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US4282389A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for the simultaneous manufacture of pure MTBE and a substantially isobutene-free mixture of C4 -hydrocarbons

Assignee: Huels AG
•
Filing: 1979-12-04
•
Granted: 1981-08-04
•
Expires: 1999-12-04
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Abstract

Abstract A process for the simultaneous manufacture of pure methyl tertiary butyl ether (MTBE) and a substantially isotubene-free mixture of C 4 -hydrocarbons, by reacting the isobutene contained in the mixture of C 4 -hydrocarbons with excess methanol in the liquid phase at elevated temperatures on strongly acid, macroporous, organic ion exchange resins. The process has the following steps: (a) methanol and isobutene are reacted in a molar ratio of 2:1 to 5:1 at temperatures between 30° and 100° C.; (b) the unconverted hydrocarbons are then removed as the top product under a pressure of 2 to 10 bars from a first rectification column; (c) the bottom product from this first column is rectified in a second column under normal pressure or under a slight excess pressure of up to 2 bars at the top of the column, the bottom product of this rectification is recycled to reaction zone (a), if necessary, after separating off a portion of the tertiary butanol formed and the C 8 -olefins; and (d) the distillate from this second column is rectified in a third rectification column under a pressure of 5 to 30 bars, the distillate thus obtained is recycled into the feed to the second column and pure methyl tertiary butyl ether is withdrawn from the bottom of the third column.

Inventors

  • 👤 Wilhelm Droste
  • 👤 Fritz Obenaus

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-25 04:28
CPC Classifications
C; C07; C07C; C07C41/00; C07C41/01; C07C41/05; C07C41/06; C07C7/00; C07C7/148; C07C7/14875; C07C7/14891

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 215 words
In a process for the simultaneous manufacture of pure methyl tertiary butyl ether and a substantially isobutene-free mixture of C 4 -hydrocarbons, by reacting isobutene contained in a mixture of C 4 -hydrocarbons with excess methanol in the liquid phase at elevated temperatures on strongly acid, macroporous, organic ion exchange resins, the improvement comprising: (a) reacting said methanol and said isobutene in a molar ratio of 2:1 to 5:1 at temperatures of between about 30° and 100° C.; (b) removing unconverted hydrocarbons as the top product under a pressure of 2 to 10 bars from a first rectification column; (c) rectifying the bottom product from said first rectification column in a second column under a pressure of about normal pressure to a pressure of about 2 bars excess at the top of the second column and recycling the bottom product of said second column to step (a); and (d) rectifying the distillate from said second column consisting essentially of an azeotrope of methanol and methyl tertiary butyl ether in a third rectification column under a pressure of about 5 to 30 bars without adding auxiliary material, recycling the distillate of said third column into the feed of said second column and withdrawing said pure methyl tertiary butyl ether from the bottom of said third column.
Claim 2
Dependent Claim 215 words
In a process for the simultaneous manufacture of pure methyl tertiary butyl ether and a substantially isobutene-free mixture of C 4 -hydrocarbons, by reacting isobutene contained in a mixture of C 4 -hydrocarbons with excess methanol in the liquid phase at elevated temperatures on strongly acid, macroporous, organic ion exchange resins, the improvement comprising: (a) reacting said methanol and said isobutene in a molar ratio of 2:1 to 5:1 at temperatures of between about 30° and 100° C.; (b) removing unconverted hydrocarbons as the top product under a pressure of 2 to 10 bars from a first rectification column; (c) rectifying the bottom product from said first rectification column in a second column under a pressure of about normal pressure to a pressure of about 2 bars excess at the top of the second column and recycling the bottom product of said second column to step (a); and (d) rectifying the distillate from said second column consisting essentially of an azeotrope of methanol and methyl tertiary butyl ether in a third rectification column under a pressure of about 5 to 30 bars without adding auxiliary material, recycling the distillate of said third column into the feed of said second column and withdrawing said pure methyl tertiary butyl ether from the bottom of said third column.
Claim 3
Dependent Claim 33 words
The process of claim 1, wherein a portion of tertiary butanol formed and C 8 -olefins are separated from the bottom product of said second column by the use of a fourth column.
Claim 4
Dependent Claim 24 words
The process of claim 1, wherein the reaction of step (a) is carried out in a temperature range of about 50° to 100° C.
Claim 5
Dependent Claim 63 words
The process of claim 1, wherein the reaction of step (a) is carried out in the front section of a catalyst bed kept at a temperature of between 50° C. and 100° C. and in a subsequent section, which comprises at least one third of the reaction zone, the temperature is kept below 50° C. down to a temperature of about 30° C.
Claim 6
Dependent Claim 22 words
The process of claim 1, wherein methanol and isobutene are employed in a molar ratio of 2.5:1 to 4:1 in step (a).
Claim 7
Dependent Claim 21 words
The process of claim 5, wherein the top product of step (b) contains less than 0.25 percent by weight of isobutene.

References Cited (Backward Citations)

US3940450A Cited
US4148695A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1984-08-03 1985-02-02 1985-08-04 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1988-08-03 1989-02-02 1989-08-04 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1992-08-03 1993-02-02 1993-08-04 $7700.00 Window Closed / Lapsed

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