Fe(VI) Oxidation of Mixed Trace Phenols: Kinetics, QSAR Modeling, and Cross-Polymerization Mechanisms

Phenolic pollutants, frequently detected in aquatic environments as trace-level mixtures, pose significant challenges for water treatment. In this study, we examined the removal of 35 trace phenol mixtures (0.1 μmol/L each) under Fe(VI) oxidation, revealing kinetic differences between single and mixed systems. Fast-reacting phenols with secondary reaction rate constant ( k app ) > 350 M −1 •s −1 experienced accelerated oxidation upon mixing, whereas slow-reacting ones ( k app ≤ 350 M −1 •s −1 ) exhibited decreased rates. The quantitative structure-activity relationship (QSAR) models were constructed to correlate the k app of these phenols with molecular descriptors, showing that higher E HOMO and lower E gap were conductive to increasing the reaction rate in the mixed system, while E LUMO had a minimal effect on the reaction. Employing molecular networking for non-targeted screening, we identified the prevalence of cross-polymerization within the mixed system, yielding various cross-polymer products. Reaction pathway analysis, TOC and COD measurements, and theoretical calculations collectively demonstrated that electrophilic attacks of Fe(VI) trigger electron loss in phenols, generating phenoxy radicals that drive cross-polymerization and accelerate reaction rates of fast-reacting phenols, aligning with QSAR model predictions. These findings can deepen our understanding of Fe(VI) oxidation mechanism on mixed trace phenols, offering valuable insights for the advancement of wastewater treatment technologies.