Open Access Research Article

Crystalinity Behaviour in Poly(e-caprolactone)-b-Poly(dimethylsiloxane) Diblock and Triblock Copolymers through FTIR and DSC

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Abstract

Well-defined block poly(e-caprolactone)-b-poly(dimethylsiloxane) (PCL-b-PDMS) copolymers with one or two PCL blocks were obtained via coordinated anionic polymerization of e-caprolactone by using hydroxy terminated PDMS oligomers both as initiators and comonomers. Molecular weights of these copolymers were varied over a wide range between 7200 and 30400 g/mol and the formation of copolymers with desired backbone composition were monitored by 1H NMR spectroscopy and SEC. DSC studies illustrated the formation of two phase morphologies, with PDMS and PCL transitions respectively and the influence of the copolymers structure on their thermal properties has been examined. Keywords: coordinated anionic ring-opening polymerization; block copolymer; crystallization

How to Cite this Article

(2009). Crystalinity Behaviour in Poly(e-caprolactone)-b-Poly(dimethylsiloxane) Diblock and Triblock Copolymers through FTIR and DSC. Materiale Plastice, 46(1).
. Crystalinity Behaviour in Poly(e-caprolactone)-b-Poly(dimethylsiloxane) Diblock and Triblock Copolymers through FTIR and DSC. Materiale Plastice. 2009;46(1).
, "Crystalinity Behaviour in Poly(e-caprolactone)-b-Poly(dimethylsiloxane) Diblock and Triblock Copolymers through FTIR and DSC,” Materiale Plastice, vol. 46, no. 1, 2009.
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