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Solid state NMR of a polymer composite and of a polymer blend
Author(s) -
Veeman W.S.
Publication year - 1993
Publication title -
makromolekulare chemie. macromolecular symposia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.257
H-Index - 76
eISSN - 1521-3900
pISSN - 0258-0322
DOI - 10.1002/masy.19930690116
Subject(s) - materials science , interphase , polymer , composite number , miscibility , composite material , solid state nuclear magnetic resonance , polymer blend , methyl methacrylate , methacrylate , polymer chemistry , chemical engineering , nuclear magnetic resonance , copolymer , genetics , physics , engineering , biology
Although nuclear magnetic resonance may not seem the technique of choice to study interfaces between components in a polymer composite or polymer blend because of its inherent low sensitivity, for certain systems solid state NMR techniques can emphasize the signals from these interfaces. In case of a composite material with an inorganic filler (particles, fibers) cross‐polarization or dipolar dephasing techniques from protons in the organic matrix or in the interphase to nuclei in the filler can be used to selectively observe the nuclei in the surface of the filler. Any changes at the filler surface caused by the presence of the matrix or coupling agent can then be detected. An example of glass reinforced nylon modelcomposites is discussed. The same techniques can also be used to study interphases in polymer blends when one of the components contains a NMR nucleus that is not present in the other component. As an example the blend poly(vinylidene fluoride)‐poly(methyl methacrylate) is studied and it is shown that such techniques can provide very detailed information about the miscibility at a molecular scale.