Understanding flame-acoustics interaction (FAI) that can potentially trigger thermoacoustic instabilities is of critical importance to mitigate the serious side effects of pressure oscillations. While FAI has been studied extensively in premixed flames, comparatively less analysis has been conducted to explore FAI mechanisms in non-premixed flames, especially under high-pressure conditions. This study aims to numerically investigate FAI in high-pressure hydrogen/air counterflow diffusion flames, with special attention on the impact of pressure on FAI. To this end, a fully compressible unsteady counterflow solver combined with Navier-Stokes Characteristic Boundary Conditions (NSCBC) is employed to capture the reflection of the acoustic waves at the boundaries. The results show that for all ambient pressures ( 1 ≤ P a ≤ 60 bar) considered here, real-gas effects on flame structures are negligible and that increasing P a would lead to a power-law dependence of density gradient on P a with an exponent of 1.5. Furthermore, all tested cases show acoustic growth with time under fully reflecting boundary conditions, which is found to be pressure dependent. The flames become less resilient to FAI when the pressure (or density gradient) is increased. The results from the spectral analysis show that for all ambient pressures, there is only a single dominant frequency at the low-density fuel side and two dominant frequencies at the high-density oxidiser side. This indicates that the pressure oscillation is more sinusoidal at the H 2 side than that at the air side. Moreover, the phase space portraits of pressure signals indicate that the dynamics of the system are becoming periodic and approaching a limit cycle. It is found that the integrated heat release rate and the pressure fluctuations are partially in phase, which is responsible for the growth of high-frequency acoustic waves at both fuel and oxidiser sides. On the other hand, the significant density gradient contributes to the growth of low-frequency acoustic waves at the oxidiser side due to the high degree of acoustic reflectivity at the density boundary.
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