Mobil Oil Corporation

Roland H Heck

Scott S Han

Frank T DiGuiseppi

Stuart S Shih

Jose G Santiesteban

Edward J Rosinski

Robert C Wilson, Jr

Jeffrey S Beck

Werner O Haag

David S Shihabi

Stephen M Oleck

Lillian A Rankel

Paul B Venuto

Gerald J Teitman

P Thomas Reischman

D Duayne Whitehurst

Heinz Heinemann

Salvatore T Viscontini

Stephen M Cleck

Tom Reischman

Michael E Ehlers

A process for the production of diesel fuel with a high cetane number at a low cloud point, which involves hydrocracking highly aromatic fractions obtained from catalytic cracking operations. The fraction of hydrocracker effluent which boils between about 400.degree. F. (205.degree. C.) and 1000.degree. F. (538.degree. C.) is subsequently catalytically dewaxed in order to obtain a cloud point of no more than 41.degree. F. (5.degree. C.). The hydrocracker effluent fraction is preferably recycled to the hydrocracking step prior to dewaxing.

Production of high cetane diesel fuel by employing hydrocracking and

The present invention relates to a process for the oligomerization of ethene to a product rich in isobutylene comprising contacting a feedstock comprising ethene under oligomerization conditions with a catalyst composition comprising a porous crystalline silicate having the structure of ZSM-35 zeolite whose surface has been at least partially deactivated for acid catalyzed reactions by a) coking or b) chemisorption of a surface-deactivating agent, e.g., collidine, which possesses an average cross section diameter greater than that of the zeolite pores.

Process for selectively converting ethene to isobutylene over

Aqueous sulfur and caustic component-containing waste streams are disposed of in an environmentally acceptable manner employing a process featuring integrated coking and gasification operations.

Process for the disposal of aqueous sulfur and caustic-containing wastes

The present invention relates to a catalyst and its use in a process for the conversion of ethene to a product rich in linear butenes, especially 2-butene, comprising contacting a feedstock comprising ethene under dimerization conditions with a catalyst composition comprising a porous crystalline silicate having the structure of ZSM-35 which has been treated by a) fluoriding, e.g., with NH.sub.4 F, and then b) at least partially surface deactivated for acid catalyzed reactions by chemisorption of a surface-deactivating agent which possesses an average cross section diameter greater than that of the zeolite pores, e.g., collidine.

Selectivated ZSM-035 catalyst and process for selectively converting

Heavy oil is hydrotreated by processing with hydrogen in the presence of a catalyst composition comprising an activated carbon component having a specified range of pore volume distribution and average pore diameter, a molybdenum or tungsten component and a cobalt or nickel component to reduce the content of nickel and vanadium therein and to achieve demetallation and conversion of the carbon residue for producing a lighter oil.

Process for treating heavy oil

Heavy oils are advantageously preconditioned by heat soaking prior to hydrotreating with a dispersed metal catalyst to reduce coking in a two stage hydrotreating process. The effluent of a hydrotreating process is filtered to recover catalytically active coke which is recovered by backflushing and recycled to the feed stream. A mild solvent deasphalting step isolates metals in a reduced volume asphaltene fraction.

Resid hydrocracking using dispersed metal catalysts

Light olefins are converted to heavier hydrocarbon products, e.g., those boiling in the gasoline, distillate, and/or lube range, under oligomerization reaction conditions in the presence of catalyst comprising zeolite MCM-49.

Process for converting olefins to higher hydrocarbons

A refinery derived spent caustic is recycled by introducing the spent caustic to a delayed coking drum while conducting delayed coking of a hydrocarbon feedstock. The alkali metal containing material accelerates coking, induces production of shot coke, alleviates the problem of a hot drum and reduces drum cooling time.

Delayed coking with refinery caustic

A surface-inactivated catalyst composition comprising acidic porous crystalline material, e.g., ZSM-23, having active internal Bronsted acid sites and containing surface-inactivating material having a boron to nitrogen bond is prepared by contacting the surface with aqueous ammonia borane solution. The catalyst may be used for organic compound conversion, e.g., oligomerization of lower olefins to produce distillate boiling range materials having reduced methyl branching and increased cetane number.

Surface modified porous acidic crystalline catalyst

A method is disclosed for the double bond isomerization of alpha olefin-containing feeds, e.g., conversion of 1-butene-containing hydrocarbon streams to 2-butene-rich product streams, wherein oligomer by-products are minimized. The process uses a catalyst composition comprising a zeolite whose surface has been at least partially deactivated for acid catalyzed reactions by chemisorption of a surface-deactivating agent, e.g., collidine, which possesses an average cross section diameter greater than that of the zeolite pores.

Double bond isomerization of olefin-containing feeds with minimal

A surface-inactivated catalyst composition comprising acidic porous crystalline material, e.g., ZSM-23, having active internal Bronsted acid sites and containing coke-inactivated external acid sites is prepared by contacting the catalyst under high pressure coking conditions, e.g. 800 psig. The catalyst may be used for organic compound conversion, e.g., oligomerization of lower olefins to produce distillate boiling range materials having reduced methyl branching and increased cetane number.

Coke-selectivated porous acidic crystalline catalyst, its preparation,

An improved hydrotreating catalyst, and a process for using thereof, comprises a conventional Group VIA and Group VIIIA metal oxide or metal sulfide, deposited on an inorganic refractory support and about 0.1% by weight to about 7% by weight of the catalyst of a promoter comprising a halogenated metal selected from the Group consisting of halogenated metals of Group IB, IIB, IIIB, titanium and tin. The presence of the promoter results in greater degree of desulfurization and in CCR reduction of hydrocarbon feedstocks, especially highly aromatic petroleum residue and synthetically-derived hydrocarbons, e.g., coal liquids.

Hydrotreating hydrocarbon feedstocks

An improved hydrotreating catalyst, and a process for using thereof, comprises a conventional Group VIA and Group VIIIA metal metal oxide or metal sulfide, deposited on an inorganic refractory support and about 0.1% by weight to about 7% by weight of the catalyst of a promoter comprising a halogenated metal selected from the Group consisting of halogenated metals of Group IB, IIB, IIIB, titanium and tin. The presence of the promoter results in greater degree of desulfurization and in CCR reduction of hydrocarbon feedstocks, especially highly aromatic petroleum residua and synthetically-derived hydrocarbons, e.g., coal liquids.

Desulfurization, denitrogenation, deoxygenation and CCR reduction of highly aromatic petroleum and coal derived liquids are conducted with hydrogen and with a refractory base catalyst incorporating at least one Group VIA metal and at least one Group VIII metal. The catalyst has a surface area of between about 100 and 300 m.sup.2 /g and a total pore volume of between about 0.3 and 1.0 cc/g and is further characterized as follows:

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Pennington, NJ, United States of America

Roland H Heck