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氟化氧化石墨烯层间距对氟化环氧树脂热性能和力学性能影响的分子动力学模拟

Molecular Dynamics Simulation for the Effect of Fluorinated Graphene Oxide Layer Spacing on the Thermal and Mechanical Properties of Fluorinated Epoxy Resin.

作者信息

Duan Qijun, Xie Jun, Xia Guowei, Xiao Chaoxuan, Yang Xinyu, Xie Qing, Huang Zhengyong

机构信息

Hebei Provincial Key Laboratory of Power Transmission Equipment Security Defense, North China Electric Power University, Baoding 071003, China.

State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources, North China Electric Power University, Beijing 102206, China.

出版信息

Nanomaterials (Basel). 2021 May 20;11(5):1344. doi: 10.3390/nano11051344.

DOI:10.3390/nano11051344
PMID:34065258
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8160737/
Abstract

Traditional epoxy resin (EP) materials have difficulty to meet the performance requirements in the increasingly complex operating environment of the electrical and electronic industry. Therefore, it is necessary to study the design and development of new epoxy composites. At present, fluorinated epoxy resin (F-EP) is widely used, but its thermal and mechanical properties cannot meet the demand. In this paper, fluorinated epoxy resin was modified by ordered filling of fluorinated graphene oxide (FGO). The effect of FGO interlayer spacing on the thermal and mechanical properties of the composite was studied by molecular dynamics (MD) simulation. It is found that FGO with ordered filling can significantly improve the thermal and mechanical properties of F-EP, and the modification effect is better than that of FGO with disordered filling. When the interlayer spacing of FGO is about 9 Å, the elastic modulus, glass transition temperature, thermal expansion coefficient, and thermal conductivity of FGO are improved with best effect. Furthermore, we calculated the micro parameters of different systems, and analyzed the influencing mechanism of ordered filling and FGO layer spacing on the properties of F-EP. It is considered that FGO can bind the F-EP molecules on both sides of the nanosheets, reducing the movement ability of the molecular segments of the materials, so as to achieve the enhancement effect. The results can provide new ideas for the development of high-performance epoxy nanocomposites.

摘要

传统环氧树脂(EP)材料在电气和电子行业日益复杂的运行环境中难以满足性能要求。因此,有必要研究新型环氧复合材料的设计与开发。目前,氟化环氧树脂(F-EP)被广泛使用,但其热性能和力学性能无法满足需求。本文通过氟化氧化石墨烯(FGO)的有序填充对氟化环氧树脂进行改性。采用分子动力学(MD)模拟研究了FGO层间距对复合材料热性能和力学性能的影响。研究发现,有序填充的FGO能显著提高F-EP的热性能和力学性能,且改性效果优于无序填充的FGO。当FGO的层间距约为9 Å时,FGO的弹性模量、玻璃化转变温度、热膨胀系数和热导率的改善效果最佳。此外,我们计算了不同体系的微观参数,并分析了有序填充和FGO层间距对F-EP性能的影响机制。认为FGO可以在纳米片两侧结合F-EP分子,降低材料分子链段的运动能力,从而实现增强效果。研究结果可为高性能环氧纳米复合材料的开发提供新思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/1dac82bdbfa6/nanomaterials-11-01344-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/d8f68e905efe/nanomaterials-11-01344-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/6582d20a57c3/nanomaterials-11-01344-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/bec9ab291e0e/nanomaterials-11-01344-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/092d104dfeb5/nanomaterials-11-01344-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/a48273758f71/nanomaterials-11-01344-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/6e1202ec6a03/nanomaterials-11-01344-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/661f151ac4ba/nanomaterials-11-01344-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/49dd7cecaa7f/nanomaterials-11-01344-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/1dac82bdbfa6/nanomaterials-11-01344-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/d8f68e905efe/nanomaterials-11-01344-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/6582d20a57c3/nanomaterials-11-01344-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/bec9ab291e0e/nanomaterials-11-01344-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/b2b45db8207f/nanomaterials-11-01344-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/092d104dfeb5/nanomaterials-11-01344-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/a48273758f71/nanomaterials-11-01344-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/6e1202ec6a03/nanomaterials-11-01344-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/661f151ac4ba/nanomaterials-11-01344-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/49dd7cecaa7f/nanomaterials-11-01344-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e748/8160737/1dac82bdbfa6/nanomaterials-11-01344-g010.jpg

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