IP Library Granted Patent US 6,939,930
Granted Patent B2
US 6,939,930 · App. 10/657,845 · Granted Sep 6, 2005

Hydrosilane additives for increased polyolefin molecular weight

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 6,939,930
App. No.
10/657,845
Granted
Sep 6, 2005
Kind
B2
Abstract

A process for polymerizing olefins is disclosed. The process uses a hydrosilane in a polymerization catalyzed by an open architecture, bridged indenoindolyl organometallic complex and an activator. Polyolefins from the process have increased molecular weight.

Claims (17)

1. A process which comprises polymerizing an olefin in the presence of a hydrosilane and a catalyst system which comprises an activator and a bridged indenoindolyl Group 4-6 transition metal complex having open archit architure, wherein the hydrosilane is used in an amount effective to increase polyolefin molecular weight.

2. The process of claim 1 wherein the transition metal complex has the general structure selected from the group consisting of:

in which M is a Group 4-6 transition metal, G is a linking group, R is alkyl, aryl, dialkylboryl, or trialkylsilyl, R 1 is C 1 -C 20 hydrocarbyl, X is alkyl, aryl, alkoxy, aryloxy, halide, dlalkylamino, or slioxy, and n satisfies the valence of M.

3. The process of claim 1 wherein the olelin is selected from the group consisting of ethylene, propylene, 1-butene, 1-pentene, 1-hexene, 1-octene and mixtures thereof.

4. The process of claim 1 wherein the activator is selected from the group consisting of alumoxanes, ionic borates, ionic aluminates, alkylaluminums, and aluminoboronates.

5. The process of claim 2 wherein M is a Group 4 transition metal.

6. The process of claim 2 wherein M is Ti or Zr, G is dimethylsilyl, and X is halide or alkyl.

7. The process of claim 1 wherein the polymerization is performed at a temperature within the range of about 30° C. to about 100° C.

8. A slurry polymerization process of claim 1 .

9. A gas-phase polymerization process of claim 1 .

10. The process of claim 1 wherein the hydrosilane has the general structure:

wherein each R 2 is independently selected from the group consisting of hydrogen, C 1 -C 10 hydrocarbyl, and trifluoroalkyl; R 3 is C 1 -C 10 hydrocarbyl; x is an integer from 0 to 200 and R 4 a selected from the group consisting of hydrogen, trialkylsiloxy and C 1 -C 10 hydrocarbyl with the proviso that when x is 0, R 4 is hydrogen.

11. The process of claim 10 wherein R 2 is C 1 -C 10 hydrocarbyl, x is 0 and R 4 is hydrogen.

12. The process of claim 10 wherein x is an integer from 5 to 100, R 2 is C 1 -C 10 hydrocarkyl, and R 4 is trialkylsiloxy.

13. The process of claim 12 wherein R 2 and R 3 are methyl and R 4 is trimethylsiloxy.

14. The process of claim 10 wherein the hydrosilane is used at a level of from about 20 to about 1000 grams of silicon per gram of transition metal.

15. The process of clam 14 wherein the hydrosilane is used at a level of from about 50 to about 500 grams of silicon per gram of transition metal.

Assignments (6)
RELEASE OF SECURITY INTEREST Recorded Mar 13, 2024
From: CITIBANK N.A., AS ADMINISTRATIVE AGENT
To: APPLIED MEDICAL RESOURCES CORPORATION
Reel/Frame 066796/0262 →
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 →