Solid-state nuclear magnetic resonance studies of vinyl polymer/silica colloidal nanocomposite particles
Solid-state nuclear magnetic resonance (NMR) has been used to characterize the interface between the organic and inorganic components of "core-shell" colloidal nanocomposite particles synthesized by in situ aqueous (co)polymerization of styrene and/or n-butyl acrylate in the presence of a...
Veröffentlicht in: | Langmuir : the ACS journal of surfaces and colloids. - 1992. - 26(2010), 19 vom: 05. Okt., Seite 15592-8 |
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Weitere Verfasser: | , , , , |
Format: | Online-Aufsatz |
Sprache: | English |
Veröffentlicht: |
2010
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Zugriff auf das übergeordnete Werk: | Langmuir : the ACS journal of surfaces and colloids |
Schlagworte: | Journal Article |
Zusammenfassung: | Solid-state nuclear magnetic resonance (NMR) has been used to characterize the interface between the organic and inorganic components of "core-shell" colloidal nanocomposite particles synthesized by in situ aqueous (co)polymerization of styrene and/or n-butyl acrylate in the presence of a glycerol-functionalized silica sol. Polymer protons are in close proximity (<5 A) to surface silanol sites in all the nanocomposites studied, indicating that either styrene or n-butyl side groups extend between the glycerol-functional silane molecules toward the surface of the silica particles. For the poly(styrene-co-n-butyl acrylate)/silica nanocomposite n-butyl acrylate residues are located closer to the surface of the silica particle than styrene residues, suggesting a specific interaction between the former and the glycerol-functionalized silica surface. The most likely explanation is a hydrogen bond between the ester carbonyl and the glycerol groups, although this cannot be observed directly. For the Bindzil CC40 glycerol-functionalized silica sol the relative intensities of (29)Si NMR lines corresponding to T and Q(3) environments imply that there are approximately twice as many unreacted silanol groups on the silica surface as attached silane molecules |
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Beschreibung: | Date Completed 03.01.2011 Date Revised 29.09.2010 published: Print Citation Status PubMed-not-MEDLINE |
ISSN: | 1520-5827 |
DOI: | 10.1021/la102298x |