Zhipeng Yang, Jiashang Yin, Yinlei Lin, Dechao Hu, Haichen Zhang, Qionghai Chen, Pengwei Duan, Xusheng Cao, Jinhao Liu, Huawen Hu, H. Z. Li
Thermoset composites are essential in modern engineering yet suffer from an intrinsic lack of recyclability due to their permanently cross-linked structures. Herein, we report a series of biobased thermoset polyimine elastomers with intrinsic self-healing and closed-loop recyclable properties, which were further employed as a polymer matrix for polyimine/carbon fiber elastomeric composites. The synthesized PIm-TFB x elastomers exhibited excellent mechanical properties (tensile strength up to 2.8 MPa and an elongation at break of 123%) and room-temperature self-healing, achieving a healing efficiency of 92.9% within 24 h at room temperature. All-atom molecular dynamics simulation models were constructed for different elastomers, providing molecular-level insight into the nonlinear dependence of tensile strength on cross-linking density and imine bond exchange in covalent adaptive networks (CANs). More importantly, the elastomers demonstrated efficient closed-loop recyclability under mild conditions, with recycled samples retaining over 92.9% of their original tensile strength and nearly unchanged T g and cross-linking density. When employed as matrices, these polyimine/carbon fiber elastomeric composites achieve a tensile strength of 10.4 MPa and maintain over 90% of their original strength after five recycling cycles, which is accompanied by the high-yield recovery of intact carbon fiber. This study combines experiments and molecular simulations to elucidate the structure–property relationships of imine-based CANs, offering a sustainable pathway for advanced recyclable thermosets.