超声
层状结构
材料科学
微晶
相位反转
相(物质)
结晶
聚合物
傅里叶变换红外光谱
氟化物
化学工程
高分子化学
差示扫描量热法
分析化学(期刊)
结晶学
复合材料
化学
有机化学
膜
热力学
物理
工程类
生物化学
无机化学
冶金
作者
Rinu Elizabeth Roy,S. Bhuvaneswari,K. P. Vijayalakshmi,Roopa Dimple,Panthaplackal Bhaskaran Soumyamol,R.S. Rajeev
摘要
ABSTRACT Self‐polarized poly(vinylidene fluoride) (PVDF) films were prepared via solution crystallization technique wherein the polymorphism of the films was controlled from α phase (>85%) to γ phase (>90%) by varying the time of ultrasonication. On increasing ultrasonication time up to 60 min, γ phase crystallites were found to be self‐aligned in the matrix while an equal proportion of α and γ phases coexist in the PVDF films ultrasonicated for 120 min. The phase conversion as well as inversion was evident from Fourier transform infrared, X‐ray diffraction, and differential scanning calorimetry analyses. Microscopic images of films ultrasonicated for 60 min showed a scrolled lamellar morphology while those sonicated for 120 min showed mixture of scrolled lamellar and spherulitic morphology. With the help of computational studies, it is explained that a large amount of energy is required for transforming trans‐gauche‐trans‐gauche into trans‐trans‐trans‐gauche conformation which is provided by ultrasonication. The mechanism of γ phase formation is proposed based on the experimental and theoretical approaches. Our studies show that just by tuning the time of ultrasonication, PVDF films with various morphologies can be processed; either one with predominantly electroactive γ phase with superior electrical properties or one with equal proportion of α and γ phases with superior mechanical properties. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2019 , 57 , 40–50
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