Zheng Bingqian, Zheng Bingjing, Carr Amanda J, Yu Xiaoxi, McClements D Julian, Bhatia Surita R
Department of Chemistry, Stony Brook University, Stony Brook, NY 11794, USA.
Department of Food Science, University of Massachusetts, Amherst, MA 01002, USA.
Inorganica Chim Acta. 2020 Aug 1;508. doi: 10.1016/j.ica.2020.119566. Epub 2020 Mar 13.
Pickering emulsions, or emulsions with solid particles at the interface, have attracted significant interest in Enhanced Oil Recovery (EOR) processes, cosmetics, and drug delivery systems due to their ability to resist coalescence. Here, a synthetic clay nanoparticle, laponite®, is utilized to create oil-in-water (o/w) emulsions, and the addition of small-molecule surfactants induces a more stable emulsion. In this study, the stability of laponite® Pickering emulsions with and without the surfactants (dodecyltrimethylammonium bromide (DTAB), Pluronic F68 (F68), and sodium dodecyl sulfate (SDS) is investigated using dynamic light scattering (DLS), -potential, optical microscopy, and rheology. With laponite® and no added surfactants, the DLS and -potential results show formation of emulsion droplets with a diameter of 3 μm and a -potential of -90 mV. With the addition of surfactants, both the droplet diameter and -potential increase, suggesting adsorption of surfactants on the surface of laponite® particle. Optical microscopy suggests that the Pickering emulsion without surfactant undergoes flocculation, while the emulsion becomes stable to coalescence and creaming with addition of surfactants due to formation of a network structure. Regardless of the formation of network structure, the laponite®-F68 emulsion rheologically behaves as a Newtonian fluid, while the laponite®-SDS and laponite®-DTAB emulsions display shear thinning behavior. The difference in the rheological behavior can be attributed to the weak adsorption of F68 on laponite® and electrostatic interactions between laponite® and charged surfactants at oil-water interface.
皮克林乳液,即界面处带有固体颗粒的乳液,因其抗聚结能力而在强化采油(EOR)工艺、化妆品和药物递送系统中引起了广泛关注。在此,利用一种合成粘土纳米颗粒锂皂石®来制备水包油(o/w)乳液,添加小分子表面活性剂可诱导形成更稳定的乳液。在本研究中,使用动态光散射(DLS)、ζ电位、光学显微镜和流变学方法研究了添加和不添加表面活性剂(十二烷基三甲基溴化铵(DTAB)、普朗尼克F68(F68)和十二烷基硫酸钠(SDS))的锂皂石®皮克林乳液的稳定性。在不添加表面活性剂的锂皂石®乳液中,DLS和ζ电位结果表明形成了直径为3μm、ζ电位为 -90 mV的乳液滴。添加表面活性剂后,液滴直径和ζ电位均增加,表明表面活性剂吸附在锂皂石®颗粒表面。光学显微镜显示,不添加表面活性剂的皮克林乳液会发生絮凝,而添加表面活性剂后,由于形成了网络结构,乳液对聚结和分层变得稳定。无论网络结构是否形成,锂皂石®-F68乳液在流变学上表现为牛顿流体,而锂皂石®-SDS和锂皂石®-DTAB乳液表现出剪切变稀行为。流变行为的差异可归因于F68在锂皂石®上的弱吸附以及锂皂石®与油水界面处带电表面活性剂之间的静电相互作用。