Exxonmobil Chemical Patents Inc.

Exxon Chemical Patents, Inc.

Exxon Research and Engineering Company

Jose M Vargas

Kenneth L Riley

Raphael Frans Caers

Magdiel Agosto

Jihad Mohammed Dakka

Stephen Harold Brown

Christopher Lynn Becker

Tan-Jen Chen

Jason D Davis

John Stephen Godsmark

Kirk C Nadler

Jörg F W Weber

Seth McConkie Washburn

Stephen Wayne Beadle

Ashley J Malik

Georges Marie K Mathys

Jon Edmond Randoph Stanat

Paul E Eberly

Ramzi Yanni Saleh

Geoffrey R Say

Yuan-Ju Chen

Arie Van Vliet

Philippe Louis Buess

Thomas R Barbee

Duane A Goetsch

Eddy Theophyle Andrea Van Driessche

Ken L Riley

Disclosed are novel processes for making cyclohexanone compositions, from a mixture comprising phenol, cyclohexanone, and cyclohexylbenzene. The process includes hydrogenation of a feed stream comprising phenol, cyclohexanone, and cyclohexylbenzene. The feed stream may be subjected to one or more pre-hydrogenation treatments, such as passing through one or more sorbents, addition of basic chemical agents, and/or addition of water, so as to improve catalyst activity, minimize undesired side reactions, and/or remove catalyst poisons from the feed stream. The feed stream may be provided to a hydrogenation reaction zone in the vapor phase, with periodic alterations to hydrogenation reaction conditions such that the feed is provided in mixed liquid and vapor phase in order to carry out liquid washing of a hydrogenation catalyst bed within the hydrogenation reaction zone.

Process for making cyclohexanone

High strength presulfided catalyst for hydrogenating hydrocarbon resins without an in situ sulfiding step. The catalyst particles have a supported metal catalyst structure with presulfided interstitial surfaces with about 20 weight percent of a low molecular weight hydrocarbon resin, based on the weight of the porous supported metal catalyst structure, filling from 90 to 95 percent of the pore volume to improve a crush strength of the catalyst particles. The presulfided catalyst can be stored and/or shipped in an airtight container with an inert atmosphere. The catalyst particles are made by preparing the oxidized catalyst, presulfiding the catalyst, contacting the catalyst with the low molecular weight hydrocarbon resin in an inert atmosphere, sealing the catalyst in a storage/shipping container, loading the reactor with the presulfided, filled catalyst, and contacting the catalyst with an unsaturated hydrocarbon resin under hydrogenation conditions.

High strength presulfided catalyst for hydrogenating hydrocarbon resins

The invention relates to series reactor beds containing different oligomerization catalysts and having independent temperature control, and processes for the oligomerization of light olefins to heavier olefins using such series reactor beds.

Series catalyst beds

The use of a controlled amount of water in a hydrogenation stage of the oxo process for the production of alcohols which uses at least two reactors in series improves the efficiency of the hydrogenation reaction and catalyst life as does a reduction in the amount of sulphur, chlorine and hydroformylation catalyst residues in the feed to hydrogenation.

Hydrogenation

An improved process for preparing alcohols by the Oxo process. More particularly this invention relates to an improvement in the hydrogenation step of the Oxo process characterized in the use of certain bulk multimetallic hydrogenation catalysts comprised of at least one Group VIII non-noble metal and at least two Group VIB metals.

Process for preparing alcohols by the Oxo process

A process for forming acids from aldehydes which comprises reacting an oxo aldehyde with water in the presence of an acid-forming catalyst and in the absence of hydrogen, and at a pressure of about 0.1 to 6.99 MPa and a temperature of about 93.degree. to 205.degree. C., thereby converting aldehyde to an oxo acid.

Process for converting aldehydes to acids

The hydrogenation steps and hydrofinishing steps of the cobalt catalyst oxo process for preparation of the alcohols by the hydroformylation of olefin are carried out using a catalyst containing Ni/Mo on alumina or silica alumina prepared by depositing an organic acid solution of Ni and Mo salts on the support, the acid being phosphorous free.

Hydrogenation catalyst for oxo alcohol process

The hydrogenation steps and hydrofinishing steps of the cobalt catalyst oxo process for preparation of the alcohols by the hydroformylation of olefin are carried out using a nickel-molybdenum catalyst on an alumina or silica alumina support which has a phosphorous content of O.1 wt. % to 1.0 wt. % phosphorus.

Hydrogenation catalyst with low phosphorous content for oxo alcohol

The hydrogenation steps and hydrofinishing steps of the cobalt catalyst oxo process for the preparation of alcohols by the hydroformylation of olefin are carried out using a trimetallic catalyst composed of metal oxides, particularly nickel oxide, molybdenum oxide and cobalt oxide supported on alumina or an alumina-silica in sulfided and non-sulfided form.

Synthesis gas is produced by the reaction of light hydrocarbons, primarily methane, in a fluid bed reaction zone of attrition resistant nickel on alpha-alumina catalyst, with steam and oxygen and the conversion level is preserved by limiting the loss of nickel from the reaction and thereby limiting the back reaction of the synthesis gas to form methane in the presence of entrained catalyst in a cooling zone.

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Baton Rouge, LA, United States of America

Jose M Vargas