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Real‐Time Characterization of Aerosol Compositions, Sources, and Aging Processes in Guangzhou During PRIDE‐GBA 2018 Campaign
Author(s) -
Chen Wei,
Ye Yuqing,
Hu Weiwei,
Zhou Huaishan,
Pan Tianle,
Wang Yingkun,
Song Wei,
Song Qicong,
Ye Chenshuo,
Wang Chaomin,
Wang Baolin,
Huang Shan,
Yuan Bin,
Zhu Ming,
Lian Xiufeng,
Zhang Guohua,
Bi Xinhui,
Jiang Fan,
Liu Junwen,
Caaco Francesco,
Prevot Andre S. H.,
Shao Min,
Wang Xinming
Publication year - 2021
Publication title -
journal of geophysical research: atmospheres
Language(s) - English
Resource type - Journals
eISSN - 2169-8996
pISSN - 2169-897X
DOI - 10.1029/2021jd035114
Subject(s) - aerosol , sulfate , nitrate , environmental chemistry , chemistry , nox , nitrogen , combustion , organic chemistry
To investigate the chemical compositions, sources, and aging processes of submicron particles (PM 1 ), a comprehensive field campaign was conducted in Guangzhou urban area of China during the autumn (October–November) of 2018. The average mass concentration of PM 1 was 35.6 ± 20.8 µg m −3 , which was mainly contributed by organic aerosols (OA, 42%), then followed by sulfate (25%) and inorganic nitrate (11%). The inorganic nitrate was found to be the main driving component (up to ∼50%) to account for the fast increase of PM 1 during the polluted periods of Guangzhou autumn. The promotion effects of sulfate, aerosol liquid water content, and particles acidity on nitrate formation were systematically discussed. Source apportionment results showed 72% of OA in Guangzhou autumn was contributed by secondary OA (SOA), and 28% of primary OA (POA), including vehicle emission related hydrocarbon‐like OA (HOA, 16%), nitrogen‐containing OA (NOA, 3%) and cooking OA (COA, 8%). To explore the aging processes of OA, the dynamic variations of OA and its oxidation level as a function of ambient photochemical age are shown. Using an in situ field‐deployed oxidation flow reactor, the heterogeneous reaction rate coefficients of ambient POA with OH radicals ( k OH ) were estimated to be 4.0–5.4 × 10 −13 cm 3 molecules −1 s −1 , which is equivalent to a lifetime of POA >2 weeks. The long heterogeneous lifetime of POA supports gas phase oxidation was the major pathway for ambient OA aging. The OH uptake coefficient ( γ OH ) was estimated to be 0.76–0.84, underlining that OH radicals can be taken up efficiently on ambient aerosols.