Abstract:
A supported cobalt-based catalyst is described, characterized in that the carrier has an average particle diameter, measured by means of Coulter LS230, ranging from 70 to 250 nullm, a surface area higher than 175 m2/g and a pore volume higher than 0.35 cm3/g, measured with the B.E.T. method. The above catalyst is particularly useful in the Fischer-Tropsch reaction.
Abstract:
A completely metallic catalyst for the oxidation of mixtures in the gaseous phase which contain carbon monoxide, hydrocarbons and/or soot, has a surface doped with a metallic element and is subjected to a second thermal treatment in an oxygen-containing atmosphere.
Abstract:
A catalytic converter including a carrier, a hydrocarbon (HC) trap layer disposed on the carrier and at least two catalyst layers comprising an inner layer disposed on the HC trap layer and an outer layer disposed on the inner layer. The inner and outer layers include catalyst noble metals, respectively. The catalyst noble metal present in the outer layer is controlled to be active earlier than the catalyst noble metal present in the inner layer during the engine warm-up operation.
Abstract:
Disclosed is an electrocatalyst for fuel cells, in which a porous carbon material including pores having a diameter smaller than a kinetic diameter of carbon monoxide is used as a support body and contact probability between an activated metal and carbon monoxide is decreased, thereby preventing fuel cell performance from being degraded by carbon monoxide. The electrocatalyst is obtained by adsorbing 10-80 parts by weight of an activated metal to 20-90 parts by weight of a porous support body, characterized in that the porous support body has a total surface area of 200-2,500 m2/g including an outer surface thereof and an inner surface of pores thereof, and has a plurality of pores penetrating into an interior of the support body with an average diameter of 2-15 nm and a total volume of 0.4-2.0 m3/g, and the activated metal is alloyed with 20-95 at % of platinum and 5-80 at % of one metal selected from among Ru, Sn, Os, Rh, Ir, Pd, V, Cr, Co, Ni, Fe and Mn. As for such an electrocatalyst, carbon monoxide does not fundamentally come in contact with the activated metal adsorbed to the inner surface of the pores of the support body, thereby minimizing degradation of fuel cell performance, thus overcoming fuel-feeding problems.
Abstract:
The present invention pertains to a catalyst comprising 7-20 wt. % of a Group VIB metal component, calculated as trioxide on the weight of the catalyst, and 0.5 to 6 wt. % of a Group VIII metal component, calculated as oxide on the weight of the catalyst, on a porous inorganic carrier. The catalyst has a specific surface area of 100-180 m2/g, a total pore volume of at least 0.55 ml/g, at least 50% of the total pore volume in pores with a diameter of at least 20 nm (200 null), 10-30% of the total pore volume in pores with a diameter of at least 200 nm (2000 null), and 0-1% of the total pore volume in pores with a diameter above 1000 nm (10000 null). The catalyst is particularly suitable for the hydroprocessing of heavy hydrocarbon feeds of which at least 50 wt. % boils above 538null C. (1000null F.). It is especially advantageous for the hydroprocessing of feedstocks of which at least 80 wt. % boils above 538null C. (1000null F.).
Abstract:
Multimetal oxide materials which contain Mo and V and, if required, one or more of the elements from the group consisting of lanthanides, transition elements of the Periodic Table of the Elements and elements of the third to sixth main group of the Periodic Table of the Elements and which are prepared in the presence of an alkali metal other than Li and have the i-phase structure are used as active material in catalysts for partial gas-phase oxidations.
Abstract:
The invention relates to a catalyst for the selective hydrodesulfurization of hydrocarbon-containing feedstocks that comprise sulfur-containing compounds and olefins. This catalyst comes in a sulfurized form and comprises a substrate that is selected from among the refractory oxides, at least one metal that is selected from the group that consists of the metals of groups VI and VII of the periodic table and carbon, whereby the carbon content is less than or equal to 2.8% by weight. The invention also relates to a method for the production of the catalyst that is described above, as well as a process that uses this catalyst for the selective hydrodesulfurization of hydrocarbon-containing feedstocks that contain sulfur-containing compounds and olefins.
Abstract:
A catalyst comprising nickel on a TiO2 support is obtainable by coprecipitation of nickel and at least one further metal selected from among Si, Zr, Hf, alkaline earth metals, Y, La and Ce, and optionally at least one dopant metal selected from groups 5 to 11 of the Periodic Table of the Elements, from a solution in which the corresponding metal salts are present onto a particulate TiO2 support, subsequent drying, calcination and reduction and optionally passivation to give the nickel-containing catalyst. It is used, in particular, for the hydrogenation of nitroaromatic compounds.
Abstract:
A process useful for the catalytic gas phase oxidation of alkanes to unsaturated aldehydes or carboxylic acids uses catalysts of particular compositions formed in a particular manner.
Abstract:
In producing a catalyst used for synthesis of an unsaturated aldehyde and an unsaturated carboxylic acid by a gas-phase catalytic oxidation, there is used a step of packing an additive-containing catalyst precursor of the catalyst into a tubular reactor, passing a gas through the tubular reactor, and elevating, in this state, the temperature of the additive-containing catalyst precursor so that a temperature of the gas at an outlet of the catalyst precursor layer becomes higher than a temperature of the gas at an inlet of the catalyst precursor layer. The step makes possible easy and highly reproducible production of a high-performance catalyst which is small in the reduction in catalytic performance caused by, for example, the thermal decomposition of the additive contained in the catalyst precursor.