Design and electrochemical study of SnO2-based mixed oxide electrodes

被引:153
作者
Adams, Brian [1 ]
Tian, Min [1 ]
Chen, Aicheng [1 ]
机构
[1] Lakehead Univ, Dept Chem, Thunder Bay, ON P7B 5E1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Nitrophenols; Electrochemical oxidation; Tin oxide; Mixed metal oxides; In situ UV/vis spectroscopy; WASTE-WATER TREATMENT; HIGH OVERVOLTAGE ANODES; P-NITROPHENOL; ELECTROCATALYTIC OXIDATION; ORGANIC POLLUTANTS; AQUEOUS-SOLUTIONS; PBO2; ELECTRODES; DEGRADATION; PHENOL; KINETICS;
D O I
10.1016/j.electacta.2008.09.034
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
For the electrochemical treatment of wastewater, it is critical to develop electrodes with a high activity for the oxidation of pollutants, long lifetimes, and low cost. In the present study. we have fabricated four different SnO2-based electrodes (Ti/SnO2-Sb2O5, Ti/SnO2-Sb2O5-PtOx, Ti/SnO2-Sb2O5-RuO2 and Ti/SnO2-Sb2O5-IrO2) using the thermal decomposition method and, for the first time, systemically Studied their stability and electrocatalytic activity towards the degradation of 2-nitrophenol (2-NPh), 3-nitrophenol (3-NPh) and 4-nitrophenol (4-NPh). Scanning electron microscope (SEM) and X-ray energy dispersive spectrometry (EDS) were used to characterize the morphology and composition of the four different SnO2-based electrocatalysts. Lifetime tests show that doping IrO2 or RuO2 greatly improves the stability of the SnO2-based electrodes. The electrochemical activities of the prepared SnO2-based electrodes were characterized using the degradation of 2-NPh, 3-NPh and 4-NPh. In situ UV/vis spectroscopy was used to monitor the concentration changes of the nitrophenols with time showing that the rate constants for the electrochemical oxidation of the nitrophenols decrease in the order of: 2-NPh > 4-NPh > 3-NPh. The effect of the applied Current densities and initial concentrations of nitrophenols have also been investigated. Our study has shown that the fabricated Ti/SnO2-Sb2O5-IrO2 electrodes are very promising for the electrochemical treatment ofwastewater. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1491 / 1498
页数:8
相关论文
共 43 条
[1]   Electrochemical oxidation of phenol using graphite anodes [J].
Awad, YM ;
Abuzaid, NS .
SEPARATION SCIENCE AND TECHNOLOGY, 1999, 34 (04) :699-708
[2]   A comparison of the electrooxidation kinetics of p-methoxyphenol and p-nitrophenol on Sb-doped SnO2 surfaces:: Concentration and temperature effects [J].
Borras, C. ;
Berzoy, C. ;
Mostany, J. ;
Herrera, J. C. ;
Scharifker, B. R. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2007, 72 (1-2) :98-104
[3]   Study of the oxidation of solutions of p-chlorophenol and p-nitrophenol on Bi-doped PbO2 electrodes by UV-Vis and FTIR in situ spectroscopy [J].
Borrás, C ;
Laredo, T ;
Mostany, J ;
Scharifker, BR .
ELECTROCHIMICA ACTA, 2004, 49 (04) :641-648
[4]   Electrochemical oxidation of phenolic wastes with boron-doped diamond anodes [J].
Cañizares, P ;
Lobato, J ;
Paz, R ;
Rodrigo, MA ;
Sáez, C .
WATER RESEARCH, 2005, 39 (12) :2687-2703
[5]   Influence of a nanoscale gold thin layer on Ti/SnO2-Sb2O5 electrodes [J].
Chen, AC ;
Nigro, S .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (48) :13341-13348
[6]   Investigation of Ti/IrO2-Sb2O5-SnO2 electrodes for O2 evolution [J].
Chen, XM ;
Chen, GH .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2005, 152 (07) :J59-J64
[7]   Comparison of Ti/BDD and Ti/SnO2-Sb2O5 electrodes for pollutant oxidation [J].
Chen, XM ;
Gao, FR ;
Chen, GH .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 2005, 35 (02) :185-191
[8]   Stable Ti/IrOx-Sb2O5-SnO2 anode for O2 evolution with low Ir content [J].
Chen, XM ;
Chen, GH ;
Yue, PL .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (20) :4623-4628
[9]   Electrocatalysis in anodic oxidation of organics with simultaneous oxygen evolution [J].
Comninellis, C ;
DeBattisti, A .
JOURNAL DE CHIMIE PHYSIQUE ET DE PHYSICO-CHIMIE BIOLOGIQUE, 1996, 93 (04) :673-679
[10]   Service life of Ti/SnO2-Sb2O5 anodes [J].
CorreaLozano, B ;
Comninellis, C ;
DeBattisti, A .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1997, 27 (08) :970-974