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氧化石墨烯功能化库阿索纤维增强环氧树脂复合材料的动态力学行为:简要报告

Dynamic Mechanical Behavior of Graphene Oxide Functionalized Curaua Fiber-Reinforced Epoxy Composites: A Brief Report.

作者信息

Costa Ulisses Oliveira, Nascimento Lucio Fabio Cassiano, Almeida Bezerra Wendell Bruno, de Oliveira Aguiar Vinícius, Pereira Artur Camposo, Monteiro Sergio Neves, Pinheiro Wagner Anacleto

机构信息

Composite Materials Group, Department of Materials Science, Military Institute of Engineering, IME, Rio de Janeiro 22290-270, Brazil.

Department of Polymer Science and Technology, Institute of Macromolecules Professor Eloisa Mano, IMA, Rio de Janeiro 21941-598, Brazil.

出版信息

Polymers (Basel). 2021 Jun 7;13(11):1897. doi: 10.3390/polym13111897.

Abstract

The coating of natural fiber by graphene oxide (GO) has, over, this past decade, attracted increasing attention as an effective way to improve the adhesion to polymer matrices and enhance the composite properties. In particular, the GO-functionalized 30 vol% curaua fiber () reinforcing epoxy composite was found to display superior tensile and thermogravimetric properties as well as higher fiber/matrix interfacial shear strength. In this brief report, dynamic mechanical analysis (DMA) was conducted in up to 50 vol% GO-functionalized curaua fiber reinforced epoxy matrix (EM) composites. The objective was not only to extend the amount incorporated but also for the first time investigate the composite viscoelastic behavior. The GO functionalization of curaua fibers (GOCF) improved the DMA storage (E') and loss (E″) modulus compared to the non-functionalized fiber composites. Values at 30 °C of both E' (13.44 GPa) and E″ (0.67 GPa) for 50 vol% GO-functionalized curaua fiber reinforced epoxy matrix composites (50GOCF/EM) were substantially higher than those of 20 GOCF/EM with E' (7.08 GPa) and E″ (0.22 GPa) as well as non-functionalized 50CF/EM with E' (11.04 GPa) and E″ (0.45 GPa). All these results are above the neat epoxy previously reported values of E' (3.86 GPa) and E″ (0.09 GPa). As for the tangent delta, the parameters associated with damping factor and glass transition temperature were not found to be significantly changed by GO functionalization, but decreased with respect to the neat epoxy due to chain mobility restriction.

摘要

在过去十年中,通过氧化石墨烯(GO)对天然纤维进行涂层处理,作为一种改善与聚合物基体的粘附性和增强复合材料性能的有效方法,已引起越来越多的关注。特别是,发现经GO功能化的30体积%的库拉索纤维增强环氧复合材料具有优异的拉伸性能和热重性能,以及更高的纤维/基体界面剪切强度。在本简要报告中,对高达50体积%的经GO功能化的库拉索纤维增强环氧基体(EM)复合材料进行了动态力学分析(DMA)。目的不仅是增加掺入量,而且首次研究复合材料的粘弹性行为。与未功能化的纤维复合材料相比,库拉索纤维的GO功能化提高了DMA储能模量(E')和损耗模量(E'')。对于50体积%的经GO功能化的库拉索纤维增强环氧基体复合材料(50GOCF/EM),在30℃时E'(13.44 GPa)和E''(0.67 GPa)的值显著高于20GOCF/EM的E'(7.08 GPa)和E''(0.22 GPa)以及未功能化的50CF/EM的E'(11.04 GPa)和E''(0.45 GPa)。所有这些结果均高于先前报道的纯环氧树脂的E'(3.86 GPa)和E''(0.09 GPa)值。至于损耗因子,与阻尼因子和玻璃化转变温度相关的参数未发现因GO功能化而有显著变化,但由于链迁移率受限,相对于纯环氧树脂有所降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0ad/8201326/174ad325e698/polymers-13-01897-g001.jpg

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