热固性聚合物
材料科学
解聚
原材料
糠醇
呋喃
聚氨酯
降级(电信)
聚合
三聚氰胺
三嗪
化学工程
催化作用
工艺工程
聚合物
有机化学
计算机科学
复合材料
高分子化学
化学
电信
工程类
作者
Zepeng Lei,Zirui Wang,Huan Jiang,Jackson R. Cahn,Hongxuan Chen,Shaofeng Huang,Yinghua Jin,Xiaohui Wang,Kai Yu,Wei Zhang
标识
DOI:10.1002/adma.202407854
摘要
Abstract Thermosets are well known for their advantages such as high stability and chemical resistance. However, developing sustainable thermosets with degradability and recyclability faces several principal challenges, including reconciling the desired characteristics during service with the recycling and reprocessing properties required at the end of life, establishing efficient methods for large‐scale synthesis, and aligning with current manufacturing process. Here a general strategy is presented for the on‐demand degradation and recycling of thermosets under mild conditions utilizing dynamic precursors with dual‐factor‐controlled reversibility. Specifically, dynamic triazine crosslinkers are introduced through dynamic nucleophilic aromatic substitution (S N Ar) into the precursor polyols used in polyurethane (PU) synthesis. Upon removal of the catalyst and alcohol, the reversibility of S N Ar is deactivated, allowing for the use of standard PU polymerization techniques such as injection molding, casting, and foaming. The resulting cyanurate‐crosslinked PUs maintain high stability and diverse mechanical properties of traditional crosslinked PUs, yet offer the advantage of easy on‐demand depolymerization for recycling by activating the reversibility of S N Ar under specific but mild conditions—a combination of base, alcohol, and mild heat. It is envisioned that this approach, involving the pre‐installation of dual‐factor‐controlled dynamic crosslinkers, can be broadly applied to current thermosetting plastic manufacturing processes, introducing enhanced sustainability.
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