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A new method to determine the 17 O isotopic abundance in CO 2 using oxygen isotope exchange with a solid oxide
This paper discusses a simple method to determine 17 O isotope excess or deficiency (‘mass‐independent isotopic composition’) in CO 2 gas. When applying conventional mass spectrometry of CO 2 ( m/z 44, 45 and 46) to determine the 17 O/ 16 O ratio, the 13 C/ 12 C ratio has to be established separatel...
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Published in: | Rapid communications in mass spectrometry 2001-12, Vol.15 (24), p.2426-2437 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | This paper discusses a simple method to determine
17
O isotope excess or deficiency (‘mass‐independent isotopic composition’) in CO
2
gas. When applying conventional mass spectrometry of CO
2
(
m/z
44, 45 and 46) to determine the
17
O/
16
O ratio, the
13
C/
12
C ratio has to be established separately. This can be achieved by analysing an aliquot of sample CO
2
before and after subjecting it to oxygen isotope exchange with a pool of oxygen with ‘normal’
17
O/
16
O ratio, i.e. with Δ
17
O≡δ
17
O−0.516 × δ
18
O = 0. Cerium oxide has been shown to be practically well suited for the exchange of CO
2
oxygen; the reagent is safe and does not produce any contamination. The CO
2
‐CeO
2
exchange reaction has 99.8 ± 0.7% recovery yield. At 650 °C this reaction reaches equilibrium in 30 min and, as tested, results in complete oxygen replacement. Δ
17
O determinations depend on accuracy of CO
2
delta measurements: the repeatability of ±0.015‰ (1σ) in δ
45
R and δ
46
R deter‐mination relative to the working reference results in an error of Δ
17
O as small as ±0.33‰. Such a precision is sufficient for Δ
17
O determination in stratospheric CO
2
. The calculated Δ
17
O value systematically depends on absolute
17
R and
13
R ratios in isotopic reference materials, which are presently not yet known with certainty (the
17
R value is most important), and may be inadequate for
17
O‐correction with a = 0.516. Within the present uncertainty, Δ
17
O determined in
17
O‐enriched CO
2
agrees with the value directly measured in the enriched O
2
from which this CO
2
was produced. Besides Δ
17
O determination, investigated CO
2
‐CeO
2
equilibration may have several other implications. Fast, complete isotopic exchange of CO
2
by reaction with CeO
2
may also be employed to get reproducible
17
O‐correction and, hence, to better monitor small δ
13
C shifts and to isotopically equilibrate mixtures of CO
2
gases. Copyright © 2001 John Wiley & Sons, Ltd. |
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ISSN: | 0951-4198 1097-0231 |
DOI: | 10.1002/rcm.529 |