IP Library Granted Patent US 8,119,849
Granted Patent B2
US 8,119,849 · App. 12/317,794 · Granted Feb 21, 2012

Propylene production

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Quick Facts
Patent No.
US 8,119,849
App. No.
12/317,794
Granted
Feb 21, 2012
Kind
B2
Abstract

A propylene production process is disclosed. The process comprises (a) reacting a feed stream comprising isobutene in the presence of a skeletal isomerization catalyst to obtain an isomerized stream comprising C 4 olefins; and (b) reacting the isomerized stream with ethylene in the presence of a metathesis catalyst to form a metathesis product stream comprising propylene, C 4 olefins, and C 5 + olefins. The metathesis reaction pressure is equal to or lower than that of the skeletal isomerization.

Claims (16)

1. A process for producing propylene comprising

(a) reacting a feed stream comprising isobutene in the presence of a skeletal isomerization catalyst to obtain an isomerized stream of isobutene comprising C 4 olefins; and

(b) reacting the isomerized stream with ethylene in the presence of a metathesis catalyst to form a metathesis product stream comprising propylene, C 4 olefins, and C 5 and higher olefins;

wherein step (b) is performed at an equal or lower pressure than step (a).

2. The process of claim 1 wherein step (a) is performed at 20 to 60 psig.

3. The process of claim 2 wherein step (b) is performed at 20 to 60 psig.

4. The process of claim 1 wherein the feed stream comprises greater than 95 wt % of C 4 olefins.

5. The process of claim 1 wherein the feed stream is produced by dehydration of tert-butyl alcohol.

6. The process of claim 1 further comprising separating the metathesis product stream into an ethylene stream, a propylene product stream, a C 4 olefins stream, and C 5 and higher olefins stream.

7. The process of claim 6 wherein step (a) is performed at 20 to 60 psig.

8. The process of claim 7 wherein step (b) is performed at 20 to 60 psig.

9. The process of claim 6 wherein the ethylene stream is recycled to step (b).

10. The process of claim 6 wherein the C 4 olefins stream is recycled to step (a).

11. The process of claim 6 wherein the feed stream comprises greater than 95 wt % C 4 olefins.

12. The process of claim 6 wherein the feed stream is produced by dehydration of tert-butyl alcohol.

13. The process of claim 1 wherein heat integration of the process is reduced compared to a process where step (b) is performed at a higher pressure than step (a).

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 Mar 2, 2009
From: SAWYER, GARY A.; AXELROD, MICHAEL G.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 022348/0599 →