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. 2019 Oct 2;10(46):10765–10771. doi: 10.1039/c9sc03917a

Fig. 2. (a) 1H-NMR spectra of the NIPAM/p-Ti3C2Tx mixture (before N2 purging) and NC hydrogel (after N2 purging and polymerization). (b) Typical 1H-NMR spectra of the different polymers initiated by p-Ti3C2Tx. PAAm: poly(acrylamide); PMMA: poly(methyl methacrylate); PHEMA: poly(hydroxyethyl methacrylate); PDMA: poly(N,N-dimethylacrylamide); solvent, DMSO-d6. The arrows denote the proton signals in the polymer backbone. The shaded areas denote the proton signals in the monomeric double bonds. (c) 1H-NMR spectra of PNIPAM initiated by p-Ti3C2Tx and (d) conversion of NIPAM to its polymer at different reaction times. All samples were polymerized using a 1.0 wt% NIPAM monomer concentration and 0.35 mg mL–1 Ti3C2Tx nanosheet concentration.

Fig. 2