首页> 外文期刊>Radiochimica Acta: International Journal for Chemical Aspects of Nuclear Science and Technology >Characterization of groundwater composition in Punjab state with special emphasis on uranium content, speciation and mobility
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Characterization of groundwater composition in Punjab state with special emphasis on uranium content, speciation and mobility

机译:旁遮普邦地下水成分的特征分析,重点是铀含量,形态和迁移率

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Groundwaters (borewell and handpump) were sampled from two districts (Bathinda and Mansa) of Punjab state and analyzed for their major ionic concentrations and uraniumisotope compositions in order to assess the possible origins of the waters and water–rock interactions that occurred in the deep aquifer system. The major ionic concentrations of waters were plotted on a Piper diagram and grouped into four dominant hydrochemical facies as (Na+K)-SO_4+Cl type (69%–73%), (Ca+Mg)-SO_4+Cl type (6%–21%), (Ca+Mg)–HCO_3 type (4%–6%) and (Na+K)-HCO_3 type (2%–19%). It was observed that mobility of uranium in groundwater was very much influenced by TDS (total dissolved solids). To investigate the various mechanisms for deriving the elevated uranium concentrations in groundwater, ~(234)U/~(238)U activity ratios (ARs) were calculated using the determined activity levels of ~(234)U and ~(238)U. ThemeanARswas found to be near unity (i.e. secular equilibrium) in the study regions confirmed that uranium in groundwaters was mainly resulted from its host/parent rocks through weathering processes. The concentration of HCO_3~? in ground water showed one order ofmagnitude higher than the total dissolved SiO_2 indicates that carbonateweathering was the dominant process due to major water–rock interaction. The uranium speciation in groundwaters was investigated by an equilibrium model calculation using MEDUSA (make equilibrium diagrams using sophisticated algorithms) under the influence of redox conditions and complexant concentration. At the observed range of pHvalues, the predominant redox speciationof uraniumwasobservedashydroxo-carbonatocomplexes of (UO_2)_2(CO_3)(OH)_3~? and hydroxyl complexes of UO_2(OH)_3~? whichmight be caused for increasing the solubility of uranium. Due to very low concentration of phosphate in groundwater, its effects on U(VI)-aqueous speciation was negligible.
机译:从旁遮普邦的两个地区(巴辛达和曼萨)抽取地下水(井筒和手泵),并分析其主要离子浓度和铀同位素组成,以评估深层含水层中可能的水源和水-岩相互作用。系统。水的主要离子浓度绘制在Piper图上,并分为四个主要的水化学相,分别为(Na + K)-SO_4 + Cl型(69%–73%),(Ca + Mg)-SO_4 + Cl型(6 %–21%),(Ca + Mg)–HCO_3类型(4%–6%)和(Na + K)-HCO_3类型(2%–19%)。据观察,铀在地下水中的迁移率受TDS(总溶解固体)的影响很大。为了研究推导地下水中铀浓度升高的各种机制,使用确定的〜(234)U和〜(238)U的活度水平计算了〜(234)U /〜(238)U活度比(ARs)。在研究区域中发现ThemetanARs接近统一(即长期平衡),这证明地下水中的铀主要来自其母体/母体岩石经过风化过程。 HCO_3〜?的浓度地下水中的碳氢化合物比溶解的SiO_2总量高一个数量级,这表明碳酸盐化风化是主要的水-岩相互作用的主要过程。在氧化还原条件和络合剂浓度的影响下,使用MEDUSA(使用复杂算法制作平衡图)通过平衡模型计算研究了地下水中的铀形态。在观察到的pH值范围内,铀的主要氧化还原形态是(UO_2)_2(CO_3)(OH)_3〜?的氢氧羰基-碳酸盐复合物。和UO_2(OH)_3〜?的羟基配合物可能是因为增加了铀的溶解度。由于地下水中磷酸盐的浓度非常低,因此其对U(VI)水溶液形态的影响可以忽略不计。

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