Oxygenated Organic Molecules over the Boundary Layer Aloft in Beijing

气溶胶 硫酸 环境化学 环境科学 成核 化学 北京 大气科学 无机化学 地质学 有机化学 地理 考古 中国
作者
Nianci Yao,Yonghong Wang,Zhiheng Liao,Yuan Liu,Pengkun Ma,Shuying Li,Jun Liu,Yongjing Ma,Qiaozhi Zha,Lei Yao,Biwu Chu,Qingxin Ma,Jiannong Quan,Douglas R. Worsnop,Markku Kulmala,Hong He
出处
期刊:Environmental Science & Technology [American Chemical Society]
卷期号:59 (27): 13892-13902
标识
DOI:10.1021/acs.est.5c01020
摘要

Oxygenated organic molecules (OOMs) originate from both direct emissions and secondary formation via the oxidation of volatile organic compounds (VOCs) emitted from biogenic and anthropogenic sources. OOMs are suggested to play a crucial role in the nucleation and growth of newly formed particles, which in turn influence climate, health and air quality. However, OOMs and the associated nucleation and growth of aerosols in the boundary layer aloft are not considered in atmospheric chemistry models owing to limited observation data. Here, by using unique measurements on the top of a 528 m building tower in Beijing, we show that a variety of OOMs existed, dominated by C6-7 and C5 compounds, which probably arose from multigeneration oxidation of aromatic compounds and isoprene, respectively. Consequently, five possible formation pathways of OOMs were identified using a machine learning approach combined with their diurnal patterns. Further analysis suggested that OOMs, together with sulfuric acid and ammonia, are highly involved in the formation of nanoparticles. Our results complement the current mechanism of ammonia-sulfuric acid nucleation in the boundary layer aloft of anthropogenically influenced regions, highlighting the important role of OOMs in the nucleation and growth of aerosol. We suggest that OOMs should be considered in atmospheric chemistry models for better prediction accuracy.
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