Temperature dependence of isotopic fractionation in the CO2 -O2 isotope exchange reaction

Updated theoretical values of α18 for equilibrium isotope exchange are lower than those derived from previous work by Richet et al. (1997). The direct sum evaluation for CO2 yields θ values higher than the canonical range maximum for mass-dependent fractionation processes. This demonstrates the need to include anharmonic effects in the calculation and definition of mass-dependent fractionation processes for poly-atomic molecules. The discrepancy between the theory and the experimental α17 and α18 values may be due to thermal diffusion associated with the temperature gradient in the reactor.

We determined experimentally the steady-state α17 and α18 fractionation factors for Pt-catalyzed CO2 -O2 oxygen isotope exchange at temperatures ranging from 500 to 1200°C. For comparison, the theoretical α18 equilibrium exchange values reported by Richet et al. (1997) have been updated using the direct sum method for CO2 and the corresponding α17 values were determined. Finally, we examined whether the steady-state fractionation factors depend on the isotopic composition of the reactants, by using CO2 and O2 differing in δ18 O value from -66 ‰ to +4 ‰.

The experimentally determined steady-state fractionation factors α17 and α18 are lower than those obtained from the updated theoretical calculations (of CO2 -O2 isotope exchange under equilibrium conditions) by 0.0024 ± 0.0001 and 0.0048 ± 0.0002, respectively. The offset is not due to scale incompatibilities between isotope measurements of O2 and CO2 nor to the neglect of non-Born-Oppenheimer effects in the calculations. There is a crossover temperature at which enrichment in the minor isotopes switches from CO2 to O2 . The direct sum evaluation yields a θ value of ~0.54, i.e. higher than the canonical range maximum for a mass-dependent fractionation process. Conclusions: Updated theoretical values of α18 for equilibrium isotope exchange are lower than those derived from previous work by Richet et al. (1997). The direct sum evaluation for CO2 yields θ values higher than the canonical range maximum for mass-dependent fractionation processes. This demonstrates the need to include anharmonic effects in the calculation and definition of mass-dependent fractionation processes for poly-atomic molecules. The discrepancy between the theory and the experimental α17 and α18 values may be due to thermal diffusion associated with the temperature gradient in the reactor.