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

Jinxia Gu, Zexin Chen, Nan Zhang, Shitao Peng, Wenjing Cui, Guangyao Huo and Feng Chen
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Jinxia Gu: School of Science, Tianjin Chengjian Unversity, Tianjin 300384, China
Zexin Chen: School of Science, Tianjin Chengjian Unversity, Tianjin 300384, China
Nan Zhang: School of Science, Tianjin Chengjian Unversity, Tianjin 300384, China
Shitao Peng: Tianjin Research Institute for Water Transport Engineering, Tianjin 300456, China
Wenjing Cui: School of Science, Tianjin Chengjian Unversity, Tianjin 300384, China
Guangyao Huo: School of Science, Tianjin Chengjian Unversity, Tianjin 300384, China
Feng Chen: School of Civil Engineering, North China Institute of Aerospace Engineering, Langfang 065000, China

IJERPH, 2022, vol. 19, issue 13, 1-18

Abstract: 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.

Keywords: atmospheric fine particles; secondary aerosol; photochemical reaction (search for similar items in EconPapers)
JEL-codes: I I1 I3 Q Q5 (search for similar items in EconPapers)
Date: 2022
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