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Vertical distribution and mobilization of arsenic in shallow alluvial aquifers of Chapai-Nawabganj, Northwestern Bangladesh

机译:孟加拉国西北部浅褐色含水层砷砷的垂直分布及动员

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Core sediments from two undisturbed boreholes and groundwater from fifty four arsenic (As)-contaminated well waters in the Chapai-Nawabganj area of northwestern Bangladesh were collected for geochemical analyses. Groundwater arsenic concentrations in the uppermost aquifer (10 to 40 m depth) range from 2.76-315 μg/L (mean 48 μg/L) whereas arsenic concentration in sediments ranges from 3.26-10 mg/kg. In January 2008, 2009 and 2010, maximum As concentration occurred at the same depth. Arsenic and Fe speciation in sediments were determined using XANES and the results imply that As(V) and Fe(III) are the dominant species in most sediments. X-ray absorption fine structure (EXAFS) analysis shows that FeOOH is the main carrier of As in the sediments. Environmental scanning electron microscopy and transmission X-ray microscopy were used to investigate the characteristics of FeOOH in sediments which adsorb arsenic. The dominant groundwater type is calcium (Ca)-bicarbonate (HCO_3~-) with high concentrations of As and iron (Fe) but low levels of nitrate (NO_3~-) and sulfate (SO_4~(-2)). Statistical analysis clearly shows that As is closely associated with Fe (R~2 = 0.64) and manganese (Mn) (R~2 = 0.91) in sediments while As is not correlated with Fe and Mn in groundwater. Comparatively low Fe and Mn concentrations in some groundwaters, suggest that probably siderite and/or rhodochrosite precipitated as secondary mineral on the surface of the sediment particles. The correlations along with results of sequential leaching experiments suggest that reductive dissolution of FeOOH and MnOOH mediated by anaerobic bacteria represents mechanism for releasing arsenic into the groundwater.
机译:从五十四个砷(AS)的核心沉积物,从五十四个砷(AS) - 在孟加拉国西北地区的Chapai-Nawabganj地区的井水域被收集进行地球化学分析。最上层含水层(10至40米深度)的地下水砷浓度为2.76-315μg/ L(平均48μg/ L),而沉积物中的砷浓度范围为3.26-10 mg / kg。 2008年1月,2009年和2010年,最大程度在相同的深度时出现。使用Xanes测定沉积物中的砷和Fe形态,结果意味着(v)和Fe(III)是大多数沉积物中的主要物种。 X射线吸收细结构(EXAFS)分析表明FeOOH是如沉积物中的主要载体。环境扫描电子显微镜和透射X射线显微镜用于研究吸附砷的沉积物中FeOOH的特性。主导地下水型是钙(Ca) - 碳酸酯(HCO_3〜 - ),具有高浓度和铁(Fe),但硝酸水平低(NO_3〜 - )和硫酸盐(SO_4〜(-2))。统计分析清楚地表明,与沉积物中的Fe(R〜2 = 0.64)和锰(Mn)(R〜2 = 0.91)密切相关,同时与地下水中的Fe和Mn相关。在一些地水中相对低的Fe和Mn浓度,表明可能在沉积物颗粒表面上作为次级矿物沉淀出来的含水极和/或罗多。相关性以及顺序浸出实验的结果表明,厌氧细菌介导的FeOH和Mnooh的还原溶解是释放砷进入地下水的机制。

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