Trace-level determination of 1,4-dioxane in water by isotopic dilution GC and GC-MS

被引:40
作者
Draper, WM [1 ]
Dhoot, JS [1 ]
Remoy, JW [1 ]
Perera, SK [1 ]
机构
[1] Calif Dept Hlth Serv, Sanitat & Radiat Lab Branch, Berkeley, CA 94704 USA
关键词
D O I
10.1039/b002345k
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The volatile and polar solvent 1,4-dioxane has recently been reported as a contaminant of ground and surface waters, establishing the need to determine this substance in drinking water. This investigation established that 1,4-dioxane can be determined in water by various techniques including direct aqueous injection (DAI) gas chromatography (GC) and purge and trap GC-mass spectrometry (MS). Purge and trap GC-MS is limited by 1,4-dioxane's poor purge efficiency, resulting in detection limits up to 100 times greater than the efficiently purged volatile organic compounds. To attain the sensitivity required for drinking water monitoring, a method based on continuous liquid-liquid extraction with dichloromethane was developed. Isotope dilution was more accurate and reproducible than quantification with external standards, and the improvement in precision led to a lower method detection limit, 0.2 mu g L-1, using a quadrupole ion trap instrument in the electron ionization mode. Isotope dilution accuracy approached 100% in ppb determinations. Isotopic dilution quantification was also possible using a non-selective GC detector owing to the high efficiency of capillary GC columns that resolve the deuterium-labeled solvent from the natural isotopes.
引用
收藏
页码:1403 / 1408
页数:6
相关论文
共 13 条
[1]   DETERMINATION OF PARTS-PER-BILLION CONCENTRATIONS OF DIOXANE IN WATER AND SOIL BY PURGE AND TRAP GAS CHROMATOGRAPHY/MASS SPECTROMETRY OR CHARCOAL TUBE ENRICHMENT GAS-CHROMATOGRAPHY [J].
EPSTEIN, PS ;
MAUER, T ;
WAGNER, M ;
CHASE, S ;
GILES, B .
ANALYTICAL CHEMISTRY, 1987, 59 (15) :1987-1990
[2]   CAPILLARY GAS-CHROMATOGRAPHY FOURIER-TRANSFORM INFRARED-SPECTROSCOPY USING AN INJECTOR TRAP AND LIQUID LIQUID EXTRACTION [J].
FEHL, AJ ;
MARCOTT, C .
ANALYTICAL CHEMISTRY, 1989, 61 (14) :1596-1598
[3]   INTERACTIVE EFFECTS OF TEMPERATURE, SALT CONCENTRATION, AND PH ON HEAD SPACE ANALYSIS FOR ISOLATING VOLATILE TRACE ORGANICS IN AQUEOUS ENVIRONMENTAL-SAMPLES [J].
FRIANT, SL ;
SUFFET, IH .
ANALYTICAL CHEMISTRY, 1979, 51 (13) :2167-2176
[4]   A REMEDIAL INVESTIGATION OF AN ORGANICALLY POLLUTED OUTWASH AQUIFER [J].
JACKSON, RE ;
PATTERSON, RJ .
GROUND WATER MONITORING AND REMEDIATION, 1989, 9 (03) :119-125
[5]   GAS-CHROMATOGRAPHY MASS-SPECTROMETRIC DETERMINATION OF TRACES OF HYDROPHILIC AND VOLATILE ORGANIC-COMPOUNDS IN WATER AFTER PRECONCENTRATION WITH ACTIVATED CARBON [J].
KADOKAMI, K ;
KOGA, M ;
OTSUKI, A .
ANALYTICAL SCIENCES, 1990, 6 (06) :843-849
[6]   OCCURRENCE AND FATE OF ORGANIC-SOLVENT RESIDUES IN ANOXIC GROUNDWATER AT THE GLOUCESTER LANDFILL, CANADA [J].
LESAGE, S ;
JACKSON, RE ;
PRIDDLE, MW ;
RIEMANN, PG .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1990, 24 (04) :559-566
[7]  
MANTICA E, 1986, 10388 EUR COMM EUR C, P89
[8]   DEVELOPMENT AND EVALUATION OF A PROCEDURE FOR DETERMINING VOLATILE ORGANICS IN WATER [J].
MICHAEL, LC ;
PELLIZZARI, ED ;
WISEMAN, RW .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1988, 22 (05) :565-570
[9]   EVALUATION OF 48 COMPOUNDS FOR POSSIBLE INCLUSION IN UNITED-STATES EPA METHOD 524.2, REVISION 3.0 - EXPANSION OF THE METHOD ANALYTE LIST TO A TOTAL OF 83 COMPOUNDS [J].
MUNCH, JW ;
EICHELBERGER, JW .
JOURNAL OF CHROMATOGRAPHIC SCIENCE, 1992, 30 (12) :471-477
[10]   BIOCHEMICAL EFFECTS ON CONTAMINANT FATE AND TRANSPORT [J].
NYER, EK ;
KRAMER, V ;
VALKENBURG, N .
GROUND WATER MONITORING AND REMEDIATION, 1991, 11 (02) :80-82