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Arsenic mobilization from synthesized Fe(III) oxides under natural conditions

机译:在自然条件下由合成的Fe(III)氧化物的砷动员

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Reductive dissolution of iron (hydr)oxides has been accepted as a major formation mechanism for high arsenic groundwater. However, few researches are available for illustrating arsenic release from different iron oxides in natural aquifer. An in-situ method was applied to elucidate mobilization of arsenate adsorbed on two-line-ferrihydrite, goethite and hematite. During the 80 d experiment, desorption of arsenate was observed in these iron oxides, but the reductive dissolution only occurred in ferrihydrite which was transformed into lepidocrocite and goethite. The redox potential and bicarbonate and DOC concentrations were the key factor controlling arsenic mobilization during desorption. At the end of the experiment, more arsenic was released from goethite than hematite.
机译:铁(氢)氧化物的还原溶解已被认为是高砷地下水的主要形成机制。然而,很少有研究用于说明从天然含水层中的不同氧化铁释放的砷释放。应用了原位方法以阐明吸附在双线 - Ferrihydite,甲酸盐和赤铁矿上的砷酸盐的动员。在80d实验期间,在这些氧化铁中观察到砷酸盐的解吸,但是在将化水晶中仅发生还原溶解,该铁矿石转化为鳞片和粘合淀粉。氧化还原电位和碳酸氢盐和DOC浓度是在解吸期间控制砷动员的关键因素。在实验结束时,更多的砷从甲酸盐释放而不是赤铁矿。

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