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首页> 外文期刊>Applied Geochemistry: Journal of the International Association of Geochemistry and Cosmochemistry >Arsenic mobilization in a freshening groundwater system formed within glaciomarine deposits
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Arsenic mobilization in a freshening groundwater system formed within glaciomarine deposits

机译:冰川海洋沉积物中形成的新鲜地下水系统中的砷动员

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Arsenic release to groundwater and conditions favoring As mobility are investigated in a system of aquifers formed within unconsolidated Quaternary sediments. The studied groundwater system is comprised of unconfined aquifers formed in glaciofluvial sediments with Ca-Mg-HCO _3 groundwater, and confined aquifers formed within glaciomarine sediments with high As(above 10μg/L)Na-HCO _3 or Na-Cl groundwater. A positive relationship of As concentrations with the Na/(Ca+Mg)ratio of groundwater indicates that As release occurs in glaciomarine sediments concurrent to cation exchange reactions related to groundwater freshening. Arsenic is mobile in confined aquifers as a result of groundwater basic pH which prevents arsenate from adsorbing to mineral surfaces, and reducing conditions that favor speciation to arsenite. Selected extractions applied to sediment core samples indicate that As occurs in sediments predominantly in sulfide minerals and in Mn oxides and/or Fe oxyhydroxides. General positive relationships between As and the reduced species Fe ~(2+), NH _3 and dissolved S ~(2-)suggest that As release occurs at increasingly reducing conditions. Despite likely As release via Fe oxyhydroxide reductive dissolution, Fe remains at relatively low concentrations in groundwater(up to 0.37mg/L)as a result of possible Fe adsorption and Fe reprecipitation as carbonate minerals favored by basic pH and high alkalinity. The presence of S ~(2-)in some samples, a negative relationship between δ ~(34)S of SO _4 and SO42- concentrations, and a positive relationship between δ ~(34)S and δ ~(18)O of SO _4 indicate that groundwater in confined aquifers is undergoing bacterial SO _4 reduction.
机译:在未固结的第四纪沉积物中形成的含水层系统中研究了砷向地下水的释放和有利于流动性的条件。所研究的地下水系统由含Ca-Mg-HCO _3地下水的河流河流沉积物中形成的无限制含水层和含高As(10μg/ L)Na-HCO _3或Na-Cl地下水的冰川海洋沉积物中形成的受限含水层组成。 As浓度与地下水的Na /(Ca + Mg)比呈正相关,表明As释放发生在与海洋淡水有关的阳离子交换反应的同时,在冰川海洋沉积物中发生。由于地下水的碱性pH值,砷可在密闭含水层中移动,从而防止了砷酸盐吸附到矿物表面,并减少了有利于形成砷酸盐的条件。对沉积物岩心样品进行的选定提取表明,As主要在硫化物矿物和Mn氧化物和/或Fe羟基氧化物中发生于沉积物中。 As与还原态Fe〜(2 +),NH_3和溶解态的S〜(2-)之间一般呈正相关关系,这表明As的释放在还原条件越来越强的条件下发生。尽管可能通过氢氧化铁还原溶解释放出Fe,但由于可能的Fe吸附和Fe再沉淀为碱性pH和高碱度所支持的碳酸盐矿物,Fe在地下水中的浓度仍相对较低(最高0.37mg / L)。样品中存在S〜(2-),SO _4的δ〜(34)S与SO42-浓度呈负相关,而δ〜(34)S与δ〜(18)O呈正相关。 SO _4表示密闭含水层中的地下水正在经历细菌SO _4的还原。

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