作者
Juliane L Fry, Danielle C Draper, Kelley C Barsanti, James N Smith, John Ortega, Paul M Winkler, Michael J Lawler, Steven S Brown, Peter M Edwards, Ronald C Cohen, Lance Lee
发表日期
2014/10/21
期刊
Environmental science & technology
卷号
48
期号
20
页码范围
11944-11953
出版商
American Chemical Society
简介
The secondary organic aerosol (SOA) mass yields from NO3 oxidation of a series of biogenic volatile organic compounds (BVOCs), consisting of five monoterpenes and one sesquiterpene (α-pinene, β-pinene, Δ-3-carene, limonene, sabinene, and β-caryophyllene), were investigated in a series of continuous flow experiments in a 10 m3 indoor Teflon chamber. By making in situ measurements of the nitrate radical and employing a kinetics box model, we generate time-dependent yield curves as a function of reacted BVOC. SOA yields varied dramatically among the different BVOCs, from zero for α-pinene to 38–65% for Δ-3-carene and 86% for β-caryophyllene at mass loading of 10 μg m–3, suggesting that model mechanisms that treat all NO3 + monoterpene reactions equally will lead to errors in predicted SOA depending on each location’s mix of BVOC emissions. In most cases, organonitrate is a dominant …
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