2018
DOI: 10.1039/c7py01840a
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Orange is the new white: rapid curing of an ethylene-glycidyl methacrylate copolymer with a Ti-bisphenolate type catalyst

Abstract: The here established crosslinking chemistry opens up a by-product free method for rapid curing of epoxy-functionalised polyethylenes.

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Cited by 12 publications
(12 citation statements)
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“…To avoid by‐products associated with peroxide crosslinking, we as well as others have recently explored alternative curing concepts based on click chemistry‐type reactions involving a statistical ethylene–glycidyl methacrylate copolymer, p(E‐ stat ‐GMA), which is commonly used as a compatibilizer for polymer blends . In particular, we found that blending of p(E‐ stat ‐GMA) with a statistical ethylene–acrylic acid copolymer, p(E‐ stat ‐AA), results in a formulation that can be extruded below 140 °C, but allows rapid curing during less than 5 min above 160 °C through a click chemistry‐type reaction between epoxy and carboxyl groups .…”
Section: Introductionmentioning
confidence: 97%
“…To avoid by‐products associated with peroxide crosslinking, we as well as others have recently explored alternative curing concepts based on click chemistry‐type reactions involving a statistical ethylene–glycidyl methacrylate copolymer, p(E‐ stat ‐GMA), which is commonly used as a compatibilizer for polymer blends . In particular, we found that blending of p(E‐ stat ‐GMA) with a statistical ethylene–acrylic acid copolymer, p(E‐ stat ‐AA), results in a formulation that can be extruded below 140 °C, but allows rapid curing during less than 5 min above 160 °C through a click chemistry‐type reaction between epoxy and carboxyl groups .…”
Section: Introductionmentioning
confidence: 97%
“…We as well as others have recently explored the viability of a click chemistry type curing of polyethylene copolymers that feature epoxy functional groups as part of a glycidyl methacrylate comonomer. [21][22][23] Such ethyleneglycidyl methacrylate copolymers are widely used for reactive processing -a common tool for the compatibilization of polymer blends -which, however, requires that the degree of crosslinking is kept low in order to not compromise the flow properties of the resin. [24][25][26][27][28] A variety of functional groups such as amines, carboxylic acids and phenols can react with oxirane rings, 29 which opens up the possibility for crosslinking with bifunctional curing agents.…”
Section: Introductionmentioning
confidence: 99%
“…22 In another study, we reduced the curing time at 200 1C to only 2 min by combining a phenol-based crosslinking agent with a titanium-based Lewis acid. 23 The electrical conductivity of click-chemistry cured copolymers has not yet been characterized. Even though the glycidyl methacrylate comonomer reduces the purity of the insulation material, the polar groups are not necessarily harmful and, in some cases, can even improve the electrical properties.…”
Section: Introductionmentioning
confidence: 99%
“…Recently, other types of copolymer blends with similar electromechanical properties to XLPE have gained interest among materials scientists [19,22,[29][30][31][32][33]. For example, [19,22] investigated polyethylene-based copolymers in terms of structural, morphological, mechanical and electrical properties.…”
Section: Introductionmentioning
confidence: 99%
“…For example, [19,22] investigated polyethylene-based copolymers in terms of structural, morphological, mechanical and electrical properties. In previous studies [29][30][31][32][33], we have introduced a byproduct-free crosslinking method based on click chemistry-type reactions for the development of polyethylene-based insulations. In these novel materials, there is no trace of detrimental by-products, and therefore the degassing process, which is a long and costly part of high-voltage cable manufacturing, is omitted.…”
Section: Introductionmentioning
confidence: 99%