IP Library Patent Application 12315605
Patent Application
App. No. 12/315,605

Diisobutylene process

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Quick Facts
Patent No.
US None
App. No.
12/315,605
Abstract

This invention is a process for producing diisobutylene from isobutylene. The process comprises first passing water through a downflow reactor containing a bed of sulfonic acid resin to produce an effluent stream having a pH of at least 5, then dimerizing isobutylene by contacting the sulfonic acid resin with a reaction feed comprising isobutylene and tertiary butyl alcohol. The downflow reactor comprises a bottom, an inlet located above the resin bed, an outlet located below the resin bed, and inert material in the space from the bottom of the reactor to at least above the outlet.

Claims (20)

1 . An isobutylene dimerization process, comprising:

(a) passing water through a downflow reactor containing a bed of sulfonic acid resin to produce an effluent stream having a pH of at least 5; and

(b) dimerizing isobutylene by contacting the sulfonic acid resin with a reaction feed comprising isobutylene and tertiary butyl alcohol to produce a product stream comprising diisobutylene,

wherein the downflow reactor comprises a bottom, an inlet located above the bed of sulfonic acid resin, an outlet located below the bed of sulfonic acid resin, and inert material in the space from the bottom of the reactor to at least above the outlet.

2 . The process of claim 1 wherein the sulfonic acid resin is contacted with the reaction feed at a temperature of 50° C. to 200° C.

3 . The process of claim 1 wherein the isobutylene is produced by dehydration of tertiary butyl alcohol.

4 . The process of claim 1 wherein the reaction feed comprises at least 2 weight percent tertiary butyl alcohol.

5 . The process of claim 1 wherein the reaction feed additionally comprises a C 3 -C 10 hydrocarbon.

6 . The process of claim 5 wherein the C 3 -C 10 hydrocarbon is a C 8 hydrocarbon.

7 . The process of claim 6 wherein the C 8 hydrocarbon is diisobutylene.

8 . The process of claim 7 wherein the reaction feed comprises 25 to 50 weight percent isobutylene, 3 to 8 weight percent tertiary butyl alcohol, and 30 to 60 weight percent diisobutylene.

9 . The process of claim 1 , further comprising hydrogenating the diisobutylene to produce isooctane.

10 . The process of claim 1 wherein the downflow reactor further comprises a drain at the bottom of reactor.

11 . The process of claim 1 wherein the product stream comprises diisobutylene, isobutylene, tertiary butyl alcohol, and water.

12 . The process of claim 11 , further comprising

(c) distilling the product stream to produce a first overhead stream comprising water and isobutylene and a first bottoms stream comprising diisobutylene and tertiary butyl alcohol;

(d) separating at least 30 percent of the water from the first overhead stream to form an isobutylene-enriched stream, and recycling the isobutylene-enriched stream back to step (b); and

(e) distilling the first bottoms stream to produce a bottoms product stream comprising diisobutylene and a second overhead stream comprising tertiary butyl alcohol and diisobutylene.

13 . The process of claim 12 wherein the water is separated from the first overhead stream by decantation.

14 . The process of claim 12 , further comprising recycling the second overhead stream back to step (b).

Assignments (14)
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: DEUTSCHE BANK TRUST COMPANY AMERICAS
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032123/0799 →
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: CITIBANK, N.A.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032125/0296 →
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032137/0156 →
APPOINTMENT OF SUCCESSOR ADMINISTRATIVE AGENT Recorded Jan 23, 2014
From: UBS AG, STAMFORD BRANCH
To: BANK OF AMERICA, N.A.
Reel/Frame 032137/0639 →
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: BANK OF AMERICA, N.A.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032138/0134 →
SECURITY AGREEMENT Recorded May 19, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 024402/0681 →
SECURITY AGREEMENT Recorded May 18, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 024397/0818 →
SECURITY AGREEMENT Recorded May 7, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 024342/0801 →
SECURITY AGREEMENT Recorded May 6, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT
Reel/Frame 024342/0421 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
To: LYONDELL CHEMICAL TECHNOLOGY, LP
Reel/Frame 024337/0285 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: LYONDELL CHEMICAL TECHNOLOGY, LP
Reel/Frame 024337/0020 →
SECURITY AGREEMENT Recorded Oct 30, 2009
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 023449/0138 →
SECURITY AGREEMENT Recorded Apr 9, 2009
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT AND COLLATERAL AGENT
Reel/Frame 022708/0830 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 4, 2008
From: ZAK, THOMAS S.; LEYSHON, DAVID W.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 021988/0995 →