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Updated: Aug 8, 2026

Automated, High-resolution Mobile Collection System for the Nitrogen Isotopic Analysis of NOx
Published on: December 20, 2016
On the N2O correction used for mass spectrometric analysis of atmospheric CO2
S S Assonov1, C A M Brenninkmeijer
1Max Planck Institute for Chemistry, P. O. Box 3060, 55020 Mainz, Germany. sergey.assonov@cec.eu.int
Abstract:
To obtain accurate values of delta(13)C(CO(2)) and delta(18)O(CO(2)) on environmental CO(2) by mass spectrometry, the raw isotope data must be corrected for the isobaric N(2)O contribution. This is one of the analytical problems limiting inter-laboratory delta(13)C(CO(2)) data consistency. The key parameter, the N(2)O relative ionisation efficiency (E(N2O)), cannot be determined with sufficient accuracy by direct measurements of pure N(2)O. The determination of (E(N2O)) by analyses on N(2)O--CO(2) mixtures of known isotope composition and mixing proportions has been recently suggested. In this work we propose a new method of N(2)O correction which uses the m/z 30 signal as a measure of the N(2)O/CO(2) ratio, so that determinations of (E(N2O)) and N(2)O content are not required. The method uses the fact that fragment-ion spectra of N(2)O and CO(2) are very specific. The formalism of the correction is considered. Various tests demonstrate that the new method is robust, stable and easy to implement in practice. The effective value (E(N2O)) (the key parameter for the new correction) has to be calibrated on known N(2)O--CO(2) mixtures by measuring (30)R signals only. The method accuracy we presently achieved is around 2.5% and any error which appears to come mostly from our N(2)O--CO(2) mixture preparation. Based on our tests and error considerations, the error of the proposed method that may be achieved is as low as +/-1.5% (relative to the correction magnitude). For tropospheric CO(2) this means +/-0.003 per thousand and +/-0.005 per thousand for delta(13)C(CO(2)) and delta(18)O(CO(2)), respectively. The proposed method may be valuable for small samples where no separate N(2)O determinations are available (e.g. ice core samples and CF-IRMS measurements) as well as for determination of (E(N2O)) and testing the 'traditional' N(2)O correction based on mass balance calculations.
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