Cross-linkable polymeric compositions, methods for making the same, and articles made therefrom
US-2015299494-A1 · Oct 22, 2015 · US
US10513625B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10513625-B2 |
| Application number | US-201214441018-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 29, 2012 |
| Priority date | Dec 29, 2012 |
| Publication date | Dec 24, 2019 |
| Grant date | Dec 24, 2019 |
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Cross-linkable polymeric compositions comprising an ethylene-based polymer, an organic peroxide, an optional cross-linking coagent, and an antioxidant. Such cross-linkable polymeric compositions are prepared by imbibing at least a portion of the organic peroxide, the optional cross-linking coagent, and the antioxidant into the ethylene-based polymer. Such cross-linkable polymeric compositions can be employed in forming coated conductors.
Opening claim text (preview).
The invention claimed is: 1. A process for preparing a cross-linkable polymeric composition, said process comprising: combining an ethylene-based polymer with an organic peroxide and an antioxidant to thereby form said cross-linkable polymeric composition, wherein said combining step comprises imbibing at least a portion of said organic peroxide and at least a portion of said antioxidant into said ethylene-based polymer, wherein said combining step employs no compounding procedure; wherein said imbibing is effected by immersing or coating at least a portion of said ethylene-based polymer, as pellets, with said organic peroxide and said antioxidant for a time and temperature sufficient to effect such imbibing. 2. The process of claim 1 , wherein said organic peroxide is selected from the group consisting of dicumyl peroxide; tert-butyl peroxybenzoate; di-tert-amyl peroxide; bis(alpha-t-butyl-peroxyisopropyl) benzene; isopropylcumyl t-butyl peroxide; t-butylcumylperoxide; di-t-butyl peroxide; 2,5-bis(t-butylperoxy)-2,5-dimethylhexane; 2,5-bis(t-butylperoxy)-2,5-dimethylhexyne-3; 1,1-bis(t-butylperoxy)3,3,5-trimethylcyclohexane; isopropylcumyl cumylperoxide; butyl 4,4-di(tert-butylperoxy)valerate; di(isopropylcumyl) peroxide; and mixtures of two or more thereof; wherein said antioxidant is a hindered phenol, a less hindered phenol, a thio compound, a siloxane, an amine, or mixtures of two or more thereof. 3. The process of claim 1 , wherein said organic peroxide is dicumyl peroxide; wherein said antioxidant comprises one or more components selected from the group consisting of distearyl thiodipropionate, dilauryl thiodipropionate, octadecyl-3,5-di-t-butyl-4-hydroxyhydrocinnamate, benzenepropanoic acid,3,5-bis(1,1-dimethylethyl)-4-hydroxy-thiodi-2,1-ehtanediyl ester, stearyl 3-(3,5-di-t-butyl-4-hydroxyphenyl) propionate, octadecyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl)-propionate, 2,4-bis(dodecylthiomethyl)-6-methylphenol, 4,4′-thiobis(6-tert-butyl-m-cresol), 4,6-bis(octylthiomethyl)-o-cresol, 1,3,5-tris(4-tert-butyl-3-hydroxy-2,6-dimethyl benzyl)- 1,3,5-triazine-2,4,6-(1H,3H,5H)-trione, pentaerythritol tetrakis(3-(3,5-di-t-butyl- 4 -hydroxyphenyl)propionate), 2′,3-bis[[3-[3,5-di-tert-butyl-4-hydroxyphenyl]propionyl]] propionohydrazide, and mixtures of two or more thereof; wherein said ethylene-based polymer is a low-density polyethylene (“LDPE”). 4. The process of claim 1 , further comprising pre-mixing said organic peroxide and said antioxidant to thereby form a mixture and thereafter at least partially immersing or coating said ethylene-based polymer in said mixture to effect said imbibing. 5. The process of claim 4 , wherein said mixture has an initial heat release temperature of at least 120° C. 6. The process of claim 1 , further comprising combining a cross-linking coagent with said ethylene-based polymer, said organic peroxide, and said antioxidant, wherein at least a portion of said cross-linking coagent is imbibed into said ethylene-based polymer. 7. The process of claim 6 , wherein said ethylene-based polymer is present in said cross-linkable polymeric composition in an amount ranging from 50 to 99 weight percent, based on the entire weight of the cross-linkable polymeric composition; wherein said organic peroxide is present in said cross-linkable polymeric composition in an amount ranging from 0.1 to 5 weight percent, based on the entire weight of the cross-linkable polymeric composition; wherein said cross-linking coagent is present in said cross-linkable polymeric composition in an amount ranging from 0.1 to 3 weight percent, based on the entire weight of the cross-linkable polymeric composition; wherein said antioxidant is present in said cross-linkable polymeric composition in an amount ranging from 0.01 to 1 weight percent based on the entire weight of the cross-linkable polymeric composition. 8. A process comprising treating at least a portion of said cross-linkable polymeric composition according to claim 1 in a heated cure zone thereby forming a cross-linked polymeric composition, wherein said cross-linked polymeric composition has a cross-link density (“MH-ML”) of at least 2.5 dN·m. 9. A process for producing a coated conductor, said process comprising: (a) premixing an organic peroxide and an antioxidant to thereby form an initial mixture; (b) at least partially immersing or coating an ethylene-based polymer, as pellets, in said initial mixture and allowing said ethylene-based polymer to at least partially imbibe said initial mixture to thereby form a cross-linkable polymeric composition comprising said ethylene-based polymer, at least a portion of said organic peroxide and at least a portion of said antioxidant; (c) coating a conductor with at least a portion of said cross-linkable polymeric composition; and (d) curing or allowing to cure at least a portion of said cross-linkable polymeric composition on said conductor, thereby forming said coated conductor wherein step (b) employs no compounding procedure. 10. The process of claim 9 , wherein said organic peroxide is dicumyl peroxide; wherein said antioxidant comprises one or more components selected from the group consisting of distearyl thiodipropionate, dilauryl thiodipropionate, octadecyl-3,5-di-t-butyl-4-hydroxyhydrocinnamate, benzenepropanoic acid,3,5-bis(1,1-dimethylethyl)-4-hydroxy-thiodi-2,1-ehtanediyl ester, stearyl 3-(3,5-di-t-butyl-4-hydroxyphenyl) propionate, octadecyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl)-propionate, 2,4-bis(dodecylthiomethyl)-6-methylphenol, 4,4′-thiobis(6-tert-butyl-m-cresol), 4,6-bis(octylthiomethyl)-o-cresol, 1,3,5-tris(4-tert-butyl-3-hydroxy-2,6-dimethyl benzyl)-1,3,5-triazine-2,4,6-(1H,3H,5H)-trione, pentaerythritol tetrakis(3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate), 2′, 3-bis[[3-[3,5-di-tert-butyl-4-hydroxyphenyl]propionyl]] propionohydrazide, and mixtures of two or more thereof; wherein said ethylene-based polymer is a low-density polyethylene (“LDPE”); wherein said imbibing of step (b) is performed at a temperature ranging from greater than the melting temperature of said initial mixture to less than the melting temperature of said ethylene-based polymer.
Phenols containing ester groups · CPC title
Homopolymers or copolymers of ethene · CPC title
from alkenes · CPC title
use in electrical wires or wirecoating · CPC title
Peroxides · CPC title
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