期刊
CHINESE CHEMICAL LETTERS
卷 34, 期 1, 页码 -出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.cclet.2022.02.058
关键词
Advanced oxidation progresses; Fe3O4; Graphene oxide; Mechanism; Reactive oxygen species
This study investigated the catalytic mechanism and performance of Fe3O4-GO(x) composites with different material ratios in three advanced oxidation processes (AOPs) for tetracycline hydrochloride (TCH) degradation. The ratio of GO in the composites showed different degradation capacities in each AOP based on distinct mechanisms. Fe3O4-rGO(20wt%) exhibited the highest catalytic performance in ozone decomposition, while Fe3O4-rGO(5wt%) showed the best performance in PDS and photo-Fenton processes. The catalytic mechanisms involving reactive oxygen species (ROS) produced by the conversion between Fe2+/Fe3+ were also analyzed.
This study explored the catalytic mechanism and performance impacted by the materials ratio of Fe3O4-GO(x) composites in three typical advanced oxidation processes (AOPs) of O-3, peroxodisulfate (PDS) and photo-Fenton processes for tetracycline hydrochloride (TCH) degradation. The ratio of GO in the Fe3O4-GO(x) composites exhibited different trends of degradation capacity in each AOPs based on different mechanisms. Fe3O4-rGO(20wt%) exhibited the optimum catalytic performance which enhanced the ozone decomposition efficiency from 33.48% (ozone alone) to 51.83% with the major reactive oxygen species (ROS) of O-2(center dot-). In PDS and photo-Fenton processes, Fe3O4-rGO(5wt%) had the highest catalytic performance in PDS and H2O2 decomposition for SO4 center dot?, and (OH)-O-center dot generation, respectively. Compared with using PDS alone, PDS decomposition rate and TCH degradation rate could be increased by 5.97 and 1.73 times under Fe3O4-rGO(5wt%) catalysis. In the photo-Fenton system, Fe3O4-rGO(5wt%) with the best catalyst performance in H2O2 decomposition, and TCH degradation rate increased by 2.02 times compared with blank group. Meantime, the catalytic mechanisms in those systems of that the ROS produced by conversion between Fe2+/Fe3+ were also analyzed. (C) 2022 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
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