Abstract
Abstract. Strong atmospheric photochemistry in summer can produce a significant amount of secondary aerosols, which may have a large impact on regional air quality and visibility. In the study reported herein, we analyzed sulfate, nitrate, and ammonium in PM2.5 samples collected using a 24-h filter system at suburban and rural sites near four major cities in China (Beijing, Shanghai, Guangzhou, and Lanzhou). Overall, the PM2.5 mass concentrations were high (with a mean value of 55–68 gμgm−3), which reflects the long-known particulate pollution in China's large urban centers. We observed very high concentrations of sulfate and nitrate at the Beijing and Shanghai sites, and, in particular, abnormally high levels of nitrate (24-h average concentration up to 42 gμgm−3 and contributing up to 25% of the PM2.5 mass) in the ammonium-poor samples. The Beijing and Shanghai aerosols were characterized by high levels of aerosol acidity (~220–390 nmol m−3) and low levels of in-situ pH (−0.77 to −0.52). In these samples, the formation of the observed high concentrations of particulate nitrate cannot be explained by homogeneous gas-phase reaction between ammonia and nitric acid. Examination of the relation of nitrate to relative humidity and aerosol loading suggests that the nitrate was most probably formed via the heterogeneous hydrolysis of N2O5 on the surface of the moist and acidic aerosols in Beijing and Shanghai. In comparison, the samples collected in Lanzhou and Guangzhou were ammonium-rich with low levels of aerosol acidity (~65–70 nmol m−3), and the formation of ammonium nitrate via the homogeneous gas-phase reaction was favored, which is similar to many previous studies. An empirical fit has been derived to relate fine nitrate to aerosol acidity, aerosol water content, aerosol surface area, and the precursor of nitrate for the data from Beijing and Shanghai.
Highlights
Atmospheric PM2.5 is linked to visibility reduction, adverse health effects, and climate change (Heintzenberg, 1989; Speizer, 1989; Dockery et al, 1993; Charlson and Heintzenberg, 1995; Vedal, 1997)
Sulfate and ammonium are the predominant water-soluble ionic species in PM2.5, whereas nitrate can be found in both PM2.5 and coarse mode (>2.5μm) particles, depending on the atmospheric conditions that support the formation of ammonium nitrate and the presence of coarse mode particles that react with nitric acid (HNO3), such as sea-salt and crustal aerosols (Seinfeld and Pandis, 2006)
Nitric acid is predominantly formed during the daytime via the homogeneous gasphase reaction of NO2+OH or via heterogeneous chemistry that involves the hydrolysis of dinitrogen-pentaoxide (N2O5) on the aerosol surface at nighttime
Summary
Atmospheric PM2.5 (particulate matter with an aerodynamic diameter of 2.5 microns or less) is linked to visibility reduction, adverse health effects, and climate change (Heintzenberg, 1989; Speizer, 1989; Dockery et al, 1993; Charlson and Heintzenberg, 1995; Vedal, 1997). Sulfate and ammonium are the predominant water-soluble ionic species in PM2.5, whereas nitrate can be found in both PM2.5 and coarse mode (>2.5μm) particles, depending on the atmospheric conditions that support the formation of ammonium nitrate and the presence of coarse mode particles that react with nitric acid (HNO3), such as sea-salt and crustal aerosols (Seinfeld and Pandis, 2006). The neutralization of acidic sulfate by ammonia is favored over the formation of ammonium nitrate via a homogeneous gas phase reaction between ammonia and nitric acid. Nitric acid is predominantly formed during the daytime via the homogeneous gasphase reaction of NO2+OH or via heterogeneous chemistry that involves the hydrolysis of dinitrogen-pentaoxide (N2O5) on the aerosol surface at nighttime
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