We describe a nearly explicit chemical mechanism for isoprene photooxidation guided by chamber studies that include time-resolved observation of an extensive suite of volatile compounds. We provide new constraints on the chemistry of the poorly-understood isoprene δ-hydroxy channels, which account for more than one third of the total isoprene carbon flux and a larger fraction of the nitrate yields. We show that thecisbranch dominates the chemistry of the δ-hydroxy channel with less than 5% of the carbon following thetransbranch. The modelled yield of isoprene nitrates is 12±3% with a large difference between the δ and β 2 branches. The oxidation of these nitrates releases about 50% of the NOx. Methacrolein nitrates (modelled yield ∼ 15±3% from methacrolein) and methylvinylketone nitrates (modelled yield ∼ 11±3% yield from methylvinylketone) are also observed. Propanone nitrate, produced with a yield of 1% from isoprene, appears to be the longest-lived nitrate formed in the total oxidation of isoprene. We find a large molar yield of formic acid and suggest a novel mechanism leading to its formation from the organic nitrates. Finally, the most important features of this mechanism are summarized in a condensed scheme appropriate for use in global chemical transport models.
CITATION STYLE
Paulot, F., Crounse, J. D., Kjaergaard, H. G., Kroll, J. H., Seinfeld, J. H., & Wennberg, P. O. (2009). Isoprene photooxidation: New insights into the production of acids and organic nitrates. Atmospheric Chemistry and Physics, 9(4), 1479–1501. https://doi.org/10.5194/acp-9-1479-2009
Mendeley helps you to discover research relevant for your work.