Exxonmobil Research and Engineering Company

Exxon Research and Engineering Company

Audi Ag

Rohm and Haas Company

Columbia University

University of Delaware

Lummus Technology Inc.

Jingguang Chen

William C Baird, Jr

Gary Brice McVicker

Michele Sue Touvelle

Edward Stanley Ellis

Darryl Patrick Klein

David E W Vaughan

Michel A Daage

James J Schorfheide

Darryl P Klein

Sylvain S Hantzer

Anne Mae Gaffney

Leo D Brown

Belabbes Merzougui

Minhua Shao

Lesia V Protsailo

David E Vaughan

Philip Jay Angevine

Chuen Yuan Yeh

Sanjay Chaturvedi

Carl W Hudson

Emanuel Hermanus Van Broekhoven

Johannes Hendrik Koegler

Michael Bruce Clark, Jr

Feng Jiao

Qi Lu

Gregory S Hutchings

William C Baird Jr

Cheun Yuan Yeh

Emmanuel Van Broekhoven

A metallic alloy includes Cu and one or more metals M selected from the group consisting of Ti, V, Cr, Mn, Fe, Co, Ni and Zn, wherein the alloy has a surface in the form of a vermiculated arrangement of irregular, nanoporous lands separated by troughs or channels. It can be made by contacting a precursor alloy including Cu, M and Al with a caustic liquid under conditions sufficient to remove the Al. Or, a metallic alloy includes Cu and one or more metals M selected from the group consisting of Ti, V, Cr, Mn, Fe, Co, Ni and Zn, wherein the one or more metals M in total constitute in a range of 3 at. % to 7 at. %, relative to the total of Cu and M. Both types of alloy can be used as an electrocatalyst in a water electrolyzer or a hydrogen fuel cell.

Electrocatalyst for hydrogen evolution and oxidation reactions

A supported catalyst includes a plurality of support particles that each include a carbon support and a layer disposed around the carbon support. The layer is selected from a metal carbide, metal oxycarbide, and combinations thereof. A catalytic material is disposed on the layers of the support particles.

Fuel cell catalyst including carbon support particles with metal carbide layer and catalytic material and fuel cell using the same

Solid acid catalysts for use in alkylation processes are described. The solid acid catalysts include a multimetallic (e.g. bimetallic, trimetallic or tetrametallic) component that performs a hydrogenating function for the reactivation (or regeneration) of the catalyst in the presence of hydrogen. The multimetallic catalyst includes a noble metal such as platinum or palladium. The invention also relates to alkylation processes using the multimetallic solid acid catalysts having a multimetallic component for hydrogenation.

Bimetallic alkylation catalysts

A supported catalyst comprising a mixed metal oxide is useful for the vapor phase oxidation of an alkane or a mixture of an alkane and an alkene to an unsaturated carboxylic acid and for the vapor phase ammoxidation of an alkane or a mixture of an alkane and an alkene to an unsaturated nitrile.

PVD supported mixed metal oxide catalyst

A process to regenerate iron-based hydrogen sulfide sorbents using steam. The steam is preferably mixed with hydrogen-containing gas and/or an inert gas, such as nitrogen. In a preferred embodiment, the sorbent is first exposed to the steam and then exposed to a hydrogen-containing gas at regeneration conditions.

Regeneration of iron-based hydrogen sulfide sorbents

Disclosed is a process for opening naphthenic rings of naphthenic ring-containing compounds, along with catalysts which can be used in that process. The ring opening is accomplished using a ring opening catalyst comprising Ir on a composite support of alumina and acidic silica-alumina molecular sieve. The ring opening activity is not significantly deactivated by exposure to oxygen at greater than about 250&deg; C.

Naphthene ring opening over an iridium ring opening catalyst

A process to regenerate metal oxide desulfurization sorbents using an oxidizing and reducing atmosphere. The sorbents may be mono- or multi-metallic in nature, and preferably comprise Cu, Ni and/or Co. If desired, secondary metals may be incorporated to increase regeneration efficiency and/or capacity. Other additives may be used to suppress hydrocarbon cracking. A sorbent containing Zn may be combined with an Fe, Co, Ni, Mo, or W catalyst or a noble metal catalyst and combinations thereof.

Regeneration of hydrogen sulfide sorbents

Disclosed is a process for opening naphthenic rings of naphthenic ring-containing compounds, along with catalysts which can be used in that process. The ring opening is accomplished using a ring opening catalyst system which combines an Ir ring opening catalyst with a Pt and Pd catalyst. The combination of the Pt and Pd-containing catalyst with an Ir-containing catalyst incorporates desirable isomerization activity and also results in substantial ring opening activity that enables Ir to be loaded at a level that is substantially below that of Ir-only ring opening processes.

Naphthene ring opening over a ring opening catalyst combination

Disclosed is a process for opening naphthenic rings of naphthenic ring-containing compounds, along with catalysts which can be used in that process. The naphthene ring opening catalyst is a catalyst which comprises at least one of a Group VIII metal selected from Ir, Pt, Pd, Rh, and Ru in an amount effective to ring open naphthene rings on naphthene ring-containing compounds, the metal being supported on a substrate comprising at least one Group IB, IIB, and IVA metal in an amount effective to moderate cracking of a naphthene ring-containing feed to form methane.

Naphthene ring opening over group VIII metal catalysts containing cracking moderators

Disclosed is a process for opening naphthenic rings of naphthenic ring-containing compounds, and catalysts which can be used in that process. The naphthene ring opening catalyst is a polymetallic catalyst comprising Group VIII metals. In a preferred embodiment the naphthene ring opening catalyst comprises Ir in combination with a Group VIII metal selected from at least one of Pt, Rh, and Ru, in an amount effective for opening a naphthene ring-containing compound at a tertiary carbon site.

Method and catalyst for opening naphthenic rings of naphthenic ring-containing compounds

A process for opening naphthenic rings of naphthenic ring-containing compounds, along with catalysts which can be used in that process. The naphthene ring opening catalyst is a catalyst comprising at least one Group VIII metal selected from Ir, Pt, Rh, and Ru, wherein these metals are supported on an alkali metal or alkaline-earth metal modified support in an amount effective for opening a naphthene ring-containing compound at a tertiary carbon site.

Ring opening with group VIII metal catalysts supported on modified substrate

A process for the hydrodesulfurization (HDS) of multiple condensed ring heterocyclic organosulfur compounds present in petroleum and petrochemical streams over noble metal-containing catalysts under relatively mild conditions. The noble metal is selected from Pt, Pd, Ir, Rh, and polymetallics thereof. The catalyst system also contains a hydrogen sulfide sorbent material.

Desulfurization process for refractory organosulfur heterocycles

A process for the hydrodesulfurization (HDS) of multiple condensed ring heterocyclic organosulfur compounds present in petroleum and petrochemical streams and the saturation of aromatics over noble metal-containing catalysts under relatively mild conditions. The noble metal is selected from Pt, Pd, Ir, Rh and polymetallics thereof. The catalyst system also contains a hydrogen sulfide sorbent material.

Desulfurization and aromatic saturation of feedstreams containing refractory organosulfur heterocycles and aromatics

A process for the hydrodesulfurization (HDS) of multiple condensed ring heterocyclic organosulftir compounds found in petroleum and petrochemical streams. HDS is preferably conducted in a mixed bed containing: (a) a Ni-based catalyst on an inorganic refractory support, and (b) a hydrogen sulfide sorbent material. The desulfurized stream can then be passed to further processing, including aromatics saturation and/or ring opening.

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Hockessin, DE, United States of America

Jingguang Chen