Formation and Stability of Pickering Emulsion Stabilized by Self-Aggregated Chitosan Particles near the pK a

皮克林乳液 壳聚糖 化学工程 吸附 聚结(物理) 材料科学 乳状液 接触角 粒子(生态学) 表面电荷 化学 润湿 高分子化学 纳米技术 粒径 化学稳定性
作者
Xintong Zhai,Mengjiao Wang,Wenfei Li,Xinyi Yin,Huiran Qi,Yuejiu Pang,Shupeng Su
出处
期刊:ACS omega [American Chemical Society]
卷期号:11 (8): 13733-13742
标识
DOI:10.1021/acsomega.5c11665
摘要

High Resolution Image Download MS PowerPoint Slide Stabilizing Pickering emulsions with highly hydrophilic biopolymers such as chitosan remains challenging due to their strong hydrophilicity. By adjusting the pH to impart minimal or zero charge, these highly hydrophilic particles can form stable Pickering emulsions. However, no consensus has been reached regarding the optimal pH to fabricate stable Pickering emulsions. Hence, this study focused on the narrow pH window near the p K a of chitosan (pH 6.1–6.9) to clarify the optimal pH and the related formation and stability mechanisms. At p K a (pH 6.5), chitosan formed self-aggregated particles with optimal amphiphilicity and moderate surface charge, facilitating robust adsorption at the oil–water interface. The resulting emulsions exhibit remarkably small droplet sizes, good fluidities, high encapsulation capacities, and exceptional stability against creaming, coalescence, flocculation, and centrifugation. In contrast, emulsions prepared at pH below 6.5 suffered from excessive hydrophilicity and poor coalescence stability, while those at pH above 6.5 experienced particle overaggregation and gelation, leading to compromised fluidity and interfacial integrity. This superior performance of Pickering emulsions at the optimal pH was attributed to the optimal hydrophilic–hydrophobic balance and moderate surface charge of the chitosan particles, facilitating smaller droplet formation and uniform particle coverage. This finding is pivotal for future applications of chitosan Pickering emulsions and offers insights for developing food-grade Pickering emulsions with other hydrophilic charged particles.

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