The present invention relates to a catalyst for hydrogenation of an aromatic compound, which is capable of greatly reducing the inactivation of a catalyst by using a support including a magnesium-based spinel structure, and a preparation method therefor.

Catalysts, catalytic systems and related synthetic methods for in situ production of H.sub.2O.sub.2 and use thereof in reaction with oxidizable substrates.

A method is disclosed for converting biomass into a fuel additive, the method comprising: liquefying the biomass to form a liquor; neutralizing the liquor; precipitating lignin out of the liquor; extracting furfural (FF) and 5-hydroxymethylfurfural (HMF) from the liquor; and hydrodeoxygenating (HDO) the extracted furfurals over a CuNi/TiO.sub.2 catalyst. The catalyst for hydrodeoxygenating (HDO) furfural (FF) and 5-hydroxymethylfurfural (HMF) to methylated furans comprises copper-nickel (CuNi) particles supported on titanium dioxide (TiO.sub.2), and wherein the copper-nickel particles form core-shell structures in which copper (Cu) is enriched at a surface of the catalyst.

The present invention discloses a core-shell structure supported tungsten composite catalyst and a preparation method and use thereof. Most of the existing synthesis methods of the main ring of quinolone drugs have the defects of many synthesis steps, cumbersome operation, large amount of three wastes, higher costs and the like. The present invention prepares a magnetic separable core-shell supported tungsten composite catalyst, WO.sub.3/SiO.sub.2/Fe.sub.3O.sub.4, by preparing Fe.sub.3O.sub.4 colloid and SiO.sub.2/Fe.sub.3O.sub.4 composite nano-particles. This magnetic separable core-shell supported tungsten composite catalyst, WO.sub.3/SiO.sub.2/Fe.sub.3O.sub.4, is used to catalyze and synthesize quinolone compounds. The present invention provides an efficient preparation method of quinolone compounds using a catalyst which can be recovered by magnetic separation and recycled. The catalyst prepared by the present invention can be reused in the preparation of quinolone compounds and still retains the original activity without deactivation, which not only greatly improves the production efficiency, but also reduces the environmental pollution.

Embodiments of the invention are directed to Z-scheme photocatalyst for efficient hydrogen generation from water. The Z-scheme photocatalyst can include a hybrid metal that includes a semiconductor material/M1/Cd.sub.xM.sub.1xS material. M1 can be transition metal and M can Zn, Fe, Cu, Sn, Mo, Ag, Pb and Ni.

A method for scaled-up synthesis of PtNi nanoparticles. Synthesizing a Pt nanoparticle catalyst comprises the steps of: synthesizing PtNi nanoparticles, isolating PtNi/substrate nanoparticles, acid leaching the PtNi/substrate, and annealing the leached PtNi/substrate nanoparticles, and forming a Pt-skin on the PtNi/substrate nanoparticles.

A method for forming catalyst particles, each of which has a core/shell structure, by a Cu-UPD method. Namely, a method of manufacturing a catalyst wherein catalyst particles, each of which has a core/shell structure composed of a shell layer that is formed of platinum and a core particle that is covered with the shell layer and is formed of a metal other than platinum, are supported on a carrier. This method is characterized by comprising: an electrolysis step wherein the carrier supporting the core particles is electrolyzed in an electrolytic solution containing copper ions, so that copper is precipitated on the surfaces of the core particles; and a substitution reaction step wherein a platinum compound solution is brought into contact with the core particles, on which copper has been precipitated, so that the copper on the surface of each core particle is substituted by platinum, thereby forming a shell layer that is formed of platinum. This method is further characterized in that the platinum compound solution in the substitution reaction step contains citric acid.

A core-shell catalyst includes a porous, palladium-based core particle and a catalytic layer on the particle. The particle can be made by providing a precursor particle that has palladium interspersed with a sacrificial material. At least a portion of the sacrificial material is then removed such that the remaining precursor particle is porous.

A carbon-platinum core-shell type catalyst for fuel cells and a method for preparing the same which includes carbon as a core and platinum as a shell which can solve durability-associated problems under proton exchange membrane fuel cells (PEMFC) operation conditions and furthermore tackle manufacturing cost-related problems and process complexity by improving acid resistance through incorporation of a carbon material rather than a transition metal into catalysts.

The present disclosure relates generally to catalyst materials and processes for making and using them. More particularly, the present disclosure relates to molybdenum, bismuth and iron-containing metal oxide catalyst materials useful, for example, in the partial oxidation or ammoxidation of propylene or isobutylene, processes for making them, and processes for making acrolein, methacrolein, acrylonitrile, and methacrylonitrile using such catalysts.