Oxidative treatment of aqueous monochlorobenzene with thermally-activated persulfate

Qishi LUO

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PDF(283 KB)
Front. Environ. Sci. Eng. ›› 2014, Vol. 8 ›› Issue (2) : 188-194. DOI: 10.1007/s11783-013-0544-x
RESEARCH ARTICLE
RESEARCH ARTICLE

Oxidative treatment of aqueous monochlorobenzene with thermally-activated persulfate

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Abstract

The oxidation of aqueous monochlorobenzene (MCB) solutions using thermally- activated persulfate has been investigated. The influence of reaction temperature on the kinetics of MCB oxidation was examined, and the Arrenhius Equation rate constants at 20°C, 30°C, 40°C, 50°C, and 60°C for MCB oxidation performance were calculated as 0, 0.001, 0.002, 0.015, 0.057 min-1, which indicates that elevated temperature accelerated the rate. The most efficient molar ratio of persulfate/MCB for MCB oxidation was determined to be 200 to 1 and an increase in the rate constants suggests that the oxidation process proceeded more rapidly with increasing persulfate/MCB molar ratios. In addition, the reactivity of persulfate in contaminated water is partly influenced by the presence of background ions such as Cl-, HCO3-, SO42-, and NO3-. Importantly, a scavenging effect in rate constant was observed for both Cl- and CO32- but not for other ions. The effective thermally activated persulfate oxidation of MCB in groundwater from a real contaminated site was achieved using both elevated reaction temperature and increased persulfate/MCB molar ratio.

Keywords

persulfate / monochlorobenzene / advanced oxidation process

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Qishi LUO. Oxidative treatment of aqueous monochlorobenzene with thermally-activated persulfate. Front Envir Sci Eng, 2014, 8(2): 188‒194 https://doi.org/10.1007/s11783-013-0544-x

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Acknowledgements

This work was financially supported by the Ministry of Environmental Protection and the Shanghai Bureau of Environmental Protection under the Research Frontiers Program (201109019; 2012-07). My colleagues, including Dr. Jie Zhu, Mr. Xiaoning Liu, Mr.Zhiqiang Liao and Dr. Liang Meng, were highly appreciated for their contributions to this work.

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2014 Higher Education Press and Springer-Verlag Berlin Heidelberg
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