Toward effective and tunable interphases in graphene oxide/epoxy composites by grafting different chain lengths of polyetheramine onto graphene oxide

被引:226
作者
Guan, Li-Zhi [1 ]
Wan, Yan-Jun [1 ]
Gong, Li-Xiu [1 ]
Yan, Dong [2 ]
Tang, Long-Cheng [1 ]
Wu, Lian-Bin [1 ]
Jiang, Jian-Xiong [1 ]
Lai, Guo-Qiao [1 ]
机构
[1] Hangzhou Normal Univ, Coll Mat Chem & Chem Engn, Key Lab Organosilicon Chem & Mat Technol, Minist Educ, Hangzhou 310012, Zhejiang, Peoples R China
[2] Beijing Univ Chem Technol, Coll Mat Sci & Engn, Dept Polymer Engn, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
ENHANCED MECHANICAL-PROPERTIES; FUNCTIONALIZED GRAPHENE; ELECTRICAL-CONDUCTIVITY; THERMAL-CONDUCTIVITY; EPOXY NANOCOMPOSITES; POLYSTYRENE; REDUCTION; DISPERSION; FRACTURE; SHEETS;
D O I
10.1039/c4ta02429j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Interface design plays a crucial role in developing superior mechanical performance of graphene/polymer nanocomposites. Herein, we report a facile approach to the fabrication of advanced polymeric nanocomposites of epoxy by the incorporation of polyetheramine-functionalized graphene oxide (PEA-f-GO). Two types of PEA molecules with different molecular lengths were used to synthesize the PEA-f-GO sheets. The chemical bonds formed between the amine functional groups on the GO surface and the epoxy resin during curing provided strong sheet/matrix interfacial adhesion. The addition of PEA-f-GO was found to produce significant enhancements in the mechanical properties of epoxy, including elastic modulus, tensile strength, elongation at break and toughness. In particular, the PEA-f-GO sheets containing shorter PEA molecules produced higher improvement in strength but smaller increases in both ductility and toughness than those containing longer PEA molecules. For example, at 0.50 wt% filler loading, two nanocomposites showed increases of 63% and 51% in tensile strength and 90% and 119% in toughness as compared to the unfilled epoxy. Our results suggest that the interphases between the GO and the polymer matrix can be tuned by varying the molecular lengths of grafted modifiers, thereby providing a new route for the rational designing and development of the GO-based composite materials.
引用
收藏
页码:15058 / 15069
页数:12
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