Glass transition temperature of functionalized graphene-polymer composites

被引:60
|
作者
Xue, Qingzhong [1 ]
Lv, Cheng [2 ,3 ]
Shan, Meixia [2 ,3 ]
Zhang, Hongxin [1 ]
Ling, Cuicui [2 ,3 ]
Zhou, Xiaoyan [2 ,3 ]
Jiao, Zhiyong [2 ,3 ]
机构
[1] Beijing Univ Posts & Telecommun, Sch Elect Engn, Beijing 100876, Peoples R China
[2] China Univ Petr, Coll Sci, Qingdao 266580, Shandong, Peoples R China
[3] China Univ Petr, Key Lab New Energy Phys & Mat Sci Univ Shandong, Qingdao 266580, Shandong, Peoples R China
关键词
Glass transition temperature; Thermal expansion; Graphene-polymer composite; Dynamic simulation; MOLECULAR-DYNAMICS SIMULATION; INTERFACIAL BONDING CHARACTERISTICS; FORCE-FIELD; POLY(ETHYLENE OXIDE); THERMAL-EXPANSION; CARBON NANOTUBES; AB-INITIO; NANOCOMPOSITES; CHEMISORPTION; MISCIBILITY;
D O I
10.1016/j.commatsci.2013.01.009
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In this study, a "cooling process", performed by molecular dynamics simulation, was used to predict the glass transition temperature (T-g) of graphene-polymer composites. It was found that the functionalization of graphene can greatly enhance T-g of graphene-polymer composites, which shows that the functionalized graphene can intensify the arrest of the polymer chains mobility. Meanwhile, it was found that the thermal expansion of the composites exhibited a relation with the phonon mode vibrations and Brownian motions of the graphene in the composites. The computational results of T-g were in good agreement with the experimental results indicating that this computational method can be used to predict effectively T-g of graphene-polymer composites. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:66 / 71
页数:6
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