Studying the Structure and Properties of Epoxy Composites Modified by Original and Functionalized with Hexamethylenediamine by Electrochemically Synthesized Graphene Oxide

Nanomaterials Pub Date : 2024-03-28 DOI:10.3390/nano14070602
A. Mostovoy, A. Bekeshev, Sergey Brudnik, A. Yakovlev, Andrey Shcherbakov, Nurgul Zhanturina, Arai K. Zhumabekova, Elena Yakovleva, Vitaly Tseluikin, M. Lopukhova
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Abstract

In this study, we used multilayer graphene oxide (GO) obtained by anodic oxidation of graphite powder in 83% sulfuric acid. The modification of GO was carried out by its interaction with hexamethylenediamine (HMDA) according to the mechanism of nucleophilic substitution between the amino group of HMDA (HMDA) and the epoxy groups of GO, accompanied by partial reduction of multilayer GO and an increase in the deformation of the carbon layers. The structure and properties of modified HMDA-GO were characterized using research methods such as scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction spectroscopy and Raman spectroscopy. The conducted studies show the effectiveness of using HMDA-OG for modifying epoxy composites. Functionalizing treatment of GO particles helps reduce the free surface energy at the polymer–nanofiller interface and increase adhesion, which leads to the improvement in physical and mechanical characteristics of the composite material. The results demonstrate an increase in the strength and elastic modulus in bending by 48% and 102%, respectively, an increase in the impact strength by 122%, and an increase in the strength and elastic modulus in tension by 82% and 47%, respectively, as compared to the pristine epoxy composite which did not contain GO-HMDA. It has been found that the addition of GO-HMDA into the epoxy composition initiates the polymerization process due to the participation of reactive amino groups in the polymerization reaction, and also provides an increase in the thermal stability of epoxy nanocomposites.
研究原始改性环氧树脂复合材料和电化学合成石墨烯功能化六亚甲基二胺复合材料的结构与性能
在这项研究中,我们使用了在 83% 的硫酸中对石墨粉进行阳极氧化而得到的多层氧化石墨烯(GO)。根据 HMDA(六甲基二胺)的氨基与 GO 的环氧基团之间的亲核取代机理,通过与六甲基二胺(HMDA)的相互作用对 GO 进行改性,伴随着多层 GO 的部分还原和碳层变形的增加。利用扫描电子显微镜(SEM)、傅立叶变换红外光谱(FTIR)、X 射线衍射光谱和拉曼光谱等研究方法对改性 HMDA-GO 的结构和性质进行了表征。研究结果表明,使用 HMDA-OG 对环氧树脂复合材料进行改性非常有效。对 GO 粒子进行功能化处理有助于降低聚合物-纳米填料界面的自由表面能,增加粘附性,从而改善复合材料的物理和机械特性。结果表明,与不含 GO-HMDA 的原始环氧树脂复合材料相比,弯曲强度和弹性模量分别提高了 48% 和 102%,冲击强度提高了 122%,拉伸强度和弹性模量分别提高了 82% 和 47%。研究发现,由于活性氨基参与了聚合反应,在环氧组合物中添加 GO-HMDA 可以启动聚合过程,还能提高环氧纳米复合材料的热稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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