Kinetic and chemical assessment of the UV/H2O2 treatment of antiepileptic drug carbamazepine

被引:297
作者
Vogna, D
Marotta, R
Andreozzi, R
Napolitano, A
d'Ischia, M
机构
[1] Univ Naples Federico II, Dept Organ Chem & Biochem, I-80126 Naples, Italy
[2] Univ Naples Federico II, Dept Chem Engn, I-80125 Naples, Italy
关键词
acridine; AOP; carbamazepine; mineralization; oxidation; UV/H2O2;
D O I
10.1016/S0045-6535(03)00757-4
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The UV/H2O2-induced degradation of carbamazepine, a worldwide used antiepileptic drug, recently found as contaminant in many municipal sewage treatment plant (STP) effluents and other aquatic environments, is investigated. The oxidation treatment caused an effective removal of the drug. At complete abatement of the substrate after 4 min treatment, a 35% value of removed total organic carbon (TOC) was obtained. A kinetic constant of (2.05 +/- 0.14) x 10(9) 1 mol(-1) s(-1) was determined for OH radical attack to carbamazepine in the UV/H2O2 process. Preparative TLC of the reaction mixture led to the isolation of acridine-9-carboxaldehyde as a reaction intermediate. HPLC and GC/MS analysis indicated formation of small amounts of acridine, salicylic acid, catechol and anthranilic acid among the reaction products. Under the same reaction conditions, synthetically prepared 10,11-epoxycarbamazepine was easily degraded to acridine as main product, suggesting that this epoxide is a likely intermediate in the oxidative conversion of carbamazepine to acridine. Under sunlight irradiation, carbamazepine in water underwent slow degradation to afford likewise acridine as main product. In view of the mutagenic properties of acridine, these results would raise important issues concerning the possible environmental impact of carbamazepine release through domestic wastewaters and support the importance of prolonged oxidation treatments to ensure complete degradation of aromatic intermediates. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:497 / 505
页数:9
相关论文
共 30 条
[1]   Advanced oxidation of phenolic compounds [J].
Alnaizy, R ;
Akgerman, A .
ADVANCES IN ENVIRONMENTAL RESEARCH, 2000, 4 (03) :233-244
[2]   Pharmaceuticals in STP effluents and their solar photodegradation in aquatic environment [J].
Andreozzi, R ;
Marotta, R ;
Paxeus, N .
CHEMOSPHERE, 2003, 50 (10) :1319-1330
[3]   Advanced oxidation processes (AOP) for water purification and recovery [J].
Andreozzi, R ;
Caprio, V ;
Insola, A ;
Marotta, R .
CATALYSIS TODAY, 1999, 53 (01) :51-59
[4]   Carbamazepine in water: persistence in the environment, ozonation treatment and preliminary assessment on algal toxicity [J].
Andreozzi, R ;
Marotta, R ;
Pinto, G ;
Pollio, A .
WATER RESEARCH, 2002, 36 (11) :2869-2877
[5]   THE PHOTOLYSIS OF HYDROGEN PEROXIDE AT HIGH LIGHT INTENSITIES [J].
BAXENDALE, JH ;
WILSON, JA .
TRANSACTIONS OF THE FARADAY SOCIETY, 1957, 53 (03) :344-356
[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]   REACTION OF 5H-DIBENZ[B,F]AZEPINE WITH TERT-BUTYL HYPOCHLORITE - AN AROMATIC NITRENIUM ION INTERMEDIATE [J].
CANN, MC ;
LEZINSKY, D .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 1988, 25 (03) :863-865
[8]   Pharmaceuticals and personal care products in the environment: Agents of subtle change? [J].
Daughton, CG ;
Ternes, TA .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1999, 107 :907-938
[9]   GAS-CHROMATOGRAPHIC DEGRADATION OF SEVERAL DRUGS AND THEIR METABOLITES [J].
FRIGERIO, A ;
BAKER, KM ;
BELVEDERE, G .
ANALYTICAL CHEMISTRY, 1973, 45 (11) :1846-1851
[10]   CARBAMAZEPINE METABOLISM TO A REACTIVE INTERMEDIATE BY THE MYELOPEROXIDASE SYSTEM OF ACTIVATED NEUTROPHILS [J].
FURST, SM ;
UETRECHT, JP .
BIOCHEMICAL PHARMACOLOGY, 1993, 45 (06) :1267-1275