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Removal of emerging contaminants by Fenton and UV-Driven Advanced Oxidation Processes

journal contribution
posted on 2015-12-08, 11:02 authored by Marco Lucas, Jose A. Peres
The removal efficiencies of four different parabens (methylparaben (MP), ethylparaben (EP), propylparaben (PP), and butylparaben (BP)) using Fenton reagent, UV irradiation, UV/H2O2, and UV/ H2O2/Fe2+ were evaluated to assess the level of paraben degradation achieved using different advanced oxidation processes (AOPs). UV irradiation by itself provided paraben conversions between 27 and 38 % after a reaction time of 180 min. The UV/ H2O2 system increased the paraben conversion to values between 62 and 92 %, and the Fenton process was revealed as inefficient in paraben degradation within the experimental conditions used. Photo- Fenton presented similar removal rates to the UV/ H2O2 process. Among the four parabens studied, butylparaben was the most easily removed, and it was possible to attain degradations higher than 90 %. In the UV/H2O2 and photo-Fenton processes, the overall kinetic constant could be split into two main components: direct oxidation by UV radiation (photolysis) and oxidation by free radicals (mainly HO•) generated from the photodecomposition of H2O2. This work reveals that UV-driven oxidation processes can be widely used to remove parabens from contaminated aqueous solutions

History

School

  • Aeronautical, Automotive, Chemical and Materials Engineering

Department

  • Chemical Engineering

Published in

Water, Air, & Soil Pollution

Volume

226

Issue

8

Citation

LUCAS, M.S. and PERES, J.A., 2015. Removal of Emerging Contaminants by Fenton and UV-Driven Advanced Oxidation Processes. Water, Air, & Soil Pollution, 226:273

Publisher

© Springer International Publishing Switzerland

Version

  • NA (Not Applicable or Unknown)

Publisher statement

This work is made available according to the conditions of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) licence. Full details of this licence are available at: https://creativecommons.org/licenses/by-nc-nd/4.0/

Publication date

2015

Notes

This paper is closed access.

ISSN

0049-6979

eISSN

1573-2932

Language

  • en

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