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Molecular-level dispersion of graphene into epoxidized natural rubber: Morphology, interfacial interaction and mechanical reinforcement

机译:石墨烯在环氧化天然橡胶中的分子水平分散:形态,界面相互作用和机械增强

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摘要

The interfacial interaction of composites dominates the properties of polymeric/inorganic nano-composites. Herein, epoxy and hydroxyl groups are introduced into the natural rubber (NR) molecular chains to anchor oxygenous functional groups on the surface of graphene oxide (GO) sheets and therefore enhance the interfacial interaction between GO and rubber. From the morphological observation and interaction analysis, it is found that epoxidized natural rubber (ENR) latex particles are assembled onto the surfaces of GO sheets by employing hydrogen bonding interaction as driving force. This self-assembly depresses restacking and agglomeration of GO sheets and leads to homogenous dispersion of GO within ENR matrix. The formation of hydrogen bonding interface between ENR and GO demonstrates a significant reinforcement for the ENR host. Compared with those of pure ENR, the composite with 0.7 wt% GO loading receives 87% increase in tensile strength and 8.7 fold increase in modulus at 200% elongation after static in-situ vulcanization. (C) 2014 Elsevier Ltd. All rights reserved.
机译:复合材料的界面相互作用主导着聚合物/无机纳米复合材料的性能。这里,将环氧和羟基基团引入天然橡胶(NR)分子链中以将含氧官能团锚定在氧化石墨烯(GO)片材的表面上,因此增强了GO与橡胶之间的界面相互作用。通过形态观察和相互作用分析,发现通过利用氢键相互作用作为驱动力,环氧化天然橡胶(ENR)胶乳颗粒被组装在GO片材的表面上。这种自组装抑制了GO片材的重新堆积和聚结,并导致GO在ENR基质中均匀分散。 ENR和GO之间氢键界面的形成证明了ENR主体的显着增强。与纯ENR相比,GO原位负载量为0.7 wt%的复合材料在静态原位硫化后,拉伸强度增加200%,拉伸强度增加87%,模量增加8.7倍。 (C)2014 Elsevier Ltd.保留所有权利。

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