Exxonmobil Chemical Patents Inc.

Exxonmobil Research and Engineering Company

Natalie Ann Fassbender

Jean Willem Beeckman

Chuansheng Bai

Adrienne J Thornburg

Stuart Leon Soled

Sabato Miseo

Randolph John Smiley

Tilman W Beutel

Ivy Dawn Johnson

Peter I Ravikovitch

Hans K T Goris

Nadya A Hrycenko

Theodore E Datz

Harry William Deckman

Roby Bearden, Jr

Jack Wayne Johnson

William Ernest Lewis

Anjaneya Sarma Kovvali

Rustom Merwan Billimoria

John P Greeley

Manuel Anthony Francisco

Ramanathan Sundararaman

Thomas Francis Degnan, Jr

Jean W L Beeckman

A method of producing a hydrogenation catalyst, for example, a phthalate hydrogenation catalyst, comprising contacting a silica support having a medium pore size of at least about 10 nm with an acid to produce a treated silica support, and depositing a noble metal, preferably ruthenium, on the treated silica support to produce a noble metal-containing silica support, and optionally contacting the noble metal-containing silica support with a chelating agent to form the hydrogenation catalyst; a hydrogenation catalyst prepared by that method; and a method of hydrogenating unsaturated hydrocarbons, such as, phthalates, in which an unsaturated hydrocarbon is contacted with hydrogen gas in the presence of the hydrogenation catalyst of the invention.

Hydrogenation catalyst, its method of preparation and use

Disclosed herein are an apparatus and a method for mixing and/or mulling a sample, the apparatus comprising at least one container made of a flexible material and containing a sample, means for holding the container, and means for impacting the container, wherein the means for holding and the means for impacting are movable relative to each other, and wherein the means for holding, the means for impacting, and the container are arranged such that the means for impacting and the container can repeatedly collide, whereby an energy of collision can be imparted to the sample, thereby mixing and/or mulling the sample. Also disclosed is an assembly for performing high throughput experiments including the apparatus for mixing and/or mulling a sample and an extruder configured to receive a sample weighing less than 100 grams.

Apparatus and method for mixing and/or mulling a sample

A method of preparing a hydrogenation catalyst, for example, a phthalate hydrogenation catalyst, comprising contacting a silica support having a median pore size of at least about 10 nm with a silylating agent to form an at least partially coated silica support, calcining said coated silica support to form a treated silica support, and depositing a noble metal, preferably ruthenium, on the treated silica support, and optionally contacting the treated silica support with an optional chelating agent to form the hydrogenation catalyst; a hydrogenation catalyst prepared by that method; and a method of hydrogenating unsaturated hydrocarbons, such as phthalates, in which an unsaturated hydrocarbon is contacted with hydrogen gas in the presence of the hydrogenation catalyst of the invention.

Systems and methods are provided for slurry hydroconversion of a heavy oil feed, such as an atmospheric or vacuum resid. The systems and methods allow for slurry hydroconversion using catalysts with enhanced activity and/or catalysts that can be recycled as a side product from a complementary refinery process.

Slurry hydroconversion using enhanced slurry catalysts

A method of preparing a hydrogenation catalyst, for example, a phthalate hydrogenation catalyst, comprising nebulizing a liquid containing a noble metal and a chelating agent comprising at least one nitrogen-containing functional group to form a nebulized liquid, and contacting the nebulized liquid with silica particles; a hydrogenation catalyst prepared by that method; and a method of hydrogenating unsaturated hydrocarbons, such as phthalates, in which an unsaturated hydrocarbon is contacted with hydrogen gas in the presence of the hydrogenation catalyst of the invention.

A composition is described comprising a molecular sieve having pores defined by channels formed by one or more 8-membered rings of tetrahedrally coordinated atoms, such as a DDR-type molecular sieve, and an amorphous deposit of a boron compound on the molecular sieve.

Boron selectivated molecular sieves and their use in sorptive separations

Methods are provided for synthesizing ZSM-58 crystals with an improved morphology and/or an improved size distribution. By controlling the conditions during synthesis of the ZSM-58 crystals, crystals of a useful size with a narrow size distribution can be generated. Steaming the H-form DDR framework type crystals at a temperature from 426&#xb1;&#xb0; C. to 1100&#xb1;&#xb0; C. for a time period from about 30 minutes to about 48 hours can attain one or more of the following properties: a CH4 diffusivity of no more than 95% of the CH4 diffusivity of the unsteamed H-form DDR framework type crystals; an N2 BET surface area from 85% to 110% of the surface area of unsteamed H-form DDR framework type crystals; and an equilibrium CO2 sorption capacity from 80% to 105% of the equilibrium CO2 sorption capacity of unsteamed H-form DDR framework type crystals.

Synthesis of ZSM-58 crystals with improved diffusivity for use in gas separations

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Nazareth, PA, United States of America

Natalie Ann Fassbender