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Read Full Article (file size: 143123 bytes) Cited by
GEOPHYSICAL RESEARCH LETTERS,
VOL. 32,
L18808,
doi:10.1029/2005GL023637,
2005
Secondary organic aerosol formation from isoprene photooxidation under high-NOx conditions
Jesse H. Kroll
Department of Environmental Science and Engineering and Department of Chemical Engineering, California Institute of Technology,
Pasadena, California, USA
Nga L. Ng
Department of Environmental Science and Engineering and Department of Chemical Engineering, California Institute of Technology,
Pasadena, California, USA
Shane M. Murphy
Department of Environmental Science and Engineering and Department of Chemical Engineering, California Institute of Technology,
Pasadena, California, USA
Richard C. Flagan
Department of Environmental Science and Engineering and Department of Chemical Engineering, California Institute of Technology,
Pasadena, California, USA
John H. Seinfeld
Department of Environmental Science and Engineering and Department of Chemical Engineering, California Institute of Technology,
Pasadena, California, USA
Abstract
The oxidation of isoprene (2-methyl-1,3-butadiene) is known to play a central role in the photochemistry of the troposphere,
but is generally not considered to lead to the formation of secondary organic aerosol (SOA), due to the relatively high volatility
of known reaction products. However, in the chamber studies described here, we measure SOA production from isoprene photooxidation
under high-NO
x
conditions, at significantly lower isoprene concentrations than had been observed previously. Mass yields are low (0.9–3.0%),
but because of large emissions, isoprene photooxidation may still contribute substantially to global SOA production. Results
from photooxidation experiments of compounds structurally similar to isoprene (1,3-butadiene and 2- and 3-methyl-1-butene)
suggest that SOA formation from isoprene oxidation proceeds from the further reaction of first-generation oxidation products
(i.e., the oxidative attack of both double bonds). The gas-phase chemistry of such oxidation products is in general poorly
characterized and warrants further study.
Received 26
May
2005;
accepted 22
August
2005;
published 23
September
2005.
Index Terms: 0305 Atmospheric Composition and Structure: Aerosols and particles (0345, 4801, 4906); 0317 Atmospheric Composition and Structure: Chemical kinetic and photochemical properties; 0365 Atmospheric Composition and Structure: Troposphere: composition and chemistry.
Read Full Article (file size: 143123 bytes) Cited by
Citation: Kroll, J. H., N. L. Ng, S. M. Murphy, R. C. Flagan, and J. H. Seinfeld
(2005),
Secondary organic aerosol formation from isoprene photooxidation under high-NOx conditions,
Geophys. Res. Lett.,
32,
L18808,
doi:10.1029/2005GL023637.
Copyright 2005 by the American Geophysical Union.
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