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Hydrocarbon elastomers peroxide vulcanization of saturated

Saturated hydrocarbon polymers are also crosslinked by the action of organic peroxides, though branching reduces the efficiency. Polyethylene is crosslinked by dicumyl peroxide at an efficiency of about 1.0, saturated EPR gives an efficiency of about 0.4, while butyl rubber cannot be cured at all. For polyethylene, the reaction scheme is similar to that of the unsaturated elastomers. [Pg.373]

However, branched polymers undergo other reactions. [Pg.373]

though the peroxide has been depleted, no crosslinks have been formed between polymer chains, and the average molecular weight of the polymer has even been reduced by scission. [Pg.374]

Sulfur, or the so-called coagents (Loan, 1963 Lenas, 1964), can be used to suppress scission. Examples of coagents are m-phenylenebismaleimide, high-1,2 (high-vinyl)polybutadiene, triallyl cyanurate, diallyl phthalate, and ethylene diacrylate. Their mechanism of action may be as follows  [Pg.374]


See other pages where Hydrocarbon elastomers peroxide vulcanization of saturated is mentioned: [Pg.373]    [Pg.359]    [Pg.250]   
See also in sourсe #XX -- [ Pg.373 ]

See also in sourсe #XX -- [ Pg.359 ]




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Elastomers hydrocarbon

Elastomers saturated

Elastomers vulcanization

Hydrocarbon saturation

Hydrocarbons, saturated

Peroxide vulcanization elastomers

Saturate hydrocarbons

Saturated hydrocarbon elastomers, peroxide

Saturated hydrocarbon elastomers, peroxide vulcanization

Vulcan

Vulcanization

Vulcanization saturated hydrocarbon

Vulcanize

Vulcanized

Vulcanized elastomer

Vulcanizing

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