Elementary Trigonometric Sums related to Quadratic Residues

Let p be a prime = 3 (mod 4). A number of elegant number-theoretical properties of the sums T(p) = \sqrt{p}sum_{n=1}^{(p-1)/2} tan(n^2\pi/p) and C(p) = \sqrt{p}sum_{n=1}^{(p-1)/2} cot(n^2\pi/p) are proved. For example, T(p) equals p times the excess of the odd quadratic residues over the even ones in the set {1,2,...,p-1}; this number is positive if p = 3 (mod 8) and negative if p = 7 (mod 8). In this revised version the connection of these sums with the class-number h(-p) is also discussed. For example, a very simple formula expressing h(-p) by means of the aforementioned excess is proved. The bibliography has been considerably enriched. This article is of an expository nature.Comment: A number of misprints have been corrected and one or two improvements have been done to the previous version of the paper with same title. The paper will appear to Elem. der Mat

The Hydrodynamic Interaction in Polymer Solutions Simulated with Dissipative Particle Dynamics

We analyzed extensively the dynamics of polymer chains in solutions simulated with dissipative particle dynamics (DPD), with a special focus on the potential influence of a low Schmidt number of a typical DPD fluid on the simulated polymer dynamics. It has been argued that a low Schmidt number in a DPD fluid can lead to underdevelopment of the hydrodynamic interaction in polymer solutions. Our analyses reveal that equilibrium polymer dynamics in dilute solution, under a typical DPD simulation conditions, obey the Zimm model very well. With a further reduction in the Schmidt number, a deviation from the Zimm model to the Rouse model is observed. This implies that the hydrodynamic interaction between monomers is reasonably developed under typical conditions of a DPD simulation. Only when the Schmidt number is further reduced, the hydrodynamic interaction within the chains becomes underdeveloped. The screening of the hydrodynamic interaction and the excluded volume interaction as the polymer volume fraction is increased are well reproduced by the DPD simulations. The use of soft interaction between polymer beads and a low Schmidt number do not produce noticeable problems for the simulated dynamics at high concentrations, except that the entanglement effect which is not captured in the simulations.Comment: 27 pages, 13 page

Application of exchange Monte Carlo method to ordering dynamics

We apply the exchange Monte Carlo method to the ordering dynamics of the three-state Potts model with the conserved order parameter. Even for the deeply quenched case to low temperatures, we have observed a rapid domain growth; we have proved the efficiency of the exchange Monte Carlo method for the ordering process. The late-stage growth law has been found to be $R(t) \sim t^{1/3}$ for the case of conserved order parameter of three-component system.Comment: 7 pages including 5 eps figures, to appear in New J. Phys. http://www.njp.or

Lattice-Gas Simulations of Minority-Phase Domain Growth in Binary Immiscible and Ternary Amphiphilic Fluid

We investigate the growth kinetics of binary immiscible fluids and emulsions in two dimensions using a hydrodynamic lattice-gas model. We perform off-critical quenches in the binary fluid case and find that the domain size within the minority phase grows algebraically with time in accordance with theoretical predictions. In the late time regime we find a growth exponent n = 0.45 over a wide range of concentrations, in good agreement with other simluations. In the early time regime we find no universal growth exponent but a strong dependence on the concentration of the minority phase. In the ternary amphiphilic fluid case the kinetics of self assembly of the droplet phase are studied for the first time. At low surfactant concentrations, we find that, after an early algebraic growth, a nucleation regime dominates the late-time kinetics, which is enhanced by an increasing concentration of surfactant. With a further increase in the concentration of surfactant, we see a crossover to logarithmically slow growth, and finally saturation of the oil droplets, which we fit phenomenologically to a stretched exponential function. Finally, the transition between the droplet and the sponge phase is studied.Comment: 22 pages, 13 figures, submitted to PR

Lattice-gas simulations of Domain Growth, Saturation and Self-Assembly in Immiscible Fluids and Microemulsions

We investigate the dynamical behavior of both binary fluid and ternary microemulsion systems in two dimensions using a recently introduced hydrodynamic lattice-gas model of microemulsions. We find that the presence of amphiphile in our simulations reduces the usual oil-water interfacial tension in accord with experiment and consequently affects the non-equilibrium growth of oil and water domains. As the density of surfactant is increased we observe a crossover from the usual two-dimensional binary fluid scaling laws to a growth that is {\it slow}, and we find that this slow growth can be characterized by a logarithmic time scale. With sufficient surfactant in the system we observe that the domains cease to grow beyond a certain point and we find that this final characteristic domain size is inversely proportional to the interfacial surfactant concentration in the system.Comment: 28 pages, latex, embedded .eps figures, one figure is in colour, all in one uuencoded gzip compressed tar file, submitted to Physical Review

A scaling theory of 3D spinodal turbulence

A new scaling theory for spinodal decomposition in the inertial hydrodynamic regime is presented. The scaling involves three relevant length scales, the domain size, the Taylor microscale and the Kolmogorov dissipation scale. This allows for the presence of an inertial "energy cascade", familiar from theories of turbulence, and improves on earlier scaling treatments based on a single length: these, it is shown, cannot be reconciled with energy conservation. The new theory reconciles the t^{2/3} scaling of the domain size, predicted by simple scaling, with the physical expectation of a saturating Reynolds number at late times.Comment: 5 pages, no figures, revised version submitted to Phys Rev E Rapp Comm. Minor changes and clarification