IP Library Patent Application 12460304
Patent Application
App. No. 12/460,304

Polyethylene compositions comprising a polar phenolic antioxidant and reduced dissipation factor, and methods thereof

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Quick Facts
Patent No.
US None
App. No.
12/460,304
Filed
Jul 16, 2009
Examiner
CHIN, HUI H
Art Unit
1762
USPC
524/287
Abstract

A polyethylene composition comprising about 0.0001% to less than 0.22% by weight of a polar phenolic antioxidant, the polar phenolic antioxidant comprising a polar phenolic moiety and a non-polar C 3 -C 30 hydrocarbon moiety, wherein the polyethylene composition comprises a reduced dissipation factor versus the same polyethylene composition comprising less of the same polar phenolic antioxidant.

Claims (28)

1 . A polyethylene composition comprising about 0.0001% to less than 0.22% by weight of a polar phenolic antioxidant, the polar phenolic antioxidant comprising a polar phenolic moiety and a non-polar C 3 -C 30 hydrocarbon moiety, wherein the polyethylene composition comprises a reduced dissipation factor versus the same polyethylene composition comprising less of the same polar phenolic antioxidant.

2 . The polyethylene composition of claim 1 , wherein the non-polar C 3 -C 30 hydrocarbon moiety is a linear or branched C 3 -C 30 alkyl, C 3 -C 30 alkenyl, C 3 -C 30 alkynyl, C 3 -C 30 cycloalkyl group, or C 3 -C 30 aryl group, the C 3 -C 30 cycloalkyl group comprising a C 3 -C 10 cycloalkyl moiety optionally comprising at least one C 1 -C 27 substituent, and the C 3 -C 30 aryl group comprising a C 3 -C 10 aryl moiety optionally comprising at least one C 1 -C 27 substituent.

3 . The polyethylene composition of claim 1 , wherein the non-polar C 3 -C 30 hydrocarbon moiety is selected from a non-polar C 8 -C 25 hydrocarbon moiety, and the C 8 -C 25 hydrocarbon moiety is a linear or branched C 8 -C 25 alkyl, C 8 -C 25 alkenyl, or C 8 -C 25 alkynyl.

4 . The polyethylene composition of claim 1 , wherein the polar phenolic antioxidant is of formula (I):

wherein:

R 1 and R 2 are the same or different, and are selected from linear or branched C 1 -C 10 aliphatic groups, or C 3 -C 10 aryl groups, the C 3 -C 10 aryl groups optionally comprising at least one linear or branched C 1 -C 10 aliphatic substituent;

m ranges from 1 to 20; and

n ranges from 3 to 30.

5 . The polyethylene composition of claim 4 , wherein:

R 1 and R 2 are the same or different, and are selected from a linear or branched C 1 -C 10 alkyl, C 1 -C 10 alkenyl, or C 1 -C 10 alkynyl groups;

m ranges from 1 to 10; and

n ranges from 8 to 25.

6 . The polyethylene composition of claim 1 , wherein the polar phenolic antioxidant is octadecyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl)-propionate.

7 . The polyethylene composition of claim 1 comprising about 0.0005% to about 0.16% by weight of the polar phenolic antioxidant.

8 . The polyethylene composition of claim 1 comprising about 0.02% to about 0.08% by weight of the polar phenolic antioxidant.

9 . The polyethylene composition of claim 1 wherein the reduced dissipation factor is normalized and correlates to the following equation at 2 GHz:

DF PE =−3.8×10 −4 *PPA ppm +(1±0.55)

wherein:

DF PE is the normalized dissipation factor of the polyethylene composition, the normalized dissipation factor being normalized with respect to a value of 1.0; and

PPA ppm is the amount of the polar phenolic antioxidant present within the polyethylene composition in parts per million (ppm).

10 . The polyethylene composition of claim 1 , wherein the reduced dissipation factor ranges from about 5×10 −6 to about 3×10 −5 at 2 GHz.

11 . The polyethylene composition of claim 1 , wherein the reduced dissipation factor ranges from about 7.50×10 −6 to about 2.75×10 −5 at 2 GHz.

12 . The polyethylene composition of claim 1 , wherein the reduced dissipation factor ranges from about 8.8×10 −6 to about 2.5×10 −5 at 2 GHz.

13 . A cable or wire comprising a polyethylene composition comprising about 0.0001% to less than 0.22% by weight of a polar phenolic antioxidant, the polar phenolic antioxidant comprising a polar phenolic moiety and a non-polar C 3 -C 30 hydrocarbon moiety, wherein the cable or wire comprises a reduced dissipation factor versus the same cable or wire comprising less of the same polar phenolic antioxidant.

14 . The cable or wire of claim 12 , wherein the cable or wire is a coaxial cable.

15 . The cable or wire of claim 12 , wherein the polar phenolic antioxidant is added in an amount of about 0.0005% to about 0.16% by weight.

16 . A method for reducing the dissipation factor of a polyethylene composition comprising adding about 0.0001% to less than 0.22% by weight of a polar phenolic antioxidant to the polyethylene composition, the polar phenolic antioxidant comprising a polar phenolic moiety and a non-polar C 3 -C 30 hydrocarbon moiety, wherein the polyethylene composition comprises a reduced dissipation factor versus the same polyethylene composition comprising less of the same polar phenolic antioxidant.

17 . The method of claim 15 , wherein the polar phenolic antioxidant is added in an amount of about 0.0005% to about 0.16% by weight.

Assignments (10)
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 16, 2009
From: HUNDLEY, MICK C.
To: EQUISTAR CHEMICALS, LP
Reel/Frame 023029/0772 →