Wang Weixing, Zhou Zhiang, Nandakumar K, Xu Zhenghe, Masliyah Jacob H
Department of Chemical and Materials Engineering, University of Alberta, Edmonton, Alberta, Canada T6G 2G6.
J Colloid Interface Sci. 2004 Jun 15;274(2):625-30. doi: 10.1016/j.jcis.2004.03.049.
A change of oil/water interfacial tension in the presence of cationic or anionic surfactants in an organic phase was observed due to the addition of charged fine solids in the aqueous phase. The charged fine solids in the aqueous phase adsorb surfactants diffused from the oil phase, thereby causing an increase in the bulk equilibrium surfactant concentration in the aqueous phase, governed by the Stern-Grahame equation. Consequently, surfactant adsorption at the oil-water interface increases, which was demonstrated from the measured reduction of the oil-water interfacial tension. The increased surfactant partition in the aqueous phase in the presence of the charged particles was confirmed by the measured decrease in the surface tension for the collected aqueous solution after solids removal, as compared with the cases without solids addition.
在有机相中,由于水相中添加了带电细颗粒,观察到在阳离子或阴离子表面活性剂存在下油/水界面张力发生了变化。水相中的带电细颗粒吸附从油相扩散而来的表面活性剂,从而导致水相中整体平衡表面活性剂浓度增加,这由斯特恩 - 格拉哈姆方程控制。因此,油水界面处的表面活性剂吸附增加,这从测量的油水界面张力降低得到证明。与未添加固体的情况相比,通过测量去除固体后收集的水溶液的表面张力降低,证实了在带电颗粒存在下水相中表面活性剂分配增加。