Freezing point depression of salt aqueous solutions using the Madrid-2019 model

冰点降低 冰点 水溶液 水模型 盐(化学) 化学 共晶体系 扩散 热力学 工作(物理) 溶解度 化学物理 电解质 力场(虚构) 分子动力学 物理 计算化学 物理化学 结晶学 微观结构 电极 量子力学
作者
Cintia P. Lamas,Carlos Vega,Eva G. Noya
出处
期刊:Journal of Chemical Physics [American Institute of Physics]
卷期号:156 (13) 被引量:27
标识
DOI:10.1063/5.0085051
摘要

Salt aqueous solutions are relevant in many fields, ranging from biological systems to seawater. Thus, the availability of a force-field that is able to reproduce the thermodynamic and dynamic behavior of salt aqueous solutions would be of great interest. Unfortunately, this has been proven challenging, and most of the existing force-fields fail to reproduce much of their behavior. In particular, the diffusion of water or the salt solubility are often not well reproduced by most of the existing force-fields. Recently, the Madrid-2019 model was proposed, and it was shown that this force-field, which uses the TIP4P/2005 model for water and non-integer charges for the ions, provides a good description of a large number of properties, including the solution densities, viscosities, and the diffusion of water. In this work, we assess the performance of this force-field on the evaluation of the freezing point depression. Although the freezing point depression is a colligative property that at low salt concentrations depends solely on properties of pure water, a good model for the electrolytes is needed to accurately predict the freezing point depression at moderate and high salt concentrations. The coexistence line between ice and several salt aqueous solutions (NaCl, KCl, LiCl, MgCl2, and Li2SO4) up to the eutectic point is estimated from direct coexistence molecular dynamics simulations. Our results show that this force-field reproduces fairly well the experimentally measured freezing point depression with respect to pure water freezing for all the salts and at all the compositions considered.
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