Tian Jin, Xu Ting, Tan Yefa, Zhang Zhongwei, Tang Binghui, Sun Zhidan
Institute of Field Engineering, Army Engineering University of PLA, Nanjing 210007, China.
National Defense Engineering Institute, Army Engineering University of PLA, Nanjing 210007, China.
Materials (Basel). 2019 Sep 23;12(19):3103. doi: 10.3390/ma12193103.
In order to improve the interfacial properties of graphene oxide (GO) and epoxy resin (EP), hyperbranched polyesters with terminal carboxyl (HBP) non-covalently functionalized graphene oxide (HBP-GO) was achieved by strong π-π coupling between hyperbranched polyesters and GO nanosheets. The effects of non-covalent functionalization of GO on the dispersibility, wettability and interfacial properties were analyzed. The mechanical properties and enhancement mechanism of HBP-GO/EP composites were investigated. The results show that the hyperbranched polyesters is embedded in the GO layer due to its highly branched structure, which forms the steric hindrance effect between the GO nanosheets, effectively prevents the agglomeration of GO nanosheets, and significantly improved the dispersibility of GO. Simultaneously, the contact angle of HBP-GO with EP is reduced, the surface energy, interfacial energy and adhesion work are increased, then the wetting property of HBP-GO is significantly improved. The main toughening mechanism of HBP-GO is microcrack deflection induced by HBP-GO and plastic deformation of the EP matrix. In the microcrack propagation zones, HBP-GO may produce the pinning effect near the microcrack tips and change their stress state, resulting in microcrack deflection and bifurcation. So, the microcrack propagation path is more tortuous, which will consume much more fracture energy. Therefore, the mechanical properties of the HBP-GO/EP composites are greatly improved.
为了改善氧化石墨烯(GO)与环氧树脂(EP)的界面性能,通过超支化聚酯与GO纳米片之间的强π-π耦合,实现了端羧基超支化聚酯(HBP)对氧化石墨烯的非共价功能化。分析了GO非共价功能化对其分散性、润湿性和界面性能的影响。研究了HBP-GO/EP复合材料的力学性能及增强机理。结果表明,超支化聚酯因其高度支化的结构而嵌入GO层中,在GO纳米片之间形成空间位阻效应,有效防止了GO纳米片的团聚,显著提高了GO的分散性。同时,HBP-GO与EP的接触角减小,表面能、界面能和粘附功增加,HBP-GO的润湿性显著改善。HBP-GO的主要增韧机理是由HBP-GO诱导的微裂纹偏转和EP基体的塑性变形。在微裂纹扩展区,HBP-GO可能在微裂纹尖端附近产生钉扎效应并改变其应力状态,导致微裂纹偏转和分支。因此,微裂纹扩展路径更加曲折,这将消耗更多的断裂能。因此,HBP-GO/EP复合材料的力学性能得到了极大的提高。