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Ex situ groundwater treatment triggering the mobilization of geogenic uranium from aquifer sediments

机译:异地地下水处理触发了含水层沉积物中动产铀的动员

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Uranium (U) concentrations in groundwater extracted for drinking water usage from a Quaternary fluvial aquifer partly exceed the German drinking water guideline of 10 μg L~(-1). Responsible sources and mobilization processes were unknown and gave rise to this study. Land use of the watershed is mainly agricultural leading to groundwater nitrate concentrations >50 mg L~(-1) and a need for water treatment prior to utilization as drinking water. This is successfully accomplished by addition of nutrients triggering bacterial nitrate reduction, followed by the addition of NaOH for water softening and CO_2 for pH adjustment, with subsequent reinfiltration into the aquifer. Three boreholes were drilled to obtain a total of 127 solid samples from Quaternary and underlying Tertiary sediments. Geochemistry and mineralogy were assessed using elemental analysis (CS, ICP-MS), X-ray diffraction and scanning electron microscopy to complement hydrochemical data and unravel U occurrence in the subsurface. Solid phase U fractionation was characterized by a sequential extraction procedure, U remobilization potential by a 137 days column experiment. Shallow Quaternary sediments yielded low U contents <1 μg g~(-1), higher values were found in depths of more than 20 m below ground surface. Here, strata of elevated Corg and C_(inorg) contain up to 14 pg g~(-1) U, mainly bound in organic and carbonate fractions. Groundwater U concentrations > 10 μg L~(-1) almost exclusively appear in this same depth range, and only in wells influenced by water treatment runoff. Results suggest that the applied water treatment approach triggers U remobilization from geogenic sources in the aquifer. The most probable mechanism is dissolution of U bearing calcite induced by CO_2 application; redox reactions and pH-driven desorption appear to play a minor role in mobilization. We conclude that groundwater treatment should carefully account for unwanted hydrogeochemical side effects triggering the mobilization of geogenic trace elements such as uranium.
机译:从第四纪河流含水层提取的用于饮用水的地下水中的铀(U)浓度部分超过了德国饮用水准则10μgL〜(-1)。负责的来源和动员过程未知,因此引起了这项研究。流域的土地利用主要是农业用途,导致地下水硝酸盐浓度> 50 mg L〜(-1),在用作饮用水之前需要进行水处理。通过添加触发细菌硝酸盐还原的营养物质,然后添加NaOH进行水软化和添加CO_2进行pH调节,然后再渗透到含水层中,可以成功实现这一目标。钻了三个钻孔,从第四纪和下层第三纪沉积物中获得了总共127个固体样品。使用元素分析(CS,ICP-MS),X射线衍射和扫描电子显微镜对地球化学和矿物学进行了评估,以补充水化学数据并揭示地下U的存在。固相U分馏的特征在于依次萃取程序,U复势潜力达137天的柱实验。浅第四纪沉积物的U含量低,<1μgg〜(-1),在地表以下20 m以上的深度发现较高的U值。在这里,升高的Corg和C_(inorg)地层最多包含14 pg g〜(-1)U,主要结合在有机和碳酸盐馏分中。地下水中U浓度> 10μgL〜(-1)几乎只出现在同一深度范围内,并且仅出现在受水处理径流影响的井中。结果表明,所应用的水处理方法触发了含水层中地源的U迁移。最可能的机理是CO_2的施加导致U形方解石溶解。氧化还原反应和pH驱动的解吸似乎在动员中起次要作用。我们得出的结论是,地下水处理应仔细考虑导致水成地球微量元素(如铀)动员的有害水文地球化学副作用。

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