TY - JOUR
T1 - Photochemical and heterogeneous photocatalytic degradation of waste vinylsulphone dyes
T2 - A case study with hydrolyzed Reactive Black 5
AU - Alaton, Idil Arslan
AU - Balcioglu, Işil Akmehmet
PY - 2001/7/2
Y1 - 2001/7/2
N2 - 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).
AB - 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).
KW - Advanced oxidation processes (AOPs)
KW - HO/UV-C treatment
KW - Langmuir-Hinshelwood type kinetic equation
KW - Reactive Black 5
KW - Textile dyestuffs
KW - TiO/UV-A treatment
UR - http://www.scopus.com/inward/record.url?scp=0035797225&partnerID=8YFLogxK
U2 - 10.1016/S1010-6030(01)00440-3
DO - 10.1016/S1010-6030(01)00440-3
M3 - Article
AN - SCOPUS:0035797225
SN - 1010-6030
VL - 141
SP - 247
EP - 254
JO - Journal of Photochemistry and Photobiology A: Chemistry
JF - Journal of Photochemistry and Photobiology A: Chemistry
IS - 2-3
ER -