Wang Feng, Zhang Yichuan, Hu Su, Zhong Xiangyu, Bai Jiangbo, Zhang Yang, Bao Jianwen
AVIC Composite Corporation Ltd., Beijing 101300, China.
Key Laboratory of Advanced Composite, Composite Technology Center, AVIC Composite Corporation Ltd., Beijing 101300, China.
Polymers (Basel). 2023 Dec 28;16(1):90. doi: 10.3390/polym16010090.
The nanocomposites with reversible cross-linking covalent bonds were prepared by reacting furfurylamine (FA)-modified diglycidyl ether of bisphenol A (DGEBA) and furfuryl-functionalized aniline trimer-modified graphene (TFAT-G) with bismaleimide (BMI) via the Diels-Alder (DA) reaction. The successful synthesis of the TFAT modifier is confirmed by nuclear magnetic resonance (NMR) hydrogen spectroscopy and IR spectroscopy tests. The structure and properties of TFAT-G epoxy nanocomposites are characterized by scanning electron microscopy (SEM), differential scanning calorimeter (DSC), tensile, and resistivity. The results show that TFAT-G was uniformly dispersed in the resin, and 1 wt% TFAT-G composites increased to 233% for tensile strength, 63% for elongation at break, 66% for modulus, and 7.8 °C for Tg. In addition, the addition of unmodified graphene degrades the mechanical properties of the composite. Overall, the graphene/self-healing resin nanocomposites have both good self-healing function and electrical conductivity by adding 1 wt% modified graphene; this allows for the maintenance of the original 83% strength and 89% electrical conductivity after one cycle of heating repair.
通过使糠胺(FA)改性的双酚A二缩水甘油醚(DGEBA)和糠基官能化的苯胺三聚体改性的石墨烯(TFAT-G)与双马来酰亚胺(BMI)经由狄尔斯-阿尔德(DA)反应,制备了具有可逆交联共价键的纳米复合材料。通过核磁共振(NMR)氢谱和红外光谱测试证实了TFAT改性剂的成功合成。通过扫描电子显微镜(SEM)、差示扫描量热仪(DSC)、拉伸试验和电阻率测试对TFAT-G环氧纳米复合材料的结构和性能进行了表征。结果表明,TFAT-G均匀分散在树脂中,1 wt% TFAT-G复合材料的拉伸强度提高到233%,断裂伸长率提高到63%,模量提高到66%,玻璃化转变温度提高到7.8℃。此外,添加未改性的石墨烯会降低复合材料的力学性能。总体而言,通过添加1 wt%的改性石墨烯,石墨烯/自修复树脂纳米复合材料兼具良好的自修复功能和导电性;在一次加热修复循环后,可保持原始强度的83%和电导率的89%。