Kinetic modeling of electro-Fenton reaction in aqueous solution

水溶液 苯酚 化学 过氧化氢 反应速率 铁质 降级(电信) 化学动力学 反应级数 反应速率常数 动力学 反应机理 无机化学 催化作用 物理化学 有机化学 物理 电信 量子力学 计算机科学
作者
Haiying Liu,X.Z. Li,Yongjun Leng,C. Wang
出处
期刊:Water Research [Elsevier]
卷期号:41 (5): 1161-1167 被引量:128
标识
DOI:10.1016/j.watres.2006.12.006
摘要

To well describe the electro-Fenton (E-Fenton) reaction in aqueous solution, a new kinetic model was established according to the generally accepted mechanism of E-Fenton reaction. The model has special consideration on the rates of hydrogen peroxide (H2O2) generation and consumption in the reaction solution. The model also embraces three key operating factors affecting the organic degradation in the E-Fenton reaction, including current density, dissolved oxygen concentration and initial ferrous ion concentration. This analytical model was then validated by the experiments of phenol degradation in aqueous solution. The experiments demonstrated that the H2O2 gradually built up with time and eventually approached its maximum value in the reaction solution. The experiments also showed that phenol was degraded at a slow rate at the early stage of the reaction, a faster rate during the middle stage, and a slow rate again at the final stage. It was confirmed in all experiments that the curves of phenol degradation (concentration vs. time) appeared to be an inverted "S" shape. The experimental data were fitted using both the normal first-order model and our new model, respectively. The goodness of fittings demonstrated that the new model could better fit the experimental data than the first-order model appreciably, which indicates that this analytical model can better describe the kinetics of the E-Fenton reaction mathematically and also chemically.

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