环氧树脂
材料科学
复合材料
氮化硼
热导率
复合数
固化(化学)
热传导
纳米颗粒
热的
纳米复合材料
共价键
双酚A
硼
复合环氧材料
填料(材料)
聚合物
热固性聚合物
电导率
作者
Xicheng Yuan,Xi Zhang,Qi Cao,Zhiqiang Wang,Chenmin Lin,Beitao Liu,Leiming Sun,F.T. Wang,Liang ZOU,Xigao Jian,Zhihuan Weng
标识
DOI:10.1021/acsapm.6c00393
摘要
Currently, enhancement of thermal conductivity in epoxy resin composites is mainly achieved by adding fillers with high thermal conductivity. However, due to weak interfacial compatibility, the thermal enhancement effect of the fillers is hampered, and other material properties may be adversely affected. Additionally, traditional epoxy cross-linked networks are incapable of self-healing damage and are nondegradable, which shortens the material lifespan and poses environmental pollution concerns. Aiming to resolve these challenges, the present work designed a one-step comodification process, where boron nitride (BN) was functionalized concurrently with polypyrrole (PPy) and silver nanoparticles to produce the target filler, denoted as MBN. This approach is simple, mild, and efficient. During the reaction, in situ generated PPy improved the compatibility at the BN/resin interface, while the silver nanoparticles collaborated with BN to form a zero-dimensional/two-dimensional synergistic thermal conduction network. Furthermore, by introducing a disulfide bond-bearing curing agent to cure bisphenol A epoxy resin (E51), a dynamic covalent network was constructed within the system. Compared with pure epoxy resin, the E51–30 wt % MBN/1 composite showed a 5.2-fold increase in thermal conductivity, reaching 0.988 W/mK. The material could self-heal 92.8% of scratch damage within 60 min and fully degraded at 80 °C, with the recovered fillers maintaining their intact morphology. This epoxy composite with high thermal conductivity and dynamic bonds demonstrates promising application prospects in thermal management fields.
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