PMMH, CNRS UMR 7636, ESPCI, 10 rue Vauquelin, F 75231 Paris Cedex 05, France.
Langmuir. 2011 Jan 18;27(2):604-11. doi: 10.1021/la1042603. Epub 2010 Dec 20.
We have performed sudden composition changes on a (surfactant + oil + water) system by adding water to a (surfactant + oil) solution. This composition change quenches the system into a metastable oil-in-water emulsion with a population in the 100 nm range. The conditions for a successful quench are as follows: the initial water content should be below a boundary called the "clearing boundary" (CB), the final water content should be sufficiently beyond CB, and the quench should be fast. We have used high purity components to avoid the complex phase separation patterns that occur with low purity ingredients: the surfactant is octaethylenehexadecyl ether (C(16)E(8)) and the oil is hexadecane (C(16)). Under these conditions, we show that the pathway for this type of quench proceeds through the swelling of the reverse micellar phase by the added water and the formation of a sponge phase. Then, further water addition causes the nucleation of oil droplets in this sponge phase, with a size that matches the spontaneous curvature of the sponge phase. Part of the surfactant remains adsorbed on these droplets, and the rest is expelled as micelles that coexist with the droplets. It is concluded that a PIC emulsification will always lead to a bimodal size distribution with surfactant "wasted" in small micelles. This is in contrast with the more efficient PIT emulsification.
我们通过向(表面活性剂+油+水)体系中加水的方式,对(表面活性剂+油)溶液进行了突然的组成变化。这种组成变化将系统淬火成具有 100nm 范围内的群体的亚稳油包水乳状液。成功淬火的条件如下:初始含水量应低于称为“澄清边界”(CB)的边界,最终含水量应充分超过 CB,并且淬火应快速。我们使用高纯度成分避免了低纯度成分中出现的复杂相分离模式:表面活性剂为辛基聚乙二醇醚(C(16)E(8)),油为十六烷(C(16))。在这些条件下,我们表明,这种淬火类型的途径是通过添加的水使反胶束相溶胀以及形成海绵相来进行的。然后,进一步加水导致在该海绵相中油滴的成核,其尺寸与海绵相的自发曲率匹配。一部分表面活性剂仍然吸附在这些液滴上,其余部分则以与液滴共存的胶束形式被排出。可以得出结论,PIC 乳化总是会导致具有表面活性剂“浪费”在小胶束中的双峰尺寸分布。这与更有效的 PIT 乳化形成对比。