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首页> 外文期刊>Applied Geochemistry: Journal of the International Association of Geochemistry and Cosmochemistry >Seasonal fluctuations and mobility of arsenic in groundwater resources, Anchorage, Alaska
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Seasonal fluctuations and mobility of arsenic in groundwater resources, Anchorage, Alaska

机译:阿拉斯加安克雷奇市地下水资源中砷的季节性波动和迁移

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摘要

There are approximately 12,000 private wells in the Municipality of Anchorage, Alaska, USA, that supply drinking water to thousands of homeowners. The results presented in this paper are from a study conducted to understand the speciation and seasonal fluctuations of As in the groundwater of Anchorage. A total of eight private drinking water wells were sampled from May to October, 2007, to determine inorganic species of As (III/V) and other physiochemical parameters of the groundwater. Arsenic concentrations above Environmental Protection Agency (EPA) drinking water standard of 10μg/L had been previously measured in all of these eight wells by the Municipality of Anchorage. Seven of the wells draw water from glaciofluvial aquifers and one well taps into the older bedrock aquifer on the mountain-side. In-situ measurements as well as groundwater samples were collected from each well and inorganic species of As (III/V) were separated in the field using anion exchange columns. Elemental analysis was conducted by inductively coupled plasma mass spectrometry (ICP-MS), major anions by ion chromatography (IC), and Fe (II) and total Fe were measured in the field with a portable spectrophotometer. The groundwater was neutral to basic ranging in pH from 7.6 to 8.8, dissolved O_2 was generally 0.1-1.0mg/L and specific conductance ranged from 300 to 1000μS/cm. Most of the groundwater is classified as Ca-Mg-HCO_3 and dissolved As concentrations ranged from below detection (~0.5μg/L) to 117μg/L with arsenite as the dominant species. Filtered and unfiltered water samples had less than 1% difference in As concentrations suggesting that most As occurs in the dissolved form. Arsenic concentrations were positively correlated with water levels indicating that the highest As concentrations occur in the aquifer during recharge events. Positive relationships with dissolved Fe and supersaturation with respect to secondary Fe oxides indicates that the As is likely associated with the Fe oxides that are partially dissociated under the dominating reducing conditions of the aquifers. There is also evidence of a positive relationship between As and SO42- which indicates that some of the As may be associated with the oxidation of Fe-bearing sulfides such as pyrite or arsenopyrite, however, this is thought to be a less important process for this system compared to Fe reduction. Most of the groundwater samples indicate supersaturation with respect to carbonates such as calcite, dolomite and siderite and there is a positive relation between As and HCO3- indicating that carbonate buffering is an important process in the groundwater geochemistry of As. In some cases homeowners filter their tap water with household water treatment systems which have a range of As removal effectiveness from about 25-100%.
机译:美国阿拉斯加安克雷奇市大约有12,000口私人水井,为数以千计的房主提供饮用水。本文介绍的结果来自于一项研究,目的是了解安克雷奇地下水中砷的形态和季节性波动。从2007年5月至10月,共采样了8口私人饮用水井,以确定砷的无机物(III / V)以及地下水的其他理化参数。此前,安克雷奇市政府在所有这八口井中都测定了高于环境保护局(EPA)饮用水标准10μg/ L的砷浓度。其中七口井从冰川河水含水层中抽水,一口井水流入山侧较老的基岩含水层。从每个井中收集现场测量值和地下水样品,并使用阴离子交换柱在现场分离出As(III / V)的无机物。通过电感耦合等离子体质谱法(ICP-MS)进行元素分析,通过离子色谱法(IC)分析主要阴离子,并使用便携式分光光度计在现场测量Fe(II)和总Fe。地下水为中性至碱性,pH范围为7.6至8.8,溶解的O_2通常为0.1-1.0mg / L,比电导范围为300至1000μS/ cm。大部分地下水归为Ca-Mg-HCO_3,溶解态As的浓度范围从低于检测值(〜0.5μg/ L)到117μg/ L,其中砷是主要物质。过滤后和未过滤的水样品中As的浓度差异小于1%,这表明大多数As以溶解形式存在。砷浓度与水位呈正相关,表明补给过程中含水层中的砷浓度最高。相对于次生Fe氧化物,与溶解的Fe和过饱和具有正相关关系,这表明As可能与在含水层的主要还原条件下部分解离的Fe氧化物有关。还有证据表明,As和SO42-之间存在正相关关系,这表明某些As可能与含Fe的硫化物(如黄铁矿或毒砂)的氧化有关,但是,这对于此过程而言不太重要。与还原铁相比。多数地下水样品表明方解石,白云石和菱铁矿等碳酸盐相对过饱和,As与HCO3-之间存在正相关关系,这表明碳酸盐缓冲作用是As地下水地球化学中的重要过程。在某些情况下,房主用家用水处理系统过滤其自来水,该系统具有大约25%至100%的砷去除效率。

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