IP Library Patent Application 12156844
Patent Application
App. No. 12/156,844

Bimodal polyethylene process and products

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Patent No.
US None
App. No.
12/156,844
Abstract

Bimodal polyethylene resins having reduced long-chain branching and suitable for use in pipe resin applications as a result of their improved SCG and RCP resistance are provided. The improved resins of the invention are produced in a two-reactor cascade slurry polymerization process using a Ziegler-Natta catalyst system and wherein an alkoxysilane modifier is present in both reactors.

Claims (20)

1 . A process for making a bimodal polyethylene resin comprising:

(a) polymerizing ethylene in the absence or substantial absence of comonomer in a first reactor in the presence of a high activity solid transition metal-containing catalyst, organoaluminum cocatalyst, hydrogen and alkoxysilane to produce a polymerizate containing a first polymer;

(b) removing substantially all hydrogen from the polymerizate and transferring to a second reactor; and

(c) adding ethylene, a C 4-8 α-olefin comonomer and hydrogen to the second reactor and continuing the polymerization to produce a bimodal polyethylene product comprised of said first polymer and a second polymer of relatively lower density and higher molecular weight than that of the first polymer.

2 . The process of claim 1 wherein the weight ratio of first polymer to second polymer is from 65:35 to 40:60.

3 . The process of claim 1 wherein the alkoxysilane has the formula R* 4-y Si (OR*) y where y is 2 or 3 and R* is independently an alkyl or cycloalkyl group.

4 . The process of claim 3 wherein the alkoxysilane is selected from the group consisting of cyclohexylmethyldimethoxysilane and methyltriethoxysilane and mixtures thereof.

5 . The process of claim 1 wherein the α-olefin comonomer is selected from the group consisting of butene-1, hexene-1 and octene-1 and mixtures thereof.

6 . The process of claim 1 wherein the polymerizations are carried out in an inert hydrocarbon.

7 . The process of claim 1 wherein the alkoxysilane is cyclohexylmethyldimethoxysilane and the α-olefin comonomer is butene-1.

8 . The process of claim 2 wherein the weight ratio of first polymer to second polymer is from 60:40 to 45:55.

9 . The process of claim 2 wherein conditions in the first reactor are maintained to target the formation of first polymer having a density of 0.964 g/cm 3 or above and MI 2 in the range 50 to 400 g/10 min and conditions in the second reactor are maintained to target a final bimodal product density of 0.946 to 0.955 g/cm 3 and final bimodal product HLMI of 3 to 16 g/10 min.

10 . The process of claim 9 wherein the polymerizations are carried out in an inert hydrocarbon, the alkoxysilane is cyclohexylmethyldimethoxysilane and the α-olefin comonomer is butene-1.

11 . A bimodal polyethylene resin comprised of a first low molecular weight high density polyethylene component and a second higher molecular weight lower density polyethylene component produced by the process of claim 1 , said resin having a density of 0.945 to 0.956 g/cm 3 , HLMI of 2 to 20 g/10 min and trefBR index of 0.001 to 0.5.

12 . The bimodal polyethylene resin of claim 11 wherein the weight ratio of first polyethylene component to second polyethylene component is from 60:40 to 45:55.

13 . The bimodal polyethylene resin of claim 11 wherein the first polyethylene component has a density of 0.964 to 0.975 g/cm 3 and MI 2 of 100 to 300 g/10 min.

14 . The bimodal polyethylene resin of claim 13 having a density of 0.947 to 0.954, HLMI from 4 to 14 g/10 min and trefBR index from 0.01 to 0.2.

15 . The bimodal resin of claim 14 wherein the second polyethylene component is a copolymer of ethylene and butene-1.

16 . A bimodal polyethylene resin produced by the process of claim 10 comprised of a first low molecular weight high density polyethylene component having a density of 0.966 to 0.975 g/cm 3 and MI 2 of 150 to 250 g/10 min and a second higher molecular weight lower density ethylene-butene-1 copolymer component, said bimodal polyethylene resin having a density from 0.947 to 0.954 g/cm 3 , HLMI from 4 to 14 g/10 min and trefBR index from 0.01 to 0.2.

17 . Extruded pipe comprising the resin of claim 11 .

Assignments (14)
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: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
To: EQUISTAR CHEMICALS, LP
Reel/Frame 024337/0186 →
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 21, 2008
From: MEHTA, SAMEER; REINKING, MARK K.; JOSEPH, SEBASTIAN; GARRISON, PHILIP J.; LEWIS, EVERTT O.; SCHWAB, THOMAS J.; YAU, WALLACE W.
To: EQUISTAR CHEMICALS
Reel/Frame 021422/0587 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 18, 2008
From: MEHTA, SAMEER D.; REINKING, MARK K.; JOSEPH, SEBASTIAN; GARRISON, PHILIP J.; LEWIS, EVERETT O.; SCHWAB, THOMAS J.; YAU, WALLACE W.
To: EQUISTAR CHEMICALS, LP
Reel/Frame 021413/0889 →