IP Library Granted Patent US 7,666,960
Granted Patent B2
US 7,666,960 · App. 11/403,296 · Granted Feb 23, 2010

Process for the production of ethylene copolymers

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Quick Facts
Patent No.
US 7,666,960
App. No.
11/403,296
Granted
Feb 23, 2010
Kind
B2
Abstract

A process for the copolymerization of ethylene and α-olefins which utilizes a mixed modifier comprised of a conjugated diene and alkoxysilane is disclosed.

Claims (12)

1. In a process for the copolymerization of ethylene with a C 3-8 α-olefin comonomer utilizing a transition metal-containing catalyst and organoaluminum cocatalyst, to modify short-chain branching characteristics, the improvement comprising conducting the copolymerization in an inert hydrocarbon medium in the presence of a mixed modifier comprised of a conjugated diene containing 4 to 12 carbon atoms and an alkoxysilane of the formula R′ 4-y Si(OR) y where y is 2 or 3, R is an alkyl group having from 1 to 10 carbon atoms and R′ is a C 1-10 alkyl or C 6-10 aryl group; said conjugated diene present in an amount from about 100 to 5000 ppm based on the weight of the hydrocarbon and said alkoxysilane present in an amount from about 1 to 50 ppm based on the weight of the hydrocarbon.

2. The process of claim 1 wherein the conjugated diene is selected from the group consisting of 1,3-butadiene, 1,3-pentadiene, 1,3-hexadiene and 2-methyl-1,3-butadiene.

3. The process of claim 1 wherein R and R′ of the alkoxysilane are C 1-6 linear or cyclic alkyl groups.

4. The process of claim 3 wherein the alkoxysilane is a monoalkyltrialkoxysilane or dialkyldialkoxysilane.

5. The process of claim 4 wherein the alkoxysilane is cyclohexylmethyldimethoxysilane.

6. The process of claim 4 wherein the alkoxysilane is methyltriethoxysilane.

7. The process of claim 1 wherein the conjugated diene is present in an amount from about 250 to 4000 ppmw and the alkoxysilane is present in an amount from about 2.5 to 40 ppmw.

8. The process of claim 1 wherein the copolymerization is conducted as one stage of a multi-stage polymerization process.

9. The process of claim 8 wherein the polymerization stages are conducted in series.

10. The process of claim 9 wherein ethylene is homopolymerized in a first stage and homopolymer produced therein fed to a second stage where the copolymerization is conducted in the presence of said homopolymer and mixed modifier.

11. The process of claim 9 wherein ethylene is copolymerized in a first stage and copolymer produced therein fed to a second stage where further copolymerization is conducted in the presence of said copolymer and mixed modifier.

12. The process of claim 8 wherein the polymerization stages are conducted in parallel.

Assignments (18)
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 →
RELEASE OF SECURITY INTEREST Recorded May 4, 2010
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: EQUISTAR CHEMICALS, LP
Reel/Frame 024329/0535 →
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 6, 2007
From: LYNCH, MICHAEL W.; REINKING, MARK K.
To: EQUISTAR CHEMICALS, LP
Reel/Frame 019553/0083 →