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Rheology of Concentrated Polymer/Ionic Liquid Solutions: An Anomalous Plasticizing Effect and a Universality in Nonlinear Shear Rheology

机译:浓缩聚合物/离子液体溶液的流变学:异常增塑效应和非线性剪切流变学的普遍性

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摘要

An anomalous plasticizing effect was observed in polymer/ionic liquid (IL) solutions by applying broad range of rheological techniques. Poly(ethylene oxide)(PEO)/IL solutions exhibit stronger dynamic temperature dependence than pure PEO, which is in conflict with the knowledge that lower-Tg solvent increases the fractional free volume. For poly(methy methacrylate)(PMMA)/IL solutions, the subtle anomaly was detected from the fact that the effective glass transition temperature Tg,eff of PMMA in IL is higher than the prediction of the self-concentration model, while in conventional polymer solutions, Tg,eff follows the original Fox equation. Observations in both solutions reveal retarded segmental dynamics, consistent with a recent simulation result (Macromolecules, 2018, 51, 5336) that polymer chains wrap the IL cations by hydrogen bonding interactions and the segmental unwrapping delays their relaxation. Start-up shear and nonlinear stress relaxation tests of polymer/IL solutions follow a universal nonlinear rheological behavior as polymer melts and solutions, indicating that the segment-cation interaction is not strong enough to influence the nonlinear chain orientation and stretch. The present work may arouse the further theoretical, experimental, and simulation interests in interpreting the effect of complex polymer-IL interaction on the dynamics of polymer/IL solutions.
机译:通过应用广泛的流变技术,在聚合物/离子液体(IL)溶液中观察到了异常的塑化效果。聚环氧乙烷(PEO)/ IL溶液比纯PEO具有更强的动态温度依赖性,这与较低Tg溶剂会增加自由体积分数的认识相矛盾。对于聚甲基丙烯酸甲酯(PMMA)/ IL溶液,从以下事实检测到微妙的异常:IL中的PMMA的有效玻璃化转变温度Tg,eff高于自浓缩模型的预测值,而在常规聚合物中解,Tg,eff遵循原始的Fox方程。两种解决方案中的观察结果都揭示了节段动力学的延迟,这与最近的模拟结果(Macromolecules,2018,51,5336)一致,即聚合物链通过氢键相互作用包裹了IL阳离子,节段的开卷延缓了其松弛。聚合物/ IL溶液的启动剪切和非线性应力松弛测试遵循普遍的非线性流变行为,即聚合物熔融和溶解,表明链段-阳离子相互作用不足以影响非线性链的取向和拉伸。当前的工作可能会引起更多的理论,实验和模拟兴趣,以解释复杂的聚合物-IL相互作用对聚合物/ IL溶液动力学的影响。

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