Energetic description of the liquid–vapor interface of water with organic coating molecules

Julien Devémy, Alain Dequidt, Pascal Renard, Laurent Deguillaume and Patrice Malfreyt
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Abstract

In situ measurements revealed the presence of a myriad of organic chemical compounds in cloud droplets. Among them, a significant fraction is composed of polar or amphiphilic compounds and these compounds have been detected in various contrasting environments (marine, biogenic, urban areas). This raises a simple question of their spatial positioning in a cloud droplet. Previous study suggested they can form an organic surface coating at the air/water interface, thus potentially perturbing the exchanges of molecules between the gaseous and aqueous phases. The present work aims at investigating the properties of the water surface at the molecular scale by selecting 4 organic compounds representative of the molecular diversity observed in clouds. Two fatty acids (cis-pinonic acid and nonanoic acid) commonly detected in the atmosphere (aerosol particles and cloud waters) were chosen. Levoglucosan is an anhydro sugar ubiquitous in the air and well-known as a tracer of biomass burning. Finally, oxalic acid, one of the most abundant di-acids in the atmosphere, has been chosen. Its ability to form a coating film was analyzed through the calculation of a free energy profile along the direction normal to the surface of water. Nonanoic and cis-pinonic acids have been shown to partition to the surface, in contrast to levoglucosan and oxalic acid that remain in water. The surface tension of the liquid–vapor (LV) interface of water was calculated as a function of surface excess of nonanoic and cis-pinonic acids. We completed this study by examining how the presence of a hydrophobic monolayer of nonanoic molecules at the surface of water can change the behavior of a hydrophilic molecules such as levoglucosan at the interface. Our results clearly indicate that levoglucosan molecules in the gas phase can be adsorbed on this organic layer. Results from this study are of particular interest for atmospheric research since by confirming the concept of organic film formation at the air/droplet interface, they lead to questions about possible heterogeneous reactivity phenomena and potential modification of compound exchanges between the gas and aqueous phases.

Abstract Image

水与有机涂层分子液气界面的能量描述
现场测量显示,云滴中存在大量有机化合物。其中,极性或两性化合物占了很大一部分,这些化合物在各种不同的环境(海洋、生物、城市)中都被检测到。这就提出了一个简单的问题,即它们在云滴中的空间定位。以前的研究表明,它们可以在空气/水界面形成有机表面涂层,从而可能扰乱气相和水相之间的分子交换。本研究旨在通过选择 4 种能代表云中分子多样性的有机化合物,研究水表面在分子尺度上的特性。我们选择了大气(气溶胶颗粒和云水)中常见的两种脂肪酸(顺式菠萝酸和壬酸)。左旋葡聚糖是空气中普遍存在的一种脱氢糖,是众所周知的生物质燃烧示踪剂。最后,我们选择了草酸,它是大气中含量最高的二元酸之一。通过计算沿水表面法线方向的自由能曲线,分析了草酸形成涂膜的能力。结果表明,壬酸和顺式蒎烯酸会分化到表面,而左旋葡聚糖和草酸则会留在水中。我们计算了水的液-气(LV)界面表面张力与壬酸和顺式蒎烯酸表面过量的函数关系。在完成这项研究的过程中,我们研究了水表面壬酸分子疏水单层的存在如何改变亲水分子(如左旋葡聚糖)在界面上的行为。我们的研究结果清楚地表明,气相中的左旋葡聚糖分子可以吸附在这个有机层上。这项研究的结果对大气研究具有特别的意义,因为通过证实空气/液滴界面有机膜形成的概念,这些结果引出了关于可能的异相反应现象以及气相和水相之间化合物交换的潜在改变的问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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