The probability density function, and related statistics, of scalar (temperature) derivative fluctuations in decaying grid turbulence with an imposed cross-stream, passive linear temperature profile, is studied for a turbulence Reynolds number range, Rel, varying from 50 to 1200, (corresponding to a Taylor Reynolds number range 30<Rλ<130). It is shown that the temperature derivative skewness in the direction of the mean gradient, Sθy has a value of 1.8±0.2 (twice the value observed in shear flows), and has no significant variation with Reynolds number. The ratio of the temperature derivative standard deviation along the gradient to that normal to it is approximately 1.2±0.1 also, with no variation with Re. The kurtosis of the derivatives increases approximately as Re0.2l. The results show that the rare, intense temperature deviations that produce the skewed scalar derivative, increase in frequency, but their area fraction (of the total field) becomes smaller as the Reynolds number increases. Thus, since Sθy remains constant, they become sharper and more intense, occurring deeper in the tails of the probability density function. Measurements in a thermal mixing layer, which has a nonlinear mean temperature profile, are also presented, and these show a similar value of Sθy to the linear profile case. The experiments broadly confirm the two-dimensional numerical simulations of Holzer and Siggia [Phys. Fluids (in press)], as well as other recent simulations, although there are some differences.
In the present study we investigate three-scalar mixing in a turbulent coaxial jet. In this flow a centre jet and an annular flow, consisting of acetone-doped air and ethylene respectively, are mixed with the co-flow air. A unique aspect of this study compared to previous studies of three-scalar mixing is that two of the scalars (the centre jet and air) are separated by the third (annular flow); therefore, this flow better approximates the mixing process in a non-premixed turbulent reactive flow. Planar laser-induced fluorescence and Rayleigh scattering are employed to measure the mass fractions of the acetone-doped air and ethylene. The results show that the most unique aspects of the three-scalar mixing occur in the near field of the flow. The mixing process in this part of the flow are analysed in detail using the scalar means, variances, correlation coefficient, joint probability density function (JPDF), conditional diffusion, conditional dissipation rates and conditional cross-dissipation rate. The diffusion velocity streamlines in scalar space representing the conditional diffusion generally converge quickly to a manifold along which they continue at a lower rate. A widely used mixing model, interaction through exchange with mean, does not exhibit such a trend. The approach to the manifold is generally in the direction of the ethylene mass fraction. The difference in the magnitudes of the diffusion velocity components for the two scalars cannot be accounted for by the difference in their dissipation time scales. The mixing processes during the approach to the manifold, therefore, cannot be modelled by using different dissipation time scales alone. While the three scalars in this flow have similar distances in scalar space, mixing between two of the scalars can occur only through the third, forcing a detour of the manifold (mixing path) in scalar space. This mixing path presents a challenging test for mixing models since most mixing models use only scalar-space variables and do not take into account the spatial (physical-space) scalar structure. The scalar JPDF and the conditional dissipation rates obtained in the present study have similarities to those of mixture fraction and temperature in turbulent flames. The results in the present study provide a basis for understanding and modelling multiscalar mixing in reactive flows.
Carbon quantum dots (CQDs) were demonstrated to have the ability to enhance the photocatalytic performance of monoclinic BiVO4 with different exposed facets under visible light.
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