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Hydrodynamic dispersion in long microchannels under conditions of electroosmotic circulation. I. Non-electrolytes

机译:在电渗循环条件下长微通道中的流体动力分散。 I.非电解质

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This study deals with the description of stationary transport of non-electrolyte molecules or electroneutral particles in straight long channels occurring due to hydrodynamic dispersion under conditions of electroosmotic flow compensated by pressure-driven counterflow (electroosmotic circulation). The electroosmotic flow is assumed to be induced due to electroosmotic slip at the charged channel walls in the presence of a buffer electrolyte with a constant concentration. It is demonstrated that for such systems, the celebrated Taylor-Aris (TA) theory is applicable locally within an inner part of the channel in a wide range of P,clet numbers (Pe). Simple analytical expressions are derived for the flux and concentration profiles inside the channel. Numerical simulations show minor deviations from analytical solutions. The breakdown of TA theory is related to the distortion of transversal concentration profiles within transition regions at the channel ends whose length increases linearly with the Pe number. Taking into account the dependence of the transition regions on Pe number, it is possible to derive simple analytical approximation for the inner concentration gradient in terms of only few parameters, determined numerically. This approximation can be used in future experimental studies.
机译:这项研究的描述是在由压力驱动的逆流(电渗循环)补偿的电渗流条件下,由于流体动力分散而在直线长通道中发生非电解质分子或电子中性粒子的平稳传输。假定在存在浓度恒定的缓冲电解质的情况下,由于在带电通道壁上发生电渗滑移而引起电渗流。事实证明,对于这样的系统,著名的泰勒-阿里斯(TA)理论可以在通道内部以广泛的P,clet数(Pe)局部应用。对于通道内部的通量和浓度分布,可以导出简单的分析表达式。数值模拟表明与解析解存在细微偏差。 TA理论的崩溃与通道末端过渡区域内横向浓度分布的畸变有关,其长度随Pe值线性增加。考虑到过渡区域对Pe数的依赖性,可以仅通过数个确定的参数得出内部浓度梯度的简单解析近似值。该近似值可用于将来的实验研究。

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