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Thermal oxidation in linear polyethylene is mainly confined to disordered regions in which scission reactions cause crystallization and eventual deterioration of mechanical properties. Gel formation is negligible at 100°C. As degradation proceeds, comparable changes occur in the intrinsic viscosities of melt and solution‐crystallized liner polymers, indicating that chain folds are regularly arranged and are resistant to oxidative scission. Breakdown is much more extensive in branched and crosslinked polymers since crosslinking retards oxidative crystallization and branching increases the volume fraction of substrate ultimately accessible to oxygen.
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Winslow et al. (1966) studied this question.
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