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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.
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页码:66 / 71
页数:6
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