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Rates of SN1 hydrolysis reactions for 2-chloro-2-methylbutane in the critical solution of isobutyric acid + water and for 2-bromo-2-methylpropane in the critical solution of triethylamine + water in the one-phase region and at various temperatures have been determined respectively by conductance measurements. It was found that the reaction rates at different temperatures for those two SN1 reactions were well described by the Arrhenius equation in the noncritical region, whereas near the critical points the critical slowing down was clearly detected. These results are inconsistent with a previous report in the literature (J. Phys. Chem. A 2003, 107, 8435 - 8443). Reanalyzing the literature data, we found that if an Arrhenius equation appropriate to either the one-phase region or the two-phase region being examined was used as the background, a critical slowing down rather than a speeding up was detected for the reaction in both the one-phase region and the two-phase region. The experimental data from different sources were fitted with a simplified crossover formalism characterizing the critical effect on the reactions to determine the critical slowing down exponents, which were found to be about 0.04, showing that only a dynamic critical slowing down could be detected for these reaction systems. This phenomenon was attributed to the fact that the SN1 hydrolysis reaction is neither a first-order nor a pseudo-first-order reaction in the reverse direction and the kinetic measurements were carried out in a region quite far from the equilibrium of the reactions.

Mixed surfactant solutions are studied to understand their synergistic effects. Here we report the micellization properties of mixed surfactant solutions of the gemini surfactant N,N'-bis(dimethyldodecyl)-1,2-ethanediammoniumdibromide (12-2-12) with the imidazolium ionic liquid 1-dodecyl-3-methylimidazolium bromide (C12mimBr) investigated by isothermal titration calorimetry (ITC), conductometry, fluorimetry, and dynamic light scattering (DLS). A two-parameter Margules model was successfully used to correlate the cmc values and calculate the compositions and activity coefficients of the two components in the mixed micelle phase for 12-2-12/C12mimBr aqueous solutions with different overall surfactant compositions. The dissociation degree of counterion, the thermodynamic quantities of micellization, and the excess thermodynamic quantities for the mixed micelle were calculated and discussed. The ITC experiment in the low overall surfactant composition region showed a second phase transition. A thermodynamic model was proposed to explore phase behaviors of two different types of micelle and their solution, which was further confirmed by fluorescence and DLS studies.