Microscopic State of Polymer Network Chains upon Swelling and Deformation
Author(s) -
Anumova,
Diana C. Agudelo,
Marcelo A. Villar,
Daniel A. Vega,
J. L. Valentín,
Kay Saalwächter
Publication year - 2019
Publication title -
macromolecules
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.994
H-Index - 313
eISSN - 1520-5835
pISSN - 0024-9297
DOI - 10.1021/acs.macromol.9b00971
Subject(s) - swelling , deformation (meteorology) , isotropy , rubber elasticity , materials science , polymer , vulcanization , composite material , dilation (metric space) , natural rubber , physics , geometry , optics , mathematics
We use low-resolution proton NMR to probe the chain deformation in swollen and nonlinearly deformed vulcanized rubber and end-linked PDMS networks on a microscopic level, extending earlier work focusing on uniaxial stretching and isotropic dilation upon swelling toward biaxial deformation and deformation of swollen samples. Previous studies have revealed that chain deformation in bulk samples is best described by tube models, and that chains in swollen samples deform affinely after an initial desinterspersion stage, upon which entanglement-related packing effects are relieved. We test whether a subsequent deformation may also be closer to affine, and find that this is not the case. Unexpectedly, nonisotropic deformation of swollen samples also follows tube-model predictions, which is explained by a dominance of structural inhomogeneities and significant reorganization of the topological constraints active in the swollen and possibly even the bulk state.
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