微尺度化学
自愈
胶粘剂
聚合物
复合数
共价键
氢键
复合材料
分子动力学
纳米技术
限制
材料科学
机械工程
化学
分子
数学
计算化学
有机化学
图层(电子)
数学教育
替代医学
医学
病理
工程类
作者
Jing Yang,Xin Zhou,Junqing Yang,Jiaoyang Chen,Zhe Sun,Yuhang Cheng,Lin Yang,Hui Wang,Guangpu Zhang,Jiajun Fu,Wei Jiang
标识
DOI:10.1016/j.cej.2022.138810
摘要
In general, robust mechanical properties require a stable strong physical or covalent network inside the polymer, limiting the mobility of molecular chains and the dynamics of physical crosslinks or reversible covalent bonds. Therefore, high healing efficiency at moderate temperature and robust mechanical properties are contradictory, which is difficult to optimize simultaneously. Therefore, this study introduced a new strategy. First, acyl semicarbazides motifs were utilized to endow energetic adhesives with strong and tough mechanical properties. Then, the asymmetric structure was introduced to regulate the hydrogen bonding array density and micro-scale trim the size of the hard domain, thereby improving the hydrogen bonding dynamics and the polymer-chains mobility. Finally, the synthesized energetic polymer adhesive (EPA) exhibited excellent comprehensive ability in terms of mechanical properties, self-healing efficiency, and energy level. Hereafter, the adhesive was further to be used with Al powder for the preparation of the EPA-based energetic composite materials (EPA/ECM), which could be mechanically comparable to commercial non-energetic adhesive-based ECMs. In addition, the high crack-healing efficiency of EPA/ECM indicated that the adhesive possessed strong application potential, which is expected to provide new ideas for improving the safety and service life of energetic composites.
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