| Popis: |
The importance of dust heterogeneous oxidation in the removal of atmospheric SO2 and formation of sulfate aerosols is not adequately understood. In this study, the Fe-, Ti-, and Al-bearing components, Na+, Cl−, K+, and Ca2+ of the dust surface, were discovered to be closely associated with the heterogeneous formation of sulfate. Regression models were then developed to make a reliable prediction of the heterogeneous reactivity based on the particle chemical compositions. Further, the recognized gas-phase, aqueous-phase, and heterogeneous oxidation routes were quantitatively assessed and kinetically compared by combining the laboratory work with a modelling study. In the presence of 55 µg m−3 airborne dust, heterogeneous oxidation accounts for approximately 28.6 % of the secondary sulfate aerosols during nighttime, while the proportion decreases to 13.1 % in the presence of solar irradiation. On the dust surface, heterogeneous drivers (e.g. transition metal constituents, water-soluble ions) are more efficient than surface-adsorbed oxidants (e.g. H2O2, NO2, O3) in the conversion of SO2, particularly during nighttime. Dust heterogeneous oxidation offers an opportunity to explain the missing sulfate source during severe haze pollution events, and its contribution proportion in the complex atmospheric environments could be even higher than the current calculation results. Overall, the dust surface drivers are responsible for the significant formation of sulfate aerosols and have profound impacts on the atmospheric sulfur cycling. |
