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首页> 外文期刊>Applied Geochemistry: Journal of the International Association of Geochemistry and Cosmochemistry >Factors affecting the occurrence of lead and manganese in untreated drinking water from Atlantic and Gulf Coastal Plain aquifers, eastern United States-Dissolved oxygen and pH framework for evaluating risk of elevated concentrations
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Factors affecting the occurrence of lead and manganese in untreated drinking water from Atlantic and Gulf Coastal Plain aquifers, eastern United States-Dissolved oxygen and pH framework for evaluating risk of elevated concentrations

机译:影响大西洋和海湾沿海普通含水层未处理饮用水中铅和锰发生的因素,东方美国溶解的氧气和pH框架,用于评估升高浓度的风险

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Groundwater samples collected during 2012 and 2013 from public-supply wells screened in the Atlantic and Gulf Coastal Plain aquifers of the eastern and southeastern U.S. rarely contained lead or manganese concentrations that exceeded drinking-water limits, despite having corrosive characteristics. Data indicate that the occurrence of dissolved lead and manganese in sampled groundwater, prior to its distribution or treatment, was related to several explanatory factors including the presence of source minerals, hydrologic position along the flow path, water-rock interactions, and associated geochemical conditions such as pH and dissolved oxygen (DO) concentrations. Elevated concentrations of lead compared to health-based benchmarks were associated with groundwater that is acidic (pH <= 6.5), oxygenated (DO >= 2 mg/L), and closer to recharge zones (relatively young water). Elevated concentrations of manganese were associated with groundwater that is acidic to neutral (pH <= 7.5), has low DO (< 2 mg/L), and further from recharge zones (relatively old). Under these geochemical conditions, minerals that could sequester lead or manganese tended to be undersaturated, and adsorption by hydrous ferric oxide was limited. Under neutral to alkaline pH conditions, precipitation of impure calcium carbonate or phosphate compounds containing traces of lead or manganese (solid solutions) could maintain low concentrations of the trace elements. Additionally, adsorption of lead or manganese cations by hydrous ferric oxides (HFO) could be another attenuating factor where conditions are oxidizing and dissolved inorganic carbon concentrations are relatively low. A DO/pH framework was developed as a screening tool for evaluating risk of elevated lead or manganese, based on the occurrence of elevated lead and manganese concentrations and the corresponding distributions of DO and pH in the Atlantic and Gulf Coastal Plain aquifers. Validation of the DO/pH framework was accomplished using an i
机译:尽管具有腐蚀性特性,但在东部和东南部的大西洋和海湾沿海普通含水层筛选的公共供应井收集的地下水样本来自2012年和2013年,从公共供应井筛选。数据表明,在其分布或治疗之前,采样地下水中的溶解铅和锰的发生与包括源矿物质的存在,沿流动路径,水岩相互作用和相关地球化学条件的存在的若干解释因素有关如pH和溶解的氧气(DO)浓度。与基于健康的基准相比升高的铅浓度与酸性(pH <= 6.5),氧化(DO> = 2mg / L)的地下水相关,更接近充电区域(相对较年轻的水)。升高的锰含有与中性酸性(pH <= 7.5)的地下水有关,具有低妥(<2mg / L),进一步来自充电区(相对较大)。在这些地球化学条件下,可以螯合铅或锰的矿物质倾向于不饱和,并通过含水氧化铁的吸附受到限制。在中性到碱性pH条件下,不纯碳酸钙或含有铅或锰(固溶体)的磷酸钙化合物的沉淀可以保持低浓度的微量元素。另外,通过含水氧化铁(HFO)对铅或锰阳离子的吸附可以是另一种衰减因子,其中条件是氧化和溶解的无机碳浓度相对较低。根据铅和锰浓度的发生以及大西洋和海湾沿海普通含水层的升高和pH相应和pH分布,作为评估升高的铅或锰风险的筛选工具作为评估升高的铅或锰的风险。使用i完成了对DO / pH框架的验证

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