Metal Speciation in Water of the Flooded Mine “Arsenic” (Karelia, Russia): Equilibrium-Kinetic Modeling with a Focus on the Influence of Humic Substances

IF 1.7 4区 地球科学 Q3 GEOCHEMISTRY & GEOPHYSICS
Elena V. Cherkasova, Artem A. Konyshev, Evgeniya A. Soldatova, Evgeniya S. Sidkina, Mikhail V. Mironenko
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引用次数: 4

Abstract

Equilibrium-kinetic modeling allows investigating metal behavior in the water–rock-organic matter system with time to evaluate anthropogenic effects on the environment. In the article, the interactions of stagnant mine drainage water of the flooded mine “Arsenic” with ore and gangue minerals were simulated using different organic matter incorporation approaches. If the model is closed to humic substances (no additional organic matter input), most fulvic acids are bound in the Fe fulvate complex. While under the removal of Fe fulvate from the model, the Cu fulvate becomes prevalent, the contribution of the fulvate complexes with Zn, Mg, and Ca also increases. This scenario simulates the organo-mineral complexes behavior well and allows identifying the sequence of metal binding to organic ligands as follows Fe > Cu > Zn > Mg > Ca. The second scenario imitates the constant input of organic matter to the model (open system regarding humic substances). The dissolved metal concentrations in the model solution are extremely high in comparison to the mine drainage water. This scenario demonstrates that excessive input of organic matter leads to the accumulation of the metals in a dissolved form and blocks the secondary mineral formation despite the faster dissolution of the primary minerals under a more acidic pH than in the first scenario. However, despite the differences between the model solution and the mine drainage water, this scenario is useful to address specific issues associated with changes in natural and anthropogenic conditions. Both scenarios show the importance of organic matter incorporation to the equilibrium-kinetic models.

Abstract Image

“砷”(卡累利阿,俄罗斯)矿井水中金属形态:平衡-动力学模型及腐殖质影响
平衡动力学模型允许随着时间的推移研究水-岩石-有机质系统中的金属行为,以评估人为对环境的影响。本文采用不同的有机质掺入方法,模拟了“砷”矿井积水与矿石、脉石矿物的相互作用。如果模型接近腐殖质(没有额外的有机物输入),大多数黄腐酸结合在黄腐酸铁络合物中。当从模型中去除富酸铁时,富酸铜变得普遍,与Zn、Mg和Ca的富酸配合物的贡献也增加。该场景很好地模拟了有机-矿物配合物的行为,并允许识别金属与有机配体结合的顺序如下:Fe > Cu > Zn > Mg > Ca。第二种情况模拟有机物对模型的持续输入(关于腐殖质的开放系统)。与矿井排水相比,模型溶液中溶解金属的浓度非常高。该情景表明,尽管在较酸性的pH值下,原生矿物的溶解速度比第一种情景更快,但有机物的过量输入导致金属以溶解形式积累,并阻碍了次生矿物的形成。然而,尽管模式解决方案与矿井排水之间存在差异,但这种情景对于处理与自然和人为条件变化有关的具体问题是有用的。这两种情况都显示了有机物加入平衡动力学模型的重要性。
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来源期刊
Aquatic Geochemistry
Aquatic Geochemistry 地学-地球化学与地球物理
CiteScore
4.30
自引率
0.00%
发文量
6
审稿时长
1 months
期刊介绍: We publish original studies relating to the geochemistry of natural waters and their interactions with rocks and minerals under near Earth-surface conditions. Coverage includes theoretical, experimental, and modeling papers dealing with this subject area, as well as papers presenting observations of natural systems that stress major processes. The journal also presents `letter''-type papers for rapid publication and a limited number of review-type papers on topics of particularly broad interest or current major controversy.
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