TY - JOUR
T1 - Measurement report
T2 - Comparison of wintertime individual particles at ground level and above the mixed layer in urban Beijing
AU - Wang, Wenhua
AU - Shao, Longyi
AU - Mazzoleni, Claudio
AU - Li, Yaowei
AU - Kotthaus, Simone
AU - Grimmond, Sue
AU - Bhandari, Janarjan
AU - Xing, Jiaoping
AU - Feng, Xiaolei
AU - Zhang, Mengyuan
AU - Shi, Zongbo
N1 - Publisher Copyright:
© Author(s) 2021. This work is distributed under the Creative Commons Attribution 4.0 License.
PY - 2021/4/7
Y1 - 2021/4/7
N2 - Beijing has been suffering from frequent severe air pollution events, with concentrations affected significantly by the mixed-layer height. Major efforts have been made to study the physico-chemical properties, compositions, and sources of aerosol particles at ground level. However, little is known about the morphology, elemental composition, and mixing state of aerosol particles above the mixed layer. In this work, we collected individual aerosol particles simultaneously at ground level (2 m above ground) and above the mixed layer in urban Beijing (within the Atmospheric Pollution and Human Health in a Chinese Megacity, APHH-Beijing, 2016 winter campaign). The particles were analyzed offline by transmission electron microscopy coupled with energy dispersive X-ray spectroscopy. Our results showed that the relative number contribution of mineral particles to all measured particles was much higher during non-haze periods (42.5 %) than haze periods (18.1 %); in contrast, internally mixed particles contributed more during haze periods (21.9 %) than non-haze periods (7.2 %) at ground level. In addition, more mineral particles were found at ground level than above the mixed-layer height. Around 20 % of individual particles showed core-shell structures during haze periods, whereas only a few core-shell particles were observed during non-haze periods (2 %). The results showed that the particles above the mixed layer were more aged, with a larger proportion of organic particles originating from coal combustion. Our results indicate that a large fraction of the airborne particles above the mixed layer come from surrounding areas influenced by coal combustion activities. This source contributes to the surface particle concentrations in Beijing when polluted air is mixed down to the ground level.
AB - Beijing has been suffering from frequent severe air pollution events, with concentrations affected significantly by the mixed-layer height. Major efforts have been made to study the physico-chemical properties, compositions, and sources of aerosol particles at ground level. However, little is known about the morphology, elemental composition, and mixing state of aerosol particles above the mixed layer. In this work, we collected individual aerosol particles simultaneously at ground level (2 m above ground) and above the mixed layer in urban Beijing (within the Atmospheric Pollution and Human Health in a Chinese Megacity, APHH-Beijing, 2016 winter campaign). The particles were analyzed offline by transmission electron microscopy coupled with energy dispersive X-ray spectroscopy. Our results showed that the relative number contribution of mineral particles to all measured particles was much higher during non-haze periods (42.5 %) than haze periods (18.1 %); in contrast, internally mixed particles contributed more during haze periods (21.9 %) than non-haze periods (7.2 %) at ground level. In addition, more mineral particles were found at ground level than above the mixed-layer height. Around 20 % of individual particles showed core-shell structures during haze periods, whereas only a few core-shell particles were observed during non-haze periods (2 %). The results showed that the particles above the mixed layer were more aged, with a larger proportion of organic particles originating from coal combustion. Our results indicate that a large fraction of the airborne particles above the mixed layer come from surrounding areas influenced by coal combustion activities. This source contributes to the surface particle concentrations in Beijing when polluted air is mixed down to the ground level.
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U2 - 10.5194/acp-21-5301-2021
DO - 10.5194/acp-21-5301-2021
M3 - Article
AN - SCOPUS:85103786869
SN - 1680-7316
VL - 21
SP - 5301
EP - 5314
JO - Atmospheric Chemistry and Physics
JF - Atmospheric Chemistry and Physics
IS - 7
ER -