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Theoretical and experimental formation of low chlorinated dibenzo-p-dioxins and dibenzofurans in the Fenton oxidation of chlorophenol solutions
The formation of chlorinated and non-chlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) has been experimentally investigated after the Fenton oxidation of 2-chlorophenol (2-CP, 15.56 mM) aqueous solutions by assessing the influence of iron concentration (0.09–2.88 mM), hydrogen peroxide dose...
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Published in: | Chemosphere (Oxford) 2016-10, Vol.161, p.136-144 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The formation of chlorinated and non-chlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) has been experimentally investigated after the Fenton oxidation of 2-chlorophenol (2-CP, 15.56 mM) aqueous solutions by assessing the influence of iron concentration (0.09–2.88 mM), hydrogen peroxide dose (40.44–202.20 mM), temperature (20–70 °C) and chloride concentration (0–56.35 mM). The presence of chloride in the medium together with room temperature and substoichiometric Fenton conditions (40.44 mM H2O2) led to an increase in total PCDD/Fs concentration from less than 1 ng L−1 to 2 μg L−1. Results showed a dominance of the dichlorinated species (DCDD/Fs) in the homologue profile of total PCDD/Fs reaching values up to 1.5 μg L−1. Furthermore, the products distribution exhibited a gradual decrease in the homologue concentration as the chlorination degree increased from di-to octachloro-substituted positions. Considering the characteristics of the reaction medium, the experimental results, and the information gathered in bibliography with regard to the generation of active radicals from 2-chlorophenol, a mechanism describing the formation of low chlorinated PCDD/Fs in a Fenton oxidizing aqueous system has been proposed.
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•Fenton oxidation reports fast degradation kinetics of aqueous 2-CP solutions.•Complete mineralization of CP is not reached especially under substoichiometric conditions.•The formation of minor byproducts such as PCDD/Fs are observed.•High concentrations of DCDD and DCDF have been detected.•A mechanism for the formation of low chlorinated PCDD/Fs in aqueous oxidation media is proposed. |
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ISSN: | 0045-6535 1879-1298 |
DOI: | 10.1016/j.chemosphere.2016.07.011 |