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水汽在有机质包裹矿物上的吸附

Water Vapor Binding on Organic Matter-Coated Minerals.

机构信息

Univ Rennes, École Nationale Supérieure de Chimie de Rennes, CNRS, ISCR - UMR6226 , F-35000 Rennes , France.

Department of Chemistry , Umeå University , SE-901 87 Umeå , Sweden.

出版信息

Environ Sci Technol. 2019 Feb 5;53(3):1252-1257. doi: 10.1021/acs.est.8b05134. Epub 2019 Jan 17.

DOI:10.1021/acs.est.8b05134
PMID:30608658
Abstract

Atmospheric water vapor binding to soils is a key process driving water availability in unsaturated terrestrial environments. Using a representative hydrophilic iron oxyhydroxide, this study highlights key mechanisms through which water vapor (i) adsorbs and (ii) condenses at mineral surfaces coated with Leonardite humic acid (LHA). Microgravimetry and vibrational spectroscopy showed that liquid-like water forms in the three-dimensional array of mineral-bound LHA when present at total C/Fe ratios well exceeding ∼73 mg C per g Fe (26 C atoms/nm). Below these loadings, minerals become even less hydrophilic than in the absence of LHA. This lowering in hydrophilicity is caused by the complexation of LHA water-binding sites to mineral surfaces, and possibly by conformational changes in LHA structure removing available condensation environments for water. An empirical relationship predicting the dependence of water adsorption densities on LHA loadings was developed from these results. Together with the molecular-level description provided in this work, this relationship should guide efforts in predicting water availability, and thereby occurrences of water-driven geochemical processes in terrestrial environments.

摘要

大气中的水汽与土壤结合是驱动非饱和陆地环境中水分可利用性的关键过程。本研究使用一种具有代表性的亲水性铁氢氧化物,强调了水汽(i)在覆盖有莱奥纳德ite 腐殖酸(LHA)的矿物表面吸附和(ii)凝结的关键机制。微量天平法和振动光谱法表明,当总 C/Fe 比远远超过约 73mg C/g Fe(26 个碳原子/纳米)时,液态水会在矿物结合的 LHA 的三维阵列中形成。在这些负载以下,矿物质的亲水性甚至比没有 LHA 时还要低。这种亲水性的降低是由于 LHA 水结合位点与矿物表面的络合,以及 LHA 结构的构象变化可能会去除水的可用凝结环境。从这些结果中开发了一个预测水吸附密度对 LHA 负载依赖性的经验关系。结合本工作提供的分子水平描述,该关系应指导预测水分可利用性的努力,从而预测陆地环境中与水分驱动的地球化学过程的发生。

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