Particle Self-Assembly in Ionic Liquid-in-Water Pickering Emulsions

被引:31
|
作者
Ma, Huan [1 ]
Dai, Lenore L. [1 ]
机构
[1] Arizona State Univ, Sch Engn Matter Transport & Energy, Tempe, AZ 85287 USA
基金
美国国家科学基金会;
关键词
SOLID PARTICLES; STABILIZED EMULSIONS; CHARGED-PARTICLES; INTERFACE; MICROPARTICLES; MICROEMULSIONS; NANOPARTICLES; SURFACTANTS; EXTRACTION; DYNAMICS;
D O I
10.1021/la103828x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report the self-assembly of a single species or a binary mixture of microparticles in ionic liquid-in-water Pickering emulsions, with emphases on the interfacial self-assembled particle structure and the partitioning preference of free particles in the dispersed and continuous phases. The particles form monolayers at ionic liquid-water interfaces and are close-packed on fully covered emulsion droplets or aggregated on partially covered droplets. In contrast to those at oil-water interfaces, no long-range-ordered colloidal lattices are observed. Interestingly, other than equilibrating at the ionic liquid-water interfaces, the microparticles also exhibit a partitioning preference in the dispersed and continuous phases: the sulfate-treated polystyrene (S-PS) and aldehyde-sulfate-treated polystyrene (AS-PS) microparticles are extracted to the ionic liquid phase with a high extraction efficiency, whereas the amine-treated polystyrene (A-PS) microparticles remain in the water phase.
引用
收藏
页码:508 / 512
页数:5
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