摘要
The peroxymonosulfate (PMS) oxidation processes have received considerable attention for water treatment. The influence of monohydrogen phosphate and dihydrogen phosphate on PMS system is still controversial. A biochar activated PMS system was constructed to investigate the HPO 4 2− /H 2 PO 4 − effects on sulfamethoxazole degradation. Results showed that the presence of H 2 PO 4 − inhibited PMS activation, while the co-existing HPO 4 2− played a positive role. Therefore, it might be inaccurate to assess the activation capacity of a catalyst for PMS activation when using phosphate as a buffer solution. Importantly, H 2 PO 4 − inhibited the function of C O, pyridine N and defects for PMS activation. However, HPO 4 2− promoted C O and graphitic N sites for sulfamethoxazole (SMX) degradation. The contributions of OH and SO 4 − to SMX degradation decreased with the increase of H 2 PO 4 − concentration. The production of SO 4 − was accelerated with the increase of HPO 4 2− concentration, promoting pollutants degradation. The contribution of 1 O 2 first increased and then decreased with the rise of HPO 4 2− /H 2 PO 4 − concentration. This study elucidated the roles of H 2 PO 4 − and HPO 4 2− in PMS system and revealed the corresponding specific influence mechanisms, promoting the application of PMS systems for antibiotic wastewater purification.
危险品化学品经营许可证(带存储)