The interactions between triblock copolymers of poly(ethylene oxide) and poly(propylene oxide), P103 and F108, EOnPOMEOn, m = 56 and n = 17 and 132, respectively, and gemini surfactants (oligooxa)-alkanediyl-alpha,w-bis(dimethyldodecylammonium bromide) (12-EOx-12),x = 0-3, have been studied in aqueous solution using isothermal titration calorimetry. The thermograms of F108 as a function of surfactant concentration show one broad peak at polymer concentrations, C-p,C- less than or equal to 0.50 omegat %, below the critical micelle concentration (cmc) of the copolymer at 25 degreesC. It is attributed to interactions between the surfactant and the triblock copolymer monomer. The critical aggregation concentration (cac) remains constant while DeltaH(max2) and the saturation concentration, C-2, increase with increasing copolymer concentration. Analysis of the cac data offers semiquantitative support that the degree of ionization of the surfactant aggregates bound to polymers is likely to be larger than that at the surfactant cmc. In P103 solutions at C-p greater than or equal to 0.05 wt %, two peaks appear in the thermograms and they are attributed to the interactions between the gemini surfactant and the micelle or monomeric forms of the copolymer. An origin-based nonlinear fitting program was employed to deconvolute the two peaks and to obtain estimates of peak properties. An estimate of the fraction of copolymer in aggregated form was also obtained. The enthalpy change due to interactions between the surfactants and P103 aggregates is very large compared to values obtained for traditional surfactants. This suggests that extensive reorganization of copolymer aggregates and surrounding solvent occurs during the interaction. Dehydration of the copolymers by the surfactant may also play an important step in the interaction. The endothermic enthalpy change reflecting interactions between the surfactant and polymer decreases more rapidly as the length and hydrophilic character of the spacer increases, suggesting that more favorable interactions occur with the P103 monomers having shorter PEO segments.
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