Preferential diffusion is very important in simulations of hydrogen flames. Flame stretch and curvature induce strong preferential diffusion effects in laminar premixed hydrogen flames, causing strong local deviations from the unburnt mixture fraction in the reaction zone. In tabulated chemistry methods, this necessitates the use of a partially premixed model even if the inlet mixture is purely premixed. Furthermore, in realistic combustion problems heat losses often play a dominant role. In this paper we derive a preferential diffusion model for constant but non-unity species Lewis numbers using three controlling variables, namely mixture fraction, progress variable and enthalpy. The model has been implemented in the Flamelet Generated Manifold (FGM) approach and validated by comparing with detailed chemistry simulations. As a test case we investigate a 2D laminar premixed hydrogen flame stabilised on an isothermal slit burner. Additionally, the model was compared with the standard treatment of preferential diffusion in FGM to show the increase in accuracy of the new model presented in this paper. The new model shows a significant improvement compared to the previous model, which can be attributed to the inclusion of cross-diffusion. The importance of the additional diffusion terms and its variation in mixture fraction for initially purely premixed hydrogen flames is highlighted.
In this study, 3D premixed turbulent ammonia-hydrogen flames in air were studied using DNS. Mixtures with 75%, 50% and 25% ammonia (by mole fraction in the fuel mixture) and equivalence ratios of 0.8, 1.0 and 1.2 were studied. The studies were conducted in a decaying turbulence field with an initial Karlowitz number of 10. The flame structure and the influence of ammonia and the equivalence ratio were first studied. It was observed that the increase in equivalence ratio smoothened out the small scale wrinkles while leading to strongly curved leading edges. Increasing the amount of hydrogen in the fuel mixtures also led to increasingly distorted flames. These effects are attributed to local increases in the equivalence ratio due to the preferential diffusion effects of hydrogen. The effects of curvature on the flame chemistry were studied by looking at fuel consumption rates and key reactions. It was observed that the highly mobile H2 and H species were responsible for differential rates of fuel consumption in the positively curved and negatively curved regions of the flame. The indication of a critical amount of hydrogen in the fuel mixture was observed, after which the trends of reactions involving H radical reactions were flipped with respect to the sign of the curvature. This also has implications on NO formation. Finally, the spatial profiles of heat release and temperature for 50% hydrogen were studied, which showed that the flame brush of the lean case increases in width and that the flame propagation is slow for stoichiometric and rich cases attributed to suppression of flame chemistry due to preferential diffusion effects.
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