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Characterization of Network Structure and Chain Dynamics of Elastomeric Ionomers by Means of 1H Low-Field NMR
Author(s) -
M. A. Malmierca,
Antonio González-Jiménez,
I. MoraBarrantes,
P. Posadas,
A. Rodrı́guez,
Luís Ibarra,
Aurora Nogales,
Kay Saalwächter,
J. L. Valentín
Publication year - 2014
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/ma501208g
Subject(s) - vulcanization , elastomer , ionic bonding , polymer chemistry , polymer , materials science , stoichiometry , nitrile rubber , thermoplastic elastomer , chemical engineering , natural rubber , telechelic polymer , chemical physics , chemistry , composite material , ion , organic chemistry , end group , copolymer , engineering
The network structure and chain dynamics of ionic elastomers based on carboxylated nitrile rubber (XNBR) cross-linked with different content of magnesium oxide (MgO) have been studied by different low-field time-domain NMR experiments. Ionic contacts created during the vulcanization tend to aggregate trapping some polymer segments that show restricted mobility as it was quantified by analyses of refocused free induction decays. Increasing the MgO content above the stoichiometric fraction has no effect on the amount of trapped polymer segments, but it increases the network cross-link density as measured by multiple-quantum (MQ) NMR experiments. The central finding of this work is that MgO addition above the stoichiometric content enhances the mechanical properties by creating a larger number of smaller ionic clusters, which act as dynamic cross-links, but are not readily seen by other techniques. Changes in the network structure and morphology of segregated thermolabile ionic domains have an impact on the ionic rearrangement dynamics and, in consequence, on the thermoplastic behavior of these materials at elevated temperatures.Peer Reviewe

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