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Kinetics of electro-Fenton ferrous regeneration (EFFR) on chlorinated organic compound degradation

机译:Fenton亚铁再生(EFFR)对氯化有机物降解的动力学

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摘要

The electro-Fenton ferrous regeneration (EFFR) process was studied for kinetic determination under various reaction conditions. A novel model equation of this process was proposed which uses 2,4-dichlorophenol (2,4-DCP) as a chlorinated organic reference for this study. The operating parameters, pH, electrical current densities, and hydrogen peroxide concentrations, were varied to validate this novel model and kinetic rate constant estimation. The kinetic rate constant of the hydroxyl radical (center dot OH) with 2,4-DCP obtained by the novel model from this experiment was between 6.76 x 10(9) and 7.82 x 10(9) M(-1)s(-1). As a result, the novel model showed a more suitable fit with the experimental data than the first-order model method. The goodness of data fit which were indicated by correlation coefficients r(2) demonstrated that the novel model can better describe the kinetics of the process for chlorinated organic compound oxidation than the first-order model. Hydroquinone, maleic, acetic, formic, and oxalic acids were the main oxidation intermediates in this experiment. A degradation pathway for chlorinated organic compound oxidation by EFFR process was proposed on the basis of the intermediate compounds detected.
机译:研究了电芬顿亚铁再生(EFFR)工艺在各种反应条件下的动力学测定。提出了该过程的新模型方程,该方程使用2,4-二氯苯酚(2,4-DCP)作为本研究的氯化有机参照物。改变操作参数,pH,电流密度和过氧化氢浓度以验证该新颖模型和动力学速率常数估计。通过新模型从该实验中获得的带有2,4-DCP的羟基自由基(中心点OH)的动力学速率常数在6.76 x 10(9)和7.82 x 10(9)M(-1)s(- 1)。结果,与一阶模型方法相比,新模型显示出更适合实验数据。相关系数r(2)表示的数据拟合优度表明,与一阶模型相比,该新模型能够更好地描述氯化有机化合物氧化过程的动力学。对苯二酚,马来酸,乙酸,甲酸和草酸是该实验中的主要氧化中间体。根据检测到的中间体化合物,提出了一种通过EFFR法降解氯代有机化合物的降解途径。

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