Abstract
Aqueous solutions of atactic poly(N-isopropylacrylamide) (a-PNIPAM) undergo complex phase transitions at 20-33 °C. In this temperature range, the a-PNIPAM solution exhibits a phase behavior of lower critical solution temperature at the binodal temperature (T(b)) and physical gel formation at the gel temperature (T(gel)). On slow heating of the one-phase solution containing linear a-PNIPAM chains, branched chains are gradually developed to proceed with the physical gelation before phase separation considering that T(gel) < T(b). Thus, the phase separation temperature determined from the conventional approaches, either by turbidity to derive the T(b) or by scattering to derive the spindal temperature (T(s)) from the Ornstein-Zernike analysis, is strictly the transition temperature associated with the a-PNIPAM hydrogel (or highly branched chains newly developed at elevated temperatures), rather than the initial a-PNIPAM solution prepared. Herein, the spinodal temperatures of a-PNIPAM hydrogels (T(s,gel)) of various concentrations were determined from rheological measurements at a heating rate of 0.2 °C/min. Analyses of the temperature dependence of loss modulus G″ and storage modulus G' give rise to the T(s,gel), based on the Fredrickson-Larson-Ajji-Choplin mean field theory. In addition, the specific temperature (T(1)) above which the one-phase solution starts to dramatically form the aggregated structure (e.g., branched chains) was also derived from the onset temperature of G' increase; this is because as solution temperature approaches the spinodal point, the concentration fluctuations become significant, which is manifested with the elastic response to enhance G' at T > T(1). Depending on the solution concentration, the measured T(s,gel) is approximately 5-10 °C higher than the derived T(1). On the other hand, T(s,gel) is independent of solution concentration to be constant at 32.8 °C. A phase diagram of the a-PNIPAM/H(2)O mixture is thoroughly constructed together with the previous data of T(gel) and T(b).