Loading…
Inorganic-organic hybrids involving poly(ε-caprolactone) and silica network: Hydrogen-bonding interactions and isothermal crystallization kinetics
Inorganic–organic hybrids mediated by hydrogen‐bonding interactions involving silicon oxide network and poly(ε‐caprolactone) (PCL) were prepared via an in situ sol–gel process of tetraethoxysilane in the presence of PCL. Fourier transform infrared spectroscopy indicated that there were hydrogen‐bond...
Saved in:
Published in: | Journal of polymer science. Part B, Polymer physics Polymer physics, 2005-09, Vol.43 (18), p.2594-2603 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Inorganic–organic hybrids mediated by hydrogen‐bonding interactions involving silicon oxide network and poly(ε‐caprolactone) (PCL) were prepared via an in situ sol–gel process of tetraethoxysilane in the presence of PCL. Fourier transform infrared spectroscopy indicated that there were hydrogen‐bonding interactions between carbonyls of PCL and silanol hydroxyls that were formed by incomplete polycondensation in the sol–gel process. In terms of the frequency shift of the hydroxyl stretching vibration bands, it is concluded that the strength of the interassociation between PCL and silicon oxide networks is weaker than that of the self‐association in the control silica network. The phenomenon of equilibrium melting point depression was observed for the PCL/silica system. The hybridization of PCL with silica network causes a considerable increase in the overall crystallization rate and dramatically influences the mechanism of nucleation and growth of the PCL crystallization. The analysis of isothermal crystallization kinetic data according to the Hoffman‐Lauritzen theory shows that with increasing silica content in the hybrids, the surface energy of extremity surfaces increases dramatically for the hybrids. © 2005 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 43: 2594–2603, 2005 |
---|---|
ISSN: | 0887-6266 1099-0488 |
DOI: | 10.1002/polb.20491 |