Water vapour effects on secondary organic aerosol formation in isoprene ozonolysis

被引:40
|
作者
Sakamoto, Yosuke [1 ,2 ]
Yajima, Ryoji [3 ]
Inomata, Satoshi [4 ]
Hirokawa, Jun [5 ]
机构
[1] Kyoto Univ, Grad Sch Global Environm Studies, Kyoto 6068501, Japan
[2] Kyoto Univ, Grad Sch Human & Environm Studies, Kyoto 6068501, Japan
[3] Hokkaido Univ, Grad Sch Environm Sci, Sapporo, Hokkaido 060, Japan
[4] Natl Inst Environm Studies, Ctr Global Environm Res, Tsukuba, Ibaraki, Japan
[5] Hokkaido Univ, Fac Environm Earth Sci, Sapporo, Hokkaido 060, Japan
基金
日本学术振兴会;
关键词
GAS-PHASE OZONOLYSIS; CONFORMER-DEPENDENT REACTIVITY; CRIEGEE INTERMEDIATE REACTIONS; VOLATILITY BASIS-SET; PARTICLE FORMATION; HYDROGEN-PEROXIDE; CARBONYL-OXIDE; OH RADICALS; HYDROXYMETHYL HYDROPEROXIDE; MONOTERPENE OZONOLYSIS;
D O I
10.1039/c6cp04521a
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
Secondary organic aerosol (SOA) formation from isoprene ozonolysis was investigated using a Teflon bag reactor under dry and humid conditions. Both the number and volume concentrations of SOA were found to be decreased by the addition of water vapour. Gas-and particle-phase product analyses with a negative ion chemical ionization mass spectrometer show that oligomers composed of stabilized Criegee intermediates as the chain units contribute to the SOA formation and that water vapour inhibits stabilized Criegee intermediates from forming the oligomers, resulting in the suppression of SOA formation. Additionally, it is suggested that a portion of stabilized Criegee intermediates other than CH2OO have low reactivity toward H2O, and thus can be involved in the oligomer and SOA formation even under humid conditions. Volatility estimation predicts that the oligomers containing even one or two stabilized Criegee intermediates can be partitioned into the aerosol phase.
引用
收藏
页码:3165 / 3175
页数:11
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