首页> 外文期刊>Applied Geochemistry: Journal of the International Association of Geochemistry and Cosmochemistry >Spatial variation in arsenic and fluoride concentrations of shallow groundwater from the town of Shahai in the Hetao basin, Inner Mongolia
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Spatial variation in arsenic and fluoride concentrations of shallow groundwater from the town of Shahai in the Hetao basin, Inner Mongolia

机译:内蒙古河套盆地沙海镇浅层地下水砷和氟化物浓度的空间变化

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Twenty-nine wells were selected for groundwater sampling in the town of Shahai, in the Hetao basin, Inner Mongolia. Four multilevel samplers were installed for monitoring groundwater chemistry at depths of 2.5-20m. Results show that groundwater As exhibits a large spatial variation, ranging between 0.96 and 720μg/L, with 71% of samples exceeding the WHO drinking water guideline value(10μg/L). Fluoride concentrations range between 0.30 and 2.57mg/L. There is no significant correlation between As and F ~- concentrations. Greater As concentrations were found with increasing well depth. However, F ~- concentrations do not show a consistent trend with depth. Groundwater with relatively low Eh has high As concentrations, indicating that the reducing environment is the major factor controlling As mobilization. Low As concentrations(<10μg/L)are found in groundwater at depths less than 10m. High groundwater As concentration is associated with aquifers that have thick overlying clay layers. The clay layers, mainly occurring at depths <10m, have low permeability and high organic C content. These strata restrict diffusion of atmospheric O _2 into the aquifers, and lead to reducing conditions that favor As release. Sediment composition is an additional factor in determining dissolved As concentrations. In aquifers composed of yellowish-brown fine sands at depths around 10m, groundwater generally has low As concentrations which is attributed to the high As adsorption capacity of the yellow-brown Fe oxyhydroxide coatings. Fluoride concentration is positively correlated with pH and negatively correlated with Ca ~(2+)concentration. All groundwater samples are over-saturated with respect to calcite and under-saturated with respect to fluorite. Dissolution and precipitation of Ca minerals(such as fluorite and calcite), and F - adsorption-desorption are likely controlling the concentration of F - in groundwater.
机译:在内蒙古河套盆地的沙海镇,选择了29口井进行地下水采样。安装了四个多级采样器,用于监测2.5-20m深度的地下水化学。结果表明,地下水As的空间变化很大,范围在0.96至720μg/ L之间,其中71%的样品超过了WHO饮用水准则(10μg/ L)。氟化物浓度范围为0.30至2.57mg / L。 As和F〜-浓度之间没有显着相关性。随着井深的增加,发现较高的As浓度。但是,F〜-浓度没有显示出与深度一致的趋势。 Eh相对较低的地下水中As含量较高,这表明还原环境是控制As迁移的主要因素。在低于10m的地下水中发现低砷浓度(<10μg/ L)。高地下水砷浓度与上覆粘土层较厚的含水层有关。粘土层主要存在于<10m的深度,渗透率低,有机碳含量高。这些地层限制了大气中O _2扩散到含水层中,并导致有利于As释放的还原条件。沉积物组成是确定溶解砷浓度的另一个因素。在深约10m的由黄棕色细砂构成的含水层中,地下水中的砷浓度通常较低,这归因于黄棕色氧化羟基铁涂层的高砷吸附能力。氟化物浓度与pH呈正相关,与Ca〜(2+)浓度呈负相关。就方解石而言,所有地下水样品都过饱和,而对于萤石而言,所有地下水样品均过饱和。 Ca矿物(如萤石和方解石)的溶解和沉淀以及F-的吸附-解吸很可能控制地下水中F-的浓度。

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