Towards mechanical robust yet self-healing polyurethane elastomers via combination of dynamic main chain and dangling quadruple

被引:121
作者
Hu, Jin [1 ]
Mo, Ruibin [1 ]
Jiang, Xiang [1 ]
Sheng, Xinxin [2 ]
Zhang, Xinya [1 ]
机构
[1] South China Univ Technol, Sch Chem & Chem Engn, Guangzhou 510640, Guangdong, Peoples R China
[2] Guangdong Univ Technol, Sch Mat & Energy, Dept Polymer Mat & Engn, Guangdong Prov Key Lab Funct Soft Condensed Matte, Guangzhou 510006, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Self-healing; Dynamic covalent bonds; Quadruple hydrogen bonds; DISELENIDE BONDS; POLYMER NETWORKS; TEMPERATURE; METATHESIS; VITRIMERS; EXCHANGE; RUBBER;
D O I
10.1016/j.polymer.2019.121912
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
One of the greatest challenges of robust self-healing materials is the confliction between high chain mobility for self-healing and a stable structure for mechanical strength. Herein, dangling 2-ureido-4[1R]-pyrimidione (UPy)-functionalized side groups were introduced into the hard segments of thermoplastic polyurethane (TPU) elastomers, where embedded the dynamic disulfide bonds in the main chain. The strong quadruple H-bonding interaction between UPy side groups acts as supramolecular crosslinkers enabling the TPU elastomer to have improved mechanical properties (tensile strength up to 25 MPa and toughness similar to 100 MJ m(-3)), and simultaneously the plasticizer effect of dangling side chain endows it with efficient healing ability at elevated temperatures (80-100 degrees C) comparable to its linear analogues. This strategy shows great potential in designing robust self-healing TPU elastomer employing weak dynamic covalent bonds, with wide promising applications as wearable electronics, coatings and adhesives.
引用
收藏
页数:11
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