Journal
CHEMICAL ENGINEERING JOURNAL
Volume 313, Issue -, Pages 815-825Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2016.12.104
Keywords
Chemical oxidation remediation; Peroxymonosulfate; Permanganate; Colloidal MnO2; Amorphous MnO2; Groundwater
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Funding
- National Natural Science Foundation of China (NSFC) [51278386]
- technological innovation from-Hubei Province [2016ACA162]
- Wuhan University [2042016kf1178]
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The present study demonstrates the effectiveness of a novel oxidant system, namely the combined use of peroxymonosulfate (PMS) and permanganate (CUPP), for the degradation of benzene and trichloroethylene (TCE) in simulated groundwater. The CUPP process exhibited favorable oxidizing capability because the in-situ generated colloidal and amorphous MnO2 linked the two oxidants. Compared with the separate use of permanganate or peroxymonosulfate, the CUPP process showed much better efficiency for the removal of refractory benzene. According to the electron paramagnetic resonance analysis and PMSactivating experiments, both colloidal and amorphous MnO2 (AM-MnO2) triggered the radical mediated oxidation, but the AM-MnO2-activated PMS showed an adsorption-dependent oxidizing capability. For the CUPP process, higher temperatures promoted the initial degradation rate of benzene, but did not change its final removal efficiency. The degradation of benzene was mostly associated with the activated PMS, and the intermediates also competed with TCE for KMnO4. The KMnO4 component played a more important role than PMS for the removal of TCE. For an aqueous mixture of 0.3 mM benzene and TCE, the combination of 2.4 mM PMS and 1.8 mM KMnO4 was optimal, achieving removal efficiencies higher than 85% for both pollutants. Regarding the degradation of benzene, chloride ions had a concentration-dependent effect, and bicarbonate ions and dihydrogen phosphate showed different levels of retarding effect. The CUPP is envisaged to be used as a remedial reagent for the in-situ chemical oxidation of groundwater contaminants. (C) 2016 Elsevier B.V. All rights reserved.
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