DETERMINATION OF VOLATILE ORGANICS IN DRINKING-WATER WITH USEPA METHOD-524.2 AND THE ION TRAP DETECTOR

被引:20
作者
EICHELBERGER, JW [1 ]
BELLAR, TA [1 ]
DONNELLY, JP [1 ]
BUDDE, WL [1 ]
机构
[1] US EPA,OFF RES & DEV,ENVIRONM MONITORING SYST LAB,26 W MARTIN LUTHER KING DR,CINCINNATI,OH 45268
关键词
D O I
10.1093/chromsci/28.9.460
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
New drinking water regulations require the monitoring of eight volatile organic compounds that have established maximum contaminant levels (MCLs) and 51 other volatile organics for which MCLs are not established. A laboratory analytical method (Method 524.2) for the determination of 58 of these compounds is investigated, and precision and accuracy data are obtained. The method uses a standard inert gas purge extraction, isolation of the volatile organics on a three-stage solid-phase trap, thermal desorption into a gas chromatograph, separation with a fused-silica capillary column, and identification and measurement with a relatively low cost, benchtop ion trap detector that functions as a mass spectrometer. At a concentration of 2 μg/L (2 parts per billion), the grand mean measurement accuracy for 54 compounds was 95% of the true value with a mean relative standard deviation (RSD) of 4%. At 0.2 μg/L (200 parts per trillion), the grand mean measurement accuracy for 52 compounds was 95% of the true value with a mean RSD of 3%.; New drinking water regulations require the monitoring of eight volatile organic compounds that have established maximum contaminant levels (MCLs) and 51 other volatile organics for which MCLs are not established. A laboratory analytical method (Method 524.2) for the determination of 58 of these compounds is investigated, and precision and accuracy data are obtained. The method uses a standard inert gas purge extraction, isolation of the volatile organics on a three-stage solid-phase trap, thermal desorption into a gas chromatograph, separation with a fused-silica capillary column, and identification and measurement with a relatively low cost, benchtop ion trap detector that functions as a mass spectrometer. At a concentration of 2 μg/L (2 parts per billion), the grand mean measurement accuracy for 54 compounds was 95% of the true value with a mean relative standard deviation (RSD) of 4%. At 0.2 μg/L (200 parts per trillion), the grand mean measurement accuracy for 52 compounds was 95% of the true value with a mean RSD of 3%.
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收藏
页码:460 / 467
页数:8
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