Influence of the Molecular Weight of the Polycarbonate Polyol on the Intrinsic Self-Healing at 20 °C of Polyurethanes

聚碳酸酯 结晶度 氢键 材料科学 自愈 碳酸盐 高分子化学 尿素 多元醇 分子质量 化学工程 聚氨酯 复合材料 化学 有机化学 分子 冶金 替代医学 病理 工程类 医学
作者
Yuliet Paez-Amieva,José Miguel Martín‐Martínez
出处
期刊:Polymers [Multidisciplinary Digital Publishing Institute]
卷期号:16 (19): 2724-2724 被引量:5
标识
DOI:10.3390/polym16192724
摘要

Different polyurethanes (PUs) were synthesized with polycarbonate polyols of molecular weights of 500, 1000, and 2000 Da. Their self-healing abilities at 20 °C were tested, and their structural, thermal, and mechanical properties were analyzed. The PUs made with polycarbonates of molecular weights 500 (YC500) and 1000 Da (YC1000) exhibited self-healing at 20 °C, and the self-healing time of YC1000 was the shortest. The absence of crystallinity and the low degree of micro-phase separation favored self-healing at 20 °C in YC500. However, the presence of tack and the existence of allophanate species and urethane–carbonate and urea–carbonate hydrogen bonds disfavored self-healing. Consequently, the self-healing time at 20 °C of YC500 was longer than expected. On the other hand, YC1000 exhibited an “equilibrium” between urethane-carbonate and urea–carbonate hydrogen bonds and carbonate–carbonate interactions among the soft segments, so a particular structural order was produced that was associated with its fastest self-healing at 20 °C. The PU made with the polycarbonate of molecular weight 2000 Da did not exhibit self-healing at 20 °C because of its significant micro-phase separation, the presence of semi-crystalline soft domains, and the lower density of hydrogen bonds.
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