Bao Tonghui, Ke Hui, Li Wanjiang, Cai Linke, Huang Yi
Engineering Research Center of Photoenergy Utilization for Pollution Control and Carbon Reduction, Ministry of Education, College of Chemistry, Central China Normal University, Wuhan 430079, China.
Nanomaterials (Basel). 2024 Aug 4;14(15):1312. doi: 10.3390/nano14151312.
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) as the catalyst in the electrically activated peroxymonosulfate (PMS) process, and the reaction kinetic constant reached 0.52 min. The redox processes of Co and Co in Co(OH) catalysts were considered to be the main pathways for PMS activation, in which O 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.
过一硫酸氢钾(PMS)活化产生活性物种是一种颇具吸引力的抗生素降解技术,但受限于低反应动力学和高成本。在本研究中,通过原位电沉积制备了一种钴基催化剂,以强化电活化PMS降解抗生素的过程。在电活化过一硫酸氢钾(PMS)过程中,以氢氧化钴(Co(OH))为催化剂,10分钟内几乎可将100%的培氟沙星(PFX)去除,反应动力学常数达到0.52 min⁻¹。Co(OH)催化剂中Co²⁺和Co³⁺的氧化还原过程被认为是PMS活化的主要途径,其中·O₂⁻是主要活性物种。此外,该策略对其他有机污染物也能实现优异的降解效率。本研究为污染物降解提供了一种有效且低成本、无二次污染的策略。