Study on structure and performance of surface-metallized carbon fibers reinforced rigid polyurethane composites

被引:8
作者
Huang, Momo [1 ]
Li, Weiwei [1 ]
Liu, Xiaojing [1 ]
Feng, Ming [1 ]
Yang, Jie [1 ]
机构
[1] Ningbo Univ, Fac Mat Sci & Chem Engn, Ningbo Key Lab Specialty Polymers, Ningbo 315211, Peoples R China
基金
美国国家科学基金会;
关键词
carbon fibers; composites; dopamine; mechanical and electrical properties; MECHANICAL-PROPERTIES; THERMAL-CONDUCTIVITY; EPOXY COMPOSITES; FOAMS; FABRICATION; NANOTUBES; BEHAVIOR; ACID;
D O I
10.1002/pat.4907
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The simultaneous promotion in mechanical and electrical properties of rigid polyurethane (RPU) is an important task for expanding potential application. In this work, carbon fibers (CFs) reinforced RPU composites were prepared with the goal of improving mechanical and electrical properties. Metallized CFs meet our performance requirements and can be easily achieved via electrodeposition. However, the weak bonding strength in fiber-metal-RPU interface restricts their application. Inspired by the reducibility and wonderful adhesion of dopamine (DA), we proposed a new and efficient electrochemical method to fabricate metallized CFs, where DA polymerization was simultaneously integrated coupled with the reduction of metal ions (Ni2+). The characterization results helped us to gain insight about the reaction mechanism, which was never reported as far as we know. Compared with pure RPU, the tensile, interlaminar shear and impact strength of polydopamine (PDA)-nickel (Ni) modified CFs/RPU composites were improved by 11.2%, 21.0%, and 78.0%, respectively, which attributed to the strong interfacial adhesion, including mechanical interlocking and chemical crosslinking between treated CFs and RPU. In addition, the PDA-Ni surface treatment method also affected the dispersion of short CFs in the RPU, which increased the possibility of conductor contact and reduced insulator between fibers networks, resulting in higher electrical conductivity.
引用
收藏
页码:1805 / 1813
页数:9
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