Publications by authors named "Jan V Sengers"

While Ising criticality in classical liquids has been firmly established both theoretically and experimentally, much less is known about criticality in liquids in which the growth of the correlation length is frustrated by finite-size effects. A theoretical approach for dealing with this issue is the random-field Ising model (RFIM). While experimental critical-exponent values have been reported for magnetic samples (here, we consider γ, ν and η), little experimental information is available for critical fluctuations in corresponding liquid systems.

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Ionic liquids have been suggested as new engineering fluids, namely in the area of heat transfer, as alternatives to current biphenyl and diphenyl oxide, alkylated aromatics and dimethyl polysiloxane oils, which degrade above 200 °C and pose some environmental problems. Recently, we have proposed 1-ethyl-3-methylimidazolium methanesulfonate, [Cmim][CHSO], as a new heat transfer fluid, because of its thermophysical and toxicological properties. However, there are some interesting points raised in this work, namely the possibility of the existence of liquid metastability below the melting point (303 K) or second order-disorder transitions (-type) before reaching the calorimetric freezing point.

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Extension of a description of mass diffusion in binary fluids based on Fick's law to multicomponent fluids requires introduction of diffusion matrices. A problem is that Fick diffusion matrices commonly adopted for multicomponent fluids depend on the velocity frame of reference. In this paper we show how one can define Fick diffusion matrices for multicomponent fluids that are frame invariant.

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We have discovered unusual behavior of polymer coils in a binary solvent (nitroethane+isooctane) near the critical temperature of demixing. The exceptionally close refractive indices of the solvent components make the critical opalescence relatively weak, thus enabling us to simultaneously observe the Brownian motion of the polymer coils and the diverging correlation length of the critical fluctuations. The polymer coils exhibit a collapse-reswelling-expansion-reshrinking transition upon approaching the critical temperature.

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We present results from an experimental dynamic light-scattering study of poly(ethylene oxide) (PEO) in both a pure solvent (water) and a mixed solvent (tert-butanol + water). The concentration dependence of the diffusive relaxation of the PEO molecules is found to be typical of polymers in a good solvent. However, the mesoscopic diffusive behavior of PEO in the mixed solvent is very different, indicating an initial collapse and subsequent reswelling of PEO caused by co-nonsolvency.

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The heat capacity of supercooled water, measured down to -37°C, shows an anomalous increase as temperature decreases. The thermal diffusivity, i.e.

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In this paper we investigate intrinsic thermally excited nonequilibrium velocity fluctuations in laminar planar Couette flow. For this purpose we have complemented the solution of the stochastic Orr-Sommerfeld equation for the intensity of the fluctuations of the wall-normal velocity, presented in a previous publication, with a solution of the stochastic Squire equation for the intensity of the fluctuations of the wall-normal vorticity. We have obtained exact solutions of these equations without boundary conditions and solutions in a Galerkin approximation when appropriate boundary conditions are included.

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The extension of the principle of critical-point universality to binary fluid mixtures, known as isomorphism of critical phenomena, has been reformulated in terms of complete scaling, a concept that properly matches asymmetric fluid-phase behavior with the symmetric Ising model. The controversial issue of the proper definition of the order parameter in binary fluid mixtures is clarified. We show that asymmetry of liquid-liquid coexistence in terms of mole fractions originates from two different sources: one is associated with a correlation between concentration and entropy fluctuations, whereas the other source is the correlation between concentration and density fluctuations.

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We present an analysis of the transverse-velocity fluctuations in an isothermal liquid layer with a uniform shear rate between two parallel horizontal boundaries as a function of the wave number and the Reynolds number. The results were obtained by solving a stochastic version of the Orr-Sommerfeld equation subject to no-slip boundary conditions in a second-order Galerkin approximation. We find that the spatial Fourier transform of the transverse-velocity fluctuations exhibits a maximum as a function of the (horizontal) wave number q(parallels).

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In this paper a simple reaction-diffusion system, namely a binary fluid mixture with an association-dissociation reaction between the two components, is considered. Fluctuations at hydrodynamic spatiotemporal scales when a temperature gradient is present in this chemically reacting system are studied. First, fluctuating hydrodynamics when the system is in global equilibrium (isothermal) is reviewed.

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In this paper we evaluate the enhancement of nonequilibrium concentration fluctuations induced by the Soret effect when a binary fluid layer is subjected to a stationary temperature gradient. Starting from the fluctuating Boussinesq equations for a binary fluid in the large-Lewis-number approximation, we show how one can obtain an exact expression for the nonequilibrium structure factor in the long-wavelength limit for a fluid layer with realistic impermeable and no-slip boundary conditions. A numerical calculation of the wave-number dependence of the nonequilibrium enhancement and of the corresponding decay rate of the concentration fluctuations is also presented.

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We report comprehensive simulations of the critical dynamics of a symmetric binary Lennard-Jones mixture near its consolute point. The self-diffusion coefficient exhibits no detectable anomaly. The data for the shear viscosity and the mutual-diffusion coefficient are fully consistent with the asymptotic power laws and amplitudes predicted by renormalization-group and mode-coupling theories provided finite-size effects and the background contribution to the relevant Onsager coefficient are suitably accounted for.

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A symmetrical binary, A+B Lennard-Jones mixture is studied by a combination of semi-grand-canonical Monte Carlo (SGMC) and molecular dynamics (MD) methods near a liquid-liquid critical temperature T(c). Choosing equal chemical potentials for the two species, the SGMC switches identities (A-->B-->A) to generate well-equilibrated configurations of the system on the coexistence curve for TT(c). A finite-size scaling analysis of the concentration susceptibility above T(c) and of the order parameter below T(c) is performed, varying the number of particles from N=400 to 12 800.

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Recently, Wada [Phys. Rev. E 69, 031202 (2004)] presented an analysis of the long-range nature of concentration fluctuations in a binary liquid mixture subjected to a concentration gradient in a uniform shear flow as a function of the wave number k of the fluctuations.

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We present experimental data and their theoretical interpretation for the decay rates of temperature fluctuations in a thin layer of a fluid heated from below and confined between parallel horizontal plates. The measurements were made with the mean temperature of the layer corresponding to the critical isochore of sulfur hexafluoride above but near the critical point where fluctuations are exceptionally strong. They cover a wide range of temperature gradients below the onset of Rayleigh-Bénard convection, and span wave numbers on both sides of the critical value for this onset.

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Ultra-high-molecular-weight polyethylene (UHMWPE) wear particles have been recognized as the cause of aseptic loosening in total joint replacement. Macrophage phagocytosis of wear particles induces human biological/physiological responses which eventually lead to bone resorption and osteolysis. However, the dependence of these reactions on the size and shape of the particles has not been elucidated and is not understood.

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We consider a horizontal fluid layer between two rigid boundaries, maintained in a stationary thermal nonequilibrium state below the convective Rayleigh-Bénard instability. We derive an explicit expression for the nonequilibrium structure factor in a first-order Galerkin approximation valid for negative and positive Rayleigh numbers R up to the critical Rayleigh number R(c) associated with the appearance of convection. The results obtained for rigid boundaries by the Galerkin-approximation method are compared with exact results previously derived for the case of free boundaries.

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