Labile Fe(III) phase mediates the electron transfer from Fe(II,III) (oxyhydr)oxides to carbon tetrachloride

Qian-Qian Jia; Xuejie Zhang; Jia Deng; Li-Zhi Huang

doi:10.1016/j.watres.2023.120636

Labile Fe(III) phase mediates the electron transfer from Fe(II,III) (oxyhydr)oxides to carbon tetrachloride

Water Res. 2023 Oct 15:245:120636. doi: 10.1016/j.watres.2023.120636. Epub 2023 Sep 16.

Authors

Qian-Qian Jia¹, Xuejie Zhang¹, Jia Deng¹, Li-Zhi Huang²

Affiliations

¹ School of Civil Engineering, Wuhan University, No. 8, East Lake South Road, Wuhan, PR China; State Key Laboratory of Water Resources and Hydropower Engineering Science, Wuhan University, Wuhan 430072, China.
² School of Civil Engineering, Wuhan University, No. 8, East Lake South Road, Wuhan, PR China; State Key Laboratory of Water Resources and Hydropower Engineering Science, Wuhan University, Wuhan 430072, China. Electronic address: lizhihuang@whu.edu.cn.

PMID: 37748348
DOI: 10.1016/j.watres.2023.120636

Abstract

Labile Fe(III) phase (includes Fe(III)_aq, Fe(III)_ads, or Fe(III)_s species) is an important intermediate during the interaction between Fe(II) and Fe(III) (oxyhydr)oxides, but how does labile Fe(III) influence the electron transfer from Fe(II) to oxidant environmental pollutant during this Fe(II)-Fe(III) interaction is unclear. In this work, the dynamic change of Fe(II,III) (oxyhydr)oxides at the same time scale is simulated by synthesizing Fe(III)-Fe(II)-I (Fe(III)+NaOH+Fe(II)+NaOH) with different Fe(II)/Fe(III) ratios. CCl₄ is used as a convenient probe to test the reduction kinetics of mixed valence Fe(II,III)(oxyhydr)oxides with different Fe(II):Fe(III) ratios. The Mössbauer spectra results reveal the Fe(III)_labile in the solid phase is in octahedral coordination. The electron-donating capability of Fe(II) was improved with increasing Fe(III) content, but suppressed when [Fe(III)] ≥ 30 mM. The reductive dechlorination of CT by Fe(III)-Fe(II)-I decreased gradually with the increase of Fe(III) content, because more amount Fe(III)_labile in solid phase is accumulated. This shows that the electron transfer from Fe(II) to Fe(III)_labile rather than to CT is enhanced with increasing Fe(III) content. FTIR data shows that the hydroxylation of Fe(II) with Fe(OH)₃ occurs preferentially in the non-hydrogen bonded hydroxyl group, causing the decrease of its reductive reactivity. The presence of [Fe(III)-O-Fe(II)]⁺ in Fe(III)-Fe(II)-I can stabilize the dichlorocarbene anion (:CCl₂^-), favouring the conversion of CT to CH₄ (13.1%). The aging experiment shows that Fe(III)_labile surface may maintain the reductive reactivity of Fe(II) during aging when [Fe(III)] = 5-20 mM. This study deepens our understanding of the mass transfer pathway of iron oxyhydroxides induced by Fe(II) and its impact on the reductive dechlorination of CT.

Keywords: Carbon tetrachloride; Fe(II,III) (oxyhydr)oxides; Labile Fe(III) phase; Reductive reactivity.