Centre de Recherche Paul Pascal, Université de Bordeaux, 115 Av. A. Schweitzer, 33600 Pessac, France.
Langmuir. 2011 Dec 6;27(23):14096-107. doi: 10.1021/la203476h. Epub 2011 Nov 11.
Emulsions were prepared using poly(N-isopropylacrylamide) microgels as thermoresponsive stabilizers. The latter are well-known for their sensitivity to temperature: they are swollen by water below the so-called volume phase transition temperature (VPTT = 33 °C) and shrink when heated above it. Most of the studies reported in the literature reveal that the corresponding emulsions are of the oil-in-water type (O/W) and undergo fast destabilization upon warming above the VPTT. In the present study, whereas O/W emulsions were obtained with a wide panel of oils of variable polarity and were all thermoresponsive, water-in-oil (W/O) emulsions were found only in the presence of fatty alcohols and did not exhibit any thermal sensitivity. To understand the peculiar behavior of emulsions based on fatty alcohols, we investigated the organization of microgels at the oil-water interface and we studied the interactions of pNIPAM microgels with octanol. By combining several microscopy methods and by exploiting the limited coalescence process, we provided evidence that W/O emulsions are stabilized by multilayers of nondeformed microgels located inside the aqueous drops. Such behavior is in contradiction with the empirical Finkle rule stating that the continuous phase of the preferred emulsion is the one in which the stabilizer is preferentially dispersed. The study of microgels in nonemulsified binary water/octanol systems revealed that octanol diffused through the aqueous phase and was incorporated in the microgels. Thus, W/O emulsions were stabilized by microgels whose properties were substantially different from the native ones. In particular, after octanol uptake, they were no longer thermoresponsive, which explained the loss of responsiveness of the corresponding W/O emulsions. Finally, we showed that the incorporation of octanol modified the interfacial properties of the microgels: the higher the octanol uptake before emulsification, the lower the amount of particles in direct contact with the interface. The multilayer arrangement was thus necessary to ensure efficient stabilization against coalescence, as it increased interface cohesiveness. We discussed the origin of this counterexample of the Finkle's rule.
乳液是使用聚(N-异丙基丙烯酰胺)微凝胶作为温敏稳定剂制备的。后者因其对温度的敏感性而广为人知:在所谓的体积相转变温度(VPTT=33°C)以下,它们会被水膨胀,而在高于该温度时会收缩。文献中报道的大多数研究表明,相应的乳液为油包水型(O/W),在高于 VPTT 时会迅速失稳。在本研究中,虽然使用各种极性不同的油获得了 O/W 乳液,且它们都是温敏的,但仅在存在脂肪醇时才能获得水包油(W/O)乳液,并且它们没有表现出任何热敏感性。为了理解基于脂肪醇的乳液的特殊行为,我们研究了微凝胶在油水界面上的组织,并研究了 pNIPAM 微凝胶与辛醇的相互作用。通过结合几种显微镜方法并利用有限的聚结过程,我们提供了证据表明,W/O 乳液是由位于水相滴内的未变形微凝胶的多层稳定的。这种行为与经验性的芬克尔规则相矛盾,该规则指出首选乳液的连续相是稳定剂优先分散的相。对非乳化二元水/辛醇体系中的微凝胶的研究表明,辛醇通过水相扩散并被纳入微凝胶中。因此,W/O 乳液是由其性质与原始微凝胶明显不同的微凝胶稳定的。特别是,在吸收辛醇后,它们不再是温敏的,这解释了相应的 W/O 乳液失去响应性的原因。最后,我们表明,辛醇的加入改变了微凝胶的界面性质:在乳化之前吸收的辛醇越多,与界面直接接触的颗粒数量越少。因此,多层排列对于确保有效的抗聚结稳定性是必要的,因为它增加了界面内聚性。我们讨论了芬克尔规则这个反例的起源。