IP Library Granted Patent US 6,908,972
Granted Patent B2
US 6,908,972 · App. 10/123,774 · Granted Jun 21, 2005

Method for making polyolefins

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Quick Facts
Patent No.
US 6,908,972
App. No.
10/123,774
Granted
Jun 21, 2005
Kind
B2
Abstract

A method for making ethylene polymers and copolymers is disclosed. The method uses a catalyst system comprising a low level of an aluminum-containing activator, a bridged indenoindolyl transition metal complex, and a treated silica support. The method enables economical preparation of ethylene copolymers having very low density. The silica-supported, bridged complexes incorporate comonomers efficiently and are valuable for a commercial slurry loop process. Use of a bridged indeno[2,1-b]indolyl complex provides exceptionally efficient comonomer incorporation, and gives polymers with a substantial and controlled level of long-chain branching. The method facilitates the production of a wide variety of polyolefins, from HDPE to plastomers.

Claims (29)

1. A method which comprises copolymerizing ethylene and a 1-olefin in the presence of a catalyst system comprising (a) an aluminum-containing activator; (b) a bridged, indenoindolyl Group 3-10 transition metal complex; and (c) an alumoxane-treated silica support, to produce a linear low density or plastomeric ethylene copolymer having a density less than 0.930 g/cm 3 , wherein the catalyst system has an aluminum:transition metal [Al:M] mole ratio less than 500.

2. The method of claim 1 wherein the complex includes a Group 4-6 transition metal.

3. The method of claim 1 wherein the complex includes an indeno[2,1-b]indolyl ligand.

4. The method of claim 1 wherein the complex includes an indeno[1 2-b]indolyl ligand.

5. The method of claim 1 wherein the complex incorporates a bridging group selected from the group consisting of methylene, dimethylene, isopropylidene, and dimethylsilyl.

6. The method of claim 1 wherein an indenoindolyl ligand of the complex is covalently bridged to a polymerization-stable ligand selected from the group consisting of cyclopentadienyl, indenyl, and fluorenyl.

7. The method of claim 1 wherein the activator is methylalumoxane or a mixture of methylalumoxane and an organoborane.

8. The method of claim 7 wherein the organoborane is tris-(pentafluorophenyl)borane.

9. The method of claim 1 wherein the [Al:M] mole ratio is less than about 250.

10. The method of claim 1 wherein the 1-olefin is selected from the group consisting of propylene, 1-butene, 1-hexene, 1-octene, and mixtures thereof.

11. The method of claim 1 wherein the ethylene copolymer has a density less than 0.920 g/cm 3 .

12. The method of claim 1 wherein the ethylene copolymer has a density less than 0.910 g/cm 3 .

13. The method of claim 1 wherein the ethylene copolymer has a density less than 0.900 g/cm 3 .

14. The method of claim 1 wherein the ethylene copolymer has a Mw/Mn<4.0.

15. The method of claim 1 performed in the presence of a chain-transfer agent selected from the group consisting of hydrogen, organozinc compounds, and organoaluminum compounds, to produce a copolymer having Mw<150,000.

16. The method of claim 15 wherein the chain-transfer agent is triethylaluminum in combination with hydrogen, and the copolymer has a Mw/Mn<3.5.

17. The method of claim 1 performed in the absence of a chain-transfer agent to produce a copolymer having Mw>400,000.

18. The method of claim 1 wherein the complex incorporates a fluorenyl ligand, and the resulting copolymer has a Mw>200,000.

19. A method which comprises polymerizing ethylene and optionally a 1-olefin in the presence of a catalyst system comprising (a) an aluminum-containing activator; (b) a bridged, indeno[2,1-b]indolyl Group 3-10 transition metal complex; and (c) an alumoxane-treated silica support, to produce an ethylene polymer or copolymer having a long-chain-branching index>0.2, wherein the catalyst system has an aluminum:transition metal [Al:M] mole ratio less than 500.

20. The method of claim 19 wherein the complex incorporates a bridging group selected from the group consisting of methylene, dimethylene, isopropylidene, and dimethylsilyl.

21. The method of claim 19 wherein an indeno[2,1-b]indolyl ligand of the complex is covalently bridged to a polymerization-stable ligand selected from the group consisting of cyclopentadienyl, indenyl, and fluorenyl.

22. The method of claim 19 wherein the [Al:M] mole ratio is less than about 250.

23. The method of claim 19 wherein the polymer or copolymer has a long-chain-branching index>0.5.

24. The method of claim 19 wherein the polymer or copolymer has a long-chain-branching index>1.0.

25. The method of claim 19 wherein the polymer or copolymer has a Mw/Mn<4.0.

26. The method of claim 19 wherein the 1-olefin is selected from the group consisting of propylene, 1-butene, 1-hexene, 1-octene, and mixtures thereof.

27. The method of claim 26 wherein the copolymer is plastomeric and has a density less than 0.915 g/cm 3 .

28. The method of claim 27 wherein the copolymer has a density less than 0.900 g/cm 3 .

29. The method of claim 19 wherein the transition metal complex incorporates a dimethylsilyl bridging group, the 1-olefin is 1-hexene, the mole ratio of 1-hexene to ethylene is at least about 0.3, and the resulting copolymer has a long-chain-branching index>1.0.

Assignments (16)
RELEASE OF SECURITY INTEREST Recorded Jan 22, 2014
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: EQUISTAR CHEMICALS, LP
Reel/Frame 032112/0786 →
APPOINTMENT OF SUCCESSOR ADMINISTRATIVE AGENT Recorded Jan 22, 2014
From: UBS AG, STAMFORD BRANCH
To: BANK OF AMERICA, N.A.
Reel/Frame 032112/0863 →
RELEASE OF SECURITY INTEREST Recorded Jan 22, 2014
From: CITIBANK, N.A.
To: EQUISTAR CHEMICALS, LP
Reel/Frame 032113/0644 →
RELEASE OF SECURITY INTEREST Recorded Jan 22, 2014
From: DEUTSCHE BANK TRUST COMPANY AMERICAS
To: EQUISTAR CHEMICALS, LP
Reel/Frame 032113/0684 →
RELEASE OF SECURITY INTEREST Recorded Jan 22, 2014
From: BANK OF AMERICA, N.A.
To: EQUISTAR CHEMICALS, LP
Reel/Frame 032113/0730 →
SECURITY AGREEMENT Recorded May 19, 2010
From: EQUISTAR CHEMICALS, LP
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 024402/0655 →
SECURITY AGREEMENT Recorded May 18, 2010
From: EQUISTAR CHEMICALS, LP
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 024397/0861 →
SECURITY AGREEMENT Recorded May 7, 2010
From: EQUISTAR CHEMICALS. LP
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 024351/0001 →
SECURITY AGREEMENT Recorded May 6, 2010
From: EQUISTAR CHEMICALS, LP
To: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT
Reel/Frame 024342/0443 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.; EQUISTAR CHEMICALS, LP
Reel/Frame 024337/0705 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
To: EQUISTAR CHEMICALS, LP
Reel/Frame 024337/0186 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.; EQUISTAR CHEMICALS, LP
Reel/Frame 024337/0856 →
SECURITY AGREEMENT Recorded Oct 30, 2009
From: EQUISTAR CHEMICALS, LP
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 023449/0687 →
SECURITY AGREEMENT Recorded Apr 9, 2009
From: EQUISTAR CHEMICALS, LP
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT AND COLLATERAL AGENT
Reel/Frame 022678/0860 →
SECURITY AGREEMENT Recorded Aug 4, 2008
From: BASELL POLYOLEFINE GMBH; ARCO CHEMICAL TECHNOLOGY L.P.; ARCO CHEMICAL TECHNOLOGY, INC.; ATLANTIC RICHFIELD COMPANY; BASELL NORTH AMERICA, INC.; BASELL POLYOLEFIN GMBH; LYONDELL CHEMICAL COMPANY; EQUISTAR CHEMICALS, L.P.
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 021354/0708 →
GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS AND PATENT APPLICATIONS Recorded Mar 26, 2008
From: BASELL POLYOLEFINE GMBH; ARCO CHEMICAL TECHNOLOGY L.P.; ARCO CHEMICAL TECHNOLOGY, INC.; ATLANTIC RICHFIELD COMPANY; BASELL NORTH AMERICA, INC.; EQUISTAR CHEMICALS. LP.; LYONDELL CHEMICAL COMPANY; LYONDELL CHEMICAL TECHNOLOGY, L.P.; LYONDELL PETROCHEMICAL COMPANY; NATIONAL DISTILLERS AND CHEMICAL CORPORATION; OCCIDENTAL CHEMICAL CORPORATION; OLIN CORPORATION; QUANTUM CHEMICAL CORPORATION; BASELL POLYOLEFIN GMBH
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 020704/0562 →