Direct gas injection method: A simple modification to an elemental analyzer/isotope ratio mass spectrometer for stable isotope analysis of N and C from N2O and CO2 gases in nanomolar concentrations
Article first published online: 21 NOV 2012
Copyright © 2012 John Wiley & Sons, Ltd.
Rapid Communications in Mass Spectrometry
Volume 27, Issue 1, pages 97–102, 15 January 2013
How to Cite
Machavaram, M. V., Beaulieu, J. J. and Mills, M. A. (2013), Direct gas injection method: A simple modification to an elemental analyzer/isotope ratio mass spectrometer for stable isotope analysis of N and C from N2O and CO2 gases in nanomolar concentrations. Rapid Commun. Mass Spectrom., 27: 97–102. doi: 10.1002/rcm.6426
- Issue published online: 21 NOV 2012
- Article first published online: 21 NOV 2012
- Manuscript Accepted: 28 SEP 2012
- Manuscript Revised: 27 SEP 2012
- Manuscript Received: 24 AUG 2012
Stable isotope analyses of trace amounts of nitrous oxide gas require special instrumentation and laborious sample preparation methods that have hindered many laboratories from measuring this potent greenhouse gas. A simple modification to an Elemental Analyzer (EA) coupled to an Isotope Ratio Mass Spectrometry (IRMS) setup that allows users to measure the N and C isotopic ratios of nitrous oxide (N2O) and carbon dioxide (CO2) by injecting the gases directly into the EA is described.
The standard EA was fitted with a gas injection port and a home-made packed column filled with Hayesep Q polymer. A gas mixture of 3.1% N2O in helium (He) was injected directly into the EA. This method allowed large volumes of sample to be injected without saturating the column.
The use of the home-made column resulted in better resolution of sample peaks and allowed smaller concentrations of the analyte to be injected. This study showed that this method produced accurate and reproducible stable isotope measurements with sample injection volumes ranging from 100 to 5000 μL, containing between 20 and 1000 nmol of analyte.
This simple, inexpensive method can be useful for the laboratories that do not have access to more advanced and expensive interfaces to analyze nanomolar quantities of N2O and CO2 from microbiological and ecological studies and offers a simple alternative for in-house measurements of these trace gases. Copyright © 2012 John Wiley & Sons, Ltd.