Hydroxyl radical initiated photodegradation of 4-chloro-3,5-dinitrobenzoic acid in aqueous solution

被引:38
作者
Lopez, JL
Einschlag, FSG
González, MC
Capparelli, AL
Oliveros, E
Hashem, TM
Braun, AM
机构
[1] Natl Univ La Plata, Fac Ciencias Exactas, Inst Invest Fisicoquim Teor & Aplicadas, RA-1900 La Plata, Argentina
[2] Univ Karlsruhe, Engler Bunte Inst, Lehrstuhl Umweltmesstech, D-76128 Karlsruhe, Germany
关键词
advanced oxidation processes (AOP); chloronitro aromatic compounds; hydroxyl radical; UV/H2O2; process; VUV photolysis; excimer lamps;
D O I
10.1016/S1010-6030(00)00357-9
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 photodegradation of 4-chloro-3,5-dinitrobenzoic acid (CDNBA) in aqueous solution was investigated using advanced oxidation processes (AOP) involving hydroxyl radical production: (i) UV-C photolysis of H2O2 using low or medium pressure Hg arcs (UV/H2O2 process) and (ii) vacuum ultraviolet (VUV) photolysis of water at 185 nm (low pressure Hg are with Suprasil envelope) and at 172 nm (Xe-excimer lamp). These processes were shown to be efficient methods for CDNBA mineralization, in contrast to CDNBA photolysis. For the UV/H2O2 process, the optimal concentration of H2O2 leading to the fastest degradation rate could be evaluated as a function of the initial CDNBA concentration using a simplified equation based on the main reactions involved in the first stages of the degradation process. Chloride ions were produced at the same rate as CDNBA was depleted, independently of the method used for the production of hydroxyl radicals. In contrast, the production of nitrate and nitrite ions was strongly process dependent, the differences being related to the formation of primary reducing intermediates by VUV photolysis of water. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:177 / 184
页数:8
相关论文
共 36 条
[21]   VUV-photolysis of aqueous systems: Spatial differentiation between volumes of primary and secondary reactions [J].
Heit, G ;
Braun, AM .
WATER SCIENCE AND TECHNOLOGY, 1997, 35 (04) :25-30
[22]   Vacuum-UV (172 nm) actinometry. The quantum yield of the photolysis of water [J].
Heit, G ;
Neuner, A ;
Saugy, PY ;
Braun, AM .
JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (28) :5551-5561
[23]  
HEIT G, 1997, THESIS U KARLSRUHE T
[24]   PHOTOOXIDATION OF 2,4-DINITROTOLUENE IN AQUEOUS-SOLUTION IN THE PRESENCE OF HYDROGEN-PEROXIDE [J].
HO, PC .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1986, 20 (03) :260-267
[25]   VACUUM-ULTRAVIOLET (VUV) PHOTOLYSIS OF WATER - OXIDATIVE-DEGRADATION OF 4-CHLOROPHENOL [J].
JAKOB, L ;
HASHEM, TM ;
BURKI, S ;
GUINDY, NM ;
BRAUN, AM .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1993, 75 (02) :97-103
[26]  
Jakob L., 1992, THESIS ECOLE POLYTEC
[27]   PHOTOCHEMICAL PROCESSES FOR WATER-TREATMENT [J].
LEGRINI, O ;
OLIVEROS, E ;
BRAUN, AM .
CHEMICAL REVIEWS, 1993, 93 (02) :671-698
[28]   FORMATION OF CONDENSATION PRODUCTS IN ADVANCED OXIDATION TECHNOLOGIES - THE PHOTOCATALYTIC DEGRADATION OF DICHLOROPHENOLS ON TIO2 [J].
MINERO, C ;
PELIZZETTI, E ;
PICHAT, P ;
SEGA, M ;
VINCENTI, M .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1995, 29 (09) :2226-2234
[29]  
NETA P, 1968, ADV CHEM SER, P222
[30]  
OLLIS DF, 1999, P 5 INT C ADV OX TEC