锰
邻苯二甲酸二甲酯
化学
降级(电信)
催化作用
砜
亚砜
氧化锰
选择性
二甲基亚砜
无机化学
污染物
核化学
有机化学
邻苯二甲酸盐
电信
计算机科学
作者
Yanhao Wang,Yunlong Sun,Mengchun Gao,Yanjun Xin,Guangshan Zhang,Peng Xu,Dong Ma
标识
DOI:10.1016/j.jhazmat.2023.132199
摘要
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.
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