Research Achievements

December 2, 2016  PRESS RELEASE

Improving the Mechanical Properties of Polymer Gels through Molecular Design

Research team develops new approach to strengthen polymer gels by changing the length of polymer "thread" per molecular "bead".

Press Released on December 1, 2016

Caption: The polymer gels, which were prepared using polyrotaxane (PR) cross-linkers of different molecular weights but the same number of cross-linking points per unit volume of gel, have almost the same Young's modulus. By contrast, the extensibility and rupture strength of the polymer gels are substantially increased with increasing molecular weight of the PR cross-linker. (c)Yukikazu Takeoka

 

Nagoya, Japan - A polymer gel consists of a three-dimensional cross-linked polymer network swollen with liquid molecules. However, most conventional polymer gels are brittle because stress concentration readily occurs in their cross-linked polymer network structure. The mechanical properties of polymer gels need to be improved to facilitate their application as, for example, molecular sieves and superabsorbent materials.

 

An international researcher team from Nagoya University and The University of Tokyo have now found a way to increase the fracture resistance of polymer gels using a design based on molecular "beads" and polymer "threads." The molecular beads are modified cyclodextrin rings, which are threaded onto polyethylene glycol (PEG) threads. The cyclodextrin rings contain groups that allow the threaded structures to be cross-linked to form a three-dimensional polymer network that can be used as a polymer gel. The findings were recently published in ChemComm.

 

"We investigated the effect of the molecular weight of PEG per cyclodextrin ring on the strain and rupture strength of the resulting gels," study coauthor Yukikazu Takeoka says.

 

The researchers found that their polymer gels are resistant to fracture because the cyclodextrin beads can slide along the PEG threads when a force is applied, preventing stress concentration. The magnitude of this effect increases with the molecular weight of PEG per cyclodextrin ring, resulting in gels with greater strain and rupture strength. That is, the ability of the cyclodextrin beads to slide along the polymer threads increases with the length of thread between beads.

 

"The ability to improve the fracture resistance of polymer gels by increasing the molecular weight of polymer units for each cross-linking cyclodextrin ring is a convenient solution to overcome the problem of the brittleness of conventional polymer gels," lead author Kana Ohmori explains.

 

This approach to improve strain and rupture strength using mobile cross-linking molecular beads threaded on polymer chains should allow polymer gels with desired mechanical properties to be fabricated.

 

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The article "Molecular weight dependency of polyrotaxane-cross-linked polymer gel extensibility" was published in ChemComm at DOI: 10.1039/c6cc07641f

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Authors: Kana Ohmori, Imran Abu Bin, Prof. Takahiro Seki, Associate Prof. Yukikazu Takeoka, Department of Molecular Design & Engineering, Graduate School of Engineering, Nagoya University, and their research colleagues at Tokyo University.

 

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Related Links:

Lab. of Department of Molecular Design and Engineering, Nagoya University

 

NU Research, "The development of novel "stimuli-sensitive" hydrogels for various applications" (Feb. 4, 2015)

 

Media Coverage: 

EurekAlert!

AlphaGalileo

ResearchSEA

Phys.org

Science Daily

Materials today

Azom.com

nano werk

Scienmag 

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Funding: ImPACT for the project ''Realizing an Ultra-Thin and Flexible Tough Polymer''

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