Articles | Volume 14, issue 5
Atmos. Chem. Phys., 14, 2497–2508, 2014
Atmos. Chem. Phys., 14, 2497–2508, 2014

Research article 11 Mar 2014

Research article | 11 Mar 2014

Fast photolysis of carbonyl nitrates from isoprene

J.-F. Müller1, J. Peeters2, and T. Stavrakou1 J.-F. Müller et al.
  • 1Belgian Institute for Space Aeronomy, Avenue Circulaire 3, 1180 Brussels, Belgium
  • 2Department of Chemistry, University of Leuven, 3001 Heverlee, Belgium

Abstract. Photolysis is shown to be a major sink for isoprene-derived carbonyl nitrates, which constitute an important component of the total organic nitrate pool over vegetated areas. Empirical evidence from published laboratory studies on the absorption cross sections and photolysis rates of α-nitrooxy ketones suggests that the presence of the nitrate group (i) greatly enhances the absorption cross sections and (ii) facilitates dissociation to a point that the photolysis quantum yield is close to unity, with O–NO2 dissociation as a likely major channel. On this basis, we provide new recommendations for estimating the cross sections and photolysis rates of carbonyl nitrates. The newly estimated photo rates are validated using a chemical box model against measured temporal profiles of carbonyl nitrates in an isoprene oxidation experiment by Paulot et al. (2009). The comparisons for ethanal nitrate and for the sum of methacrolein- and methyl vinyl ketone nitrates strongly supports our assumptions of large cross-section enhancements and a near-unit quantum yield for these compounds. These findings have significant atmospheric implications: the photorates of key carbonyl nitrates from isoprene are estimated to be typically between ~ 3 and 20 times higher than their sink due to reaction with OH in relevant atmospheric conditions. Moreover, since the reaction is expected to release NO2, photolysis is especially effective in depleting the total organic nitrate pool.

Final-revised paper