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To gain insight into a recent observation that the prominent, Debye-type relaxation process observed for a primary alcohol may not be the α-relaxation process associated with molecular diffusion of a liquid [Europhys. Lett. 40, 549 (1997), J. Chem. Phys. 107, 1086 (1997)], the dielectric spectra of an uncrystallizable secondary alcohol, 5-methyl-2-hexanol, has been investigated by broadband spectroscopy. Measurements made over a temperature range from 110 to 298 K showed that three relaxation processes occur. Processes I and II have a non-Arrhenius variation of the relaxation rate with temperature, and process III an Arrhenius. Only process I, the slowest of the three, has a single relaxation rate, the other two, a broad distribution. The contribution to permittivity from process II was 0.8, i.e., ∼3% of the static permittivity, and from process III, the fastest was 0.1, i.e., ∼0.3%. It is argued that the mechanism of process I is the breaking followed by dipolar reorientation and reforming of the H-bonds...

The exponential dielectric relaxation dynamics in a secondary alcohol’s supercooled liquid and glassy states