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从海洋环境中提取的溶解有机物的酸碱性质。

Acid-base properties of dissolved organic matter extracted from the marine environment.

机构信息

GEOMAR Helmholtz Centre for Ocean Research Kiel, Wischhofstraße 1-3, 24148 Kiel, Germany.

Departament de Química, Universitat de Lleida and AGROTECNIO, Rovira Roure 191, 25198 Lleida, Spain.

出版信息

Sci Total Environ. 2020 Aug 10;729:138437. doi: 10.1016/j.scitotenv.2020.138437. Epub 2020 Apr 19.

DOI:10.1016/j.scitotenv.2020.138437
PMID:32371203
Abstract

Marine dissolved organic matter (DOM) plays a key role in the current and future global carbon cycle, which supports life on Earth. Trace metals such as iron, an essential micronutrient, compete with protons and major ions for the binding to DOM. These competitive effects and the DOM binding capacity are related to the DOM acid-base properties, which also influence DOM transport and reactivity in marine waters. Here we present the results of a complete set of acid-base titration experiments of a pre-concentrated marine DOM sample in the range 0.01 ≤ I ≤ 0.7 M and 3 ≤ pH ≤ 10. We characterize the obtained proton binding curves using a combination of the non-ideal competitive adsorption (NICA) isotherm and Donnan electrostatic model. Within the main chemical groups of marine DOM, the carboxylic distribution was accurately characterized from the obtained data (Q=2.52 mol·kg, logk¯ = 3.26, m = 0.69 and b = 0.70). This carboxylic mode was found to be less acidic and more homogeneous than a generic fulvic acid, but the differences are consistent with the reported variability of fulvic acids of freshwater and terrestrial origin. We find that changes in temperature (down to 5.5 °C), and the presence of calcium or magnesium (at 0.01 M) resulted in no significant modification of the proton ion binding curves obtained at 25 °C and 0.7 or 0.1 M ionic strength, respectively. We demonstrate the relevance of proton binding parameters for the modelling of the system iron/marine DOM throughout a wide range of salinity and acidity conditions in the context of different future ocean scenarios.

摘要

海洋溶解有机质 (DOM) 在当前和未来的全球碳循环中起着关键作用,为地球上的生命提供支持。铁等痕量金属是一种必需的微量元素,与质子和主要离子竞争与 DOM 结合。这些竞争效应和 DOM 结合能力与 DOM 的酸碱性质有关,这些性质也会影响 DOM 在海洋水中的传输和反应性。在这里,我们展示了一系列完整的海洋 DOM 预浓缩样品在 0.01≤I≤0.7 M 和 3≤pH≤10 范围内的酸碱滴定实验结果。我们使用非理想竞争吸附(NICA)等温线和 Donnan 静电模型组合来描述获得的质子结合曲线。在所研究的海洋 DOM 的主要化学基团中,从获得的数据准确地描述了羧酸的分布(Q=2.52 mol·kg,logk¯ = 3.26,m=0.69 和 b=0.70)。与通用富里酸相比,这种羧酸模式的酸性较小且更均匀,但差异与淡水和陆地来源的富里酸的报道变异性一致。我们发现,温度变化(低至 5.5°C)和钙或镁的存在(0.01 M)分别在 25°C 和 0.7 或 0.1 M 离子强度下不会导致质子离子结合曲线发生显著变化。我们证明了质子结合参数在不同未来海洋情景下,在广泛的盐度和酸度条件下,对铁/海洋 DOM 系统建模的相关性。

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