Photocatalytic and sonolytic oxidation of acid orange 7 in aqueous solution

被引:122
作者
Velegraki, T
Poulios, I
Charalabaki, M
Kalogerakis, N
Samaras, P
Mantzavinos, D [1 ]
机构
[1] Tech Univ Crete, Dept Environm Engn, GR-73100 Khania, Greece
[2] Aristotle Univ Thessaloniki, Dept Chem, Lab Phys Chem, GR-54006 Thessaloniki, Greece
[3] Technol Educ Inst W Macedonia, Dept Pollut Control Technol, GR-50100 Kozani, Greece
关键词
acid orange 7; intermediates; photocatalysis; toxicity; TiO2; ultrasound; wastewater;
D O I
10.1016/j.apcatb.2005.07.007
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The oxidation of 50 mg/L azodye acid orange 7 (AO7) in water was investigated by means of hotocatalysis in the presence of various semiconducting catalysts and ultrasound irradiation. The UVA-induced photocatalytic degradation over TiO2 anatase suspensions was found to increase with increasing catalyst concentration, decreasing solution pH, as well as in the presence of dissolved oxygen. The presence of 1,4-benzoquinone, sodium azide or sodium chloride in the reaction mixture decreased degradation due to the scavenging of radicals and other reactive moieties. Interestingly, addition of hydrogen peroxide at various concentrations from 21 to 1050 mg/L also inhibited degradation. The sonochemical degradation of AO7 was found to increase with increasing frequency and decreasing temperature. Under similar treatment conditions, ultrasound irradiation resulted in higher conversion than photocatalysis; moreover, the sonochemically irradiated solution consistently contained low aliphatic intermediates, while the photocatalytically treated solution mainly consisted of aromatic intermediates as confirmed by GC-MS analysis. The acute toxicity to marine bacteria V. fischeri decreased following oxidation with either process. Furthermore, deep sonochemical treatment slightly improved the aerobic biodegradability as assessed by shake flask tests. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:159 / 168
页数:10
相关论文
共 30 条
[1]   Sonochemistry: Environmental science and engineering applications [J].
Adewuyi, YG .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2001, 40 (22) :4681-4715
[2]   Fenton oxidation of reactive black 5: Effect of mixing intensity and reagent addition strategy [J].
Aris, A ;
Sharratt, PN .
ENVIRONMENTAL TECHNOLOGY, 2004, 25 (05) :601-612
[3]   Azo-dyes photocatalytic degradation in aqueous suspension of TiO2 under solar irradiation [J].
Augugliaro, V ;
Baiocchi, C ;
Prevot, AB ;
García-López, E ;
Loddo, V ;
Malato, S ;
Marcí, G ;
Palmisano, L ;
Pazzi, M ;
Pramauro, E .
CHEMOSPHERE, 2002, 49 (10) :1223-1230
[4]   Enhancing sonochemical activity in aqueous media using power-modulated pulsed ultrasound: an initial study [J].
Casadonte, DJ ;
Flores, M ;
Petrier, C .
ULTRASONICS SONOCHEMISTRY, 2005, 12 (03) :147-152
[5]  
CHEN LC, 1993, J MOL CATAL, V85, P201
[6]   UV-induced photocatalytic degradation of azo dyes by organic-capped ZnO nanocrystals immobilized onto substrates [J].
Comparelli, R ;
Fanizza, E ;
Curri, ML ;
Cozzoli, PD ;
Mascolo, G ;
Agostiano, A .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2005, 60 (1-2) :1-11
[7]   Photocatalytic degradation of azo dyes by organic-capped anatase TiO2 nanocrystals immobilized onto substrates [J].
Comparelli, R ;
Fanizza, E ;
Curri, ML ;
Cozzoli, PD ;
Mascolo, G ;
Passino, R ;
Agostiano, A .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2005, 55 (02) :81-91
[8]   Decolorization of orange II by electrocoagulation method [J].
Daneshvar, N ;
Ashassi-Sorkhabi, H ;
Tizpar, A .
SEPARATION AND PURIFICATION TECHNOLOGY, 2003, 31 (02) :153-162
[9]   Semiconductor-sensitized photodegradation of dichlorvos in water using TiO2 and ZnO as catalysts [J].
Evgenidou, E ;
Fytianos, K ;
Poulios, I .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2005, 59 (1-2) :81-89
[10]   Degradation of azo-dye Orange II by a photoassisted Fenton reaction using a novel composite of iron oxide and silicate nanoparticles as a catalyst [J].
Feng, JY ;
Hu, XJ ;
Yue, PL ;
Zhu, HY ;
Lu, GQ .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2003, 42 (10) :2058-2066