TY - JOUR
T1 - Application of a novel semiconductor catalyst, CT, in degradation of aromatic pollutants in wastewater
T2 - Phenol and catechol
AU - Chen, Xiao
AU - Zhang, Yanling
AU - Zhou, Xuefei
AU - Ichimura, Shoji
AU - Tong, Guoxiu
AU - Chen, Xi
AU - ZHOU, Qiming
AU - Wang, Wenzhao
AU - Liang, Yan
N1 - Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 2014
Y1 - 2014
N2 - Water-soluble phenol and phenolic compounds were generally removed via advanced oxidation processes. A novel semiconductor catalyst, CT, was the first-time employed in the present study to degrade phenol and catechol. The phenolic compounds (initial concentration of 88 mg L-1) were completely mineralized by the CT catalytic nanoparticles (1%) within 15 days, under acidic condition and with the presence of mild UV radiation (15 w, the emitted wavelength is 254 nm and the light intensity <26 μw/cm 2). Under the same reaction condition, 1% TiO2 (mixture of rutile and anatase, nanopowder, <100 nm) and H2O2 had lower removal efficiency (phenol: <42%; catechol: <60%), whereas the control (without addition of catalysts/H2O2) only showed <12% removal. The processes of phenol/catechol removal by CT followed pseudo-zero-order kinetics. The aromatic structures absorbed the UV energy and passed to an excited state, which the CT worked on. The pollutants were adsorbed on the CT's surface and oxidized via charge-transfer and hydroxyl radical generation by CT. Given low initial concentrations, a circumstance encountered in wastewater polishing, the current set-up should be an efficient and less energy- and chemical-consumptive treatment method.
AB - Water-soluble phenol and phenolic compounds were generally removed via advanced oxidation processes. A novel semiconductor catalyst, CT, was the first-time employed in the present study to degrade phenol and catechol. The phenolic compounds (initial concentration of 88 mg L-1) were completely mineralized by the CT catalytic nanoparticles (1%) within 15 days, under acidic condition and with the presence of mild UV radiation (15 w, the emitted wavelength is 254 nm and the light intensity <26 μw/cm 2). Under the same reaction condition, 1% TiO2 (mixture of rutile and anatase, nanopowder, <100 nm) and H2O2 had lower removal efficiency (phenol: <42%; catechol: <60%), whereas the control (without addition of catalysts/H2O2) only showed <12% removal. The processes of phenol/catechol removal by CT followed pseudo-zero-order kinetics. The aromatic structures absorbed the UV energy and passed to an excited state, which the CT worked on. The pollutants were adsorbed on the CT's surface and oxidized via charge-transfer and hydroxyl radical generation by CT. Given low initial concentrations, a circumstance encountered in wastewater polishing, the current set-up should be an efficient and less energy- and chemical-consumptive treatment method.
UR - http://www.scopus.com/inward/record.url?scp=84899928199&partnerID=8YFLogxK
U2 - 10.1155/2014/524141
DO - 10.1155/2014/524141
M3 - Journal article
AN - SCOPUS:84899928199
SN - 1687-4110
VL - 2014
JO - Journal of Nanomaterials
JF - Journal of Nanomaterials
M1 - 524141
ER -