草酸
氧化还原
缺氧水域
尾矿
化学
溶解
磁铁矿
钒
无机化学
结晶
磷酸盐
环境化学
再分配(选举)
转化(遗传学)
矿物氧化还原缓冲液
铁质
铁酸盐
二价
钛铁矿
鳞片岩
草酸盐
钛
化学工程
配体(生物化学)
污染物
作者
Chun-dan Gan,Jin-yan Yang,Jiali Li,Xinyue Du,Jen-How Huang,Xun Wang,Sabry M Shaheen,Jörg Rinklebe
标识
DOI:10.1021/acs.est.5c11078
摘要
Vanadium(V) is a primary pollutant in vanadium-titanium magnetite tailings, with its geochemical behavior strongly shaped by redox dynamics. To date, how Fe transformations and organic acids regulate V mobilization and sequestration in tailings under repeated redox fluctuations has not yet been sufficiently studied. Here, we examined the coupled effects of Fe (hydr)oxides and oxalic acid (OA) on V transformation and (im)mobilization in vanadium-titanium magnetite tailings over 56 days across four redox cycles. Under anoxic conditions, OA promoted the dissolution of Fe (hydr)oxides, releasing substantial dissolved Fe(II) and comobilizing V. During subsequent redox cycles, progressive crystallization of secondary Fe phases (e.g., hematite) markedly immobilized V. Oxalic acid not only mediated Fe transformation but also facilitated redox-driven V(V) reduction and redistribution among acid-soluble, reducible, oxidizable, and residual fractions. In moderate (0.5 mM) and high (5.0 mM) V treatments, OA significantly promoted V immobilization by shifting acid-soluble V into the reducible fraction, particularly under anoxic conditions in the moderate case at the end of the experiment. These findings highlight the dual role of OA in promoting short-term V mobilization while enhancing its long-term sequestration through Fe (hydr)oxides transformations over repeated redox cycling, providing new insights into redox-driven stabilization strategies for V-bearing tailings.
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