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Numerical Investigation of Oxidizer Dilution Effects on Autoignited Laminar Lifted Methane/Hydrogen Jet Flames

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This study uses detailed 2D simulations to examine how oxygen dilution influences autoignited lifted methane/hydrogen jet flames under MILD combustion conditions. Results show that decreasing oxygen mole fraction amplifies the trend of reduced lift-off height with increasing jet velocity, due to shifts in reactive zones and enhanced differential diffusion effects, promoting earlier ignition and faster edge flame propagation, with findings robust across various parameters.

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ABSTRACT Flame stabilization of autoignited lifted jet flames under oxygen-diluted conditions relevant to MILD combustion remains challenging. Motivated by the counterintuitive trend—namely, a decrease in liftoff height, H L , of methane/hydrogen jet flame with increasing jet velocity, U 0 , due to differential diffusion—we investigate whether this effect can be leveraged to enhance the stabilization of laminar autoignited lifted methane/hydrogen jet flames under MILD combustion conditions. Two-dimensional numerical simulations are performed using a detailed kinetic mechanism involving 57 species over a wide range of oxidizer oxygen mole fractions, X O 2 . The results show that the decreasing trend of H L with increasing U 0 becomes more pronounced as X O 2 decreases. At sufficiently high U 0 , H L even decreases with decreasing X O 2 , contrary to expectations based on conventional flame behavior in fuel/air mixtures. Complementary one- and two-dimensional simulations reveal that, as X O 2 decreases, the most reactive zone shifts toward the coflow, strengthening the differential diffusion effect. This shift increases the local hydrogen ratio, R H , upstream of the flamebase, thereby promoting earlier local ignition and a higher edge flame propagation speed, S e . The combined effects of enhanced local reactivity and increased edge flame propagation lead to a reduction in H L as X O 2 decreases. Sensitivity tests over inlet temperature and chemical-kinetic mechanisms further indicate that these trends are robust rather than confined to a narrow parameter window.

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