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Hydroxyl-Terminated Triazine Derivatives Grafted Graphene Oxide for Epoxy Composites: Enhancement of Interfacial and Mechanical Properties

机译:羟基封端的三嗪衍生物接枝的氧化石墨烯用于环氧复合材料:界面和机械性能的增强

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摘要

An effective approach to the fabrication of progressive epoxy nanocomposites by the incorporation of hydroxyl-terminated dendrimers functionalized graphene oxide (GO-TCT-Tris) is reported. The relationship between surface grafting, chemical construction, morphology, dispersion, and interfacial interaction as well as the corresponding mechanical properties of the composites were studied in detail. It was shown that hydroxyl-terminated triazine derivatives have been resoundingly bonded onto the GO surface through covalent bonding, which effectively improved the dispersion and compatibility of GO sheets in epoxy resin. The tensile and flexural tests manifested that the GO-TCT-Tris/epoxy composites exhibited greater tensile/flexural strength and modulus than either the pure epoxy or the GO/epoxy composites. For GO-TCT-Tris (0.10 wt%)/epoxy composite, the tensile strength and elastic modulus increased from 63 ± 4 to 89 ± 6 MPa (41.27%) and from 2.8 ± 0.1 to 3.6 ± 0.2 GPa (28.57%), and the flexural strength and modulus increased from 106 ± 5 to 158 ± 6 MPa (49.06%) and from 3.0 ± 0.1 to 3.5 ± 0.2 GPa (16.67%), respectively, compared to the pure epoxy matrix. Moreover, the fractographic analysis also illustrated the ameliorative interfacial interaction between GO-TCT-Tris and epoxy matrix.
机译:报道了通过掺入羟基封端的树枝状大分子官能化的氧化石墨烯(GO-TCT-Tris)来制备渐进环氧纳米复合材料的有效方法。详细研究了表面接枝,化学结构,形态,分散和界面相互作用之间的关系,以及复合材料的相应力学性能。结果表明,羟基末端的三嗪衍生物已通过共价键牢固地键合在GO表面,有效地改善了GO片在环氧树脂中的分散性和相容性。拉伸和挠曲测试表明,GO-TCT-Tris /环氧树脂复合材料比纯环氧树脂或GO /环氧树脂复合材料具有更高的拉伸/挠曲强度和模量。对于GO-TCT-Tris(0.10 wt%)/环氧树脂复合材料,拉伸强度和弹性模量从63±4到89±6 MPa(41.27%)和从2.8±0.1到3.6±0.2 GPa(28.57%)增加,与纯环氧基质相比,抗弯强度和模量分别从106±5 MPa增至158±6 MPa(49.06%)和从3.0±0.1增至3.5±0.2 GPa(16.67%)。此外,分形分析还显示了GO-TCT-Tris与环氧基质之间的界面改善作用。

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