Importance of direction of vibration on the onset of Soret-driven convection under gravity or weightlessness

This paper considers the influence of the direction of vibration on the stability threshold of two-dimensional Soret-driven convection. The configuration is an infinite layer filled with a binary mixture, which can be heated from below or from above. The limiting case of high-frequency and small-amplitude vibration is considered for which the time-averaged formulation has been adopted. The linear stability analysis of the quasi-mechanical equilibrium shows that the problem depends on five non-dimensional parameters. These include the thermal Rayleigh number ( Ra_T), the vibrational parameter (R), the Prandtl number ( Pr), the Lewis number (Le), the separation ratio (S) and the orientation of vibration with respect to the horizontal heated plate (). For different sets of parameters, the bifurcation diagrams are plotted Ra_c = f (S) and k_c = g(S), which are the critical thermal Rayleigh and the critical wave numbers, respectively. Our results indicate that, relative to the classical case of static gravity, vibration may affect all regions in Ra_c-S stability diagram. In the case of mono-cellular convection, by using a regular perturbation method, a closed-form relation for the critical Rayleigh number is found. Several physical situations in the presence or in the absence of gravity (micro-gravity) are discussed.     

Transient-state method for coupled evaluation of Soret and Fick coefficients,and related tortuosity factors,using free and porous packed thermodiffusion cells: Application to CuSO4 aqueous solution ( 0.25M)

The measurement of Soret coefficients in liquids is not easy and usually not very precise because the resulting concentration gradient is small and moreover can be perturbed by undesired convection currents. In order to suppress, or to drastically reduce these convection currents, the use of a porous medium is sometimes suggested. The question arises as to whether the Soret coefficient is the same in free fluid and in porous medium. This is the aim of this paper. To this end, for a given liquid mixture, the time evolution of the vertical concentration gradient is experimentally measured in the same thermodiffusion cell filled first with the free liquid and next with a porous medium followed by saturation by the liquid mixture. Both the isothermal diffusion (Fick) coefficient and the Soret coefficient can be deduced, providing that a correct working equation is used. The proposed equation results from integration of the general mass conservation equation with realistic boundary conditions (zero mass flux at the boundaries) and some simplifying assumptions rendering this equation more tractable than the one proposed some decades ago by Bierlein (J.A. Bierlein, J. Chem. Phys. 23, 10 (1955)). The method is applied here to an electrolytic solution (CuSO4, 0.25 M) at a mean temperature of 37^°C. The Soret coefficients in free and porous medium (zircon microspheres in the range of 250- 315 ^. 10^-6m) may be considered to be equal ( S_T = 13.2±0.5 ^. 10^-3 K^-1) and the tortuosity factors for the packed medium are the same relative to thermodiffusion and Fick coefficients ( = 1.51±0.02).     

Transient oscillations in Soret-driven convection in a colloidal suspension

We present measurements of the transient stage of Soret-driven convective instability. The sample is a diluted colloidal suspension of silica spheres in water with an unusually large negative Soret coefficient S_T. A large temperature gradient (heating from above) is rapidly applied over the sample, while a shadowgraph imaging technique provides images of the convective flow. From the processing of the variance of the intensity of the images we are able to recover the time evolution of the overall intensity of the convective flow. A typical evolution of such signal exhibits, after a latency time, a peak followed by some damped oscillations leading to a steady-state value. Both the onset time _p (the temporal position of the first peak), and the oscillation period _osc show a power law dependence as a function of the solutal Rayleigh number R_s. The exponents found are compared with predictions from existing models.     

The role of heat-conducting walls in the measurement of heat and mass transport in transient grating experiments

We present a two-dimensional model to account for the role of heat-conducting walls in the measurement of heat transport and Soret-effect-driven mass transport in transient holographic grating experiments. Heat diffusion into the walls leads to non-exponential decay of the temperature grating. Under certain experimental conditions it can be approximated by an exponential function and assigned an apparent thermal diffusivity D_{th, app} < D_{th, s}, where D_th,s is the true thermal diffusivity of the sample. The ratio D_{th, app}/D_{th, s} depends on only three dimensionless parameters, d /l_s, κ_s/κ_w, and D_{th, s}/D_{th, w}. d is the grating period, l_s the sample thickness, κ_s and κ_w the thermal conductivities of sample and wall, respectively, and D_th,w the thermal diffusivity of the wall. If at least two measurements are performed at different d /l_s, both D_th,s and κ_s can be determined. Instead of costly solving PDEs, D_th,s can be obtained by finding the zero of an analytic function. For thin samples and large grating periods, heat conduction into the walls plays a predominant role and the concentration grating in binary mixtures is no longer one-dimensional. Nevertheless, the normalized heterodyne diffraction efficiency of the concentration grating remains unaffected and the true thermal and collective diffusion coefficient and the correct Soret coefficient are still obtained from a simple one-dimensional model.     

Influence of ion implantation on the thermal diffusivity of semiconductors

The influence of ion implantation on the thermal diffusivities of semiconductors are studied using the mirage effect. The dependences of the thermal diffusivities on the implantation doses are obtained. For silicon wafers implanted by boron, phosphorus and arsenic ions, with constant implantation energy, the thermal diffusivities decrease with increasing dose, when the doses are less than some critical values. The theoretical calculation results by using a one-dimensional multilayer model are in good agreement with the experimental ones. On the other hand, for gallium-arsenide wafers implanted with silicon ions, it is found experimentally that the thermal diffusivity increases with the implantation dose.     

Anomalous viscosity exponent in a discretized model for a chain diffusion in one dimension

We present a one-dimensional Monte Carlo simulation for the diffusion motion of a chain of N beads. We found that the scaling exponent for the viscosity can be smaller or greater than 3. This anomalous behavior cannot be attributed to the diffusivity scaling or the length fluctuations but is due to the chain dynamics details during diffusion in which the end beads play the key role. The viscosity exponent 3 and its expected relation with the diffusivity exponent are recovered in the asymptotic regime (N ↦∞). Received 24 September 2001 and Received in final form 28 January 2002     

The nonlinear Fokker-Planck equation with state-dependent diffusion - a nonextensive maximum entropy approach

Nonlinear Fokker-Planck equations (e.g., the diffusion equation for porous medium) are important candidates for describing anomalous diffusion in a variety of systems. In this paper we introduce such nonlinear Fokker-Planck equations with general state-dependent diffusion, thus significantly generalizing the case of constant diffusion which has been discussed previously. An approximate maximum entropy (MaxEnt) approach based on the Tsallis nonextensive entropy is developed for the study of these equations. The MaxEnt solutions are shown to preserve the functional relation between the time derivative of the entropy and the time dependent solution. In some particular important cases of diffusion with power-law multiplicative noise, our MaxEnt scheme provides exact time dependent solutions. We also prove that the stationary solutions of the nonlinear Fokker-Planck equation with diffusion of the (generalized) Stratonovich type exhibit the Tsallis MaxEnt form. Received 26 February 1999     

Single-particle thermal diffusion of charged colloids: Double-layer theory in a temperature gradient

The double-layer contribution to the single-particle thermal diffusion coefficient of charged, spherical colloids with arbitrary double-layer thickness is calculated and compared to experiments. The calculation is based on an extension of the Debye-Hückel theory for the double-layer structure that includes a small temperature gradient. There are three forces that constitute the total thermophoretic force on a charged colloidal sphere due to the presence of its double layer: i) the force F _W that results from the temperature dependence of the internal electrostatic energy W of the double layer, ii) the electric force F _el with which the temperature-induced non-spherically symmetric double-layer potential acts on the surface charges of the colloidal sphere and iii) the solvent-friction force F _sol on the surface of the colloidal sphere due to the solvent flow that is induced in the double layer because of its asymmetry. The force F _W will be shown to reproduce predictions based on irreversible-thermodynamics considerations. The other two forces F _el and F _sol depend on the details of the temperature-gradient-induced asymmetry of the double-layer structure which cannot be included in an irreversible-thermodynamics treatment. Explicit expressions for the thermal diffusion coefficient are derived for arbitrary double-layer thickness, which complement the irreversible-thermodynamics result through the inclusion of the thermophoretic velocity resulting from the electric- and solvent-friction force.     

Monte-Carlo analysis of tracer diffusion mechanisms in YBa2Cu3O6+c

A method for estimating, via the Monte-Carlo simulation, the most often realized diffusion mechanisms in 2D ordered structures is presented. Taking as an example the diffusion of oxygen ions in high temperature superconductor we propose several diffusion mechanisms and show to what extent they depend on the temperature and concentration of the diffusing particles. Our results are compared with the ones proposed earlier on the basis of energy arguments. We find also additional trajectories, different from those earlier reported in that system. Received 9 November 1998     

New problems of particle transfer in ferrocolloids: Magnetic Soret effect and thermoosmosis

The paper deals with critical reviewing of the experiments on thermodiffusion in ferrocolloids. The observed magnetic Soret effect is much stronger than that predicted theoretically. It is shown that the main reason of that is the influence of the magnetic field on mass diffusion. Besides, some measurements are affected by uncontrolled thermal and solutal magnetic convection. In porous media, when macroscopic convection is suppressed, thermodiffusion is accompanied by thermoosmosis as well as by a microconvective mass transfer induced by particle magnetophoresis on filter grains.     

Cooperative motions in a finite size model of liquid silica: an anomalous behavior

Finite size effects on dynamical heterogeneity are studied in liquid silica with Molecular Dynamics simulations using the BKS potential model. When the system size decreases relaxation times are found to increase in accordance with previous results in finite-size simulations and confined liquids. It has been suggested that this increase may be related to a modification of the spatially heterogeneous dynamics in confined liquids. In agreement with this hypothesis we observe a decrease of the spatially heterogeneous dynamics when the size decreases. The spatially heterogeneous dynamics is usually characterized by the dynamical aggregation of the most or the least mobile atoms. However we find that the decrease of the dynamical aggregation associated to the least mobile atoms is much more important than the decrease associated to the most mobile atoms when the size decreases. This result associated with a slowing down of the liquid is surprising as it is expected that the dynamical aggregation of the least mobile atoms should increase the slowing down of the liquid dynamics. The decrease of the heterogeneous behaviour is also in contradiction with the increase of the spatially heterogeneous dynamics observed in liquids confined inside nanopores. However, an increase of the non-Gaussian parameter appears both for the confinement inside nanopores and for the finite size simulations. As the non-Gaussian parameter is usually associated with the heterogeneous dynamics, the increase of the non-Gaussian parameter together with a decrease of the spatially heterogeneous dynamics is also surprising.     

Diffusion and rheology in a model of glassy materials

We study self-diffusion within a simple hopping model for glassy materials. (The model is Bouchaud's model of glasses (J.-P. Bouchaud, J. Phys. I France 2, 1705 (1992)), as extended to describe rheological properties (P. Sollich, F. Lequeux, P. Hébraud, M.E. Cates, Phys. Rev. Lett. 78, 2020 (1997)).) We investigate the breakdown, near the glass transition, of the (generalized) Stokes-Einstein relation between self-diffusion of a tracer particle and the (frequency-dependent) viscosity of the system as a whole. This stems from the presence of a broad distribution of relaxation times of which different moments control diffusion and rheology. We also investigate the effect of flow (oscillatory shear) on self-diffusion and show that this causes a finite diffusivity in the temperature regime below the glass transition (where this was previously zero). At higher temperatures the diffusivity is enhanced by a power law frequency dependence that also characterises the rheological response. The relevance of these findings to soft glassy materials (foams, emulsions etc.) as well as to conventional glass-forming liquids is discussed. Received 31 August 1998 and Received in final form 25 January 1999     

Forced diffusion in magnetic fluids under the influence of a strong magnetic field gradient

We have investigated the forced diffusion of magnetic nanoparticles suspended in a carrier liquid under the influence of a magnetic field gradient. A cylindrical layer of the suspension was exposed to an azimuthal magnetic field with radial gradient. The radial distribution of the concentration of magnetic particles was determined for different times. The obtained experimental data are compared with a numerical solution of the diffusion equation and good agreement has been observed.     

Segregation in desiccated sessile drops of biological fluids

It is shown here that concurrence between advection and diffusion in a drying sessile drop of a biological fluid can produce spatial redistribution of albumen and salt. The result gives an explanation for the patterns observed in the dried drops of the biological fluids.     

Correlation between the Soret coefficient and the static structure factor in a polymer blend

Mutual mass diffusion and thermal diffusion has been investigated in poly(dimethylsiloxane)/ poly(ethylmethylsiloxane) (PDMS/PEMS) polymer blends of equal weight fractions. Molar masses ranged from below 1 to over 20 kg/mol. Both the mutual mass (D) and the thermal diffusion (D_T) coefficient contain a thermally activated factor with an activation temperature of 1415 K. The molar mass dependence of D_T is due to an end-group effect of the local friction coefficient. The thermal diffusion coefficient in the limit of long chains and infinite temperature is D_T^0, = - 1.69×10^-7cm²(sK)^-1. The Soret coefficient S_T of blends far enough away from a critical point is proportional to the static structure factor S(q = 0).     

Target ion source and charge exchange cell development for the EXCYT facility

The EXCYT facility at the INFN-LNS is based on a K-800 superconducting cyclotron delivering stable ion beams on a Target Ion Source (TIS) assembly to produce the required nuclear species, and on a 15 MV Tandem for post-accelerating the radioactive beams. For some ion beams such as for Li, the extraction efficiency from the TIS is higher when obtained by positive ionisation, while the injection into the Tandem is possible only after a charge exchange to obtain negative ions. In this work we present the procedures together with the results of the production of ^6,7,8,9Li beams extracted at EXCYT during the last year. The production of the radioactive elements was performed by sending a ¹³C⁴⁺ primary beam of 45 MeV/u on a graphite target. The ionisation of the production species was achieved by a tungsten positive surface ioniser. The Li⁺ has been extracted from TIS at different energies to cross-check the transmission and the charge exchange efficiency. To perform the conversion from positive to negative ions we employed a Charge Exchange Cell (CEC) containing Cs vapours. The Li beam interacts with the latter in a two-step reaction, thus converting its charge from +1 to –1. The CEC was already characterised during off-line tests; the results obtained at EXCYT confirmed both the isotopic shift effect and the efficiency values at several given extraction energies. Future improvements of the TIS and the CEC are discussed.     

Time evolution of near membrane layers

The near membrane layer is a region where the concentration of the substance transported across the membrane is significantly decreased. Its thickness is defined as a length over which the concentration drops k times with k being an arbitrary large number. The time evolution of such a layer is studied experimentally by means of the laser interferometric method. It is shown that within the experimental errors the thickness of the near membrane layer grows in time for any k as with the coefficient a being independent of the initial concentration and the membrane permeability. Time evolution of the near membrane layers is also analyzed theoretically. The regularities found experimentally are naturally described within the model which has been earlier developed by one of us. In particular, a scales as . Received 12 November 1999 and Received in final form 3 July 2000     

Water and its energy landscape

We present an overview of the recent studies on the properties of the potential energy surface for a simple model of water. We emphasize the relations between PES properties and dynamics in supercooled states for the model and discuss possible future application of the PES studies. Received 13 March 2002     

Phase transitions in materials with thermal memory: The case of unequal conductivities

A model for thermally induced phase transitions in materials with thermal memory was recently proposed, where the equations determining heatflow were assumed to be the same in both phases. In this work, the model is generalized to the case of phase dependent heatflow relations. The temperature (or coldness) gradient is decomposed into two parts, each zero on one phase and equal to the temperature (or coldness) gradient on the other. However, they vary smoothly over the transition zone. These are treated as separate independent quantities in the derivation of field equations from thermodynamics. Heat flux is given by an integral over the history of the temperature gradient, with different kernels on each phase. Asymptotic analysis is carried out to obtain generalizations of previous results. These involve the jump in temperature across the transition zone and the normal derivatives of the temperature on each phase boundary, which are related to the velocity of the transition zone and a latent heat dependent on this velocity, as well as the speeds of thermal disturbances in the two phases.