The present disclosure provides a catalyst for reducing CO and HC which is a core-shell particle including a core and a shell surrounding the core, the core includes metal oxide nanoparticles and noble metal nanoparticles fixed to the metal oxide nanoparticles, and the shell includes zirconia (ZrO.sub.2), and a layer from which the metal oxide is removed between the core and the shell is included.

The present disclosure provides a catalyst for a water gas shift reaction at middle temperature, the catalyst comprising a catalytically active component containing 40 to 80 mol % of copper (Cu), 15 to 50 mol % of zinc (Zn), and 1 to 13 mol % of aluminum (Al), relative to all metals of the catalyst, wherein an aluminum-rich layer is present in a surface layer of a particle of the catalyst. Furthermore, the present disclosure provides a preparation method of the catalyst, and a hydrogen preparation method using the same.

Disclosed here is a supported catalyst comprising a thermally stable core, wherein the thermally stable core comprises a metal oxide support and nickel disposed in the metal oxide support, wherein the metal oxide support comprises at least one base metal oxide and at least one transition metal oxide or rare earth metal oxide mixed with or dispersed in the base metal oxide. Optionally the supported catalyst can further comprise an electrolyte removing layer coating the thermally stable core and/or an electrolyte repelling layer coating the electrolyte removing layer, wherein the electrolyte removing layer comprises at least one metal oxide, and wherein the electrolyte repelling layer comprises at least one of graphite, metal carbide and metal nitride. Also disclosed is a molten carbonate fuel cell comprising the supported catalyst as a direct internal reforming catalyst.

A carbon-coated transition metal nanocomposite material includes carbon-coated transition metal particles having a core-shell structure. The shell layer of the core-shell structure is a graphitized carbon layer doped with oxygen and/or nitrogen, and the core of the core-shell structure is a transition metal nanoparticle. The nanocomposite material has a structure rich in mesopores, is an adsorption/catalyst material with excellent performance, can be used for catalyzing various hydrogenation reduction reactions, or used as a catalytic-oxidation catalyst useful for the treatment of volatile organic compounds in industrial exhaust gases.

The manufacturing method provided by the present invention provides a powder material substantially comprising Ag—Pd core-shell particles consisting of Ag core particles containing silver as a principal constituent element and a Pd shell containing palladium as a principal constituent element covering at least part of the surface of the Ag core particles, wherein hydroquinone and/or a quinone is attached to the surface of the Ag—Pd core-shell particles. Typically, when the powder material is in a dispersed state in a specific medium, a Z average particle diameter (D.sub.DLS) based on the dynamic light scattering (DLS) method is 0.1 μm to 2 μm, and the polydispersity index (PDI) based on the dynamic light scattering method is 0.4 or lower.

The present disclosure provides a method for preparing an organophosphorus degrading enzyme based multifunctional catalyst and an organophosphorus degrading enzyme based multifunctional catalyst and use thereof. In the present disclosure, the preparation method includes: directly adding a composite yolk-shell-structured nanomaterial into a crude enzyme solution of organophosphorus degrading enzyme with an affinity tag, and mixing, to obtain a mixture, and then subjecting the mixture to a separation, to obtain an organophosphorus degrading enzyme based multifunctional catalyst. According to the present disclosure, the method for preparing an organophosphorus degrading enzyme based multifunctional catalyst is simple in operation, and has a low cost; the multifunctional catalyst prepared by the same has low requirement for the purity of enzyme, support of which could be directionally binded with enzyme, and could be used for detecting an organophosphorus pesticide, and also for a cascade degradation of an organophosphorus pesticide. The final product p-aminophenol has important application value.

Embodiments of the present disclosure are directed to methods of producing a hydrogen-selective oxygen carrier material comprising combining one or more core material precursors and one or more shell material precursors to from a precursor mixture and heat-treating the precursor mixture at a treatment temperature to form the hydrogen-selective oxygen carrier material. The treatment temperature is greater than or equal to 100° C. less than the melting point of a shell material, and the hydrogen-selective oxygen carrier material comprises a core comprising a core material and a shell comprising the shell material. The shell material may be in direct contact with at least a majority of an outer surface of the core material.

The present disclosure provides a catalyst for reducing CO and HC which is a core-shell particle including a core and a shell surrounding the core, the core includes metal oxide nanoparticles and noble metal nanoparticles fixed to the metal oxide nanoparticles, and the shell includes zirconia (ZrO.sub.2), and a layer from which the metal oxide is removed between the core and the shell is included.

Disclosed are a heterogeneous catalyst, a production method thereof, and a method for producing a lignin-derived high-substituted aromatic monomer from a woody biomass material using the heterogeneous catalyst. The heterogeneous catalyst includes a carrier; and a Ni—Al nano-particle supported on the carrier.

A method of forming a nanomaterial catalyst mesh and a nanomaterial catalyst mesh formed by the method. The nanomaterial catalyst mesh comprises a copper support mesh and a nanoparticle layer disposed on the copper support mesh. The nanoparticle layer comprises Cu.sub.2O and CuO. The method involves treating the copper mesh support with a plant extract to form a treated mesh and annealing the treated mesh at 210 to 500° C. The nanomaterial catalyst mesh is used in a method of photodegrading an organic pollutant, preferably a dye, involving hydrogen peroxide and visible light.