In situ Polymerization of Polyamide 6/Boron Nitride Composites to Enhance Thermal Conductivity and Mechanical Properties via Boron Nitride Covalently Grafted Polyamide 6

被引:17
|
作者
Fang, Hui [1 ,2 ,3 ]
Li, Denghui [1 ]
Wu, Fangjuan [1 ,2 ]
Peng, Xiangfang [1 ,2 ]
Chen, Anlin [1 ]
Zhang, Lingjie [1 ]
Chen, Sheng [1 ]
机构
[1] Fujian Univ Technol, Coll Mat Sci & Engn, Fuzhou, Peoples R China
[2] Fujian Univ Technol, Key Lab Polymer Mat & Prod Univ Fujian, Fuzhou, Peoples R China
[3] Fujian Univ Technol, Fujian Prov Key Lab Adv Mat Proc & Applicat, Fuzhou, Peoples R China
来源
POLYMER ENGINEERING AND SCIENCE | 2020年 / 60卷 / 04期
基金
中国国家自然科学基金;
关键词
FUNCTIONALIZATION; FABRICATION; NETWORK;
D O I
10.1002/pen.25329
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Polyamide 6/boron nitride (PA6/BN) composites were synthesized via anionic ring-opening polymerization using epsilon-caprolactam as the monomer and functional boron nitride (f-BN) as the thermal conductive filler. Besides the homopolymerized PA6, some PA6 molecule chains would grow from the f-BN sheets through the "grafting from" strategy. Compared with unfunctional hexagonal BN (h-BN), the introduction of f-BN not only improved the dispersion of f-BN in the matrix but also enhanced the interface bonding between f-BN and PA6. The homogeneous dispersion of f-BN in the PA6/f-BN composite favored the formation of the continuous thermal conductive paths or network at a low f-BN loading, and the good interface bonding reduced the phonon scattering in the interface, which improved the thermal conductivity (TC) of the PA6/f-BN composite by 66.0% compared with that of the pure PA6, when only 5 wt% f-BN was added. In contrast, with the same content of unfunctional h-BN loading, the TC of the corresponding composite merely improved by 29.7%. Moreover, Young's modulus and yield strength of PA6/f-BN composites had increased obviously with the introduction of f-BN, whereas those of PA6/h-BN composites showed small fluctuation with the same contents of BN. POLYM. ENG. SCI., 2020. (c) 2020 Society of Plastics Engineers
引用
收藏
页码:710 / 716
页数:7
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