化学
聚合物
聚氨酯
胶粘剂
弹性体
分子内力
降级(电信)
劈理(地质)
氧代碳
侧链
高分子化学
化学工程
有机化学
复合材料
材料科学
催化作用
亲核细胞
工程类
电信
图层(电子)
断裂(地质)
计算机科学
作者
Ephraim G. Morado,Mara L. Paterson,Douglas G. Ivanoff,Hsuan-Chin Wang,Alayna M. Johnson,Darius Daniels,Aoon Rizvi,Nancy R. Sottos,Steven C. Zimmerman
出处
期刊:Nature Chemistry
[Nature Portfolio]
日期:2023-03-02
卷期号:15 (4): 569-577
被引量:31
标识
DOI:10.1038/s41557-023-01151-y
摘要
A major challenge in developing recyclable polymeric materials is the inherent conflict between the properties required during and after their life span. In particular, materials must be strong and durable when in use, but undergo complete and rapid degradation, ideally under mild conditions, as they approach the end of their life span. We report a mechanism for degrading polymers called cyclization-triggered chain cleavage (CATCH cleavage) that achieves this duality. CATCH cleavage features a simple glycerol-based acyclic acetal unit as a kinetic and thermodynamic trap for gated chain shattering. Thus, an organic acid induces transient chain breaks with oxocarbenium ion formation and subsequent intramolecular cyclization to fully depolymerize the polymer backbone at room temperature. With minimal chemical modification, the resulting degradation products from a polyurethane elastomer can be repurposed into strong adhesives and photochromic coatings, demonstrating the potential for upcycling. The CATCH cleavage strategy for low-energy input breakdown and subsequent upcycling may be generalizable to a broader range of synthetic polymers and their end-of-life waste streams.
科研通智能强力驱动
Strongly Powered by AbleSci AI