Reversible Emulsions from Polyoxometalate-Polymer: A Robust Strategy to Cyclic Emulsion Catalysis and High-Internal-Phase Emulsion Materials

被引:14
作者
Wan, Chuchu [1 ]
Wu, Yutian [1 ]
Cheng, Quanyong [1 ]
Yu, Xiang [1 ]
Song, Yuhang [1 ]
Guan, Chengshu [1 ]
Tan, Xuemei [1 ]
Huang, Caili [1 ]
Zhu, Jintao [1 ]
Russell, Thomas P. [2 ,3 ]
机构
[1] Huazhong Univ Sci & Technol HUST, Sch Chem & Chem Engn, Key Lab Mat Chem Energy Convers & Storage, Minist Educ HUST, Wuhan 430074, Peoples R China
[2] Univ Massachusetts, Dept Polymer Sci & Engn, Amherst, MA 01003 USA
[3] Lawrence Berkeley Natl Lab, Mat Sci Div, Berkeley, CA 94720 USA
基金
中国国家自然科学基金;
关键词
HYDROPHOBIZED IN-SITU; PICKERING EMULSIONS; JANUS PARTICLES; NANOPARTICLES; INVERSION; PHOTOCHROMISM; SEPARATION; DROPLETS; DESIGN;
D O I
10.1021/jacs.3c10005
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Reversible Pickering emulsions, achieved by switchable, interfacially active colloidal particles, that enable on-demand emulsification/demulsification or phase inversion, hold substantial promise for biphasic catalysis, emulsion polymerization, cutting fluids, and crude oil pipeline transportation. However, particles with such a responsive behavior usually require complex chemical syntheses and surface modifications, limiting their extensive use. Herein, we report a simple route to generate emulsions that can be controlled and reversibly undergo phase inversion. The emulsions are prepared and stabilized by the interfacial assembly of polyoxometalate (POM)-polymer, where their electrostatic interaction at the interface is dynamic. The wettability of the POMs that dictates the emulsion type can be readily regulated by tuning the number of polymer chains bound to POMs, which, in turn, can be controlled by varying the concentrations of both components and the water/oil ratio. In addition, the number of polymer chains anchored to the POMs can be varied by controlling the number of negative charges on the POMs through an in situ redox reaction. As such, a reversible inversion of the emulsions can be triggered by switching between exposure to ultraviolet light and the introduction of oxygen. Combining the functions of POM itself, a cyclic interfacial catalysis system was realized. Inversion of the emulsion also affords a pathway to high-internal-phase emulsions. The diversity of the POMs, the polymers, and the responsive switching groups open numerous new, simple strategies for designing a wide range of responsive soft matter for cargo loading, controlled release, and delivery in biomedical and engineering applications without time-consuming particle syntheses.
引用
收藏
页码:25431 / 25439
页数:9
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