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Occurrence of arsenic in core sediments and groundwater in the Ghapai-Nawabganj District, northwestern Bangladesh

机译:孟加拉国西北部Ghapai-Nawabganj区核心沉积物和地下水中砷的存在

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Groundwater and core sediments of two boreholes (to a depth of 50 m) from the Chapai-Nawabganj area in northwestern Bangladesh were collected for arsenic concentration and geochemical analysis. Groundwater arsenic concentrations in the uppermost aquifer (10-40 m of depth) range from 2.8 μg L~(-1) to 462.3 μg L~(-1). Groundwater geochemical conditions change from oxidized to successively more reduced, higher As concentration with depth. Higher sediment arsenic levels (55 mg kg~(-1)) were found within the upper 40 m of the drilled core samples. X-ray absorption near-edge structure spectroscopy was employed to elucidate the arsenic speciation of sediments collected from two boreholes. Environmental scanning electron microscopy and transmission X-ray microscopy were used to investigate the characteristics of FeOOH in sediments which adsorb arsenic. In addition, a pH-Eh diagram was drawn using the Geochemist's Workbench (GWB) software to elucidate the arsenic speciation in groundwater. The dominant groundwater type is Ca-HCO_3 with high concentrations of As, Fe and Mn but low levels of NO_3~- and SO_4~(2-). Sequential extraction analysis reveals that Mn and Fe hydroxides and organic matter are the major leachable solids carrying As. High levels of arsenic concentration in aquifers are associated with finegrained sediments. Fluorescent intensities of humic substances indicate that both groundwater and sediments in this arsenic hotspot area contain less organic matter compared to other parts of Bengal basin. Statistical analysis clearly shows that As is closely associated with Fe and Mn in sediments while As is better correlated with Mn in groundwater. These correlations along with results of sequential leaching experiments suggest that reductive dissolution of MnOOH and FeOOH mediated by anaerobic bacteria represents an important mechanism for releasing arsenic into the groundwater.
机译:收集了孟加拉西北部Chapai-Nawabganj地区两个钻孔(深度为50 m)的地下水和岩心沉积物,以进行砷浓度和地球化学分析。最上层含水层(深度为10-40 m)中的地下水砷浓度范围为2.8μgL〜(-1)至462.3μgL〜(-1)。地下水的地球化学条件从氧化变化为还原,随着深度的增加,砷的浓度逐渐升高。在钻探的岩心样品的上部40 m内发现较高的沉积物砷含量(55 mg kg〜(-1))。 X射线吸收近边缘结构光谱用于阐明从两个钻孔收集的沉积物的砷形态。使用环境扫描电子显微镜和透射X射线显微镜研究吸附砷的沉积物中FeOOH的特征。此外,使用地球化学家的工作台(GWB)软件绘制了pH-Eh图,以阐明地下水中的砷形态。地下水的主要类型为Ca-HCO_3,其中As,Fe和Mn的浓度较高,而NO_3〜-和SO_4〜(2-)的含量较低。顺序萃取分析表明,Mn和Fe的氢氧化物和有机物是携带As的主要可浸出固体。含水层中高浓度的砷与细颗粒沉积物有关。腐殖质的荧光强度表明,与孟加拉盆地的其他部分相比,该砷热点地区的地下水和沉积物都含有较少的有机物。统计分析清楚地表明,As与沉积物中的Fe和Mn密切相关,而As与地下水中的Mn相关性更好。这些相关性以及顺序浸出实验的结果表明,厌氧细菌介导的MnOOH和FeOOH的还原溶解代表了将砷释放到地下水中的重要机制。

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