Oxidation of sulfur dioxide by nitrogen dioxide accelerated at the interface of deliquesced aerosol particles

Although the multiphase chemistry of SO2 in aerosol particles is of great importance to air quality under polluted haze conditions, a fundamental understanding of the pertinent mechanisms and kinetics is lacking. In particular, there is considerable debate on the importance of NO2 in the oxidation of SO2 in aerosol particles. Here experiments with atmospherically relevant deliquesced particles at buffered pH values of 4-5 show that the effective rate constant for the reaction of NO2 with SO32- ((1.4 +/- 0.5) x 10(10) M-1 s(-1)) is more than three orders of magnitude larger than the value in dilute solutions. An interfacial reaction at the surface of aerosol particles probably drives the very fast kinetics. Our results indicate that oxidation of SO2 by NO2 at aerosol surfaces may be an important source of sulfate aerosols under polluted haze conditions.

Automated summary

This study demonstrates that the rate of reaction between NO2 and SO2 in dense atmospheric particles is significantly higher than in dilute solutions, indicating that the surface of aerosol particles may be the driving force behind this rapid reaction kinetics. These results suggest that the oxidation of SO2 by NO2 at aerosol surfaces could be an important source of sulfate aerosols under polluted haze conditions.