Triclosan reactivity chloraminated waters

被引:52
作者
Greyshock, AE [1 ]
Vikesland, PJ [1 ]
机构
[1] Virginia Polytech Inst & State Univ, Dept Civil & Environm Engn, Blacksburg, VA 24060 USA
关键词
D O I
10.1021/es051952d
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Triclosan, widely employed as an antimicrobial additive in many household personal care products, has recently been detected in wastewater treatment plant effluents and in source waters used for drinking water supplies. Chloramines used either as alternative disinfectants in drinking water treatment or formed during chlorination of nonnitrified wastewater effluents have the potential to react with triclosan. This study examined triclosan reactivity in chloraminated waters over the pH range of 6.5-10.5. Experimental and modeling results show that monochloramine directly reacts with the phenolate form of triclosan; however, the reaction is relatively slow as evinced by the second-order rate constant k(Ar0-NH2Cl) = 0.025 M-1 s(-1). Kinetic modeling indicates that for pH values less than 9.5, reactions between triclosan and two monochloramine autodecomposition intermediates, hypochlorous acid (k(Ar0-HOCl) = 5.4 x 10(3) M-1 s(-1)) and dichloramine (k(Ar0-NHCl2) = 60 M-1 s(-1)), are responsible for a significant percentage of the observed triclosan decay. The products of these reactions include three chlorinated triclosan byproducts as well as 2,4- dichlorophenol and 2,4,6-trichlorophenol. Low levels of chloroform were detected after 1 week at pH values of 6.5 and 7.5. The slow reactivity of triclosan in the presence of chloramines explains the recalcitrance of this species in nonnitrified wastewater effluents.
引用
收藏
页码:2615 / 2622
页数:8
相关论文
共 41 条
[1]   Evaluation of triclosan and biphenylol in marine sediments and urban wastewaters by pressurized liquid extraction and solid phase extraction followed by gas chromatography mass spectrometry and liquid chromatography mass spectrometry [J].
Agüera, A ;
Fernández-Alba, AR ;
Piedra, L ;
Mézcua, M ;
Gómez, MJ .
ANALYTICA CHIMICA ACTA, 2003, 480 (02) :193-205
[2]   Production of macromolecular chloramines by chlorine-transfer reactions [J].
Bedner, M ;
MacCrehan, WA ;
Helz, GR .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2004, 38 (06) :1753-1758
[3]   Fate of triclosan and triclosan-methyl in sewage treatment plants and surface waters [J].
Bester, K .
ARCHIVES OF ENVIRONMENTAL CONTAMINATION AND TOXICOLOGY, 2005, 49 (01) :9-17
[4]   Transformation of the antibacterial agent sulfamethoxazole in reactions with chlorine: Kinetics mechanisms, and pathways [J].
Dodd, MC ;
Huang, CH .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2004, 38 (21) :5607-5615
[5]  
DODD MC, 2005, ENV SCI TECHNOL, V39
[6]   Modeling monochloramine loss in the presence of natural organic matter [J].
Duirk, SE ;
Gombert, B ;
Croué, JP ;
Valentine, RL .
WATER RESEARCH, 2005, 39 (14) :3418-3431
[7]   Chlorination of phenols: Kinetics and formation of chloroform [J].
Gallard, H ;
Von Gunten, U .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2002, 36 (05) :884-890
[8]  
Greenberg A. E., 1992, STANDARD METHODS EXA
[9]   KINETICS AND MECHANISMS OF THE DECOMPOSITION OF DICHLORAMINE IN AQUEOUS-SOLUTION [J].
HAND, VC ;
MARGERUM, DW .
INORGANIC CHEMISTRY, 1983, 22 (10) :1449-1456
[10]   Investigations of the reactions of monochloramine and dichloramine with selected phenols: Examination of humic acid models and water contaminants [J].
Heasley, VL ;
Fisher, AM ;
Herman, EE ;
Jacobsen, FE ;
Miller, EW ;
Ramirez, AM ;
Royer, NR ;
Whisenand, JM ;
Zoetewey, DL ;
Shellhamer, DF .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2004, 38 (19) :5022-5029