We have used differential scanning calorimetry (DSC) to investigate the thermodynamic and kinetic properties of the glass transition of simple amine and alcohol solutions of inorganic salts. Although the glass-transition temperature (T-g) increases with the addition of salts, in common with other solutions, the concentration dependence of the heat-capacity change (C-p) at T-g and the kinetic fragility index (m) are quite different for the amine and alcohol solutions. The thermodynamic and kinetic properties depend more strongly on the solvents than on the solutes. By comparing the DSC data with Raman results, we suggest that the glass-transition thermodynamics and kinetics are controlled mainly by the strength or stability of hydrogen-bond structures and the properties of dominant intermolecular interactions in the solutions.
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