References

ACPD

Atmospheric Chemistry and Physics Discussions

ACPD

1680-7375

Copernicus GmbH

Göttingen, Germany

10.5194/acpd-9-5231-2009

A product study of the isoprene+NO3 reaction

Perring

A. E.

¹ Wisthaler

² ⁶ Graus

² Wooldridge

P. J.

¹ Lockwood

A. L.

⁴ Mielke

L. H.

⁴ Shepson

P. B.

³ ⁴ Hansel

² Cohen

R. C.

¹ ⁵

Department of Chemistry, University of California Berkeley, Berkeley, CA, USA

Institut fuer Ionenphysik und Angewandte Physik, University of Innsbruck, Innsbruck, Austria

Purdue Climate Change Research Center, Purdue University, West Lafayette, IN, USA

Department of Chemistry, Purdue University, West Lafayette, IN, USA

Department of Earth and Planetary Sciences, University of California Berkeley, Berkeley, CA, USA

equally contributing author

27 02 2009

9 1 5231 5261

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Oxidation of isoprene through reaction with NO3 is a significant sink for isoprene that persists after dark. The products of the reaction are multifunctional nitrates. These nitrates constitute a significant NOx sink in the nocturnal boundary layer and they likely play an important role in formation of secondary organic aerosol. Products of the isoprene+NO3 reaction will, in many locations, be abundant enough to affect nighttime radical chemistry and to persist into daytime where they may represent a source of NOx. Product formation in the isoprene+NO3 reaction was studied in a smog chamber at Purdue University. Isoprene nitrates and other hydrocarbon products were observed using Proton Transfer Reaction-Mass Spectrometry (PTR-MS) and reactive nitrogen products were observed using Thermal Dissociation–Laser Induced Fluorescence (TD-LIF). The organic nitrate yield is found to be 62±6% and the combined yield of MACR+MVK is found to be ~10%. Additional hydrocarbon products, thought to be primarily C4 and C5 carbonyl compounds, were observed by the PTR-MS at various m/z ratios and their yields quantified. These other oxidation products are used as additional constraints on the reaction mechanism.

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