Jump to main content
Jump to site search

Issue 19, 2015
Previous Article Next Article

Poly(lactide)-block-poly(ε-caprolactone-co-ε-decalactone)-block-poly(lactide) copolymer elastomers

Author affiliations

Abstract

Batch ring opening transesterification copolymerization of ε-caprolactone and ε-decalactone was used to generate statistical copolymers over a wide range of compositions and molar masses. Reactivity ratios determined for this monomer pair, rCL = 5.9 and rDL = 0.03, reveal ε-caprolactone is added preferentially regardless of the propagating chain end. Relative to poly(ε-caprolactone) the crystallinity and melting point of these statistical copolymers were depressed by the addition of ε-decalactone; copolymers containing greater than 31 mol% (46 wt%) ε-decalactone were amorphous. Poly(lactide)-block-poly(ε-caprolactone-co-ε-decalactone)-block-poly(lactide) triblock polymers were also prepared and used to explore the influence of midblock composition on the temperature dependent Flory-Huggins interaction parameter (χ). In addition, uniaxial extension tests were used to determine the effects of midblock composition, poly(lactide) content, and molar mass on the mechanical properties of these new elastomeric triblocks.

Graphical abstract: Poly(lactide)-block-poly(ε-caprolactone-co-ε-decalactone)-block-poly(lactide) copolymer elastomers

Back to tab navigation

Supplementary files

Publication details

The article was received on 08 Feb 2015, accepted on 02 Apr 2015 and first published on 17 Apr 2015


Article type: Paper
DOI: 10.1039/C5PY00202H
Author version available: Download Author version (PDF)
Citation: Polym. Chem., 2015,6, 3641-3651
  •   Request permissions

    Poly(lactide)-block-poly(ε-caprolactone-co-ε-decalactone)-block-poly(lactide) copolymer elastomers

    D. K. Schneiderman, E. M. Hill, M. T. Martello and M. A. Hillmyer, Polym. Chem., 2015, 6, 3641
    DOI: 10.1039/C5PY00202H

Search articles by author

Spotlight

Advertisements