Polymer dynamics under cylindrical confinement featuring a locally repulsive surface: A quasielastic neutron scattering study

Autor(en): Krutyeva, M.
Pasini, S.
Monkenbusch, M.
Allgaier, J.
Maiz, J.
Mijangos, C.
Hartmann-Azanza, B.
Steinhart, M. 
Jalarvo, N.
Richter, D.
Stichwörter: BLENDS; CHAINS; Chemistry; Chemistry, Physical; DIFFUSION; MOLECULAR-DYNAMICS; NANOCOMPOSITES; Physics; Physics, Atomic, Molecular & Chemical; RELAXATION; THIN
Erscheinungsdatum: 2017
Herausgeber: AMER INST PHYSICS
Journal: JOURNAL OF CHEMICAL PHYSICS
Volumen: 146
Ausgabe: 20
Zusammenfassung: 
We investigated the effect of intermediate cylindrical confinement with locally repulsive walls on the segmental and entanglement dynamics of a polymer melt by quasielastic neutron scattering. As a reference, the corresponding polymer melt was measured under identical conditions. The locally repulsive confinement was realized by hydrophilic anodic alumina nanopores with a diameter of 20 nm. The end-to-end distance of the hydrophobic infiltrated polyethylene-alt-propylene was close to this diameter. In the case of hard wall repulsion with negligible local attraction, several simulations predicted an acceleration of segmental dynamics close to the wall. Other than in attractive or neutral systems, where the segmental dynamics is slowed down, we found that the segmental dynamics in the nanopores is identical to the local mobility in the bulk. Even under very careful scrutiny, we could not find any acceleration of the surface-near segmental motion. On the larger time scale, the neutron spin-echo experiment showed that the Rouse relaxation was not altered by confinement effects. Also the entanglement dynamics was not affected. Thus at moderate confinement conditions, facilitated by locally repulsive walls, the dynamics remains as in the bulk melt, a result that is not so clear from simulations. Published by AIP Publishing.
ISSN: 00219606
DOI: 10.1063/1.4974836

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