材料科学
聚氨酯
弹性体
韧性
自愈
氢键
极限抗拉强度
复合材料
自愈材料
粘结强度
聚合物
延伸率
胶粘剂
有机化学
分子
化学
医学
替代医学
病理
图层(电子)
作者
Yue Gu,Hongjun Tu,Z. F. Zhou,Ziyang Wan,Bo Pu,Xiaodong Yi,Liangliang Xia,Ming Zhou
标识
DOI:10.1177/14658011251345248
摘要
In order to explore new high-strength polymer materials that can achieve self-healing of damage under more mild conditions, the high-strength room temperature self-healing polyurethane elastomers with multiple hydrogen bonds/aromatic disulphide bonds (PU PIPMD ) were constructed by using the strategy of multiple repair networks. Through the interaction between the carbamate group (-NH-C(=O)-O-), pyridine and urea group (-NH-CO-NH-) to form a multiple of different strength hydrogen bond, the reversible covalent bond-disulphide bond (-S-S-) was introduced into the molecular chain at the same time to build the target amorphous structure products. The prepared room temperature self-healing polyurethane elastomer had outstanding mechanical properties with strain-strengthening behaviour. In addition, it also exhibits strain-strengthening behaviour. After 48 h of static repair at room temperature, the tensile strength, elongation at break, and toughness of prepared polyurethane elastomer can be well restored, with a synchronous self-healing efficiency of over 80%. Achieving a dual improvement in mechanical strength and room temperature self-healing performance. And further enhanced the service life and reusability of the polyurethane elastomer material.
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