Liu Zhonghua, Wang Wei, Stadler Florian J, Yan Zhi-Chao
College of Materials Science and Engineering, Shenzhen Key Laboratory of Polymer Science and Technology, Guangdong Research Center for Interfacial Engineering of Functional Materials, Nanshan District Key Lab for Biopolymers and Safety Evaluation, Shenzhen University, Shenzhen 518055, China.
Polymers (Basel). 2019 May 14;11(5):877. doi: 10.3390/polym11050877.
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- 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 of PMMA in IL is higher than the prediction of the self-concentration model, while in conventional polymer solutions, follows the original Fox equation. Observations in both solutions reveal retarded segmental dynamics, consistent with a recent simulation result (, 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.
通过应用广泛的流变学技术,在聚合物/离子液体(IL)溶液中观察到了异常的增塑效应。聚环氧乙烷(PEO)/IL溶液表现出比纯PEO更强的动态温度依赖性,这与低溶剂会增加自由体积分数的认知相矛盾。对于聚甲基丙烯酸甲酯(PMMA)/IL溶液,从PMMA在IL中的有效玻璃化转变温度高于自浓度模型预测这一事实中检测到了微妙的异常,而在传统聚合物溶液中,遵循原始的福克斯方程。两种溶液中的观察结果都揭示了链段动力学的迟缓,这与最近的模拟结果(2018年,51卷,5336页)一致,即聚合物链通过氢键相互作用包裹IL阳离子,链段的解缠延迟了它们的松弛。聚合物/IL溶液的起始剪切和非线性应力松弛测试遵循与聚合物熔体和溶液相同的通用非线性流变行为,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。目前的工作可能会激发人们在解释复杂的聚合物-IL相互作用对聚合物/IL溶液动力学的影响方面,进一步开展理论、实验和模拟研究。