Abstract

A variable temperature ATR–FTIR study of the gelation behaviour of a thermo-responsive ABA triblock copolymer (A=poly(N-isopropylacrylamide) and B=poly[2-(methacryloyloxy)ethyl phosphorylcholine]) is reported. Close inspection of selected copolymer and water bands in the temperature resolved spectra provides evidence for the dehydration of the poly(N-isopropylacrylamide) chains above a critical gelation temperature of approximately 37°C, while the central poly[2-(methacryoyloxy)ethyl phosphorylcholine]) chains remain hydrated. A blue shift in the amide I peak and a red shift in the amide II band indicate a reduction in the hydrogen bonding between the PNIPAM amide functional group and the solvent water. This is corroborated by a decrease in the intensity of the amide I peak above the gel point. Evidence of hydrophobic interactions and an indication of the source of the gelation mechanism were observed in the form of a red shift in the antisymmetric CH vibration with increasing temperature. These findings are consistent with the formation of a micellar gel network by the copolymer chains.

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