The present invention provides a technique capable of adjusting the loading positions of gold and palladium in a VAM catalyst by a method of producing a palladium-gold loaded catalyst for vinyl acetate synthesis. The method includes a step of impregnating a spherical porous molded carrier of an inorganic oxide with a mixed aqueous solution containing a palladium precursor as a catalytically active species and a gold precursor as a co-catalyst component, and subsequently impregnating the resultant spherical porous molded carrier with an aqueous alkaline solution to water-insolubilize the palladium precursor and the gold precursor in the spherical porous molded carrier to obtain a palladium-gold immobilized spherical porous molded carrier; and a subsequent step of adjusting the moisture content of the palladium-gold immobilized spherical porous molded carrier.

The presently disclosed and claimed inventive concept(s) generally relates to a method of making a solid catalyst component comprising a zeolite with a modifier and at least one Group VIII metal alloyed with at least one transition metal and a process of converting mixed waste plastics into low molecular weight organic compounds using the solid catalyst component. The process of converting mixed waste plastics into low molecular weight organic compounds may employ the use of a non-thermal catalytic plasma reactor, which may be configured as a fluid bed reactor or fixed bed reactor.

Disclosed are a low-temperature de-NO.sub.x catalyst using a ceria-alumina complex support, and a method of manufacturing the same. According to the present invention, provided is a low-temperature de-NO.sub.x catalyst using a ceria-alumina complex support, manufactured by impregnating noble metal and metal oxides into a ceria-alumina complex support synthesized by treating a ceria precursor and an alumina precursor in a predetermined mass ratio by a co-precipitation method.

Catalysts and processes for producing catalysts for neopentane production are provided herein. A process includes reducing a catalyst precursor comprising a transition metal and an inorganic support at a temperature less than 500° C. to produce a catalyst. Also provided herein are processes to produce neopentane using the catalysts described herein and neopentane compositions produced therefrom.

The present disclosure features a high metal cation content zeolite-based binary catalyst (e.g., a high copper and/or iron content zeolite-based binary catalyst, where the zeolite can be a chabazite) for NO.sub.x reduction, having relatively low N.sub.2O make, and having low corresponding metal oxide content; where the metal in the metal oxide corresponds to the metal of the metal cation. The present disclosure also describes the synthesis of the zeolite-based binary catalyst having high metal cation content.

A hydrogenolysis/hydrogenation catalyst includes copper oxide, calcium oxide, silicon dioxide, and sodium oxide, wherein the hydrogenolysis/hydrogenation catalyst is a powder, tablet, or extrudate, the hydrogenolysis/hydrogenation catalyst is substantially free of chromium, the hydrogenolysis/hydrogenation catalyst exhibits a crystallite phase of CuO and an additional crystallite phase selected from the group consisting of cubic SiO.sub.2, rhombohedral calcium carbonate CaCO.sub.3, anorthic calcium silicate CaCO.sub.3, calcium silicate hydroxide hydrate (Ca.sub.14Si.sub.24O.sub.58(OH).sub.8.Math.5H.sub.2O), calcium silicate hydrate 4CaO.Math.5 SiO.sub.2.Math.5H.sub.2O, alumina, and combinations of two or more thereof.

Various uses of monochlorotrifluoropropenes, in combination with one or more other components, including other fluoroalkenes, hydrocarbons; hydrofluorocarbons (HFCs), ethers, alcohols, aldehydes, ketones, methyl formate, formic acid, water, trans-1,2-dichloroethylene, carbon dioxide and combinations of any two or more of these, in a variety of applications, including as blowing agents, are disclosed.

Disclosed are a chemochromic nanoparticle, a method for manufacturing the chemochromic nanoparticle, and a hydrogen sensor comprising the chemochromic nanoparticle. In particular, the chemochromic nanoparticle has a core-shell structure such that the chemochromic nanoparticle and comprises a core comprising a hydrated or non-hydrated transition metal oxide; and a shell comprising a transition metal catalyst.

A process for the methanation of carbon monoxide and/or carbon dioxide in a feed stream containing carbon monoxide and/or carbon dioxide is disclosed. This is achieved by a process for the methanation of carbon monoxide and/or carbon dioxide in a feed stream containing carbon monoxide and/or carbon dioxide, hydrogen and more than 1 ppb of sulfur, using a catalyst comprising aluminum oxide, an Ni active composition and Mn. It has surprisingly The Mn-containing Ni catalyst has a high sulfur resistance and also a high sulfur capacity.

Direct conversion of syngas to light olefins is carried out in a fixed bed or a moving bed reactor with a composite catalyst A+B. The active ingredient of catalyst A is active metal oxide; and catalyst B is one or more than one of zeolite of CHA and AEI structures or metal modified CHA and/or AEI zeolite. A spacing between geometric centers of the active metal oxide of the catalyst A and the particle of the catalyst B is 5 m-40 mm. A spacing between axes of the particles is preferably 100 m-5 mm, and more preferably 200 m-4 mm. A weight ratio of the active ingredients in the catalyst A and the catalyst B is within a range of 0.1-20 times, and preferably 0.3-5.