Atmos. Chem. Phys. Discuss., 7, 2937-2960, 2007
www.atmos-chem-phys-discuss.net/7/2937/2007/
doi:10.5194/acpd-7-2937-2007
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This discussion paper has been under review for the journal Atmospheric Chemistry and Physics (ACP). Please refer to the corresponding final paper in ACP.
Estimating the NH3:H2SO4ratio of nucleating clusters in atmospheric conditions using quantum chemical methods
T. Kurtén1, L. Torpo1, M. R. Sundberg2, V.-M. Kerminen3, H. Vehkamäki1, and M. Kulmala1
1Division of Atmospheric Sciences, Department of Physical Sciences, P.O.Box 64, FI-00014 University of Helsinki, Finland
2Laboratory of Inorganic Chemistry, Department of Chemistry, P.O. Box 55, FI-00014 University of Helsinki, Finland
3Finnish Meteorological Institute, Air Quality Research, Sahaajankatu 20 E, FI-00880 Helsinki, Finland

Abstract. We study the ammonia addition reactions of H2SO4·NH3 molecular clusters containing up to four ammonia and two sulfuric acid molecules using the ab initio method RI-MP2 (Resolution of Identity 2nd order Møller-Plesset perturbation theory). Together with results from previous studies, we use the computed values to estimate an upper limit for the ammonia content of small atmospheric clusters, without having to explicitly include water molecules in the quantum chemical simulations. Our results indicate that the NH3:H2SO4 mole ratio of small molecular clusters in typical atmospheric conditions is probably around 1:2. High ammonia concentrations or low temperatures may lead to the formation of ammonium bisulfate (1:1) clusters, but our results rule out the formation of ammonium sulfate clusters (2:1) anywhere in the atmosphere. A sensitivity analysis indicates that the qualitative conclusions of this study are not affected even by relatively large errors in the calculation of electronic energies or vibrational frequencies.

Citation: Kurtén, T., Torpo, L., Sundberg, M. R., Kerminen, V.-M., Vehkamäki, H., and Kulmala, M.: Estimating the NH3:H2SO4ratio of nucleating clusters in atmospheric conditions using quantum chemical methods, Atmos. Chem. Phys. Discuss., 7, 2937-2960, doi:10.5194/acpd-7-2937-2007, 2007.
 
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