Isocyanate-free Route to Starch-graft-Polycaprolactone via Carbonyldiimidazole (CDI)-mediated End Group Conversion

This paper reports on the synthesis of biodegradable starch-graft-poly ε-caprolactone (starch-g-PCL) in two steps. First, poly ε-caprolactone (PCL) was modified on the terminal groups by using carbodiimidazole (CDI) as coupling agent. Then, the starch graft copolymers with PCL were prepared through...

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Veröffentlicht in:Die Stärke 2010-02, Vol.62 (2), p.90-101
Hauptverfasser: Najemi, Loubna, Jeanmaire, Thomas, Zerroukhi, Amar, Raihane, Mustapha
Format: Artikel
Sprache:eng
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Zusammenfassung:This paper reports on the synthesis of biodegradable starch-graft-poly ε-caprolactone (starch-g-PCL) in two steps. First, poly ε-caprolactone (PCL) was modified on the terminal groups by using carbodiimidazole (CDI) as coupling agent. Then, the starch graft copolymers with PCL were prepared through a carbonate bond using carboimidazole function. Monofunctional and bifunctional reactive end-group PCL terminated with carboimidazole groups were prepared and reacted with hydroxyl groups of starch. The resulting starch-g-PCL copolymers were characterized by FT-IR, NMR, HR-MAS-NMR, DSC, MEB and XRD.
ISSN:0038-9056
1521-379X
DOI:10.1002/star.200900192