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Vertical distribution of As(Ⅲ) and As(ⅴ) in a coastal sandy aquifer: Marine clays, a potential reservoir for arsenic in coastal groundwater systems

机译:沿海砂质含水层中As(Ⅲ)和As(ⅴ)的垂直分布:海洋粘土,沿海地下水系统中砷的潜在储层

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Arsenic species were measured in a bundled-piezometer installed in the Holocene barrier sand deposits of the Stuarts Point coastal sands aquifer, Northern New South Wales, Australia. Vertical distribution shows two peaks of elevated arsenic concentration. At a depth 10-11 m below ground surface (bgs), As~(Tot), As(ⅴ) and As(Ⅲ) are in the range of 52-85, 38-67 and 14-18 μg/L respectively and the ratio of As(ⅴ)/As(Ⅲ) is well above 1 at 3.7-2.7. The second peak at a depth 24-26 m bgs shows the highest concentrations of As~(Tot), As(ⅴ) and As(Ⅲ). At 25 m bgs As~(Tot), As(ⅴ) and As(Ⅲ) are at 337, 125 and 212 μg/L respectively and the ratio is below 1 at 0.6-0.7. High As~(Tot) and As(ⅴ) concentrations in shallower depths are associated with acidic conditions and very low concentration of all ions. Desorption of As from Al hydroxides and As enriched Fe oxyhydroxides are the possible mechanisms releasing As into the aquatic system. The high concentrations of As~(Tot) and As(Ⅲ) at 25 m are concordant with high pH values and high HCO_3~- and Cl~- concentrations. The high concentration of As at this depth is possibly attributed to HCO_3~- competition with HAsO_4~(2-) which is reducing the possible extent of As sorption on Fe and Mn oxyhydroxides. The hydrochemistry of As at this depth shows its source to be potentially influenced by the mixing of saline water leaching from adjacent Holocene marine clay deposits into the adjacent groundwater system.
机译:砷的种类通过安装在澳大利亚新南威尔士州北部Stuarts Point沿海砂含水层的全新世屏障砂矿中的成束比气计进行测量。垂直分布显示出砷浓度升高的两个峰。在地下(bgs)下方10-11 m的深度处,As〜(Tot),As(and)和As(Ⅲ)分别在52-85、38-67和14-18μg/ L的范围内, As(ⅴ)/ As(Ⅲ)的比值在3.7-2.7时远高于1。深度为24-26 m bgs的第二个峰显示了As〜(Tot),As(As)和As(Ⅲ)的最高浓度。在25 m bgs下,As〜(Tot),As(ⅴ)和As(Ⅲ)分别为337、125和212μg/ L,比率在0.6-0.7以下小于1。较浅深度的高As〜(Tot)和As(ⅴ)浓度与酸性条件和所有离子的浓度极低有关。砷从氢氧化铝和富砷氢氧化铁中解吸是将砷释放到水生系统中的可能机理。 25 m时高浓度的As〜(Tot)和As(Ⅲ)与高pH值,高HCO_3〜-和Cl〜-浓度相吻合。 As在此深度的高浓度可能归因于HCO_3与HAsO_4〜(2-)的竞争,这降低了As在Fe和Mn羟基氧化物上的吸附程度。在此深度的砷的水化学表明,其来源可能受到从全新世海洋黏土沉积物浸出到相邻地下水系统中的盐水混合的影响。

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