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D M Heyes

Publications and source records attributed to D M Heyes.

3 recordsLinked to original sources

Time correlation functions of hard sphere and soft sphere fluids.

We explore the transition between soft particle fluids of increasing steepness to the hard sphere limit. We analyze the analytic forms of the time correlation functions used in determining transport coefficients in Green-Kubo formulas for fluids composed of particles interacting through a repulsive r(-n) potential. We focus on the steeply repulsive n--> infinity limit where the potential tends to the hard sphere interaction. Dufty [Mol. Phys. 100, 2331 (2002)] developed a theoretical framework that can be used to characterize the transition from a steeply repulsive continuous potential toward the hard sphere potential for the shear stress time correlation function. This function was shown to consist of a rapidly decaying contribution (which is singular in the steeply repulsive limit) and a slowly decaying nonsingular part which can be reasonably well represented by Enskog's prediction on times of order and in excess of the mean collision time. We extend this treatment to the bulk viscosity and thermal conductivity. We focus on the bulk viscosity (pressure) correlation function as it is purely singular for hard spheres, and has no kinetic or cross term contributions in this limit. There is no relaxation of this correlation function on the mean collision or Enskog time scale for hard spheres. We show that it is not possible to represent the steeply repulsive behavior of this function entirely in terms of a sech function, i.e., C(B)(t)=sech(a(n)t/tau(n)), where a(n) is a numerical factor, t is time, and tau(n) is a relaxation time proportional to n(-1). An additional singular function, which we call w(t), is required to obtain the correct short-time behavior of C(B)(t) and the Enskog value for the bulk viscosity. With this additional function, the value of a(n) in the n--> infinity limit is a(n)=square root of 2 which is consistent with the second moment of the time expansion of the time correlation function. We compute this function for large n and extrapolate it to n--> infinity, determining one possible analytic form. The shear stress correlation function also gives a(n)=square root of 2 in the hard sphere limit for the singular part when the sech and w functions are used. This function has a nonsingular component, even in the hard sphere limit. We explore various forms for the crossover function X(t/tau(n)) introduced by Dufty, which weights the limiting singular and nonsingular contributions to C(S)(t) particularly at intermediate times. The qualitative behavior for the heat flux time correlation function (used to obtain the thermal conductivity) is much the same as the shear case. The w(t) derived by several self-consistent extrapolations appears, within the simulation statistics, to be the same for the bulk and shear viscosity, and for the thermal conductivity cases.

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Algorithms for Brownian dynamics computer simulations: multivariable case.

Several Brownian numerical schemes for treating stochastic differential equations at the position Langevin level are analyzed from the point of view of their algorithmic efficiency for large-N systems. The algorithms are tested using model colloidal fluids of particles interacting via the Yukawa potential. Limitations in the conventional Brownian dynamics algorithm are shown and it is demonstrated that much better accuracy for dynamical and static quantities can be achieved with an algorithm based on the stochastic expansion and second-order stochastic Runge-Kutta algorithms. The importance of the various terms in the stochastic expansion is analyzed, and the relative merits of second-order algorithms are discussed.

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Effects of bead-bead interactions on the static and dynamical properties of model polymer solutions.

The effects of segment-segment interactions on the static and dynamical properties of model polymer solutions are examined by Brownian dynamics simulations in the free-draining limit over a wide concentration range. A bead-and-spring model is used to describe the polymer chains at a coarse-grained level, in which segment-segment interactions are represented by a bead-bead pair potential with a Gaussian analytic form, beta u(ev)(r)=A exp(-r(2)/2 sigma(2)), where beta=1/k(B)T and A and sigma are characteristic energy and distance scales, respectively. The chain dimensions, self-diffusion coefficient, and viscosity of the systems are studied as functions of number density of beads of the system, rho, at given excluded-volume potential parameters, A and sigma. Our results show that in the limit of infinite dilution even for short chains (N approximately 10) there is statistically significant scaling behavior in the static and dynamical properties. For a system with given values of A and sigma the change in polymer coil size shows a realistic trend as the concentration of the system increases. In the dilute and concentrated regions the coil size decreases as a result of increasing interchain repulsions, while in the highly concentrated region the coil size increases again, showing a return to Rouse-like behavior because the intrapolymer and interpolymer segment-segment interactions become effectively indistinguishable for an arbitrary bead and to a large extent are "balanced out." In the limit of infinite dilution, the self-diffusion coefficient of the center of mass, D(cm), depends on N only and not on the potential parameter A, while in contrast the specific viscosity eta(sp) depends on both N and A. As the concentration increases D(cm) decreases and eta(sp) increases consistent with the behavior of real polymers. When the system becomes highly concentrated, however, both D(cm) and eta(sp) unrealistically return to the Rouse limit. This suggests that from the concentrated region upward in concentration, the entanglement or the topological constraints caused by the physical connectivity of the chains significantly influence their dynamical behavior. The mean-field segment-segment interactions or excluded-volume effects incorporated in the current coarse-grained bead-spring approach cannot capture this entanglement effect, and therefore give rise to unrealistic dynamical behavior in the concentrated regime.

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