In this study, first polyacrylamide hydrogels were synthesized by free‐radical crosslinking polymerization of acrylamide monomer with N,N′‐methylenebis(acrylamide) as a crosslinker in an aqueous solution at 22°C. Then, a series of hydrogels at various charge densities were prepared by partial hydrolysis of polyacrylamide precursors in a 0.1M sodium hydroxide solution at 60°C. The hydrolysis time was varied between 20 and 180 min. The chemical structures and internal morphologies of the hydrogels before and after alkaline hydrolysis were characterized with attenuated total reflectance/Fourier transform infrared and scanning electron microscopy measurements. The swelling ratio of the hydrolyzed hydrogels was measured in buffer solutions at various pHs. From differential curves of dQv/dpH versus pH (where Qv is the equilibrium swelling ratio of the hydrogels), the volume phase transition pH of the hydrogels was found to be 4.33 ± 0.05, regardless of the charge density of the hydrogels. In water at 22°C, the hydrogels with greater charge density showed a more rapid swelling rate because of their higher porosity and hydrophilicity. Moreover, in buffer solutions with the pH changing from 9.0 to 2.0 at 22°C, the hydrogels with greater charge density also exhibited a more rapid deswelling rate than the hydrogels with less charge density. In conclusion, the postmodification method is a good way of preparing pH‐sensitive hydrogels with fast responsiveness.
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Turan et al. (2008) studied this question.
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