Reaction of FeaqII with Peroxymonosulfate and Peroxydisulfate in the Presence of Bicarbonate: Formation of FeaqIV and Carbonate Radical Anions

Many advanced oxidation processes (AOPs) use Fenton-like reactions to degrade organic pollutants by activating peroxymonosulfate (HSO₅^-, PMS) or peroxydisulfate (S₂O₈^2-, PDS) with Fe(H₂O)₆²⁺ (Fe_aq^II). This paper presents results on the kinetics and mechanisms of reactions between Fe_aq^II and PMS or PDS in the absence and presence of bicarbonate (HCO₃^-) at different pH. In the absence of HCO₃^-, Fe_aq^IV, rather than the commonly assumed SO₄^•-, is the dominant oxidizing species. Multianalytical methods verified the selective conversion of dimethyl sulfoxide (DMSO) and phenyl methyl sulfoxide (PMSO) to dimethyl sulfone (DMSO₂) and phenyl methyl sulfone (PMSO₂), respectively, confirming the generation of Fe_aq^IV by the Fe_aq^II-PMS/PDS systems without HCO₃^-. Significantly, in the presence of environmentally relevant concentrations of HCO₃^-, a carbonate radical anion (CO₃^•-) becomes the dominant reactive species as confirmed by the electron paramagnetic resonance (EPR) analysis. The new findings suggest that the mechanisms of the persulfate-based Fenton-like reactions in natural environments might differ remarkably from those obtained in ideal conditions. Using sulfonamide antibiotics (sulfamethoxazole (SMX) and sulfadimethoxine (SDM)) as model contaminants, our study further demonstrated the different reactivities of Fe_aq^IV and CO₃^•- in the Fe_aq^II-PMS/PDS systems. The results shed significant light on advancing the persulfate-based AOPs to oxidize pollutants in natural water.