材料科学
极限抗拉强度
聚氨酯
延伸率
单体
弹性体
聚合物
复合材料
自愈材料
共聚物
氢键
自愈
拉伸试验
共价键
分子
有机化学
医学
病理
化学
替代医学
作者
Chenyuan Zhang,Liu Zhiqiang,Zhijia Zhang,Wenjun Zhou,Wang Guojun,Songsong Zhang,Hao Wei,Qiang Wang,Teng Ma,Rui Li
标识
DOI:10.1016/j.mtcomm.2023.105747
摘要
In practical applications, the scratch or damage of materials are inevitable. Self-healing materials are beneficial to the sustainable use of materials. Herein, the dual cross-linked self-healing polyurethane (PU-xUPy) were prepared by copolymerization of diisocyanate monomers, quadruple hydrogen bond chain extender based on 2‐ureido‐4[1H]‐pyrimidinone (UPy) and triol monomers. The PU-xUPy exhibit excellent mechanical properties owing to the covalent cross-linking via triol monomer and the noncovalent-linking via UPy. The tensile strength and elongation at break of PU-75UPy were 9.6 MPa and 420.1%, respectively. The self-healing efficiency of the tensile strength and elongation at break were achieved to 73% (the tensile strength is 7.0 MPa) and 72.7% (the elongation at break is 306.6%) after 24 h of healing at 40 ℃, respectively. Moreover, the cyclic fatigue tensile test provided the evidences of the breaking and recombination of hydrogen bonds. These promising outcomes are expected to promote the development of the sustainable application of polyurethane elastomers.
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