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具有多重刺激响应性的可再加工、可返工及机械变色聚六氢三嗪热固性材料

Reprocessable, Reworkable, and Mechanochromic Polyhexahydrotriazine Thermoset with Multiple Stimulus Responsiveness.

作者信息

Chen Li, Zhu Siyao, Toendepi Innocent, Jiang Qiuran, Wei Yi, Qiu Yiping, Liu Wanshuang

机构信息

Shanghai Collaborative Innovation Center for High Performance Fiber Composites, Center for Civil Aviation Composites, Donghua University, 2999 North Renmin Road, Shanghai 201620, China.

Key Laboratory of Textile Science &Technology, Ministry of Education, College of Textiles, Donghua University, 2999 North Renmin Road, Shanghai 201620, China.

出版信息

Polymers (Basel). 2020 Oct 15;12(10):2375. doi: 10.3390/polym12102375.

Abstract

Developing recyclable, reworkable, and intelligent thermosetting polymers, as a long-standing challenge, is highly desirable for modern manufacturing industries. Herein, we report a polyhexahydrotriazine thermoset (PHT) prepared by a one-pot polycondensation between 4-aminophenyl disulfide and paraformaldehyde. The PHT has a glass transition temperature of 135 °C and good solvent resistance. The incorporation of dual stimuli-responsive groups (disulfide bond and hexahydrotriazine ring) endows the PHT with re-processability, re-workability, and damage monitoring function. The PHT can be repeatedly reprocessed by hot pressing, and a near 100% recovery of flexural strength is achieved. The PHT can also degrade in inorganic acid or organic thiol solutions at room temperature. The thermally reworkable test demonstrates that, after heating the PHT at 200 °C for 1 h, the residuals can be easily wiped off. Finally, the PHT exhibits a reversible mechanochromic behavior when damaged.

摘要

开发可回收、可返工且智能的热固性聚合物,作为一项长期挑战,是现代制造业非常渴望实现的目标。在此,我们报道了一种通过4-氨基苯基二硫化物与多聚甲醛一锅法缩聚制备的聚六氢三嗪热固性材料(PHT)。该PHT的玻璃化转变温度为135℃,且具有良好的耐溶剂性。双刺激响应基团(二硫键和六氢三嗪环)的引入赋予了PHT可再加工性、可返工性和损伤监测功能。PHT可通过热压反复再加工,并实现了近100%的弯曲强度恢复。PHT在室温下也能在无机酸或有机硫醇溶液中降解。热返工测试表明,将PHT在200℃加热1小时后,残留物可轻松擦除。最后,PHT在受损时表现出可逆的机械变色行为。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2370/7602728/6a4653ac57ea/polymers-12-02375-g001.jpg

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