Xingna Yu 1,2, Li Shen1, Sihan Xiao1, Jia Ma3, Rui Lü1, Bin Zhu1, Jianlin Hu4, Kui Chen1, Jun Zhu1


Key Laboratory of Meteorological Disaster, Ministry of Education (KLME)/Joint International Research Laboratory of Climate and Environment Change (ILCEC)/Collaborative Innovation Center on Forecast and Evaluation of Meteorological Disasters (CIC-FEMD)/Key Laboratory for Aerosol-Cloud-Precipitation of China Meteorological Administration, Nanjing University of Information Science and Technology, Nanjing 210044, China
Shanghai Key Laboratory of Atmospheric Particle Pollution and Prevention (LAP3), Shanghai 200433, China
Guangzhou Hexin Analytical Instrument Company Limited, Guangzhou 510530, China
Collaborative Innovation Center of Atmospheric Environment and Equipment Technology, Jiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution Control, School of Environmental Science and Engineering, Nanjing University of Information Science and Technology, Nanjing 210044, China



Received: December 29, 2017
Revised: April 19, 2018
Accepted: April 19, 2018
Download Citation: ||https://doi.org/10.4209/aaqr.2017.12.0572  

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Cite this article:
Yu, X., Shen, L., Xiao, S., Ma, J., Lü, R., Zhu, B., Hu, J., Chen, K. and Zhu, J. (2019). Chemical and Optical Properties of Atmospheric Aerosols during the Polluted Periods in a Megacity in the Yangtze River Delta, China. Aerosol Air Qual. Res. 19: 103-117. https://doi.org/10.4209/aaqr.2017.12.0572


HIGHLIGHTS

  • Aerosol chemical and optical properties were observed in Nanjing.
  • Secondary formation dominated PM2.5 pollution were discussed.
  • Contributions of aerosol chemical components to light extinction were quantified.

ABSTRACT


The chemical composition and optical properties of particulate matter (PM) were characterized in an urban-industrial area of Nanjing, China, in January 2015, when heavily polluted periods frequently occurred. Only 30% of the days fulfilled the National Ambient Air Quality Standards of China. The average scattering and absorption coefficients at 532 nm during the polluted periods were 620 ± 320 Mm–1 and 102 ± 57 Mm–1. An increasing relative fraction of the large size PM during the polluted periods can be deduced from the variations of the scattering Ångström exponent, backscattering ratio, and asymmetry factor. The mean mass concentrations of NO3, SO42– and NH4+ in PM2.5 during the polluted periods were 32.87 ± 17.76 µg m–3, 23.6 ± 13.2 µg m–3, and 19.4 ± 10.1 µg m–3, respectively. NO3, SO42– and NH4+ were the dominant water-soluble ions (WSIs) and accounted for 87% of the total ion concentration. Nitrate and organic matter (OM) dominated the aerosol composition during the polluted periods. The averaged organic carbon/elementary carbon ratios during the polluted and the cleaner periods were 3.6 and 4.3, respectively, consistent with a mix of primary emissions and secondary organic aerosol formation. Organic matter and ammonium nitrate (AN) were the dominant species contributing to light extinction during the polluted periods, contributing values of 159 ± 63 Mm–1 and 156 ± 91 Mm–1, respectively.


Keywords: Air pollution; Aerosol chemical composition; Aerosol optical properties; Atmospheric extinction.

 


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