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dc.contributor.authorRamos, Javier-
dc.contributor.authorVega, Juan Francisco-
dc.contributor.authorMartínez-Salazar, Javier-
dc.date.accessioned2017-06-05T07:38:11Z-
dc.date.available2017-06-05T07:38:11Z-
dc.date.issued2016-03-09-
dc.identifierdoi: 10.1039/C5SM03080C-
dc.identifierissn: 1744-6848-
dc.identifier.citationSoft Matter 12: 3929-3936 (2016)-
dc.identifier.urihttp://hdl.handle.net/10261/150884-
dc.description8 págs.; 6 figs.; 4 tabs.-
dc.description.abstractExtensive molecular dynamics simulations of the macromolecular conformation and the melt dynamics for model polymers of different molecular weights have been carried out. The selected models are hydrogenated polybutadienes with a 2% content of ethyl branches and linear polyethylene. It will be shown that the density and chain stiffness are clearly affected by both the molecular weight and the presence of ethyl branches. Furthermore, the results obtained from the simulations on the molecular size and, more remarkably, chain dynamics, perfectly match the neutron scattering experiments performed by Zamponi et al. in hydrogenated polybutadienes. We observe a clear chain contraction and a slow dynamics for the hydrogenated polybutadiene with respect to the linear chain of the same molecular length. Using the Likhtman¿McLeish definitions, the obtained values of the entanglement relaxation time (¿e) and the tube diameter (a) are found to be in agreement with the available experimental data (by rheology and neutron spin echo) as well as with those obtained by the simulations. Finally, a very good agreement of diffusion coefficients as a function of the molecular weight between simulations and experiments is observed. Therefore, there exists a clear difference between the results obtained for branched and linear polyethylene, accounting for a definitive effect of the short chain branching on the conformational properties and the melt dynamics of polyolefins. ©The Royal Society of Chemistry 2016-
dc.description.sponsorshipThanks are due to the CICYT (Project MAT2012-36341) for financial support. J. Ramos acknowledges financial support through the Ramón y Cajal program (Contract RYC-2011-09585). The authors also thank the ‘‘Centro de Supercomputación de Galicia (CESGA)’’ for CPU allocation time.-
dc.publisherRoyal Society of Chemistry (UK)-
dc.relationMINECO/MAT2012-36341-
dc.rightsclosedAccess-
dc.titleA new insight into the conformation and melt dynamics of hydrogenated polybutadiene as revealed by computer simulations-
dc.typeartículo-
dc.identifier.doi10.1039/C5SM03080C-
dc.relation.publisherversionhttp://doi.org/10.1039/C5SM03080C-
dc.date.updated2017-06-05T07:38:11Z-
dc.description.versionPeer Reviewed-
dc.language.rfc3066eng-
dc.contributor.funderComisión Interministerial de Ciencia y Tecnología, CICYT (España)-
dc.contributor.funderCentro de Supercomputación de Galicia-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100007273es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
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