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Dynamical behavior of highly concentrated trehalose water solutions: a dielectric spectroscopy study

AutorPagnotta, S. E.; Alegría, Ángel ; Colmenero de León, Juan
Fecha de publicación2012
EditorRoyal Society of Chemistry (Great Britain)
CitaciónPhysical Chemistry Chemical Physics 14(9): 2991-2996 (2012)
ResumenTrehalose solutions were investigated by means of broadband dielectric spectroscopy at different water contents, ranging from an anhydrous sample to wC = 40%. While the structural α-relaxation was detectable only in the low hydration and dry samples, and in a quite limited range of temperatures, two secondary processes were presented and characterized in all the solutions investigated. In particular, the fastest secondary process displayed a characteristic behavior widely observed in other small organic glass formers. It had an Arrhenius-like temperature dependence, it sped up and increased the dielectric strength when adding water and finally it possessed an activation energy compatible with the breaking/formation of two hydrogen bonds. From all these indications it was plausible to attribute it to water dipole reorientation dynamics. The slower secondary process was again well described by an Arrhenius-like function, now the relaxation time at high temperature was only slightly dependent on the exact water amount but the activation energy was markedly dependent on it. The molecular origin of this process was tentatively attributed to the motion of the entire molecule involving rotation of the two monosugar rings around the glycosidic bond. 2012 The Owner Societies.
URIhttp://hdl.handle.net/10261/50541
DOI10.1039/c2cp22402j
Identificadoresdoi: 10.1039/c2cp22402j
issn: 1463-9076
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