Sonochemical degradation of azo dyes in aqueous solution: a new heterogeneous kinetics model taking into account the local concentration of OH radicals and azo dyes

被引:224
作者
Okitsu, K
Iwasaki, K
Yobiko, Y
Bandow, H
Nishimura, R
Maeda, Y
机构
[1] Osaka Prefecture Univ, Grad Sch Engn, Dept Appl Mat Sci, Sakai, Osaka 5998531, Japan
[2] Technol Res Inst Osaka Prefecture, Osaka 5941157, Japan
关键词
sonochemical degradation; azo dye; C. I. reactive red 22; methyl orange; heterogeneous reaction kinetics;
D O I
10.1016/j.ultsonch.2004.01.038
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
The sonochemical decolorization and decomposition of azo dyes, such as C. I. Reactive Red 22 and methyl orange, were performed from the viewpoints of wastewater treatment and to determine the reaction kinetics. A low concentration of the azo dye solution was irradiated with a 200 kHz and 1.25 W/cm(2) ultrasound in a homogeneous aqueous solution. The azo dye solutions were readily decolorized by the irradiation. The sonochemical decolorization was also depressed by the addition of the t-butyl alcohol radical scavenger. These results indicated that azo dye molecules were mainly decomposed by OH radicals formed from the water sonolysis. In this paper, we propose a new kinetics model taking into account the heterogeneous reaction kinetics similar to a Langmuir-Hinshelwood mechanism or an Eley-Rideal mechanism. The proposed kinetics model is based on the local reaction site at the interface region of the cavitation bubbles, where azo dye molecules are quickly decomposed because an extremely high concentration of OH radicals exists in this region. To confirm the proposed kinetics model, the effects of the initial concentration of azo dyes, irradiated atmosphere and pH on the decomposition rates were investigated. The obtained results were in good agreement with the proposed kinetics model. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:255 / 262
页数:8
相关论文
共 32 条
[1]   Sonochemistry: Environmental science and engineering applications [J].
Adewuyi, YG .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2001, 40 (22) :4681-4715
[2]   The effect of pH on multibubble sonoluminescence from aqueous solutions containing simple organic weak acids and bases [J].
Ashokkumar, M ;
Mulvaney, P ;
Grieser, F .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (32) :7355-7359
[3]  
Crum LA., 1999, Sonochemistry And Sonoluminescence, DOI DOI 10.1007/978-94-015-9215-4
[4]   Sonochemical destruction of trichloroethylene in water [J].
Cyr, PJ ;
Paraskewich, MR ;
Suri, RPS .
WATER SCIENCE AND TECHNOLOGY, 1999, 40 (4-5) :131-136
[5]   Synergistic effects of sonolysis combined with ozonolysis for the oxidation of azobenzene and methyl orange [J].
Destaillats, H ;
Colussi, AJ ;
Joseph, JM ;
Hoffmann, MR .
JOURNAL OF PHYSICAL CHEMISTRY A, 2000, 104 (39) :8930-8935
[6]   Molecular structure effects on the kinetics of hydroxyl radical addition to azo dyes [J].
Destaillats, H ;
Turjanski, AG ;
Estrin, DA ;
Hoffmann, MR .
JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, 2002, 15 (05) :287-292
[7]   Hot spot conditions during cavitation in water [J].
Didenko, YT ;
McNamara, WB ;
Suslick, KS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (24) :5817-5818
[8]   RADICAL SCAVENGING IN THE SONOLYSIS OF AQUEOUS-SOLUTIONS OF I-, BR-, AND N3- [J].
GUTIERREZ, M ;
HENGLEIN, A ;
IBANEZ, F .
JOURNAL OF PHYSICAL CHEMISTRY, 1991, 95 (15) :6044-6047
[9]   SCAVENGING OF OH RADICALS PRODUCED IN THE SONOLYSIS OF WATER [J].
HENGLEIN, A ;
KORMANN, C .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1985, 48 (02) :251-258
[10]  
HIRAI K, 1996, ULTRASON SONOCHEM, V3, P205