Purpose. To address the lack of fundamental thermophysical data for tr
ehalose and its aqueous systems by measuring equilibrium and nonequili
brium properties of such systems. Methods/Results. Differential scanni
ng calorimetry (DSC) and dynamic mechanical analysis were used to meas
ure glass transition temperatures of trehalose and its solutions. X-ra
y diffractometry was used to verify the structure of amorphous trehalo
se. Controlled-stress rheometry was used to measure viscosity of sever
al aqueous trehalose systems at ambient and sub-ambient temperatures.
Over this temperature range, the density of these solutions was also m
easured with a vibrating tube densimeter. The equilibrium phase diagra
m of aqueous trehalose was determined by measuring the solubility and
freezing point depression. Conclusions. Our solubility measurements, w
hich have allowed long times for attainment of chemical equilibrium, a
re substantially different from those reported earlier that used diffe
rent techniques. Our measurements of the glass transition temperature
of trehalose are higher than reported values. A simple model for the g
lass transition is presented to describe our experimental observations
.