酯交换
聚酯纤维
催化作用
化学
共价键
高分子化学
高分子科学
有机化学
材料科学
作者
Shengke Zhao,Yuanyuan Liu,Haiyue Zhao,Kangwen Ma,Yuxiang Fu,Y.-L. Dong,Jialong Li,Chengcai Pang
标识
DOI:10.1021/acs.macromol.4c02025
摘要
Most vitrimers based on transesterification (TER) require external catalysts. Moreover, their slow relaxation rates necessitate a high reprocessing temperature and prolonged reprocessing time, resulting in issues like degradation or side reactions. Herein, a spider-like bisenol tetraester (E4) is investigated as a building block to synthesize dynamic covalent networks (DCNs). One of the highlights of E4 is that it can undergo a catalyst-free TER following the dissociative pathway at high temperatures. Using this dissociative TER, a series of DCNs were prepared by melt curing of E4 and different alkanediols. Remarkably, these DCNs exhibit ultrafast stress relaxation rates at 190 °C, with rather short relaxation times (1.4–3.1 s) and relatively high viscous flow activation energies (142.7–167.1 kJ mol–1). This allows for fast reprocessing of them at 180 °C within 8–10 s, a considerably shorter time frame as compared to the long reprocessing time required for vitrimers based on conventional TER. Lastly, the catalyst-free TER allows highly selective depolymerization of these DCNs and the carbon fiber-reinforced polymers (CFRPs) based on them, achieving eco-friendly and low-cost recovery of initial monomers from the mixed plastic waste stream.
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