水溶液电解质在弯曲几何中浓度富集的电渗透不稳定性

Bingrui Xu, Zhibo Gu, Wei Liu, P. Huo, Yueting Zhou, S. Rubinstein, M. Bazant, B. Zaltzman, I. Rubinstein, D. Deng
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引用次数: 2

摘要

我们报告了水溶液电解质在弯曲几何中浓度富集的电渗透不稳定性,与众所周知的相反,只在富集界面(阳极)开始,而不是在耗尽界面(阴极)开始。对于这种不稳定性,线电荷奇点产生的强电场消除了平面几何中不现实的高材料佩莱特数的限制。在同心圆形电极的模型设置中,我们通过稳定性分析、数值模拟和实验可视化表明,不稳定性发生在内部阳极,低于临界曲率半径。稳定性判据也用临界电场的形式表示,并通过保角映射扩展到任意(2d)几何形状。这一发现表明,在受盐富集限制的过程中,如反渗透,通过针状电极触发这种不稳定性,可能会增强转运。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electro-osmotic instability of concentration enrichment in curved geometries for an aqueous electrolyte
We report that an electro-osmotic instability of concentration enrichment in curved geometries for an aqueous electrolyte, as opposed to the well-known one, is initiated exclusively at the enriched interface (anode), rather than at the depleted one (cathode). For this instability, the limitation of unrealistically high material Peclet number in planar geometry is eliminated by the strong electric field arising from the line charge singularity. In a model setup of concentric circular electrodes, we show by stability analysis, numerical simulation, and experimental visualization that instability occurs at the inner anode, below a critical radius of curvature. The stability criterion is also formulated in terms of a critical electric field and extended to arbitrary (2d) geometries by conformal mapping. This discovery suggests that transport may be enhanced in processes limited by salt enrichment, such as reverse osmosis, by triggering this instability with needle-like electrodes.
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