School for Engineering of Matter, Transport and Energy, Arizona State University, 501 East Tyler Mall, Tempe, AZ 85287, USA.
School for Engineering of Matter, Transport and Energy, Arizona State University, 501 East Tyler Mall, Tempe, AZ 85287, USA.
Adv Colloid Interface Sci. 2014 Apr;206:92-105. doi: 10.1016/j.cis.2013.09.004. Epub 2013 Oct 1.
This review presents an overview of the nature of ionic liquid (IL)-based interfaces and self-assembled particle morphologies of IL-in-water, oil- and water-in-IL, and novel IL-in-IL Pickering emulsions with emphasis on their unique phenomena, by means of experimental and computational studies. In IL-in-water Pickering emulsions, particles formed monolayers at ionic liquid-water interfaces and were close-packed on fully covered emulsion droplets or aggregated on partially covered droplets. Interestingly, other than equilibrating at the ionic liquid-water interfaces, microparticles with certain surface chemistries were extracted into the ionic liquid phase with a high efficiency. These experimental findings were supported by potential of mean force calculations, which showed large energy drops as hydrophobic particles crossed the interface into the IL phase. In the oil- and water-in-IL Pickering emulsions, microparticles with acidic surface chemistries formed monolayer bridges between the internal phase droplets rather than residing at the oil/water-ionic liquid interfaces, a significant deviation from traditional Pickering emulsion morphology. Molecular dynamics simulations revealed aspects of the mechanism behind this bridging phenomenon, including the role of the droplet phase, surface chemistry, and inter-particle film. Novel IL-in-IL Pickering emulsions exhibited an array of self-assembled morphologies including the previously observed particle absorption and bridging phenomena. The appearance of these morphologies depended on the particle surface chemistry as well as the ILs used. The incorporation of particle self-assembly with ionic liquid science allows for new applications at the intersection of these two fields, and have the potential to be numerous due to the tunability of the ionic liquids and particles incorporated, as well as the particle morphology by combining certain groups of particle surface chemistry, IL type (protic or aprotic), and whether oil or water is incorporated.
这篇综述通过实验和计算研究,介绍了基于离子液体(IL)的界面的性质以及 IL 水、油 IL 和新型 IL 内 IL Pickering 乳液中自组装颗粒形态,重点介绍了它们独特的现象。在 IL 水 Pickering 乳液中,颗粒在 IL-水界面上形成单层,并在完全覆盖的乳液液滴上紧密排列或在部分覆盖的液滴上聚集。有趣的是,除了在 IL-水界面上达到平衡之外,具有特定表面化学性质的微粒还可以高效率地被提取到离子液体相中。这些实验结果得到了平均势能计算的支持,该计算显示疏水颗粒穿过界面进入 IL 相时会有很大的能量下降。在油 IL 和水 IL Pickering 乳液中,具有酸性表面化学性质的微粒在内部相液滴之间形成单层桥,而不是位于油/水-IL 界面上,这与传统的 Pickering 乳液形态有很大的偏离。分子动力学模拟揭示了这种桥接现象背后的机制方面,包括液滴相、表面化学和粒子间膜的作用。新型 IL 内 IL Pickering 乳液表现出多种自组装形态,包括先前观察到的粒子吸收和桥接现象。这些形态的出现取决于粒子表面化学性质以及所使用的 IL。将粒子自组装与离子液体科学相结合,可以在这两个领域的交叉点上开辟新的应用,并且由于所包含的离子液体和粒子的可调节性、粒子形态以及粒子表面化学、IL 类型(质子或非质子)以及是否包含油或水等因素的组合,具有很大的潜力。