摘要
Fe2+is widely used for effective peroxymonosulfate (PMS) activation to eliminate refractory organics. However, Fe2+/PMS process suffers from difficulty on Fe2+regeneration. Herein, we report an Fe2+/PMS process by using gallic acid (GA) as an effective promotor for efficient degradation of bisphenol A (BPA). The process exhibited considerable oxidation performance in the pH range of 3.0-10.0. Higher concentration of Fe2+/GA complex exhibited better BPA degradation performance whereby BPA could be completely degraded within 4 mins. Reactive oxidation species (ROS) quenching experiments, electron paramagnetic resonance (EPR) analysis, and methyl phenyl sulfoxide (PMSO) probing experiments revealed that sulfate radical (SO4 -), hydroxyl radical (HO ), and ferryl species are involved and responsible for the BPA degradation. Electrochemical analysis and density function theory (DFT) calculation explored that the self-oxidation of GA boosted the reduction of Fe2+into Fe2+for continuous activation of PMS. The GA boosted Fe2+/PMS system reached an intriguing mineralization efficiency of 86.4%. Findings from this work proposed references to improve the oxidation performance of Fenton-like reaction and provided new sight into the Fe2+/Fe2+cycling.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 4852-4863 |
| 页数 | 12 |
| 期刊 | Water Supply |
| 卷 | 22 |
| 期 | 5 |
| DOI | |
| 出版状态 | 已出版 - 1 5月 2022 |
学术指纹
探究 'Gallic acid enhanced bisphenol A degradation through Fe2+/peroxymonosulfate process' 的科研主题。它们共同构成独一无二的指纹。引用此
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