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Poly(acrylamide-co-acrylic acid) nanocomposite physical(P(AAm-co-AAc)NCP) hydrogels have been prepared through the in situ free radical solution polymerization based on a “single network, dual cross-linkings” strategy. The P(AAm-co-AAc) NCP hydrogels are composed of nanobrushes of P(AAm-co-AAc) chains grafted on the surface of vinylhybrid silica nanoparticles(VSNPs). In the hydrogel system, the VSNPs act as the “analogous chemical cross-linking points”once the hydrogen bonds formed between the P(AAm-co-AAc) chains of the nanobrushes, thus leading to the fabrication of high-strength P(AAm-co-AAc) NCP hydrogels. Compared with conventional thermosensitive P(AAm-co-AAc) hydrogels,the P(AAm-co-AAc) NCP hydrogels have a broader range of phase transition temperature, which can be adjusted by altering the monomer ratio, the VSNPs concentration, the addition of urea and N,N-dimethylacrylamide(DMAAm). At the same time, the mechanical properties of the P(AAm-co-AAc) NCP hydrogels have been improved significantly by the introduction of VSNPs. Furthermore, both the phase transition and the tensile strength of the P(AAm-co-AAc) NCP hydrogels are largely influenced when Fe3+ ions are introduced as the ionic crosslinkers into the hydrogel networks.
Poly (acrylamide-co-acrylic acid) nanocomposite physical (P (AAm-co-AAc) NCP) hydrogels have been prepared through the in situ free radical solution polymerization based on a “single network, dual cross-linkings” strategy. In the hydrogel system, the VSNPs act as the “analogous (AAm-co-AAc) chemical cross-linking points ”once the hydrogen bonds formed between the P (AAm-co-AAc) chains of the nanobrushes, thus leading to the fabrication of high-strength P (AAm-co- AAc) NCP hydrogels. The thermosensitive P (AAm-co-AAc) hydrogels, the P (AAm-co-AAc) NCP hydrogels have a broader range of phase transition temperatures, which can be adjusted by altering the monomer ratio, the VSNPs concentration, the addition of urea and N, N-dimethylacrylamide (DMAAm). At the same time, the mechanical properties of the P (AAm-co-AAc) NCP hydrogels have been im significantly significantly by the introduction of VSNPs. Both, the phase transition and the tensile strength of the P (AAm-co-AAc) NCP hydrogels are largely influenced when Fe3 + ions are introduced as the ionic crosslinkers into the hydrogel networks.