Structure and evolution of ordered domains in deeply quenched polyethylene melt

POLY 463

Naida Lacevic, lacevic2@llnl.gov, Richard H. Gee, and Laurence E. Fried. Chemistry, Materials and Life Sciences Directorate, Lawrence Livermore National Laboratory, Mail Code L-268, 7000 East Avenue, Livermore, CA 94550
Solidification of polymeric materials, a complex process in which the entangled polymer melt becomes a composite of amorphous and crystalline domains, strongly depends on how the melt is cooled below its crystallization temperature. If cooling is at moderate rates, the most common and well understood mechanism is via nucleation and growth of spherulites, but special cases exist where crystallization is preceded by a pre-transition state induced by density fluctuations. Such multi-step crystallization scenarios are suggested by many experiments, and recent theoretical and simulation work. We have conducted the largest and longest timescale simulations of polyethylene to date. These elucidate the initial separation of a metastable, mesomorphic phase. Via energetic and geometric analyses, we have examined the structure of mesomorphic domains and the dynamics of their formation and evolution, including atomic scale details of molecular addition to ordered domains, as well as particle dynamics in the system, including high mobility jumps in the ordered domains at wavelengths matching the monomer spacing.
 

Polymers and Liquid Crystals
6:00 PM-8:00 PM, Tuesday, August 21, 2007 BCEC -- Exhibit Hall - B2, Poster

Division of Polymer Chemistry

The 234th ACS National Meeting, Boston, MA, August 19-23, 2007