在流体界面上不可逆转的粒子吸附的动力学
Marina Pasquet1, Yu Fu2, Peiyao Wu2
1Chemical and Biomolecular Engineering Department, University of California, Berkeley, Berkeley, 94760, California, United States; Biofisika Institute (CSIC, UPV/EHU) and Department of Biochemistry and Molecular Biology, University of the Basque Country, Leioa, 48940, Spain.
Journal of colloid and interface science
|February 28, 2026
概括
在流体界面上的粒子吸附从扩散受限转变为动力受限动力学. 一个新的模型解释了不可逆转的吸附和粒子阻断,这对于乳液稳定和材料组装至关重要.
科学领域:
- 合体和表面科学科学
- 材料科学 材料科学 材料科学
- 物理化学 物理化学
背景情况:
- 在流体界面上的合物颗粒的动态吸附对于乳液稳定等应用来说是关键.
- 由于不可逆转的吸附和颗粒拥挤,现有的扩散有限模型在更高的表面覆盖率下失败.
- 粒子阻断和不可逆向吸附需要超出平衡假设的先进建模.
研究的目的:
- 开发一种统一的模型,用于流体界面上的体粒子吸附动力学.
- 为了捕捉从扩散受限到动力受限吸附模式的过渡.
- 为了研究表面覆盖面对吸附动力学的影响.
主要方法:
- 开发了一个统一的合扩散模型与随机序列吸附 (RSA) 边界条件.
- 采用微电压计和悬挂滴压计来测量动态界面张力.
- 在不同条件下,研究了烯/水界面上的3 - 甲酸 (TPM) 颗粒.
主要成果:
- 吸附流被增加的表面覆盖面积阻碍,与RSA预测保持一致.
- 计算了泰勒模块,以量化吸附动力学与扩散的比率.
- 确定了一个关键的表面覆盖面,触发了向反应有限吸附动态的过渡.
结论:
- 统一模型准确地描述了粒子吸附,超越了平衡扩散有限的假设.
- 由于粒子阻断,吸附动力学在高表面覆盖率下变得受到反应限制.
- 这个框架为界面粒子组装和稳定应用提供了预测能力.
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