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High‐precision continuous‐flow isotope ratio mass spectrometry
Author(s) -
Brenna J. Thomas,
Corso Thomas N.,
Tobias Herbert J.,
Caimi Richard J.
Publication year - 1997
Publication title -
mass spectrometry reviews
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.035
H-Index - 126
eISSN - 1098-2787
pISSN - 0277-7037
DOI - 10.1002/(sici)1098-2787(1997)16:5<227::aid-mas1>3.0.co;2-j
Subject(s) - chemistry , isotope ratio mass spectrometry , isotope analysis , mass spectrometry , isotope , chromatography , analytical chemistry (journal) , stable isotope ratio , isotopes of carbon , isotope fractionation , gas chromatography , elemental analysis , fractionation , environmental chemistry , organic chemistry , total organic carbon , ecology , physics , quantum mechanics , biology
Although high‐precision isotope determinations are routine in many areas of natural science, the instrument principles for their measurements have remained remarkably unchanged for four decades. The introduction of continuous‐flow techniques to isotope ratio mass spectrometry (IRMS) instrumentation has precipitated a rapid expansion in capabilities for high‐precision measurement of C, N, O, S, and H isotopes in the 1990s. Elemental analyzers, based on the flash combustion of solid organic samples, are interfaced to IRMS to facilitate routine C and N isotopic analysis of unprocessed samples. Gas/liquid equilibrators have automated O and H isotopic analysis of water in untreated aqueous fluids as complex as urine. Automated cryogenic concentrators permit analysis at part‐per‐million concentrations in environmental samples. Capillary gas chromatography interfaced to IRMS via on‐line microchemistry facilitates compound‐specific isotope analysis (CSIA) for purified organic analytes of 1 nmol of C, N, or O. GC‐based CSIA for hydrogen and liquid chromatography‐based interfaces to IRMS have both been demonstrated, and continuing progress promises to bring these advances to routine use. Automated position‐specific isotope analysis (PSIA) using noncatalytic pyrolysis has been shown to produce fragments without appreciable carbon scrambling or major isotopic fractionation, and shows great promise for intramolecular isotope ratio analysis. Finally, IRMS notation and useful elementary isotopic relationships derived from the fundamental mass balance equation are presented. © 1998 John Wiley & Sons, Inc., Mass Spectrom Rev 16, 227–258, 1997