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Effect of irrigation on Fe(III)-SO42- redox cycling and arsenic mobilization in shallow groundwater from the Datong basin, China: Evidence from hydrochemical monitoring and modeling

机译:灌溉对大同盆地浅层地下水中Fe(III)-SO42-氧化还原循环和砷迁移的影响:来自水化学监测和模拟的证据

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Seasonal hydrochemical monitoring has been conducted at a well-known arsenic (As) contaminated site to understand the critical controlling processes on As mobilization and enrichment in groundwater. The hydrochemical results indicate that the water chemistry at the studied site is mainly controlled by evaporates dissolution, and redox reactions during irrigation and non-irrigation periods, respectively. The measured redox-sensitive components indicate that the groundwater experienced periodic redox changes from irrigation to non-irrigation periods and that an enhanced reducing environment prevailed during the non-irrigation period. The observed high As concentration and the strong positive correlation between As and Fe support the conclusion that the Fe oxides/hydroxides reduction and Fe sulfide oxidation releases As during the irrigation period. However, the relatively low As concentration and the close inverse correlation between As, Fe and SO42- show that Fe(III) and SO42- reduction accompanied by the formation of Fe sulfide precipitates, retains As during the non-irrigation periods. The geochemical inverse modeling performed for the selected wells confirms that Fe oxide/hydroxide and Fe sulfide dissolution as well as siderite precipitation are the dominant processes related to the mobilization of As during the water evolution from the pre-irrigation to irrigation period, while Fe sulfide precipitation immobilize As during the groundwater evolution from the irrigation to the post-irrigation period. In general, the combined results of the hydrochemical monitoring and the geochemical inverse modeling support the conclusion that the Fe(III)-SO42- redox cycling induced by periodic irrigation practices controls the mobilization of As in groundwater at this site. (C) 2015 Elsevier B.V. All rights reserved.
机译:已在一个著名的砷污染地点进行了季节性水化学监测,以了解对地下水中砷的富集和富集的关键控制过程。水化学结果表明,研究地点的水化学主要受蒸发和非灌溉期间蒸发溶解和氧化还原反应的控制。测得的对氧化还原敏感的成分表明,从灌溉到非灌溉期间,地下水经历了周期性的氧化还原变化,并且在非灌溉期间,还原环境普遍存在。观测到的高砷浓度和砷与铁之间的强正相关关系支持以下结论:灌溉期间铁氧化物/氢氧化物的还原和铁硫化物的氧化释放出砷。但是,相对较低的砷浓度以及砷,铁和SO42-之间的紧密反相关关系表明,在非灌溉期间,Fe(III)和SO42-的还原伴随着硫化铁沉淀的形成而保留了As。对选定的井进行的地球化学逆向模型证实,从灌溉前到灌溉期的水演化过程中,Fe氧化物/氢氧化物和Fe硫化物的溶解以及菱铁矿的沉淀是与As迁移有关的主要过程。在从灌溉到灌溉后的地下水演化过程中,降水固定化为As。一般而言,水化学监测和地球化学反演模型的综合结果支持以下结论:定期灌溉实践引起的Fe(III)-SO42-氧化还原循环控制了该地点地下水中As的迁移。 (C)2015 Elsevier B.V.保留所有权利。

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