The characteristics of fine aerosol particles were investigated at an urban site in Beijing during an atmospheric pollution accumulation process. The organics, sulfate and BC were the dominant components in fine particles in the clear air, and the concentrations of organics, sulfate, nitrate and ammonium increased during the haze formation. The mass concentrations of primary species (chloride and BC) in the clear air were similar to those in the haze. The morphology, mixing state and aging status of fine particles in the clear air were different from those in the haze. Accumulation secondary particles were detected with high frequency and accumulation secondary particles with coating were rare in all the samples. The frequency of soot particles with coating in the clear air was lower than that in the haze. The number ratio of accumulation secondary particles to soot containing particles changed from 3:1 in clear air to 2:3 in the haze. These results indicated that the number frequency of accumulation secondary particles decreased while that of the soot containing particles increased with the air pollutants accumulating. The core-shell ratio of coated soot particles ranged between 0.1–0.6 was 62% in the clear air, and 82% in the haze. The mode sizes for the core and the shell of soot particles were 0.35 μm and 0.55 μm in the clear air, and 0.35 μm and 1.0 μm in the haze, respectively. The mean diameters of the core and the shell were 0.3 μm and was 0.6 μm in the clear air, and 0.4 μm and 1.0 μm in the haze, respectively. These results indicated that with the air pollution accumulating, the frequency of accumulation secondary particles decreased while the soot containing particles increased. The aging process of soot particles was stronger in the haze, and resulted in greater hygroscopicity for soot particles in the haze.
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1 February 2015
Research Article|
February 01 2015
Evolution of atmospheric aerosol particles during a pollution accumulation process: a case study
Hongya Niu;
Hongya Niu
*
1
Key Laboratory of Resource Exploration Research of Hebei Province; Hebei University of Engineering, Handan 056038, Heibei, China.
2
State Key Joint Laboratory of Environmental Simulation and Pollution Control, College of Environmental Sciences and Engineering, Peking University, Beijing 100871, China.
*E-mail: niuhongya@126.com
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Wei Hu;
Wei Hu
2
State Key Joint Laboratory of Environmental Simulation and Pollution Control, College of Environmental Sciences and Engineering, Peking University, Beijing 100871, China.
3
Faculty of Environmental and Symbiotic Sciences, Prefectural University of Kumamoto, Kumamoto 862-8502, Japan.
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Wei Pian;
Wei Pian
1
Key Laboratory of Resource Exploration Research of Hebei Province; Hebei University of Engineering, Handan 056038, Heibei, China.
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Jingsen Fan;
Jingsen Fan
4
Hebei Collaborative Innovation Center of Coal Exploitation, Hebei University of Engineering, Handan 056038, Hebei, China.
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Jinxi Wang
Jinxi Wang
1
Key Laboratory of Resource Exploration Research of Hebei Province; Hebei University of Engineering, Handan 056038, Heibei, China.
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*E-mail: niuhongya@126.com
Publisher: Emerald Publishing
Received:
October 02 2014
Accepted:
December 05 2014
Online ISSN: 2515-8082
Print ISSN: 1708-5284
World Journal of Engineering (2015) 12 (1): 51–60.
Article history
Received:
October 02 2014
Accepted:
December 05 2014
Citation
Niu H, Hu W, Pian W, Fan J, Wang J (2015), "Evolution of atmospheric aerosol particles during a pollution accumulation process: a case study". World Journal of Engineering, Vol. 12 No. 1 pp. 51–60, doi: https://doi.org/10.1260/1708-5284.12.1.51
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