Reduced volatility of aerosols from surface emissions to the top of the planetary boundary layer
<p>Aerosols from surface emission can be transported upwards through convective mixing in the planetary boundary layer (PBL), which subsequently interact with clouds, serving as important sources to nucleate droplets or ice particles. However, the evolution of aerosol composition during this v...
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Format: | Article |
Language: | English |
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Copernicus Publications
2021-10-01
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Series: | Atmospheric Chemistry and Physics |
Online Access: | https://acp.copernicus.org/articles/21/14749/2021/acp-21-14749-2021.pdf |
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record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Q. Liu D. Liu Y. Wu K. Bi W. Gao P. Tian D. Zhao S. Li C. Yu G. Tang Y. Wu K. Hu S. Ding Q. Gao F. Wang S. Kong H. He H. He M. Huang M. Huang D. Ding |
spellingShingle |
Q. Liu D. Liu Y. Wu K. Bi W. Gao P. Tian D. Zhao S. Li C. Yu G. Tang Y. Wu K. Hu S. Ding Q. Gao F. Wang S. Kong H. He H. He M. Huang M. Huang D. Ding Reduced volatility of aerosols from surface emissions to the top of the planetary boundary layer Atmospheric Chemistry and Physics |
author_facet |
Q. Liu D. Liu Y. Wu K. Bi W. Gao P. Tian D. Zhao S. Li C. Yu G. Tang Y. Wu K. Hu S. Ding Q. Gao F. Wang S. Kong H. He H. He M. Huang M. Huang D. Ding |
author_sort |
Q. Liu |
title |
Reduced volatility of aerosols from surface emissions to the top of the planetary boundary layer |
title_short |
Reduced volatility of aerosols from surface emissions to the top of the planetary boundary layer |
title_full |
Reduced volatility of aerosols from surface emissions to the top of the planetary boundary layer |
title_fullStr |
Reduced volatility of aerosols from surface emissions to the top of the planetary boundary layer |
title_full_unstemmed |
Reduced volatility of aerosols from surface emissions to the top of the planetary boundary layer |
title_sort |
reduced volatility of aerosols from surface emissions to the top of the planetary boundary layer |
publisher |
Copernicus Publications |
series |
Atmospheric Chemistry and Physics |
issn |
1680-7316 1680-7324 |
publishDate |
2021-10-01 |
description |
<p>Aerosols from surface emission can be transported upwards through convective mixing in the planetary boundary layer (PBL), which subsequently interact with clouds, serving as important sources to nucleate droplets or ice particles. However, the evolution of aerosol composition during this vertical transport has yet to be explicitly understood. In this study, simultaneous measurements of detailed aerosol compositions were conducted at two sites, namely urban Beijing (50 m above sea level – a.s.l.) and Haituo mountain (1344 m a.s.l.) during wintertime, representing the anthropogenically polluted surface environment and the top of the PBL, respectively. The pollutants from surface emissions were observed to reach the mountain site on daily basis through daytime PBL convective mixing. From the surface to the top of PBL, we found efficient transport or formation of lower-volatility species (black carbon, sulfate, and low-volatile organic aerosol, OA); however, a notable reduction in semivolatile substances, such as the fractions of nitrate and semivolatile OA reduced by 74 % and 76 %, respectively,
during the upward transport. This implies that the mass loss of these
semivolatile species was driven by the evaporation process, which
repartitioned the condensed semivolatile substances to the gas phase when
aerosols were transported and exposed to a cleaner environment. In
combination with the oxidation processes, these led to an enhanced oxidation state of OA at the top of the PBL compared to surface environment, with an increase of oxygen to carbon atomic ratio by 0.2. Such a reduction in aerosol volatility during vertical transport may be important in modifying its viscosity, nucleation activity, and atmospheric lifetime.</p> |
url |
https://acp.copernicus.org/articles/21/14749/2021/acp-21-14749-2021.pdf |
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doaj-f9d2c3db85034561bf3794e28009b6fb2021-10-05T13:48:22ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242021-10-0121147491476010.5194/acp-21-14749-2021Reduced volatility of aerosols from surface emissions to the top of the planetary boundary layerQ. Liu0D. Liu1Y. Wu2K. Bi3W. Gao4P. Tian5D. Zhao6S. Li7C. Yu8G. Tang9Y. Wu10K. Hu11S. Ding12Q. Gao13F. Wang14S. Kong15H. He16H. He17M. Huang18M. Huang19D. Ding20State Key Laboratory of Severe Weather & Key Laboratory of Atmospheric Chemistry of CMA, Chinese Academy of Meteorological Sciences, Beijing 100081, ChinaDepartment of Atmospheric Sciences, School of Earth Sciences, Zhejiang University, Hangzhou, Zhejiang, 310027, ChinaDepartment of Atmospheric Sciences, School of Earth Sciences, Zhejiang University, Hangzhou, Zhejiang, 310027, ChinaBeijing Weather Modification Office, Beijing 100089, ChinaState Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100029, ChinaBeijing Weather Modification Office, Beijing 100089, ChinaBeijing Weather Modification Office, Beijing 100089, ChinaDepartment of Atmospheric Sciences, School of Earth Sciences, Zhejiang University, Hangzhou, Zhejiang, 310027, ChinaCentre for Atmospheric Sciences, School of Earth and Environmental Sciences, University of Manchester, Manchester M13 9PL, UKState Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100029, ChinaKey Laboratory of Middle Atmosphere and Global Environment Observation (LAGEO), Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100029, ChinaDepartment of Atmospheric Sciences, School of Earth Sciences, Zhejiang University, Hangzhou, Zhejiang, 310027, ChinaDepartment of Atmospheric Sciences, School of Earth Sciences, Zhejiang University, Hangzhou, Zhejiang, 310027, ChinaBeijing Weather Modification Office, Beijing 100089, ChinaBeijing Weather Modification Office, Beijing 100089, ChinaDepartment of Atmospheric Science, School of Environmental Studies, China University of Geosciences, Wuhan 430074, ChinaBeijing Weather Modification Office, Beijing 100089, ChinaField experiment base of cloud and precipitation research in North China, China Meteorological Administration, Beijing 101200, ChinaBeijing Weather Modification Office, Beijing 100089, ChinaField experiment base of cloud and precipitation research in North China, China Meteorological Administration, Beijing 101200, ChinaBeijing Weather Modification Office, Beijing 100089, China<p>Aerosols from surface emission can be transported upwards through convective mixing in the planetary boundary layer (PBL), which subsequently interact with clouds, serving as important sources to nucleate droplets or ice particles. However, the evolution of aerosol composition during this vertical transport has yet to be explicitly understood. In this study, simultaneous measurements of detailed aerosol compositions were conducted at two sites, namely urban Beijing (50 m above sea level – a.s.l.) and Haituo mountain (1344 m a.s.l.) during wintertime, representing the anthropogenically polluted surface environment and the top of the PBL, respectively. The pollutants from surface emissions were observed to reach the mountain site on daily basis through daytime PBL convective mixing. From the surface to the top of PBL, we found efficient transport or formation of lower-volatility species (black carbon, sulfate, and low-volatile organic aerosol, OA); however, a notable reduction in semivolatile substances, such as the fractions of nitrate and semivolatile OA reduced by 74 % and 76 %, respectively, during the upward transport. This implies that the mass loss of these semivolatile species was driven by the evaporation process, which repartitioned the condensed semivolatile substances to the gas phase when aerosols were transported and exposed to a cleaner environment. In combination with the oxidation processes, these led to an enhanced oxidation state of OA at the top of the PBL compared to surface environment, with an increase of oxygen to carbon atomic ratio by 0.2. Such a reduction in aerosol volatility during vertical transport may be important in modifying its viscosity, nucleation activity, and atmospheric lifetime.</p>https://acp.copernicus.org/articles/21/14749/2021/acp-21-14749-2021.pdf |