AC-driven electro-osmotic flow in charged nanopores

被引:7
|
作者
Catalano, J. [1 ]
Biesheuvel, P. M. [2 ]
机构
[1] Aarhus Univ, Dept Engn, Hangovej 2, DK-8200 Aarhus, Denmark
[2] Wetsus, European Ctr Excellence Sustainable Water Technol, Oostergoweg 9, NL-8911 MA Leeuwarden 9, Netherlands
关键词
ELECTROKINETIC ENERGY-CONVERSION; ION-EXCHANGE MEMBRANES; REVERSE ELECTRODIALYSIS; ULTRAFINE CAPILLARIES; CARBON NANOTUBES; POWER-GENERATION; MASS-TRANSPORT; EFFICIENCY; MODEL; SYSTEMS;
D O I
10.1209/0295-5075/123/58006
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
In this paper we report the theory describing the electro-osmotic flow in charged nanopores with constant radius and charge density driven by alternating current. We solve the ion and solution transport in unsteady conditions as described by the Navier-Stokes and Nernst-Planck equations considering the electrical potential inside the charged nanopore uniform in the radial direction (Uniform Potential model approximation). We derive the transport equation system in the case in which the pore is connected to two boundary diffusion layers and the cations and anions have different diffusion coefficients. This approach allows the theoretical description of the characteristic frequency dependence of the phase shift between the applied current density and the electro-osmotic flow. Additionally we show how the analysis of the dynamic response of the electro-osmotic coupling factor vs. the AC frequency allows us to quantify the apparent ion diffusion coefficient in membranes. Notably, the frequency window where the phase shift is predicted is well inside the commonly used sampling rate for electro-osmotic flow experiments f epsilon [10(-4) ,10(1)] Hz, hence the proposed method can be useful to determine the apparent diffusion coefficient of ions (such as redox complex for flow batteries) in charged membranes. Copyright (C) EPLA, 2018
引用
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页数:7
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