首页> 外文期刊>Journal of the Geological Society of India >Hydrochemistry and Arsenic Contamination of Shallow Aquifers in Bidyananda and Nazimkhan Unions, Rajarhat Upazilla, Kurigram, Bangladesh
【24h】

Hydrochemistry and Arsenic Contamination of Shallow Aquifers in Bidyananda and Nazimkhan Unions, Rajarhat Upazilla, Kurigram, Bangladesh

机译:Bidyananda和Nazimkhan工会浅含水层的水化和砷污染,Rajarhat Upazilla,Kurigram,孟加拉国

获取原文
获取原文并翻译 | 示例
           

摘要

In this study, the spatial distribution and hydrochemistry of arsenic (As) in shallow alluvial aquifers of Bidyananda and Nazimkhan Union of Rajarhat opazilla, Kurigram district of Bangladesh have been evaluated. Nineteen groundwater samples (depth: 10 to 50 m) were collected from the studied area for physical and chemical analysis. Based on analytical data of chemical analysis, a Piper trilinear diagram have been prepared which revealed that the groundwater of the studied area is CaHCO 3 type, where Ca is the dominant metal. Physical data and permeability index values indicate good quality of the groundwater for drinking and irrigation. The concentrations of Fe, Mn and As in almost all samples exceed the WHO and Bangladesh national standard indicating significant pollutions. Groundwater As concentrations in the aquifer (10-50 m of depth) ranged from <0.005 to 0.323 mgL-1 and geochemical conditions changed from oxidized to successively more reduced, higher As concentrations with depth. Correlation studies revealed a good correlation between As and Mn (R2= 0.20) in groundwater implying that natural reductive dissolution of MnO(OH) and FeO(OH) may be responsible for As release into the groundwater. However, a poor correlation between As and Fe (R2 = 0.0084) in groundwater is probably due to the precipitation of dissolved Fe and Mn as siderite (FeCO 3) and rhodochrosite (MnCO 3), respectively, under reducing conditions. The poor correlations among dissolved As, Fe and SO 42- concentrations (As vs. SO 42- R2 = 0.0674; Fe vs. SO 42-, R2=0.1542) in groundwater suggest that pyrite/sulfide oxidation is not the dominant process for As release. A high concentration of As, Fe and Mn indicate that the natural reductive dissolution of iron oxyhydroxides is probably the dominant process for As mobilization in the groundwater of the studied area.
机译:在这项研究中,评估了孟加拉国Kurigram地区的Bidyananda和纳粹Khan联盟的浅尘含水层砷(AS)的空间分布和水化学。从研究区域收集19个地下水样品(深度:10至50米)以进行物理和化学分析。基于化学分析的分析数据,已经制定了一种吹笛式三轴图,显示研究区域的地下水是CAHCO 3型,其中CA是优势金属。物理数据和渗透率指标值表示饮用和灌溉的地下水的良好质量。 Fe,Mn的浓度和几乎所有样品的浓度超过了世卫组织和孟加拉国国家标准,表明显着的污染。作为含水层中的浓度(深度10-50米)的地下水范围为<0.005至0.323 MgL-1,地球化学条件从氧化变为连续减少,随着深度的浓度更高。相关性研究揭示了地下水中的良好相关性和Mn(R2 = 0.20),这意味着MnO(OH)和FeO(OH)的自然还原溶解可能是作为释放到地下水中的负责的。然而,在地下水中的和​​Fe(R2 = 0.0084)之间的相关性差可能是由于分别在还原条件下溶解的Fe和Mn和菱形(MNCO 3)和菱氯橡胶(MNCO 3)的沉淀。地下水中溶解的溶解作为,Fe等42-浓度(如42- r2 = 0.0674; Fe 42-,R2 = 0.1542)表明黄铁矿/硫化物氧化不是主要的过程释放。高浓度的AS,Fe和Mn表明铁羟基氧化铁的自然还原溶解可能是在研究区域的地下水中动员的主导过程。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号