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 |
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Hauptverfasser: | , , , |
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. |
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ISSN: | 0038-9056 1521-379X |
DOI: | 10.1002/star.200900192 |