CO2-Switchable Phase Separation of Nonaqueous Surfactant-Free Ionic Liquid-Based Microemulsions

微乳液 离子液体 微型反应器 化学 相(物质) 化学工程 动态光散射 溶解度 肺表面活性物质 有机化学 材料科学 纳米技术 催化作用 纳米颗粒 生物化学 工程类
作者
Xiaoyan Pei,Zhiyong Li,Jianji Wang,Qiuju Zhou,Zuodong Liu,Jianji Wang
出处
期刊:ACS Sustainable Chemistry & Engineering [American Chemical Society]
卷期号:10 (5): 1777-1785 被引量:16
标识
DOI:10.1021/acssuschemeng.1c05737
摘要

Surfactant-free microemulsions (SFMEs) have shown great potential in many aspects such as chemical reactions and material preparation. Ionic liquid (IL)-based SFME is a promising member in this family. However, switchable phase separation of nonaqueous IL SFMEs has not been reported up to now although it is of great importance for the separation of products and recycling of the systems. Herein, a new kind of CO2-responsive SFMEs composed of quaternary ammonium IL, dimethyl sulfoxide, and ethyl acetate has been developed. It is worth noting that the microemulsion can be reversibly switched between emulsification and complete phase separation upon alternative CO2 and N2 bubbling at atmospheric pressure. The microstructures and phase behavior of the systems before and after CO2 bubbling have been systematically studied by phase diagrams, electrical conductivity, dynamic light scattering, optical microscopy, and atomic force microscopy, respectively. Mechanism studies verify that the reversible switching is attributed to the generation and restoration of more hydrophilic carbamate salts from the reaction of CO2 with IL anions, which results in poor solubility of ILs in the nonaqueous microemulsions and thus reversible breaking and rebuilding of the microemulsions. Based on this unique phase behavior, the CO2-switchable SFMEs are used as a microreactor for room temperature synthesis of Zn-based metal–organic frameworks, and effective reaction and microemulsion recycling have been achieved. This study may provide a new strategy for the integration of reaction, separation, and recycling procedures to obtain sustainable chemical processes.
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