期刊
ATMOSPHERIC RESEARCH
卷 54, 期 1, 页码 41-57出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/S0169-8095(00)00038-7
关键词
aerosol particles; heterogeneous reactions; aerosol dynamics; sulfur chemistry
In the atmosphere, oxidation of sulfur dioxide (SO2) to sulfate may occur in the gas phase, in cloud or fog droplets, or in the aerosol phase on the surface or inside aerosol particles. While aerosol phase reactions have been studied in the case of supermicron sea-salt and crustal particles, very few investigations regarding submicron particles are available. In this paper, the importance of aerosol phase sulfate production to the dynamics of submicron particle populations was examined. The investigation was based on model simulations and theoretical evaluations regarding potential SO2 oxidation reactions. None of the relatively well-quantified aqueous phase reactions was rapid enough to make small nuclei grow to cloud condensation nuclei (CCN) size within the particle lifetime in the lower troposphere. This is consistent with the few observations showing that the smallest atmospheric particles are enriched in organics rather than sulfate. The amount of submicron particulate matter could be enhanced significantly by certain aerosol phase reactions, but this is likely to require a particle population having a pH close to 7. Aerosol phase reactions could partly explain the apparently too low SO2-to-sulfate conversion rates predicted by several chemical transport models over polluted regions. In addition to the bulk aerosol phase, SO2-to-sulfate conversion might involve physical adsorption of SO2 or a compound reacting with it by the particle surface, or it could take place in a liquid surface layer that usually covers atmospheric particles. Reactions involving physical adsorption seem to have negligible influence on the dynamics of submicron atmospheric particle populations. Aerosol phase reactions worth future investigation are those occurring in particle surface layers and those occurring in cloud interstitial particles. (C) 2000 Elsevier Science B.V. All rights reserved.
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