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Mackinawite(FeS) Reduces Mercury(II) under SulfidicConditions

机译:麦金刚石(FeS)还原硫化物下的汞(II)条件

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摘要

Mercury (Hg) is a toxicant of global concern that accumulates in organisms as methyl Hg. The production of methyl Hg by anaerobic bacteria may be limited in anoxic sediments by the sequestration of divalent Hg [Hg(II)] into a solid phase or by the formation of elemental Hg [Hg(0)]. We tested the hypothesis that nanocrystalline mackinawite (tetragonal FeS), which is abundant in sediments where Hg is methylated, both sorbs and reduces Hg(II). Mackinawite suspensions were equilibrated with dissolved Hg(II) in batch reactors. Examination of the solid phase using Hg LIII-edge extended X-ray absorption fine structure (EXAFS) spectroscopy showed that Hg(II) was indeed reduced in FeS suspensions. Measurement of purgeable Hg using cold vapor atomic fluorescence spectrometry (CVAFS) from FeS suspensions and control solutions corroborated the production of Hg(0) that was observed spectroscopically. However, a fraction of the Hg(II) initially added to the suspensions remained in the divalent state, likely in the form of β-HgS-like clusters associated with the FeS surface or as a mixture of β-HgSand surface-associated species. Complexation by dissolved S(-II) inanoxic sediments hinders Hg(0) formation, but, by contrast, Hg(II)–S(-II)species are reduced in the presence of mackinawite, producing Hg(0)after only 1 h of reaction time. The results of our work support theidea that Hg(0) accounts for a significant fraction of the total Hgin wetland and estuarine sediments.
机译:汞(Hg)是一种全球关注的有毒物质,它以甲基汞的形式累积在生物体内。通过将二价汞[Hg(II)]螯合成固相或形成元素汞[Hg(0)],厌氧细菌产生的甲基汞可能会限制在缺氧沉积物中。我们测试了以下假说:纳米晶马基钠铁矿(四方FeS)在Hg甲基化的沉积物中含量丰富,既吸附又还原Hg(II)。在间歇反应器中将Mackinawite悬浮液与溶解的Hg(II)平衡。使用Hg LIII边缘扩展X射线吸收精细结构(EXAFS)光谱检查固相表明,Fes悬浮液中的Hg(II)确实减少了。使用冷蒸气原子荧光光谱法(CVAFS)从FeS悬浮液和对照溶液中测量可净化的Hg,证实了通过光谱法观察到的Hg(0)的产生。但是,最初添加到悬浮液中的一部分Hg(II)保持二价状态,可能以与FeS表面相关的类β-HgS簇的形式或以β-HgS的混合物形式存在和与表面有关的物种。通过溶解的S(-II)络合缺氧沉积物阻碍了Hg(0)的形成,但是相反,Hg(II)–S(-II)麦基钠铁矿存在时,汞物种减少,产生汞(0)仅反应1小时后。我们的工作结果支持认为汞(0)占汞总量的很大一部分在湿地和河口沉积物中。

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