Key Laboratory of Ministry of Education on Pollution Control and Ecosystem Restoration in Industry Clusters, Guangdong Provincial Key Laboratory of Solid Wastes Pollution Control and Recycling, School of Environment and Energy, South China University of Technology, Guangzhou 510006 Guangdong, China.
Key Laboratory of Ministry of Education on Pollution Control and Ecosystem Restoration in Industry Clusters, Guangdong Provincial Key Laboratory of Solid Wastes Pollution Control and Recycling, School of Environment and Energy, South China University of Technology, Guangzhou 510006 Guangdong, China; Institute of Environmental and Ecological Engineering, Guangdong University of Technology, Guangzhou 510006, China.
J Hazard Mater. 2022 Feb 5;423(Pt B):127240. doi: 10.1016/j.jhazmat.2021.127240. Epub 2021 Sep 16.
The effects of organic acids on hexavalent chromium (Cr(VI)) removal by reduced iron-based materials have been extensively studied. Nevertheless, the promotion mechanism from the perspective of the electron transfer process is still unclear. Herein, sulfidated nanoscale zero-valent iron (S-nZVI) and the selected organic acids, citric acid (containing both -OH and -COOH groups) and oxalic acid (containing only -COOH groups), showed significant synergistic promotion effects in Cr(VI) removal. The FeS and FeS on S-nZVI surface could enhance the Cr(VI) reduction as the reductive entity and electron conductor. Furthermore, even though the reactivity of FeS with Cr(VI) is higher than that with FeS, the Cr(VI) removal efficiency by FeS was much higher than that by FeS with organic acids. Under neutral and alkaline conditions (pH 6.0-8.0), organic acids promoted the diffusion, adsorption and complexation of Cr(VI) on S-nZVI surface, thus enhancing the electron selectivity towards Cr(VI). However, when the solution pH changed to acidic conditions (pH 4.0), organic acids facilitated the dissolution of Fe(II) ions from S-nZVI and enhanced the electron utilization towards Cr(VI) via the fast Fe(III) reduction process. This study provided a new insight into the Cr(VI) removal, which was beneficial to understand the application boundaries of S-nZVI for Cr(VI) remediation.
有机酸对还原铁基材料去除六价铬(Cr(VI))的影响已得到广泛研究。然而,从电子传递过程的角度来看,其促进机制仍不清楚。本文中,硫化纳米零价铁(S-nZVI)和选定的有机酸,柠檬酸(含有-OH 和-COOH 基团)和草酸(仅含有-COOH 基团),在 Cr(VI)去除方面表现出显著的协同促进作用。S-nZVI 表面的 FeS 和 FeS 可以增强 Cr(VI)的还原作用,作为还原实体和电子导体。此外,尽管 FeS 与 Cr(VI)的反应性高于 FeS,但在有有机酸存在的情况下,FeS 对 Cr(VI)的去除效率远高于 FeS。在中性和碱性条件(pH 6.0-8.0)下,有机酸促进了 Cr(VI)在 S-nZVI 表面的扩散、吸附和络合,从而增强了对 Cr(VI)的电子选择性。然而,当溶液 pH 值变为酸性条件(pH 4.0)时,有机酸促进了 S-nZVI 中 Fe(II)离子的溶解,并通过快速的 Fe(III)还原过程增强了对 Cr(VI)的电子利用。本研究为 Cr(VI)的去除提供了新的见解,有助于理解 S-nZVI 在 Cr(VI)修复中的应用界限。