Abstract
The reduction process of Cr(VI) and NO3−-N by sulfidized nanoscale zerovalent iron (S-nZVI) under coexistence conditions has yet to be investigated. This study innovatively confirmed that NO3−-N and Cr(VI) could be reduced synchronously or selectively by synthesizing diverse montmorillonite-supported S-nZVI (S-nZVI@MMT) to meet different remediation requirements. Concretely speaking, S-nZVI@MMT at low S/Fe could synchronously reduce NO3−-N and Cr(VI) to NH4+-N and Cr(III). S-nZVI@MMT at high S/Fe selectively removed Cr(VI). The vital roles of Fe(II) and S0 in S-nZVI@MMT were clearly revealed. Fe(II) mainly involved in the generation of Fe3O4 during the reaction at low S/Fe, while participating in the transformation of amorphous phases of Fe3O4, FeS, and FeS2 at high S/Fe. The Fe0 and converted Fe3O4 were the primary reactive sites for the synchronous removal of NO3−-N and Cr(VI) while the surface-bound Fe(II) and converted amorphous phases of Fe3O4 and FeSx determined the selective removal of Cr(VI). Meanwhile, the high contents of S0 in S-nZVI@MMT at high S/Fe mediated the generation of FeSx during the reaction and blocked the adsorption and reduction of NO3−-N which was critical for the selective removal of Cr(VI). The variations in the reactive species of S-nZVI@MMT at different S/Fe led to discrepant Cr(VI) reaction pathways. The findings provided new insights and strategies for the practical applicability of S-nZVI. SynopsisStudy provides a new insight into the synchronous/selective removal of Cr(VI) and NO3−-N by S-nZVI to meet the remediation requirements for different application scenarios.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.