期刊
SEPARATION AND PURIFICATION TECHNOLOGY
卷 300, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.seppur.2022.121822
关键词
Co5Mn-LDH; Formation mechanism; Peroxymonosulfate; Norfloxacin; Catalytic mechanism
资金
- Technology Innovation Project ofHebei Normal University [L2018K06]
In this study, Co5Mn-layered double hydroxide (Co5Mn-LDH) was synthesized by hydrothermal process. The investigation on Co5Mn-LDH revealed its potential as a heterogeneous Fenton-like catalyst for efficient degradation of norfloxacin (NOR) using peroxymonosulfate (PMS) activation. The mechanism of Co5Mn-LDH in PMS activation and Co2+/Mn3+ and Co3+/Mn4+ transformation was also studied.
In this study, Co5Mn-layered double hydroxide (Co5Mn-LDH) was synthesized by hydrothermal process. The SEM image of Co5Mn-LDH shows the urchin-like sphere with the approximate diameter of 7.0-8.0 mu m assembled by the numerous rods with a width of about 30-40 nm. Investigation on the formation mechanism of Co5Mn-LDH indicated that NH4F dosage and reaction time played an essential role in modulating the morphology and structure of Co5Mn-LDH. Co5Mn-LDH, as a heterogeneous Fenton-like catalyst, could efficiently activate peroxymonosulfate (PMS) and degrade norfloxacin (NOR) in the pH range of 3.0-9.0. The degradation efficiency of NOR was 98.7% at its natural pH, and the COD removal rate reached 83.3% within 8 min. On the one hand, the abundant Co2+ and Mn3+ in Co5Mn-LDH can simultaneously react with PMS to generate various reactive oxygen species (ROS), while the resulted Co3+ and Mn4+ could convert to original Co2+ and Mn3+, behaving similarly to the Harber-Weiss cycle. On the other hand, the regeneration of Co2+ could also rely on the oxidation and reduction between Co3+/Co2+ and Mn4+/Mn3+. Co(OH)(6) octahedron structure and rich surface hydroxyl groups within LDH are favorable to the transformation between Co2+/Mn3+ and Co3+/Mn4+. Such mechanism provides new insights into the nature of reactions in heterogeneous Fenton-like system.
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