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Improved reduction efficiency, cycling performance, and removal rate of hexavalent chromium by adding water-soluble salts
Environmental Science and Pollution Research Pub Date : 2023-10-18 , DOI: 10.1007/s11356-023-30138-y
Junfeng He 1 , Yuheng Liang 1 , Hao Huang 1 , Wangjian Zhai 1 , Qinyu He 1
Affiliation  

Recently, the reaction speed and cycle performance of hexavalent chromium reduction over microsized zero-valent iron (ZVI) with an Fe0 core and iron oxide (FeOx) shell structure have been improved by activating the Fe0-core electrons through electromagnetic coupling between Fe0-core electrons and charges (hexavalent chromium in solution, double-charge layers of the ZVI/solution interface). Herein, the abovementioned electromagnetic coupling was greatly increased by adding salt (CH3COONa, NaCl, NaNO3, and Na2SO4) in the hexavalent chromium solution to increase the charge response. Adding salt greatly improved the reaction speed and cycle performance of hexavalent chromium reduction. It took 8 min to reduce hexavalent chromium with CH3COONa to below the discharge standard of wastewater in the first cycle and 20 min after reducing for 20 cycles. The best apparent rate of constant value (0.416 (min)-1) is nearly four times larger than those without salts. X-ray diffraction and X-ray photoelectron spectroscopy revealed the production of amorphous iron oxide shell with salt. The salt improves the hexavalent chromium reduction speed and cycle performance and impedes the Fe0-core-electron transfer via the produced Fe2O3, resulting in existence of an optimized salt dosage. This work aims to provide an effective route for enhancing the removal efficiency and cycle performance of heavy-metal–ion reduction via Fe0. And this work also proposes a novel viewpoint that adding salt in waste water would increase the electromagnetic coupling between the charges in solution and Fe0-core electrons which could finally activate the redox reaction.



中文翻译:


通过添加水溶性盐提高还原效率、循环性能和六价铬去除率



最近,通过Fe 0核和氧化铁(FeO x )壳结构的微米级零价铁(ZVI)还原六价铬的反应速度和循环性能,通过之间的电磁耦合激活Fe 0核电子得到了提高。 Fe 0 -核心电子和电荷(溶液中的六价铬,ZVI/溶液界面的双电荷层)。在此,通过在六价铬溶液中添加盐(CH 3 COONa、NaCl、NaNO 3和Na 2 SO 4 )以增加电荷响应,大大增加了上述电磁耦合。添加盐大大提高了六价铬还原的反应速度和循环性能。首次循环用CH 3 COONa还原六价铬需要8 min,达到废水排放标准以下,还原20个循环后需要20 min。最佳表观恒定值速率(0.416(min) -1 )比无盐的大近四倍。 X射线衍射和X射线光电子能谱揭示了带有盐的无定形氧化铁壳的产生。该盐提高了六价铬的还原速度和循环性能,并阻碍了通过产生的Fe 2 O 3的Fe 0核电子转移,从而导致存在优化的盐剂量。本工作旨在为提高Fe 0还原重金属离子的去除效率和循环性能提供有效途径。 这项工作还提出了一个新的观点,即在废水中添加盐会增加溶液中电荷与Fe 0核电子之间的电磁耦合,最终激活氧化还原反应。

更新日期:2023-10-18
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