Crystallization of alkanes under quiescent and shearing conditions

We report molecular dynamics simulation of crystallization of model alkane systems conducted under constant pressure conditions. We have studied crystallization of n-eicosane (C20H42) and n-hexacontane (C60 H122) under quiescent and shearing conditions. We find preshearing before subjecting the melt to quiescent crystallization enhances the crystallization of higher molecular weight hexacontane, whereas, for low molecular weight eicosane, no significant change can be detected. For both alkanes applying steady planar shear significantly speeds up the crystallization. The crystal growth rate increases with the shear rate. However, we find that the critical shear rate above which the crystallization is enhanced, is inversely proportional to the size of the chains. In all cases the Weissenberg numbers of the sheared systems are moderate. We estimate them to be in the range of 0.01–10. Our quiescent simulations for eicosane predict crystallization temperature and lattice parameters of the crystalline phase in good agreement with experimental measurements. We have compared an order parameter used in the simulations against one analogous to that used in dilatometry experiments. Using this order parameter as a measure of crystallinity we predict the crystal growth rate of n-eicosane to be a maximum at ∼300 K in good agreement with experiments. Fitting crystallization growth data to Avrami's model we have calculated Avrami growth functions and exponents for many cases. For quiescent crystallization of n-eicosane we found the Avrami exponent calculated using our order parameter for defining degree of crystallinity, agrees well with that obtained in the experiments. For C60 the crystallization process is very slow at quiescent conditions; however preshearing enhances the crystal growth.