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Reduction of Chromium(VI) mediated by zero-valent magnesium under neutral pH conditions

机译:零价镁在中性pH条件下还原铬(VI)

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In an effort to assess the potential use of ZVMg in contaminant treatments, we examined Cr(VI) reduction mediated by ZVMg particles under neutral pH conditions. The reduction of Cr(VI) was tested with batch experiments by varying [Cr(VI)]_0 (4.9,9.6,49.9 or 96.9 μM) in the presence of 50 mg/L ZVMg particles ([Mg~0]_0 = 2.06 mM) at pH 7 buffered with 50 mM Na-MOPS. When [Cr(VI)]_0 = 4.9 or 9.6 μM, Cr(VI) was completely reduced within 60 min. At higher [Cr(VI)]_0 (49.9 or 96.9 μM), by contrast, the reduction became retarded at >120 min likely due to rapid ZVMg dissolution in water and surface precipitation of Cr(III) on ZVMg particles. Surface precipitation was observed only when [Cr(VI)]_0 = 49.9 or 96.9 μM and increased with increasing [Cr(VI)]_0. The effect of dissolved oxygen was negligible on the rate and extent of Cr(VI) reduction. Experimental results indicated that Cr(VI) was reduced not directly by ZVMg but by reactive intermediates produced from ZVMg-water reaction under the experimental conditions employed in this study. In addition, the observed rates of Cr(VI) reduction appeared to follow an order below unity (0.19) with respect to [Cr(VI)]_0. These results imply that ZVMg-mediated Cr(VI) reduction likely occurred via an alternative mechanism to the direct surface-mediated reduction typically observed for other zero-valent metals. Rapid and complete Cr(VI) reduction was achieved when a mass ratio of [ZVMg]_0:[Cr(VI)]_0≥ 100 at neutral pH under both oxic and anoxic conditions. Our results highlights the potential for ZVMg to be used in Cr(VI) treatments especially under neutral pH conditions in the presence of dissolved oxygen.
机译:为了评估ZVMg在污染物处理中的潜在用途,我们研究了ZVMg颗粒在中性pH条件下介导的Cr(VI)还原。在50 mg / L ZVMg颗粒([Mg〜0] _0 = 2.06)存在的情况下,通过改变[Cr(VI)] _ 0(4.9、9.6、49.9或96.9μM),通过批量实验测试了Cr(VI)的还原pH值为7(mM),并用50 mM Na-MOPS缓冲。当[Cr(VI)] _ 0 = 4.9或9.6μM时,Cr(VI)在60分钟内完全还原。相反,在较高的[Cr(VI)] _ 0(49.9或96.9μM)下,还原可能在> 120分钟时延迟,这可能是由于ZVMg在水中的快速溶解和Cr(III)在ZVMg颗粒上的表面沉淀所致。仅当[Cr(VI)] _ 0 = 49.9或96.9μM时才观察到表面沉淀,并且随着[Cr(VI)] _ 0的增加而增加。溶解氧对Cr(VI)还原速率和程度的影响可以忽略不计。实验结果表明,在本研究采用的实验条件下,ZVMg不能直接还原Cr(VI),ZVMg-水反应产生的反应性中间体可以还原Cr(VI)。此外,相对于[Cr(VI)] _ 0,观察到的Cr(VI)还原速率似乎低于一个单位(0.19)。这些结果表明,ZVMg介导的Cr(VI)还原可能是通过对其他零价金属通常观察到的直接表面介导还原的替代机制而发生的。当在有氧和无氧条件下,中性pH值下[ZVMg] _0:[Cr(VI)] _0≥100的质量比达到Cr(VI)的快速和完全还原。我们的结果强调了ZVMg在Cr(VI)处理中使用的潜力,尤其是在存在溶解氧的中性pH条件下。

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