Effect of tunable styrene content on achieving high-performance poly (styrene-b-ethylene-ran-butylene-b-styrene)/graphene oxide nanocomposites

被引:12
|
作者
Wang, Jianfeng [1 ]
Jin, Xiuxiu [3 ]
Zhang, Xiaomeng [1 ]
Wu, Hong [1 ,2 ]
Guo, Shaoyun [1 ]
机构
[1] Sichuan Univ, Polymer Res Inst, State Key Lab Polymer Mat Engn, Chengdu 610065, Sichuan, Peoples R China
[2] Sichuan Univ WuXi, Res Ctr Applicat Graphene, Wuxi 214000, Peoples R China
[3] Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Chengdu 610065, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Polymer-matrix composites (PMCs); Interface; Surface treatments; Mechanical performance; REDUCED GRAPHENE OXIDE; MECHANICAL-PROPERTIES; DIELECTRIC-PROPERTIES; CARBON NANOTUBE; FUNCTIONALIZATION; POLYCARBONATE; TOUGHNESS; STRENGTH;
D O I
10.1016/j.compscitech.2018.05.041
中图分类号
TB33 [复合材料];
学科分类号
摘要
In this paper, two poly(styrene-b-ethylene-ran-butylene-b-styrene) (SEBS) with different styrene segment content were adopted to explore the relationship between varying pi-pi stacking interaction and the mechanical performance of polymer composites. The results showed that the high styrene content on SEBS (SEBS-30, 30 wt% styrene segment) endows SEBS a stronger pi-pi stacking interaction with GO and a better dispersion of GO in the matrix than that in SEBS with low styrene content (SEBS-12, 12 wt% styrene segment), resulting in a high efficiency on enhancing the performance of SEES. By adding 0.5 wt% GO, the tensile strength and modulus of SEBS-30 was increased by 44% and 64%, respectively, while that of SEBS-12 was increased by 24% and 39%. Furthermore, the GO also exhibited the ability to toughen SEBS via forming microcrack and GO-induced fibrillation of SEBS during the fracture process. The elongation at break and fracture toughness of SEBS-30 was increased by 10% and 64%, respectively. This study gives us a deep insight into the influence of varying pi-pi stacking interaction between graphene oxide (GO) and polymer on achieving high-performance polymer nanocomposites.
引用
收藏
页码:229 / 237
页数:9
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