Effect of hydrophobic primary organic aerosols on secondary organic aerosol formation from ozonolysis of α-pinene

被引:81
|
作者
Song, Chen
Zaveri, Rahul A.
Alexander, M. Lizabeth
Thornton, Joel A.
Madronich, Sasha
Ortega, John V.
Zelenyuk, Alla
Yu, Xiao-Ying
Laskin, Alexander
Maughan, David A.
机构
[1] Pacific NW Natl Lab, Atmospher Sci & Global Change Div, Richland, WA 99352 USA
[2] Pacific NW Natl Lab, Environm Mol Sci Lab, Richland, WA 99352 USA
[3] Natl Ctr Atmospher Res, Div Atmospher Chem, Boulder, CO 80307 USA
[4] Univ Washington, Dept Atmospher Sci, Seattle, WA 98195 USA
关键词
MASS-SPECTROMETER; OXIDATION; MODEL; CHEMISTRY; EMISSIONS;
D O I
10.1029/2007GL030720
中图分类号
P [天文学、地球科学];
学科分类号
07 ;
摘要
Semi-empirical secondary organic aerosol (SOA) models typically assume a well-mixed organic aerosol phase even in the presence of hydrophobic primary organic aerosols (POA). This assumption significantly enhances the modeled SOA yields as additional organic mass is made available to absorb greater amounts of oxidized secondary organic gases than otherwise. We investigate the applicability of this critical assumption by measuring SOA yields from ozonolysis of a-pinene ( a major biogenic SOA precursor) in a smog chamber in the absence and in the presence of dioctyl phthalate (DOP) and lubricating oil seed aerosol. These particles serve as surrogates for urban hydrophobic POA. The results show that these POA did not enhance the SOA yields. If these results are found to apply to other biogenic SOA precursors, then the semiempirical models used in many global models would predict significantly less biogenic SOA mass and display reduced sensitivity to anthropogenic POA emissions than previously thought.
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页数:5
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