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Enhancement of Arsenic Adsorption during Mineral Transformation from Siderite to Goethite: Mechanism and Application

机译:矿物从菱铁矿向针铁矿转变过程中砷吸附的增强:机理与应用

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摘要

Synthesized siderite was used to remove As(Ⅲ) and As(V) from water solutions under anoxic conditions and oxic conditions. Results showed that As adsorption on synthetic siderite under anoxic conditions was around 10 mg/g calculated with Langmuir isotherm. However, the calculated As adsorption on synthetic siderite under oxic conditions ranged between 115 and 121 mg/g, which was around 11 times higher than that under anoxic conditions. It was found that 75% siderite was transformed into goethite during oxic adsorption. However, synthetic goethite had lower As adsorption capacity than siderite under oxic conditions, although its adsorption capacity was a little higher than siderite under anoxic conditions. It suggested that the coexistence of goethite and siderite bimineral during mineral transformation probably contributed to the robust adsorption capacity of siderite under oxic conditions. Results of extended X-ray absorption fine structure (EXAF) spectroscopy indicated both As(Ⅲ) and As(V) formed inner-sphere complexes on the surface of As-treated solid regardless of substrates, including the bidentate binuclear corner-sharing (~2C) complexes and the monodentate mononudear corner-sharing (~1V) complexes. Monodenate (~1V) and bidentate (~2C) complexes would be related to high As adsorption capacity of siderite under oxic conditions. It showed that more Fe atoms were coordinated with As atom in the monodentate complexes and the bidentate complexes of As (V)/As (Ⅲ)treated siderite under oxic conditions, in comparison with As(V)/As(Ⅲ)-treated siderite under anoxic conditions and As(V)/ As (Ⅲ)-treated goethite. Calcinations of natural siderite resulting in the coexistence of goethite and siderite greatly increased As adsorption on the solid, which confirmed that the coexistence of bimineral during mineral transformation from siderite to goethite greatly enhanced As adsorption capacity of siderite adsorbent. The observation can be applied for modification of natural siderite for As removal from high As waters.
机译:在缺氧条件和有氧条件下,用合成的菱铁矿去除水溶液中的As(Ⅲ)和As(V)。结果表明,根据Langmuir等温线计算,在缺氧条件下合成菱铁矿上的As吸附约为10 mg / g。然而,在有氧条件下计算得出的合成菱铁矿的As吸附量介于115和121 mg / g之间,比无氧条件下高约11倍。发现在氧吸附期间75%的菱铁矿转化为针铁矿。但是,合成针铁矿在有氧条件下的吸附能力比菱铁矿低,尽管在缺氧条件下其吸附能力比菱铁矿略高。这表明针铁矿和菱铁矿矿物共存在矿物转化过程中可能有助于在氧气条件下强大的菱铁矿吸附能力。扩展X射线吸收精细结构(EXAF)光谱的结果表明,无论底物包括二齿双核角共享(〜),As(Ⅲ)和As(V)都在经过As处理的固体表面上形成内球络合物。 2C)复合物和单齿单核角共享(〜1V)复合物。单价酸盐(〜1V)和二齿酸盐(〜2C)的络合物与氧条件下菱铁矿的高As吸附能力有关。结果表明,与As(V)/ As(Ⅲ)处理的菱铁矿相比,在有氧条件下,As(V)/ As(Ⅲ)处理的菱铁矿的单齿配合物和二齿配合物中更多的Fe原子与As原子配位。在缺氧条件下和经As(V)/ As(Ⅲ)处理的针铁矿。天然针铁矿的煅烧导致针铁矿和菱铁矿的共存大大增加了As在固体上的吸附,这证实了矿物从铁菱铁矿转变为针铁矿的过程中双矿物的共存大大提高了菱铁矿吸附剂对As的吸附能力。该观察结果可用于改性天然菱铁矿,以便从高砷水中去除砷。

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  • 来源
    《Environmental Science & Technology》 |2013年第2期|1009-1016|共8页
  • 作者单位

    State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences, Beijing 100083, P.R.China,School of Water Resources and Environment, China University of Geosciences, Beijing 100083, P.R. China;

    School of Water Resources and Environment, China University of Geosciences, Beijing 100083, P.R. China;

    School of Water Resources and Environment, China University of Geosciences, Beijing 100083, P.R. China;

    State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences, Beijing 100083, P.R.China,School of Water Resources and Environment, China University of Geosciences, Beijing 100083, P.R. China;

    State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences, Beijing 100083, P.R.China,School of Water Resources and Environment, China University of Geosciences, Beijing 100083, P.R. China;

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