Gliding arc plasma assisted photocatalytic degradation of anthraquinonic acid green 25 in solution with TiO2

被引:83
作者
Ghezzar, M. R. [1 ]
Abdelmalek, F. [1 ]
Belhadj, M. [1 ]
Benderdouche, N. [1 ]
Addou, A. [1 ]
机构
[1] Univ Mostaganem, Fac Sci Ingn, Lab Sci & Tech Environm & Valorisat, Mostaganem 27000, Algeria
关键词
anthraquinonic dye; degradation; gliding arc; plasmacatalysis; TiO2;
D O I
10.1016/j.apcatb.2006.11.008
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
Anthraquinonic acid green 25 (AG 25) removal was investigated by plasmachemistry using non-thermal gliding arc at atmospheric pressure. The gaseous species formed in the discharge, and especially OH center dot radicals, induce strong oxidizing effects in the target solution. The removal of the dye was carried out in the absence and presence of TiO2 as photocatalyst. The decolourization of AG 25 was followed by UV-vis spectrometry (at 643 nm), while the degradation was followed by COD measurements. The effects, of operating variables such as initial concentration of AG 25 and catalyst concentration were investigated. Experiments were carried out to optimise the amount of TiO2. The results showed that maximum degradation was attained for 2 g L-1 TiO2 concentration. At this optimum concentration, the dye (80 mu M) was totally decolourized within 15 min of plasma-treatment time, and 93% removal of initial COD was attained after a 180-min plasma-treatment time. In the absence of catalyst, colour removal was 46% after 15 min, while COD abatement reached 84% after 180 min. The extent of degradation decreased with initial concentration and the time required for complete degradation increased. In all cases, the plasma-treated samples in the presence or absence of catalyst were found to follow pseudo-first order reaction kinetics. The TiO2-mediated plasmachemical process showed potential application for the treatment of dye solutions, resulting in the mineralization of the dye confirmed by sulfate ion formation. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:304 / 313
页数:10
相关论文
共 38 条
[1]   Bleaching and degradation of textile dyes by nonthermal plasma process at atmospheric pressure [J].
Abdelmalek, F ;
Ghezzar, MR ;
Belhadj, M ;
Addou, A ;
Brisset, JL .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2006, 45 (01) :23-29
[2]   Plasmachemical degradation of azo dyes by humid air plasma: Yellow Supranol 4 GL, Scarlet Red Nylosan F3 GL and industrial waste [J].
Abdelmalek, F ;
Gharbi, S ;
Benstaali, B ;
Addou, A ;
Brisset, JL .
WATER RESEARCH, 2004, 38 (09) :2339-2347
[3]   Advanced chemical oxidation of reactive dyes in simulated dyehouse effluents by ferrioxalate-Fenton/UV-A and TiO2/UV-A processes [J].
Arslan, I ;
Balcioglu, IA ;
Bahnemann, DW .
DYES AND PIGMENTS, 2000, 47 (03) :207-218
[4]   Degradation/decoloration of concentrated solutions of Orange II. Kinetics and quantum yield for sunlight induced reactions via Fenton type reagents [J].
Bandara, J ;
Morrison, C ;
Kiwi, J ;
Pulgarin, C ;
Peringer, P .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1996, 99 (01) :57-66
[5]   Density and rotational temperature measurements of the OH° and NO° radicals produced by a gliding arc in humid air [J].
Benstaali, B ;
Boubert, P ;
Cheron, BG ;
Addou, A ;
Brisset, JL .
PLASMA CHEMISTRY AND PLASMA PROCESSING, 2002, 22 (04) :553-571
[6]   Heterogeneous photocatalytic degradation of the anthraquinonic dye, Acid Blue 25 (AB25): a kinetic approach [J].
Bouzaida, I ;
Ferronato, C ;
Chovelon, JM ;
Rammah, ME ;
Herrmann, JM .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2004, 168 (1-2) :23-30
[7]  
Brisset, 2005, ORIENT J CHEM, V21, P21
[8]   Reducing degradation of azo dye by zero-valent iron in aqueous solution [J].
Cao, JS ;
Wei, LP ;
Huang, QG ;
Wang, LS ;
Han, SK .
CHEMOSPHERE, 1999, 38 (03) :565-571
[9]  
Cisneros RL, 2002, CHEMOSPHERE, V48, P393
[10]   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