Affiliation:
1. Laboratoire des Sciences et Technologies de l’Environnement , Faculté des Sciences Exactes, Département de Chimie, Université Frères Mentouri Constantine 1 , 25000 Constantine , Algeria
Abstract
Abstract
In the present work, a comparative study of the photooxidation of an aqueous solution of Methyl Orange (MeO) has been realized using H2O2 and IO3
−, BrO3
−, ClO3
−, ClO4
−, BO3
− ions in the presence of UV low pressure mercury lamp (UV-C light at λ
max = 254 nm). The initial concentration of MeO in all experiments was 6 × 10−5 mol L−1. The degradation rate of MeO follows pseudo-first-order kinetics in all UV/Oxidant systems. The highest degradation rate of MeO was in the BrO3
−/UV254nm system. Different systems were compared for an oxidant concentration of 10−2 mol L−1 and the obtained results showed that decolorization followed the decreasing order: BrO
3
−
/UV
254 nm
> IO
3
−
/UV
254 nm
> H
2
O
2
/UV
254 nm
> BO
3
−
/UV
254 nm
> ClO
3
−
/UV
254 nm
= ClO
4
−
/UV
254 nm
= UV
254 nm
. The optimization of oxidants concentration for each process was determined (10−2 mol L−1 for IO3
− which gives almost the same k
app for 5 × 10−3, 10−2 mol L−1 for BO3
− and 5 × 10−2 mol L−1 for H2O2). No degradation of MeO in presence of ClO3
− and ClO4
− because these ions do not absorb at 254 nm, therefore they do not generate radical species which degrade organic pollutants. The mineralization was also studied where it was reached 97% after 5 h of irradiation for both H2O2/UV254 nm and BO3
−/UV254 nm systems.
Subject
General Chemical Engineering
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3 articles.
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