Smog chamber study of the role of NH3 in new particle formation fromphoto-oxidation of aromatic hydrocarbons

Abstract Ammonia (NH 3 ) is a major contributor to secondary aerosol in the atmosphere and can alter the kinetics of their formation. However, systematic studies related to the role of NH 3 in aerosol nucleation processes and further particle size growth under complex scenarios are lacking. In this study, we conducted 16 experiments in the CSIRO smog chamber under dry conditions using aromatic hydrocarbons (toluene, o -/ m -/ p -xylene) and different concentrations of NH 3 . The presence of NH 3 did not change the gas-phase chemistry or nucleation onset time, but slowed the nucleation rate (5%–94%) once it began. From the response of nitrogen oxides (NOx) measurement and mechanism modeling results, we hypothesised that the surface reaction between NH 3 and nitric acid played a central role in aerosol nucleation and further growth. After nucleation, the subsequently formed ammonium nitrate and organic condensation vapours may partition together into the initial growth process of new particles, thus increasing the aerosol initial growth rate (8%–90%) and size growth potentials (7%–108%), and leading to high aerosol mass formation. Further investigation implied that the initial growth and further growth rate determine the aerosol mass concentration, rather than the nucleation rate. We conclude that both the initial NOx concentration and volatile organic compound (VOC)/NOx ratio are crucial for the initial and further growth, and aerosol mass of new particles, when NH 3 levels are high. Our results provide crucial insights into the complex chemistry of VOC/NOx/NH 3 in the atmosphere, and highlight the importance of NH 3 reduction for particulate matter control.