首页> 外文期刊>Journal of Contaminant Hydrology >Evaluating mobilization and transport of arsenic in sediments and groundwaters of Aquia aquifer, Maryland, USA
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Evaluating mobilization and transport of arsenic in sediments and groundwaters of Aquia aquifer, Maryland, USA

机译:评价美国马里兰州阿基亚含水层沉积物和地下水中砷的动员和运输

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Groundwater and sediment samples were collected along a flow path in the Aquia aquifer (Paleocene), Maryland in order to examine and study the factors influencing "evolution" of arsenic (As) in these groundwaters. The Aquia crops out near Washington, DC, where it is unconfined, and extends approximately 90 km down dip to the south and east towards and beneath the Chesapeake Bay. The studied flow path was chosen owing to (ⅰ) the number of accessible wells, (ⅱ) differences in total dissolved As concentrations in groundwaters from some of the sampled wells, which reach values ≥ 667 nmol kg~(-1) or ≥50 ppb, and (ⅲ) the distinct difference in total dissolved As concentrations in Aquia groundwaters between the northern and southern portions of the study area. In groundwater samples, in situ separation of inorganic As species [As(III) and As(V)] were performed by using anion exchange chromatography. Subsequently, As concentrations were determined by inductively coupled plasma mass spectrometry. In situ measurements of Fe concentrations and speciation, dissolved S(-II) concentrations, pH, alkalinity, and oxidation-reduction potential (Eh) were determined to establish the oxidation-reduction conditions and solution chemistry along the flow path. Concentrations of As in 12 analyzed groundwater samples range from ~ 0.75 to 1072 nmol kg~(-1), and As(III) concentrations ranging from 0.24 to 980 nmol kg~(-1) appears to be the dominant form of As in solution. 50% of the studied wells yielded groundwaters with concentrations that exceed the US EPA's Maximum Contaminant Level for As in drinking water of 133 nmol kg~(-1) or 10 ppb. In order to examine the solid phase speciation of As within the aquifer sediments, we collected a number of Aquia sediment samples from a drill core that was archived at the Maryland Geological Survey. These sediment samples were evaluated using a previously established sequential extractions procedure. Solid phase As concentrations range between 973 and 2,012 nmol kg~(-1). Additionally, petrographic, X-Ray diffraction and diffuse reflectance spectroscopy analyses of the Aquia sediments reveal presence of glauconite, and smectite along with goethite and hematite within the samples. Here, we present the possible mechanisms responsible for the elevated As concentrations in the studied groundwaters of the Aquia aquifer.
机译:沿着马里兰州Aquia含水层(古新世)的流动路径收集了地下水和沉积物样本,以便研究和研究影响这些地下水中砷(As)“释放”的因素。阿奎亚(Aquia)在不受限制的华盛顿特区附近播种,并向南和向东延伸至切萨皮克湾(Chesapeake Bay)和下方,向下延伸约90公里。选择研究流径的原因是:(ⅰ)一些可利用的井的数量,(ⅱ)某些取样井的地下水中总溶解砷浓度的差异,达到≥667 nmol kg〜(-1)或≥50 ppb和(ⅲ)研究区北部和南部之间阿奎亚(Aquia)地下水中总溶解砷浓度的明显差异。在地下水样品中,通过使用阴离子交换色谱法原位分离无机As物种[As(III)和As(V)]。随后,通过电感耦合等离子体质谱法测定As浓度。对铁浓度和形态进行原位测量,确定溶解的S(-II)浓度,pH,碱度和氧化还原电位(Eh),以建立沿流路的氧化还原条件和溶液化学性质。所分析的12个地下水样品中As的浓度范围为0.75〜1072 nmol kg〜(-1),As(III)的浓度范围为0.24至980 nmol kg〜(-1)似乎是溶液中As的主要形式。 。所研究的井中有50%产生的地下水浓度超过了美国EPA的饮用水中133 nmol kg〜(-1)或10 ppb的最大砷污染水平。为了检查含水层沉积物中As的固相形态,我们从钻芯采集了许多Aquia沉积物样品,这些样品已在马里兰州地质调查局存档。使用先前建立的顺序萃取程序评估这些沉积物样品。固相As的浓度在973和2,012 nmol kg〜(-1)之间。此外,对阿基亚(Aquia)沉积物的岩石学,X射线衍射和漫反射光谱分析表明,样品中存在青石,蒙脱石以及针铁矿和赤铁矿。在这里,我们介绍了造成含水层含水量升高的砷浓度的可能机理。

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