Disclosed is a method of preparing an intermetallic catalyst that includes irradiating ultrasonic waves to a precursor admixture including a noble metal precursor, a transition metal precursor, and a carrier to form core-shell particles including a transition metal oxide coating layer; the annealing the core-shell particles to form intermetallic particles including a transition metal oxide coating layer; and the removing the transition metal oxide coating layer from the intermetallic particles.

Provided is a preparation method of a coating material. The method includes: using an aluminum salt and a silicon source as precursors; and performing hydrothermal crystallization and calcination treatments successively under an action of a template agent to obtain the coating material, wherein the template agent is used to cause the coating material to form a porous spherical structure. In the embodiments of the present disclosure, the preparation process of the coating material is simple and the cost is low, and the specific surface area of the prepared coating material is large.

A catalyst of the present invention contains a first transition metal oxide (A1) represented by the general formula M.sup.1O.sub.x, wherein M.sup.1 represents a transition metal element, and x represents a positive real number, and a metal compound (B1) capable of adsorbing carbon dioxide. The first transition metal oxide (A1) is supported on the metal compound (B1), and the first transition metal oxide (A1) can produce a compound represented by the general formula M.sup.1O.sub.x-n by reduction, wherein M.sup.1 and x are as defined above, and n represents a positive real number equal to or less than x.

The present disclosure relates to the technical field of Fischer-Tropsch synthesis reaction catalysts, and discloses a supported ε/ε′ iron carbide catalyst for Fischer-Tropsch synthesis reaction, preparation method thereof and Fischer-Tropsch synthesis process, wherein the method comprises the following steps: (1) dipping a catalyst carrier in a ferric salt aqueous solution, drying and roasting the dipped carrier to obtain a catalyst precursor; (2) subjecting the catalyst precursor and H.sub.2 to a precursor reduction at the temperature of 300-550° C.; (3) pretreating the material obtained in the step (2) with H.sub.2 and CO at the temperature of 90-185° C., wherein the molar ratio of H.sub.2/CO is 1.2-2.8:1; (4) preparing carbide with the material obtained in the step (3), H.sub.2 and CO at the temperature of 200-300° C., wherein the molar ratio of H.sub.2/CO is 1.0-3.2:1. The preparation method has the advantages of simple and easily obtained raw materials, simple and convenient operation steps, being capable of preparing the catalyst with 100% pure phase ε/ε′ iron carbide as the active phase, the catalyst has lower selectivity of CO.sub.2 and CH.sub.4 and higher selectivity of effective products.

A catalyst composition and its use as a dehydrogenation catalyst to increase normal olefin selectivity and reduce undesirable aromatic selectivity. The reduction in aromatic production allows for the elimination of a unit to remove aromatic compounds. The catalyst has a layered composition comprising an inner core, an outer layer bonded to the inner core, the outer layer comprising one or more transition alumina with at least two diffraction angle peaks between 32.0 and 70.0 2, wherein a first diffraction angle peak in that range is at 32.70.4 2, a second diffraction angle peak is at 50.80.4 2, and having a thickness of less than about 100 microns and having uniformly dispersed thereon said platinum catalyst and at least one promoter metal and having a concentration of the platinum catalyst of from about 0.00006 to 0.0005 gram of the platinum group metal on an elemental basis per meter square surface area of the outer layer.

A method of synthesizing TiO.sub.2/Co.sub.3O.sub.4 core-shell photocatalysts is provided. The method includes preparing SiO.sub.2 hollow nanospheres via sol-gel synthesis in the presence of a triblock copolymer surfactant and a cationic surfactant; adding titanium sec-butoxide to a solution containing the SiO.sub.2 hollow nanospheres to provide a first combined sample; calcinating the first combined sample to provide hollow mesoporous TiO.sub.2 nanospheres; adding cobalt nitrate to a solution comprising the hollow mesoporous TiO.sub.2 nanospheres to provide a second combined sample; and calcinating the second combined sample to provide TiO.sub.2/Co.sub.3O.sub.4 core-shell photocatalysts. Methods of producing hydrogen by water-splitting using TiO.sub.2/Co.sub.3O.sub.4 core-shell photocatalysts are also provided. Such methods include photodepositing platinum onto the photocatalysts during the reaction.

A method of forming a fuel cell catalyst system, the method includes providing an anticorrosive, conductive catalyst support material having oxygen vacancies and a formula (I):

MgTi.sub.2O.sub.5-(I),

where .sub. is any number between 0 and 3 optionally including a fractional part denoting the oxygen vacancies, coating the catalyst support material with a polymeric film, attaching a catalyst material onto the polymeric film, removing the polymeric film, and providing additional material onto the support material to increase physical, electrical, and/or mechanical contact between the catalyst material and the catalyst support material.

The invention concerns particles which may include a catalytically active component, in the form of a three-dimensional ellipsoidal shape having three major axes at least two of which axes are of different lengths. Beds of such particles are useful for forming particle beds through which a fluid may flow.

The present invention relates to a method for producing automobile exhaust gas catalytic converters, to the catalytic converters as such and to the use thereof. In particular, the method comprises a step which results in a smaller particle size of the catalytically active material used.

An exhaust gas purification catalyst including particles of a catalyst metal supported on secondary particles of an inorganic oxide, wherein when scanning transmission electron microscope-energy dispersive X-ray line analysis is performed from a surface of the secondary particles toward a center thereof, a support density of the catalyst metal on a surface side of the secondary particles is greater than the support density of the catalyst metal in a center part of the secondary particles.