化学
电解
高锰酸盐
锰
水溶液
硝基苯
阴极
过硫酸盐
阳极
电合成
核化学
苯酚
无机化学
电化学
电极
催化作用
有机化学
物理化学
电解质
作者
Yunhua Zhu,Xuxu Wang,Jing Zhang,Lei Ding,Junfeng Li,Huaili Zheng,Chun Zhao
标识
DOI:10.1021/acs.est.9b01510
摘要
Our study on the synergetic effect of electrolysis and permanganate (E-PM) revealed a novel alternative method for generating active Mn(III)aq heterogeneously by electrochemically activating PM with Mn2+ as promoter and stabilizer. We systematically explored the generation mechanism of Mn(III)aq. It indicated that all three components (electrolysis + PM + Mn2+) were necessary to facilitate the generation of active Mn(III) in the E-PM-Mn2+ process. It was worth noting that Mn2+, as essential promoter and Mn(III)aq stabilizer, could considerably enhance the concentration of Mn(III) in the E-PM-Mn2+ process. Further study revealed that the active Mn(III) was mainly produced on cathode rather than in aqueous solution or on anode. In addition, the soluble Mn(III)aq generated in the E-PM-Mn2+ process was demonstrated to be very efficient for the degradation and mineralization of diclofenac (DCF) as well as methyl blue, carbamazepine, phenol, sulfamethoxazole, and nitrobenzene. Moreover, the effects of the main operating parameters (Mn2+ dosage, PM dosage, applied current density, pH of solution, and contaminant concentration) and different water matrices on the E-PM-Mn2+ process were investigated systematically. Possible degradation pathways of DCF in the E-PM-Mn2+ process were also proposed. The results demonstrated that the E-PM-Mn2+ system based on active Mn(III)aq could create a more efficient, sustainable, and less energy costing technology for water treatment.
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