Comparing calorimetric and dielectric polarization modes in viscous 2-ethyl-1-hexanol

Dielectric relaxation and dynamic heat capacity measurements are compared for 2-ethyl-1-hexanol near its glass transition temperature T-g in order to further clarify the origin of the prominent Debye-type loss peak observed in many monohydroxy alcohols and other hydrogen-bonding liquids. While the dielectric spectrum epsilon(') displays two distinct polarization processes that are separated by a factor of 2000 in terms of the peak frequency, the heat capacity c(p)(') shows only a single peak. The dielectric process with lower amplitude and higher peak frequency coincides with the calorimetric signal, whereas the large dielectric Debye signal is not associated with calorimetric modes. The authors conclude that the Debye process corresponds to a transition among states which differ in energy only in the case of an external electric field.