Photodegradation processes of the Antiepileptic drug carbamazepine, relevant to estuarine waters

被引:246
作者
Chiron, Serge
Minero, Claudio
Vione, Davide
机构
[1] Univ Aix Marseille 1, Lab Chim & Environm, F-13331 Marseille 3, France
[2] Univ Turin, Dipartimento Chim Analit, I-10125 Turin, Italy
关键词
D O I
10.1021/es060502y
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The photodegradation of carbamazepine was studied in artificial estuarine water, under conditions relevant to the Rhone delta. Chloride substantially enhances the photodegradation of carbamazepine, most likely because of the interaction between Fe(III) colloids and Cl- ions under irradiation, yielding Cl-2(center dot-). For a given compound, prerequisites for the described degradation enhancement by chloride to be significant are faster degradation via reaction with Cl-2(center dot-) compared to charge-transfer processes on the surface of Fe(III) colloids and an important role of indirect phototransformation compared to direct photolysis. A major photodegradation intermediate of carbamazepine is acridine, formed by direct photolysis, while hydroxylated/oxidized compounds are formed in the presence of (OH)-O-center dot, and chloroderivative formation is observed in the presence of Fe(III) and chloride.
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收藏
页码:5977 / 5983
页数:7
相关论文
共 47 条
[1]  
BOULE P, 2005, ENV PHOTOCHEMISTRY 1, V2
[2]   MECHANISM OF IRON REMOVAL IN ESTUARIES [J].
BOYLE, EA ;
EDMOND, JM ;
SHOLKOVITZ, ER .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1977, 41 (09) :1313-1324
[3]   Nitrate-induced photolysis in natural waters: Controls on concentrations of hydroxyl radical photo-intermediates by natural scavenging agents [J].
Brezonik, PL ;
Fulkerson-Brekken, J .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1998, 32 (19) :3004-3010
[4]   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
[5]   Photoinduced halophenol formation in the presence of iron(III) species or cadmium sulfide [J].
Calza, P ;
Maurino, V ;
Minero, C ;
Pelizzetti, E ;
Sega, M ;
Vincenti, A .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2005, 170 (01) :61-67
[6]   Photosensitizer method to determine rate constants for the reaction of carbonate radical with organic compounds [J].
Canonica, S ;
Kohn, T ;
Mac, M ;
Real, FJ ;
Wirz, J ;
Von Gunten, U .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2005, 39 (23) :9182-9188
[7]   Quantitative structure-activity relationships for oxidation reactions of organic chemicals in water [J].
Canonica, S ;
Tratnyek, PG .
ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY, 2003, 22 (08) :1743-1754
[8]   Electron-rich phenols for probing the photochemical reactivity of freshwaters [J].
Canonica, S ;
Freiburghaus, M .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (04) :690-695
[9]   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
[10]   Photosensitized degradation of bisphenol a by dissolved organic matter [J].
Chin, YP ;
Miller, PL ;
Zeng, LK ;
Cawley, K ;
Weavers, LK .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2004, 38 (22) :5888-5894