Hussein Sheik Abdulkadir, Bandulasena Himiyage Chaminda Hemaka, Starov Victor, Trybala Anna
Department of Chemical Engineering, Loughborough University, Loughborough, UK.
Electrophoresis. 2017 Oct;38(20):2554-2560. doi: 10.1002/elps.201600549. Epub 2017 Apr 18.
Fluid flow profiles in free liquid films stabilised by anionic and cationic surfactants under an external electric field were investigated. Depthwise velocity fields were measured at the mid region of the free liquid film by confocal micron-resolution particle image velocimetry and corresponding numerical simulations were performed using Finite Element Method to model the system. Depthwise change in velocity profiles was observed with electroosmotic flow dominating in the vicinity of the gas-liquid and solid-liquid interfaces while backpressure drives fluid in the opposite direction at the core of the film. It was also found that the direction of the flow at various sections of the films depends on the type of surfactant used, but flow features remained the same. Numerical simulations predicted the flow profiles with reasonable accuracy; however, asymmetry of the actual film geometry caused deviations at the top half of the computational domain. Overall, electroosmotic flow profiles within a free liquid film are similar to that of the closed-end solid microchannel. However, the flow direction and features of the velocity profiles can be changed by selecting various types of surfactants. The free liquid films thickness was selected to match dimensions of foam Plateau border. Hence, these findings will be useful in developing a separation system based on foam electrokinetics.
研究了在外部电场作用下,由阴离子和阳离子表面活性剂稳定的自由液膜中的流体流动剖面。通过共焦微米分辨率粒子图像测速技术在自由液膜的中部区域测量了深度方向的速度场,并使用有限元方法进行了相应的数值模拟,以对该系统进行建模。观察到速度剖面在深度方向上的变化,其中电渗流在气液和固液界面附近占主导地位,而背压在液膜核心处驱动流体向相反方向流动。还发现,液膜不同截面处的流动方向取决于所用表面活性剂的类型,但流动特征保持不变。数值模拟以合理的精度预测了流动剖面;然而,实际膜几何形状的不对称导致计算域上半部分出现偏差。总体而言,自由液膜内的电渗流剖面与封闭端固体微通道的相似。然而,通过选择不同类型的表面活性剂,可以改变速度剖面的流动方向和特征。选择自由液膜的厚度以匹配泡沫Plateau边界的尺寸。因此,这些发现将有助于开发基于泡沫电动学的分离系统。