TY - JOUR
T1 - Photoelectrochemical degradation of dye wastewater on TiO2-coated titanium electrode prepared by electrophoretic deposition
AU - Liu, Ching Fang
AU - Huang, C. P.
AU - Hu, Chi Chang
AU - Juang, Yaju
AU - Huang, Ch-Hpin
N1 - Publisher Copyright:
© 2016 Elsevier B.V. All rights reserved.
PY - 2016/6/13
Y1 - 2016/6/13
N2 - The degradation of azo dye Orange G (OG) on TiO2/Ti electrode was studied using a photoelectrocatalytic system. TiO2/Ti electrode was prepared by electrophoretic deposition (EPD) process. Results of surface analyses, namely, X-ray diffraction (XRD), SEM, X-ray photoelectron spectroscopy (XPS), and linear sweep voltammetry (LSV), revealed that the optimal EPD condition was a deposition potential of 180 V for 1 min and annealed at 350 °C. The TiO2/Ti electrode was used as photoanode and a graphite cathode for the degradation of OG. The coupling effect of photocatalytic and electrochemical oxidation processes was evaluated in terms of the decolorization of OG. The degradation of OG increased in the following increasing order: photocatalysis < electrochemical oxidation < photoelectrochemical degradation. A decolorization of 54.3% was achieved at an applied current density of 75 μA cm-2. The degradation of Orange G follows the first-order kinetics in those three treatment processes, which suggests the participation of OH radicals in the decolorization reaction.
AB - The degradation of azo dye Orange G (OG) on TiO2/Ti electrode was studied using a photoelectrocatalytic system. TiO2/Ti electrode was prepared by electrophoretic deposition (EPD) process. Results of surface analyses, namely, X-ray diffraction (XRD), SEM, X-ray photoelectron spectroscopy (XPS), and linear sweep voltammetry (LSV), revealed that the optimal EPD condition was a deposition potential of 180 V for 1 min and annealed at 350 °C. The TiO2/Ti electrode was used as photoanode and a graphite cathode for the degradation of OG. The coupling effect of photocatalytic and electrochemical oxidation processes was evaluated in terms of the decolorization of OG. The degradation of OG increased in the following increasing order: photocatalysis < electrochemical oxidation < photoelectrochemical degradation. A decolorization of 54.3% was achieved at an applied current density of 75 μA cm-2. The degradation of Orange G follows the first-order kinetics in those three treatment processes, which suggests the participation of OH radicals in the decolorization reaction.
KW - Electrochemical oxidation
KW - Electrophoretic deposition
KW - Orange G
KW - Photocatalysis
KW - Photoelectrocatalysis
UR - http://www.scopus.com/inward/record.url?scp=84962426676&partnerID=8YFLogxK
U2 - 10.1016/j.seppur.2016.03.045
DO - 10.1016/j.seppur.2016.03.045
M3 - Article
AN - SCOPUS:84962426676
SN - 1383-5866
VL - 165
SP - 145
EP - 153
JO - Separation and Purification Technology
JF - Separation and Purification Technology
ER -