Utility of three types of mass spectrometers for determining elemental compositions of ions formed from chromatographically separated compounds

被引:22
作者
Grange, AH [1 ]
Genicola, FA
Sovocool, GW
机构
[1] US EPA, NERL, Div Environm Sci, Las Vegas, NV 89193 USA
[2] NJ Dept Enviornm Protect, Div Sci Res & Technol, Trenton, NJ 08625 USA
关键词
D O I
10.1002/rcm.842
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Concentration factors of 1000 and more reveal dozens of compounds in extracts of water supplies. Library mass spectra for most of these compounds are not available, and alternative means of identification are needed. Determination of the elemental compositions of the ions in mass spectra makes feasible searches of commercial and chemical literature that often lead to compound identification. Instrumental capabilities that constrain the utility of a mass spectrometer for determining ion compositions for compounds that elute from a chromatographic column are scan speed, mass accuracy, linear dynamic range, and resolving power. Mass peak profiling from selected ion recording data (MPPSIRD) performed with a double-focusing mass spectrometer provides the best combination of these capabilities. This technique provides unique ion compositions for ions of higher mass from compounds eluting from a gas chromatograph than can be obtained by orthogonal acceleration time-of-flight (oa-TOF) or Fourier transform ion cyclotron resonance mass spectrometry. Multiple compositions are usually possible for an ion with a mass exceeding 150 Da within the error limits of the mass measurement. The correct composition is selected based on measured exact masses of the mass peak profiles resulting from isotopic ions higher in mass by 1 and 2 Da and accurate measurement of the summed abundances of these isotopic ions relative to the monoisotopic ion. A profile generation model (PGM) automatically determines which compositions are consistent with measured exact masses and relative abundances. The utility of oa-TOF and double-focusing mass :spectrometry using ion composition elucidation (MPPSIRD plus the PGM) are considered for determining ion compositions of two compounds found in drinking water extracts and a third Compound from a monitoring well at a landfill. Published in 2002 by John Wiley Sons, Ltd.
引用
收藏
页码:2356 / 2369
页数:14
相关论文
共 47 条
[11]   Determination of elemental compositions from mass peak profiles of the molecular ion (M) and the M+1 and M+2 ions [J].
Grange, AH ;
Donnelly, JR ;
Sovocool, GW ;
Brumley, WC .
ANALYTICAL CHEMISTRY, 1996, 68 (03) :553-560
[12]  
Grange AH, 1998, RAPID COMMUN MASS SP, V12, P1161, DOI 10.1002/(SICI)1097-0231(19980915)12:17<1161::AID-RCM288>3.3.CO
[13]  
2-B
[14]   MASS MEASUREMENTS BY AN ACCURATE AND SENSITIVE SELECTED-ION RECORDING TECHNIQUE [J].
GRANGE, AH ;
DONNELLY, JR ;
BRUMLEY, WC ;
BILLETS, S ;
SOVOCOOL, GW .
ANALYTICAL CHEMISTRY, 1994, 66 (24) :4416-4421
[15]   PLOTTING MASS-PEAK PROFILES FROM SELECTED-ION RECORDING DATA [J].
GRANGE, AH ;
BRUMLEY, WC .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 1992, 6 (01) :68-70
[16]  
Grange AH, 1999, J AOAC INT, V82, P1443
[17]   A mass peak profile generation model to facilitate determination of elemental compositions of ions based on exact masses and isotopic abundances [J].
Grange, AH ;
Brumley, WC .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1997, 8 (02) :170-182
[18]   Ion composition elucidation (ICE): an investigative tool for characterization and identification of compounds of regulatory importance [J].
Grange, AH ;
Osemwengie, LI ;
Brilis, GM ;
Sovocool, GW .
ENVIRONMENTAL FORENSICS, 2001, 2 (01) :61-74
[19]   Tandem mass spectrometric accurate mass performance of time-of-flight and Fourier transform ion cyclotron resonance mass spectrometry: a case study with pyridine derivatives [J].
Hau, J ;
Stadler, R ;
Jenny, TA ;
Fay, LB .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2001, 15 (19) :1840-1848
[20]  
Hogenboom AC, 1999, RAPID COMMUN MASS SP, V13, P125, DOI 10.1002/(SICI)1097-0231(19990130)13:2<125::AID-RCM473>3.3.CO