Turbulent Mixing with Chemical Reaction in the Planetary Boundary Layer

R. I. Sykes ARAP Group, Titan Research and Technology Division, Titan Corporation, Princeton, New Jersey

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S. F. Parker ARAP Group, Titan Research and Technology Division, Titan Corporation, Princeton, New Jersey

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D. S. Henn ARAP Group, Titan Research and Technology Division, Titan Corporation, Princeton, New Jersey

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W. S. Lewellen Physics and Atmospheric Science, Drexel University, Philadelphia, Pennsylvania

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Abstract

Detailed statistics of the fluctuating concentration field produced by large-eddy simulations (LES) of the chemically reactive mixing of two species in a convectively driven mixed layer are presented. The effect of the turbulent mixing on the effective reaction rate between the species is analysed. The segregation between the species is shown to be significant for fast reactions, and therefore correct model predictions of the evolution of the species concentration requires an estimate of the segregation coefficient. Some simple modeling concepts for one-point second-order turbulence closure schemes are examined and compared with the LES results. The results are a promising indication that second-order closure schemes can be extended to provide a practical calculation of the turbulent mixing effects on fast chemical reactions.

Abstract

Detailed statistics of the fluctuating concentration field produced by large-eddy simulations (LES) of the chemically reactive mixing of two species in a convectively driven mixed layer are presented. The effect of the turbulent mixing on the effective reaction rate between the species is analysed. The segregation between the species is shown to be significant for fast reactions, and therefore correct model predictions of the evolution of the species concentration requires an estimate of the segregation coefficient. Some simple modeling concepts for one-point second-order turbulence closure schemes are examined and compared with the LES results. The results are a promising indication that second-order closure schemes can be extended to provide a practical calculation of the turbulent mixing effects on fast chemical reactions.

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