Worthen Andrew J, Foster Lynn M, Dong Jiannan, Bollinger Jonathan A, Peterman Adam H, Pastora Lucinda E, Bryant Steven L, Truskett Thomas M, Bielawski Christopher W, Johnston Keith P
McKetta Department of Chemical Engineering, ‡Department of Chemistry and Biochemistry, and §Department of Petroleum and Geosystems Engineering, University of Texas at Austin , Austin, Texas 78712-0231, United States.
Langmuir. 2014 Feb 4;30(4):984-94. doi: 10.1021/la404132p. Epub 2014 Jan 21.
Oil-in-water emulsions were formed and stabilized at low amphiphile concentrations by combining hydrophilic nanoparticles (NPs) (i.e., bare colloidal silica) with a weakly interacting zwitterionic surfactant, caprylamidopropyl betaine, to generate a high hydrophilic-lipophilic balance. The weak interaction of the NPs with surfactant was quantified with contact angle measurements. Emulsions were characterized by static light scattering to determine the droplet size distributions, optical photography to quantify phase separation due to creaming, and both optical and electron microscopy to determine emulsion microstructure. The NPs and surfactant acted synergistically to produce finer emulsions with a greater stability to coalescence relative to the behavior with either NPs or surfactant alone. As a consequence of the weak adsorption of the highly hydrophilic surfactant on the anionic NPs along with the high critical micelle concentration, an unusually large surfactant concentration was available to adsorb at the oil-water interface and lower the interfacial tension. The synergy for emulsion formation and stabilization for the two amphiphiles was even greater in the case of a high-salinity synthetic seawater aqueous phase. Here, higher NP adsorption at the oil-water interface was caused by electrostatic screening of interactions between (1) NPs and the anionic oil-water interface and (2) between the NPs. This greater adsorption as well as partial flocculation of the NPs provided a more efficient barrier to droplet coalescence.
通过将亲水性纳米颗粒(NPs)(即裸露的胶体二氧化硅)与弱相互作用的两性离子表面活性剂辛酰氨基丙基甜菜碱相结合,形成了水包油乳液,并在低两亲物浓度下使其稳定,以产生高亲水亲油平衡。通过接触角测量对纳米颗粒与表面活性剂之间的弱相互作用进行了量化。通过静态光散射表征乳液以确定液滴尺寸分布,通过光学摄影量化由于乳析引起的相分离,并通过光学显微镜和电子显微镜确定乳液微观结构。与单独使用纳米颗粒或表面活性剂的情况相比,纳米颗粒和表面活性剂协同作用产生了更细的乳液,对聚结具有更高的稳定性。由于高亲水性表面活性剂在阴离子纳米颗粒上的弱吸附以及高临界胶束浓度,有异常大量的表面活性剂可用于吸附在油水界面并降低界面张力。在高盐度合成海水水相的情况下,两种两亲物形成乳液和使其稳定的协同作用甚至更大。在这里,纳米颗粒在油水界面的更高吸附是由以下相互作用的静电屏蔽引起的:(1)纳米颗粒与阴离子油水界面之间的相互作用,以及(2)纳米颗粒之间的相互作用。这种更大的吸附以及纳米颗粒的部分絮凝为液滴聚结提供了更有效的屏障。