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Triple-Shape Capability of Thermo-sensitive Nanocomposites from Multiphase Polymer Networks and Magnetic Nanoparticles

Published online by Cambridge University Press:  31 January 2011

Narendra Kumar Uttamchand
Affiliation:
narendra.uttamchand@gkss.de, Center for Biomaterial Development, Institute for Polymer Research, GKSS Forschungszentrum Geesthacht GmbH and Berlin-Brandenburg Center for Regenerative Therapies (BCRT), Kantstrasse 55, Teltow, 14513, Germany, 0049 3328 352 248, 0049 3328 352 452
Karl Kratz
Affiliation:
karl.kratz@gkss.de, Center for Biomaterial Development, Institute for Polymer Research, GKSS Forschungszentrum Geesthacht GmbH, Head of the Analytics Department, Teltow, Germany
Marc Behl
Affiliation:
marc.behl@gkss.de, Center for Biomaterial Development, Institute for Polymer Research, GKSS Forschungszentrum Geesthacht GmbH, Head of Active Polymers Department, Teltow, Germany
Andreas Lendlein
Affiliation:
lendlein@online.de, United States
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Abstract

Thermo-sensitive multiphase polymer networks with triple-shape capability have been recently introduced as a new class of active polymers that can change on demand from a first shape A to a second shape B and from there to a permanent shape C. Such multiphase polymer networks consist of covalent cross-links that determine shape C and at least two phase-segregated domains with distinct thermal transitions Ttrans,A and Ttrans,B , that are associated to shape A and B. In general the application of a two step programming or a one step programming procedure is required for creation of triple-shape functionality. In this study we report about a series of CLEGC nanocomposites consisting of silica coated nanoparticles (SNP) incorporated in a multiphase graft polymer network matrix from crystallisable poly(ε-caprolactone) diisocyanatoethyl methacrylate (PCLDIMA) and poly(ethylene glycol) monomethyl ether monomethacrylate (PEGMA) forming crystallisable side chains. These CLEGC nanocomposites were designed to enabling non contact activation of triple-shape effect in alternating magnetic field. Composites with variable PCLDIMA content ranging from 30 wt-% and 70 wt-% and different SNP amounts (0 wt-%, 2.5 wt-%, 5 wt-% and 10 wt-%) were realized by thermally induced polymerization. The thermal and mechanical properties of the CLEG nanocomposites were explored by means of DSC, DMTA and tensile tests. The triple-shape properties were quantified in cyclic, thermomechanical experiments, which consisted of a two step programming procedure and a recovery module under stress-free conditions for recovery of shapes B and C. While the thermal properties and the Young’s modulus of the investigated polymer networks were found to be independent from the incorporated amount of SNP, the elongation at break (εB) decreases with increasing nanoparticle content. All investigated composites exhibit excellent triple-shape properties showing a well separated two step shape recovery process.

Type
Research Article
Copyright
Copyright © Materials Research Society 2009

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