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US4242526A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for the direct separation of isobutylene from mixtures of hydrocarbons

Assignee: Magyar Asvanyolaj es Foldgaz Kiserleti Intezet
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Filing: 1978-03-08
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Granted: 1980-12-30
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Expires: 1998-03-08
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Abstract

Abstract Methyl tertiary butyl ether is produced from a mixture of C 4 hydrocarbons containing isobutylene and butadiene. The isobutylene is selectively reacted with a greater than stoichiometric amount of methanol at a temperature of 50 to 120 degrees C., in a homogeneous liquid phase and in the presence of a catalytic amount of sulfuric acid. The sulfuric acid is present in an amount less than 20% by weight based on the weight of the reaction mixture. The homogeneous liquid phase is maintained throughout the reaction whereby a reaction mixture containing methyl tertiary butyl ether is produced and undesired polymerization of the badadiene is avoided. The reaction mixture is cooled then reaction mixture which has been washed free of methanol, or separated unreacted C 4 fraction which is isobutylene-free, is added. An upper phase containing hydrocarbons and methyl tertiary butyl ether and a part of the methanol and a lower phase containing methanol and 10 to 50% sulfuric acid is formed. The lower phase is recirculated as a catalyst to the step of selectively reacting the isobutylene with methanol.

Inventors

  • 👤 Janos Laky
  • 👤 Rezso Csikos
  • 👤 Lajos Peterfy
  • 👤 Lajos Szvetelszky
  • 👤 Istvan Pallay

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-01 05:21
CPC Classifications
C; C07; C07C; C07C41/00; C07C41/01; C07C41/05; C07C41/06

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 184 words
A process for producing methyl tertiary butyl ether from a mixture of C 4 hydrocarbons containing isobutylene and butadiene, comprising the steps of selectively reacting the isobutylene with a greater than stoichiometric amount of methanol, at a temperature of 50 to 120 degrees C., in a homogeneous liquid phase and in the presence of a catalytic amount of sulfuric acid, said sulfuric acid being present in an amount less than 20% by weight based on the weight of the reaction mixture, said homogeneous liquid phase being maintained throughout the reaction, whereby a reaction mixture containing methyl tertiary butyl ether is produced and undesired polymerization of the budadiene is avoided; cooling the reaction mixture then adding to it reaction mixture which has been washed free of methanol or separated unreacted C 4 fraction which is isobutylene-free whereby an upper phase containing hydrocarbons and methyl tertiary butyl ether and a part of the methanol and a lower phase containing methanol and 10 to 50% sulfuric acid is formed; and recirculating the lower phase as a catalyst to said step of selectively reacting the isobutylene with methanol.
Claim 2
Dependent Claim 184 words
A process for producing methyl tertiary butyl ether from a mixture of C 4 hydrocarbons containing isobutylene and butadiene, comprising the steps of selectively reacting the isobutylene with a greater than stoichiometric amount of methanol, at a temperature of 50 to 120 degrees C., in a homogeneous liquid phase and in the presence of a catalytic amount of sulfuric acid, said sulfuric acid being present in an amount less than 20% by weight based on the weight of the reaction mixture, said homogeneous liquid phase being maintained throughout the reaction, whereby a reaction mixture containing methyl tertiary butyl ether is produced and undesired polymerization of the budadiene is avoided; cooling the reaction mixture then adding to it reaction mixture which has been washed free of methanol or separated unreacted C 4 fraction which is isobutylene-free whereby an upper phase containing hydrocarbons and methyl tertiary butyl ether and a part of the methanol and a lower phase containing methanol and 10 to 50% sulfuric acid is formed; and recirculating the lower phase as a catalyst to said step of selectively reacting the isobutylene with methanol.

References Cited (Backward Citations)

US2139359A Cited
US1968601A Cited
US2067385A Cited
US2391084A Cited
US2721222A Cited
US3121124A Cited
US3846088A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1983-12-30 1984-06-30 1984-12-30 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1987-12-30 1988-06-30 1988-12-30 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1991-12-30 1992-06-30 1992-12-30 $7700.00 Window Closed / Lapsed

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