Crystallization kinetics of PVDF filled with multi wall carbon nanotubes modified by amphiphilic ionic liquid
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  • 作者:Ali Bahader ; Haoguan Gui ; Yu Li ; Pei Xu ; Yunsheng Ding
  • 关键词:poly(vinylidene fluoride) (PVDF) ; crystallization kinetics ; ionic liquids ; MWCNT and nucleation
  • 刊名:Macromolecular Research
  • 出版年:2015
  • 出版时间:March 2015
  • 年:2015
  • 卷:23
  • 期:3
  • 页码:273-283
  • 全文大小:1,054 KB
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  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Chemistry
    Physical Chemistry
    Polymer Sciences
    Characterization and Evaluation of Materials
    Soft and Granular Matter, Complex Fluids and Microfluidics
    Nanochemistry
    Nanotec
  • 出版者:The Polymer Society of Korea, co-published with Springer
  • ISSN:2092-7673
文摘
The special electric properties of the poly(vinylidene fluoride) (PVDF) is strongly dependent on its crystalline structural morphology. In this study, modification in the crystal structure of PVDF was achieved by utilizing the long alkyl chain ionic liquid (1-hexadecyl-3-methylimidazolium bromide, [C16mim][Br]) and ionic liquid modified multiwalled carbon nanotubes (MWCNT). The developed crystal pattern was analyzed by XRD and the compatibility and dispersion characteristics of MWCNT in the matrix was observed by FESEM. The isothermal and non-isothermal crystallization kinetics were studied by DSC and different models namely; Avrami, Jeziorny and Ozawa were applied to fit the data. The results demonstrate that crystal structure of PVDF is significantly changed and the dispersion of MWCNT was enhanced with the addition of ionic liquid (IL). Kinetically, the crystallization was influenced and became fast due to the presence of [C16mim][Br] at the PVDF/MWCNT interface. Furthermore, the data well fitted in the model with significant linearity. The positive effect on the crystallization of PVDF may be ascribed to not only due to the existence of π-cation interaction between the imidazolium cation and the aromatic multiwall carbon nanotubes structure, but also due to the electrostatic interaction between the > CF2 of the polymer backbone and imidazolium cation, which speed up the crystallization kinetics.

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