Study of compressibility effects in mixing layer by numerical simulation

1990 ◽  
Author(s):  
ITARU HATAUE
AIAA Journal ◽  
2000 ◽  
Vol 38 ◽  
pp. 2210-2218 ◽  
Author(s):  
Christopher Bogey ◽  
Christopher Bailly ◽  
Daniel Juve

Author(s):  
Ruru Matsuo ◽  
Ryosuke Matsumoto

This study focused on the diffusion and mixing phenomena investigated by using luminol chemiluminescence (CL) to estimate the local chemical reaction rate in the T-junction microchannel. Generally, the degree of mixing in microchannel is calculated by the deviation of the obtained concentration profiles from the uniform concentration profile by using fluorescence technique. Thus, the degree of mixing is a macroscopic estimate for the whole microchannel, which is inappropriate for understanding the diffusion and mixing phenomena in the mixing layer. In this study, the luminol CL reaction is applied to visualize the local chemical reaction and to estimate the local diffusion and mixing phenomena at an interface between two liquids in microchannel. Luminol emits blue chemiluminescence when it reacts with the hydrogen peroxide at the mixing layer. Experiments were carried out on the T-junction microchannel with 200 microns in width and 50 microns in depth casted in the PDMS chip. The chemiluminescence intensity profiles clearly show the mixing layer at an interface between two liquids. The experimental results are compared with the results of numerical simulation that involves solving the mass transport equations including the chemical reaction term. By calibrating CL intensity to the chemical reaction rate estimated by the numerical simulation, the local chemical reaction profile can be quantitatively estimated from the CL intensity profile.


AIAA Journal ◽  
10.2514/2.906 ◽  
2000 ◽  
Vol 38 (12) ◽  
pp. 2210-2218 ◽  
Author(s):  
Christophe Bogey ◽  
Christophe Bailly ◽  
Daniel Juve

2000 ◽  
Vol 421 ◽  
pp. 229-267 ◽  
Author(s):  
JONATHAN B. FREUND ◽  
SANJIVA K. LELE ◽  
PARVIZ MOIN

This work uses direct numerical simulations of time evolving annular mixing layers, which correspond to the early development of round jets, to study compressibility effects on turbulence in free shear flows. Nine cases were considered with convective Mach numbers ranging from Mc = 0.1 to 1.8 and turbulence Mach numbers reaching as high as Mt = 0.8.Growth rates of the simulated mixing layers are suppressed with increasing Mach number as observed experimentally. Also in accord with experiments, the mean velocity difference across the layer is found to be inadequate for scaling most turbulence statistics. An alternative scaling based on the mean velocity difference across a typical large eddy, whose dimension is determined by two-point spatial correlations, is proposed and validated. Analysis of the budget of the streamwise component of Reynolds stress shows how the new scaling is linked to the observed growth rate suppression. Dilatational contributions to the budget of turbulent kinetic energy are found to increase rapidly with Mach number, but remain small even at Mc = 1.8 despite the fact that shocklets are found at high Mach numbers. Flow visualizations show that at low Mach numbers the mixing region is dominated by large azimuthally correlated rollers whereas at high Mach numbers the flow is dominated by small streamwise oriented structures. An acoustic timescale limitation for supersonically deforming eddies is found to be consistent with the observations and scalings and is offered as a possible explanation for the decrease in transverse lengthscale.


Author(s):  
Tomomi Uchiyama ◽  
Naohiro Otsuki

This paper presents a particle method for free turbulent reacting flows. The vorticity and concentration fields are discretized into the vortex and concentration elements, respectively, and the behavior of the elements is calculated with the Lagrangian method. The chemical reaction is estimated through the Lagrangian calculation for the strength of concentration element. The particle method is applied to simulate a plane mixing layer with a single-step and irreversible chemical reaction of non-premixed reactants so as to discuss the applicability.


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