摘要
Safe treatment of antibiotics requires efficient removal of both antibiotics and their degraded intermediates. In this study, we demonstrate that FeC 2 O 4 •2H 2 O enables the more sustainable conversion of H 2 O 2 to • OH than commonly used FeSO 4 •7H 2 O, promoting the detoxification of a typical antibiotic sulfadimidine. It was found that the FeC 2 O 4 /H 2 O 2 system could completely degrade 250 mg L −1 of sulfadimidine within 40 min at pH 3.0, along with decreasing the contents of chemical oxygen demand and total organic carbon by 295.0 and 33.5 mg L −1 , respectively, more efficient than those in a classical Fenton system (FeSO 4 /H 2 O 2 ). Analysis of sulfadimidine degraded intermediates and toxicity evaluation suggested that the FeC 2 O 4 /H 2 O 2 treatment could more effectively decrease the overall toxicity of the sulfadimidine solution than the FeSO 4 /H 2 O 2 counterpart. The sustainability of FeC 2 O 4 •2H 2 O in H 2 O 2 conversion to • OH was attributed to its controlled release of Fe 2+ into the solution to prevent the quenching of • OH by excessive Fe 2+ , as well as the simultaneous release of C 2 O 4 2− to complex with Fe 2+ and Fe 3+ , which could inhibit iron sludge formation and accelerate Fe 3+ /Fe 2+ redox cycle. This study provides a promising Fenton system for the safe treatment of antibiotics and sheds light on the potential of FeC 2 O 4 •2H 2 O in environmental remediation.
危险品化学品经营许可证(带存储)