表面活性剂溶液在微孔疏水膜上的接触角解释

IF 4.9 Q1 ENGINEERING, CHEMICAL
Yu-Xi Huang , Zhangxin Wang , Thomas Horseman , Joshua L. Livingston , Shihong Lin
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引用次数: 10

摘要

几乎每一项关于膜的实验研究都涉及到接触角(CA)的测量,以量化膜的润湿特性。然而,CA的解释有时会很棘手。在这项研究中,我们研究了表面活性剂溶液在微孔疏水膜上的CA现象。具体来说,表面张力非常低的表面活性剂溶液在微孔疏水膜上具有意想不到的高CA。相反,具有相同表面张力的水/乙醇混合物完全吸干膜(即零CA)。两种表面张力相同的液体之间CA的巨大差异是由于表面活性剂在润湿边界的快速吸附大大降低了局部表面活性剂浓度,增加了局部表面张力。同样的理论也可以用来解释两种液体在毛细管上升和液体进入压力方面的显著差异。本研究的结果对表面张力在理解表面活性剂溶液与大比表面积固体接触时的润湿行为中的作用提出了重大质疑,并对表面活性剂溶液在微孔疏水膜上测量CA的效用提出了重要问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Interpreting contact angles of surfactant solutions on microporous hydrophobic membranes

Interpreting contact angles of surfactant solutions on microporous hydrophobic membranes

Almost every single experimental study regarding membranes involves the measurement of contact angle (CA) to quantify the membrane wetting property. However, the interpretation of CA can sometimes be tricky. In this study, we investigate an interesting phenomenon about the CA of a surfactant solution on a microporous hydrophobic membrane. Specifically, a surfactant solution with a very low surface tension can have an unexpectedly high CA on a microporous hydrophobic membrane. In contrast, a water/ethanol mixture with the same surface tension completely wicks the membrane (i.e., zero CA). The drastic difference in CA between the two types of liquid of the same surface tension results from the rapid adsorption of surfactants at the wetting frontier which substantially reduces the local surfactant concentration and increases the local surface tension. The same theory can also be applied to explain the striking difference between the two liquids in capillary rise and liquid entry pressure. The results from this study cast significant doubt on the role of surface tension in understanding the wetting behavior of surfactant solutions when they are in contact with solid with large specific area and raise important questions regarding the utility of measuring CA for surfactant solutions on microporous hydrophobic membranes.

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