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Interfacial effects on the NMR of composite polymers
Author(s) -
Douglass Dean C.,
McBrierty Vincent J.
Publication year - 1979
Publication title -
polymer engineering and science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.503
H-Index - 111
eISSN - 1548-2634
pISSN - 0032-3888
DOI - 10.1002/pen.760191414
Subject(s) - materials science , polycarbonate , polyvinylidene fluoride , polymer , nanometre , composite material , crystallinity , composite number , elastomer , styrene butadiene , copolymer , polymer science , styrene
Several NMR experiments can provide estimates of the scale of spatial inhomogeneity in solid materials in the range of nanometers to microns. The effects underlying these experiments their interpretation, and models used in their interpretation are discussed and illustrated with applications to polymers. Examples chosen from the literature include semicrystalline polymers (polyethylene, polyvinylidene fluoride, polychlorotrifluoroethylene), filled elastomers (carbon‐filled butadiene), copolymers (styrene: butadiene, dimethylsiloxane: bisphenol‐A polycarbonate, polyurethane) and blends (polymethylmethacrylate‐polystyreneacrylonitrile, polyvinylidene fluoride‐polymethylmethacrylate). Comparison of examples directs attention to the similarity in anisotropic motional behavior of highly constrained interfacial material in semicrystalline and filled polymers. While no one experiment is applicable to all dimensions, or all systems, NMR has proven especially useful for dimensions in the range of tens of nanometers, where other techniques are often less revealing.