Articles | Volume 4, issue 1
Atmos. Chem. Phys., 4, 95–110, 2004
https://doi.org/10.5194/acp-4-95-2004

Special issue: Atmospheric chemistry in the Earth system: from regional pollution...

Atmos. Chem. Phys., 4, 95–110, 2004
https://doi.org/10.5194/acp-4-95-2004

  26 Jan 2004

26 Jan 2004

The role of transition metal ions on HOx radicals in clouds: a numerical evaluation of its impact on multiphase chemistry

L. Deguillaume1, M. Leriche1, A. Monod2, and N. Chaumerliac1 L. Deguillaume et al.
  • 1Laboratoire de Météorologie Physique (LaMP), CNRS, Université Blaise Pascal, 24 av. des Landais, 63177 Aubière, Cedex, France
  • 2Laboratoire Chimie et Environnement, Université de Provence, Case 293, place Victor Hugo,13331 Marseille Cedex 3, France

Abstract. A new modelling study of the role of transition metal ions on cloud chemistry has been performed. Developments of the Model of Multiphase Cloud Chemistry (M2C2; Leriche et al., 2001) are described, including the transition metal ions reactivity emission/deposition processes and variable photolysis in the aqueous phase. The model is then applied to three summertime scenarios under urban, remote and marine conditions, described by Ervens et al. (2003).

Chemical regimes in clouds are analyzed to understand the role of transition metal ions on cloud chemistry and especially, on HxOy chemistry, which consequently influences the sulphur and the VOCs chemistry in droplets. The ratio of Fe(II)/Fe(III) exhibits a diurnal variation with values in agreement with the available measurements of Fe speciation. In the urban case, sensitivity tests with and without TMI chemistry, show an enhancement of OH concentration in the aqueous phase when TMI chemistry is considered.

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