IP Library Granted Patent US 6,992,152
Granted Patent B2
US 6,992,152 · App. 10/922,181 · Granted Jan 31, 2006

Apparatus and method for controlling olefin polymerization process

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Quick Facts
Patent No.
US 6,992,152
App. No.
10/922,181
Granted
Jan 31, 2006
Kind
B2
Abstract

Apparatus for olefin polymerization includes one or more shell and tube olefin polymerization reactors, each of which has an olefin polymerization reaction mixture inlet connection and a crude polyolefin product outlet connection. Each reactor is equipped with a recirculation system including a pump arranged to circulate a reaction mixture through the tube side of the reactor independently of the introduction of olefin polymerization reaction mixture into the reactor. The apparatus may also include an inlet reaction mixture distribution manifold and an outlet polymerization reaction mixture collection manifold interconnecting the reactors for operation in parallel. The apparatus also includes catalyst composition and catalyst modifier inlets for each reactor arranged such that a catalyst modifier to may be introduced into each reactor at a rate which is independent of the introduction of catalyst composition.

Claims (56)

1. A method for conducting an olefin polymerization reaction comprising:

recirculating an olefin polymerization reaction mixture in a reaction zone of an olefin polymerization reactor;

introducing an olefin containing feedstock into said recirculated olefin polymerization reaction mixture, said olefin polymerization reaction mixture being recirculated at a flow rate which is independent of the rate of introduction of said feedstock into said zone;

introducing a catalyst composition comprising a catalyst and a catalyst modifier into said reaction mixture;

subjecting said polymerization reaction mixture to exothermic olefin polymerization reaction conditions in said zone in the presence of said catalyst composition; and

introducing a catalyst modifier into said recirculating olefin polymerization reaction mixture at a rate which is independent of the rate of introduction of said catalyst composition into said zone.

2. A liquid phase polymerization process for preparing polyisobutylene, said process comprising:

providing a feedstock comprising isobutylene;

providing a catalyst composition comprising a complex of BF 3 and a complexing agent;

introducing said feedstock and said catalyst composition into a reaction mixture in a reaction zone;

intimately intermixing said reaction mixture, said feedstock and said catalyst composition to present an intimately intermixed reaction admixture in said reaction zone;

maintaining the intimately intermixed reaction admixture in its intimately intermixed condition while the same is in said reaction zone, to thereby cause the isobutylene therein to undergo polymerization to form polyisobutylene;

introducing an additional amount of said complexing agent into said intimately intermixed reaction admixture at a rate which is independent of the rate of introduction of said catalyst composition; and

withdrawing a product stream comprising polyisobutylene from said reaction zone.

3. A process as set forth in claim 2 , said reaction zone comprising a loop reactor wherein the reaction admixture is continuously recirculated at a first volumetric flow rate, and said feedstock and said catalyst composition are continuously introduced at a combined second volumetric flow rate.

4. A process as set forth in claim 3 , wherein said complexing agent comprises methanol.

5. A process as set forth in claim 4 , wherein the product is a highly reactive polyisobutylene and the ratio of BF 3 to methanol in said catalyst composition is no less than about 0.59:1.

6. A process as set forth in claim 4 , wherein the product is a highly reactive polyisobutylene and the ratio of BF 3 to methanol in said catalyst composition is in the range of from about 0.59:1 to about 0.62:1.

7. A process as set forth in claim 5 , wherein the product is a highly reactive polyisobutylene and a sufficient amount of methanol is independently introduced to cause the ratio of BF 3 to methanol in said intimately intermixed reaction admixture catalyst composition to be maintained in the range of from about 0.59:1 to about 0.60:1 during the course of the reaction.

8. A process as set forth in claim 6 , wherein a sufficient amount of methanol is independently introduced to cause the ratio of BF 3 to methanol in said intimately intermixed reaction admixture catalyst composition to be maintained at approximately 0.59:1 to about 0.62:1 during the course of the reaction.

9. A process as set forth in claim 3 , wherein said intimately intermixed reaction admixture catalyst composition is maintained at a temperature of at least about 0° C. while the same is in said reaction zone.

10. A process as set forth in claim 3 , including controlling the introduction of said feedstock into said reaction zone and the withdrawal of said product stream from the reaction zone such that the residence time of the isobutylene undergoing polymerization in the reaction zone is no greater than about 4 minutes.

11. A process as set forth in claim 9 , including controlling the introduction of said feedstock into said reaction zone and the withdrawal of said product stream from the reaction zone such that the residence time of the isobutylene undergoing polymerization in the reaction zone is no greater than about 4 minutes.

12. A process as set forth in claim 10 , wherein the introduction of said feedstock into said reaction zone and the withdrawal of said product stream from the reaction zone are controlled such that the residence time of the isobutylene undergoing polymerization in the reaction zone is no greater than about 3 minutes.

13. A process as set forth in claim 11 , wherein the introduction of said feedstock into said reaction zone and the withdrawal of said product stream from the reaction zone are controlled such that the residence time of the isobutylene undergoing polymerization in the reaction zone is no greater than about 3 minutes.

14. A process as set forth in claim 10 , wherein the introduction of said feedstock into said reaction zone and the withdrawal of said product stream from the reaction zone are controlled such that the residence time of the isobutylene undergoing polymerization in the reaction zone is no greater than about 200 seconds.

15. A process as set forth in claim 11 , wherein the introduction of said feedstock into said reaction zone and the withdrawal of said product stream from the reaction zone are controlled such that the residence time of the isobutylene undergoing polymerization in the reaction zone is no greater than about 200 seconds.

16. A process as set forth in claim 4 , wherein the product is a mid-range vinylidene content polyisobutylene and the ratio of BF 3 to methanol in said catalyst composition is about 1:1.

17. A process as set forth in claim 5 , wherein the product is a mid-range vinylidene content polyisobutylene and a sufficient amount of methanol is independently introduced to cause the ratio of BF 3 to methanol in said intimately intermixed reaction admixture catalyst composition to be maintained at approximately 1:1 during the course of the reaction.

18. A single-stage liquid phase polymerization process for preparing a polyolefin product having preselected properties, said process comprising:

providing a liquid feedstock comprising at least one olefinic component;

providing a catalyst composition comprising a complex of BF 3 and a complexing agent therefor, said complexing agent comprising a glycol or an aliphatic alcohol having a primary hydroxyl group and no hydrogen on a beta carbon, said complex being stable at temperatures needed to produce said polyolefin product;

introducing said feedstock and said catalyst composition into a residual reaction mixture in a loop reactor reaction zone;

recirculating the residual reaction mixture with the feedstock and the catalyst composition therein in said zone at a recirculation rate sufficient to cause intimate intermixing of the residual reaction mixture, the feedstock and the catalyst composition to thereby present a recirculating, intimately intermixed reaction admixture of the residual reaction mixture, the feedstock and the catalyst composition in said reaction zone;

maintaining the recirculating intimately intermixed reaction admixture in its intimately intermixed condition and removing heat of reaction from the reaction admixture at a rate calculated to provide a substantially constant reaction temperature in the reaction admixture while the same is recirculating in said reaction zone, said constant reaction temperature being at a level appropriate for causing olefinic components introduced in said feedstock to undergo polymerization to form said polyolefin product in the presence of said catalyst composition;

providing a catalyst modifier and introducing the same into said residual reaction mixture separately from said catalyst composition;

withdrawing a product stream comprising polyolefin product and catalyst composition from said reaction zone; and

controlling the introduction of said feedstock into said reaction zone and the withdrawal of said product stream from the reaction zone such that the residence time of the olefinic components undergoing polymerization in the reaction zone is appropriate for production of said polyolefin product.

19. A liquid phase polymerization process for preparing low molecular weight, highly reactive polyisobutylene, said process comprising: providing a feedstock comprising isobutylene; providing a catalyst composition comprising a complex of BF 3 and a complexing agent therefor; introducing said feedstock and said catalyst composition into a residual reaction mixture in a reaction zone; intimately intermixing said residual reaction mixture, said feedstock and said catalyst composition to present an intimately intermixed reaction admixture in said reaction zone; maintaining the intimately intermixed reaction admixture in its intimately intermixed condition and keeping it at a temperature of at least about 0° C. while the same is in said reaction zone, to thereby cause the isobutylene therein to undergo polymerization to form said polyisobutylene; providing a catalyst modifier and introducing the same into said residual reaction mixture separately from said catalyst composition; withdrawing a product stream comprising low molecular weight, highly reactive polyisobutylene from said reaction zone; and controlling the introduction of said feedstock into said reaction zone and the withdrawal of said product stream from the reaction zone such that the residence time of the isobutylene undergoing polymerization in the reaction zone is no greater than about 4 minutes.

20. A liquid phase polymerization process as set forth in claim 19 , wherein said polyisobutylene has an average molecular weight in the range of from about 500 to about 5000 and a vinylidene content of at least 70%, said catalyst composition comprises a complex of BF 3 and a C 1 to C 8 primary alcohol, and the amount of catalyst complex introduced into said reaction zone is controlled such that about 0.1 to about 10 millimoles of BF 3 are introduced for each mole of isobutylene introduced in said feedstock.

21. A liquid phase polymerization process as set forth in claim 19 , wherein said polyisobutylene has an average molecular weight in the range of from about 950 to about 1050, a polydispersity within the range of from about 1.3 to about 1.5 and a vinylidene content of at least about 80%, said feedstock comprises at least about 40% by weight isobutylene, said catalyst composition comprises a complex of BF 3 and methanol, the amount of catalyst complex introduced into said reaction zone is controlled such that about 0.5 to about 2 millimoles of BF 3 are introduced for each mole of isobutylene introduced in said feedstock, and the introduction of said feedstock into said reaction zone and the withdrawal of said product stream from the reaction zone are controlled such that the residence time of the isobutylene undergoing polymerization in the reaction zone is within the inclusive range of from about 45 to about 90 seconds.

22. A process as set forth in claim 19 , said reaction zone comprising a loop reactor wherein the reaction admixture is continuously recirculated at a first volumetric flow rate, and said feedstock and said catalyst composition are continuously introduced at a combined second volumetric flow rate.

23. A process as set forth in claim 20 , said reaction zone comprising a loop reactor wherein the reaction admixture is continuously recirculated at a first volumetric flow rate, and said feedstock and said catalyst composition are continuously introduced at a combined second volumetric flow rate.

24. A process as set forth in claim 21 , said reaction zone comprising a loop reactor wherein the reaction admixture is continuously recirculated at a first volumetric flow rate, and said feedstock and said catalyst composition are continuously introduced at a combined second volumetric flow rate.

25. A process as set forth in claim 18 or 19 , wherein said catalyst modifier comprises essentially the same composition as said complexing agent.

26. A process as set forth in claim 18 or 19 , wherein said catalyst modifier comprises a C 1 to C 8 primary alcohol.

27. A process as set forth in claim 18 or 19 , wherein said complexing agent comprises a C 1 to C 8 primary alcohol.

28. A process as set forth in claim 25 , wherein said same composition comprises a C 1 to C 8 primary alcohol.

29. A process as set forth in claim 18 or 19 , wherein said catalyst modifier comprises methanol.

30. A process as set forth in claim 18 or 19 , wherein said complexing agent comprises methanol.

31. A process as set forth in claim 25 , wherein said same composition comprises methanol.

32. A process as set forth in claim 19 , 22 , 23 or 24 , wherein said feedstock comprises at least about 30% by weight of said isobutylene.

33. A process as set forth in claim 18 , 19 , 20 or 21 , wherein the reaction zone is a tube side of a shell-and-tube reactor and the heat of reaction is removed simultaneously with its generation by circulation of a coolant in the shell side of the exchanger.

34. A process as set forth in claim 29 , wherein a heat transfer coefficient U of at least about 50 Btu/min ft 2 ° F. is maintained in the reaction zone.

35. A process as set forth in claim 18 , 19 , 20 or 21 , wherein said recirculation rate is sufficient to establish a Reynolds number of at least about 2000 in said zone.

36. A process as set forth in claim 18 , 19 , 20 or 21 , wherein is included a step of adding a quenching material capable of killing the catalyst to the withdrawn product stream.

Assignments (32)
RELEASE OF SECURITY INTEREST Recorded Dec 16, 2024
From: GLAS TRUST COMPANY LLC
To: TPC GROUP LLC
Reel/Frame 069602/0182 →
TERMINATION AND RELEASE OF SUPPLEMENTAL GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS AT REEL/FRAME 055119/0158 Recorded Dec 20, 2022
From: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS SUCCESSOR COLLATERAL AGENT TO U.S. BANK NATIONAL ASSOCIATION
To: TPC GROUP LLC
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TERMINATION AND RELEASE OF SUPPLEMENTAL GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS AT REEL/FRAME 049949/0024 Recorded Dec 20, 2022
From: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS SUCCESSOR COLLATERAL AGENT TO U.S. BANK NATIONAL ASSOCIATION
To: TPC GROUP LLC
Reel/Frame 062171/0658 →
TERMINATION AND RELEASE OF GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS AT REEL/FRAME 060287/0820 Recorded Dec 20, 2022
From: GLAS AMERICAS LLC, AS COLLATERAL AGENT
To: TPC GROUP LLC
Reel/Frame 062171/0674 →
SECURITY INTEREST Recorded Dec 16, 2022
From: TPC GROUP LLC
To: ECLIPSE BUSINESS CAPITAL LLC, AS COLLATERAL AGENT
Reel/Frame 062130/0001 →
SECURITY INTEREST Recorded Dec 16, 2022
From: TPC GROUP LLC
To: GLAS TRUST COMPANY LLC, AS COLLATERAL AGENT
Reel/Frame 062130/0137 →
RELEASE OF SECURITY INTEREST AT REEL/FRAME 60113/0169 Recorded Dec 16, 2022
From: ECLIPSE BUSINESS CAPITAL LLC, AS AGENT
To: TPC GROUP LLC
Reel/Frame 062142/0523 →
RELEASE OF SECURITY INTEREST AT REEL/FRAME 29644/0870 Recorded Jun 8, 2022
From: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
To: TPC GROUP LLC
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GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS Recorded Jun 6, 2022
From: TPC GROUP LLC
To: GLAS AMERICAS LLC, AS COLLATERAL AGENT
Reel/Frame 060287/0820 →
SECURITY INTEREST Recorded Jun 6, 2022
From: TPC GROUP LLC
To: ECLIPSE BUSINESS CAPITAL LLC, AS AGENT
Reel/Frame 060113/0169 →
SECURITY INTEREST Recorded Feb 2, 2021
From: TPC GROUP LLC
To: U.S. BANK NATIONAL ASSOCIATION, AS AGENT
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TERMINATION AND RELEASE OF SECURITY INTEREST IN UNITED STATES TRADEMARKS AND PATENTS Recorded Aug 6, 2019
From: U.S. BANK NATIONAL ASSOCIATION, AS SUCCESSOR COLLATERAL AGENT TO WELLS FARGO BANK, NATIONAL ASSOCIATION
To: TPC GROUP LLC
Reel/Frame 049970/0375 →
CONFIRMATION OF SUCCESSION OF AGENCY Recorded Aug 5, 2019
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
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TERMINATION AND RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY Recorded Aug 2, 2019
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CONFIRMATION OF TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENT RIGHTS Recorded Aug 2, 2019
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SECURITY AGREEMENT Recorded Aug 2, 2019
From: TPC GROUP LLC
To: U.S. BANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 049949/0024 →
SECURITY INTEREST Recorded Jan 15, 2016
From: TPC GROUP LLC
To: RIVERSTONE CREDIT PARTNERS, L.P.
Reel/Frame 037499/0246 →
RELEASE OF SECURITY INTEREST Recorded Jan 16, 2013
From: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT
To: TPC GROUP LLC
Reel/Frame 029639/0200 →
SECURITY AGREEMENT Recorded Jan 16, 2013
From: TPC GROUP LLC
To: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 029644/0870 →
SECURITY AGREEMENT Recorded Jan 16, 2013
From: TPC GROUP LLC
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 029644/0910 →
SECURITY AGREEMENT Recorded Oct 14, 2010
From: TPC GROUP LLC (F/K/A TEXAS PETROCHEMICALS LP)
To: DEUTSCHE BANK TRUST COMPANY AMERICAS
Reel/Frame 025137/0398 →
RELEASE OF SECURITY INTEREST Recorded Oct 13, 2010
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CERTIFICATE OF CONVERSION Recorded May 25, 2010
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CHANGE OF NAME Recorded May 25, 2010
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RELEASE OF SECURITY INTEREST IN U.S. PATENTS Recorded May 5, 2010
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CHANGE OF NAME Recorded Feb 1, 2010
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To: TPC GROUP LLC
Reel/Frame 023870/0598 →
CONVERSION OF TEXAS PETROCHEMICALS LP Recorded Dec 18, 2008
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To: TEXAS PETROCHEMICALS LLC
Reel/Frame 021998/0966 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 28, 2005
From: BAXTER JR., C. EDWARD; REID SR., RUSSELL E.
To: TEXAS PETROCHEMICALS LP
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ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 3, 2005
From: BAXTER, JR., C. EDWARD; REID, SR., RUSSELL E.
To: TEXAS PETROCHEMICALS LP
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ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 19, 2004
From: LOBUE, CHRISTOPHER; VALDEZ, GILBERT; HERNDON, DANIEL
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