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首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Macroscopic Differentiators for Microscopic Structural Nonideality in Binary Ionic Liquid Mixtures
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Macroscopic Differentiators for Microscopic Structural Nonideality in Binary Ionic Liquid Mixtures

机译:二元离子液体混合物中微观结构非直观性的宏观分子

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Combining two ionic liquids to form a binary ionic liquid mixture is a simple yet effective strategy to not only expand the number of ionic liquids but also precisely control various physicochemical properties of resultant ionic liquid mixtures. From a fundamental thermodynamic point of view, it is not entirely clear whether such mixtures can be classified as ideal solutions. Given a large number of binary ionic liquid mixtures that emerge, the ability to predict the presence of nonideality in such mixtures a priori without the need for experimentation or molecular simulationbased calculations is immensely valuable for their rational design. In this research report, we demonstrate that the difference in the molar volumes (Delta V) of the pure ionic liquids and the difference in the hydrogen-bonding ability of anions (Delta beta) are the primary determinants of nonideal behavior of binary ionic liquid mixtures containing a common cation and two anions. Our conclusion is derived from a comparison of microscopic structural properties expressed in terms of radial, spatial, and angular distributions for binary mixtures and those of the corresponding pure ionic liquids. Molecular dynamics simulations of 16 binary ionic liquid mixtures, containing a common cation 1-n-butyl-3-methylimidazolium [C(4)mim](+) and combinations of (less basic) fluorinated {trifluoromethylacetate [TFA](-), trifluoromethanesulfonate [TFS](-), bis(trifluoromethanesulfonyl) imide [NTf2](-), and tris (pentafluoroethyl) trifluorophosphate [eFAP](-)} versus (more basic) nonfluorinated {chloride Cl-, acetate [OAC](-), methylsulfate [MeSO4](-), and dimethylphosphate [Me2PO4](-)} anions, were conducted. The large number of binary ionic liquid mixtures examined here enabled us to span a broad range of Delta V and Delta beta values. The results indicate that binary mixtures of two ionic liquids for which Delta V > 60 cm(3)/mol and Delta beta > 0.4 are expected to be microscopically nonideal. On the other hand, Delta V < 60 cm(3)/mol and Delta beta < 0.4 will lead to molecular structures that are not differentiated from those of their pure ionic liquid counterparts.
机译:组合两种离子液体以形成二元离子液体混合物是一种简单而有效的策略,不仅膨胀离子液体的数量,而且精确地控制所得离子液体混合物的各种物理化学性质。从根本的热力学的角度来看,它并不完全清楚这些混合物是否可以被归类为理想的解决方案。给定大量的二元离子液体混合物,其在这种混合物中预测非前熟存在的能力优先于没有实验或分子模拟的计算的优先考虑对其合理设计非常有价值。在本研究报告中,我们证明了纯离子液体的摩尔体积(Delta V)的差异和阴离子的氢键能力(Delta Beta)的差异是二元离子液体混合物的非膜行为的主要决定因素含有常见的阳离子和两个阴离子。我们的结论是衍生自用于二元混合物的径向,空间和角度分布而表达的微观结构特性的比较和相应的纯离子液体的显微结构特性。 16二元离子液体混合物的分子动力学模拟,含有常见的阳离子1-正丁基-3-甲基咪唑鎓[C(4)MIM](+)和(较少碱性)氟化的组合(三氟甲基乙酸酯[TFA]( - ),三氟甲磺酸磺酸盐[TFS]( - ),双(三氟甲磺酰基)酰亚胺[NTF2]( - ),和三(五氟乙基)三氟磷酸η( - )( - )非氟磷酸酯}与(更碱性)非氟化含量(氯化物Cl-,乙酸酯[OAC]( - ),进行甲基硫酸盐[Meso4]( - )和二甲基磷酸磷酸磷酸磷酸酯[ME2PO4]( - )}阴离子。介绍的大量二元离子液体混合物使我们能够跨越广泛的ΔV和Δβ值。结果表明,预期ΔV> 60cm(3)/ mol和Deltaβ> 0.4的两种离子液体的二元混合物预期是显微镜的。另一方面,δV<60cm(3)/ mol和Deltaβ<0.4将导致不与纯离子液体对应物的分子结构。

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