Tpc Group LLC

Celanese International Corporation

Uop Lcc

Michael O Nutt

Joseph G Duff

Jillian M Horn

Clifford Alan Maat

Peggy J Macatangay

André M Gobin

Rajeev Kumar

Ronald David Shaver

G Paull Torrence

Tianshu Pan

Mark P Kaminsky

Brian W Hokkanen

George Pappas

John Joseph Senetar

Liana Caciula

Wayne Ouellette

Randall V Redd

Leonard M Czupski

James A Hopson

Charles P Luebke

Gilbert D Valdez

Jeannie Mee Blommel

Dana K Sullivan

Gus K Georgeton

Robert Z Confair

Joseph A Comeaux

David S Hager

Baiyi Zhao

Isobutylene copolymer includes repeat units derived from isobutylene and one or more comonomers selected from isoprene, butadiene, cyclopentadiene, dicyclopentadiene, limonene, substituted styrenes, and C4 to C10 dienes other than isoprene, butadiene, limonene, cyclopentadiene, or dicyclopentadiene, wherein the molar ratio of isobutylene derived repeat units to the comonomer derived repeat units is from 75:1 to 1.5:1. The copolymers have a molecular weight, Mn, of from 200 to 20,000 Daltons and typically have a high double bond content and a high vinylidene double bond content when diene monomers are utilized.

Isobutylene copolymers, method for making isobutylene copolymers and isobutylene copolymer products

Non-random isobutylene copolymer includes repeat units derived from isobutylene and one or more comonomers selected from isoprene, butadiene, cyclopentadiene, dicyclopentadiene, limonene, substituted styrenes, and C4 to C10 dienes other than isoprene, butadiene, limonene, cyclopentadiene, or dicyclopentadiene, wherein the molar ratio of isobutylene derived repeat units to the comonomer derived repeat units is from 75:1 to 1.5:1. The non-random copolymers have a molecular weight, Mn, of from 200 to 20,000 Daltons and typically have a high double bond content and a high vinylidene double bond content when diene monomers are utilized.

Non-random isobutylene copolymers

A flexible manufacturing system for selectively producing different alpha-olefins from ethylene includes: (a) a reaction sectionwith ethylene feed operative to oligomerize ethylene; (b) a catalyst feed systemcomprising a plurality of independent homogeneous catalyst feeders connected with the reaction section for alternatively providing different selective homogeneous catalyst compositions to the reaction section; (c) an ethylene recycle columncoupled to the reaction section and adapted to receive crude product and unreacted ethylene therefrom, the recycle column being operative to separate ethylene and optionally lower oligomers from the crude product which are recycled to the ethylene feed to the reaction section, the ethylene recycle column being further operative to provide a crude product bottoms stream; (d) a catalyst removal sectioncoupled to the reaction section adapted to remove spent catalyst from the system; and (e) a first product separation columnconnected to the recycle column receiving the crude product stream therefrom, the product separation column being operative to separate purified oligomer from the crude product stream. Optionally provided is a second product separation column

Flexible manufacturing system for selectively producing different linear alpha olefins

A dehydrogenation system includes a plurality of dehydrogenation reactors valved to operate in alternating dehydrogenation modes and regeneration modes in a timed sequence in a system cycle by way of the plurality of valves; a digital programmable controller connected to the plurality of valves for sequencing the reactors; and means for determining the productivity characteristics of each reactor over a system cycle. The digital controller is operable to re-sequence the reactors to reduce either peak productivity or productivity deltas over an initial system cycle. After resequencing, production may be increased with the more uniform productivity profile of the re-sequenced system without exceeding system limits, such as compressor operating limits.

Dehydrogenation process and system with reactor re-sequencing

The process to recover heat in oxidative dehydrogenation of butene to butadiene is presented. The process utilizes heat recovered in oxidative dehydrogenation of butene to butadiene to generate steam. The process utilizes the circulated water stream generated in oxidative dehydrogenation of butene to butadiene for steam generation. A feedstream comprising butene is mixed with steam and preheated air at the inlet of the oxidative dehydrogenation reactor.

Heat recovery in the process of production of butadiene

A process is presented for the production of butadienes. The process includes the separation of oxygenates from the product stream from an oxidative dehydrogenation reactor. The process includes quenching the product stream and solvent and oxygenates from the product stream. The oxygenates are stripped from the solvent with an inert gas to reduce the energy consumption of the process, and the solvent is recycled and reused in the process.

Use of C4 absorber overhead for stripping aldehydes

A method of oxidatively dehydrogenating a dehydrogenation reactant includes providing a first gaseous feed stream to a first adiabatic, catalytic reaction zone with less than a stoichiometric amount of oxygen and superheated steam, oxidatively dehydrogenating dehydrogenation reactant in said first adiabatic, catalytic reaction zone and subsequently cooling the effluent, adding additional oxygen and reacting the effluent stream in at least one subsequent adiabatic reaction zone. The dehydrogenation system enables higher conversion and yield per pass and in some cases greatly reduces steam usage and energy costs. In a preferred integrated process, ethylene is converted to n-butene which is then oxidatively dehydrogenated to butadiene.

Multi-stage oxidative dehydrogenation process with inter-stage cooling

The present invention discloses a process to treat a ferrite based catalyst useful in the oxidative dehydrogenation of monololefins and diolefins which process includes a preheat step prior to use of the catalyst in the OXO-D reactor. The catalyst is preferably a zinc ferrite catalyst for the production of butadiene. It has been observed that substantially no nitrogen oxide emissions result from the use of this treated catalyst in the reactor unit during the oxidative dehydrogenation reaction.

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Oxidative dehydrogenation includes: (a) providing a gaseous feed stream to a catalytic reactor, the feed stream comprising a dehydrogenation reactant, oxygen, superheated steam, hydrocarbon moderator gas and optionally nitrogen, wherein the molar ratio of moderator gas to oxygen in feed stream is typically from 4:1 to 1:1 and the molar ratio of oxygen to nitrogen in the feed stream is at least 2; (b) oxidatively dehydrogenating the reactant in the reactor to provide a dehydrogenated product enriched effluent product stream; and (c) recovering dehydrogenated product from the effluent product stream. One preferred embodiment is a process for making butadiene including dimerizing ethylene to n-butene in a homogeneous reaction medium to provide a hydrocarbonaceous n-butene rich feed stream and oxidatively dehydrogenating the n-butene so formed.

Oxidative dehydrogenation process with hydrocarbon moderator gas and reduced nitrogen feed

A method of making a low-fluoride reactive PIB composition includes (a) providing a modified C4 feedstock by way of blending a mixed C4 feedstock with a second feedstock having a lower LB/IsoB ratio; or providing a C4 feedstock with an LB/IsoB index of less than 10%; (b) feeding the modified C4 feedstock or the C4 feedstock with an LB/IsoB index of less than 10% to a CSTR with a homogeneous catalyst comprising BFand a modifier selected from alcohols, ethers and mixtures thereof; (c) polymerizing the modified C4 feedstock or the C4 feedstock with an LB/IsoB index of less than 10% in the reactor while maintaining the reactor at a temperature above &#x2212;15&#xb0; C. and utilizing a residence time less than 45 minutes to produce a crude PIB composition in a polymerization mixture; and (d) recovering a purified PIB composition from the polymerization mixture having a molecular weight, Mn, from 250 to 5000 Daltons and an alpha vinylidene content of at least 50 mol %. The crude PIB composition suitably has a fluoride content of less than 100 ppm and the purified PIB composition has a fluoride content of less than 20 ppm in preferred embodiments. In the most preferred embodiments, ammonium salts are used to neutralize the catalyst and fluoride salts are sublimed from the product at elevated temperatures.

Low-fluoride, reactive polyisobutylene

A method of making a low-fluoride reactive PIB composition includes in one embodiment: a) providing an isobutylene-enriched C4 feedstock by way of blending a first mixed C4 feedstock with a second feedstock having a lower LB/IsoB index; (b) feeding the isobutylene-enriched C4 feedstock to a polymerization reactor with a catalyst complex comprising BFand a modifier selected from alcohols, ethers and mixtures thereof; (c) polymerizing the isobutylene-enriched C4 feedstock in the reactor while maintaining the reactor at a temperature above &#x2212;40&#xb0; C. and most preferably above &#x2212;15&#xb0; C. and utilizing a residence time less than 45 minutes to produce a crude PIB composition in a polymerization mixture; and (d) recovering a purified PIB composition from the polymerization mixture having a molecular weight, Mn, from 250 to 5000 Daltons and an alpha vinylidene content of at least 50 mol %. The crude PIB composition suitably has a fluoride content of less than 100 ppm and the purified PIB composition has a fluoride content of less than 20 ppm. In another aspect, ammonium salts are used to neutralize the catalyst and fluoride salts are sublimed from the product at elevated temperatures.

A process for producing acetic acid comprising the steps of reacting carbon monoxide and at least one of methanol and a methanol derivative in a first reactor under conditions effective to produce a crude acetic acid product; separating the crude acetic acid product into at least one derivative stream, at least one of the at least one derivative stream comprising residual carbon monoxide; and reacting at least a portion of the residual carbon monoxide with at least one of methanol and a methanol derivative over a metal catalyst in a second reactor to produce additional acetic acid.

Production of acetic acid with high conversion rate

A method of producing butadiene includes: (1) dimerizing ethylene to butene followed by (2) oxidatively dehydrogenating the butene to butadiene and (3) recovering the butadiene by (i) absorbing the product with a hydrocarbon absorber oil and (ii) stripping a crude product stream from the absorber oil. The absorber oil is selected so as to be effective to sequester ethylene dimerization-derived impurities from the system.

Manufacture of butadiene from ethylene

The present invention is to a process for producing acetic acid comprising the step of reacting a carbon monoxide feed and methanol and/or a methanol derivative in a first reactor to produce a crude acetic acid product. The carbon monoxide may comprise less than 99.5 mol % carbon monoxide. The process further comprises the step of purging a carbon monoxide purge stream comprising a first amount of residual carbon monoxide and one or more impurities. Preferably, the first amount is greater than 20 mol %. The process further comprises the step of separating the crude acetic acid product into at least one derivative stream comprising a second amount of residual carbon monoxide. The process further comprises the step of reacting at least a portion of the second amount of residual carbon monoxide and methanol and/or a methanol derivative in a second reactor to produce additional acetic acid.

Growing community of inventors

Pearland, TX, United States of America

Michael O Nutt