Sakamoto Yosuke, Yajima Ryoji, Inomata Satoshi, Hirokawa Jun
Graduate School of Global Environmental Studies, Kyoto University, Kyoto, Japan.
Graduate School of Environmental Science, Hokkaido University, Sapporo, Japan.
Phys Chem Chem Phys. 2017 Jan 25;19(4):3165-3175. doi: 10.1039/c6cp04521a.
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 CHOO have low reactivity toward HO, 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.
在干燥和潮湿条件下,使用特氟龙袋式反应器研究了异戊二烯臭氧分解生成二次有机气溶胶(SOA)的过程。研究发现,添加水蒸气会使SOA的数量浓度和体积浓度均降低。利用负离子化学电离质谱仪进行的气相和颗粒相产物分析表明,以稳定的Criegee中间体作为链单元组成的低聚物有助于SOA的形成,并且水蒸气会抑制稳定的Criegee中间体形成低聚物,从而导致SOA形成受到抑制。此外,研究表明,除CHOO之外的一部分稳定的Criegee中间体对HO的反应活性较低,因此即使在潮湿条件下也可参与低聚物和SOA的形成。挥发性估算预测,即使含有一两个稳定的Criegee中间体的低聚物也可分配到气溶胶相中。