IP Library Granted Patent US 7,122,497
Granted Patent B1
US 7,122,497 · App. 11/221,287 · Granted Oct 17, 2006

Olefin polymerization catalyst system

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Quick Facts
Patent No.
US 7,122,497
App. No.
11/221,287
Granted
Oct 17, 2006
Kind
B1
Abstract

A catalyst system useful for polymerizing olefins is disclosed. The catalyst system comprises a cocatalyst and a supported transition metal prepared from a halogen-containing Group 4–6 transition metal compound and an organoaluminum-siloxane containing mixture. The latter mixture, which is prepared from an organoaluminum compound and an organomagnesium-siloxane reaction product, incorporates a chelating ligand. The invention includes a method for making the catalyst system and a process for polymerizing olefins using the catalyst system. The process is convenient and avoids expensive catalyst components used in known olefin polymerization processes.

Claims (25)

1. A catalyst system which comprises:

a) a cocatalyst selected from the group consisting of trialkylaluminums, dialkylaluminum halides, and alkylaluminum dihalides; and

b) a supported transition metal comprising the reaction product of:

1) a halogen-containing Group 4–6 transition metal compound; and

2) an organoaluminum-siloxane containing mixture comprising the reaction product of:

(a) an organoaluminum compound; and

(b) the reaction product of a polymethylhydrosiloxane and an organic magnesium halide;

wherein at least one of the organoaluminum compound or the organic magnesium halide incorporates a chelating ligand.

2. The catalyst system of claim 1 wherein the organic magnesium halide incorporates the chelating ligand.

3. The catalyst system of claim 2 wherein the chelating ligand is derived from a hydroxyl compound.

4. The catalyst system of claim 3 wherein the hydroxyl compound is selected from the group consisting of hydroxylamines, 2-hydroxypyridines, 8-hydroxyquinolines, hydroxyimines prepared from 2-hydroxyanilines, and hydroxyimines prepared from 2-hydroxybenzaldehydes.

5. The catalyst system of claim 4 wherein the hydroxyl compound is a hydroxylamine.

6. The catalyst system of claim 1 wherein the organoaluminum compound incorporates a chelating ligand.

7. The catalyst system of claim 6 wherein the chelating ligand is derived from a hydroxyl compound.

8. The catalyst system of claim 7 wherein the hydroxyl compound is selected from the group consisting of hydroxylamines, 2-hydroxypyridines, 8-hydroxyquinolines, hydroxyimines prepared from 2-hydroxyanilines, and hydroxyimines prepared from 2-hydroxybenzaldehydes.

9. The catalyst system of claim 8 wherein the hydroxyl compound is a hydroxylamine.

10. A method for making a catalyst system, comprising:

(a) reacting a polymethylhydrosiloxane with an organic magnesium halide to produce an organomagnesium siloxane;

(b) reacting the organomagnesium siloxane with an organoaluminum compound to produce an organoaluminum-siloxane containing mixture;

(c) reacting the organoaluminum-siloxane containing mixture with a halogen-containing Group 4–6 transition metal compound to produce a supported transition metal; and

(d) combining the supported transition metal with a cocatalyst selected from the group consisting of trialkylaluminums, dialkylaluminum halides, and alkylaluminum dihalides;

wherein at least one of the organic magnesium halide or the organoaluminum compound incorporates a chelating ligand.

11. A process comprising polymerizing an olefin using the catalyst system of claim 1 .

12. The process of claim 11 wherein the olefin is selected from the group consisting of ethylene, propylene, 1-butene, 1-hexene, 1-octene, and mixtures thereof.

13. A slurry polymerization process of claim 11 .

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 Dec 22, 2005
From: NAGY, SANDOR; TSUIE, BARBARA M.
To: EQUISTAR CHEMICALS, LP
Reel/Frame 017383/0637 →