Enhancing the pre-polymerization coordination of 1-vinylimidazole

被引:6
|
作者
Hamilton, Jackie R. [1 ]
Abedini, Asghar [1 ]
Zhang, Zhongtao [1 ]
Whitley, John W. [1 ]
Bara, Jason E. [1 ]
Turner, C. Heath [1 ]
机构
[1] Univ Alabama, Dept Chem & Biol Engn, Tuscaloosa, AL 35487 USA
基金
美国国家科学基金会;
关键词
Ionic liquid; Polymerization; Molecular dynamics; Simulation; Imidazole; TEMPERATURE IONIC LIQUIDS; MOLECULAR-FORCE FIELD; METHYL-METHACRYLATE; PHOTOPOLYMERIZATION; POLYVINYLIMIDAZOLE; DYNAMICS; SALT; ACCELERATION; SIMULATION; COMPOSITE;
D O I
10.1016/j.ces.2015.08.045
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Recent experimental investigations have found that the rate and conversion of the photopolymerization of 1-vinylimidazole (Vim) can be significantly accelerated with the addition of lithium bistrifiimide (LiTf2N). However, the underlying molecular-level interactions responsible for this phenomenon are unclear. The two components, Vim and L1Tf(2)N, are miscible over a wide range of concentrations and form liquid phases at ambient temperature, and if the fundamental behavior of this mixture can be clearly quantified, there are significant opportunities for tuning the polymerization dynamics, polymer structure, and properties. In this work, molecular dynamics (MD) simulations are used to model the underlying pre-polymerization structure of VIm+LiTf2N mixtures at several different concentrations. It is found that the Li+ enhances the site-site interactions of key functional groups involved in the polymerization, and this is suggested to play a major role in the experimentally-observed enhancement of the polymerization behavior. (C) 2015 Elsevier Ltd. All rights reserved.
引用
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页码:646 / 654
页数:9
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