Two-dimensional on-line detection of brominated and iodinated volatile organic compounds by ECD and ICP-MS after GC separation

被引:34
作者
Schwarz, A [1 ]
Heumann, KG [1 ]
机构
[1] Univ Mainz, Inst Inorgan Chem & Analyt Chem, D-55099 Mainz, Germany
关键词
brominated and iodinated volatile organic; compounds; gas chromatography; two-dimensional detection; inductively coupled plasma mass spectrometry; electron capture detector;
D O I
10.1007/s00216-002-1422-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Inductively coupled plasma-mass spectrometry (ICP-MS) was coupled to a gas chromatographic (GC) system with electron capture detector (ECD), which enables relatively easy characterization and quantification of brominated and iodinated (halogenated) volatile organic compounds (HVOCs) in aquatic and air samples. The GC-ECD system is connected in series with an ICP-MS by a directly heated transfer line and an outlet port-hole for elimination of the ECD make-up gas during ignition of the plasma. The hyphenated GC-ECD/ICP-MS system provides high selectivity and sensitivity for monitoring individual HVOCs under fast chromatographic conditions. The ECD is most sensitive for the detection of chlorinated and brominated but the ICP-MS for iodinated compounds. The greatest advantage of the use of an ICP-MS is its element-specific detection, which allows clear identification of compounds in most cases. The absolute detection limits for ICP-MS are 0.5 pg for iodinated, 10 pg for brominated, and 50 pg for chlorinated HVOCs with the additional advantage that calibration is almost independent on different compounds of the same halogen. In contrast to that detection limits for ECD vary for the different halogenated compounds and lie in the range of 0.03-11 pg. The two-dimensional GC-ECD/ICP-MS instrumentation is compared with electron impact mass spectrometry (EI-MS) and microwave induced plasma atomic emission detection (MIP-AED). Even if EI-MS has additional power in identifying unknown peaks by its scan mode, the detection limits are much higher compared with GC-ECD/ICP-MS, whereas the selective ion monitoring mode (SIM) reaches similar detection limits. The MIP-AED detection limits are at the same level as EI-MS in the scan mode.
引用
收藏
页码:212 / 219
页数:8
相关论文
共 28 条
[1]   DETERMINATION OF BIOGENIC AND ANTHROPOGENIC VOLATILE HALOCARBONS IN SEA-WATER BY LIQUID-LIQUID-EXTRACTION AND CAPILLARY GAS-CHROMATOGRAPHY [J].
ABRAHAMSSON, K ;
KLICK, S .
JOURNAL OF CHROMATOGRAPHY, 1990, 513 :39-45
[2]  
Baker JM, 2001, CHEMOSPHERE GLOBAL C, V3, P93, DOI DOI 10.1016/S1465-9972(00)00021-0
[3]   OZONE DESTRUCTION AND PHOTOCHEMICAL-REACTIONS AT POLAR SUNRISE IN THE LOWER ARCTIC ATMOSPHERE [J].
BARRIE, LA ;
BOTTENHEIM, JW ;
SCHNELL, RC ;
CRUTZEN, PJ ;
RASMUSSEN, RA .
NATURE, 1988, 334 (6178) :138-141
[4]   Novel biogenic iodine-containing trihalomethanes and other short-lived halocarbons in the coastal East Atlantic [J].
Carpenter, LJ ;
Malin, G ;
Liss, PS ;
Küpper, FC .
GLOBAL BIOGEOCHEMICAL CYCLES, 2000, 14 (04) :1191-1204
[5]  
CARPENTER LJ, 2001, ATMOS CHEM PHYS DISC, V1, P193
[6]   MEASUREMENTS OF ATMOSPHERIC METHYL-BROMIDE AND BROMOFORM [J].
CICERONE, RJ ;
HEIDT, LE ;
POLLOCK, WH .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1988, 93 (D4) :3745-3749
[7]   CHEMISTRY OF ORGANIC TRACES IN AIR .8. SOURCES AND DISTRIBUTION OF BROMOCHLOROMETHANES AND BROMOCHLOROMETHANES IN MARINE AIR AND SURFACEWATER OF THE ATLANTIC-OCEAN [J].
CLASS, TH ;
BALLSCHMITER, K .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 1988, 6 (1-2) :35-46
[8]   Sodium tetra(n-propyl)borate:: a novel aqueous in situ derivatization reagent for the simultaneous determination of organomercury, -lead and -tin compounds with capillary gas chromatography inductively coupled plasma mass spectrometry [J].
De Smaele, T ;
Moens, L ;
Dams, R ;
Sandra, P ;
Van der Eycken, J ;
Vandyck, J .
JOURNAL OF CHROMATOGRAPHY A, 1998, 793 (01) :99-106
[9]   Validation of methylmercury determinations in aquatic systems by alkyl derivatization methods for GC analysis using ICP-IDMS [J].
Demuth, N ;
Heumann, KG .
ANALYTICAL CHEMISTRY, 2001, 73 (16) :4020-4027
[10]   A flexible interface for the coupling of capillary gas chromatography with inductively coupled plasma mass spectrometry [J].
DeSmaele, T ;
Verrept, P ;
Moens, L ;
Dams, R .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 1995, 50 (11) :1409-1416