Primary and secondary organic aerosols in summer 2016 in Beijing
To improve air quality, the Beijing government has employed several air pollution control measures since the 2008 Olympics. In order to investigate organic aerosol sources after the implementation of these measures, ambient fine particulate matter was collected at a regional site in Changping (CP) a...
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Veröffentlicht in: | Atmospheric chemistry and physics 2018-03, Vol.18 (6), p.4055-4068 |
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Zusammenfassung: | To improve air quality, the Beijing government has employed several air
pollution control measures since the 2008 Olympics. In order to investigate
organic aerosol sources after the implementation of these measures, ambient
fine particulate matter was collected at a regional site in Changping (CP) and
an urban site at the Peking University Atmosphere Environment Monitoring Station (PKUERS)
during the “Photochemical Smog in China” field campaign in summer
2016. Chemical mass balance (CMB) modeling and the tracer yield method
were used to apportion primary and secondary organic sources. Our results
showed that the particle concentration decreased significantly during the
last few years. The apportioned primary and secondary sources explained
62.8 ± 18.3 and 80.9 ± 27.2 % of the measured OC at CP and
PKUERS, respectively. Vehicular emissions served as the dominant source.
Except for gasoline engine emissions, the contributions of all the other primary
sources decreased. In addition, the anthropogenic SOC, i.e., toluene SOC, also
decreased, implying that deducting primary emissions can reduce anthropogenic
SOA. In contrast to the SOA from other regions in the world where biogenic
SOA was dominant, anthropogenic SOA was the major contributor to SOA,
implying that deducting anthropogenic VOC emissions is an efficient way to
reduce SOA in Beijing. Back-trajectory cluster analysis results showed that
high mass concentrations of OC were observed when the air mass was from
the south. However, the contributions of different primary organic sources were
similar, suggesting regional particle pollution. The ozone concentration
and temperature correlated well with the SOA concentration. Different
correlations between day and night samples suggested different SOA
formation pathways. Significant enhancement of SOA with increasing particle
water content and acidity was observed in our study, suggesting that aqueous-phase acid-catalyzed reactions may be the important SOA formation mechanism
in summer in Beijing. |
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ISSN: | 1680-7324 1680-7316 1680-7324 |
DOI: | 10.5194/acp-18-4055-2018 |