Field Observation of Important Nonactivation Scavenging of Black Carbon by Clouds

The in-cloud scavenging of black carbon containing (BCc) aerosols by cloud condensation nuclei (CCN) activation is considered to be the primary mechanism for wet scavenging. By measuring the particle-resolved mixing state of BCc in the residues of orographic clouds downstream of a ground-based counter-flow virtual impactor, we found that a fraction of 30-90% of BCc could be in clouds by a collision/coalescence process without satisfying the conventional Köhler theory for CCN activation. These non-CCN BCc in clouds occupied a larger fraction of total in-cloud BCc when cloud droplets were larger, e.g., the non-CCN BCc fraction in clouds increased from 40% to 80% when the effective diameter of droplets increased from about 7.6 to 15.8 μm. This collision/coalescence process among droplets and BCc tended to be more efficient for larger droplets, which is also supported by microscopy images that one droplet could capture more than one BC cores. Larger droplets corresponded to lower ambient water supersaturation, under which conditions the removal of BCc in clouds by collision/coalescence may override CCN activation. By in situ measurements, the results here for the first time separated and quantified the BCc in clouds between activation and nonactivation processes, which provides insights into evaluating the wet removal and aging of atmospheric BC.

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Publication Details

Journal
Environmental Science & Technology
Published
2025-05-06
DOI
https://doi.org/10.1021/acs.est.5c00199
Citations
5
Primary Topic
Atmospheric chemistry and aerosols
Type
article
Field-Weighted Citation Impact
6.50

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article

Field Observation of Important Nonactivation Scavenging of Black Carbon by Clouds

Xiaocong Peng, Weiqi Xu, Baiwan Pan, Yele Sun et al.
5 citations
Environmental Science & Technology
Atmospheric chemistry and aerosols
6.50
article

Field Observation of Important Nonactivation Scavenging of Black Carbon by Clouds

Xiaocong Peng, Weiqi Xu, Baiwan Pan, Yele Sun, Yunfei Wu, Xiaomi Teng, Xinhui Bi, Lanzhong Liu, Yangzhou Wu, Shuo Ding, Dantong Liu, Ping Tian, Zifa Wang, Xiaole Pan, Guohua Zhang, Weijun Li, Yi Zhang, Siyuan Li, Shitong Zhao
article en
5 citations

Abstract

The in-cloud scavenging of black carbon containing (BCc) aerosols by cloud condensation nuclei (CCN) activation is considered to be the primary mechanism for wet scavenging. By measuring the particle-resolved mixing state of BCc in the residues of orographic clouds downstream of a ground-based counter-flow virtual impactor, we found that a fraction of 30-90% of BCc could be in clouds by a collision/coalescence process without satisfying the conventional Köhler theory for CCN activation. These non-CCN BCc in clouds occupied a larger fraction of total in-cloud BCc when cloud droplets were larger, e.g., the non-CCN BCc fraction in clouds increased from 40% to 80% when the effective diameter of droplets increased from about 7.6 to 15.8 μm. This collision/coalescence process among droplets and BCc tended to be more efficient for larger droplets, which is also supported by microscopy images that one droplet could capture more than one BC cores. Larger droplets corresponded to lower ambient water supersaturation, under which conditions the removal of BCc in clouds by collision/coalescence may override CCN activation. By in situ measurements, the results here for the first time separated and quantified the BCc in clouds between activation and nonactivation processes, which provides insights into evaluating the wet removal and aging of atmospheric BC.

Environmental Science & TechnologyVol. 59(19)
Chinese Academy of Sciences (CN), Institute of Geochemistry (CN), Jilin Weather Modification Office (CN), Czech Academy of Sciences, Institute of Atmospheric Physics (CZ), China Jiliang University (CN), Zhejiang University (CN)
National Natural Science Foundation of China, Chinese Academy of Sciences, Natural Science Foundation of Zhejiang Province, Science Fund for Distinguished Young Scholars of Zhejiang Province
Openalex Percentile: Top 3%
Atmospheric chemistry and aerosols
6.50
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