CO2-Switchable High Internal Phase Pickering Emulsions Stabilized by Small-Molecular Surfactants and Hydrophilic Silica Nanoparticles

皮克林乳液 化学工程 阳离子聚合 流变学 肺表面活性物质 粘度 材料科学 纳米颗粒 提高采收率 水溶液 相(物质) 吸附 双水相体系 纳米技术 有机化学 化学 高分子化学 复合材料 工程类
作者
Wanqing Zhang,Miao Lv,Jin Shi,Jianzhong Jiang
出处
期刊:ACS Sustainable Chemistry & Engineering [American Chemical Society]
卷期号:13 (1): 692-699
标识
DOI:10.1021/acssuschemeng.4c09490
摘要

High internal phase Pickering emulsions (HIPPEs) have received increasing attention recently due to their unique viscosity and rheological characteristics. Nevertheless, their high viscosity might limit their applications in the transportation field. Developing HIPPEs with adjustable stability, controllable viscosity, and easy preparation remains a challenge. Here, we reported an O/W HIPPEs costabilized by a novel CO2-switchable nonionic surfactant (NCOEO3) and hydrophilic silica nanoparticles with low concentrations, facilitated by the adsorption of NCOEO3 onto the nanoparticles through hydrogen bonding. Upon increasing the NCOEO3 concentration to 1 mM, the oil volume fraction of the emulsions can be adjusted to 92%. The HIPPEs demonstrate remarkable CO2 responsiveness due to the reversible transformation of the surfactant structure between nonionic (NCOEO3) and cationic-nonionic (N+COEO3) forms triggered by CO2. This responsiveness enables efficient demulsification at room temperature as well as the recycling and recovery of the surfactant within the aqueous phase. More importantly, the inverted highly viscous HIPPEs could be reversibly converted into flowable low viscous HIPPEs through the CO2 trigger. This research offers an effective method for preparing intelligent HIPPEs with adjustable properties, such as stability, viscosity, and an aqueous recyclable emulsifier, which can meet various practical application needs.
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