Datta S, Conlisk A T, Li H F, Yoda M
201 W 19th Avenue, Mechanical Engineering, Scott Laboratory, Ohio State University, Columbus, OH 43210 (
Mech Res Commun. 2009 Jan;36(1):65-74. doi: 10.1016/j.mechrescom.2008.07.006.
The electroosmotic flow (EOF) rate in fused silica microchannels is experimentally found to decrease when trace quantities of salts containing the divalent cations Ca(2+) and Mg(2+) are added to a constant ionic strength background electrolytic solution (BGE) flowing in a channel having negatively charged walls. Moreover, the observed effect is quantitatively different for the two ions Ca(2+) and Mg(2+). Since electrostatic interactions are identical for ions of the same valence modeled as point charges, a description of the electric double layer (EDL) based on the Poisson-Boltzmann equation alone cannot account for these experimental observations. New experimental observations on electroosmotic flow in presence of Ca(2+) and Mg(2+) are reported in this work. A site binding model that accounts for the chemical interactions of the BGE ions with the silica surface is developed. The model predictions are in good agreement with the experimental observations on divalent cations as well as data from the literature on how properties such as pH and ionic strength affect electroosmotic flow rates for a BGE with monovalent cations.
实验发现,当向在带负电荷壁面的通道中流动的具有恒定离子强度的背景电解质溶液(BGE)中添加痕量含有二价阳离子Ca(2+)和Mg(2+)的盐时,熔融石英微通道中的电渗流(EOF)速率会降低。此外,对于Ca(2+)和Mg(2+)这两种离子,观察到的效应在数量上有所不同。由于对于建模为点电荷的相同价态离子,静电相互作用是相同的,仅基于泊松 - 玻尔兹曼方程对双电层(EDL)的描述无法解释这些实验观察结果。本文报道了在存在Ca(2+)和Mg(2+)情况下电渗流的新实验观察结果。开发了一个考虑BGE离子与二氧化硅表面化学相互作用的位点结合模型。该模型预测与关于二价阳离子的实验观察结果以及文献中关于pH和离子强度等性质如何影响含有单价阳离子的BGE的电渗流速率的数据高度吻合。