Abstract
Model elastomeric networks were prepared by trifunctionally end linking hydroxyl-terminated chains of polyisobutylene having number-average molecular weights in the range 10−3Mn = 2.4 – 10.7 g mol−1. Their stress-strain isotherms in elongation at 25°C in the unswollen state showed significant increases or upturns in modulus at high elongations, due to strain-induced crystallization. Increase in degree of cross-linking (decrease in Mn) was found to decrease the elongation required to initiate crystallization and the maximum extensibility, but to increase the magnitude of the upturn in modulus.
Published Version
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