A dual-responsive
hydrogel based on graphene oxide (GO) was prepared
by in situ radical copolymerization of N-isopropyl
acrylamide (NIPAM) as a temperature-sensitive component and acrylic
acid (AA) as a pH-sensitive unit. The resulting hydrogels (GO/poly(NIPAM-co-AA)
(PNA) were systematically characterized by Fourier transform infrared
spectroscopy, X-ray photoelectron spectroscopy, Raman spectroscopy,
thermogravimetric analysis, differential scanning calorimetry, and
scanning electron microscopy. With the change of AA content, the lower
critical solution temperature of hydrogels changed from 26.91 to 24.38 °C.
The swelling ratio under alkaline condition was higher than that under
acidic condition. The adsorption of rhodamine B (RB) followed Langmuir
isotherm model and pseudo-second-order model, and nearly 93% of RB
could be released within 10 h at pH 4.01 and 60 °C. With imidacloprid
as the model drug, the higher cumulative release rate of the GO/PNA
hydrogel was obviously observed at pH = 4.01 than at pH = 9.18. On
the basis of their good adsorption–desorption, loading-releasing,
and regeneration ability, the GO/PNA hydrogel as a multifunctional
adsorbent might have broad application prospects in environmental
protection and biomedical engineering.