材料科学
纳米复合材料
碳纳米管
结晶
渗流阈值
复合材料
有机粘土
三元运算
成核
极限抗拉强度
电阻率和电导率
化学工程
工程类
程序设计语言
化学
有机化学
电气工程
计算机科学
标识
DOI:10.1016/j.matchemphys.2013.09.054
摘要
Binary and ternary poly(vinylidene fluoride) (PVDF) nanocomposites filled with organoclay (15A) and/or multi-walled carbon nanotubes (MWNTs) were successfully prepared. MWNTs were dispersed more homogeneously than 15A within PVDF matrix, and the presence of MWNTs facilitated the dispersibility of 15A. The 15A addition induced β -form PVDF crystal formation, but MWNTs hardly changed the α -form crystal development. Both nanofillers facilitated the nucleation of PVDF (up to 12.3 °C increase), and the efficiency of enhancing PVDF crystallization followed the sequence MWNT > 15A/MWNT > 15A. The nanocomposites possess higher T m ° than neat PVDF. In particular, adding 15A led to a T m ° ( β -form) increase of no less than 11 °C. A rheological percolation threshold at 1 wt.% MWNT loading was determined. The electrical resistivity dropped by more than 13 orders of magnitude at 5 wt.% MWNT loading. The nanocomposites exhibited enhanced tensile modulus (up to 83% increase with MWNTs inclusion) compared with neat PVDF. • Properties of binary and ternary PVDF nanocomposites were compared. • PVDF crystallization rise followed the order of adding MWNT > nanoclay/MWNT > nanoclay. • Nanoclay induced the β -form crystals; MWNT hardly changed the α -form crystals. • Higher equilibrium melting temperatures were observed in the nanocomposites. • Electrical percolation threshold was at 0.5 wt.% MWNT loading.
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