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Ph Effects On Iron-catalyzed Oxidation Using Fenton's Reagent

机译:Ph对Fenton试剂对铁催化氧化的影响

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This work extends investigations into the development and use of a kinetic model to simulate and improve the iron-catalyzed oxidation of organic compounds using Fenton's reagent.While a number of recent studies have successfully modeled the kinetics and species behavior in simple Fenton systems,none have extended and applied the model to examine the effect of operating parameters such as pH on treatment performance.The purpose of this work is to investigate the effect of pH in Fenton-based oxidation systems and to use kinetic modeling to gain insight into the reaction mechanism and speciation of the iron catalyst.Laboratory experiments were conducted across a range of starting concentrations of Fe(Ⅱ) and H_2O_2 at pHs of 2.5,3.0,and 4.0,both in the presence and absence of a target organic,formic acid (HCOOH).With minor modifications,the model presented is capable of accurately describing changes in Fe(Ⅱ) concentrations over a wide range of reaction conditions and,provided account is taken of additional hydroxyl radical scavenging pathways,also accounts for the oxidation of formic acid over extended reaction times at all pHs considered.The use of composite values for rate constants of reactions involving weakly acidic species is shown to be appropriate,and analysis of the model reveals the catalytic role iron plays in the oxidation process.Experimental and simulated data at the different pHs highlights the effect the catalytic redox cycling of iron has on the performance and oxidation capacity of the Fenton system.
机译:这项工作扩展了对动力学模型的开发和使用的研究,以使用芬顿试剂模拟和改善铁催化的有机化合物的氧化。尽管最近的许多研究已经成功地模拟了简单芬顿体系中的动力学和物种行为,但是还没有研究扩展并应用该模型以检查pH等操作参数对处理性能的影响。本工作的目的是研究pH在基于Fenton的氧化系统中的影响,并使用动力学模型深入了解反应机理和在存在和不存在目标有机甲酸(HCOOH)的条件下,在2.5、3.0和4.0的pH范围内,对Fe(Ⅱ)和H_2O_2的起始浓度范围进行了实验室实验。只需稍作修改,所提供的模型就可以准确地描述在宽范围的反应条件下Fe(Ⅱ)浓度的变化,并且提供了额外的羟基自由基清除途径,也考虑到了在所有pH值下,甲酸在延长的反应时间内都会发生氧化。使用弱酸性物质的反应速率常数的复合值被证明是合适的,并且对该模型进行了分析在不同pH值下的实验和模拟数据突显了铁的催化氧化还原循环对Fenton系统的性能和氧化能力的影响。

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