Deciphering the Novel Picolinate-Mn(II)/peroxymonosulfate System for Sustainable Fenton-like Oxidation: Dominance of the Picolinate-Mn(IV)-peroxymonosulfate Complex.

Abstract

A highly efficient and sustainable water treatment system was developed herein by combining Mn(II), peroxymonosulfate (PMS), and biodegradable picolinic acid (PICA). The micropollutant elimination process underwent two phases: an initial slow degradation phase (0-10 min) followed by a rapid phase (10-20 min). Multiple evidence demonstrated that a PICA-Mn(IV) complex (PICA-Mn(IV)*) was generated, acting as a conductive bridge facilitating the electron transfer between PMS and micropollutants. Quantum chemical calculations revealed that PMS readily oxidized the PICA-Mn(II)* to PICA-Mn(IV)*. This intermediate then complexed with PMS to produce PICA-Mn(IV)-PMS*, elongating the O-O bond of PMS and increasing its oxidation capacity. The primary transformation mechanisms of typical micropollutants mediated by PICA-Mn(IV)-PMS* include oxidation, ring-opening, bond cleavage, and epoxidation reactions. The toxicity assessment results showed that most products were less toxic than the parent compounds. Moreover, the Mn(II)/PICA/PMS system showed resilience to water matrices and high efficiency in real water environments. Notably, PICA-Mn(IV)* exhibited greater stability and a longer lifespan than traditional reactive oxygen species, enabling repeated utilization. Overall, this study developed an innovative, sustainable, and selective oxidation system, i.e., Mn(II)/PICA/PMS, for rapid water decontamination, highlighting the critical role of in situ generated Mn(IV).