IP Library Granted Patent US 6,884,858
Granted Patent B2
US 6,884,858 · App. 10/208,234 · Granted Apr 26, 2005

Process for preparing polyolefin products

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Quick Facts
Patent No.
US 6,884,858
App. No.
10/208,234
Granted
Apr 26, 2005
Kind
B2
Abstract

A novel liquid phase polymerization process for preparing a polyolefin product having preselected properties is disclosed. The process includes the steps of providing a liquid feedstock which contains an olefinic component and a catalyst composition consisting of a stable complex of BF 3 and a complexing agent therefor. The feedstock may comprise any one or more of a number of olefins including branched olefins such as isobutylene, C 3 to C 15 linear alpha olefins and C 4 to C 15 reactive non-alpha olefins. The feedstock and the catalyst composition are introduced into a residual reaction mixture recirculating in a loop reactor reaction zone provided in the tube side of a shell and tube heat exchanger at a recirculation rate sufficient to cause intimate intermixing of the residual reaction mixture, the added feedstock and the added catalyst composition. The heat of the polymerization reaction is removed from the recirculating intimately intermixed reaction admixture at a rate calculated to provide a substantially constant reaction temperature therein while the same is recirculating in said reaction zone. The conditions in the reactor are appropriate for causing olefinic components introduced in said feedstock to undergo polymerization to form the desired polyolefin product in the presence of the catalyst composition. A product stream containing the desired polyolefin product is withdrawn from the reaction zone. The introduction of the feedstock into the reaction zone and the withdrawal of the product stream from the reaction zone are controlled such that the residence time of the olefinic components undergoing polymerization in the reaction zone is appropriate for production of the desired polyolefin product.

Claims (61)

1. 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, said reaction zone comprising a tube side of a shell-and-tube heat exchanger;

recirculating the residual reaction mixture with the feedstock and the catalyst composition therein in said zone at a recirculation rate sufficient to establish a Reynolds number of at least about 2000 in the zone and thereby 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;

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

adding a quenching material capable of killing the catalyst to the withdrawn product stream; 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.

2. A process as set forth in claim 1 , wherein said heat of reaction is removed simultaneously with its generation by circulation of a coolant in the shell side of the exchanger.

3. A process as set forth in claim 1 , wherein said residence time is no greater than 4 minutes.

4. A process as set forth in claim 1 , wherein said residence time is no greater than 3 minutes.

5. A process as set forth in claim 1 , wherein said residence time is no greater than 2 minutes.

6. A process as set forth in claim 1 , wherein said residence time is no greater than 1 minute.

7. A process as set forth in claim 1 , where said complexing agent comprises an alcohol.

8. A process as set forth in claim 7 , where said complexing agent comprises a C 1 -C 8 alcohol.

9. A process as set forth in claim 7 , where said alcohol comprises methanol.

10. A process as set forth in claim 7 , where said alcohol comprises neopentanol.

11. A process as set forth in claim 1 , where said complexing agent comprises a glycol.

12. A process as set forth in claim 11 , where said complexing agent comprises ethylene glycol.

13. A process as set forth in claim 1 , wherein the molar ratio of BF 3 to complexing agent in said complex ranges from approximately 0.5:1 to approximately 5:1.

14. A process as set forth in claim 1 , wherein the molar ratio of BF 3 to complexing agent in said complex ranges from approximately 0.5:1 to approximately 2:1.

15. A process as set forth in claim 1 , wherein the molar ratio of BF 3 to complexing agent in said complex ranges from approximately 0.5:1 to approximately 1:1.

16. A process as set forth in claim 1 , wherein the molar ratio of BF 3 to complexing agent in said complex is approximately 1:1.

17. A process as set forth in claim 1 , wherein the molar ratio of BF 3 to complexing agent in said complex is approximately 0.75:1.

18. A process as set forth in claim 1 , wherein from about 0.1 to about 10 millimoles of BF 3 are introduced into said reaction admixture with said catalyst composition for each mole of olefinic component introduced into said admixture in said feedstock.

19. A process as set forth in claim 1 , wherein from about 0.5 to about 2 millimoles of BF 3 are introduced into said reaction admixture with said catalyst composition for each mole of olefinic component introduced into said admixture in said feedstock.

20. A process as set forth in claim 1 , wherein the reaction admixture is recirculated at a first volumetric flow rate, and said feedstock and said catalyst composition are introduced at a combined second volumetric flow rate.

21. A process as set forth in claim 20 , wherein the ratio of said first volumetric flow rate to said second volumetric flow rate is such that the concentrations of ingredients in the reaction admixture remain essentially constant.

22. A process as set forth in claim 20 , wherein the ratio of said first volumetric flow rate to said second volumetric flow rate is such that essentially isothermal conditions are established and maintained in said reaction admixture.

23. A process as set forth in claim 20 , wherein said feedstock and said catalyst composition are premixed and introduced into the reaction zone together as a single stream at said second volumetric flow rate.

24. A process as set forth in claim 20 , wherein said feedstock and said catalyst composition are introduced into the reaction zone separately as two streams, the flow rates of which together add up to said second volumetric flow rate.

25. A process as set forth in claim 20 , wherein turbulent flow is maintained in said reaction zone.

26. A process as set forth in claim 25 , wherein a heat transfer coefficient U of at least about 50 Btu/min ft 2 °F. is maintained in said reaction zone.

27. A process as set forth in claim 1 , wherein said feed stock comprises at least 30% by weight of said olefinic component.

28. A process as set forth in claim 1 , wherein said feed stock comprises a non-reactive hydrocarbon diluent.

29. A process as set forth in claim 28 , wherein said feed stock comprises at least 30% by weight of said olefinic component.

30. A process as set forth in claim 1 , wherein said polyolefin product has a molecular weight of no more than 5000.

31. A process as set forth in claim 30 , wherein said polyolefin product has a molecular weight of at least about 350.

32. A process as set forth in claim 31 , wherein the olefinic component comprises isobutylene and the polyolefin product comprises polyisobutylene.

33. A process as set forth in claim 32 , wherein said polyisobutylene has a vinylidene content of at least 50%.

34. A process as set forth in claim 32 , wherein said liquid feedstock comprises a raff-1 stream.

35. A process as set forth in claim 32 , wherein said feed stock comprises an isobutylene concentrate.

36. A process as set forth in claim 32 , wherein said feed stock comprises a dehydro effluent.

37. A process as set forth in claim 30 , wherein said polyolefin product has a molecular weight of at least 250.

38. A process as set forth in claim 1 , wherein said liquid feedstock comprises a raff-1 stream.

39. A process as set forth in claim 1 , wherein said feed stock comprises an isobutylene concentrate.

40. A process as set forth in claim 1 wherein said feed stock comprises a dehydro effluent.

41. A process as set forth in claim 20 , wherein the ratio of said first volumetric flow rate to said second volumetric flow rate ranges from about 20:1 to about 50:1.

42. A process as set forth in claim 41 , wherein the ratio of said first volumetric flow rate to said second volumetric flow rate ranges from about 25:1 to about 40:1.

43. A process as set forth in claim 42 , wherein the ratio of said first volumetric flow rate to said second volumetric flow rate ranges from about 28:1 to about 35:1.

44. A process as set forth in claim 41 , wherein said feed stock comprises at least 30% by weight of said olefinic component.

45. A process as set forth in claim 41 , wherein said feed stock comprises an isobutylene concentrate.

46. A process as set forth in claim 41 wherein said feed stock comprises a dehydro effluent.

47. A process as set forth in claim 41 wherein said feed stock comprises a raff-1 stream.

48. A process as set forth in claim 7 , wherein the olefinic component comprises a C 3 to C 15 linear alpha olefin.

49. A process as set forth in claim 7 , wherein the olefinic component comprises a C 4 to C 15 non-alpha olefin.

50. A process as set forth in claim 49 wherein the olefinic component is 2-butene.

51. A process as set forth in claim 11 , wherein the olefinic component comprises a C 3 to C 15 linear alpha olefin.

52. A process as set forth in claim 11 , wherein the olefinic component comprises a C 4 to C 15 non-alpha olefin.

53. A process as set forth in claim 52 , wherein the olefinic component is 2-butene.

Assignments (32)
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
Reel/Frame 062171/0666 →
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 →
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 →
SECURITY INTEREST Recorded Dec 16, 2022
From: TPC GROUP LLC
To: ECLIPSE BUSINESS CAPITAL LLC, AS COLLATERAL AGENT
Reel/Frame 062130/0001 →
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
Reel/Frame 060307/0955 →
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
Reel/Frame 055119/0158 →
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
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 049962/0956 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY Recorded Aug 2, 2019
From: RIVERSTONE CREDIT PARTNERS, L.P.
To: TPC GROUP, LLC
Reel/Frame 049949/0259 →
SECURITY AGREEMENT Recorded Aug 2, 2019
From: TPC GROUP LLC
To: U.S. BANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 049949/0024 →
CONFIRMATION OF TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENT RIGHTS Recorded Aug 2, 2019
From: DEUTSCHE BANK TRUST COMPANY AMERICAS
To: TPC GROUP LLC
Reel/Frame 049949/0182 →
SECURITY INTEREST Recorded Jan 15, 2016
From: TPC GROUP LLC
To: RIVERSTONE CREDIT PARTNERS, L.P.
Reel/Frame 037499/0246 →
SECURITY AGREEMENT Recorded Jan 16, 2013
From: TPC GROUP LLC
To: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 029644/0870 →
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: 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
From: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT
To: TPC GROUP LLC
Reel/Frame 025126/0712 →
RELEASE OF SECURITY INTEREST RECORDED AT REEL/FRAME 013974/0271 Recorded Jun 16, 2010
From: BANK OF AMERICA, N.A.
To: TEXAS PETROCHEMICALS LP (FORMERLY TEXAS PETROCHEMICALS CORPORATION)
Reel/Frame 024547/0076 →
CERTIFICATE OF CONVERSION Recorded May 25, 2010
From: TEXAS PETROCHEMICALS LP
To: TEXAS PETROCHEMICALS LLC
Reel/Frame 024434/0263 →
CHANGE OF NAME Recorded May 25, 2010
From: TEXAS PETROCHEMICALS LLC
To: TPC GROUP LLC
Reel/Frame 024434/0363 →
RELEASE OF SECURITY INTEREST IN U.S. PATENTS Recorded May 5, 2010
From: U.S. BANK NATIONAL ASSOCIATION
To: TEXAS PETROCHEMICALS LP
Reel/Frame 024337/0518 →
GRANT OF SECURITY INTEREST IN U.S. PATENTS (TERM LOAN) Recorded May 4, 2010
From: TPC GROUP LLC
To: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT
Reel/Frame 024329/0236 →
GRANT OF SECURITY INTEREST IN U.S. PATENTS (REVOLVING LOAN) Recorded May 4, 2010
From: TPC GROUP LLC
To: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT
Reel/Frame 024329/0223 →
CHANGE OF NAME Recorded Feb 1, 2010
From: TEXAS PETROCHEMICALS LLC
To: TPC GROUP LLC
Reel/Frame 023870/0598 →
CONVERSION OF TEXAS PETROCHEMICALS LP Recorded Dec 18, 2008
From: TEXAS PETROCHEMICALS LP
To: TEXAS PETROCHEMICALS LLC
Reel/Frame 021998/0966 →
TERMINATION Recorded Jun 2, 2004
From: CREDIT SUISSE FIRST BOSTON, AS ADMINISTRATIVE AGENT
To: TEXAS PETROCHEMICALS LP
Reel/Frame 015386/0071 →
SECURITY INTEREST Recorded Jun 2, 2004
From: TEXAS PETROCHEMICALS LP
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 015400/0093 →
SECURITY INTEREST Recorded Apr 17, 2003
From: TEXAS PETROCHEMICALS LP
To: BANK OF AMERICA, N.A.
Reel/Frame 013974/0271 →
GRANT OF PATENT SECURITY INTEREST Recorded Nov 26, 2002
From: TEXAS PETROCHEMICALS L.P, A TEXAS LIMITED PARTNERSHIP
To: CREDIT SUISSE FIRST BOSTON, AS ADMINISTRATIVE AGENT
Reel/Frame 013532/0567 →