Microphysical Processes Affecting Stratospheric Aerosol Particles

Patrick Hamill Theoretical and Planetary Studies Branch, Ames Research Center, NASA, Moffett Field, Calif. 94035

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O. B. Toon Theoretical and Planetary Studies Branch, Ames Research Center, NASA, Moffett Field, Calif. 94035

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C. S. Kiang National Center for Atmospheric Research, Boulder, Colo. 80303

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Abstract

Physical processes which affect stratospheric aerosol particles include nucleation, condensation, evaporation, coagulation and sedimentation. We carry out quantitative studies of these mechanisms to determine if they can account for some of the observed properties of the aerosol. We show that the altitude range in which nucleation of H2SO4-H2O solution droplets can take place corresponds to that region of the stratosphere where the aerosol is generally found. Since heterogeneous nucleation is the dominant nucleation mechanism, the stratospheric solution droplets are mainly formed on particles which have been mixed up from the troposphere or injected into the stratosphere by volcanoes or meteorites. Particle growth by heteromolecular condensation can account for the observed increase in mixing ratio of large particles in the stratosphere. Coagulation is important in reducing the number of particles smaller than 0.05 µm radius. Growth by condensation, applied to the mixed nature of the particles, shows that available information is consistent with ammonium sulfate being formed by liquid phase chemical reactions in the aerosol particles. The upper altitude limit of the aerosol layer is probably due to the evaporation of sulfuric acid aerosol particles, while the lower limit is due to mixing across the tropopause.

Abstract

Physical processes which affect stratospheric aerosol particles include nucleation, condensation, evaporation, coagulation and sedimentation. We carry out quantitative studies of these mechanisms to determine if they can account for some of the observed properties of the aerosol. We show that the altitude range in which nucleation of H2SO4-H2O solution droplets can take place corresponds to that region of the stratosphere where the aerosol is generally found. Since heterogeneous nucleation is the dominant nucleation mechanism, the stratospheric solution droplets are mainly formed on particles which have been mixed up from the troposphere or injected into the stratosphere by volcanoes or meteorites. Particle growth by heteromolecular condensation can account for the observed increase in mixing ratio of large particles in the stratosphere. Coagulation is important in reducing the number of particles smaller than 0.05 µm radius. Growth by condensation, applied to the mixed nature of the particles, shows that available information is consistent with ammonium sulfate being formed by liquid phase chemical reactions in the aerosol particles. The upper altitude limit of the aerosol layer is probably due to the evaporation of sulfuric acid aerosol particles, while the lower limit is due to mixing across the tropopause.

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