Real-time measurement of oligomeric species in secondary organic aerosol with the aerosol time-of-flight mass spectrometer

被引:76
作者
Gross, DS
Gälli, ME
Kalberer, M
Prevot, ASH
Dommen, J
Alfarra, MR
Duplissy, J
Gaeggeler, K
Gascho, A
Metzger, A
Baltensperger, U
机构
[1] Carleton Coll, Dept Chem, Northfield, MN 55057 USA
[2] TSI Inc, Shoreview, MN 55126 USA
[3] ETH, Dept Chem & Appl Biosci, CH-8093 Zurich, Switzerland
[4] Paul Scherrer Inst, Lab Atmospher Chem, CH-5232 Villigen, Switzerland
关键词
D O I
10.1021/ac060138l
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Real-time detection of oligomers in secondary organic aerosols has been carried out with an aerosol time-of-flight mass spectrometer sampling particles generated in a smog chamber. The photooxidation products of 1,3,5-trimethylbenzene and NO, were studied over a range of initial 1,3,5-trimethylbenzene concentrations (137-1180 ppb), while keeping the 1,3,5-trimediylbenzene to NO, ratio nearly constant. The photooxidation products of a mixture of a-pinene (initial concentration 191 ppb), 1,3,5-trimethylbenzene (60 ppb), and NO,, were also investigated. In both systems, ions were observed in the single-particle mass spectra up to 750 Da; the species observed differed in the two systems. These high-mass ions occur with characteristic spacing of 14 and 16 Da, indicative of oligomeric species. The results obtained agree well with off-line (matrix-assisted) laser desorption/ionization mass spectrometry results. The real-time capabilities of the aerosol time-of-flight mass spectrometer make it possible to investigate the temporal development of the oligomers with 5-min time resolution and also demonstrate that there are certain ions within the oligomer population that occur in nearly all of the particles and with relatively high signal intensity, suggesting that these ions have higher stability or that the species are formed preferentially.
引用
收藏
页码:2130 / 2137
页数:8
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