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表面张力:哪个相更重要,液体还是蒸汽?

Tension at the surface: which phase is more important, liquid or vapor?

机构信息

Department of Chemical Engineering, University of Waterloo, Waterloo, Ontario, Canada.

出版信息

PLoS One. 2009 Dec 14;4(12):e8281. doi: 10.1371/journal.pone.0008281.

Abstract

Tension at the surface is a most fundamental physicochemical property of a liquid surface. The concept of surface tension has widespread implications in numerous natural, engineering and biomedical processes. Research to date has been largely focused on the liquid side; little attention has been paid to the vapor--the other side of the surface, despite over 100 years of study. However, the question remains as to whether the vapor plays any role, and to what extent it affects the surface tension of the liquid. Here we show a systematic study of the effect of vapor on the surface tension and in particular, a surprising observation that the vapor, not the liquid, plays a dominant role in determining the surface tension of a range of common volatile organic solutions. This is in stark contrast to results of common surfactants where the concentration in the liquid plays the major role. We further confirmed our results with a modified adsorption isotherm and molecular dynamics simulations, where highly structured, hydrogen bonded networks, and in particular a solute depletion layer just beneath the Gibbs dividing surface, were revealed.

摘要

表面张力是液体表面最基本的物理化学性质。表面张力这一概念在众多自然、工程和生物医学过程中具有广泛的应用。迄今为止,研究主要集中在液相方面;尽管已经进行了 100 多年的研究,但对气相(表面的另一面)的关注甚少。然而,目前仍存在一个问题,即气相是否发挥作用,以及它在多大程度上影响液体的表面张力。在这里,我们对蒸汽对表面张力的影响进行了系统的研究,特别是一个令人惊讶的观察结果,即蒸汽而不是液体在决定一系列常见挥发性有机溶液的表面张力方面起着主导作用。这与常见表面活性剂的结果形成鲜明对比,在常见表面活性剂中,液体中的浓度起着主要作用。我们进一步通过改进的吸附等温线和分子动力学模拟证实了我们的结果,其中揭示了高度结构化的氢键网络,特别是在吉布斯分割面下的溶质耗尽层。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2698/2788621/651d0d26a73e/pone.0008281.g001.jpg

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