Computer Simulation of Three-Phase Equilibria for Some Water/-Alkane Binary Systems.

In this work, the vapor-liquid-liquid equilibrium (VLLE) of the water/-pentane, water/-hexane, water/-octane, and water/-decane binary systems is calculated by computer simulation using the NVT-Gibbs ensemble (in the version of three simulation boxes) combined with the configurational bias Monte Carlo method. The combination of both methods, the molecular potential models used, and the simulation details allowed us to calculate the triphasic equilibrium properties of the systems studied: the densities of the three phases in equilibrium, their compositions, and potential energies. In previous works, these simulations were not carried out at a temperature range nor water/-alkanes systems simulated in this work, probably because they are highly nonideal systems; so, to the best of our knowledge, this is the first time that this phenomenon is studied in detail.

Structure factor and rheology of chain molecules from molecular dynamics.

Equilibrium and non-equilibrium molecular dynamics were performed to determine the relationship between the static structure factor, the molecular conformation, and the rheological properties of chain molecules. A spring-monomer model with Finitely Extensible Nonlinear Elastic and Lennard-Jones force field potentials was used to describe chain molecules. The equations of motion were solved for shear flow with SLLOD equations of motion integrated with Verlet's algorithm.

Dynamic evolution of supported metal nanocatalyst/carbon structure during single-walled carbon nanotube growth.

Single-walled carbon nanotubes (SCWNTs) have outstanding properties that depend on structural features such as their chirality. Thus, developing a strategy to control chirality during SWCNT synthesis is critical for the exploitation of nanotube-based technologies in fields such as electronics and biomedicine. In response to this need, tuning the nanocatalyst structure has been envisioned as a means to control the nanotube structure.

Nonequilibrium molecular dynamics of the rheological and structural properties of linear and branched molecules. Simple shear and poiseuille flows; instabilities and slip.

Nonequilibrium molecular-dynamics simulations are performed for linear and branched chain molecules to study their rheological and structural properties under simple shear and Poiseuille flows. Molecules are described by a spring-monomer model with a given intermolecular potential. The equations of motion are solved for shear and Poiseuille flows with Lees and Edward's [A.

Critical flocculation density of dilute water-in-CO2 emulsions stabilized with block copolymers.

The critical flocculation density (CFD), that is, the CO(2) density below which flocculation occurs, was studied for dilute water-in-CO(2) (W/C) miniemulsions stabilized with poly(1,1-dihydroperfluorooctyl methacrylate)-b-poly(ethylene oxide) (PFOMA-b-PEO) surfactants. The CFD, which was measured by turbidimetry, decreased as the PFOMA molecular weight was increased, the average droplet size was decreased, the surfactant loading was increased, and the temperature was increased. A simple model, which addressed both the van der Waals attraction between droplets and osmotic solvent-tail interactions, was in good qualitative agreement with the experimentally observed trends for the CFD and predicted a decrease in emulsion stability as the CO(2) density was lowered toward the theta density for PFOMA in bulk CO(2).