The present invention relates to a catalyst for producing chlorine by oxidation of hydrogen chloride and a method for preparing the same. The catalyst comprises a support and active ingredients that comprise 1-20 wt % of copper, 0.01-5 wt % of boron, 0.1-10 wt % of alkali metal element(s), 0.1-15 wt % of one or more rare earth elements, and 0-10 wt % of one or more elements selected from magnesium, calcium, barium, manganese, iron, nickel, cobalt, zinc, ruthenium or titanium based on the total weight of the catalyst. The catalyst is prepared by a two-step impregnation method. Comparing with the available catalysts of the same type, the catalyst according to the present invention has greatly improved conversion and stability.

In accordance with one or more embodiments of the present disclosure, a catalyst composition includes a catalyst support and at least one hydrogenative component disposed on the catalyst support. The catalyst support includes at least one USY zeolite having a framework substituted with titanium and zirconium. The framework-substituted USY zeolite comprises at least one rare earth element. Methods of making and using such a catalyst in a hydrocracking process are also disclosed.

Catalytic system which can be used in processes for the hydroconversion of heavy oils by means of hydrotreatment in slurry phase, characterized in that it comprises: a catalyst, having the function of hydrogenating agent, containing MoS.sub.2 or WS.sub.2 or mixtures thereof in lamellar form or an oil-soluble precursor thereof; a co-catalyst, having nanometric or micronic particle-sizes, selected from cracking and/or denitrogenation catalysts. The co-catalyst preferably consists of zeolites having small-sized crystals and with a low aggregation degree between the primary particles, and/or oxides or sulfides or precursors of sulfides of Ni and/or Co in a mixture with Mo and/or W.

A nanostructured porous catalyst for rubber vulcanization, the catalyst comprising a high surface area.

Disclosed are a phosphorus-containing high-silica molecular sieve, its preparation and application thereof, wherein the molecular sieve comprises about 86.5-99.8 wt % of silicon, about 0.1-13.5 wt % of aluminum and about 0.01-6 wt % of phosphorus, calculated as oxides and based on the dry weight of the molecular sieve, the molecular sieve has an XRD pattern with at least three diffraction peaks, the first strong peak is present at a diffraction angle of about 5.9-6.9°, the second strong peak is present at a diffraction angle of about 10.0-11.0°, and the third strong peak is present at a diffraction angle of about 15.6-16.7°. The phosphorus-containing high-silica molecular sieve shows an improved hydrocracking activity in the presence of nitrogen-containing species when used in the preparation of hydrocracking catalysts.

To be able to produce an SCR catalyst (2), in particular one having a zeolite fraction (Z) as catalytically active fraction, in a reliable process and at the same time achieve good catalytic activity of the catalyst (2), an inorganic binder fraction (B) which is catalytically inactive in the starting state and has been treated to develop catalytic activity is mixed into a catalyst composition (4). The inorganic binder component for the binder fraction (B) is, in the starting state, preferably porous particles (10), in particular diatomaceous earth, which display mesoporosity. To effect catalytic activation, the individual particles (10) are either coated with a catalytically active layer (12) or transformed into a catalytically active zeolite (14) with maintenance of the mesoporosity.

To be able to produce an SCR catalyst (2), in particular one having a zeolite fraction (Z) as catalytically active fraction, in a reliable process and at the same time achieve good catalytic activity of the catalyst (2), an inorganic binder fraction (B) which is catalytically inactive in the starting state and has been treated to develop catalytic activity is mixed into a catalyst composition (4). The inorganic binder component for the binder fraction (B) is, in the starting state, preferably porous particles (10), in particular diatomaceous earth, which display mesoporosity. To effect catalytic activation, the individual particles (10) are either coated with a catalytically active layer (12) or transformed into a catalytically active zeolite (14) with maintenance of the mesoporosity.

The present invention provides a novel process and system in which a mixture of carbon monoxide and hydrogen synthesis gas, or syngas, is converted into hydrocarbon mixtures composed of high quality gasoline components, aromatic compounds, and lower molecular weight gaseous olefins in one reactor or step. The invention utilizes a novel molybdenum-zeolite catalyst in high pressure hydrogen for conversion, as well as a novel rhenium-zeolite catalyst in place of the molybdenum-zeolite catalyst, and provides for use of the novel catalysts in the process and system of the invention.

Methods for processing paraffinic naphtha include contacting a paraffinic naphtha feedstock with a catalyst system in a dehydrogenation reactor. The catalyst system includes a framework-substituted ultra-stable Y (USY)-type zeolite to produce a dehydrogenated product stream. The catalyst system includes a framework-substituted ultra-stable Y (USY)-type zeolite. The framework-substituted USY-type zeolite has a modified USY framework. The modified USY framework includes a USY aluminosilicate framework modified by substituting a portion of framework aluminum atoms of the USY aluminosilicate framework with substitution atoms independently selected from the group consisting of titanium atoms, zirconium atoms, hafnium atoms, and combinations thereof. A dehydrogenation catalyst for dehydrogenating a paraffinic naphtha includes the framework-substituted ultra-stable Y (USY)-type zeolite.

The present invention relates to a hydrocarbon conversion catalyst, comprising: a first composition comprising a dehydrogenation active metal on a solid support, and a second composition comprising a transition metal and a doping agent, wherein the doping agent is selected from zinc, gallium, indium, lanthanum, and mixtures thereof, on an inorganic support.