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A product study of the isoprene+NO3 reaction

  • A. E. Perring
  • , A. Wisthaler
  • , M. Graus
  • , P. J. Wooldridge
  • , A. L. Lockwood
  • , L. H. Mielke
  • , P. B. Shepson
  • , A. Hansel
  • , R. C. Cohen
  • University of California at Berkeley
  • University of Innsbruck
  • Purdue University

Research output: Contribution to journalArticlepeer-review

75 Scopus citations

Abstract

Oxidation of isoprene through reaction with NO3 radicals is a significant sink for isoprene that persists after dark. The main 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 65±12% of which the majority was nitrooxy carbonyls and the combined yield of methacrolein and methyl vinyl ketone (MACR+MVK) is found to be ∼ 10%. PTR-MS measurements of nitrooxy carbonyls and TD-LIF measurements of total organic nitrates agreed well. The PTR-MS also observed a series of minor oxidation products which were tentatively identified and their yields quantified These other oxidation products are used as additional constraints on the reaction mechanism.

Original languageEnglish
Pages (from-to)4945-4956
Number of pages12
JournalAtmospheric Chemistry and Physics
Volume9
Issue number14
DOIs
StatePublished - 2009

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