Vapor-phase addition of methanol to isobutene on a macroporous resin. A kinetic study

The authors describe a study of the kinetics of the vapor-phase addition of methanol to isobutene to give methyl tert-butyl ether (MTBE) on the ion-exchange resin Amberlyst 15. Rate data were obtained in a continuous differential reactor operated at atmospheric pressure and 41-61.5{sup 0}C. The best...

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Veröffentlicht in:Industrial & engineering chemistry research 1989-09, Vol.28 (9), p.1269-1277
Hauptverfasser: Tejero, Javier, Cunill, Fidel, Izquierdo, Jose F
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container_issue 9
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container_title Industrial & engineering chemistry research
container_volume 28
creator Tejero, Javier
Cunill, Fidel
Izquierdo, Jose F
description The authors describe a study of the kinetics of the vapor-phase addition of methanol to isobutene to give methyl tert-butyl ether (MTBE) on the ion-exchange resin Amberlyst 15. Rate data were obtained in a continuous differential reactor operated at atmospheric pressure and 41-61.5{sup 0}C. The best-fitting Langmuir-Hinshelwood-Hougen-Watson (LHHW) rate equation is derived from a mechanism whose rate-determining step is the reaction between the methanol adsorbed molecularly on one center and the isobutene adsorbed on two centers. This mechanism is thermodynamically consistent.
doi_str_mv 10.1021/ie00093a001
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A kinetic study</atitle><jtitle>Industrial &amp; engineering chemistry research</jtitle><addtitle>Ind. Eng. Chem. Res</addtitle><date>1989-09-01</date><risdate>1989</risdate><volume>28</volume><issue>9</issue><spage>1269</spage><epage>1277</epage><pages>1269-1277</pages><issn>0888-5885</issn><eissn>1520-5045</eissn><coden>IECRED</coden><abstract>The authors describe a study of the kinetics of the vapor-phase addition of methanol to isobutene to give methyl tert-butyl ether (MTBE) on the ion-exchange resin Amberlyst 15. Rate data were obtained in a continuous differential reactor operated at atmospheric pressure and 41-61.5{sup 0}C. The best-fitting Langmuir-Hinshelwood-Hougen-Watson (LHHW) rate equation is derived from a mechanism whose rate-determining step is the reaction between the methanol adsorbed molecularly on one center and the isobutene adsorbed on two centers. This mechanism is thermodynamically consistent.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ie00093a001</doi><tpages>9</tpages></addata></record>
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ispartof Industrial & engineering chemistry research, 1989-09, Vol.28 (9), p.1269-1277
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language eng
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source American Chemical Society Journals
subjects 10 SYNTHETIC FUELS
100300 - Synthetic Fuels- Properties & Composition- (1990-)
400201 - Chemical & Physicochemical Properties
ALCOHOLS
ALKENES
BUTENES
BUTYL ETHER
CHEMICAL REACTION KINETICS
CHEMICAL REACTORS
Chemistry
EQUATIONS
ETHERS
Exact sciences and technology
HYDROCARBONS
HYDROXY COMPOUNDS
INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY
ION EXCHANGE
KINETICS
Kinetics and mechanisms
METHANOL
Organic chemistry
ORGANIC COMPOUNDS
ORGANIC OXYGEN COMPOUNDS
ORGANIC POLYMERS
PETROCHEMICALS
PETROLEUM PRODUCTS
POLYMERS
REACTION KINETICS
Reactivity and mechanisms
RESINS
SYNTHESIS
title Vapor-phase addition of methanol to isobutene on a macroporous resin. A kinetic study
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