Ge.

Disclosed is a catalyst for producing ethylbenzene in one-step by vapor phase alkylation reaction of ethanol and benzene. The catalyst has the following features for the reaction: high alkylation reaction activity, high selectivity of ethylbenzene in an alkylation product, high hydrothermal stability and stable catalytic performance. The catalyst comprises a mesoporous-microporous composite TNU-9 molecular sieve and the silicon to aluminum molar ratio, SiO.sub.2/Al.sub.2O.sub.3, of the meso-microporous composite TNU-9 molecular sieve ranges from 50 to 200.

A catalyst including an amorphous matrix of a metallic glass including iron and phosphorous; wherein when the catalyst performs a catalytic reaction with a reactant, the metallic glass catalyst activates at least some of the reactant, and at least a portion of the catalyst at a surface of the metallic glass matrix transforms to a surface layer including a material property different from that of the metallic glass matrix being covered by the surface layer; and wherein the surface layer is arranged to maintain an amorphous structure of the metallic glass matrix and to facilitate the catalytic reaction to occur at the surface layer.