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In Situ Characterization and Interfacial Viscoelastic Properties of Pickering Emulsions Stabilized by AIE-Active Modified Alginate and Chitosan Complexes

皮克林乳液 石英晶体微天平 壳聚糖 粘弹性 润湿 材料科学 化学工程 吸附 乳状液 扫描电子显微镜 胶体 纳米技术 化学 复合材料 有机化学 纳米颗粒 工程类
作者
Sihui Wan,Qu Zeng,Shujuan Yang,Xinyu Zhao,Qiyan Wen,Haiyun Tang,Yamei Zhang,Junhao Huang,Gaobo Yu,Yuhong Feng,Jiacheng Li
出处
期刊:ACS Sustainable Chemistry & Engineering [American Chemical Society]
卷期号:10 (31): 10275-10285 被引量:13
标识
DOI:10.1021/acssuschemeng.2c02299
摘要

Pickering emulsions stabilized by polysaccharide–polysaccharide complexes are attractive in many applications. However, how interface films formed by soft particles affect the stability of Pickering emulsions has not been well explored. Herein, we designed aggregation-induced emission (AIE)-active modified alginate (Alg-AIE)/chitosan (CS) polyelectrolyte complex (Alg-AIE/CS complex) colloidal particles that are used to stabilize Pickering emulsions. To explore the relationship between the interface film structure and emulsification properties, the microstructure of emulsions was directly visualized by a combination of confocal laser scanning microscopy (CLSM) and scanning electron microscopy (SEM). The wetting properties of Alg-AIE/CS complexes were regulated by changing the amount of CS, which further regulated the aggregation behavior of the interface. The interfacial adsorption behavior of the particles and the physical stability of the emulsions were determined by combining stability analysis and employing a quartz crystal microbalance with dissipation monitoring (QCM-D). The results showed that the addition of CS resulted in more Alg-AIE/CS complexes that could be adsorbed at the oil–water interface, forming thicker and stronger viscoelastic interface films, which improved the stability of the emulsion. Most importantly, in situ visualization technology provided a new way to understand the interfacial properties of Pickering emulsions.
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