Amoco Corporation

Frederick T Clark

Simon G Kukes

Albert L Hensley, Jr

P Donald Hopkins

David Lyzinski

Lisa M Green

George A Huff

Muin S Haddad

James L Taylor

Lawrence B Peck

Mary C Springman

David C Arters

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A method is disclosed for optimizing the pressure drop in the catalytic conversion of a feed in a bed of catalyst particles in a vertically arranged reactor by grading the catalyst particles within the bed by pressure drop.

Method for grading cylindrical catalyst particles in a bed to reduce

A process and catalyst are provided for the hydrogenation of a hydrocarbon feedstock consisting essentially of hydrocarbon boiling between about 150.degree. F. and 700.degree. F. at atmospheric pressure. The process comprises reacting the feedstock with hydrogen at hydrogenation conditions in the presence of a catalyst comprising hydrogenation metals and a support comprising beta zeolite. The hydrogenation metals comprise from about 0.1 percent by weight to about 2.0 percent by weight each of palladium and platinum measured as a percentage of the catalyst. The beta zeolite comprises from about 1 ppm by weight to about 3.0 percent by weight sodium calculated as a percentage of said beta zeolite.

Distillate hydrogenation catalyst

A process and catalyst is provided for the hydrogenation of a hydrocarbon feedstock comprising a substantial portion of a distillate hydrocarbon feedstock, wherein said distillate hydrocarbon feedstock consists essentially of material boiling between about 150.degree. F. and about 700.degree. F. at atmospheric pressure, which comprises reacting the feedstock with hydrogen at hydrogenation conditions in the presence of a catalyst comprising from about 0.1% to about 2.0% by weight of palladium and from about 0.1% to about 2.0% by weight of platinum and a support comprising borosilicate, for producing a hydrogenated product.

Distillate hydrogenation

Distillate hydrogenation utilizing a catalyst comprising platinum,

A process and catalyst are provided for hydrogenation of a hydrocarbon feedstock consisting essentially of material boiling between about 150.degree. F. and about 700.degree. F. which comprises reacting the feedstock with hydrogen at hydrogenation conditions in the presence of a catalyst comprising hydrogenation metals and a support comprising zeolite Y. The hydrogenation metals comprise from about 0.1 percent to about 2.0 percent by weight each of palladium and platinum calculated as a percentage of the catalyst. The zeolite Y further comprises sodium in an amount ranging from about 1.5 to about 8.0 percent of the zeolite Y by weight. The process of the present invention provides substantially improved dearomatization performance, increased desulfurization and denitrogenation, increased distillate product cetane number, and increased distillate volume expansion.

A method is provided for regenerating a molecular sieve-free resid hydroprocessing catalyst for use with an ebullated bed reaction process comprising at least one hydrogenation metal and at least one Group IIA metal deposited on an inorganic oxide support wherein the catalyst contains a pore volume of pores having a diameter greater than 1200 Angstroms of at least 0.05 cc/gm. The method comprises the steps of contacting the molecular sieve-free resid hydroprocessing catalyst with a contaminant metal-containing hydrocarbon feedstream in a first contacting step at conditions sufficient to deposit contaminant metals and coke onto the catalyst; and contacting the coke-deactivated, contaminant metal-containing, molecular sieve-free catalyst with an oxygen-containing gas in a second contacting step at oxidation conditions sufficient to remove a substantial amount of the coke from the coke-deactivated, contaminant metal-containing, molecular sieve-free catalyst. The loss on attrition of the regenerated molecular sieve-free resid hydroprocessing catalyst after the second contacting step is less than 10 weight percent fines per day calculated based on a regeneration temperature of about 900.degree. F.

Process for regenerating a spent resid hydroprocessing catalyst using a

A method for reducing the pour point of a hydrocarbon feedstock that contains aromatic compounds, sulfur-containing compounds and nitrogen-containing compounds is provided. The method involves solvent extraction and utilizes a catalytic hydrodewaxing zone with a first section having a shape-selective molecular sieve-containing catalyst composition which is substantially free of Group VIII metals and a second section having a Group VIII metal-containing hydrogenation catalyst composition with a porous support material substantially free of acidic crystalline molecular sieve material.

Manufacture of lubricating oils

A method of regenerating a contaminant metal-containing, coke deactivated, molecular sieve-free catalyst having at least one hydrogenation metal and at least one Group IV metal deposited on an inorganic oxide support comprising contacting the catalyst with an oxygen-containing gas under conditions sufficient to remove a substantial amount of the coke from the catalyst.

Process for regenerating a spent resin hydroprocessing catalyst using a

A process and catalyst are provided for hydrogenation of a hydrocarbon feedstock consisting essentially of material boiling between about 150.degree. F. and about 700.degree. F. which comprises reacting the feedstock with hydrogen at hydrogenation conditions in the presence of a catalyst comprising from about 0.1% to about 2.0% by weight each of palladium and platinum and a support comprising mordenite. The process of the present invention provides substantially improved dearomatization performance, increased desulfurization and denitrogenation, increased distillate product cetane number, increased distillate volume expansion, and utilizes a more durable catalyst.

A hydroprocessing catalyst and process of using such catalyst wherein such catalyst has at least one hydrogenation metal deposited on an inorganic oxide support and is further characterized by a surface area of greater than about 220 m.sup.2 /g, a pore volume of about 0.23-0.30 cc/g in pores greater than about 600 Angstroms radius, an average pore radius of about 30-70 Angstroms in pores less than 600 Angstroms, and an incremental pore volume curve with a maximum at about 25-50 Angstroms radius.

Hydroprocessing catalyst

The present invention relates to a hydroprocessing process that employs a catalyst that has been regenerated by subjecting the catalyst to an initial partial decoking step, followed by impregnation with a Group IIA metal-containing component and then subjected to a final decoking step.

Hydroprocessing using regenerated spent heavy hydrocarbon catalyst

A process and catalyust are provided for hydrogenation of a hydrocarbon feedstock consisting essentially of material boiling between about 150.degree. F. and about 700.degree. F. which comprises reacting the feedstock with hydrogen at hydrogenation conditions in the presence of a catalyst comprising from about 0.1% to about 2.0% by weight each of palladium and platinum and a support comprising mordenite. The process of the present invention provides substantially improved dearomatization performance, increased desulfurization and denitrogenation, increased distillate product cetane number, increased distllate volume expansion, and utilizes a more durable catalyst.

A process and catalyst are provided for hydrogenation of a hydrocarbon feedstock consisting essentially of material boiling between about 150.degree. F. and about 700.degree. F. which comprises reacting the feedstock with hydrogen at hydrogenation conditions in the presence of a catalyst comprising hydrogenation metals and a support comprising zeolite Y. The hydrogenation metals comprise from about 0.1 percent to about 2.0 percent by weight each of palladium and platinum calculated as a percnetage of the catalyst. The zeolite Y further comprises sodium in an amount ranging from about 1.5 to about 8.0 percent of the zeolite Y by weight. The process of the present invention provides substantially improved dearomatization performance, increased desulfurization and denitrogenation, increased distillate product cetane number, and increased distillate volume expansion.

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Wheaton, IL, United States of America

Frederick T Clark