A novel catalyst includes a plurality of nanoparticles, each nanoparticle including a core made of a catalytic metal and a porous shell surrounding the core, made of metal oxide, the porous shell preserving a catalytic function of the core and reducing reduction of the core and coalescence of the nanoparticles.

Shaped porous carbon products and processes for preparing these products are provided. The shaped porous carbon products can be used, for example, as catalyst supports and adsorbents. Catalyst compositions including these shaped porous carbon products, processes of preparing the catalyst compositions, and various processes of using the shaped porous carbon products and catalyst compositions are also provided.

Porous particles comprising an active ingredient and a coating exhibiting greater dissolution rate in aqueous media than in alcoholic media are disclosed. A process for the manufacture of the particles is also disclosed, as well as tamper-proof particles and solid dosage forms comprising the coated particles. The differential solubility characteristics of the particle coating allow the particles to be incorporated into abuse-deterrent medicaments.

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.

The present invention relates to an SCR-active material, comprising a small-pore zeolite, aluminum oxide and copper, characterized in that it contains 5 to 25 wt-% of aluminum oxide in relation to the entire material and that the copper is present on the aluminum oxide in a first concentration and on the small-pore zeolite in a second concentration.

The present invention relates to the field of isobutylene preparation. Disclosed are a catalyst and preparation method thereof, and method for preparing isobutylene by applying the same; the catalyst has a core-shell structure, the core an amorphous silica-alumina particle and/or an aggregate molding thereof, and the shell aluminum oxide comprising silicon and tin; the weight ratio of aluminum oxide comprising silicon and tin to amorphous silica-alumina is 1:60-1:3; in the aluminum oxide comprising silicon and tin, on basis of the weight of aluminum oxide comprising silicon and tin, the content of silicon is 0.5-2 wt %, and of tin is 0.2-1 wt %. The catalyst of the present invention is used to catalyze a mixture of MTBE and TBA to prepare isobutylene, enabling the MTBE cleavage and TBA dehydration reactions to be conducted simultaneously to generate isobutylene, achieving higher conversion rates of TBA and MTBE, and higher selectivity for generating isobutylene.

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 NiAl nano-particle supported on the carrier.

A method of making silica-layered double hydroxide microspheres having the formula I: (i) wherein, M.sup.z+ and M.sup.y+ are two different charged metal cations; z=1 or 2; y=3 or 4; 0<x<0.9; b is 0 to 10; c is 0 to 10; P>0, q>0, X.sup.n is an anion; with n>0 a=z(1x)+xy2; and the AMO-solvent is an 100% aqueous miscible organic solvent; comprises the steps: (a) contacting silica microspheres and a metal ion containing solution containing metal ions M.sup.z+ and M.sup.y+ in the presence of a base and an anion solution; (b) collecting the product; and (c) optionally treating the product with AMO-solvent and recovering the solvent treated material to obtain the silica-layered double hydroxide microspheres. Preferably, M in the formula I is Li, Mg, Ni or Ca. Preferably, M in formula I is Al. The invention further provides silica-layered double hydroxide microspheres having the formula I. The silica-layered double hydroxide microspheres may be used as catalysts and/or catalyst supports.
(SiO.sub.2).sub.p@{[M.sup.z+.sub.(1-x)M.sup.y+.sub.x(OH).sub.2].sup.a+(X.sup.n).sub.a/n.bH.sub.2O.c(AMO-solvent)}.sub.q(I)

A composite photocatalyst is provided. The composite photocatalyst includes a nanomotor and a plurality of cocatalysts, the nanomotor comprises a shell formed by porous material, at least one inner core formed by a photocatalyst, and a cavity between the shell and the at least one inner core, the plurality of cocatalysts are located in the cavity. The plurality of cocatalysts are selected from the group consisting of metal nanoparticles, metal oxide nanoparticles, metal sulfide nanoparticles, phosphate nanoparticles, up-conversion material nanoparticles, and any combination thereof. A method for making the composite photocatalyst and application thereof are further provided. The plurality of cocatalysts and the nanomotor forms a photocatalytic synergistic reaction system, improving photo-catalytic activity of the composite photocatalyst.

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.