Evaluation of thermal, mechanical, and electrical properties of PVDF/GNP binary and PVDF/PMMA/GNP ternary nanocomposites

被引:65
作者
Chiu, Fang-Chyou [1 ]
Chen, Ying-Jing [1 ]
机构
[1] Chang Gung Univ, Dept Chem & Mat Engn, Taoyuan 333, Taiwan
关键词
Nano-structures; Polymer-matrix composites (PMCs); Thermal properties; Mechanical properties; WALLED CARBON NANOTUBES; POLY(VINYLIDENE FLUORIDE); PHYSICAL-PROPERTIES; POLY(METHYL METHACRYLATE); RHEOLOGICAL PROPERTIES; LAYERED SILICATE; BETA-PHASE; BLENDS; CRYSTALLIZATION; POLYMORPHISM;
D O I
10.1016/j.compositesa.2014.09.019
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Graphene nanoplatelet (GNP) was incorporated into poly(vinylidene fluoride) (PVDF) and PVDF/poly (methyl methacrylate) (PMMA) blend to achieve binary and ternary nanocomposites. GNP was more randomly dispersed in binary composites compared with ternary composites. GNP exhibited higher nucleation efficiency for PVDF crystallization in ternary composites than in binary composites. GNP addition induced PVDF crystals with higher stability; however, PMMA imparted opposite effect. The binary composite exhibited lower thermal expansion value than PVDF; the value further declined (up to 28.5% drop) in the ternary composites. The storage modulus of binary and ternary composites increased to 23.1% and 53.9% (at 25 degrees C), respectively, compared with PVDF. Electrical percolation threshold between 1 phr and 2 phr GNP loading was identified for the two composite systems; the ternary composites exhibited lower electrical resistivity at identical GNP loadings. Rheological data confirmed that the formation of GNP (pseudo)network structure was assisted in the ternary system. (C) 2014 Elsevier Ltd. All rights reserved.
引用
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页码:62 / 71
页数:10
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