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Geochemical changes in individual sediment grains during sequential arsenic extractions

机译:连续抽砷过程中单个沉积物颗粒的地球化学变化

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摘要

High concentrations of As in groundwater frequently occur throughout the world. The dissolved concentration, however, is not necessarily determined by the amount of As in the ambient sediment but rather by the partitioning of As between different minerals and the type of fixation. Sequential extractions are commonly applied to determine associations and binding forms of As in sediments. Due to the operational nature of the extracted fractions, however, the results do not provide insight into how and where precisely As is bound within mineral grains and no information about elemental associations or involved mineral phases can be gained. Furthermore, little is known about possible geochemical alterations that actually occur within a single grain during sequential extraction. Therefore, micro-synchrotron X-ray fluorescence analysis was applied to study the micro-scale distribution of As and other elements in single sediment grains. Arsenic was found to be mainly enriched in Fe oxy-hydroxide coatings along with other heavy metals resulting in high correlations. Phosphate leached 34-66% of As from the studied grains. The release of As in this leaching step was accompanied by the disappearance of correlations between As and Fe as well as by a higher Fe/As ratio compared to untreated samples. During the Fe-leaching step the coatings were largely dissolved leading to much lower concentrations of As and Fe. The correlation between As and Fe was preserved only in association with K, indicating the presence of both elements in silicate structures. Several distinctive features were observed such as the release of Fe, Mn and Cr during phosphate leaching as well as the lowering of mean K concentrations due to the Fe-leaching which indicates that not only target mineral phases were dissolved in these extraction steps. The importance of re-precipitation processes during sequential extraction was indicated by a consistently observed increase of the Fe/As ratio from the untreated to the Fe-leached samples.
机译:全世界地下水中砷的浓度很高。但是,溶解的浓度不一定取决于周围沉积物中砷的含量,而取决于不同矿物之间的砷分配和固定类型。顺序提取通常用于确定沉积物中As的缔合和结合形式。但是,由于所提取馏分的操作性质,结果无法提供对As在矿物颗粒中的结合方式和精确位置的了解,也无法获得有关元素缔合或涉及的矿物相的信息。此外,对于在顺序提取过程中单个晶粒内实际发生的可能的地球化学变化知之甚少。因此,采用微同步辐射X射线荧光分析法研究了单沉积颗粒中As等元素的微观分布。发现砷主要与其他重金属一起富集在羟基氧化铁涂层中,从而导致高度相关。磷酸盐从研究谷物中浸出34-66%的As。与未经处理的样品相比,在该浸出步骤中As的释放伴随着As和Fe之间的相关性消失以及更高的Fe / As比。在铁浸出步骤中,涂层大量溶解,导致砷和铁的浓度大大降低。仅与K结合保留了As和Fe之间的相关性,表明硅酸盐结构中同时存在这两种元素。观察到一些独特的特征,例如在磷酸盐浸出过程中释放Fe,Mn和Cr,以及由于Fe浸出而导致平均K浓度降低,这表明在这些萃取步骤中不仅溶解了目标矿物相。连续观察到,从未经处理的样品到浸出Fe的样品中,Fe / As比值的增加表明了在连续萃取过程中再沉淀过程的重要性。

著录项

  • 来源
    《Water Research》 |2010年第19期|p.5545-5555|共11页
  • 作者单位

    Institute of Mineralogy & Geochemistry, Karlsruhe Institute 0f Technology, 76131 Karlsruhe, Germany;

    rnInstitute of Mineralogy & Geochemistry, Karlsruhe Institute 0f Technology, 76131 Karlsruhe, Germany;

    rnEauag, Suriss Federal Institute 0f Aquatic Science and Technology, 8600 Duebendorf, Switzerland;

    rnInstitute of Mineralogy & Geochemistry, Karlsruhe Institute 0f Technology, 76131 Karlsruhe, Germany;

    rnInstitute of Mineralogy & Geochemistry, Karlsruhe Institute 0f Technology, 76131 Karlsruhe, Germany;

    rnInstitute of Mineralogy & Geochemistry, Karlsruhe Institute 0f Technology, 76131 Karlsruhe, Germany;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    groundwater arsenic contamination; mobility; sediment leaching; re-precipitation; micro-synchrotron X-ray; fluorescence analysis (Μs-XRF); vietnam;

    机译:地下水砷污染;流动性沉淀物浸出;再沉淀微型同步辐射X射线;荧光分析(MS-XRF);越南;

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