Reductive dehalogenation in groundwater by Si-Fe(II) co-precipitates enhanced by internal electric field and low vacancy concentrations.

Fe(II) and silicate can form Si-Fe(II) co-precipitates in anoxic groundwater and sediments, but their phase composition and reactivity towards subsurface pollutants are largely unknown. Three types of Si-Fe(II) co-precipitations with the same chemical composition, namely Si-Fe(II)-I, Si-Fe(II)-II, and Si-Fe(II)-III, have been synthesized by different hydroxylation sequences in this work. It was found that Si-Fe(II)-III reduce carbon tetrachloride (CT) much faster (k=0.04419 min) than Si-Fe(II)-I (0 min) and Si-Fe(II)-II (7.860 × 10 min). XRD results show that the main component of Si-Fe(II)-III is ferrous silicate (FeSiO), which is quite different from that of Si-Fe(II)-I and Si-Fe(II)-II. The unique arrangement of hydroxyl coordination, the less distorted octahedral structure, the polyhedral morphology and the absence of Si-A center vacancies in Si-Fe(II)-III are responsible for its high reductive dehalogenation reactivity. The highest redox activity of Si-Fe(II)-III was shown by electrochemical characterization. The [Fe-O-Si] in Si-Fe(II)-III may stabilize the dichlorocarbene anion (˸CCl), which favors the transformation of CT to methane (9.2%). The Si-Fe(II) co-precipitates consist of countless internal electric fields, and the transformation of hydroxyl and CT both consumed electrons. The coexistence of hydroxyl and CT increases the electron density in the electron-rich region due to their electronegativity, enhancing their electron-accepting capabilities. This study deepens our understanding of the phase composition and electronic structure of Si-Fe(II) co-precipitates, which fills the gap in the reductive dehalogenation of halides by Si-Fe(II) co-precipitates.