Physical Chemistry Department, Kuban State University, 149 Stavropolskaya str., 350040 Krasnodar, Russia.
Adv Colloid Interface Sci. 2010 Oct 15;160(1-2):101-23. doi: 10.1016/j.cis.2010.08.001. Epub 2010 Aug 18.
Usually in electrochemical systems, the direct current densities not exceeding the limiting current density are applied. However, the recent practice of electrodialysis evidences the interest of other current modes where either the imposed direct current is over the limiting one or a non-constant asymmetrical (such as pulsed) current is used. The paper is devoted to make the mechanisms of mass transfer under these current regimes more clear. The theoretical background for mathematical modelling of mass transfer at overlimiting currents is described. Four effects providing overlimiting current conductance are examined. Two of them are related to water splitting: the appearance of additional charge carriers (H(+) and OH(-) ions) and exaltation effect. Two others are due to coupled convection partially destroying the diffusion boundary layer: gravitational convection and electroconvection. These effects result from formation of concentration gradients (known as concentration polarization) caused by the current flowing under conditions where ionic transport numbers are different in the membrane and solution. Similar effects take place not only in electrodialysis membrane systems, but in electrode ones, in electrophoresis and electrokinetic micro- and nanofluidic devices such as micropumps. The relation of these effects to the properties of the membrane surface (the chemical nature of the fixed groups, the degree of heterogeneity and hydrophobicity, and the geometrical shape of the surface) is analyzed. The interaction between the coupled effects is studied, and the conditions under which one or another effect becomes dominant are discussed. The application of intensive current modes in electrodialysis, the state-of-the-art and perspectives, are considered. It is shown that the intensive current modes are compatible with new trends in water treatment oriented towards Zero Liquid Discharge (ZLD) technologies. The main idea of these hybrid schemes including pressure- and electro-driven processes as well as conventional methods is to provide the precipitation of hardness salts before the membrane modules and that of well dissolved salts after.
通常在电化学系统中,施加的直流密度不超过极限电流密度。然而,最近电渗析的实践证明了其他电流模式的兴趣,其中要么施加的直流超过极限电流,要么使用非恒定不对称(如脉冲)电流。本文致力于使这些电流模式下的传质机制更加清晰。描述了极限电流下传质的数学建模的理论背景。考察了提供过限电流电导的四种效应。其中两种与水分解有关:额外电荷载流子(H(+)和 OH(-)离子)的出现和激发效应。另外两种是由于耦合对流部分破坏了扩散边界层:重力对流和电对流。这些效应是由在膜和溶液中离子迁移数不同的条件下电流流动引起的浓度梯度(称为浓差极化)形成的。类似的效应不仅发生在电渗析膜系统中,而且发生在电极系统、电泳和电动微纳流控装置中,如微泵。分析了这些效应与膜表面性质(固定基团的化学性质、异质性和疏水性程度以及表面的几何形状)之间的关系。研究了耦合效应之间的相互作用,并讨论了一个或另一个效应占主导地位的条件。考虑了在电渗析中应用强电流模式的现状和前景。结果表明,强电流模式与面向零液体排放(ZLD)技术的水处理新趋势兼容。这些混合方案的主要思想包括压力和电动过程以及传统方法,旨在在膜组件之前沉淀硬度盐,在膜组件之后沉淀溶解良好的盐。