School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China.
State Key Laboratory of Silkworm Genome Biology, Key Laboratory of Sericultural Biology and Genetic Breeding, Ministry of Agriculture and Rural Affairs, College of Sericulture, Textile and Biomass Sciences, Southwest University, Chongqing 400715, China.
Int J Mol Sci. 2023 Mar 16;24(6):5702. doi: 10.3390/ijms24065702.
A magnetic copper ferrite and biochar composite (CuFeO@BC) catalyst was prepared by an improved sol-gel calcination method and initially used for the removal of antibiotics ciprofloxacin (CIP) by activated peroxymonosulfate (PMS). Using CuFeO@BC as the activator, 97.8% CIP removal efficiency could be achieved in 30 min. After a continuous degradation cycle, CuFeO@BC catalyst still exhibited great stability and repeatability and could also be quickly recovered by an external magnetic field. Meanwhile, the CuFeO@BC/PMS system presented good stability for metal ion leaching, which was far less than the leaching of metal ions in the CuFeO/PMS system. Moreover, the effects of various influencing factors, such as initial solution pH, activator loading, PMS dosage, reaction temperature, humic acid (HA), and the inorganic anions were explored. The quenching experiments and the electron paramagnetic resonance (EPR) analysis manifested that hydroxyl radical (•OH), sulfate radical (SO), superoxide radical (O), and singlet oxygen (O) were generated in the CuFeO@BC/PMS system, while O and O are mainly involved in the degradation process. The synergistic effect between CuFeO and BC enhanced the structural stability and electrical conductivity of the material, which promoted the bonding between the catalyst and PMS, resulting in the enhanced catalytic activity of CuFeO@BC. This indicates that CuFeO@BC activating PMS is a promising remediation technique for CIP-contaminated water.
一种磁性铜铁氧体和生物炭复合材料(CuFeO@BC)催化剂通过改进的溶胶-凝胶煅烧法制备,并首次用于通过活化过一硫酸盐(PMS)去除抗生素环丙沙星(CIP)。以 CuFeO@BC 为活化剂,在 30 分钟内可实现 97.8%的 CIP 去除效率。经过连续降解循环后,CuFeO@BC 催化剂仍表现出优异的稳定性和可重复性,并且可以通过外部磁场快速回收。同时,CuFeO@BC/PMS 体系对金属离子浸出表现出良好的稳定性,远低于 CuFeO/PMS 体系中金属离子的浸出。此外,还考察了各种影响因素,如初始溶液 pH 值、活化剂负载量、PMS 用量、反应温度、腐殖酸(HA)和无机阴离子的影响。猝灭实验和电子顺磁共振(EPR)分析表明,在 CuFeO@BC/PMS 体系中生成了羟基自由基(•OH)、硫酸根自由基(SO)、超氧自由基(O)和单线态氧(O),而 O 和 O 主要参与降解过程。CuFeO 和 BC 之间的协同效应增强了材料的结构稳定性和导电性,促进了催化剂与 PMS 之间的键合,从而提高了 CuFeO@BC 的催化活性。这表明 CuFeO@BC 活化 PMS 是一种有前途的用于处理 CIP 污染水的修复技术。