Combustion Reactions in Silane–Air Flames II. Counterflow Diffusion Flame

Abstract

Abstract A detailed chemical reaction scheme and a full set of governing equations for fluid dynamics were used to elucidate the chemical and physical phenomena involved in a silane–air counterflow diffusion flame, where the fuel and air issue from the lower and upper nozzles, respectively. It was found that a stagnation surface, where the axial velocities fall down to zero, is kept in a position slightly shifted to the upper side, dividing the system into two zones: the upper air side and the lower fuel side; after leaving the nozzle silane begins to dissociate itself into SiH2 and H2 when it reaches the region of rising temperature; oxygen penetrates into the fuel side by diffusion and reacts with H2 forming OH radicals and H atoms. The produced SiH2 is further dehydrogenated to SiO via HSiO; comparing with premixed flames, the diffusion flames have large local equivalence ratios, so that the combustion reactions in the latter flames occur through a different mechanism.