甲基丙烯酸酯
共聚物
甲基丙烯酸甲酯
共价键
丙烯酸乙酯
丙烯酸酯
材料科学
丙烯酸丁酯
热塑性塑料
聚合物
高分子化学
异构化
化学
复合材料
有机化学
催化作用
作者
Siyang Wang,Lei Li,Qianhui Liu,Marek W. Urban
出处
期刊:Macromolecules
[American Chemical Society]
日期:2022-06-03
卷期号:55 (11): 4703-4709
被引量:29
标识
DOI:10.1021/acs.macromol.2c00739
摘要
Combining autonomous self-healing and reprocessing in one material offers an extended life span and enables shape configuration changes. We developed commodity poly((2-acetoacetoxy)ethyl methacrylate/methyl methacrylate/n-butyl acrylate) [p(AAEMA/MMA/nBA)] copolymer networks that are capable of both self-healing without intervention as well as reprocessing. The thermoplastic p(AAEMA/MMA/nBA) was obtained by copolymerizing (2-acetoacetoxy)ethyl methacrylate (AAEMA), methyl methacrylate (MMA), and n-butyl acrylate (nBA), followed by cross-linking with tristriaminoethyl amine (TREN) to form covalently adaptable networks (CANs). This copolymer network exhibits self-healability under ambient conditions and reprocessibility by compression molding at 120 °C. Using an array of thermo-mechanical and spectroscopic tools, these studies show that reprocessibility is achieved by the exchange reactions of dynamic cross-links, whereas self-healing is facilitated by the recovery of energetically favorable inter-chain van der Waals interactions accompanied by the reversible E ⇌ Z isomerization of the C═C bonds in vinylogous urethane moieties of the network.
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