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Mechanical properties of supramolecular elastomers prepared from polymer-grafted polyrotaxane
Supramolecular slide-ring (SR) elastomers without solvent were fabricated by cross-linking of polymer-grafted polyrotaxane in which α-cyclodextrins (CDs) with poly-ε-caprolactone (PCL) side chains are threaded on a polyethylene glycol (PEG) axial linear chain. The cross-links in the SR elastomers ar...
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Published in: | Polymer (Guilford) 2017-10, Vol.128, p.386-391 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Supramolecular slide-ring (SR) elastomers without solvent were fabricated by cross-linking of polymer-grafted polyrotaxane in which α-cyclodextrins (CDs) with poly-ε-caprolactone (PCL) side chains are threaded on a polyethylene glycol (PEG) axial linear chain. The cross-links in the SR elastomers are capable of sliding along the backbone in response to applied stress. Mechanical properties of the SR elastomers with different cross-linking densities were compared with those of fixed cross-link (FC) elastomers prepared from PCL-grafted hydroxypropyl cellulose (HPC) to understand the influence of the slidable cross-links. The SR elastomers are found to undergo less strain-hardening at large strains and demonstrate higher strains at break than the conventional FC elastomers with the same Young's moduli.
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•Supramolecular slide-ring (SR) elastomers exhibit smaller Young's moduli than fixed cross-link (FC) elastomers.•SR elastomers show less strain-hardening and larger strains at break compared with FC elastomers.•The softness and high deformability of SR elastomers are attributed to the slidability of the cross-links. |
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ISSN: | 0032-3861 1873-2291 |
DOI: | 10.1016/j.polymer.2017.02.090 |