Center for Complex Fluids Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, United States.
Department of Chemical Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, United States.
Langmuir. 2021 Oct 5;37(39):11573-11581. doi: 10.1021/acs.langmuir.1c01889. Epub 2021 Sep 23.
While the concept of interfacial tension synergism in surfactant mixtures is well established, little attention has been paid to the possibility of synergistic effects on the interfacial rheology of mixed surfactant systems. Furthermore, interfacial tension synergism is most often investigated for mixtures of surfactants residing in a single phase. Here, we define dilatational modulus synergism and report a study of interfacial tension isotherms and complex dilatational moduli for a binary surfactant system with the two surfactants accessing the oil/water interface from opposite sides. Using an oil-soluble fatty acid surfactant (palmitic acid, PA) that may be ionized at the oil/water interface and a quaternary ammonium water-soluble cationic surfactant (tetradecyltrimethylammonium bromide, TTAB), the binary interfacial interaction was tuned by the aqueous phase pH. Interfacial tensions and dilatational moduli were measured by the pendant drop method for the binary surfactant system as well as the corresponding single-surfactant systems to identify synergistic effects. The possible occurrence of dilatational modulus synergism was probed from two perspectives: one for a fixed total surfactant concentration and the other for a fixed interfacial tension. The aqueous pH was found to have a controlling effect on both interfacial tension synergism and the dilatational modulus synergism. The conditions for interfacial tension synergism coincided with those for the storage modulus synergism: both tension and storage modulus synergisms were observed under all conditions tested at pH 7 where PA was mostly deprotonated, for both perspectives examined, but not for any conditions tested at pH 3 where PA is mostly protonated. The loss modulus synergism exhibited more complex behaviors, such as frequency and interfacial tension dependences, but again was only observed at pH 7. The tension and modulus synergism at pH 7 were attributed to the increased attraction between ionized PA and cationic TTAB and the formation of catanionic complexes at the oil/water interface.
虽然表面活性剂混合物的界面张力协同作用的概念已经得到很好的确立,但很少有人关注混合表面活性剂体系的界面流变学可能存在协同效应。此外,界面张力协同作用通常是针对处于单一相的表面活性剂混合物进行研究的。在这里,我们定义了拉伸模量协同作用,并报告了一种研究具有两种表面活性剂从相反侧进入油水界面的二元表面活性剂体系的界面张力等温线和复拉伸模量的研究结果。使用一种可能在油水界面上电离的油溶性脂肪酸表面活性剂(棕榈酸,PA)和一种季铵水溶性阳离子表面活性剂(十四烷基三甲基溴化铵,TTAB),通过水相 pH 值来调节二元界面相互作用。通过悬滴法测量了二元表面活性剂体系以及相应的单表面活性剂体系的界面张力和拉伸模量,以识别协同效应。从两个角度探讨了拉伸模量协同作用的可能性:一种是在固定总表面活性剂浓度的情况下,另一种是在固定界面张力的情况下。发现水相 pH 值对界面张力协同作用和拉伸模量协同作用都有控制作用。界面张力协同作用的条件与储能模量协同作用的条件一致:在 pH 7 下,PA 大部分去质子化时,所有测试条件下都观察到张力和储能协同作用,但在 pH 3 下,PA 大部分质子化时,任何测试条件下都没有观察到。损耗模量协同作用表现出更复杂的行为,如频率和界面张力依赖性,但也仅在 pH 7 下观察到。在 pH 7 时,张力和模量协同作用归因于离子化 PA 和阳离子 TTAB 之间的吸引力增加以及在油水界面上形成的反胶束复合物。