Search arXiv⌕ Search

arXiv · cond-mat/0007344

Hysteretic transition from laminar to vortex shedding flow in soap films

Abstract

There are different ways for fluid flow to become turbulent, but usually many instabilities take place before that. Among these instabilities the transition from laminar flow to vortex shedding carries significant practical importance. Here we study a flow, where at high enough flow rates, vortices are generated by a fixed obstacle (cylinder), which penetrates a flowing, quasi-two dimensional soap film. We present experimental results that demonstrate that the transition from laminar flow to a periodic Kármán vortex street can be hysteretic, i.e. changing the mean flow rate $\bar V$ vortices can survive at velocities lower than the velocity needed to generate them. This is an unexpected result since 3D experiments are well described by the Hopf equation, which is incompatible with hysteresis. Beyond that, our data cannot be satisfactorily fitted by the generic model of hysteresis, i.e. the 5th order Landau equation. It is found that a phenomenological model describes our experimental findings very well. Evidences are presented that wetting properties of the rod, mechanical instabilities (i.e. vibrations) of the setup, and the effect of the surrounding air are not the cause of the hysteresis. To reduce three dimensional effects, the rod was replaced by a disk having a thickness roughly eight times that of the film. The replacement of the rod by a disk increases the gap width and the shedding frequency. Behaviour of the system (for instance the unstable trajectory) in the hysteretic gap is investigated by means of transient measurements.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Viktor K. Horváth, J. Rob Cressman, Walter I. Goldburg, Xiao-Lun Wu. 2000-07-21. Hysteretic transition from laminar to vortex shedding flow in soap films. https://arxiv.org/abs/cond-mat/0007344

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Control of filament network rigidity by the condensation of crowding molecules

Understanding how liquid-liquid phase separation impacts the mechanics of filament networks is a fundamental physical problem at the heart of biological cellular processes and soft material design. While a few theoretical mechanisms have been proposed, a clear demonstration of the direct coupling of phase separation to the overall network stiffness is missing. We report experiments that reveal a universal mechanism by which the condensation of macromolecular crowders induces a rigidity transition in a model filament network. We reconstituted stiff sterically interacting helical filaments and polymeric crowders. Initially, the macromolecules were uniformly dissolved and the filaments formed bundles that assembled a rigid entangled network. Once the crowders condensed into droplets, the network structure lost its rigidity and its mechanical response weakened by an order-of-magnitude. The subsequent dissolution of the condensates was accompanied by the re-establishment of rigidity. Our results show that crowder phase separation modulates the mechanics of filament networks by tuning the osmotic pressure holding the network together. This principle may serve as a paradigm for devising dynamically tunable filamentous materials.

cond-mat.soft↗

Speed up of passive tracers in mixtures with active chemical reactions

Diffusivity of passive tracers in complex mixtures is widely relevant for industrial applications and for probing biological systems. Interactions with the surrounding medium typically generate a drag force that suppresses tracer diffusion, although self-propulsion can accelerate tracers via active fluctuations. Similar effects are not understood in mixtures with particle conversion and exchange, although these are particularly relevant in biological contexts, where actively driven reactions prevail. By studying a thermodynamically consistent model of chemical reactions in mixtures, we show that reactions provide an additional relaxation pathway that suppresses interaction-induced memory, reducing the drag on tracers and restoring their diffusivity toward the value expected in the absence of solutes. Moreover, active reactions generate nonequilibrium fluctuations that can push tracer diffusivity beyond this limit, an effect we confirm with particle-based simulations. Our results identify chemical activity as a distinct route to controlling mass transport and offer a framework for interpreting microrheology experiments in chemically active mixtures.

cond-mat.soft↗

Diffusion of charged rods across 3D varying section channels

We analyze the transport of rod-like particles by diffusion and drift in a three-dimensional channel with varying circular or elliptic cross section. Applying the Fick-Jacobs approximation to the transport equation of the particles' probability distribution, we derive an effective one-dimensional substitute model and the associated free energy profile. Our results show that the data for the mean first passage time of rods, once expressed as a function of the effective free energy barrier, collapse onto the same master curve as obtained for point or spherical particles. The observed universality provides a simple framework for predicting transport times of anisotropic particles in confined geometries without resolving the full multidimensional dynamics.

cond-mat.soft↗