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[离子液体+聚乙二醇]混合物中温度依赖性协同动态粘度和探针报告的微观粘度揭示的相互作用。

Interactions within a [ionic liquid + poly(ethylene glycol)] mixture revealed by temperature-dependent synergistic dynamic viscosity and probe-reported microviscosity.

机构信息

Department of Chemistry, Indian Institute of Technology, Delhi, Hauz Khas, New Delhi, India.

出版信息

J Phys Chem B. 2011 Jun 9;115(22):7405-16. doi: 10.1021/jp203079p. Epub 2011 May 17.

DOI:10.1021/jp203079p
PMID:21591689
Abstract

Mixtures of ionic liquid (IL) with poly(ethylene glycol) (PEG) may afford media with favorable properties. Dynamic viscosities of mixtures of a common and popular IL 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim][PF(6)]) with PEGs of average molecular weight (MW) 200 (PEG200), average MW 400 (PEG400), number-average MW M(n) 570-630 (PEG600), and number-average MW M(n) 950-1050 (PEG1000) over a complete composition range at 10° intervals in the temperature range of 10-90 °C are measured. The temperature dependence of the dynamic viscosity shows ([bmim][PF(6)] + PEG) mixtures to behave as Newtonian fluids and is found to follow Arrhenius-type behavior. In the IL-rich region, excess logarithmic viscosities for the ([bmim][PF(6)] + PEG200) mixture are found to be negative and independent of the temperature. Mixtures of ([bmim][PF(6)] + PEG600) and ([bmim][PF(6)] + PEG1000) show rare and unusual viscosity "synergism" or "hyperviscosity" in the sense that the mixture viscosity is observed to be significantly higher than the viscosity of both the neat components forming the mixture, giving rise to large positive excess logarithmic viscosities. These positive excess logarithmic viscosities decrease with increasing temperature. Formation of extensive H-bonding between the IL and PEG more than compensates for the losses in Coulombic attractive and van der Waals interactions within [bmim][PF(6)] and PEG600/PEG1000, respectively, giving rise to viscosity synergism. This compensation is not enough for ([bmim][PF(6)] + PEG200) and ([bmim][PF(6)] + PEG400) mixtures. The evidence for H-bonding in the mixtures is provided by FTIR absorbance data. The product of the monomer-to-excimer emission intensity ratio and the lifetime of the intramolecular excimer fluorescence of a microfluidity probe, 1,3-bis(1-pyrenyl)propane (BPP), is used as a reflection of the microviscosity of the mixture at different temperatures. The microviscosity shows synergistic effects in all four ([bmim][PF(6)] + PEG) mixtures. The contribution of H-bonding to the microviscosity reported by BPP is observed to be more then that as compared to contributions of Coulombic and van der Waals interactions. Synergism in the dynamic viscosity and microviscosity of ([bmim][PF(6)] + PEG) mixtures is a complex interplay of inter- and intramolecular H-bonding as well as Coulombic and van der Waals type interactions.

摘要

离子液体(IL)与聚乙二醇(PEG)的混合物可能提供具有良好性质的介质。在 10-90°C 的温度范围内以 10°C 的间隔测量常见且受欢迎的 IL 1-丁基-3-甲基咪唑六氟磷酸盐([bmim][PF(6))与平均分子量(MW)为 200(PEG200)、平均 MW 为 400(PEG400)、数均 MW M(n) 为 570-630(PEG600)和数均 MW M(n) 为 950-1050(PEG1000)的 PEG 混合物在整个组成范围内的动态粘度。动态粘度的温度依赖性表明,([bmim][PF(6)] + PEG)混合物表现为牛顿流体,并发现其遵循阿累尼乌斯型行为。在 IL 丰富的区域,([bmim][PF(6)] + PEG200)混合物的过量对数粘度为负,且与温度无关。([bmim][PF(6)] + PEG600)和([bmim][PF(6)] + PEG1000)混合物表现出罕见且不寻常的粘度“协同作用”或“超粘性”,因为观察到混合物的粘度明显高于形成混合物的两种纯组分的粘度,导致大的正过量对数粘度。这些正过量对数粘度随温度升高而降低。IL 与 PEG 之间形成广泛的氢键,足以补偿[bmim][PF(6)]和 PEG600/PEG1000 内库仑吸引和范德华相互作用的损失,从而导致粘度协同作用。这对于([bmim][PF(6)] + PEG200)和([bmim][PF(6)] + PEG400)混合物来说是不够的。混合物中氢键的证据由 FTIR 吸光度数据提供。微流动性探针 1,3-双(1-芘基)丙烷(BPP)的单体-激基发射强度比与分子内激基荧光寿命的乘积用作不同温度下混合物微粘度的反映。微粘度在四种([bmim][PF(6)] + PEG)混合物中均表现出协同效应。BPP 报告的氢键对微粘度的贡献被观察到大于库仑和范德华相互作用的贡献。([bmim][PF(6)] + PEG)混合物的动态粘度和微粘度的协同作用是分子间和分子内氢键以及库仑和范德华型相互作用复杂相互作用的结果。

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