Effective and fast convergence toward an equilibrium state for long-chain polymer melts is realized by a hybrid method coupling molecular dynamics and the elastic continuum. The required simulation time to achieve the equilibrium state is reduced compared with conventional equilibration methods. The polymers move on a wide range phase space due to large-scale fluctuation generated by the elastic continuum. A variety of chain structures is generated in the polymer melt which results in the fast convergence to the equilibrium state.Peer reviewe
In ultra-high molecular weight polyethylene (UHMW-PE), it is possible to obtain single chain forming...
No abstract.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/55922/1/11064_ftp.pd
In polymers, it is possible to obtain single chain forming single crystals. It is feasible to melt t...
Effective and fast convergence toward an equilibrium state for long-chain polymer melts is realized ...
2005-2006 > Academic research: refereed > Publication in refereed journalVersion of RecordPublishe
Journal ArticleParallel tempering molecular dynamics simulations have been performed for 1,4-polybut...
Several methods for preparing well equilibrated melts of long chains polymers are studied. We show t...
The coarse-grained molecular dynamics simulations of linear polyethylene (PE) melts were ranging in ...
Journal ArticleWe have investigated chain dynamics of an unentangled polybutadiene melt via molecula...
Extensive molecular-dynamics simulations have been performed to study the effect of chain conformati...
Journal ArticleWe present a novel simulation algorithm based on tempering a fraction of relaxation-l...
Polymer crystal melting kinetics is simulated by using molecular dynamics. A simplified molecular mo...
We study the dynamics of flexible, semiflexible, and self-avoiding polymer chains moving under a Kra...
Kremer-Grest model polymer melts of highly entangled linear chains. Each melt has approximately 500 ...
We study the onset of chain stretch and emergent extension hardening in the nonlinear rheological re...
In ultra-high molecular weight polyethylene (UHMW-PE), it is possible to obtain single chain forming...
No abstract.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/55922/1/11064_ftp.pd
In polymers, it is possible to obtain single chain forming single crystals. It is feasible to melt t...
Effective and fast convergence toward an equilibrium state for long-chain polymer melts is realized ...
2005-2006 > Academic research: refereed > Publication in refereed journalVersion of RecordPublishe
Journal ArticleParallel tempering molecular dynamics simulations have been performed for 1,4-polybut...
Several methods for preparing well equilibrated melts of long chains polymers are studied. We show t...
The coarse-grained molecular dynamics simulations of linear polyethylene (PE) melts were ranging in ...
Journal ArticleWe have investigated chain dynamics of an unentangled polybutadiene melt via molecula...
Extensive molecular-dynamics simulations have been performed to study the effect of chain conformati...
Journal ArticleWe present a novel simulation algorithm based on tempering a fraction of relaxation-l...
Polymer crystal melting kinetics is simulated by using molecular dynamics. A simplified molecular mo...
We study the dynamics of flexible, semiflexible, and self-avoiding polymer chains moving under a Kra...
Kremer-Grest model polymer melts of highly entangled linear chains. Each melt has approximately 500 ...
We study the onset of chain stretch and emergent extension hardening in the nonlinear rheological re...
In ultra-high molecular weight polyethylene (UHMW-PE), it is possible to obtain single chain forming...
No abstract.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/55922/1/11064_ftp.pd
In polymers, it is possible to obtain single chain forming single crystals. It is feasible to melt t...