Kinetics of aqueous ozone-induced oxidation of some endocrine disruptors

被引:157
作者
Deborde, M
Rabouan, S
Duguet, JP
Legube, B
机构
[1] CNRS, Lab Chim Eau & Environm, UMR 6008, Ecole Super Ingn Poitiers, F-86022 Poitiers, France
[2] Fac Med & Pharm, F-86005 Poitiers, France
[3] SAGEP, Direct Qual & Environm Eau Paris, F-75675 Paris, France
关键词
D O I
10.1021/es0501619
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This study investigated aqueous ozone-induced oxidation of six endocrine disruptors (EDs: 4-n-nonylphenol, bisphenol A, 17 alpha-ethinylestradiol, 17 beta-estradiol, estrone, and estriol). In the first part, ED ozonation kinetics were studied over a pH range of 2.5-10.5 at 20 +/- 2 degrees C and in the presence of tert-butyl alcohol. Under these conditions, for each studied compound, the apparent ozone rates presented minima at acidic pH (PH < 5) and maxima at basic PH (PH > 10). In the second part, to explain this PH dependence, elementary reactions, i.e., reactions of ozone with neutral and ionized ED species, were proposed, and the intrinsic constants of each of them were calculated. The reactivity of ozone with ionized EDs (i.e. 1.06 x 10(9)-6.83 x 10(9) M-1 s(-1)) was found to be 10(4)-10(5) times higher than with neutral EDs (i.e. 1.68 x 10(4) M-1 s(-1)-2.21 x 10(5) M-1 s(-1)). At PH > 5, ozone reacted to the greatest extent with dissociated ED forms. Finally, to assess the potential of ozone for inducing ED oxidation in water treatment conditions, the expected removal rates for each of the studied EDs were determined on the basis of the kinetic study at PH = 7 and 20 +/- 2 degrees C. For all EDs considered, 03 exposures of only similar to 2 x 10(-3) Mg min L-1 were calculated to achieve >= 95% removal efficiency. The ozonation process could thus highly oxidize the studied EDs under water treatment conditions.
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收藏
页码:6086 / 6092
页数:7
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[1]   BEHAVIOR OF ALKYLPHENOL POLYETHOXYLATE SURFACTANTS IN THE AQUATIC ENVIRONMENT .2. OCCURRENCE AND TRANSFORMATION IN RIVERS [J].
AHEL, M ;
GIGER, W ;
SCHAFFNER, C .
WATER RESEARCH, 1994, 28 (05) :1143-1152
[2]   THE RELEVANCE OF THE PRESENCE OF CERTAIN SYNTHETIC STEROIDS IN THE AQUATIC ENVIRONMENT [J].
AHERNE, GW ;
BRIGGS, R .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1989, 41 (10) :735-736
[3]   PHYSIOLOGICAL DISTURBANCES IN FISH LIVING IN COASTAL WATER POLLUTED WITH BLEACHED KRAFT PULP-MILL EFFLUENTS [J].
ANDERSSON, T ;
FORLIN, L ;
HARDIG, J ;
LARSSON, A .
CANADIAN JOURNAL OF FISHERIES AND AQUATIC SCIENCES, 1988, 45 (09) :1525-1536
[4]   DETERMINATION OF OZONE IN WATER BY THE INDIGO METHOD [J].
BADER, H ;
HOIGNE, J .
WATER RESEARCH, 1981, 15 (04) :449-456
[5]   Monitoring natural and synthetic estrogens at activated sludge sewage treatment plants and in a receiving river water [J].
Baronti, C ;
Curini, R ;
D'Ascenzo, G ;
Di Corcia, A ;
Gentili, A ;
Samperi, R .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2000, 34 (24) :5059-5066
[6]   Analysis and occurrence of estrogenic hormones and their glucuronides in surface water and waste water in The Netherlands [J].
Belfroid, AC ;
Van der Horst, A ;
Vethaak, AD ;
Schäfer, AJ ;
Rijs, GBJ ;
Wegener, J ;
Cofino, WP .
SCIENCE OF THE TOTAL ENVIRONMENT, 1999, 225 (1-2) :101-108
[7]   CONCENTRATIONS OF ALKYLPHENOLS IN RIVERS AND ESTUARIES IN ENGLAND AND WALES [J].
BLACKBURN, MA ;
WALDOCK, MJ .
WATER RESEARCH, 1995, 29 (07) :1623-1629
[8]   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
[9]  
CLARKE EGC, 1986, CLARKS ISOLATION IDE
[10]   Fate of natural estrogen conjugates in municipal sewage transport and treatment facilities [J].
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Di Corcia, A ;
Gentili, A ;
Mancini, R ;
Mastropasqua, R ;
Nazzari, M ;
Samperi, R .
SCIENCE OF THE TOTAL ENVIRONMENT, 2003, 302 (1-3) :199-209