Your browser doesn't support javascript.
loading
The carbonaceous aerosol levels still remain a challenge in the Beijing-Tianjin-Hebei region of China: Insights from continuous high temporal resolution measurements in multiple cities.
Ji, Dongsheng; Gao, Meng; Maenhaut, Willy; He, Jun; Wu, Cheng; Cheng, Linjun; Gao, Wenkang; Sun, Yang; Sun, Jiaren; Xin, Jinyuan; Wang, Lili; Wang, Yuesi.
Afiliación
  • Ji D; State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100191, China; Atmosphere Sub-Center of Chinese Ecosystem Research Network, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beij
  • Gao M; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138, USA.
  • Maenhaut W; Department of Chemistry, Ghent University, Gent 9000, Belgium. Electronic address: Willy.Maenhaut@UGent.be.
  • He J; International Doctoral Innovation Centre, Department of Chemical and Environmental Engineering, University of Nottingham Ningbo China, Ningbo 315100, China.
  • Wu C; Institute of Mass Spectrometer and Atmospheric Environment, Jinan University, Guangzhou 510632, China; Guangdong Provincial Engineering Research Center for On-Line Source Apportionment System of Air Pollution, Guangzhou 510632, China.
  • Cheng L; China National Environmental Monitoring Center, Beijing 100012, China.
  • Gao W; State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100191, China.
  • Sun Y; State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100191, China; Atmosphere Sub-Center of Chinese Ecosystem Research Network, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beij
  • Sun J; South China Institute of Environmental Sciences, Ministry of Environmental Protection, Guangzhou 510655, China.
  • Xin J; State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100191, China; Atmosphere Sub-Center of Chinese Ecosystem Research Network, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beij
  • Wang L; State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100191, China; Atmosphere Sub-Center of Chinese Ecosystem Research Network, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beij
  • Wang Y; State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100191, China; Atmosphere Sub-Center of Chinese Ecosystem Research Network, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beij
Environ Int ; 126: 171-183, 2019 05.
Article en En | MEDLINE | ID: mdl-30798198
ABSTRACT
Carbonaceous aerosols in high emission areas attract worldwide attention of the scientific community and the public due to their adverse impacts on the environment, human health and climate. However, long-term continuous hourly measurements are scarce on the regional scale. In this study, a one-year hourly measurement (from December 1, 2016 to November 30, 2017) of organic carbon (OC) and elemental carbon (EC) in airborne fine particles was performed using semi-continuous OC/EC analyzers in Beijing, Tianjin, Shijiazhuang and Tangshan in the Beijing-Tianjin-Hebei (BTH) region in China, which is one of high emission areas in China, even in the world. Marked spatiotemporal variations were observed. The highest concentrations of OC (22.8 ±â€¯30.6 µg/m3) and EC (5.4 ±â€¯6.5 µg/m3) occurred in Shijiangzhuang while the lowest concentrations of OC (11.0 ±â€¯10.7 µg/m3) and EC (3.1 ±â€¯3.6 µg/m3) were obtained in Beijing and Tianjin, respectively. Pronounced monthly, seasonal and diurnal variations of OC and EC were recorded. Compared to published data from the past two decades for the BTH region, our OC and EC levels were lower, implying some effect of recent measures for improving the air quality. Significant correlations of OC versus EC (p < 0.001) were found throughout the study period with high slopes and correlation coefficients in winter, but low slopes and correlation coefficients in summer. The estimated secondary OC (SOC), based on the minimum R squared (MRS) method, represented 29%, 47%, 38% and 48% of the OC for Beijing, Tianjin, Shijiazhuang and Tangshan, respectively. These percentages are larger than previous ones obtained for the BTH region in the past decade. There were obvious differences in the potential source regions of OC and EC among the four cities. Obvious prominent potential source areas of OC and EC were observed for Beijing, which were mainly located in the central and western areas of Inner Mongolia and even extended to the Mongolian regions, which is different from the findings in previous studies. For all sites, adjacent areas of the main provinces in northern China were found to be important potential source areas.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Carbono / Contaminantes Atmosféricos / Material Particulado País/Región como asunto: Asia Idioma: En Revista: Environ Int Año: 2019 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Carbono / Contaminantes Atmosféricos / Material Particulado País/Región como asunto: Asia Idioma: En Revista: Environ Int Año: 2019 Tipo del documento: Article