Consolute Critical Phenomena in Dilute Silica Gel

1992 ◽  
Vol 290 ◽  
Author(s):  
B. J. Frisken ◽  
Fabio Ferri ◽  
David S. Cannell

AbstractThe effect of even dilute silica networks on the critical phenomena of binary liquid mixtures is profound. The network preferentially adsorbs one component, preventing a portion of the mixture from participating in critical fluctuations. Fluctuations in the remaining mixture are found to decay with a non-exponential correlation function near the consolute point. A correlation function consisting of the sum of an exponential decay and a non-exponential term of either an activated or stretched exponential form fits the data well. In the presence of the silica network, the mixtures are observed to phase separate near the critical temperature of the pure system, but while still in the one-phase region of the pure system.

Entropy ◽  
2018 ◽  
Vol 20 (12) ◽  
pp. 936
Author(s):  
Andrea Lamorgese ◽  
Roberto Mauri

We discuss numerical results of diffusion-driven separation into three phases of a symmetric, three-component highly viscous liquid mixture after an instantaneous quench from the one-phase region into an unstable location within the tie triangle of its phase diagram. Our theoretical approach follows a diffuse-interface model of partially miscible ternary liquid mixtures that incorporates the one-parameter Margules correlation as a submodel for the enthalpic (so-called excess) component of the Gibbs energy of mixing, while its nonlocal part is represented based on a square-gradient (Cahn–Hilliard-type) modeling assumption. The governing equations for this phase-field ternary mixture model are simulated in 3D, showing the segregation kinetics in terms of basic segregation statistics, such as the integral scale of the pair-correlation function and the separation depth for each component. Based on the temporal evolution of the integral scales, phase separation takes place via the simultaneous growth of three phases up until a symmetry-breaking event after which one component continues to separate quickly, while phase separation for the other two seems to be delayed. However, inspection of the separation depths reveals that there can be no symmetry among the three components at any instant in time during a triphase segregation process.


Author(s):  
Nicola Molinari ◽  
Jonathan P. Mailoa ◽  
Boris Kozinsky

We show that strong cation-anion interactions in a wide range of lithium-salt/ionic liquid mixtures result in a negative lithium transference number, using molecular dynamics simulations and rigorous concentrated solution theory. This behavior fundamentally deviates from the one obtained using self-diffusion coefficient analysis and agrees well with experimental electrophoretic NMR measurements, which accounts for ion correlations. We extend these findings to several ionic liquid compositions. We investigate the degree of spatial ionic coordination employing single-linkage cluster analysis, unveiling asymmetrical anion-cation clusters. Additionally, we formulate a way to compute the effective lithium charge that corresponds to and agrees well with electrophoretic measurements and show that lithium effectively carries a negative charge in a remarkably wide range of chemistries and concentrations. The generality of our observation has significant implications for the energy storage community, emphasizing the need to reconsider the potential of these systems as next generation battery electrolytes.<br>


2012 ◽  
Vol 26 (29) ◽  
pp. 1250146 ◽  
Author(s):  
BHASKAR SEN GUPTA ◽  
SHANKAR P. DAS

The renormalized dynamics described by the equations of nonlinear fluctuating hydrodynamics (NFH) treated at one loop order gives rise to the basic model of the mode coupling theory (MCT). We investigate here by analyzing the density correlation function, a crucial prediction of ideal MCT, namely the validity of the multi step relaxation scenario. The equilibrium density correlation function is calculated here from the direct solutions of NFH equations for a hard sphere system. We make first detailed investigation for the robustness of the correlation functions obtained from the numerical solutions by varying the size of the grid. For an optimum choice of grid size we analyze the decay of the density correlation function to identify the multi-step relaxation process. Weak signatures of two step power law relaxation is seen with exponents which do not match predictions from the one loop MCT. For the final relaxation stretched exponential (KWW) behavior is seen and the relaxation time grows with increase of density. But apparent power law divergences indicate a critical packing fraction much higher than the corresponding MCT predictions for a hard sphere fluid.


Author(s):  
Eldred H. Chimowitz

The critical point of mixtures requires a more intricate set of conditions to hold than those at a pure-fluid critical point. In contrast to the pure-fluid case, in which the critical point occurs at a unique point, mixtures have additional thermodynamic degrees of freedom. They, therefore, possess a critical line which defines a locus of critical points for the mixture. At each point along this locus, the mixture exhibits a critical point with its own composition, temperature, and pressure. In this chapter we investigate the critical behavior of binary mixtures, since higher-order systems do not bring significant new considerations beyond those found in binaries. We deal first with mixtures at finite compositions along the critical locus, followed by consideration of the technologically important case involving dilute mixtures near the solvent’s critical point. Before taking up this discussion, however, we briefly describe some of the main topographic features of the critical line of systems of significant interest: those for which nonvolatile solutes are dissolved in a solvent near its critical point. The critical line divides the P–T plane into two distinctive regions. The area above the line is a one-phase region, while below this line, phase transitions can occur. For example, a mixture of overall composition xc will have a loop associated with it, like the one shown in figure 4.1, which just touches the critical line of the mixture at a unique point. The leg of the curve to the “left” of the critical point is referred to as the bubble line; while that to the right is termed the dew line. Phase equilibrium occurs between two phases at the point where the bubble line at one composition intersects the dew line; this requires two loops to be drawn of the sort shown in figure 4.1. A question naturally arises as to whether or not all binary systems exhibit continuous critical lines like that shown. In particular we are interested in the situation involving a nonvolatile solute dissolved in a supercritical fluid of high volatility.


1996 ◽  
Vol 54 (18) ◽  
pp. R12669-R12672 ◽  
Author(s):  
A. H. Bougourzi ◽  
M. Couture ◽  
M. Kacir

1975 ◽  
Vol 30 (8) ◽  
pp. 1060-1070
Author(s):  
Keiichiro Nasu

Abstract A theory of the optical band shape for A1g - T1u transitions is developed based on the method of the characteristic function. It covers the region of weak coupling between the electrons and the phonon modes of a1g , eg and t2g symmetries, and takes account of the phonon dispersion. It is bound that the cumulant function of the characteristic function can be described by a two-time phonon correlation function which includes the multi-phonon correlation due to the Jahn-Teller effect. A Dyson equation of the phonon correlation function is solved under specific conditions where the contribution from the eg modes is neglected and the phonons have a Lorentzian dispersion. Analytical expressions are given for intensity, peak shift and broadening of a few lower phonon side bands, and it is found that the one phonon side band of the t2g mode shifts to higher frequencies than that of the a1g mode.


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