Abstract
Aqueous solutions of hydrolyzed Reactive Black 5 (RB5) dye, a well-known surrogate for non-biodegradable azo dyes, were photochemically and photocatalytically treated by employing the H2O2/UV-C and TiO2/UV-A advanced oxidation systems, respectively. The observed effects of reaction pH, oxidant dose and initial dyestuff concentration were used to explain the OH· induced color disappearance kinetics empirically. Accordingly, the waste dyestuff solutions could be completely decolorized (kd, max=0.155min-1; H2O2/UV-C system) and effectively mineralized (kTOC, max=0.01min-1; H2O2/UV-C system), with an average overall TOC removal of 78% after 120min advanced oxidation at the specified optimized reaction conditions. The treatment via H2O2/UV-C was mainly governed by OH· type oxidation rather than direct UV-C or UV-A photolysis, and the bleaching effect of the TiO2/UV-A process could be successfully fitted to the empirical Langmuir-Hinshelwood (L-H) kinetic model (kL-H=4.47mgl-1min-1; KL-H=2.01lmg-1).
Original language | English |
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Pages (from-to) | 247-254 |
Number of pages | 8 |
Journal | Journal of Photochemistry and Photobiology A: Chemistry |
Volume | 141 |
Issue number | 2-3 |
DOIs | |
Publication status | Published - 2 Jul 2001 |
Externally published | Yes |
Keywords
- Advanced oxidation processes (AOPs)
- HO/UV-C treatment
- Langmuir-Hinshelwood type kinetic equation
- Reactive Black 5
- Textile dyestuffs
- TiO/UV-A treatment