期刊
SOFT MATTER
卷 10, 期 35, 页码 6658-6665出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4sm00709c
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资金
- Japan Society for the Promotion of Science (JSPS)
- Center for Medical System Innovation (CMSI)
- Graduate Program for Leaders in Life Innovation (GPLLI)
- International Core Research Center for Nanobio
- Core-to-Core Program
- A. The Advanced Research Networks
- Funding Program for World-Leading Innovative R&D on Science and Technology (FIRST program)
- Ministry of Education, Culture, Sports, Science, and Technology in Japan (MEXT) through the Center for NanoBio Integration (CNBI)
- MEXT [23700555, 24240069]
- Japan Science and Technology Agency (JST) through the S-innovation program
- COI STREAM
- Grants-in-Aid for Scientific Research [25708033, 14J06390, 23700555] Funding Source: KAKEN
Recently, polymer gels have drawn much attention as scaffolds for regenerative medicines, soft actuators, and functional membranes. These applications need tough and robust polymer gels as represented by the double network gels. To fully understand this mechanism and develop further advanced polymer gels, we need to fully understand the molecular origin of fracture energy for conventional polymer gels, which is inhibited by the inherent heterogeneity. In this paper, we show the experimental results on the fracture of model polymer gels with controlled network structure, and discuss the mechanism of the fracture of polymer gels.
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