培氟沙星
催化作用
降级(电信)
钴
化学
污染物
反应速率常数
氧化还原
化学工程
电极
动力学
无机化学
有机化学
抗生素
计算机科学
物理化学
工程类
物理
电信
氧氟沙星
环丙沙星
量子力学
生物化学
作者
Tonghui Bao,Hui Ke,Wanjiang Li,Linke Cai,Yi Huang
出处
期刊:Nanomaterials
[Multidisciplinary Digital Publishing Institute]
日期:2024-08-04
卷期号:14 (15): 1312-1312
摘要
The activation of PMS to produce active species is an attractive technique for antibiotic degradation but is restricted to the low reaction kinetics and high costs. In this work, a cobalt-based catalyst was prepared by in situ electrodeposition to enhance the electrically activated PMS process for the degradation of antibiotics. Almost 100% of pefloxacin (PFX) was removed within 10 min by employing Co(OH)2 as the catalyst in the electrically activated peroxymonosulfate (PMS) process, and the reaction kinetic constant reached 0.52 min−1. The redox processes of Co2+ and Co3+ in Co(OH)2 catalysts were considered to be the main pathways for PMS activation, in which 1O2 was the main active species. Furthermore, this strategy could also achieve excellent degradation efficiency for other organic pollutants. This study provides an effective and low-cost strategy with no secondary pollution for pollutant degradation.
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