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Compressible Rayleigh–Taylor turbulent mixing layer between Newtonian miscible fluids

Published online by Cambridge University Press:  29 September 2017

Serge Gauthier*
Affiliation:
CEA, DAM, DIF, 91297 Arpajon, France
*
†Email address for correspondence: Serge.Gauthier@orange.fr

Abstract

Rayleigh–Taylor instability induced turbulence between two compressible miscible Newtonian fluids is studied in a strongly stratified configuration at a moderate Atwood number. A direct numerical simulation has been carried out with an auto-adaptive multidomain Chebyshev–Fourier–Fourier numerical method. The spatial resolution is increased up to $(9\times 100)\times 1000^{2}=900M$ collocation points. These numerical data are compared with those obtained from a simulation carried out at a lower Reynolds number and at the same Atwood number, and those obtained from a simulation carried out within the Boussinesq approximation at the same Reynolds number. A comprehensive data analysis is reported. Physical-variable mean profiles – density, concentration, temperature, entropy, velocity, vorticity, helicity and palinstrophy – are provided. Anisotropy is studied in the spectral space. The intermediate-scale isotropy and the small-scale anisotropy are exhibited for the scalars, i.e. concentration and temperature. Velocity is anisotropic at all scales but this anisotropy is more marked at small scales. The data are also analysed with the Favre-averaged equations. Sources of the turbulent kinetic energy, mass flux, root-mean-square density and energy equations are analysed. Compressibility effects are discussed in particular with the Kovàsznay-mode decomposition. A statistical study is reported where skewnesses, flatnesses and probability density functions (PDFs) are displayed and commented. A flow visualization is also given. Finally, the temperature field appears to be the slave of the mixing. This conclusion is drawn from the comparison of power spectra, anisotropy spectra, skewnesses, flatnesses, PDFs and correlation coefficients. There is however a significant time lag between the density and temperature evolution.

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Papers
Copyright
© 2017 Cambridge University Press 
Figure 0

Table 1. List of parameter values used in the three simulations. The specific heat ratios of the two fluids are equal, $\unicode[STIX]{x1D6FE}_{H}=\unicode[STIX]{x1D6FE}_{L}=\unicode[STIX]{x1D6FE}_{r}=5/3$.

Figure 1

Table 2. Characteristics of the numerical simulation $Sr6\text{-}Re6\times 10^{4}$: the Atwood number, the stratification, the Reynolds number, the speeds of sound in the heavy ($H$) and light ($L$) fluids, the density-gradient length scales and the ratios of the densities and pressures between the top and the bottom of the domain.

Figure 2

Figure 1. (a) Initial equilibrium state: density (blue) and pressure (green) profiles for a stratification parameter value $Sr=6$ and an Atwood number $At=0.25$. The density jump is located at $z=0$. (b) Dispersion curves for the Rayleigh–Taylor equilibrium state given in equation (3.1), for two values of the Reynolds number $Re=6\times 10^{4}$ (blue) and $Re=3\times 10^{4}$ (green). The vertical dashed lines define the spectral domain of the initial condition.

Figure 3

Figure 2. (a) Zoom of the mean density profiles, $\overline{\unicode[STIX]{x1D70C}}(z,t)$, at six selected times. (b) The large-scale Atwood number, $A_{LS}(t)$, as a function of time. The initial value $A_{LS}(t=0)$, is slightly below the value of the simulation $A_{t}=0.25$, due to the regularization of the initial density jump (see equation (3.1)) with the small-scale Atwood number, $A_{SS}(t)$, defined by the root-mean-square density.

Figure 4

Figure 3. (a) Mean concentration profiles, $\overline{c}(z,t)$, at six different times. After the baroclinic source term is turned off, the turbulence homogenizes the mixing. (b) Mean temperature profiles $\overline{T}(z,t)$ at the six times selected.

Figure 5

Figure 4. (a) Mean velocity profiles, $\widetilde{u}(z,t)$, versus the vertical coordinate $z$. (b) Entropy profiles, $\overline{s}_{m}(z,t)$, at six different times. The dashed black lines stand for the entropy of the ideal initial state. Unstable regions correspond to negative entropy gradient, $\text{d}\overline{s}_{m}/\text{d}z<0$.

Figure 6

Figure 5. Thickness of the turbulent mixing layer versus time, in linear (a) and log–log (b) scales computed from $h(t)=3\langle \overline{c}(1-\overline{c})\rangle$. The full lines correspond to the $Sr6\text{-}Re6\times 10^{4}$ simulation and the dashed lines to the $Sr6\text{-}Re3\times 10^{4}$ simulation. The dashed black line stands for the $t^{2}$-scaling.

Figure 7

Figure 6. Taylor-based Reynolds number, $Re_{Tx,z}$. (a) The vertical and the horizontal Taylor–Reynolds numbers. The dashed black curve stands for the mean effective Atwood number ($80A_{LS}(t)/A_{LS}(0)$). (b) Comparison of the vertical Taylor–Reynolds number for the three simulations, $Sr6\text{-}Re6\times 10^{4}$, $Sr6\text{-}Re3\times 10^{4}$ and $Sr0\text{-}Re3\times 10^{4}$.

Figure 8

Figure 7. Total kinetic energy, $\overline{\unicode[STIX]{x1D70C}}\widetilde{K}=\overline{\unicode[STIX]{x1D70C}u_{i}u_{i}}/2$. (a) Two-dimensional map in the plane $(t,z)$. The two maxima are clearly visible. (b) Vertical profiles at six selected times.

Figure 9

Figure 8. (a) Mach numbers. Turbulent Mach number $M_{t}$ defined by (4.6) (blue, $Re=6\times 10^{4}$). Flow Mach number $M_{f}$ defined by (4.6), for the $Sr6\text{-}Re6\times 10^{4}$ simulation and $\unicode[STIX]{x1D6FD}=0.8$ (dashed red) and $\unicode[STIX]{x1D6FD}=0.2$ (yellow). Turbulent Mach number $M_{t}$ for the $Sr6\text{-}Re3\times 10^{4}$ simulation (dashed green). (b) Two-dimensional vertical velocity $\widetilde{u}_{z}$ map in the plane $(t,z)$. This map reveals an acoustic wave system stronger in the heavy fluid (upper side) than in the light fluid (lower side).

Figure 10

Figure 9. (a) Molecular mixing fraction $\langle \unicode[STIX]{x1D703}\rangle _{\unicode[STIX]{x1D6FD}}=\langle \overline{c(1-c)}/\overline{c}(1-\overline{c})\rangle _{\unicode[STIX]{x1D6FD}}$ versus time, for two values of $\unicode[STIX]{x1D6FD}$, $0.8$ (blue) and $0.2$ (green). (b) The r.m.s. concentration, normalized by its maximum in time (blue), the mixing fraction (green) and the averaged Atwood number, $A_{t}/A_{t}(0)$ (black dashed).

Figure 11

Figure 10. Vorticity and baroclinic vorticity production evolution. (a) Vorticity and baroclinic norms and their components. Baroclinic terms have been divided by 10 for the sake of clarity. The mean effective Atwood number evolution is represented by the dashed black curve. (b) Same quantities normalized by their maximum in time.

Figure 12

Figure 11. Helicity. (a) Helicity evolution versus time of the three simulations, $Sr6\text{-}Re6\times 10^{4}$, $Sr6\text{-}Re3\times 10^{4}$ and $Sr0\text{-}Re3\times 10^{4}$. The helicity of the $Sr0\text{-}Re3\times 10^{4}$ simulation has been divided by 10 for the sake of clarity. The helicity strongly decays during the RT regime and in a second step due to acoustic waves. In the FD regime, helicity vanishes slowly. (b) Helicity source terms of (4.9), corresponding to the simulation $Sr6\text{-}Re6\times 10^{4}$. Baroclinic source term (blue), pressure source term (green) and dissipation (red). The detailed behaviour of these three contributions depends on the value of $\unicode[STIX]{x1D6FD}$ (not included), but not the global evolution.

Figure 13

Figure 12. (a) Comparison of the evolution of the palinstrophy norm in linear–log scales for the three simulations, $Sr6\text{-}Re6\times 10^{4}$, $Sr6\text{-}Re3\times 10^{4}$ and $Sr0\text{-}Re3\times 10^{4}$. (b) Palinstrophy isosurface at time $t=4.35$, coloured by the concentration.

Figure 14

Figure 13. (a) Density fluctuation spectra. The dashed straight line represents the $-5/3$ power law. (b) Pressure fluctuation spectra. The dashed straight line represents the $-7/3$ power law. The vertical dashed lines stand for the horizontal and vertical Taylor wavenumbers and the horizontal and vertical Taylor mixing wavenumbers, respectively.

Figure 15

Figure 14. Velocity fluctuation spectra. (a) Horizontal velocity, $\sqrt{\unicode[STIX]{x1D70C}}u_{x}$, spectra. The dashed straight line represents the $-$5/3 power law. The vertical dashed lines stand for the horizontal and vertical Taylor wavenumbers and the horizontal and vertical Taylor mixing wavenumbers, respectively. (b) Vertical velocity, $\sqrt{\unicode[STIX]{x1D70C}}u_{z}$, spectra.

Figure 16

Figure 15. Spectra of concentration (a) and temperature (b) fluctuations. The dashed straight line represents the $-$17/3 power law. The vertical dashed lines stand for the horizontal and vertical Taylor wavenumbers and the horizontal and vertical Taylor mixing wavenumbers, respectively. These two sets of spectra are very close to each other.

Figure 17

Figure 16. Reynolds stress anisotropy tensor defined by (5.1). (a) Vertical profiles of the diagonal component $\unicode[STIX]{x1D609}_{zz}$, at six different times. (b) Evolution of the $\unicode[STIX]{x1D623}_{zz}$ (black), $\unicode[STIX]{x1D623}_{yy}$ (green) and $\unicode[STIX]{x1D623}_{yz}$ (blue) components, as defined in (5.1).

Figure 18

Figure 17. Velocity spectral anisotropy, as defined by (5.2), at four different times, $t=4.35$ (first vorticity maximum), $t=6.85$ (second vorticity maximum), $t=7.45$ (kinetic energy maximum) and $t=11$ (within the FD regime).

Figure 19

Figure 18. Concentration-gradient spectral anisotropy, as defined by (5.3), at four different times, $t=4.35$, $6.85$, $7.45$ and $11$.

Figure 20

Figure 19. Temperature-gradient spectral anisotropy, as defined by (5.3), at four different times, $t=4.35$, $6.85$, $7.45$ and $11$.

Figure 21

Figure 20. (a) Turbulent kinetic energy $\overline{\unicode[STIX]{x1D70C}}\widetilde{k}=\overline{\unicode[STIX]{x1D70C}u_{i}^{\prime \prime }u_{i}^{\prime \prime }}/2$. Comparison between results obtained from simulations $Sr6\text{-}Re6\times 10^{4}$ (blue), $Sr6\text{-}Re3\times 10^{4}$ (green) and $Sr0\text{-}Re3\times 10^{4}$ (red). (b) Dissipation rate. Comparison between results obtained from simulations $Sr6\text{-}Re6\times 10^{4}$ (blue), $Sr6\text{-}Re3\times 10^{4}$ (green) and $Sr0\text{-}Re3\times 10^{4}$ (red).

Figure 22

Figure 21. Mean profiles related to (6.1). (a) Turbulent kinetic energy $\overline{\unicode[STIX]{x1D70C}}\widetilde{k}$, dissipation rate $\overline{\unicode[STIX]{x1D70C}}\widetilde{\unicode[STIX]{x1D700}}$, pressure source term $-1/Sr\overline{u_{z}^{\prime }}\unicode[STIX]{x2202}_{z}\overline{p}$ and pressure–velocity divergence correlation $1/Sr\overline{p^{\prime }\unicode[STIX]{x2202}_{i}u_{i}^{\prime }}$. The mean effective Atwood number $3\times 10^{-3}A_{t}(t)/A_{t}(0)$ versus time is represented by the black dashed curve. (b) Disequilibrium as defined by (6.3) for two values of $\unicode[STIX]{x1D6FD}=0.8$; (blue) and $\unicode[STIX]{x1D6FD}=0.2$ (green). The black dashed line is located at the ordinate 1, the equilibrium value.

Figure 23

Figure 22. Vertical mean profiles of the r.m.s.-density source terms (equation (6.4)). (a) Density-gradient source term $-2\overline{\unicode[STIX]{x1D70C}^{\prime }u_{z}^{\prime }}\unicode[STIX]{x2202}_{z}\bar{\unicode[STIX]{x1D70C}}$. (b) Velocity-gradient source term $-2\overline{\unicode[STIX]{x1D70C}^{\prime 2}}\unicode[STIX]{x2202}_{z}\tilde{u} _{z}$.

Figure 24

Figure 23. Mass flux source terms of equation (6.5). (b) Mean values of the three production terms proportional to the density, vertical velocity and pressure gradients, respectively. The pressure-gradient term is dominant and reaches its maximum at $t=3.25$. (b) Vertical profiles of the mass flux source term proportional to the pressure at six different times.

Figure 25

Figure 24. Vertical profiles of r.m.s. thermodynamic fluctuations, density $\unicode[STIX]{x1D70C}_{rms}/\overline{\unicode[STIX]{x1D70C}}$ (blue), pressure $p_{rms}/\overline{p}$ (green), temperature $T_{rms}/\overline{T}$ (red) and concentration $c_{rms}/2$ (yellow), at times $t=3.25$; 4.15; 6.85; 7.45; 8.15; and 18.55.

Figure 26

Figure 25. (a) Evolution of r.m.s. density, $\langle \unicode[STIX]{x1D70C}_{rms}/\overline{\unicode[STIX]{x1D70C}}\rangle _{\unicode[STIX]{x1D6FD}}$, pressure, $\langle p_{rms}/\overline{p}\rangle _{\unicode[STIX]{x1D6FD}}$, temperature, $\langle T_{rms}/\overline{T}\rangle _{\unicode[STIX]{x1D6FD}}$ and concentration fluctuations, $\langle c_{rms}\rangle _{\unicode[STIX]{x1D6FD}}/2$ versus time. (b) Entropic and acoustic modes of the density and temperature versus time, i.e. $\langle \overline{\unicode[STIX]{x1D70C}_{en}^{\prime 2}}^{1/2}/\overline{\unicode[STIX]{x1D70C}}\rangle _{\unicode[STIX]{x1D6FD}}$ (blue), $\langle \overline{\unicode[STIX]{x1D70C}_{ac}^{\prime 2}}^{1/2}/\overline{\unicode[STIX]{x1D70C}}\rangle _{\unicode[STIX]{x1D6FD}}$ (green), $\langle \overline{T_{en}^{\prime 2}}^{1/2}/\overline{T}\rangle _{\unicode[STIX]{x1D6FD}}$ (red), $\langle \overline{T_{ac}^{\prime 2}}^{1/2}/\overline{T}\rangle _{\unicode[STIX]{x1D6FD}}$ (yellow), respectively.

Figure 27

Figure 26. Acoustic-mode vertical profiles of the density $\overline{\unicode[STIX]{x1D70C}_{ac}^{\prime 2}}^{1/2}/\overline{\unicode[STIX]{x1D70C}}$ (a) and temperature $\overline{T_{ac}^{\prime 2}}^{1/2}/\overline{T}$ (b).

Figure 28

Figure 27. (a) Density–pressure correlation, $R_{\unicode[STIX]{x1D70C}}(\unicode[STIX]{x1D70C},p)$, defined by (7.5) as a function of the vertical coordinate $z$, at five different times. (b) Density–temperature correlation, $S(\unicode[STIX]{x1D70C},T)$, defined by (7.7) as a function of the vertical coordinate $z$, at three different times.

Figure 29

Figure 28. Velocity statistics. Skewness, $\overline{u_{z}^{\prime 3}}/\overline{u_{z}^{\prime 2}}^{3/2}$ (a) and flatness, $\overline{u_{z}^{\prime 4}}/\overline{u_{z}^{\prime 2}}^{2}$ (b), of the vertical velocity. The flatness of the Gaussian process is represented by the horizontal dashed line.

Figure 30

Figure 29. Velocity PDFs. (a) Horizontal velocity, $u_{x}^{\prime }$ and vertical velocity, $u_{z}^{\prime }$. (b) Vertical gradient of the horizontal velocity and vertical velocity components. On each plot, the dashed lines show Gaussian distribution with the same mean and variance.

Figure 31

Figure 30. (a) Pressure PDFs for two different intervals defined by the mean concentration $\overline{c}$. (b) PDF of the horizontal and vertical potential vorticity components.

Figure 32

Figure 31. Mixing statistics. Skewness, $\overline{c^{\prime 3}}/\overline{c^{\prime 2}}^{3/2}$ (a) and flatness, $\overline{c^{\prime 4}}/\overline{c^{\prime 2}}^{2}$ (b), of the concentration fluctuation at six different times, $t=$ 3.25, 4.15, 4.35, 6.85, 7.45 and 8.30. The horizontal black dashed line stands for the Gaussian process flatness.

Figure 33

Figure 32. Mixing statistics. Flatness of the concentration fluctuation gradient versus the vertical coordinate $z$ at six different times, $t=3.25$, 4.15, 4.35, 6.85, 7.45 and 8.30. (a) Horizontal gradient $\overline{(\unicode[STIX]{x2202}_{x}c^{\prime })^{4}}/\overline{(\unicode[STIX]{x2202}_{x}c^{\prime })^{2}}^{2}$. (b) Vertical gradient $\overline{(\unicode[STIX]{x2202}_{z}c^{\prime })^{4}}/\overline{(\unicode[STIX]{x2202}_{z}c^{\prime })^{2}}^{2}$. The horizontal black dashed line stands for the Gaussian process flatness.

Figure 34

Figure 33. Mixing statistics. (a) PDFs of the concentration fluctuations $c^{\prime }$ at time $t=7.45$, for two different intervals. (b) PDFs of the concentration fluctuation $x$- and $z$-gradients, at the same time.

Figure 35

Figure 34. Density statistics. (a) PDFs of the density fluctuations $c^{\prime }$ at time $t=7.45$, for two different intervals defined by the mean concentration $\overline{c}$. (b) Density fluctuation $x$- and $z$-gradient PDFs, at the same time.

Figure 36

Figure 35. Temperature statistics. Skewness $\overline{T^{\prime 3}}/\overline{T^{\prime 2}}^{3/2}$ (a) and flatness $\overline{T^{\prime 4}}/\overline{T^{\prime 2}}^{2}$ (b) of the temperature fluctuations versus the vertical coordinate $z$, at six different times, $t=3.25$, 4.15, 4.35, 6.85, 7.45 and 8.30. The horizontal black dashed line stands for the Gaussian process flatness.

Figure 37

Figure 36. Temperature statistics. Flatness of the temperature fluctuation $x$- and $z$ gradients versus the vertical coordinate $z$, at six different times, $t=$ 3.25, 4.15, 4.35, 6.85, 7.45 and 8.30. (a) Horizontal gradient $\overline{(\unicode[STIX]{x2202}_{x}T^{\prime })^{4}}/\overline{(\unicode[STIX]{x2202}_{x}T^{\prime })^{2}}^{2}$. (b) Vertical gradient $\overline{(\unicode[STIX]{x2202}_{z}T^{\prime })^{4}}/\overline{(\unicode[STIX]{x2202}_{z}T^{\prime })^{2}}^{2}$. The horizontal black dashed line stands for the Gaussian process flatness.

Figure 38

Figure 37. Temperature statistics. (a) PDFs of the temperature fluctuations $T^{\prime }$ at time $t=7.45$, for two different intervals defined by the mean concentration, $\overline{c}$. (b) PDFs of the temperature fluctuation $x$- and $z$-gradient, at the same time.

Figure 39

Figure 38. Statistics. PDFs of the cosine of the angle between various quantities at time $t=7.45$, the turbulent kinetic energy maximum. (a) Superimposition of the PDFs of the cosine of the angle between vorticity and temperature (blue), density (green) and concentration (red) gradient, respectively. (b) PDFs of the cosine of the angle between vorticity and pressure gradient (blue) and the gradients of density and concentration (green) and density and pressure (red).

Figure 40

Figure 39. Visualization. (a) Temperature isosurfaces (top view) $T=0.95$ (blue) and $T=1.05$ (red). Temperature at rest is $T=1$. Time is $t=4.6$. (b) Helicity isosurfaces for the two values, ${\mathcal{H}}=\pm 0.20$, coloured by the concentration, at time $t=4.35$, top view.