Journalartikel

Jahr der Veröffentlichung: 2004

Seiten: 9811-9820

Zeitschrift: Langmuir

Bandnummer: 20

Heftnummer: 22

ISSN: 0743-7463

DOI Link: https://doi.org/10.1021/la048962x

Verlag: American Chemical Society

Abstract: 
Mesostructured lamellar nanocomposite films with alternating silica and organic layers containing poly(N-isopropropyl acrylamide) (PNIPAM) were prepared using evaporation-induced self-assembly. A suitable theoretical approach to analyze the small-angle X-ray scattering (SAXS) patterns of oriented lamellar two-phase systems was applied to the SAXS data of films of varying composition, providing details on the self-assembly process, the composition, and the polymerization. In particular, this approach allowed an accurate determination of the thickness of the silica and the organic layer. The applicability of the SAXS approach was carefully tested with simulated data and verified by thermogravimetric analysis (TGA). TGA and C-13 NMR were used to study the polymerization and linkage to the silica matrix. SAXS and time-resolved grazing incidence SAXS revealed that the phase transition of PNIPAM at ca. 32 degreesC leads to a reversible expansion/contraction perpendicular to the layers on a time scale of ca. 30 min.

Harvard-Zitierstil: Garnweitner, G., Smarsly, B., Assink, R., Dunphy, D., Scullin, C. and Brinker, C. (2004) Characterization of self-assembled lamellar thermoresponsive silica-hydrogel nanocomposite films, Langmuir, 20(22), pp. 9811-9820. https://doi.org/10.1021/la048962x

APA-Zitierstil: Garnweitner, G., Smarsly, B., Assink, R., Dunphy, D., Scullin, C., & Brinker, C. (2004). Characterization of self-assembled lamellar thermoresponsive silica-hydrogel nanocomposite films. Langmuir. 20(22), 9811-9820. https://doi.org/10.1021/la048962x