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黑暗及光助Co2+催化过一硫酸盐体系对酸性橙7的氧化脱色及矿化动力学

Kinetics of oxidative decolorization and mineralization of Acid Orange 7 by dark and photoassisted Co2+-catalyzed peroxymonosulfate system.

作者信息

Chen Xiaoyang, Qiao Xianliang, Wang Degao, Lin Jing, Chen Jingwen

机构信息

Department of Environmental Science and Technology, Dalian University of Technology, Linggong Road 2, Dalian, Liaoning Province 116024, PR China.

出版信息

Chemosphere. 2007 Mar;67(4):802-8. doi: 10.1016/j.chemosphere.2006.10.032. Epub 2006 Dec 6.

Abstract

A kinetic model was proposed and used to interpret the experimental data for degradation of Acid Orange 7 (AO7) in aqueous solution induced by Co(2+)/peroxymonosulfate (Co/PMS) reagent in terms of both decolorization and mineralization. The pseudo first-order decolorization rate constants are related to [Co(2+)], [PMS], reciprocal of [H(+)] and AO7. Activation energy of the AO7 decolorization process was determined to be 75.7 kJ mol(-1). UV and visible light can accelerate the decolorization and mineralization process due to different mechanisms. In the combined UV/Co/PMS system, UV light can decompose PMS to generate hydroxyl (()OH) and sulfate radicals (SO(4)(-)), while in the Vis/Co/PMS system, excited AO7 molecules can transfer electrons to PMS or Co(3+) and thus accelerate the decomposition of PMS and catalytic cycle of Co(3+)/Co(2+).

摘要

提出了一个动力学模型,用于从脱色和矿化两方面解释Co(2+)/过一硫酸盐(Co/PMS)试剂诱导酸性橙7(AO7)在水溶液中降解的实验数据。准一级脱色速率常数与[Co(2+)]、[PMS]、[H(+)]的倒数以及AO7有关。AO7脱色过程的活化能确定为75.7 kJ mol(-1)。紫外光和可见光由于不同的机制可以加速脱色和矿化过程。在UV/Co/PMS组合体系中,紫外光可分解PMS生成羟基自由基(()OH)和硫酸根自由基(SO(4)(-)),而在Vis/Co/PMS体系中,激发态的AO7分子可将电子转移给PMS或Co(3+),从而加速PMS的分解和Co(3+)/Co(2+)的催化循环。

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