Abstract
Stable carbon isotope analysis of methane ( 13C
of CH4) on atmospheric samples is one key method to constrain
the current and past atmospheric CH4 budget. A frequently
applied measurement technique is gas chromatography
(GC) isotope ratio mass spectrometry (IRMS) coupled to
a combustion-preconcentration unit. This report shows that
the atmospheric trace gas krypton (Kr) can severely interfere
during the mass spectrometric measurement, leading to significant
biases in 13C of CH4, if krypton is not sufficiently
separated during the analysis. According to our experiments,
the krypton interference is likely composed of two individual
effects, with the lateral tailing of the doubly charged
86Kr peak affecting the neighbouring m/z 44 and partially
the m/z 45 Faraday cups. Additionally, a broad signal affecting
m/z 45 and especially m/z 46 is assumed to result from
scattered ions of singly charged krypton. The introduced bias
in the measured isotope ratios is dependent on the chromatographic
separation, the krypton-to-CH4 mixing ratio in the
sample, the focusing of the mass spectrometer as well as
the detector configuration and can amount to up to several
per mil in 13C. Apart from technical solutions to avoid this
interference, we present correction routines to a posteriori
remove the bias.
| Original language | English |
|---|---|
| Pages (from-to) | 1425-1445 |
| Number of pages | 21 |
| Journal | Atmospheric Measurement Techniques |
| Volume | 6 |
| DOIs | |
| Publication status | Published - 2013 |
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