摘要
The decay of free radicals involved in side reactions is one of the challenges faced by electrochemical degradation of organic pollutants. To this end, a non-radical oxidation system was constructed by a natural air diffusion cathode (ADC) and a Ti-based dimensional stable anode coated by RuO 2 (RuO 2 -Ti anode) for cathodic hydrogen peroxide activation by anodic chlorine evolution. The ADC fabricated by the carbon black of BP2000 produced a stable concentration of hydrogen peroxide of 339.94 mg L −1 (current efficiency of 73.4%) without aeration, which was superior to the cathode made by the XC72 carbon black. The flow-by ADC-RuO 2 system consisted of an ADC and a RuO 2 -Ti anode showed high selectivity to aniline (AN) compared to benzoate (BA) in a NaCl electrolyte, whose degradation efficiencies were 97.72% and 1.3%, respectively. Rapid degradations of a mixture of emerging pollutants and AN were also observed in the ADC-RuO 2 system, with pseudo-first-order kinetic constants of 0.51, 1.29, 0.89, and 0.99 min −1 for Bisphenol A (BPA), tetracycline (TC), sulfamethoxazole (SMX) and AN, respectively. Quenching experiments revealed the main reactive oxygen species for the pollutant degradation was singlet oxygen ( 1 O 2 ), which was also identified by the electron spin resonance (ESR) analysis. Finally, the steady-stable content of 1 O 2 was quantitatively determined to be 6.25 × 10 −11 M by the method of furfuryl alcohol (FFA) probe. Our findings provide a fast, low energy consumption and well controlled electrochemical oxidation method for selective degradation of organic pollutants. Graphical abstract H 2 O 2 generated on an air diffusion cathode by naturally diffused O 2 , reacts with ClO − produced from chloride oxidation on the RuO 2 -Ti anode to form singlet oxygen ( 1 O 2 ). The electrochemical system shows an efficient oxidation to electron-rich emerging pollutants including bisphenol A, tetracycline, sulfamethoxazole and aniline, but a poor performance on the electron-deficient compounds (e.g., benzoate).
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