Particle self-assembly in oil-in-ionic liquid Pickering emulsions

被引:22
|
作者
Walker, Elizabeth M. [1 ]
Frost, Denzil S. [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
Particle assembly; Ionic liquid; Pickering emulsions; Microparticle bridging; Emulsion stability; MICROPARTICLES; DYNAMICS; WATER;
D O I
10.1016/j.jcis.2011.07.056
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We have studied polydimethylsiloxane (PDMS)-in-1-butyl-3-methylimidazolium hexafluorophosphate ([BMIM][PF6]) Pickering emulsions stabilized by polystyrene microparticles with different surface chemistry. Surprisingly, in contrast to the consensus originating from oil/water Pickering emulsions in which the solid particles equilibrate at the oil-water droplet interfaces and provide effective stabilization, here the polystyrene microparticles treated with sulfate, aldehyde sulfate, or carboxylate dissociable groups mostly formed monolayer bridges among the oil droplets rather than residing at the oil-ionic liquid interfaces. The bridge formation inhibited individual droplet-droplet coalescence; however, due to low density and large volume (thus the buoyant effect), the aggregated oil droplets actually promoted oil/ionic liquid phase separation and distressed emulsion stability. Systems with binary heterogeneous polystyrene microparticles exhibited similar, even enhanced (in terms of surface chemistry dependence), bridging phenomenon in the PDMS-in-[BMIM][PF6] Pickering emulsions. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:307 / 313
页数:7
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