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Urethane Ionic Groups Induced Rapid Crystallization of Biodegradable Poly(ethylene succinate)
Jian-Bing Zeng1, Fang Wu1, Cai-Li Huang1
1Center for Degradable and Flame-Retardant Polymeric Materials (ERCPM-MoE), College of Chemistry, State Key Laboratory of Polymer Materials Engineering, National Engineering Laboratory of Eco-Friendly Polymeric Materials (Sichuan), Sichuan University, Chengdu 610064, China.
Abstract:
Novel urethane ionic groups were incorporated into biodegradable poly(ethylene succinate) (PES) by chain extension reaction of PES diol (HO-PES-OH) and diethanolamine hydrochloride (DEAH) using hexamethylene diisocyanate (HDI) as a chain extender. The synthesized polymer was a novel segmented poly(ester urethane) ionomer (PESI) in which the soft segments were formed by reaction of HO-PES-OH with HDI and the hard segments that contained ionic groups were derived from reaction of DEAH with HDI. The crystallization rate of PESI was dramatically accelerated when 3 mol % urethane ionic groups were incorporated. However, the crystallization mechanism did not change. The significant acceleration in crystallization rate was attributed to the improved nucleation efficiency by incorporation of the urethane ionic group, because PESI showed significantly enhanced nucleation density but slightly slowed spherurlitic growth rate in comparison with PES which was synthesized by chain extension reaction of HO-PES-OH with HDI. The increased nucleation efficiency was ascribed to the aggregation of hard segments of PESI induced by the ionic interactions.
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