Abstract

Abstract. Aerosol particles play important roles in air quality and global climate change. In this study, we analyze the measurements of particle size distribution from 12 March to 6 April 2016 in Beijing to characterize new particle formation (NPF) using the observational data of sulfuric acid, meteorological parameters, solar radiation, and the mass concentration of fine particles (PM2.5, particulate matter with diameters less than 2.5 µm). During this 26 d campaign, 11 new particle formation events are identified with obvious bursts of sub-3 nm particle number concentrations and subsequent growth of these nucleated particles. It is found that sulfuric acid concentration in Beijing does not have a significant difference between NPF event and non-event days. Low relative humidity (RH) and high daily total solar radiation appear to be favorable for the occurrence of NPF events, which is quite obvious in this campaign. The simulations using four nucleation schemes, i.e., H2SO4–H2O binary homogeneous nucleation (BHN), H2SO4–H2O–NH3 ternary homogeneous nucleation (THN), H2SO4–H2O–ion binary ion-mediated nucleation (BIMN), and H2SO4–H2O–NH3–ion ternary ion-mediated nucleation (TIMN), based on a global chemistry transport model (GEOS-Chem) coupled with an advanced particle microphysics (APM) model, are conducted to study the particle number concentrations and new particle formation process. Our comparisons between measurements and simulations indicate that the BHN scheme and BIMN scheme significantly underestimate the observed particle number concentrations, and the THN scheme captures the total particle number concentration on most NPF event days well but fails to capture the noticeable increase in particle number concentrations on 18 March and 1 April. The TIMN scheme has obvious improvement in terms of total and sub-3 nm particle number concentrations and nucleation rates. This study provides a basis for further understanding of the nucleation mechanism in Beijing.

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