Phase transformation of Cr(VI) host-mineral driven by citric acid-aided mechanochemical approach for advanced remediation of chromium ore processing residue-contaminated soil.

The slow release of Cr(VI) from chromium ore processing residue-contaminated soil (COPR-soil) poses a significant environmental and health risk, yet advanced remediation techniques are still insufficient. Here, the slow-release behavior of Cr(VI) in COPR-soil is observed and attributed to the embedded Cr(VI) in the lattice of vaterite due to the isomeric substitution of CrO 4 2- for CO 3 2-. A citric acid-aided mechanochemical approach with FeS 2 /ZVI as reductive material was developed and found to be highly effective in remediating COPR-soil. Almost all Cr(VI) in COPR-soil, including Cr(VI) embedded in the minerals, are reduced with a reduction efficiency of 99.94%. Cr(VI) reduction kinetics indicate that the Cr(VI) reduction rate constant in the presence of citric acid was 4.8 times higher compared to its absence. According to the Raman spectroscopy, X-ray diffraction (XRD), and Electron Probe X-ray Micro-Analyzer (EPMA) analysis, the reduction of Cr(VI) embedded in vaterite was mainly attributed to the citric acid-induced protonation effect. That is, under the protonation effect, the embedded Cr(VI) could be released from vaterite through its phase transformation to calcite, whose affinity to Cr(VI) is low. While the reduction of released Cr(VI) could be promoted due to the complexation of citric acid with disulfide groups on FeS 2 /ZVI. The results of long-term stability tests demonstrated that the remediated COPR-soil exhibited excellent long-term stability, which may also be associated with improved utilization of available carbon and electron donors by the Cr(VI) reducing bacteria (Proteobacteri a)-dominated microbial community in the presence of citric acid, thereby promoting to establish a stable reducing microenvironment. Collectively, these findings will further our understanding of the reduction remediation of COPR-soil, especially in the case of Cr(VI) embedded in minerals. [Display omitted] • Vaterite was identified as a key Cr(VI) host-mineral in COPR-soil. • 99.94% Cr(VI) was reduction by citric acid-aided mechanochemical approach. • The embedded Cr(VI) was released by the transformation of vaterite to calcite. • Citric acid-induced complexation effect accelerated the reduced of released Cr(VI). • Proteobacteri a-dominated microbial community facilitate remediated soil stability. [ABSTRACT FROM AUTHOR]