Summary
Nano zero-valent iron (nZVI) is extensively used as a peroxymonosulfate (PMS) activator but suffers from the ease of oxidation and agglomeration due to its high surface energy and inherent magnetism. Here, green and sustainable yeast was selected as a support material to firstly in-situ prepare yeast-supported Fe-0@Fe2O3 and used for activating PMS to degrade tetracycline hydrochloride (TCH), one of the common antibiotics. Due to the anti-oxidation ability of the Fe2O3 shell and the support effect of yeast, the prepared Fe0@Fe2O3/YC exhibited a superior catalytic activity for the removal of TCH as well as some other typical refractory contaminants. The chemical quenching experiments and EPR results demonstrated SO4 center dot was the main reactive oxygen species while O-2(sic) O-1(2) and center dot OH played a minor role. Importantly, the crucial role of the Fe2+/Fe3+ cycle promoted by the Fe0 core and surface iron hydroxyl species in PMS activation was elucidated in detail. The TCH degradation pathways were proposed by LC-MS and density functional theory (DFT) calculation. In addition, the outstanding magnetic separation property, anti-oxidation ability, and high environmental resistance of the catalyst were demonstrated. Our work may inspire the development of green, efficient, and robust nZVI-based materials for wastewater treatment.