The role of alkaline mineral aerosol in controlling HNO3 partitioning betwe
en gas and aerosol phases is explored using a comprehensive, process orient
ed three-dimensional model. Simulation results for March 1994, a period fro
m the PEM West B experiment, are presented. It is found that in the dust im
pacted regions of the boundary layer and free troposphere, more than 50% of
HNO3 is partitioned onto dust particles; while 10 similar to 50% of HNO3 i
n the boundary layer and 10 similar to 30% of HNO3 in the free troposphere
is partitioned onto sea-salt particles. This higher capacity of mineral dus
t to uptake HNO3 is due to the fact that carbonate in the dust particles is
more volatile (thus easily replaced by nitrate) than chloride in the sea-s
alt particles. When this process of nitric acid partitioning onto alkaline
particles is included in the analysis, model predicted HNO3-to-NOx ratios a
re much closer to observed values that typically range between 1 and 9.