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关断电流后对瞬态膜电位的测量作为研究支撑薄纳米多孔层电化学性质的一种工具。

Measurements of transient membrane potential after current switch-off as a tool to study the electrochemical properties of supported thin nanoporous layers.

作者信息

Yaroshchuk Andriy, Karpenko Larisa, Ribitsch Volker

机构信息

Institut für Chemie, Karl-Franzens-Universität Graz, Heinrichstr. 28, 8010 Graz, Austria.

出版信息

J Phys Chem B. 2005 Apr 28;109(16):7834-42. doi: 10.1021/jp040599f.

Abstract

We have studied the potential of chronopotentiometry after current switch-off as a tool for electrochemical characterization of thin supported nanoporous layers. Within the scope of this technique, a thin supported electrochemically active layer is polarized by direct electric current until a steady state is reached. After that, the current is switched-off in a stepwise manner, and the reading of transient membrane potential begins. A linear non-steady-state theory of the method has been developed in terms of a model-independent approach of network thermodynamics. The measurements of transient membrane potential after current switch-off have been carried out in KCl solutions of various concentrations for a commercially available nanofiltration membrane (Desal5 DK). Such membranes consist of micron-thick active (or barrier) nanoporous layers and much thicker (100-200 microm) and coarse-porous supports (the pore size usually is 0.1-5 microm). The reproducibility of the method has been found to be quite reasonable especially in not too dilute electrolyte solutions and at not too short times (> or = 10 ms). The relaxation measurements have been complemented by the measurements of the steady-state membrane potential and by sample measurements of salt rejection in the pressure-driven mode, which enabled us to carry out a self-consistent interpretation of the experimental data. This has revealed, in particular, that the ion rejection mechanism related to the fixed electric charges is not the dominant one in the case of the Desal5 DK nanofiltration membrane. Proceeding from a quantitative interpretation of relaxation patterns, we could also determine some properties of membrane support, namely, the porosity and the salt diffusivity. They have been found to have reasonable values remarkably independent of salt concentration, which confirms the self-consistency of our interpretations.

摘要

我们研究了关断电流后计时电位法作为一种用于表征负载型纳米多孔薄膜电化学性质的工具的潜力。在该技术范围内,通过直流电流对负载型薄电化学活性层进行极化,直至达到稳态。此后,逐步关断电流,并开始读取瞬态膜电位。该方法的线性非稳态理论是根据网络热力学的模型无关方法发展而来的。对于市售的纳滤膜(Desal5 DK),在不同浓度的KCl溶液中进行了关断电流后瞬态膜电位的测量。此类膜由微米厚的活性(或阻挡)纳米多孔层以及更厚(100 - 200微米)且孔径较大(通常为0.1 - 5微米)的粗孔支撑层组成。已发现该方法的重现性相当不错,尤其是在不太稀的电解质溶液中以及不太短的时间(≥10毫秒)内。通过稳态膜电位测量以及压力驱动模式下盐截留率的样品测量对弛豫测量进行了补充,这使我们能够对实验数据进行自洽解释。这尤其表明,对于Desal5 DK纳滤膜而言,与固定电荷相关的离子截留机制并非主导机制。从弛豫模式的定量解释出发,我们还能够确定膜支撑体的一些性质,即孔隙率和盐扩散率。已发现它们具有相当合理的值,且显著独立于盐浓度,这证实了我们解释的自洽性。

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