纳米笼
化学
介孔材料
催化作用
锰
吸附
无机化学
钴
浸出(土壤学)
激进的
水溶液中的金属离子
光化学
金属
有机化学
土壤水分
土壤科学
环境科学
作者
Jing Deng,Yongqing Cheng,Yuan Lü,John C. Crittenden,Shiqing Zhou,Naiyun Gao,Jun Li
标识
DOI:10.1016/j.cej.2017.07.149
摘要
Mesoporous MnxCo3 − xO4 nanocages with high cobalt content, large surface area and high pore volume were synthesized through a self-assembly method. The as-prepared MnxCo3 − xO4 nanocages displayed satisfactory catalytic activity toward peroxymonosulfate (PMS) and the metal ions leaching concentration could be negligible. Sulfate radical was identified as the predominant active species through radical quenching experiments and electron spin resonance spin-trapping technique. The kinetics of the oxidation process was of pseudo-first order. The increasing cobalt content in MnxCo3 − xO4 NCs was in favor of enhancing the decomposition of PMS. MnxCo3 − xO4 nanocages dosage, PMS concentration and reaction temperature put the promoting effect on the degradation, while initial CBZ concentration had the retarding impact. MnxCo3 − xO4 nanocages could efficiently operate over a wide pH range of 5.0–8.0. Coexisting chloride ions exerted a dual role in the decomposition of PMS and this role was concentration-dependent. XPS analysis confirmed the reversible valence equilibrium between metal ions and the recovery of surface adsorbed oxygen, which ensured their sustainable catalytic activity even after five consecutive runs. Based on the main intermediates identified by liquid chromatography-tandem mass spectrometry, a possible pathway of CBZ oxidation was proposed. The potential risk resulting from the highly toxic intermediates can also be effectively controlled by MnxCo3 − xO4 NCs activated PMS system.
科研通智能强力驱动
Strongly Powered by AbleSci AI