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Rates and Dynamics of Mercury Isotope Exchange between Dissolved Elemental Hg(0) and Hg(Ⅱ) Bound to Organic and Inorganic Ligands

机译:溶解元素HG(0)和Hg(Ⅱ)与有机和无机配体结合的汞同位素交换的速率和动力学

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摘要

Mercury (Hg) isotope exchange is a common process in biogeochemical transformations of Hg in the environment, but it is unclear whether and at what rates dissolved elemental Hg(0)_(aq) may exchange with divalent Hg(Ⅱ) bound to various organic and inorganic ligands in water. Using enriched stable isotopes, we investigated the rates and dynamics of isotope exchange between ~(202)Hg(0)_(aq) and ~(201)Hg(Ⅱ) bound to organic and inorganic ligands with varying chemical structures and binding affinities. Time-dependent exchange reactions were followed by isotope compositional changes using both inductively coupled plasma mass spectrometry and Zeeman cold vapor atomic absorption spectrometry. Rapid, spontaneous isotope exchange (<1 h) was observed between ~(202)Hg(0)_(aq) and ~(201)Hg(Ⅱ) bound to chloride (Cl~-), ethylenediaminetetraacetate (EDTA), and thiols, such as cysteine (CYS), glutathione (GSH), and 2,3-dimercaptopropane-sulfonic acid (DMPS) at a thiol ligand-to-Hg(Ⅱ) molar ratio of 1:1. Without external reductants or oxidants, the exchange resulted in transfer of two electrons and redistribution of Hg isotopes bound to the ligand but no net changes of chemical species in the system. However, an increase in the ligand-to-Hg(Ⅱ) ratio decreased the exchange rates due to the formation of 2:1 or higher thiol:Hg(Ⅱ) chelated complexes, but had no effects on exchange rates with ~(201)Hg(Ⅱ) bound to EDTA or Cl~-. The exchange between ~(202)Hg(0)_(aq) and Hg(Ⅱ) bound to dissolved organic matter (DOM) showed an initially rapid followed by a slower exchange rate, likely resulting from Hg(Ⅱ) complexation with both low- and high-affinity binding functional groups on DOM (e.g., carboxylates vs bidentate thiolates). These results demonstrate that Hg(0)_(aq) readily exchanges with Hg(Ⅱ) bound to various ligands and highlight the importance of considering exchange reactions in experimental enriched Hg isotope tracer studies or in natural abundance Hg isotope studies in environmental matrices.
机译:汞(Hg)同位素交换是环境中Hg生物地球化学转化的常见方法,但目前尚不清楚溶解的元素Hg(0)_(aq)可以与二价Hg(Ⅱ)交换到各种有机物和水中无机配体。使用富集的稳定同位素,我们研究了同位素交换的率和动力学在与有机和无机配体结合的〜(202)Hg(0)_(AQ)和〜(Ⅱ)与具有不同化学结构和结合亲和力的〜(Ⅱ)。使用电感耦合等离子体质谱和塞曼冷蒸气原子吸收光谱法随后是时间依赖的交换反应。在与氯化物(Cl〜 - ),乙二胺四乙酸乙酯(EDTA)结合的〜(202)Hg(0)℃和〜(201)Hg(Ⅱ)之间观察到快速,自发同位素交换(<1 h)。 ,如半胱氨酸(Cys),谷胱甘肽(GSH)和2,3-二巯基丙烷 - 磺酸(DMP),如硫醇配体 - 至Hg(Ⅱ)摩尔比为1:1。没有外部还原剂或氧化剂,交换导致转移两种电子,并重新分布于与配体结合的Hg同位素,但系统中没有化学物质的净变化。然而,由于形成2:1或更高的硫醇:Hg(Ⅱ)螯合的复合物,抗亚藻(Ⅱ)比的增加降低了汇率:Hg(Ⅱ)螯合络合物,但与〜(201)没有对汇率的影响Hg(Ⅱ)与EDTA或Cl〜 - 。 〜(202)Hg(0)℃和Hg(Ⅱ)与溶解有机物质(DOM)的交换显示最初迅速,其次是较慢的汇率,可能由Hg(Ⅱ)络合与低 - DOM上的高亲和力结合官能团(例如,羧酸盐与二齿硫醇酸盐)。这些结果表明,Hg(0)_(aq)易于与各种配体结合的Hg(Ⅱ)交换,并突显了考虑实验富集的Hg同位素示踪研究中的交换反应的重要性或在环境基质中的天然丰度Hg同位素研究。

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  • 来源
    《Environmental Science & Technology》 |2020年第23期|15534-15545|共12页
  • 作者单位

    Key Laboratory of Wet Ecology and Environment Northeast Institute of Geography and Agroecology Chinese Academy of Sciences Changchun 130102 China Environmental Sciences Division Oak Ridge National Laboratory Oak Ridge Tennessee 37830 United States;

    Environmental Sciences Division Oak Ridge National Laboratory Oak Ridge Tennessee 37830 United States;

    Environmental Sciences Division Oak Ridge National Laboratory Oak Ridge Tennessee 37830 United States;

    Environmental Sciences Division Oak Ridge National Laboratory Oak Ridge Tennessee 37830 United States;

    Environmental Sciences Division Oak Ridge National Laboratory Oak Ridge Tennessee 37830 United States;

    Institute of Surface-Earth System Science School of Earth System Science Tianjin University Tianjin 300072 China Environmental Sciences Division Oak Ridge National Laboratory Oak Ridge Tennessee 37830 United States;

    Environmental Sciences Division Oak Ridge National Laboratory Oak Ridge Tennessee 37830 United States;

    Environmental Sciences Division Oak Ridge National Laboratory Oak Ridge Tennessee 37830 United States Department of Biosystems Engineering and Soil Science University of Tennessee Knoxville Tennessee 37996 United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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