Evidence and evolution of Criegee intermediates, hydroperoxides and secondary organic aerosols formed via ozonolysis of α-pinene

被引:15
|
作者
Bagchi, Arnab [1 ,2 ]
Yu, Youqing [1 ,4 ]
Huang, Jhih-Hong [1 ,2 ]
Tsai, Cheng-Cheng [3 ]
Hu, Wei-Ping [3 ]
Wang, Chia C. [1 ,2 ]
机构
[1] Natl Sun Yat Sen Univ, Dept Chem, Kaohsiung, Taiwan
[2] Natl Sun Yat Sen Univ, Aemsol Sci Res Ctr, Kaohsiung, Taiwan
[3] Natl Chung Cheng Univ, Dept Chem & Biochem, Chiayi, Taiwan
[4] Yangtze Normal Univ, Green Intelligence Environm Sch, Chongqing 408100, Peoples R China
关键词
GAS-PHASE; MULTIFUNCTIONAL COMPOUNDS; TEMPERATURE-DEPENDENCE; INFRARED DETECTION; OPTICAL-PROPERTIES; POTENTIAL SOURCE; MATRIX-ISOLATION; BETA-PINENE; CH2OO; ALKENES;
D O I
10.1039/c9cp06306d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
alpha-Pinene, the most abundant monoterpene in the atmosphere, accounts for more than 50% of global monoterpene emission. Though its reaction with ozone has been generally perceived as a major source of secondary organic aerosols (SOAs), direct evidence of its reaction intermediates (RI) and their evolution remain lacking. Here we study the ozonolysis of alpha-pinene between 180 and 298 K using a long-path, temperature-variable aerosol cooling chamber coupled to a rapid-scan time-resolved Fourier transform infrared spectrometer. The spectroscopic signatures of large Criegee intermediates (CIs) and hydroperoxides (HPs) were found for the first time. The aerosol size evolution during the reaction was also measured. In contrast to a previous perception, we show that temperature plays a determinant role in the ozonolysis kinetics. Finally, we show that the formation of HPs is an energetically favorable pathway to dissipate CIs. This study provides new insights into the ozonolysis of alpha-pinene and its contribution to SOA formation.
引用
收藏
页码:6528 / 6537
页数:10
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