Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.jhazmat.2007.06.073
Title: Degradation of C.I. Reactive Red 2 (RR2) using ozone-based systems: Comparisons of decolorization efficiency and power consumption
Authors: Wu, C.-H.
Ng, H.-Y. 
Keywords: C.I. Reactive Red 2
Decolorization
Ferric
Hydrogen peroxide
Ozone
Power consumption
Issue Date: 21-Mar-2008
Source: Wu, C.-H., Ng, H.-Y. (2008-03-21). Degradation of C.I. Reactive Red 2 (RR2) using ozone-based systems: Comparisons of decolorization efficiency and power consumption. Journal of Hazardous Materials 152 (1) : 120-127. ScholarBank@NUS Repository. https://doi.org/10.1016/j.jhazmat.2007.06.073
Abstract: This study investigated the decolorization efficiency of C.I. Reactive Red 2 (RR2) in O3, O3/H2O2, O3/Fe3+, O3/H2O2/Fe3+, UV/O3, UV/O3/Fe3+, UV/O3/H2O2 and UV/O3/H2O2/Fe3+ systems at various pHs. The effective energy consumption constants and the electrical energy per order of pollutant removal (EE/O) were also determined. The experimental results indicated that the energy efficiency was highest at [H2O2]0 = 1000 mg/l and [Fe3+]0 = 25 mg/l. Accordingly, the H2O2 and Fe3+ doses in the hybrid ozone- and UV/ozone-based systems were controlled at these values. This work suggests that the dominant reactant in O3, O3/Fe3+ and O3/H2O2 systems was O3 and that in the O3/H2O2/Fe3+ system was H2O2/Fe3+. The experimental results revealed that the combinations of Fe3+ or H2O2/Fe3+ with O3 at pH 4 and of H2O2 or H2O2/Fe3+ with UV/O3 at pH 4 or 7 yielded a higher decolorization rate than O3 and UV/O3, respectively. At pH 4, the EE/O results demonstrated that the UV/O3/H2O2/Fe3+ system reduced 85% of the energy consumption compared with the UV/O3 system. Moreover, the O3/H2O2/Fe3+ system reduced 62% of the energy consumption compared with the O3 system. At pH 7, the EE/O results revealed that the UV/O3/H2O2/Fe3+ system consumed half the energy of the UV/O3 system. © 2007 Elsevier B.V. All rights reserved.
Source Title: Journal of Hazardous Materials
URI: http://scholarbank.nus.edu.sg/handle/10635/87477
ISSN: 03043894
DOI: 10.1016/j.jhazmat.2007.06.073
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