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Tough supramolecular hydrogels with excellent self-recovery behavior mediated by metal-coordination interaction
- Source :
- Polymer. 171:201-210
- Publication Year :
- 2019
- Publisher :
- Elsevier BV, 2019.
-
Abstract
- Based on the strategy of dynamic metal-coordination for improving mechanical properties, a further ideal was taken to prepare the tough hydrogels with the combination of self-crosslinking monomer and metal-coordination complexes. Herein, a series of hydrogels of poly(acrylamide-co-acrylic acid-co- N-hydroxymethyl acrylamide) (P(AM-co-AAc-co-NMAM)) consisting the chemical crosslinking induced by NMAM units and the physical crosslinking derived from the coordination complexes of carboxyl-Fe3+ were prepared. The molecular structure was investigated with the ATR-FTIR, Raman and UV-vis spectra. These hydrogels with different water content of 57–93% possess good mechanical performances. The optimal hydrogels possess high tensile strength (8.56 MPa), prominent modulus (15.5 MPa), remarkable toughness (37.85 MJ/m3) and superb tearing energy (7062 J/m2). The tough hydrogels also display excellent self-recovery (95% toughness recovery within 50 min), pH-triggered healing, shape memory and plasticity abilities. These hydrogels having high strength and toughness may broaden range of potential applications in load-bearing soft actuators, flexible electronics, etc.
- Subjects :
- Toughness
Materials science
Polymers and Plastics
Organic Chemistry
Modulus
02 engineering and technology
010402 general chemistry
021001 nanoscience & nanotechnology
01 natural sciences
Flexible electronics
0104 chemical sciences
chemistry.chemical_compound
symbols.namesake
Monomer
chemistry
Chemical engineering
Ultimate tensile strength
Self-healing hydrogels
Materials Chemistry
symbols
Molecule
0210 nano-technology
Raman spectroscopy
Subjects
Details
- ISSN :
- 00323861
- Volume :
- 171
- Database :
- OpenAIRE
- Journal :
- Polymer
- Accession number :
- edsair.doi...........cd1096b103bb8ff276f222bcaa643ea3
- Full Text :
- https://doi.org/10.1016/j.polymer.2019.03.061