Disclosed is a composition useful in the hydrolysis of sulfur compounds that are contained in a gas stream. The composition comprises a calcined co-mulled mixture of psuedoboehmite, a cobalt compound, and a molybdenum compound such that the composition comprises gamma-alumina, at least 7.5 wt. % molybdenum, and at least 2.75 wt. % cobalt. The composition is made by forming into an agglomerate a co-mulled mixture pseudoboehmite, a cobalt component, and a molybdenum component followed by drying and calcining the agglomerate to provide a catalyst composition comprising gamma-alumina, at least 7.5 wt. % molybdenum, and at least 2.75 wt. % cobalt.

An object of the present invention is to provide an exhaust gas purification catalyst which can exhibit high durability and warm-up performance. The present invention relates to an exhaust gas purification catalyst comprising a substrate and a catalyst coating layer formed on the substrate, wherein the catalyst coating layer comprises catalyst particles, the catalyst coating layer having an upstream region extending by 40 to 60% of the entire length of the substrate from an upstream end of the catalyst in the direction of an exhaust gas flow and a downstream region corresponding to the remainder portion of the catalyst coating layer, the composition of the catalyst particle of the upstream region being different from that of the downstream region. The upstream region in the direction of an exhaust gas flow has a structure where a void is included in a large number, and furthermore high-aspect-ratio pores having an aspect ratio of 5 or more account for a certain percentage or more of the whole volume of voids. Thus, the exhaust gas purification catalyst exhibits enhanced purification performance.

A method of reducing nitrogen oxides in exhaust gas of an internal combustion engine by selective catalytic reduction (SCR) comprises contacting the exhaust gas also containing ammonia and oxygen with a catalytic converter comprising a catalyst (2) comprising at least one crystalline small-pore molecular sieve catalytically active component (Z.sub.M,I) having a maximum ring opening of eight tetrahedral basic building blocks, which crystalline small-pore molecular sieve catalytically active component (Z.sub.M,I) comprising mesopores.

Embodiments of processes for producing propylene utilize a dual catalyst system comprising a mesoporous silica catalyst impregnated with metal oxide and a mordenite framework inverted (MFI) structured silica catalyst downstream of the mesoporous silica catalyst, where the mesoporous silica catalyst includes a pore size distribution of at least 2.5 nm to 40 nm and a total pore volume of at least 0.600 cm.sup.3/g, and the MFI structured silica catalyst has a total acidity of 0.001 mmol/g to 0.1 mmol/g. The propylene is produced from the butene stream via metathesis by contacting the mesoporous silica catalyst and subsequent cracking by contacting the MFI structured silica catalyst.

Provided is a NaY molecular sieve and a method for preparing the NaY molecular sieve, an HY molecular sieve and a method for preparing the HY molecular sieve, a hydrocracking catalyst, and a hydrocracking method. The average grain diameter of the NaY molecular sieve is 2-5 m, and the sum of pore volumes of pores in 1-10 nm diameter accounts for 70-90% of the total pore volume of the NaY molecular sieve. The HY molecular sieve obtained from the large-grain NaY molecular sieve can be used as an acidic component in the hydrocracking catalyst. When the hydrocracking catalyst containing the HY molecular sieve is applied in the hydrocracking reaction of heavy oils that contain macromolecules, it can provide better cracking activity and product selectivity in the hydrocracking reaction.

The present invention provides a catalyst carrier with shift and adsorption purification performance, comprising modified bauxite in the raw material components which fluxing and pore forming effects. Most iron oxide contained in the bauxite is removed after modification, so that there are a large amount of highly active aluminosilicate compounds in the modified bauxite. When preparing the catalyst, the aluminosilicate compound serves as a low melting point flux and can significantly increase the migration rate of magnesium and aluminum ions during the calcinating process and promote the generation of MgAl.sub.2O.sub.4 at low temperatures, thereby the catalyst carrier of the present invention has strong anti-hydration capacity and mechanical strength. In addition, when the modified bauxite is used as macroporous hard template for the preparation of the catalyst, macro pores can be formed in the structure of the catalyst carrier after calcinating treatment, so that the catalyst carrier of the present invention has strong adsorption purification ability on macromolecular particles including oil pollution and dust.

The invention relates to an improved catalyst based on a tableted molded catalyst body, containing a metal-containing mixture, containing copper, zinc, and aluminum, with calcium aluminate as a binder material with a weight fraction of calcium aluminate in the range of 1.0% to 30.0%, for synthesizing methanol from synthesis gas. The invention further relates to the production of the catalyst and to the use of the catalyst in the synthesis of methanol from synthesis gas.

The invention relates to an oxygen carrier solid, its preparation and its use in a method of combustion of a hydrocarbon feedstock by active mass chemical-looping oxidation-reduction, i.e. chemical-looping combustion (CLC). The solid, which is in the form of particles, comprises an oxidation-reduction active mass composed of metal oxide(s) dispersed in a ceramic matrix comprising at least one oxide with a melting point higher than 1500 C., such as alumina, and has, initially, a specific macroporous texture. The oxygen carrier solid is prepared from an aqueous suspension containing precursor oxide grains for the ceramic matrix that have a specific size, by a spray-drying technique.

A porous body is provided with enhanced fluid transport properties that is capable of performing or facilitating separations, or performing reactions and/or providing areas for such separations or reactions to take place. The porous body includes at least 80 percent alpha alumina and has a pore volume from 0.3 mL/g to 1.2 mL/g and a surface area from 0.3 m.sup.2/g to 3.0 m.sup.2/g. The porous body further includes a pore architecture that provides at least one of a tortuosity of 7.0 or less, a constriction of 4.0 or less and a permeability of 30 mdarcys or greater. The porous body can be used in a wide variety of applications such as, for example, as a filter, as a membrane or as a catalyst carrier.

A porous material comprises at least 60 wt % of a calcium-deficient hydroxyapatite having a Ca/P molar ratio of less than 1.67, having a specific BET surface area of at least 110 m.sup.2/g and a pore volume of at least 0.41 cm.sup.3/g, both measured after heat treatment at 120 C. A catalyst composition for catalytic reduction of NO.sub.x compounds, comprising an active catalyst component: Cu and/or CuO deposited on the porous material as support. A deNOx process according to which an ammonia source is injected into a combustion waste gas stream containing NOx; and to which the catalyst composition is brought into contact with the waste gas stream at a temperature of at least 100 C. and preferably at most 600 C. to carry out, in the presence of O.sub.2, a reduction by NH.sub.3 of at least a portion of the NOx.