Degradation of p-hydroxyphenylacetic acid by photoassisted Fenton reaction

被引:13
作者
Acero, JL [1 ]
Benítez, FJ [1 ]
Real, FJ [1 ]
Leal, AI [1 ]
机构
[1] Univ Extremadura, Dept Ingn Quim & Energet, E-06071 Badajoz, Spain
关键词
Fenton's reagent; OH radicals; photo-Fenton system; p-hydroxyphenylacetic acid;
D O I
10.2166/wst.2001.0245
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The chemical decomposition of p-hydroxyphenylacetic acid, a phenolic pollutant present in agroindustrial plant effluents, has been investigated by means of the Fenton's reaction and the photoassisted Fenton's reaction, the so-called photo-Fenton system. The degradation levels achieved have been compared to those obtained by applying other Advanced Oxidation Processes, such as the combination UV/H2O2. The optimum pH to carry out the decomposition of this organic compound by either Fenton or photo-Fenton systems was found to be pH = 3. The presence of buffers such as phosphate impedes these processes due to the formation of ferric complexes. A reaction mechanism, which allows calculating the contribution of the radical reaction to the global process, has been proposed, According to this mechanism, the dominant way of degradation of p-hydroxyphenylacetic acid is through its reaction with the OH radicals originated in the photolysis of H2O2 and, especially, in the Fenton's reaction.
引用
收藏
页码:31 / 38
页数:8
相关论文
共 19 条
[1]   PHOTOMETRIC-METHOD FOR THE DETERMINATION OF LOW CONCENTRATIONS OF HYDROGEN-PEROXIDE BY THE PEROXIDASE CATALYZED OXIDATION OF N,N-DIETHYL-P-PHENYLENEDIAMINE (DPD) [J].
BADER, H ;
STURZENEGGER, V ;
HOIGNE, J .
WATER RESEARCH, 1988, 22 (09) :1109-1115
[2]  
BALICE V., 1990, RIV ITAL SOSTANZE GR, V67, P9
[3]  
BALZANI CH, 1970, PHOTOCHEMISTRY COORD
[4]   ACUCHEM - A COMPUTER-PROGRAM FOR MODELING COMPLEX CHEMICAL-REACTION SYSTEMS [J].
BRAUN, W ;
HERRON, JT ;
KAHANER, DK .
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 1988, 20 (01) :51-62
[5]   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
[6]   OZONE OXIDATION OF COMPOUNDS RESISTANT TO BIOLOGICAL DEGRADATION [J].
CALVOSA, L ;
MONTEVERDI, A ;
RINDONE, B ;
RIVA, G .
WATER RESEARCH, 1991, 25 (08) :985-993
[7]   Chemical degradation of aromatic amines by Fenton's reagent [J].
Casero, I ;
Sicilia, D ;
Rubio, S ;
PerezBendito, D .
WATER RESEARCH, 1997, 31 (08) :1985-1995
[8]   A kinetic model for H2O2/UV process in a completely mixed batch reactor [J].
Crittenden, JC ;
Hu, SM ;
Hand, DW ;
Green, SA .
WATER RESEARCH, 1999, 33 (10) :2315-2328
[9]   Effect of pH on the oxidation rate of organic compounds by FeII/H2O2.: Mechanisms and simulation [J].
Gallard, H ;
de Laat, J ;
Legube, B .
NEW JOURNAL OF CHEMISTRY, 1998, 22 (03) :263-268
[10]   ADVANCED OXIDATION PROCESSES - A KINETIC-MODEL FOR THE OXIDATION OF 1,2-DIBROMO-3-CHLOROPROPANE IN WATER BY THE COMBINATION OF HYDROGEN-PEROXIDE AND UV-RADIATION [J].
GLAZE, WH ;
LAY, Y ;
KANG, JW .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1995, 34 (07) :2314-2323