摘要
The integration of ceramic fillers with high thermal conductivity into polymer fiber insulating paper enhances both thermal conductivity and dielectric strength. Nonetheless, elevated filler loadings augment the filler-matrix interface, thereby intensifying phonon scattering. Additionally, filler agglomeration, driven by van der Waals forces, impedes the formation of a continuous thermal network and introduces defects that facilitate electrical treeing. This research draws inspiration from “brick-and-mortar” architectures, employing high-surface-area thermotropic liquid crystal polyarylate (PAR) nanofibers as the continuous mortar and surface-modified hexagonal boron nitride (TMS@h-BN) nanoplates as the bricks. A scalable papermaking process is employed to fabricate high-thermal-conductivity insulating paper with a high filler content. The three-dimensional network structure of PAR nanofibers spatially confines the h-BN nanoplates, effectively preventing their agglomeration. Furthermore, π-π conjugation between the aromatic structures of PAR and the benzene rings of h-BN enhances interfacial bonding by facilitating the diffusion and entanglement of PAR molecular chains during thermal pressing. This results in a dense interfacial structure that provides an efficient pathway for phonon transport, thereby enhancing thermal conductivity and minimizing electrical distortion. At a filler loading of 70 wt%, the TMS@h-BN/PAR nanocomposite paper exhibits superior mechanical performance and flexibility, achieving an in-plane thermal conductivity of 14.19 W·m −1 ·K −1 and a breakdown field strength of 111.17 kV/mm, which represent significant improvements over commercial insulating paper. Additionally, it demonstrates exceptional thermal stability and flame retardancy, with minimal dimensional changes following heat treatment.
危险品化学品经营许可证(带存储)