Degradation of dimethyl phthalate by morphology controlled β-MnO2 activated peroxymonosulfate: The overlooked roles of high-valent manganese species

Abstract

Activated peroxymonosulfate (PMS) processes have emerged as an efficient advanced oxidation process to eliminate refractory organic pollutants in water. This study synthesized a novel spherical manganese oxide catalyst (0.4KBr-β-MnO2) via a simple KBr-guided approach to activate PMS for degrading dimethyl phthalate (DMP). The 0.4KBr-β-MnO2/PMS system enhanced DMP degradation under different water quality conditions, exhibiting an ultrahigh and stable catalytic activity, outperforming equivalent quantities of pristine β-MnO2 by 8.5 times. Mn(V) was the dominant reactive species that was revealed by the generation of methyl phenyl sulfone from methyl phenyl sulfoxide oxidation. The selectivity of Mn(V) was demonstrated by the negligible inhibitory effects of Inorganic anions. Theoretical calculations confirmed that Mn (V) was more prone to attack the CO bond of the side chain of DMP. This study revealed the indispensable roles of high-valent manganese species in DMP degradation by the 0.4KBr-β-MnO2/PMS system. The findings could provide insight into effective PMS activation by Mn-based catalysts to efficiently degrade pollutants in water via the high-valent manganese species.