Articles | Volume 9, issue 19
Atmos. Chem. Phys., 9, 7531–7550, 2009
Atmos. Chem. Phys., 9, 7531–7550, 2009

  09 Oct 2009

09 Oct 2009

Investigation of ship-plume chemistry using a newly-developed photochemical/dynamic ship-plume model

H. S. Kim1, C. H. Song1, R. S. Park1, G. Huey2, and J. Y. Ryu3 H. S. Kim et al.
  • 1Dept. of Environmental Science and Engineering, Gwangju Institute of Science and Technology (GIST), Gwangju, Korea
  • 2School of the Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, Georgia, USA
  • 3Korea Environmental Industry and Technology Institute (KEITI), Seoul, Korea

Abstract. A photochemical/dynamic ship-plume model, which can consider the ship-plume dynamics and ship-plume chemistry, simultaneously, was developed to gain a better understanding of atmospheric impact of ship emissions. The model performance was then evaluated by a comparison with the observation data measured on a NOAA WP-3D flight during the Intercontinental Transport and Chemical Transformation 2002 (ITCT 2K2) airborne field campaign. The simulation conditions and parameters, such as meteorological conditions, emission rates, and background gas and particulate species concentrations, were obtained directly and/or inferred indirectly from the ITCT 2K2 observation data. The model-predicted concentrations showed good agreement with the observed concentrations of five ambient species (NOx, NOy, ozone, HNO3, and H2SO4) at the eight plume transects by the WP-3D flight with strong correlations around the 1:1 line (0.64≤R≤0.85). In addition, a set of tests were carried out to approximate the magnitude of the reaction probability of HNO3 onto sea-salt particles in the model-observation comparison framework. These results suggest that the reaction probability of HNO3 onto sea-salt particles may be in the order of 0.05–0.1. The equivalent NOx lifetime throughout the "entire plume" was also estimated from photochemical/dynamic ship-plume modeling. The NOx lifetimes estimated throughout the entire ship plume ranged from 2.64 h to 3.76 h under stable to neutral stability conditions. The short NOx lifetime over the entire ship plume clearly shows that the ship-plume chemistry shortens the NOx lifetime considerably. Therefore, the ship-plume chemistry model should be used to model the changes in ship-plume chemical compositions and better evaluate the atmospheric impact of ocean-going ship emissions.

Final-revised paper