Enhanced ferrate oxidation of organic pollutants in the presence of Cu (II) Ion

In this study, we found that the introduction of Cu(II) (several mu M, close to the concentration level of some real water/wastewater) in ferrate (Fe(VI)) oxidation can remarkably accelerate the abatement of various organic pollutants under slightly alkaline conditions. The results show that 5 mu M sulfamethoxazole (SMX) can be completely degraded by Fe(VI) (50 mu M) in the presence of 20 mu M Cu(II) within 10 min at pH 8.0, which was 1.65 times higher than that by Fe(VI) alone. High-valent iron intermediates (i.e. Fe(V), Fe(IV)) and Cu(III) were generated as reactive species in the Cu(II)/Fe(VI) system, all of which contributed to the enhanced oxidation of SMX. Common water components, except for HCO3- and humic acid, exhibited no influence on SMX removal. Additionally, the enhanced removal of SMX by Cu(II)/Fe(VI) was also observed in real water with the benefit of total removal of Cu(II) by the ferrate resultant particles. Due to the presence of highly reactive and selective oxidant, the Cu(II)/Fe(VI) system could react readily with organic pollutants containing electron-rich moieties, such as phenol, olefin or amino groups. This study provided a simple, selective, and practical strategy for the abatement of organic pollutants and a simultaneous removal of Cu(II).

Automated summary

In this study, the introduction of Cu(II) in ferrate oxidation was found to greatly accelerate the abatement of various organic pollutants under slightly alkaline conditions. The presence of highly reactive and selective oxidants in the Cu(II)/Fe(VI) system contributed to the enhanced oxidation of organic pollutants. This study provides a simple, selective, and practical strategy for the abatement of organic pollutants and simultaneous removal of Cu(II).