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弱荷多孔介质的机械化学效应。

Mechano-chemical effects in weakly charged porous media.

机构信息

Institute of Bio-Colloid Chemistry of Ukrainian Academy of Sciences, Vernadskogo, 42, 03142 Kiev, Ukraine.

ICREA &Department d'Enginyeria Química (EQ), Universitat Politècnica de Catalunya, Av. Diagonal, 647, Edifici H, 4a planta, 08028 Barcelona, Spain.

出版信息

Adv Colloid Interface Sci. 2015 Aug;222:779-801. doi: 10.1016/j.cis.2014.09.006. Epub 2014 Oct 2.

Abstract

The paper is concerned with mechano-chemical effects, namely, osmosis and pressure-driven separation of ions that can be observed when a charged porous medium is placed between two electrolyte solutions. The study is focused on porous systems with low equilibrium interfacial potentials (about 30 mV or lower). At such low potentials, osmosis and pressure-driven separation of ions noticeably manifest themselves provided that the ions in the electrolyte solutions have different diffusion coefficients. The analysis is conducted by combining the irreversible thermodynamic approach and the linearized (in terms of the normalized equilibrium interfacial potential) version of the Standard Electrokinetic Model. Osmosis and the pressure-driven separation of ions are considered for an arbitrary mixed electrolyte solution and various porous space geometries. It is shown that the effects under consideration are proportional to a geometrical factor which, for all the considered geometries of porous space, can be expressed as a function of porosity and the Λ- parameter of porous medium normalized by the Debye length. For all the studied geometries, this function turns out to be weakly dependent on both the porosity and the geometry type. The latter allows for a rough evaluation of the geometrical factor from experimental data on electric conductivity and hydraulic permeability without previous knowledge of the porous space geometry. The obtained results are used to illustrate how the composition of electrolyte solution affects the mechano-chemical effects. For various examples of electrolyte solution compositions, the obtained results are capable of describing positive, negative and anomalous osmosis, positive and negative rejection of binary electrolytes, and pressure-driven separation of binary electrolyte mixtures.

摘要

本文研究了力学-化学效应,即在置于两种电解质溶液之间的带电多孔介质中观察到的渗透和离子的压力驱动分离。研究重点是平衡界面势(约 30 mV 或更低)较低的多孔系统。在如此低的电势下,如果电解质溶液中的离子具有不同的扩散系数,则渗透和离子的压力驱动分离会明显表现出来。该分析通过结合不可逆热力学方法和标准动电模型的线性化(按归一化平衡界面势)版本进行。研究了任意混合电解质溶液和各种多孔空间几何形状的渗透和离子的压力驱动分离。结果表明,所考虑的效应与一个几何因子成正比,对于所有考虑的多孔空间几何形状,该因子可以表示为孔隙率和多孔介质的 Λ 参数与德拜长度之比的函数。对于所有研究的几何形状,该函数对孔隙率和几何形状类型的依赖性都很弱。后者允许从电导率和水力渗透率的实验数据中粗略评估几何因子,而无需事先了解多孔空间的几何形状。所得结果用于说明电解质溶液的组成如何影响力学-化学效应。对于各种电解质溶液组成的例子,可以用所得结果描述正渗透、负渗透和反常渗透、二元电解质的正渗透和负排斥以及二元电解质混合物的压力驱动分离。

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