Surface density function evolution and the influence of strain rates during turbulent boundary layer flashback of hydrogen-rich premixed combustion

Abstract

The statistical behavior of the magnitude of the reaction progress variable gradient [alternatively known as the surface density function (SDF)] and the strain rates, which govern the evolution of the SDF, have been analyzed for boundary layer flashback of a premixed hydrogen-air flame with an equivalence ratio of 1.5 in a fully developed turbulent channel flow. The non-reacting part of the channel flow is representative of the friction velocity based Reynolds number Reτ = 120. A skeletal chemical mechanism with nine chemical species and twenty reactions is employed to represent hydrogen-air combustion. Three definitions of the reaction progress variable (RPV) based on the mass fractions of H2, O2, and H2O have been considered to analyze the SDF statistics. It is found that the mean variations of the SDF and the displacement speed Sd depend on the choice of the RPV and the distance away from the wall. The preferential alignment of the RPV gradient with the most extensive principal strain rate strengthens with an increase in distance from the cold wall, which leads to changes in the behaviors of normal and tangential strain rates from the vicinity of the wall toward the middle of the channel. The differences in displacement speed statistics for different choices of the RPV and the wall distance affect the behaviors of the normal strain rate due to flame propagation and curvature stretch. The relative thickening/thinning of the reaction layers of the major species has been explained in terms of the statistics of the effective normal strain rate experienced by the progress variable isosurfaces for different wall distances and choices of RPVs.