| Literature DB >> 35650803 |
Chang Liu1, Hirokazu Kadono1, Koichi Mayumi1, Kazuaki Kato1, Hideaki Yokoyama1, Kohzo Ito1.
Abstract
In this study, the quasi-static fracture behavior of slide-ring gels (SR gels), in which movable cross-links can slide on polymer chains, is for the first time investigated and compared to that of conventional polymer gels with fixed cross-links (FC gels). For the usual FC gels, there is a trade-off relation between toughness (fracture energy [Formula: see text]) and stiffness (Young's modulus E): with increasing cross-linking density, the Young's modulus E increases, while fracture energy [Formula: see text] decreases. However, SR gels show an unusual fracture behavior that contradicts this trade-off relation. The fracture energy of SR gels is independent of the Young's modulus, in other words, the cross-linking density; moreover, it rises with increasing slidable range of movable cross-links on polymer chains. A new molecular model is proposed by attributing the unusual fracture properties of SR gels to the relative sliding movement between polymer chains and cross-links. Utilizing this concept, simultaneous fulfillment of high stiffness and high toughness in polymer gels can be realized.Entities:
Year: 2017 PMID: 35650803 DOI: 10.1021/acsmacrolett.7b00729
Source DB: PubMed Journal: ACS Macro Lett ISSN: 2161-1653 Impact factor: 6.903