IP Library Granted Patent US 7,060,787
Granted Patent B2
US 7,060,787 · App. 10/846,735 · Granted Jun 13, 2006

Extraction of impurities from grafted polyolefins

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Quick Facts
Patent No.
US 7,060,787
App. No.
10/846,735
Granted
Jun 13, 2006
Kind
B2
Abstract

A process for purifying grafted polyolefins by extraction is disclosed. The purified grafted polyolefins have improved color and adhesion properties. The extraction is performed with an azeotropic solvent that is strong enough to extract impurities but does not cause sticking of the grafted polyolefin. The azeotropic solvent can be easily recycled.

Claims (20)

1. A process which comprises extracting a mixture comprising a grafted polyolefin and low molecular weight impurities with an azeotropic solvent and drying the purified grafted polyolefin, wherein the azeotropic solvent is a liquid mixture of two or more substances that behaves like a single substance in that vapor produced by partial evaporation of the liquid mixture has the same composition as that of the liquid mixture.

2. The process of claim 1 wherein the used azeotropic solvent is distilled to recover a purified azeotropic solvent.

3. The process of claim 1 wherein the grafted polyolefin is a grafted polypropylene or a grafted propylene copolymer.

4. The process of claim 1 wherein the grafted polyolefin is made by grafting a polyolefin with an alkene-containing grafting agent selected from the group consisting of vinyl silanes, dienes, and alkene-containing carboxylic acids and carboxylic acid derivatives.

5. The process of claim 4 wherein the alkene-containing grafting agent is maleic anhydride.

6. The process of claim 1 wherein the grafted polyolefin is polypropylene grafted with maleic anhydride.

7. The process of claim 1 wherein the azeotropic solvent is a binary azeotrope.

8. The process of claim 7 wherein the solvent is a mixture of a C 5 –C 8 hydrocarbon with a C 1 –C 10 oxygen-containing compound.

9. The process of claim 8 wherein the C 1 –C 10 oxygen-containing compound is an aliphatic alcohol, an aliphatic ketone, or an aliphatic ester.

10. The process of claim 9 wherein the oxygen-containing compound is an alkyl acetate.

11. The process of claim 10 wherein the hydrocarbon is hexane and the alkyl acetate is ethyl acetate.

12. The process of claim 1 wherein the grafted polyolefin is extracted with the azeotropic solvent for a period of 3 to 12 hours.

13. The process of claim 1 wherein the azeotropic solvent is boiled through a column containing the grafted polyolefin and low molecular weight impurities.

14. The process of claim 1 wherein the azeotropic solvent has a boiling point from about 35° C. to about 100° C.

15. The process of claim 1 wherein the amount of azeotropic solvent is more than 3 to about 10 parts by weight per grafted polyolefin.

16. A process which comprises extracting a mixture comprising a grafted polyolefin and low molecular weight impurities with an azeotropic solvent, washing the extracted grafted polyolefin with additional azeotropic solvent, and drying the purified grafted polyolefin.

17. A process Which comprises (a) extracting a mixture comprising a maleic anhydride-grafted polypropylene or a maleic anhydride-grafted propylene copolymer and low molecular weight impurities with an azeotropic solvent comprising a hydrocarbon and an alkyl acetate; (b) drying the purified grafted polyolefin; and (c) distilling the used azeotropic solvent to recover a purified azeotropic solvent; wherein the azeotropic solvent is a liquid mixture of two or more substances that behaves like a single substance in that vapor produced by partial evaporation of the liquid mixture has the same composition as that of the liquid mixture.

18. The process of claim 17 wherein after step (a), the extracted mixture is washed with additional azeotropic solvent.

19. The process of claim 18 wherein step (a) is done by immersing the mixture in boiling azeotropic solvent, condensing the vapors that exit the top of the column, and pumping the condensed solvent back to the bottom of the column.

20. The process of claim 19 wherein an inert gas is fed from the bottom of the column in step (a).

Assignments (19)
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: DEUTSCHE BANK TRUST COMPANY AMERICAS
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032123/0799 →
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: CITIBANK, N.A.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032125/0296 →
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032137/0156 →
APPOINTMENT OF SUCCESSOR ADMINISTRATIVE AGENT Recorded Jan 23, 2014
From: UBS AG, STAMFORD BRANCH
To: BANK OF AMERICA, N.A.
Reel/Frame 032137/0639 →
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: BANK OF AMERICA, N.A.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032138/0134 →
SECURITY AGREEMENT Recorded May 19, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 024402/0681 →
SECURITY AGREEMENT Recorded May 18, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 024397/0818 →
SECURITY AGREEMENT Recorded May 7, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 024342/0801 →
SECURITY AGREEMENT Recorded May 6, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT
Reel/Frame 024342/0421 →
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 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: LYONDELL CHEMICAL TECHNOLOGY, LP
Reel/Frame 024337/0285 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: LYONDELL CHEMICAL TECHNOLOGY, LP
Reel/Frame 024337/0020 →
SECURITY AGREEMENT Recorded Oct 30, 2009
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 023449/0138 →
SECURITY AGREEMENT Recorded Apr 9, 2009
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT AND COLLATERAL AGENT
Reel/Frame 022708/0830 →
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 →
CHANGE OF NAME Recorded Feb 3, 2006
From: ARCO CHEMICAL TECHNOLOGY, L.P.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 017118/0140 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 26, 2004
From: GUPTA, VIJAI P.; CAREY, EDWARD P.
To: ARCO CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 015601/0996 →