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In order to evaluate the pollution characterization of PM 2.5 (particles with aerodynamic diameters less than or equal to 2.5 μm) and secondary aerosol formation under the different photochemical activity levels, CO was used as a tracer for primary aerosol, and hourly maximum of O 3 (O 3,max ) was used as an index for photochemical activity. Results showed that under the different photochemical activity levels of L, M, LH and H, the mass concentration of PM 2.5 were 29.8 ± 17.4, 32.9 ± 20.4, 39.4 ± 19.1 and 42.2 ± 18.9 μg/m 3 , respectively. The diurnal patterns of PM 2.5 were similar under the photochemical activity and they increased along with the strengthening of photochemical activity. Especially, the ratios of estimated secondary aerosol to the observed PM 2.5 were more than 58.6% at any hour under the photochemical activity levels of LH and H. The measured chemical composition included water soluble inorganic ions, organic carbon (OC), and element carbon (EC), which accounted for 73.5 ± 14.9%, 70.3 ± 24.9%, 72.0 ± 21.9%, and 65.8 ± 21.2% in PM 2.5 under the photochemical activities of L, M, LH, and H, respectively. Furthermore, the sulfate (SO 4  2- ) and nitrate (NO 3  - ) were nearly neutralized by ammonium (NH 4  + ) with the regression slope of 0.71, 0.77, 0.77, and 0.75 between [NH 4  + ] and 2[SO 4  2- ] + [NO 3  - ]. The chemical composition of PM 2.5 was mainly composed of SO 4  2- , NO 3  - , NH 4  + and secondary organic carbon (SOC), indicating that the formation of secondary aerosols significantly contributed to the increase in PM 2.5 . The formation mechanism of sulfate in PM 2.5 was the gas-phase oxidation of SO 2 to H 2 SO 4 . Photochemical production of nitric acid was intense during daytime, but particulate nitrate concentration was low in the afternoon due to high temperature.

international journal of environmental  research and public health/international journal of environmental research and public health

Characterization of Atmospheric Fine Particles and Secondary Aerosol Estimated under the Different Photochemical Activities in Summertime Tianjin, China