Heine Nadja, Arata Caleb, Goldstein Allen H, Houle Frances A, Wilson Kevin R
Chemical Sciences Division , Lawrence Berkeley National Laboratory , Berkeley , California 94720 , United States.
Department of Chemistry , University of California , Berkeley , California 94720 , United States.
J Phys Chem Lett. 2018 Jun 21;9(12):3504-3510. doi: 10.1021/acs.jpclett.8b01171. Epub 2018 Jun 13.
Here we report a new multiphase reaction mechanism by which Criegee intermediates (CIs), formed by ozone reactions at an alkene surface, convert SO to SO to produce sulfuric acid, a precursor for new particle formation (NPF). During the heterogeneous ozone reaction, in the presence of 220 ppb SO, an unsaturated aerosol (squalene) undergoes rapid chemical erosion, which is accompanied by NPF. A kinetic model predicts that the mechanism for chemical erosion and NPF originate from a common elementary step (CI + SO) that produces both gas phase SO and small ketones. At low relative humidity (RH = 5%), 20% of the aerosol mass is lost, with 17% of the ozone-surface reactions producing SO. At RH = 60%, the aerosol shrinks by 30%, and the yield of SO is <5%. This multiphase formation mechanism of HSO by CIs is discussed in the context of indoor air quality and atmospheric chemistry.
在此,我们报告了一种新的多相反应机制,通过该机制,在烯烃表面由臭氧反应形成的克里吉中间体(CIs)将SO转化为SO以生成硫酸,硫酸是新粒子形成(NPF)的前体。在非均相臭氧反应过程中,在220 ppb SO存在的情况下,一种不饱和气溶胶(角鲨烯)会经历快速化学侵蚀,并伴有NPF。动力学模型预测,化学侵蚀和NPF的机制源自一个共同的基本步骤(CI + SO),该步骤会同时产生气相SO和小酮。在低相对湿度(RH = 5%)下,20%的气溶胶质量损失,其中17%的臭氧-表面反应产生SO。在RH = 60%时,气溶胶收缩30%,SO的产率<5%。本文在室内空气质量和大气化学的背景下讨论了CIs形成HSO的这种多相形成机制。