IP Library Granted Patent US 6,984,677
Granted Patent B2
US 6,984,677 · App. 10/268,636 · Granted Jan 10, 2006

Flame retardant insulation composition having improved scorch resistance

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Quick Facts
Patent No.
US 6,984,677
App. No.
10/268,636
Granted
Jan 10, 2006
Kind
B2
Abstract

Crosslinkable, flame retardant insulation compositions having improved resistance to scorch are provided. The compositions are comprised of a base resin, hydrated inorganic filler, coupling agent and stabilizer and formulated with a peroxide/scorch retardant combination, specifically, a combination of α,α′-bis(t-butylperoxy)diisopropyl benzene and 2,4-diphenyl-4-methyl-1-pentene.

Claims (17)

1. A crosslinkable, flame retardant insulation composition having improved scorch resistance comprising:

1) 20 to 60 wt. % of a base resin selected from the group consisting of ethylene-vinyl carboxylate copolymer, ethylene-alkyl acrylate copolymer and ethylene-alkyl methacrylate copolymer, and having a melt index of 0.1 to 10 g/10 min.;

2) 35 to 75 wt. % hydrated inorganic filler;

3) 0.1 to 2.5 weight percent alkoxysilane coupling agent having 2 or 3 C 1-3 alkoxy substituents;

4) 0.2 to 4.0 wt. % stabilizer comprising at least one hindered phenol stabilizer selected from the group consisting of 4,4′-methylenebis(2,6-di-t-butylphenol); tetrakis[methylene(3,5-di-t-butyl-4-hydroxyhydrocinnamate)]methane; 3,5-trimethyl-2,4,6-tris(3,5-di-t-butyl-4-hydroxybenzyl)-benzene; 1,3,5-tris(3,5-di-t-butyl-4-hydroxybenzyl)-s-triazine 2,4,6(1H,3H,5H)trione; N,N′-bis[3-(3,5-di-t-butyl-4-hydroxyphenyl)propanyl]-hydrazine; octadecyl 3,5-di-t-butyl-4-hydroxyhydrocinnamate; and thiodiethylene bis(3,5-di-tert-butyl-4-hydroxyhydrocinnamate); and

5) 0.4 to 8.0 wt. % of a crosslinking component comprised of α,α′-bis(t-butylperoxy)diisopropyl benzene and 2,4-diphenyl-4-methyl-1-pentene present at a weight ratio of 10:1 to 1:1.

2. The composition of claim 1 wherein the crosslinking component additionally contains a multifunctional crosslinking coagent, the weight ratio of α,α′-bis(t-butylperoxy)diisopropyl benzene to multifunctional crosslinking agent ranging from 10:1 to 1:1.

3. The composition of claim 2 wherein the multifunctional crosslinking agent is selected from the group consisting of triallyl cyanurate, triallyl isocyanurate, diallyl phthalate, trimethylolpropane trimethacrylate, and N,N′-m-phenylene dimaleimide and the weight ratio of α,α′-bis(t-butylperoxy)diisopropyl benzene to multifunctional crosslinking agent is from 3:1 to 1:1.

4. The composition of claim 1 wherein the hydrated inorganic filler is aluminum trihydrate.

5. The composition of claim 1 wherein the alkoxysilane coupling agent is vinyltrimethoxysilane or vinyltriethoxysilane.

6. The composition of claim 1 wherein one or more additional stabilizers selected from the group consisting of thioesters, zinc salts of mercaptobenzimidazoles, aromatic secondary amines, bis alkyl sulfides, polymerized 1,2-dihydro-2,2,4-trimethyl quinoline and tris(3,5-di-t-butyl-4-hydroxybenzyl) isocyanurate are present with the hindered phenol.

7. The composition of claim 1 wherein (1) is present from 40 to 50 wt. %, (2) is present from 50 to 60 wt. %, (3) is present from 0.4 to 1.0 wt. %, (4) is present from 0.75 to 1.5 wt. %, and (5) is present from 1.0 to 4.0 wt. %.

8. The composition of claim 1 wherein the base resin is a copolymer of ethylene and a vinyl ester of a C 2 –C 6 aliphatic carboxylic acid.

9. The composition of claim 8 wherein the base resin has a melt index of 0.3 to 5.0 g/10 min.

10. The composition of claim 8 wherein the base resin is a copolymer of ethylene and 5 to 45 wt. % vinyl acetate.

11. The composition of claim 1 wherein the base resin is a copolymer of ethylene and 10 to 45 wt. % n-butyl acrylate.

12. The composition of claim 11 wherein the base resin has a melt index of 0.3 to 5.0 g/10 min.

Assignments (17)
RELEASE OF SECURITY INTEREST Recorded Jan 22, 2014
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: EQUISTAR CHEMICALS, LP
Reel/Frame 032112/0786 →
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 →
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 →
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 024337/0856 →
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 024337/0705 →
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 →