Strategies comparison of eliminating the passivation of non-aromatic intermediates in degradation of Orange II by Fe3+/H2O2

被引:19
作者
Chen, Feng [1 ]
Li, Yan
Guo, Liqin
Zhang, Jinlong
机构
[1] E China Univ Sci & Technol, Adv Mat Lab, Shanghai 200237, Peoples R China
关键词
Fenton; Orange II; Non-aromatic intermediate; Aluminum ion; TOC; WEIGHT ORGANIC-ACIDS; FENTON TYPE REAGENTS; AQUEOUS-SOLUTION; AZO-DYE; AROMATIC-COMPOUNDS; HYDROGEN-PEROXIDE; 2,4-DICHLOROPHENOXYACETIC ACID; VISIBLE IRRADIATION; HYDROXYL RADICALS; QUANTUM YIELD;
D O I
10.1016/j.jhazmat.2009.04.007
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The degradation kinetics of Orange II by Fe3+/H2O2 was examined under various conditions in the presence of the non-aromatic organic intermediates such as malonic acid (MA), oxalic acid (OX) and EDTA. Various strategies were adopted to eliminate the passivation of the non-aromatic organic intermediates in the Fenton-like degradation of Orange II. UV irradiation, visible irradiation, hydroquinone (HQ) additive and their hybrid were used to accelerate the decoloration of Orange II; however, some of them were failed to show a good performance in the presence of non-aromatic organics, especially for the mineralization of Orange II. Aluminum ions additive released the ferric ions via a competitive chelation process, and accelerated the reaction obviously. From the decoloration and the mineralization data of Orange II, UV irradiation combined with Al3+ ion additive was regarded as the most favorable strategy for deep mineralization of Orange II by Fe3+/H2O2 in the presence of non-aromatic intermediates. However, by considering the decoloration of Orange H with moderate mineralization, the combination of visible irradiation and Al3+ ion additive might present the best performance. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:711 / 718
页数:8
相关论文
共 39 条
[1]   ECOTOXICOLOGY OF DYESTUFFS - JOINT EFFORT BY INDUSTRY [J].
ANLIKER, R .
ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, 1979, 3 (01) :59-74
[2]   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
[3]   Biological decolorization of the azo dye reactive red 2 under various oxidation-reduction conditions [J].
Beydilli, MI ;
Pavlostathis, SG ;
Tincher, WC .
WATER ENVIRONMENT RESEARCH, 2000, 72 (06) :698-705
[4]   New evidence against hydroxyl radicals as reactive intermediates in the thermal and photochemically enhanced fenton reactions [J].
Bossmann, SH ;
Oliveros, E ;
Göb, S ;
Siegwart, S ;
Dahlen, EP ;
Payawan, L ;
Straub, M ;
Wörner, M ;
Braun, AM .
JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (28) :5542-5550
[5]   Photoformation of low-molecular-weight organic acids from brown water dissolved organic matter [J].
Brinkmann, T ;
Hörsch, P ;
Sartorius, D ;
Frimmel, FH .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2003, 37 (18) :4190-4198
[6]   CRITICAL-REVIEW OF RATE CONSTANTS FOR REACTIONS OF HYDRATED ELECTRONS, HYDROGEN-ATOMS AND HYDROXYL RADICALS (.OH/.O-) IN AQUEOUS-SOLUTION [J].
BUXTON, GV ;
GREENSTOCK, CL ;
HELMAN, WP ;
ROSS, AB .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1988, 17 (02) :513-886
[7]   Fenton degradation of malachite green catalyzed by aromatic additives [J].
Chen, F ;
Ma, WH ;
He, JJ ;
Zhao, JC .
JOURNAL OF PHYSICAL CHEMISTRY A, 2002, 106 (41) :9485-9490
[8]   Photo-Fenton degradation of malachite green catalyzed by aromatic compounds under visible light irradiation [J].
Chen, F ;
He, JJ ;
Zhao, JC ;
Yu, JC .
NEW JOURNAL OF CHEMISTRY, 2002, 26 (03) :336-341
[9]   Role of quinone intermediates as electron shuttles in Fenton and photoassisted Fenton oxidations of aromatic compounds [J].
Chen, RZ ;
Pignatello, JJ .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (08) :2399-2406
[10]   DETERMINATION OF THE QUANTUM YIELD OF THE FERRIOXALATE ACTINOMETER WITH ELECTRICALLY CALIBRATED RADIOMETERS [J].
DEMAS, JN ;
BOWMAN, WD ;
ZALEWSKI, EF ;
VELAPOLDI, RA .
JOURNAL OF PHYSICAL CHEMISTRY, 1981, 85 (19) :2766-2771