Sujuan Zhang,Jianjun Yi,Jiming Chen,Yong Li,Baoliang Liu,Zaijun Lu
Graphical In this study, imine-containing polybenzoxazine vitrimer (C-ABZ) was synthesized through a condensation reaction between an aldehyde-containing benzoxazine oligomer (O-ABZ) and 1,12-dodecanediamine. The dynamic exchangeable characteristics of imine bonds impart C-ABZ with weldabilities and reprocessabilities. At the same time, the hydrophobic polybenzoxazine backbone significantly improve the water resistance of imine bonds. Traditional polybenzoxazine thermosets cannot be reprocessed or recycled due to the permanent crosslinked networks. The dynamic exchangeable characteristics of imine bonds can impart the networks with reprocessabilities and recyclabilities. This study reported a weldable, reprocessable, and water-resistant polybenzoxazine vitrimer (C-ABZ) crosslinked by dynamic imine bonds. It was synthesized through a condensation reaction between an aldehyde-containing benzoxazine oligomer (O-ABZ) and 1,12-dodecanediamine. The resulting C-ABZ was able to be welded and reprocessed due to the dynamic exchange of imine bonds. The tensile strengths of the welded C-ABZ and the reprocessed C-ABZ after three cycles of hot-pressing were 76.7, 81.3, 70.8, and 58.1 Mpa, with corresponding tensile strength recovery ratios of 74.1 %, 78.6 %, 68.4 %, and 56.1 %, respectively. Furthermore, the polybenzoxazine backbone significantly improved the water resistance of the imine bonds. After immersing in water for 30 days at room temperature, the weight gain of C-ABZ was less than 1 % with corresponding tensile strength and tensile strength retention ratio of 59.5 Mpa and 57.5 %, respectively. Although the heat resistance of C-ABZ decreased slightly with increased hot-pressing cycles, a glass transition temperature ( T g, tanδ ) of 150 °C was retained after the third hot-pressing. Overall, these findings demonstrate that the C-ABZ possesses excellent comprehensive performances.
The demand for renewable fiber-based epoxy composites is increasing rapidly as a sustainable alternative to conventional synthetic composites. However, limited attention has been directed toward the degradation and reprocessing of the epoxy resin matrix, which could further enhance the environmental benefits of natural fiber-reinforced epoxy composites. This study utilized delignified basswood as a porous template to in situ synthesize epoxy vitrimers based on dynamic ester exchange reactions through vacuum impregnation, successfully preparing a Wood/Epoxy Vitrimers Composite (WEPVC). Unlike traditional wood–epoxy resin composites, WEPVC demonstrated thermally activated topological rearrangement behavior at 180 °C, achieving thermal welding repair and three cycles of mechanical crushing and hot-press reprocessing. In ethylene glycol solution, the material could be completely degraded within 240 min to recycle both the wood template and resin oligomers. The composite simultaneously exhibited excellent mechanical properties (tensile strength 73.21 MPa), thermal stability (degradation onset temperature 273 °C), and water resistance (water contact angle 82°). These combined properties make the WEPVC developed in this study an environmentally friendly, cost-effective candidate for sustainable structural materials.