Yury A. Budkov, Nikolai N. Kalikin, Petr E. Brandyshev
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引用次数: 0
Abstract
We determine the surface tension of aqueous electrolyte solutions in contact with non-polar dielectric media using a thermomechanical approach, which involves deriving the stress tensor from the thermodynamic potential of an inhomogeneous fluid. To obtain the surface tension, we calculate both the normal and tangential pressures using the components of the stress tensor, recently derived by us [Y. A. Budkov and P. E. Brandyshev, J. Chem. Phys. 159, 174103 (2023)] within the framework of Wang’s variational field theory. Using this approach, we derive an analytical expression for the surface tension in the linear approximation. At low ionic concentrations, this expression represents the classical Onsager–Samaras limiting law. By utilizing only one fitting parameter, which is related to the affinity of anions to the dielectric boundary, we successfully approximated experimental data on the surface tension of several aqueous electrolyte solutions. This approximation applies to both the solution–air and solution–dodecane interfaces, covering a wide range of electrolyte concentrations.
我们采用热力学方法测定了与非极性介质接触的电解质水溶液的表面张力,该方法包括从非均相流体的热力学势中推导出应力张量。为了获得表面张力,我们使用应力张量的分量计算法向和切向压力,这些分量是我们最近在王氏变分场理论框架内推导出来的 [Y. A. Budkov and P. E. Brandyshev, J. Chem. Phys.利用这种方法,我们得出了线性近似表面张力的分析表达式。在低离子浓度下,该表达式代表了经典的 Onsager-Samaras 极限定律。通过仅使用一个与阴离子对介电边界的亲和力有关的拟合参数,我们成功地近似了几种电解质水溶液的表面张力实验数据。这种近似方法适用于溶液-空气界面和溶液-十二烷界面,涵盖了广泛的电解质浓度范围。