Degradation of benzene, toluene ethylbenzene and p-xylene (BTEX) in aqueous solutions using UV/H2O2 system
Journal of Chemical Technology and Biotechnology • 2004
Publication Information
Authors
Abdel Hakim AM Daifullah1∗ and Mohamed Mokhtar Mohamed2
Keywords
Not Available
Journal
Journal of Chemical Technology and Biotechnology
Publisher
Not Available
Volume
79:468–474
Issue
79
Pages
Society of Chemical Industry
publication.type
International
Paper Link
Not Available
Supplementary Materials
Not Available
Abstract
The homogeneous degradation of benzene (B), toluene (T), ethylbenzene (E) and p-xylene
(X) (BTEX) was studied in aqueous solutions, at pH 3.0, of hydrogen peroxide (5.8mM) under UV
irradiation in a photoreactor equipped with a 300nm lamp of light intensity 3.5 × 10−5 Ein L−1 min−1. BTEX
was substantially degraded by the H2O2/UV system, with >90% disappearing in 10min of irradiation.
The decomposition of BTEX was studied either as single or as multi-component systems. The effects
of irradiation time, amounts of H2O2 in molar ratios, rate of degradation and competition between
components were thoroughly examined. It can be stated that the rate of BTEX degradation in mixture was
higher than those for the individual components due to external effects of the absorption of UV light by the
mixture, and their effects on enhancing the formation of OH• radicals. The appropriate figure of merit,
the electrical energy per mass (EE/M), was estimated at various molar ratios and it was confirmed that
the best value was the one depicted for p-xylene (0.065kWhkg−1). A theoretical model for the degradation
pathway was proposed.
(X) (BTEX) was studied in aqueous solutions, at pH 3.0, of hydrogen peroxide (5.8mM) under UV
irradiation in a photoreactor equipped with a 300nm lamp of light intensity 3.5 × 10−5 Ein L−1 min−1. BTEX
was substantially degraded by the H2O2/UV system, with >90% disappearing in 10min of irradiation.
The decomposition of BTEX was studied either as single or as multi-component systems. The effects
of irradiation time, amounts of H2O2 in molar ratios, rate of degradation and competition between
components were thoroughly examined. It can be stated that the rate of BTEX degradation in mixture was
higher than those for the individual components due to external effects of the absorption of UV light by the
mixture, and their effects on enhancing the formation of OH• radicals. The appropriate figure of merit,
the electrical energy per mass (EE/M), was estimated at various molar ratios and it was confirmed that
the best value was the one depicted for p-xylene (0.065kWhkg−1). A theoretical model for the degradation
pathway was proposed.
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