Abstract: A hydroprocessing catalyst with improved performance has been produced that involves an intimately mixed unsupported metal oxide with a zeolite or other acid function. The intimate mixing allows an intimate interaction between the unsupported metal oxide and the acid function. The hydroprocessing catalyst may be used alone or may be incorporated with a portion of a conventional hydrocracking catalyst.

Abstract: A hydroprocessing catalyst with improved performance has been produced that involves an intimately mixed unsupported metal oxide with a zeolite or other acid function. The intimate mixing allows an intimate interaction between the unsupported metal oxide and the acid function. The hydroprocessing catalyst may be used alone or may be incorporated with a portion of a conventional hydrocracking catalyst.

Abstract: An extruded C8 alkylaromatic isomerization catalyst is described. The catalyst has an average pore diameter in a range of about 110 ? to about 155 ? measured by BJH adsorption method and a pore volume less than about 0.62 cc/g measured by N2 porosimetry. A process for isomerizing a non-equilibrium C8 aromatic feed to provide an isomerized product is also described.

Abstract: An extruded C8 alkylaromatic isomerization catalyst is described. The catalyst has an average pore diameter in a range of about 110 ? to about 155 ? measured by BJH adsorption method and a pore volume less than about 0.62 cc/g measured by N2 porosimetry. A process for isomerizing a non-equilibrium C8 aromatic feed to provide an isomerized product is also described.

Abstract: Catalysts comprise a combination of molecular sieve having a pore diameter of from about 4 to 8 angstroms and a catalytically-effective amount of molybdenum hydrogenation component and a sufficient amount of at least one platinum group metal hydrogenation component to enhance the isomerization activity of the catalyst.

Abstract: Catalysts comprising a combination of molecular sieve having a pore diameter of from about 4 to 8 angstroms and a catalytically-effective amount of molybdenum hydrogenation component in an amorphous aluminum phosphate binder provide processes for isomerizing xylene and dealkylating ethylbenzene in feed streams that exhibit stability, selectivity and low ring loss.

Abstract: Catalysts comprising a combination of molecular sieve having a pore diameter of from about 4 to 8 angstroms and a catalytically-effective amount of molybdenum hydrogenation component in an amorphous aluminum phosphate binder provide processes for isomerizing xylene and dealkylating ethylbenzene in feed streams that exhibit stability, selectivity and low ring loss.

Abstract: A process for preparing a transalkylation catalyst, the catalyst itself, and a transalkylation process for using the catalyst are herein disclosed. The catalyst comprises rhenium metal on a solid-acid support such as mordenite, which has been treated with a sulfur-based agent. Such treatment reduces the amount of methane produced by metal hydrogenolysis in a transalkylation process wherein heavy aromatics like A9+ are reacted with toluene to produce xylenes. Reduced methane production relative to total light ends gas production results in lower hydrogen consumption and lower reactor exotherms.

Abstract: Reduced co-production of toluene and C9 and higher aromatics such as trimethylbenzene, methylethylbenzene, and diethylbenzene is achieved in processes for the isomerization of xylenes to close to equilibrium using a layered catalyst having a thin outer layer of molecular sieve and hydrogenation metal component on a core, wherein at least about 75 mass-% of the hydrogenation metal component is in the outer layer.

Abstract: Catalysts of certain combinations of platinum, tin, acidic molecular sieve and aluminum phosphate binder achieve the isomerization and dealkylation activities characteristic of platinum-containing catalysts yet enjoy the low net C6 naphthenes make properties.

Abstract: Catalysts of certain combinations of platinum, tin, acidic molecular sieve and aluminum phosphate binder achieve the isomerization and dealkylation activities characteristic of platinum-containing catalysts yet enjoy the low net C6 naphthenes make properties.

Abstract: Catalysts of certain combinations of platinum, tin, acidic molecular sieve and aluminum phosphate binder achieve the isomerization and dealkylation activities characteristic of platinum-containing catalysts yet enjoy the low net C6 naphthenes make properties.

Abstract: Hydrocarbon conversion processes using a new family of zeolites identified as UZM-8HS are described. The UZM-8HS zeolite are derived from UZM-8 zeolites by treating the UZM-8 with a fluoro-silicate salt, an acid, etc. The UZM-8HS zeolites have unique x-ray diffraction patterns. These zeolites can be used in alkylation of aromatics, transalkylation of aromatics, isomerization of aromatics and alkylation of isoparaffins.

Abstract: A process for isomerizing ethylbenzene into xylenes such as para-xylene using a zeolitic catalyst system based on low Si/Al2 MTW-type zeolite that preferably is substantially free of mordenite. The catalyst may be bimetallic where the two metals are platinum and tin.

Abstract: A process for preparing a transalkylation catalyst, the catalyst itself, and a transalkylation process for using the catalyst are herein disclosed. The catalyst comprises rhenium metal on a solid-acid support such as mordenite, which has been treated with a sulfur-based agent. Such treatment reduces the amount of methane produced by metal hydrogenolysis in a transalkylation process wherein heavy aromatics like A9+ are reacted with toluene to produce xylenes. Reduced methane production relative to total light ends gas production results in lower hydrogen consumption and lower reactor exotherms.

Abstract: The use of transalkylation catalysts to react heavy aromatic compounds of carbon number nine (and heavier carbon numbers) with benzene to form carbon number eight aromatics is disclosed. The catalyst system preserves ethyl-group species on the heavier aromatics that are otherwise de-ethylated over most gas-phase transalkylation catalysts to form undesired ethane gas with benzene or toluene. The catalyst system also promotes methyl-group species transalkylation at selected conditions. Thus, by using the transalkylation system, a greater yield of para-xylene or other carbon number eight aromatics may be achieved overall within an integrated aromatics complex.

Abstract: A process for isomerizing ethylbenzene into paraxylene using a zeolitic catalyst system based on MTW-type zeolite that is substantially free of mordenite. The invention obtains an improved yield of paraxylene without excess benzene production by dealkylation. The zeolitic silica-to-alumina ratio ranges from 20 to 45. Elimination of mordenite in the catalyst improves yields and integrated aromatics complex economics by reducing undesirable aromatic ring-loss reactions as well.

Abstract: A process for isomerizing ethylbenzene into xylenes such as para-xylene using a bimetallic zeolitic catalyst system based on MTW-type zeolite is disclosed. Preferably the two metals are platinum and tin. The invention obtains a stable and improved yield of xylenes such as para-xylene without excess benzene production by dealkylation. The zeolitic silica-to-alumina ratio ranges from 20 to 45. Use of MTW substantially free of mordenite improves yields and integrated aromatics complex economics by reducing undesirable aromatic ring-loss reactions.