Sakai Kenichi, Iijima Satoshi, Ikeda Ryosuke, Endo Takeshi, Yamazaki Takahiro, Yamashita Yuji, Natsuisaka Makoto, Sakai Hideki, Abe Masahiko, Sakamoto Kazutami
Department of Pure and Applied Chemistry in Faculty of Science and Technology, and Research Institute for Science and Technology, Tokyo University of Science, Noda, Chiba 278-8510, Japan.
J Oleo Sci. 2013;62(7):505-11. doi: 10.5650/jos.62.505.
We have recently proposed a new general concept regarding amphiphilic materials that have been named as "active interfacial modifier (AIM)." In emulsion systems, an AIM is essentially insoluble in both water and organic solvents; however, it possesses moieties that are attracted to each of these immiscible liquid phases. Hence, an AIM practically stays just at the interface between the two phases and makes the resulting emulsion stable. In this study, the effects of silicone oil species on the dispersion stability of water-in-oil (W/O) emulsions in the presence of an AIM sample were evaluated in order to understand the destabilization mechanism in such emulsion systems. The AIM sample used in this study is an amphiphilic polymer consisting of a silicone backbone modified with hydrocarbon chains and hydrolyzed silk peptides. The Stokes equation predicts that the sedimentation velocity of water droplets dispersed in a continuous silicone oil phase simply depends on the expression (ρ - ρ₀)/η assuming that the droplet size is constant (where ρ is the density of the dispersed water phase, ρ₀ is the density of the continuous silicone oil phase, and η is the viscosity of the oil phase). The experimental results shown in this paper are consistent with the Stokes prediction: i.e., in the low-viscous genuine or quasi-Newtonian fluid region, the dispersion stability increases in the following order: dodecamethylpentasiloxane (DPS) < decamethylcyclopentasiloxane (D₅) ≤ dodecamethylcyclohexasiloxane (D₆). This order agrees well with the order obtained by using the expression (ρ - ρ₀)/η as DPS > D₅ > D₆. This indicates that our emulsion system experiences destabilization through sedimentation, but hardly any coalescence occurs owing to the presence of an additional third phase consisting of the AIM that stabilizes the silicone oil/water interface in the emulsions.
我们最近提出了一个关于两亲性材料的新的通用概念,这类材料被命名为“活性界面改性剂(AIM)”。在乳液体系中,AIM在水和有机溶剂中基本都不溶;然而,它具有能被这两种互不相溶的液相各自吸引的部分。因此,AIM实际上就停留在两相之间的界面处,并使所得乳液稳定。在本研究中,评估了硅油种类对在存在AIM样品的情况下油包水(W/O)乳液分散稳定性的影响,以了解此类乳液体系中的失稳机制。本研究中使用的AIM样品是一种两亲性聚合物,由用烃链改性的硅氧烷主链和水解丝肽组成。斯托克斯方程预测,假设液滴尺寸恒定,分散在连续硅油相中的水滴沉降速度仅取决于表达式(ρ - ρ₀)/η(其中ρ是分散水相的密度,ρ₀是连续硅油相的密度,η是油相的粘度)。本文所示的实验结果与斯托克斯预测一致:即在低粘度的纯液体或准牛顿流体区域,分散稳定性按以下顺序增加:十二甲基戊硅氧烷(DPS)< 十甲基环戊硅氧烷(D₅)≤ 十二甲基环己硅氧烷(D₆)。这个顺序与使用表达式(ρ - ρ₀)/η得到的顺序(DPS > D₅ > D₆)非常吻合。这表明我们的乳液体系通过沉降发生失稳,但由于存在由AIM组成的额外第三相稳定了乳液中的硅油/水界面,几乎没有发生聚并。