Trace determination of triazine herbicides by means of coupled-column liquid chromatography and large volume injection

被引:44
作者
Hidalgo, C [1 ]
Sancho, JV [1 ]
Hernandez, F [1 ]
机构
[1] UNIV JAUME 1,DEPT EXPT SCI,CASTELLO DE PLANA 12080,SPAIN
关键词
liquid chromatography; triazines; simazine; atrazine; terbuthylazine; terbutryn; coupled column LC (LC-LC); large volume injection (LVI); waters; pesticide residue analysis;
D O I
10.1016/S0003-2670(96)00455-2
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Coupled-column liquid chromatography (LC-LC) with ultraviolet detection was used for the trace-level determination of simazine, atrazine, terbuthylazine and terbutryn in environmental water samples. A sample volume of 2 mi was directly injected in the chromatographic system, using two reversed-phase C-18 coupled columns. The mobile phases consisted of two mixtures CH3CN/H2O, one with 40% of acetonitrile (M-1) and one with 70% (M-2). As a result, a rapid procedure with detection Limits down to 0.1 mu g l(-1) was developed. The method was validated by means of recovery experiments. Drinking and surface water samples were spiked at 4 and 0.4 mu g l(-1) yielding average recoveries between 86-104% (n=5) with coefficients of variation between 1-6%. The overall procedure allowed a sample throughput of up to 60 samples per day. Surface water samples from a wet area of Castellon (Spain) were analyzed by means of the proposed LC-LC procedure, thus simazine, terbuthylazine and terbutryn were detected at sub-mu g l(-1) levels. Lower detection limits, between 0.02-0.05 mu g l(-1) were reached by preconcentration of 100 mi of water samples on C-18 bonded phase solid phase extraction (SPE) cartridges. Drinking water samples spiked at 0.1 mu g l(-1) were preconcentrated and analyzed by LC-LC yielding average recoveries between 84-103% (n=3) with coefficients of variation between 2-5%.
引用
收藏
页码:223 / 229
页数:7
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