Flow-induced Density Fluctuation assisted Nucleation in Polyethylene

The nucleation process of polyethylene under quiescent and shear flow conditions are comparatively studied with all_atom molecular dynamical simulations. At both conditions, nucleation are demonstrated to be two_step processes, which, however, proceed via different intermediate orders. Quiescent nucleation is assisted by local structure order coupling conformational and local rotational symmetric orderings, while flow_induced nucleation is promoted by density fluctuation, which is a coupling effect of conformational and orientation orderings. Flow drives the transformation from flexible chains to rigid conformational ordered segments and circumvents the entropic penalty, which is the most peculiar and rate_limited step in polymer crystallization. Current work suggests that flow accelerates nucleation in orders of magnitude is not simply due to flow_induced entropic reduction of melt as early models proposed, which is mainly attributed to the different kinetic pathway via conformational/orientational ordering_density fluctuation_nucleation.