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纳米尺度对十六烷/水乳液中表面活性剂吸附和界面电荷的影响

Nanoscale Effects on the Surfactant Adsorption and Interface Charging in Hexadecane/Water Emulsions.

作者信息

Glikman Dana, Braunschweig Björn

机构信息

Institute of Physical Chemistry and Center for Soft Nanoscience, Westfälische Wilhelms-Universität Münster, Corrensstraße 28/30, 48149 Münster, Germany.

出版信息

ACS Nano. 2021 Dec 28;15(12):20136-20147. doi: 10.1021/acsnano.1c08038. Epub 2021 Dec 13.

Abstract

Nanoscale properties at interfaces play a key role in the colloidal stability of emulsions and other soft matter materials where physical properties need to be controlled from the nano to macroscopically visible length scales. Our molecular level understanding of oil-water interfaces arises mostly from results at extended interfaces and the common view that emulsions are stabilized by a large number of surfactant molecules at the droplet's interface which, however, has been recently challenged. In this work, we show that the particle size and the curvature of oil droplets at the nanoscale is of great importance for the interface adsorption of dodecyl sulfate surfactants and possible counterion condensation at the charged hexadecane-water interface. Using second-harmonic scattering, we have studied the surface charge of oil droplets in nanoemulsions where we systematically varied the particle size between 80 and 270 nm and demonstrate that the surface charge density σ changes drastically with size: For sizes >200 nm, σ is similar to what can be expected at flat extended interfaces, while σ is dramatically reduced by almost an order of magnitude when the particle size of the oil droplet is 80 nm. Using a theoretical approach that considers counterion condensation, we quantify the nanoscale effects on the change in surface charge with particle size and find excellent agreement with our experimental result. Modeling of the experimental results also implies that the charge per particle remains constant and depends on a critical balance of surfactant adsorption and ion condensation.

摘要

界面处的纳米尺度性质在乳液和其他软物质材料的胶体稳定性中起着关键作用,在这些材料中,物理性质需要从纳米尺度控制到宏观可见的长度尺度。我们对油水界面的分子水平理解主要源于在扩展界面上的研究结果,以及一种普遍观点,即乳液通过大量表面活性剂分子在液滴界面处实现稳定,然而,这种观点最近受到了挑战。在这项工作中,我们表明纳米尺度下油滴的粒径和曲率对于十二烷基硫酸盐表面活性剂在界面的吸附以及在带电荷的十六烷 - 水界面处可能发生的反离子凝聚非常重要。利用二次谐波散射,我们研究了纳米乳液中油滴的表面电荷,系统地改变了粒径在80至270纳米之间,并证明表面电荷密度σ随粒径急剧变化:对于粒径大于200纳米时,σ类似于在平坦扩展界面上预期的值,而当油滴粒径为80纳米时,σ显著降低了近一个数量级。使用考虑反离子凝聚的理论方法,我们量化了纳米尺度效应导致的表面电荷随粒径的变化,并发现与我们的实验结果非常吻合。对实验结果的建模还表明,每个粒子的电荷保持恒定,并且取决于表面活性剂吸附和离子凝聚的临界平衡。

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