Direct detection of trace haloacetates in drinking water using microbore ion chromatography - Improved detector sensitivity using a hydroxide gradient and a monolithic ion-exchange type suppressor

被引:15
作者
Barron, L [1 ]
Paull, B [1 ]
机构
[1] Dublin City Univ, Sch Chem Sci, Natl Ctr Sensor Res, Dublin 9, Ireland
关键词
atlas suppressor; water analysis; environmental analysis; haloacetates; halogenated compounds; disinfectant by-products; organochlorine compounds; organobromine compounds; organofluorine compounds;
D O I
10.1016/j.chroma.2004.06.100
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A highly sensitive gradient microbore ion chromatographic method was developed with electrolytically generated hydroxide eluents for the determination of low mug/L levels of chloroacetate, bromoacetate, trifluoroacetate, dichloroacetate, chlorodifluoroacetate, dibromoacetate, trichloroacetate, bromodichloroacetate and dibromochloroacetate disinfectant by-products formed as a result of chlorination of drinking waters. The possibility of using a packed bed Dionex Atlas suppressor with a hydroxide gradient at microbore flow rates was investigated in order to reduce baseline noise levels. The Atlas suppressor displayed a very significant reduction in noise levels compared to the standard alternative ASRS Ultra suppressor, reducing noise by a factor of 15-20 in some cases, allowing trace haloacetic acids (HAs) to be seen with the direct injection of 100 muL of treated water, with prior chloride and sulfate removal. To lower detection limits even further, a solid phase extraction was employed to preconcentrate HAs, resulting in detection limits of between 0.09 and 21.5 mug/L. The method was applied to the determination of HAs in environmental samples and standard addition curves for three drinking water samples were carried out for both direct injection and preconcentration methods. R-2 values in both cases were greater than or equal to0.98. Combined content for US Environmental Protection Agency regulated HAs in the three drinking water samples from Dublin City University; New Ross, Co. Wexford and Drogheda, Co. Louth were 46.5, 58.3 and 12.6 mug/L, respectively. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:205 / 212
页数:8
相关论文
共 17 条
[1]   IDENTITY AND YIELDS OF MAJOR HALOGENATED PRODUCTS OF AQUATIC FULVIC-ACID CHLORINATION [J].
CHRISTMAN, RF ;
NORWOOD, DL ;
MILLINGTON, DS ;
JOHNSON, JD ;
STEVENS, AA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1983, 17 (10) :625-628
[2]   Haloacetic acids (HAAs) formation in desalination processes from disinfectants [J].
Dalvi, AGI ;
Al-Rasheed, R ;
Javeed, MA .
DESALINATION, 2000, 129 (03) :261-271
[3]  
HODGESON J, 1990, 5520 EPA NAT EXP RES
[4]   Determination of bromate and chlorinated haloacetic acids in bottled drinking water with chromatographic methods [J].
Liu, YJ ;
Mou, S .
CHEMOSPHERE, 2004, 55 (09) :1253-1258
[5]   Determination of trace levels of haloacetic acids and perchlorate in drinking water by ion chromatography with direct injection [J].
Liu, YJ ;
Mou, SF .
JOURNAL OF CHROMATOGRAPHY A, 2003, 997 (1-2) :225-235
[6]   Simultaneous determination of trace level bromate and chlorinated haloacetic acids in bottled drinking water by ion chromatography [J].
Liu, YJ ;
Mou, SF .
MICROCHEMICAL JOURNAL, 2003, 75 (02) :79-86
[7]   Evaluation of different electrolyte systems and on-line preconcentrations for the analysis of haloacetic acids by capillary zone electrophoresis [J].
Martínez, D ;
Borrull, F ;
Calull, M .
JOURNAL OF CHROMATOGRAPHY A, 1999, 835 (1-2) :187-196
[8]   Comparative study of a solid-phase extraction system coupled to capillary electrophoresis in the determination of haloacetic compounds in tap water [J].
Martínez, D ;
Borrull, F ;
Calull, M .
JOURNAL OF CHROMATOGRAPHY A, 1998, 827 (01) :105-112
[9]  
Munch D. J., 1995, 5522 EPA NAT EXP RES
[10]   DETERMINATION OF HALOACETIC ACIDS BY ION CHROMATOGRAPHY [J].
NAIR, LM ;
SAARINORDHAUS, R ;
ANDERSON, JM .
JOURNAL OF CHROMATOGRAPHY A, 1994, 671 (1-2) :309-313