Please use this identifier to cite or link to this item: https://idr.l3.nitk.ac.in/jspui/handle/123456789/12177
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dc.contributor.authorGe, T.
dc.contributor.authorKalathi, J.T.
dc.contributor.authorHalverson, J.D.
dc.contributor.authorGrest, G.S.
dc.contributor.authorRubinstein, M.
dc.date.accessioned2020-03-31T08:38:45Z-
dc.date.available2020-03-31T08:38:45Z-
dc.date.issued2017
dc.identifier.citationMacromolecules, 2017, Vol.50, 4, pp.1749-1754en_US
dc.identifier.urihttp://idr.nitk.ac.in/jspui/handle/123456789/12177-
dc.description.abstractThe motion of nanoparticles (NPs) in entangled melts of linear polymers and nonconcatenated ring polymers are compared by large-scale molecular dynamics simulations. The comparison provides a paradigm for the effects of polymer architecture on the dynamical coupling between NPs and polymers in nanocomposites. Strongly suppressed motion of NPs with diameter d larger than the entanglement spacing a is observed in a melt of linear polymers before the onset of Fickian NP diffusion. This strong suppression of NP motion occurs progressively as d exceeds a and is related to the hopping diffusion of NPs in the entanglement network. In contrast to the NP motion in linear polymers, the motion of NPs with d > a in ring polymers is not as strongly suppressed prior to Fickian diffusion. The diffusion coefficient D decreases with increasing d much slower in entangled rings than in entangled linear chains. NP motion in entangled nonconcatenated ring polymers is understood through a scaling analysis of the coupling between NP motion and the self-similar entangled dynamics of ring polymers. 2017 American Chemical Society.en_US
dc.titleNanoparticle Motion in Entangled Melts of Linear and Nonconcatenated Ring Polymersen_US
dc.typeArticleen_US
Appears in Collections:1. Journal Articles

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