Evidence of heterogeneous HONO formation from aerosols and the regional photochemical impact of this HONO source

Abstract

Large missing daytime HONO sources have been reported by many previous studies around the world. Possible HONO sources include ground heterogeneous conversion, aerosol heterogeneous formation, soil emission, and photochemical production. In this study, a consistent 1D framework based on regional and 3D chemical transport models (CTMs) was used to analyze the unknown daytime HONO sources in 14 cases worldwide. We assume that the source of HONO from aerosols is through NO2 hydrolysis (not including its oxidation products) and that non-local mixing effect is negligible. Assuming all the missing unknown HONO source is from the ground, it would imply a NO2-to-HONO ground heterogeneous conversion exceeding 100% in daytime, which is unphysical. In contrast, a strong R2 reaching up to 0.92 is found between the unknown HONO sources and the products of aerosol wet surface area and short-wave radiation. Because the largest unknown daytime HONO sources are found in China due to high concentrations of aerosols and NO2, we derive an optimized NO2 uptake coefficient on the basis of these measurements. The 3D CTM simulations suggest that in some regions of central, eastern, and southwestern (e.g. SiChuan province) China, the aerosol HONO source has the greatest effects on ozone (>10 ppbv) and OH (>200%) in winter. In January, the simulated particulate sulfate level over these three regions increases by 6–10 μg m−3 after including the aerosol-HONO source, which helps reduce the previous model underestimation of sulfate production in winter. Additional measurement studies that target the daytime HONO sources will be essential to a better understanding of the mechanisms and resulting effects on atmospheric oxidants.