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稀电解质浓度范围内的胶体热泳:从理论到实验

Colloid thermophoresis in the dilute electrolyte concentration regime: from theory to experiment.

作者信息

Pu Di, Panahi Amirreza, Natale Giovanniantonio, Benneker Anne M

机构信息

Department of Chemical and Petroleum Engineering, 2500 University Drive NW, Calgary, Alberta, T2N 1N4, Canada.

出版信息

Soft Matter. 2023 May 17;19(19):3464-3474. doi: 10.1039/d2sm01668k.

Abstract

Colloid thermophoresis in aqueous media is vital for numerous applications in nanoscience and life sciences. To date, a general description of colloid thermophoresis in DI water has not been determined. Here, we describe a theoretical model within the framework of the Fokker-Planck formalism and the flickering cluster concept to describe the hydration entropy effect on the thermophoretic behaviour of colloids suspended in DI water and compare this to new experimental results. We built an experimental platform to allow for rapid and robust temperature control and investigate the thermophoretic behaviour of silica microspheres with different sizes at various background temperatures for comparison. In this work, the ionic shielding effect is accounted for by using the well-known Duhr-Dhont's model, and the hydration layer effect is determined using the developed theoretical model. For the latter, our model reveals that the sign of the Soret coefficient is governed by the interplay between the binding energy and the chemical potential of water molecules, which were found to be in the same order of magnitude. We show that our analysis accurately describes the experimental behaviour of colloidal particles that opens a new avenue for developing versatile trapping and separation techniques for various colloidal particles in aqueous systems according to their size and background temperature.

摘要

水介质中的胶体热泳对于纳米科学和生命科学中的众多应用至关重要。迄今为止,尚未确定去离子水中胶体热泳的一般描述。在此,我们在福克 - 普朗克形式体系和闪烁簇概念的框架内描述了一个理论模型,以描述水合熵对悬浮在去离子水中的胶体热泳行为的影响,并将其与新的实验结果进行比较。我们构建了一个实验平台,以实现快速且稳定的温度控制,并研究不同尺寸的二氧化硅微球在不同背景温度下的热泳行为以作比较。在这项工作中,通过使用著名的杜尔 - 东特模型来考虑离子屏蔽效应,并使用所开发的理论模型来确定水合层效应。对于后者,我们的模型表明,索雷特系数的符号由结合能与水分子化学势之间的相互作用决定,发现它们处于相同的数量级。我们表明,我们的分析准确地描述了胶体颗粒的实验行为,这为根据其尺寸和背景温度开发用于水体系中各种胶体颗粒的通用捕获和分离技术开辟了一条新途径。

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