过氧乙酸
双金属片
废水
环境修复
衍生工具(金融)
化学
核化学
废物管理
材料科学
有机化学
业务
催化作用
污染
过氧化氢
工程类
生物
生态学
财务
作者
Shengmei Tan,Liuwei Zhang,Zhiliang Cheng,Yan Peng,Jinshan Tang,Hongrui Zhu,Facheng Qiu
标识
DOI:10.1038/s41545-025-00465-3
摘要
Abstract This study introduces a hydrogenated FeCo-MOF derivative catalyst (HC-FeCo@C350) to activate peracetic acid (PAA) for efficient degradation dye wastewater. Rhodamine B (RhB) as a model pollutant, the HC-FeCo@C350/PAA achieved a 99.33% removal efficiency within 20 min, with a rate constant 18 times higher than the non-hydrogenated system. Liquid chromatography-mass spectrometry (LC-MS) and the toxicity evaluation software (T.E.S.T.) confirmed reduced intermediate toxicity. Quenching experiments, electron paramagnetic resonance (EPR) tests, and density functional theory (DFT) calculation show that HC-FeCo@C350 can effectively activate PAA to produce 1O2, CH3C(O)O•, and CH3C(O)OO•. The magnetically recoverable catalyst maintained over 80% efficiency after 4 cycles. In actual dye wastewater treatment, the RE of chemical oxygen demand (COD), ammonia nitrogen (NH3-N), total nitrogen (TN), total phosphorus (TP) could reach approximately 53.57%, 53.23%, 29.25%, 19.2%, respectively, with reduced toxicity validated by mungbean germination experiment. This technology offers a promising approach for refractory dye wastewater treatment and reuse.
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