Abstract
Stable isotope methods are potentially quite useful for validating natural or enhanced mineral degradation of contaminants, For this
reason, a continuous flow gas chromatograph (GC), isotope ratio mass
spectrometer (IRMS) has been coupled with a quadrupole mass selective
detector (MSD) to allow simultaneous mass spectral and stable carbon
isotope ratio data to be obtained from a single chromatographic
analysis. This allows the target contaminant and any extra-cellular
degradation intermediates to be both qualified and quantified.
Previously acceptable limits of precision (0.3 parts per mil) are
undesirable given the small fractionation observed during aerobic
degradation. To further understand the fate of organic contaminants and
to gain information about the metabolic degradative pathway employed by
a microorganism, routine isotopic analyses on a range of analytes have
been performed. Quantities of sample producing mass-44 ion beam signal
(I-44) of 2 x 10(-10) fo 1 x 10(-8) A were analysed. When the IRMS was
tuned for high sensitivity, ion source nonlinearities were overcome by
peak height correction from an algorithm that was produced using known
isotopic standards of varying concentrations. This led to sample
accuracy of <0.01 parts per thousand and sample precision of 0.1 parts
per thousand. Copyright (C) 1999 John Wiley & Sons, Ltd.
Original language | English |
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Pages (from-to) | 1231-1236 |
Number of pages | 6 |
Journal | Rapid Communications in Mass Spectrometry |
Volume | 13 |
Issue number | 13 |
DOIs | |
Publication status | Published - 1999 |
Keywords
- gas chromatography
- mass spectrometry