IP Library Granted Patent US 8,470,939
Granted Patent B2
US 8,470,939 · App. 11/809,688 · Granted Jun 25, 2013

Preparation of polyethylene

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Quick Facts
Patent No.
US 8,470,939
App. No.
11/809,688
Granted
Jun 25, 2013
Kind
B2
Abstract

A process for preparing a polyethylene in a multi-stage process is described. The process comprises pre-treating a Ziegler catalyst in a first stage in the presence of a 1-olefin/ethylene mixture or a 1-olefin to produce a LLDPE or VLDPE, which have the characteristics of a polymer prepared with a single-site catalyst, e.g. high levels of short-chain branching that are uniformly distributed. The contents of the first stage are then transferred to a second stage where an ethylene or an ethylene/1-olefin mixture is polymerized in the presence of the pre-treated catalyst to form a polyethylene with good processability.

Claims (17)

1. A process of preparing a polyethylene, the process comprising:

(a) in a first stage, pre-treating a Ziegler catalyst by contacting the Ziegler catalyst and co-catalyst with a 1-olefin or a 1-olefin/ethylene mixture having a molar ratio of 1-olefin/ethylene within the range of about 0.8 to about 4.0, at a temperature within the range of about 55° C. to about 120° C., and for a time of from about 15 seconds to about 15 minutes; and

(b) in a second stage, polymerizing ethylene or an ethylene/1-olefin mixture having a molar ratio of ethylene/1-olefin within the range of about 1/0.001 to about 1/0.2, in the presence of the pre-treated catalyst,

wherein the Ziegler catalyst comprises a transition metal and an alkyl magnesium silyl amide complex, wherein the transition metal is selected from the group consisting of Ti, Zr, V, Cr and mixtures thereof, and an alkyl aluminum co-catalyst, and wherein a polymer produced in the first stage has a density within the range of about 0.88 g/cm 3 to about 0.92 g/cm 3 , a molecular weight distribution less than or equal to about 4.0, and an ER within the range of about 1.0 to about 3.0, and wherein the first and second stages are gas-phase or super-critical phase processes.

2. The process of claim 1 , wherein the catalyst is pretreated for about 30 seconds to about 8 minutes.

3. The process of claim 1 , wherein the catalyst is pretreated for about 45 seconds to about 5 minutes.

4. The process of claim 1 , wherein the temperature in the first stage is within the range of about 60° C. to about 95° C.

5. The process of claim 1 , wherein the amount of the polymer produced in the first stage is less than about 3 wt. % of the total amount of the polyethylene, produced in the first and second stages.

6. The process of claim 1 , wherein the polymer produced in the first stage has a density within the range of about 0.89 g/cm 3 to about 0.91 g/cm 3 .

7. The process of claim 1 , wherein the polymer produced in the first stage has an amount of short chain branching (SCB) within the range of about 30 to about 60 SCB/1000 carbon atoms.

8. The process of claim 7 , wherein the SCB is concentrated in the high molecular weight region of the polyethylene.

9. The process of claim 1 , wherein the co-catalyst is selected from the group consisting of alkyl alumoxanes, alkylaluminum compounds, aluminoboronates, organoboranes, ionic borates, ionic aluminates, and mixtures thereof.

10. The process of claim 1 , wherein the co-catalyst is an alumoxane or a derivative thereof.

11. The process of claim 1 , wherein the co-catalyst is diisobutyl alumoxane.

12. The process of claim 1 , wherein the polyethylene produced from the first and second stages has a density of about 0.910 g/cm 3 to about 0.968 g/cm 3 .

13. The process of claim 1 , wherein the 1-olefin in the first stage and second stage is independently selected from the group consisting of propylene, 1-butene, 1-pentene, 1-hexane, 1-octene, 4-methyl-1-pentene, and mixtures thereof.

14. The process of claim 1 , wherein the molar ratio of ethylene/1-olefin in the second stage is within the range of about 1/0.07 to about 1/0.15.

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 Jun 1, 2007
From: LYNCH, MICHAEL W.; MEVERDEN, CRAIG C.
To: EQUISTAR CHEMICALS, LP
Reel/Frame 019942/0271 →