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Register a new userCurvature suppresses the Rayleigh-Taylor instability
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The dynamics of a thin liquid film on the underside of a curved cylindrical substrate is studied. The evolution of the liquid layer is investigated as the film thickness and the radius of curvature of the substrate are varied. A dimensionless parameter (a modified Bond number) that incorporates both geometric parameters, gravity, and surface tension is identified, and allows the observations to be classified according to three different flow regimes: stable films, films with transient growth of perturbations followed by decay, and unstable films. Experiments and theory confirm that, below a critical value of the Bond number, curvature of the substrate suppresses the Rayleigh-Taylor instability.
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Rayleigh-Taylor-instability(RTI) induced flow and mixing are of great importance in both nature and engineering scenarios. To capture the underpinning physics, tracers are introduced to make a supplement to discrete Boltzmann simulation of RTI in compressible flows. Via marking two types of tracers with different colors, the tracer distribution provides a clear boundary of two fluids during the RTI evolution. Fine structures of the flow and thermodynamic nonequilibrium behavior around the interface in a miscible two-fluid system are delineated. Distribution of tracers in its velocity phase space makes a charming pattern showing quite dense information on the flow behavior, which opens a new perspective for analyzing and accessing significantly deep insights into the flow system. RTI mixing is further investigated via tracer defined local mixedness. The appearance of Kelvin-Helmholtz instability is quantitatively captured by mixedness averaged align the direction of the pressure gradient. The role of compressibility and viscosity on mixing are investigated separately, both of which show two-stage effect. The underlying mechanism of the two-stage effect is interpreted as the development of large structures at the initial stage and the generation of small structures at the late stage. At the late stage, for a fixed time, a saturation phenomenon of viscosity is found that further increase of viscosity cannot see an evident decline in mixedness. The mixing statues of heavy and light fluids are not synchronous and the mixing of a RTI system is heterogenous. The results are helpful for understanding the mechanism of flow and mixing induced by RTI.
In this paper, the coupled Rayleigh-Taylor-Kelvin-Helmholtz instability(RTI, KHI and RTKHI, respectively) system is investigated using a multiple-relaxation-time discrete Boltzmann model. Both the morphological boundary length and thermodynamic nonequilibrium (TNE) strength are introduced to probe the complex configurations and kinetic processes. In the simulations, RTI always plays a major role in the later stage, while the main mechanism in the early stage depends on the comparison of buoyancy and shear strength. It is found that, both the total boundary length $L$ of the condensed temperature field and the mean heat flux strength $D_{3,1}$ can be used to measure the ratio of buoyancy to shear strength, and to quantitatively judge the main mechanism in the early stage of the RTKHI system. Specifically, when KHI (RTI) dominates, $L^{KHI} > L^{RTI}$ ($L^{KHI} < L^{RTI}$), $D_{3,1}^{KHI} > D_{3,1}^{RTI}$ ($D_{3,1}^{KHI} < D_{3,1}^{RTI}$); when KHI and RTI are balanced, $L^{KHI} = L^{RTI}$, $D_{3,1}^{KHI} = D_{3,1}^{RTI}$. A second sets of findings are as below: For the case where the KHI dominates at earlier time and the RTI dominates at later time, the evolution process can be roughly divided into two stages. Before the transition point of the two stages, $L^{RTKHI}$ initially increases exponentially, and then increases linearly. Hence, the ending point of linear increasing $L^{RTKHI}$ can work as a geometric criterion for discriminating the two stages. The TNE quantity, heat flux strength $D_{3,1}^{RTKHI}$, shows similar behavior. Therefore, the ending point of linear increasing $D_{3,1}^{RTKHI}$ can work as a physical criterion for discriminating the two stages.
Rayleigh-Taylor (RT) instability widely exists in nature and engineering fields. How to better understand the physical mechanism of RT instability is of great theoretical significance and practical value. At present, abundant results of RT instability have been obtained by traditional macroscopic methods. However, research on the thermodynamic non-equilibrium (TNE) effects in the process of system evolution is relatively scarce. In this paper, the discrete Boltzmann method based on non-equilibrium statistical physics is utilized to study the effects of the specific heat ratio on compressible RT instability. The evolution process of the compressible RT system with different specific heat ratios can be analyzed by the temperature gradient and the proportion of the non-equilibrium region. Firstly, as a result of the competition between the macroscopic magnitude gradient and the non-equilibrium region, the average TNE intensity first increases and then reduces, and it increases with the specific heat ratio decreasing; the specific heat ratio has the same effect on the global strength of the viscous stress tensor. Secondly, the moment when the total temperature gradient in y direction deviates from the fixed value can be regarded as a physical criterion for judging the formation of the vortex structure. Thirdly, under the competition between the temperature gradients and the contact area of the two fluids, the average intensity of the non-equilibrium quantity related to the heat flux shows diversity, and the influence of the specific heat ratio is also quite remarkable.
Understanding the mechanics of detrimental convective instabilities in drying polymer solutions is crucial in many applications such as the production of film coatings. It is well known that solvent evaporation in polymer solutions can lead to Rayleigh-Benard or Marangoni-type instabilities. Here we reveal another mechanism, namely that evaporation can cause the interface to display Rayleigh-Taylor instabilities due to the build-up of a dense layer at the air-liquid interface. We study experimentally the onset time ($t_p$) of the instability as a function of the macroscopic properties of aqueous polymer solutions, which we tune by varying the polymer concentration ($c_0$), molecular weight and polymer type. In dilute solutions, $t_p$ shows two limiting behaviors depending on the polymer diffusivity. For high diffusivity polymers (low molecular weight), the pluming time scales as $c_0^{-2/3}$. This result agrees with previous studies on gravitational instabilities in miscible systems where diffusion stabilizes the system. On the other hand, in low diffusivity polymers the pluming time scales as $c_0^{-1}$. The stabilizing effect of an effective interfacial tension, similar to those in immiscible systems, explains this strong concentration dependence. Above a critical concentration, $hat{c}$, viscosity delays the growth of the instability, allowing time for diffusion to act as the dominant stabilizing mechanism. This results in $t_p$ scaling as $( u/c_0)^{2/3}$.
We studied turbulence induced by the Rayleigh-Taylor (RT) instability for 2D immiscible two-component flows by using a multicomponent lattice Boltzmann method with a Shan-Chen pseudopotential implemented on GPUs. We compare our results with the extension to the 2D case of the phenomenological theory for immiscible 3D RT studied by Chertkov and collaborators ({it Physical Review E 71, 055301, 2005}). Furthermore, we compared the growth of the mixing layer, typical velocity, average density profiles and enstrophy with the equivalent case but for miscible two-component fluid. Both in the miscible and immiscible cases, the expected quadratic growth of the mixing layer and the linear growth of the typical velocity are observed with close long-time asymptotic prefactors but different initial transients. In the immiscible case, the enstrophy shows a tendency to grow like $propto t^{3/2}$, with the highest values of vorticity concentrated close to the interface. In addition, we investigate the evolution of the typical drop size and the behavior of the total length of the interface in the emulsion-like state, showing the existence of a power law behavior compatible with our phenomenological predictions. Our results can also be considered as a first validation step to extend the application of lattice Boltzmann tool to study the 3D immiscible case.
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