Electrocatalytically enhanced Cu(II)/peroxymonosulfate (PMS) oxidation: Focus on electrically-induced sustained Cu(II)/Cu(I)/Cu(III) cycling and suppression of singlet oxygen (1O2) production

Abstract

Numerous azo dyes are discharged into industrial wastewater annually, posing significant threats to ecology and human health. In this study, an applied electric field was implemented in a trace copper-activated peroxymonosulfate system (EC/Cu(II)/PMS), achieving high removal efficiency (95.40 %) of Congo red (CR). The electron-donating effect of the cathode greatly enhanced the redox cycling of Cu(II)/Cu(I). Almost complete activation of PMS occurred during the entire reaction with an electrical consumption of merely 0.85 kWh/m3. Using electron paramagnetic resonance (EPR), quenching experiments, and chemical probes, the reactive substance that dominate CR removal, including Cu(III), sulfate radical (SO4•−), hydroxyl radical (HO∙), and singlet oxygen (1O2), were investigated. Cu(III) was identified as the main reactive substance, contributing over 90 %, and was primarily formed through double electron transfer of Cu(I). HO∙ can emerge as a secondary oxide of Cu(III). SO4•− originated mainly from the electroactivation of PMS. It was noted that 1O2 can be physically quenched by water, and thus 1O2 was considered as a side reaction product of PMS. Applying an electric field lowered the overall production of 1O2 and markedly mitigated the inefficient consumption of PMS. Moreover, the degradation pathways proposed for CR, based on mass spectrometry analysis, were in agreement with the predictions made by density functional theory (DFT). The toxicological characteristics of both CR and its intermediates were comprehensively analyzed as well. The study presents a straightforward and efficient strategy for PMS activation with versatile application potential for dye wastewater treatment.