Oscillatory Thermocapillary Convection

Stability analysis of thermocapillary convection in rectangular cavities is performed using direct numerical simulation. The influence of the Reynolds number (Re), the fluid Prandtl number (Pr) and cavity aspect ratio (Ar) on the motion is investigated. Neutral stability curves for transition to time-dependent convection are delineated in the Re-Ar plane for fluids with Pr=1.0, 4.4, 6.78, and 10. Several interesting features of these diagrams are discussed. One important conclusion is that Ar(epsilon tau) increases as Pr decreases. Thus large values of both Ar and Re are necessary to induce thermocapillary oscillations for small Pr fluids such as liquid metals and semiconductor melts. Energy analysis is also performed for the oscillatory flow in the neighborhood of critical points in order to gain insight into the mechanisms leading to instability

Oscillatory thermocapillary convection

We study thermocapillary and buoyant thermocapillary convection in rectangular cavities with aspect ratio A = 4 and Pr = 0.015. Two separate problems are considered. The first is combined buoyant thermocapillary convection with a nondeforming interface. We establish neutral curves for transition to oscillatory convection in the Re-Gr plane. It is shown that while pure buoyant convection exhibits oscillatory behavior for Gr is greater than Gr(sub cr) (where Gr(sub cr) is defined for the pure buoyant problem), pure thermocapillary convection is steady within the range of parameters tested. In the second problem, we consider the influence of surface deformation on the pure thermocapillary problem. For the range of parameters considered, thermocapillary convection remained steady

Autocatalytic plume pinch-off

A localized source of buoyancy flux in a non-reactive fluid medium creates a plume. The flux can be provided by either heat, a compositional difference between the fluid comprising the plume and its surroundings, or a combination of both. For autocatalytic plumes produced by the iodate-arsenous acid reaction, however, buoyancy is produced along the entire reacting interface between the plume and its surroundings. Buoyancy production at the moving interface drives fluid motion, which in turn generates flow that advects the reaction front. As a consequence of this interplay between fluid flow and chemical reaction, autocatalytic plumes exhibit a rich dynamics during their ascent through the reactant medium. One of the more interesting dynamical features is the production of an accelerating vortical plume head that in certain cases pinches-off and detaches from the upwelling conduit. After pinch-off, a new plume head forms in the conduit below, and this can lead to multiple generations of plume heads for a single plume initiation. We investigated the pinch-off process using both experimentation and simulation. Experiments were performed using various concentrations of glycerol, in which it was found that repeated pinch-off occurs exclusively in a specific concentration range. Autocatalytic plume simulations revealed that pinch-off is triggered by the appearance of accelerating flow in the plume conduit.Comment: 10 figures. Accepted for publication in Phys Rev E. See also http://www.physics.utoronto.ca/nonlinear/papers_chemwave.htm

Double diffusive instabilities of autocatalytic chemical fronts

info:eu-repo/semantics/publishe

On the classification of buoyancy-driven chemo-hydrodynamic instabilities of chemical fronts.

Exothermic autocatalytic fronts traveling in the gravity field can be deformed by buoyancy-driven convection due to solutal and thermal contributions to changes in the density of the product versus the reactant solutions. We classify the possible instability mechanisms, such as Rayleigh-Benard, Rayleigh-Taylor, and double-diffusive mechanisms known to operate in such conditions in a parameter space spanned by the corresponding solutal and thermal Rayleigh numbers. We also discuss a counterintuitive instability leading to buoyancy-driven deformation of statically stable fronts across which a solute-light and hot solution lies on top of a solute-heavy and colder one. The mechanism of this chemically driven instability lies in the coupling of a localized reaction zone and of differential diffusion of heat and mass. Dispersion curves of the various cases are analyzed. A discussion of the possible candidates of autocatalytic reactions and experimental conditions necessary to observe the various instability scenarios is presented.Journal ArticleSCOPUS: ar.jinfo:eu-repo/semantics/publishe