IP Library Granted Patent US 7,659,346
Granted Patent B2
US 7,659,346 · App. 11/528,411 · Granted Feb 9, 2010

Process for maleating polymerization residues and products

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Quick Facts
Patent No.
US 7,659,346
App. No.
11/528,411
Granted
Feb 9, 2010
Kind
B2
Abstract

A process for converting distillation residues obtained from polymerization processes to useful maleated products is provided.

Claims (22)

1. A process for the maleation of a distillation residue containing 4 to 10 weight percent hydrocarbon diluent, 5 to 20 weight percent polyethylene having a density of 0.940 to 0.955 g/cm 3 and melt index according to ASTM D 1238-01, condition 190/2.16 of 0.02 to 0.3 g/10 min, 60 to 90 weight percent polyethylene wax having a number average molecular weight from 100 to 30000 and 0.2 to 1 weight percent catalyst residue, comprising:

(a) treating the distillation residue to remove hydrocarbon diluent;

(b) incorporating 1 to 10 weight percent maleic anhydride, based on the weight of the distillation residue;

(c) incorporating 0.25 to 6 weight percent organic peroxide, based on the weight of the distillation residue;

(d) heating the mixture above the decomposition temperature of the organic peroxide until the maleic anhydride is reacted; and

(e) recovering the maleated product.

2. The process of claim 1 wherein the hydrocarbon diluent is hexane.

3. The process of claim 1 wherein (a) is conducted at a temperature in the range 120° C. to 150° C.

4. The process of claim 1 wherein the residue treated in accordance with (a) contains less than 200 ppm hydrocarbon.

5. The process of claim 1 wherein the maleic-anhydride incorporation is carried out in the melt state.

6. The process of claim 5 wherein the amount of maleic anhydride incorporated is from 1.5 to 8 weight percent.

7. The process of claim 1 wherein the organic peroxide incorporation is carried out in the melt state at a temperature below the decomposition temperature of the organic peroxide.

8. The process of claim 7 wherein the amount of the organic peroxide incorporated is from 0.5 to 5 weight percent.

9. The process of claim 1 wherein (d) is conducted at a temperature in the range 103° C. to 200° C.

10. The maleated product produced by the process of claim 1 which contains from 0.5 to 7 weight percent bound maleic anhydride.

11. The maleated product of claim 10 further characterized by having shear dependent viscosity.

12. A process for the maleation of a distillation residue obtained from a process for the polymerization of ethylene, said distillation residue containing 4 to 10 weight percent hydrocarbon diluent, 5 to 20 weight percent polyethylene having a density of 0.940 to 0.955 g/cm 3 and melt index according to ASTM D 1238-01, condition 190/2.16 of 0.02 to 0.3 g/10 mm, 60 to 90 weight percent polyethylene waxes having a number average molecular weight from 100 to 30000 and 0.2 to 1 weight percent catalyst residue, comprising:

(a) heating the distillation residue at a temperature of 120° C. to 150° C. to remove hydrocarbon diluent;

(b) maintaining the residue obtained from (a) containing less than 200 ppm hydrocarbon diluent in a molten state and incorporating from 1 to 10 weight percent maleic anhydride;

(c) incorporating 0.25 to 6 weight percent organic peroxide into the melt containing the maleic anhydride from (b) while maintaining the temperature of said melt below the decomposition temperature of the organic peroxide;

(d) increasing the temperature of the mixture from (c) above the decomposition temperature of the organic peroxide and maintaining until the maleic anhydride is reacted; and

(e) recovering the maleated product.

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 Nov 20, 2006
From: LEE, CHUN D.; JONES, JEFFREY A.
To: EQUISTAR CHEMICALS, LP
Reel/Frame 018581/0462 →