Elemental analysis of chamber organic aerosol using an aerodyne high-resolution aerosol mass spectrometer

被引:128
作者
Chhabra, P. S. [1 ]
Flagan, R. C. [1 ,2 ]
Seinfeld, J. H. [1 ,2 ]
机构
[1] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
[2] CALTECH, Div Engn & Appl Sci, Pasadena, CA 91125 USA
关键词
ALPHA-PINENE; GAS-PHASE; CHEMICAL-COMPOSITION; HYDROXYL RADICALS; AMBIENT AEROSOL; MEXICO-CITY; AROMATIC-HYDROCARBONS; SOURCE APPORTIONMENT; SECONDARY AEROSOLS; AQUEOUS GLYOXAL;
D O I
10.5194/acp-10-4111-2010
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The elemental composition of laboratory chamber secondary organic aerosol (SOA) from glyoxal uptake, alpha-pinene ozonolysis, isoprene photooxidation, single-ring aromatic photooxidation, and naphthalene photooxidation is evaluated using Aerodyne high-resolution time-of-flight mass spectrometer data. SOA O/C ratios range from 1.13 for glyoxal uptake experiments to 0.30-0.43 for alpha-pinene ozonolysis. The elemental composition of alpha-pinene and naphthalene SOA is also confirmed by offline mass spectrometry. The fraction of organic signal at m/z 44 is generally a good measure of SOA oxygenation for alpha-pinene/O-3, isoprene/high-NOx, and naphthalene SOA systems. The agreement between measured and estimated O/C ratios tends to get closer as the fraction of organic signal at m/z 44 increases. This is in contrast to the glyoxal uptake system, in which m/z 44 substantially underpredicts O/C. Although chamber SOA has generally been considered less oxygenated than ambient SOA, single-ring aromatic- and naphthalene-derived SOA can reach O/C ratios upward of 0.7, well within the range of ambient PMF component OOA, though still not as high as some ambient measurements. The spectra of aromatic and isoprene-high-NOx SOA resemble that of OOA, but the spectrum of glyoxal uptake does not resemble that of any ambient organic aerosol PMF component.
引用
收藏
页码:4111 / 4131
页数:21
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