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摘要
以间甲酚(MC)为对象,研究了Fe (Ⅵ)/H2O2体系对其的降解效果及机理。考察了Fe (Ⅵ)投加量、H2O2浓度、pH和温度等因素对间甲酚降解率的影响;利用HPLC、GC-MS等方法对其进行分析与表征,解析Fe (Ⅵ)/H2O2体系降解MC过程中的产物并推测可能的降解路径。结果表明,当Fe (Ⅵ)和间甲酚物质的量比为5:1、H2O2浓度为40 mmol/L、pH为4、温度为25℃时,反应16.5 min后间甲酚的降解率可达到100%,最终矿化度为23.85%。Fe (Ⅵ)氧化MC阶段,起氧化作用的主要为中间高价态铁;后期类Fenton氧化阶段,·OH起主要作用,反应符合准一级动力学模型,反应速率常数为0.358 32。
Abstract
The degradation effect and mechanism of m-cresol by Fe(Ⅵ)/H2O2 system is studied,and the effects of Fe(Ⅵ) dosage,H2O2 dosage,pH and temperature on the degradation rate of m-cresol are investigated.HPLC,GC-MS and other methods is employed to characterize the products generated in the degradation process of m-cresol by Fe(Ⅵ)/H2O2 system,and speculate the possible degradation pathways.The results show that the degradation rate of m-cresol reaches 100% and the final mineralization rate is 23.85% when the molar ratio of Fe(Ⅵ) to m-cresol is 5:1,the reaction has performed for 16.5 min,the dosage of H2O2 is 40 mmol·L-1,pH is 4,and the temperature is 25℃.The intermediate high valence iron plays a major role in the oxidation of m-cresol by Fe(Ⅵ),while ·OH has primary effect in subsequent Fenton-like oxidation process,which conforms to the quasi-first-order kinetic model with a reaction rate constant of 0.358 32.
关键词
Fe (Ⅵ)/H2O2体系
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矿化度
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羟基自由基
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动力学
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间甲酚
Key words
Fe(Ⅵ)/H2O2 system
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mineralization rate
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hydroxyl radical
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kinetics
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m-cresol
Author summay
冯卓(1997-),男,硕士研究生,研究方向为废水处理技术,747153151@qq.com
Fe (Ⅵ)/H2O2体系氧化降解间甲酚的效能研究[J].
现代化工, 2022, 42(11): 194-200 DOI:10.16606/j.cnki.issn0253-4320.2022.11.036