Hygroscopic growth and activation changed submicron aerosol composition and properties in the North China Plain

被引:1
|
作者
Xu, Weiqi [1 ]
Kuang, Ye [2 ]
Xu, Wanyun [3 ,4 ]
Zhang, Zhiqiang [1 ,5 ]
Luo, Biao [2 ]
Zhang, Xiaoyi [3 ,4 ,6 ]
Tao, Jiangchuang [2 ]
Qiao, Hongqin [2 ]
Liu, Li [7 ]
Sun, Yele [1 ,5 ]
机构
[1] Chinese Acad Sci, Inst Atmospher Phys, State Key Lab Atmospher Boundary Layer Phys & Atmo, Beijing 100029, Peoples R China
[2] Jinan Univ, Coll Environm & Climate, Inst Environm & Climate Res, Guangzhou 511443, Peoples R China
[3] Chinese Acad Meteorol Sci, Inst Atmospher Composit, State Key Lab Severe Weather, Beijing 100081, Peoples R China
[4] Chinese Acad Meteorol Sci, Inst Atmospher Composit, Key Lab Atmospher Chem, Beijing 100081, Peoples R China
[5] Univ Chinese Acad Sci, Coll Earth & Planetary Sci, Beijing 100049, Peoples R China
[6] Fudan Univ, Dept Atmospher & Ocean Sci, Shanghai 200438, Peoples R China
[7] China Meteorol Adm, Inst Trop & Marine Meteorol, Key Lab Reg Numer Weather Predict, Guangzhou 510080, Peoples R China
基金
中国国家自然科学基金;
关键词
SECONDARY ORGANIC AEROSOL; POSITIVE MATRIX FACTORIZATION; MASS-SPECTROMETER; PARTICULATE MATTER; AQUEOUS-PHASE; CHEMICAL-COMPOSITION; RELATIVE-HUMIDITY; WINTERTIME; CHEMISTRY; INSIGHTS;
D O I
10.5194/acp-24-9387-2024
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Aerosol hygroscopic growth and activation under high-relative-humidity (RH) conditions significantly influence the physicochemical properties of submicron aerosols (PM1). However, this process remains poorly characterized due to limited measurements. To address this gap, we deployed an advanced aerosol-fog sampling system that automatically switched between PM1, PM2.5 and total suspended particulate (TSP) inlets at a rural site in the North China Plain in the cold season. The results revealed that aerosol swelling due to water vapor uptake influenced aerosol sampling under high-RH conditions by shifting the cut-off size of impactors. At subsaturated high RH (> 90 %), over 25 % of aerosol mass with dry diameters below 1 mu m resided in supermicron ranges, while in supersaturated foggy conditions, more than 70 % of submicron aerosol migrated to supermicron ranges. Hygroscopic growth and activation particularly affected highly hydrophilic inorganic salts, shifting a significant number of submicron sulfate and nitrate particles to supermicron ranges, with 27 %-33 % at 95 % <= RH <= 99 % and more than 78 % under supersaturated foggy conditions. Moreover, more than 10 % of submicron biomass burning organic aerosols grew beyond 2.5 mu m during fog events, while fossil-fuel-related organic aerosol (FFOA) remained dominantly in submicron ranges, suggesting inefficient aqueous conversion of FFOA. The two secondary organic aerosol (SOA) factors (OOA1 and OOA2) behaved differently under supersaturated conditions, with OOA2 exhibiting a higher activated fraction despite a lower oxygen carbon ratio. A substantial increase in organic nitrate and organosulfur mass concentrations in activated droplets during fog events suggested aqueous conversions and formations of brown carbon with potential radiative impacts. Overall, our study highlights remarkably different cloud and fog processing behaviors between primary and secondary aerosols, which would benefit a better understanding of aerosol-cloud interactions under distinct atmospheric conditions.
引用
收藏
页码:9387 / 9399
页数:13
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