Do you want to publish a course? Click here

Considerations about universality in phase-ordering of binary liquids

67   0   0.0 ( 0 )
 Added by Alexander J. Wagner
 Publication date 2000
  fields Physics
and research's language is English
 Authors A.J. Wagner




Ask ChatGPT about the research

In this article we show that the phase-ordering scaling state for binary fluids is not necessarily unique and that local correlations in the initial conditions can be responsible for selecting the scaling state. We describe a new scaling state for symmetric volume fractions that consists of drops of the one component suspended in a matrix of the other. The underlying reason for the existence of the newly observed scaling state is that the main coarsening mechanism of binary fluids which is the deformation of interfaces by flow is not acting, and this leads to a new scaling law. An initial droplet state can be formed by a number of physical phenomena. In a unified description this can be undestood as local correlations in the initial conditions. Local correlations with length $xi$ are believed to be irrelevant when the typical length scale L of the system is large ($Lgg xi$). Our result shows that these initial correlations, contrary to current thinking, can be important even at late times.



rate research

Read More

The range of the magnitude of the liquid viscosity as a function of the temperature (T) is one of the most impressive of any physical property, changing by approximately 17 orders of magnitude from its extrapolated value at infinite temperature to that at the glass transition. We present experimental measurements of containerlessly processed metallic liquids that reveal that the ratio of the viscosity to its extrapolated infinite temperature value follows a universal function of Tcoop/T. The temperature Tcoop corresponds to the onset of cooperative motion and is strongly correlated with the glass transition temperature. On average the extrapolated infinite temperature viscosity is found to be nh, where h is Plancks constant and n is the particle number density. A surprising universality in the viscosity of metallic liquids and its relation to the glass transition is demonstrated.
The growth of surface plasmonic microbubbles in binary water/ethanol solutions is experimentally studied. The microbubbles are generated by illuminating a gold nanoparticle array with a continuous wave laser. Plasmonic bubbles exhibit ethanol concentration-dependent behaviors. For low ethanol concentrations (f_e) of < 67.5%, bubbles do not exist at the solid-liquid interface. For high f_e values of >80%, the bubbles behave as in pure ethanol. Only in an intermediate window of 67.5% < f_e < 80% do we find sessile plasmonic bubbles with a highly nontrivial temporal evolution, in which as a function of time three phases can be discerned. (1) In the first phase, the microbubbles grow, while wiggling. (2) As soon as the wiggling stops, the microbubbles enter the second phase in which they suddenly shrink, followed by (3) a steady reentrant growth phase. Our experiments reveal that the sudden shrinkage of the microbubbles in the second regime is caused by a depinning event of the three phase contact line. We systematically vary the ethanol concentration, laser power, and laser spot size to unravel water recondensation as the underlying mechanism of the sudden bubble shrinkage in phase 2.
266 - P.-L. Giscard 2009
We present a method for calculating the Aharonov-Anandan phase for time-independent Hamiltonians that avoids the calculation of evolution operators. We compare the generic method used to calculate the Aharonov-Anandan phase with the method proposed here through four examples; a spin-1/2 particle in a constant magnetic field, an arbitrary infinite-sized Hamiltonian with two known eigenvalues, a Fabry-Perot cavity with one movable mirror and a three mirrors cavity with a slightly transmissive movable middle mirror.
We study the phase-ordering kinetics following a temperature quench of O(N) continuous symmetry models with and 4 on graphs. By means of extensive simulations, we show that the global pattern of scaling behaviours is analogous to the one found on usual lattices. The exponent a for the integrated response function and the exponent z, describing the growing length, are related to the large scale topology of the networks through the spectral dimension and the fractal dimension alone, by means of the same expressions as are provided by the analytic solution of the inifnite N limit. This suggests that the large N value of these exponents could be exact for every N.
148 - Gyula I. Toth 2016
In this paper general dynamic equations describing the time evolution of isothermal quasi-incompressible multicomponent liquids are derived in the framework of the classical Ginzburg-Landau theory of first order phase transformations. Based on the fundamental {equations of continuum mechanics}, a general convection-diffusion dynamics is set up first for compressible liquids. The constitutive relations for the diffusion fluxes and the capillary stress are determined in the framework of gradient theories. {Next the general definition of incompressibility is given}, which is taken into account {in the derivation} by using the Lagrange multiplier method. To validate the theory, the dynamic equations are solved numerically for the quaternary quasi-incompressible Cahn-Hilliard system. It is demonstrated that variable density (i) has no effect on equilibrium (in case of a suitably constructed free energy functional), {and (ii) can} influence non-equilibrium pattern formation significantly.
comments
Fetching comments Fetching comments
Sign in to be able to follow your search criteria
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا