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深共熔溶剂固液平衡的活度建模

Activity modelling of the solid-liquid equilibrium of deep eutectic solvents.

作者信息

Kollau Laura J B M, Vis Mark, van den Bruinhorst Adriaan, de With Gijsbertus, Tuinier Remco

机构信息

Laboratory of Physical Chemistry, Department of Chemical Engineering and Chemistry, Eindhoven University of Technology, P.O. Box 513, 5600MB Eindhoven, The Netherlands.

Institute for Complex Molecular Systems, Eindhoven University of Technology, Eindhoven, The Netherlands.

出版信息

Pure Appl Chem. 2019 May 21;91(8):1341-1349. doi: 10.1515/pac-2018-1014. eCollection 2019 Aug.

Abstract

Compared to conventional solvents used in the chemical industry, deep eutectic solvents (DESs) are considered as promising potentially sustainable solvents. DESs are binary mixtures and the resulting liquid mixture is characterized by a large melting point depression with respect to the melting temperatures of its constituents. The relative melting point depression becomes larger as the two components have stronger attractive interactions, resulting in non-ideal behavior. The compositional range over which such binary mixtures are liquids is set by the location of the solid-liquid phase boundary. Here we present experimental phase diagrams of various recent and new DESs that vary in the degree of non-ideality. We investigate whether thermodynamic models are able to describe the solid-liquid equilibria and focus on relating the parameters of these models to the non-ideal behavior, including asymmetric behavior of the activity coefficients. It is shown that the orthogonal Redlich-Kister-like polynomial (OP) expansion, including an additional first order term, provides an accurate description. This theory can be considered as an extension of regular solution theory and enables physical interpretation of the fit parameters.

摘要

与化学工业中使用的传统溶剂相比,深共熔溶剂(DESs)被认为是有潜力的可持续溶剂。DESs是二元混合物,所得液体混合物的特征是相对于其组分的熔点有较大的熔点降低。随着两种组分具有更强的吸引相互作用,相对熔点降低变得更大,导致非理想行为。这种二元混合物为液体的组成范围由固 - 液相边界的位置确定。在此,我们展示了各种近期和新型DESs的实验相图,这些DESs在非理想程度上有所不同。我们研究热力学模型是否能够描述固 - 液平衡,并着重将这些模型的参数与非理想行为相关联,包括活度系数的不对称行为。结果表明,包括一个额外一阶项的正交类Redlich - Kister多项式(OP)展开提供了准确的描述。该理论可被视为正规溶液理论的扩展,并能够对拟合参数进行物理解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2a8/11670871/415fbd4b8a54/j_pac-2018-1014_fig_003.jpg

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