聚合
聚丙烯腈
聚吡咯
材料科学
纳米纤维
化学工程
单体
高分子化学
动力学
原位聚合
界面聚合
吡咯
静电纺丝
聚合物
化学
复合材料
有机化学
工程类
物理
量子力学
作者
Yifu Li,Hesheng Yu,Yi Zhang,Y. Zhou,Zhongchao Tan
标识
DOI:10.1016/j.cej.2021.133531
摘要
Polypyrrole (PPy) is a conductive polymer that can be fabricated into various structures via in-situ polymerization for different applications. However, a kinetics study of its in-situ polymerization is needed for a better understanding of the mechanisms of pyrrole polymerization. This paper develops two different kinetics models based on existing PPy polymerization mechanisms. The most suitable mechanism is first identified by comparing the model results with experimental data. Then, in-situ polymerizations of PPy on electrospun fibrous polyacrylonitrile (PAN) templates were produced at temperatures ranging from 273 to 285 K. The results show that the overall reaction rate of the in-situ polymerization process in the presence of electrospun fibrous template is faster than that without the template. Further investigation confirms that the increase in the overall reaction rate is attributed to the enhanced reactions between oxidized pyrrole oligomers and neutral pyrrole monomers, as the corresponding reaction rate constant and activation entropy increased by 158.2–209.6% and 37.7%, respectively. The reason is that the considerable number of available reaction sites between oxidized oligomers and neutral monomers are created by the fibrous template. In addition, the composite membrane obtained from the in-situ polymerization exhibited well-developed fibrous nanostructure, good electrical conductivity (0.29 ± 0.04 S∙m−1), sufficient mechanical strength (UTS of 8.7 MPa) and relatively stable thermal properties (up to 250 °C).
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