Journal cover Journal topic
Atmospheric Chemistry and Physics An interactive open-access journal of the European Geosciences Union
Atmos. Chem. Phys., 8, 6699-6706, 2008
© Author(s) 2008. This work is distributed under
the Creative Commons Attribution 3.0 License.
20 Nov 2008
Determination of the evaporation coefficient of D2O
W. S. Drisdell1,2, C. D. Cappa3, J. D. Smith2, R. J. Saykally1,2, and R. C. Cohen1,4 1Department of Chemistry, UC Berkeley, Berkeley, CA, USA
2Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA
3Department of Civil and Environmental Engineering, UC Davis, Davis, CA, USA
4Department of Earth and Planetary Science, UC Berkeley, Berkeley, CA, USA
Abstract. The evaporation rate of D2O has been determined by Raman thermometry of a droplet train (12–15 μm diameter) injected into vacuum (~10-5 torr). The cooling rate measured as a function of time in vacuum was fit to a model that accounts for temperature gradients between the surface and the core of the droplets, yielding an evaporation coefficient (γe) of 0.57±0.06. This is nearly identical to that found for H2O (0.62±0.09) using the same experimental method and model, and indicates the existence of a kinetic barrier to evaporation. The application of a recently developed transition-state theory (TST) model suggests that the kinetic barrier is due to librational and hindered translational motions at the liquid surface, and that the lack of an isotope effect is due to competing energetic and entropic factors. The implications of these results for cloud and aerosol particles in the atmosphere are discussed.

Citation: Drisdell, W. S., Cappa, C. D., Smith, J. D., Saykally, R. J., and Cohen, R. C.: Determination of the evaporation coefficient of D2O, Atmos. Chem. Phys., 8, 6699-6706,, 2008.
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