Using septum-capped vials with continuous-flow isotope ratio mass spectrometric analysis of atmospheric CO2 for Keeling plot applications

Citation
Kp. Tu et al., Using septum-capped vials with continuous-flow isotope ratio mass spectrometric analysis of atmospheric CO2 for Keeling plot applications, RAP C MASS, 15(12), 2001, pp. 952-956
Citations number
6
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences
Journal title
RAPID COMMUNICATIONS IN MASS SPECTROMETRY
ISSN journal
09514198 → ACNP
Volume
15
Issue
12
Year of publication
2001
Pages
952 - 956
Database
ISI
SICI code
0951-4198(2001)15:12<952:USVWCI>2.0.ZU;2-9
Abstract
Recent advances in continuous-flow isotope ratio mass spectrometry have mad e possible automated analysis of delta C-13 and delta O-18 in CO2 in air fr om 10-mL septum-capped vials. With the potential to collect, transport, and analyze a large number of air samples using these small inexpensive vials, the opportunity exists for routine and statistically robust sampling of CO 2 for Keeling plot applications. With the above-mentioned objectives in mind, we measured the precision of c arbon and oxygen stable isotope ratios in the CO2 of air within septum-capp ed vials using a Finnigan MAT Delta(plus) XL continuous-flow isotope ratio mass spectrometer (CF-IRMS) interfaced to a GasBench II. The standard devia tion of 45 delta C-13(PDB) and delta O-18(VSMOW) measurements from five via ls filled with identical tank air was 0.08 parts per thousand and 0.14 part s per thousand, respectively. This translated into a measurement precision (standard error; SE) of 0.01 parts per thousand delta C-13(PDB) and 0.02 pa rts per thousand delta O-18(VSMOW). This precision was similar to that obta ined with the tank air introduced directly into the GasBench II by bypassin g the vials/autosampler (also with a SE = 0.01 parts per thousand for both delta C-13(PDB) and delta O-18(VSMOW))] suggesting minimal vial-related eff ects with no storage time at ambient pressure and CO2 concentration. Furthe r, puncturing the butyl rubber septa during filling just prior to analysis did not affect the precision (SE = 0.01 parts per thousand for both delta C -13(PDB) and delta O-18(VSMOW), II = 45). After nine days of storage in vials with unpunctured septa, neither delta C -13(PDB) nor delta O-18(VSMOW) changed significantly, although the precisio n decreased to similar to0.04 parts per thousand for both delta C-13(PDB) a nd delta O-18(VSMOW) A greater decrease in precision was observed for vials with punctured septa (from 0.01 parts per thousand to 0.10 parts per thous and SE for both delta C-13(PDB) and delta O-18(VSMOW)). Further, whereas vi als with punctured septa showed no change in delta O-18(VSMSW), delta C-13( PDB) decreased by 0.07 parts per thousand /day (r(2) = 0.96). In practice, such storage-related effects could be accounted for based on concurrent cha nges in reference standards. These results suggest that air may be collected and stored in 10-mL septum- capped vials and analyzed in an automated fashion with the Gas Bench II/Del ta(plus) with sufficient precision for Keeling plot applications. Further, a relatively high sample throughput of about 4 vials per hour or about 100 vials or 2000 injections per day offers the potential for high precision wi th large sample sizes. Higher throughput should permit experimental advance s that were not possible before. Copyright (C) 2001 John Wiley & Sons, Ltd.