Efficient peroxymonosulfate activation of immobilized Fe–N–C catalyst on ceramsite for the continuous flow removal of phenol

Abstract

Nowadays, developing environmentally friendly catalysts with both low cost and high efficiency was still a challenge in actual organic wastewater purification. Herein, the Fe–N–C catalyst was successfully immobilized on solid waste derived ceramsite for efficient degradation of phenol under continuous flow conditions by activating peroxymonosulfate (PMS). After the introduction of ceramsite, the microstructure of Fe–N–C catalyst was changed from granular structure to worm-like structure, promoting the dispersion of the nanoscale catalyst and providing more reactive sites. Therefore, the phenol removal rate and mineralization rate of the obtained 0.5FNNC within 30 min were up to 96.79% and 71.79%, respectively. In addition, the degradation rate of the optimal composite (0.5FNNC)/PMS system was about 4.06 times higher than that of bare Fe–N–C/PMS system. Intriguingly, the Fe ion leaching from 0.5FNNC during the degradation reaction was significantly lower than bare Fe–N–C owing to the strong catalyst-support chemical bonding. Based on electron paramagnetic resonance, quenching experiments, X-ray photoelectron spectroscopy analysis and electrochemical analysis, it was indicated that the non-radical processes (1O2 and high valent iron-oxo species) should be responsible for the phenol degradation. Meanwhile, the possible phenol degradation pathways were proposed, and the intermediates were evaluated for ecotoxicity by ECOSAR. Finally, a preliminary economic analysis of this process was carried out. Overall, this work would provide a new strategy for the construction of ceramsite based multi-pore composite catalysts and the large-scale application of persulfate oxidation technology in organic wastewater treatment.