RESUMO
The crystal growth kinetics and interfacial properties of titanium (Ti) are studied using molecular dynamics computer simulation. The interactions between the Ti atoms are modeled via an embedded atom method potential. First, the free solidification method (FSM) is used to determine the melting temperature Tm at zero pressure where the transition from liquid to body-centered cubic crystal occurs. From the simulations with the FSM, the kinetic growth coefficients are also determined for different orientations of the crystal, analyzing how the coupling to the thermostat affects the estimates of the growth coefficients. At Tm, anisotropic interfacial stiffnesses and free energies as well as kinetic growth coefficients are determined from capillary wave fluctuations. The so-obtained growth coefficients from equilibrium fluctuations and without the coupling of the system to a thermostat agree well with those extracted from the FSM calculations.
RESUMO
A new correlation method for the surface tension of fluids is proposed, which is based on friction theory applied to the interface of a two-phase system. The substance properties enter the model by a regular equation of state. Here we derive the method and test it with the Lennard-Jones 12-6 fluid as the reference system using molecular dynamics simulations of the vapor-liquid interface in combination with a new Lennard-Jones 12-6 equation of state. Further correlations of experimental surface tension data based on the Peng-Robinson and the PC-SAFT equations of state are presented. As a result, we find that the method allows an accurate correlation of the surface tension of pure fluids.