The kinetics of dehydration of lignite have been characterized by isot
hermal measurements of the water evolved under vacuum at 273-313 K. Th
e rate of water release at low relative pressures is deceleratory and
data are well expressed by the contracting volume rate equation. When
the water vapour pressure, p, approaches the saturated value, p(o), th
e rate becomes controlled by the relative vapour pressure, beta = p/p(
o). These controls are combined in the kinetic analysis of the isother
mal yield-time data. It is shown that the evaporation of water from li
gnite is satisfactorily expressed by the equation, dp/dt = k(1 - alpha
)2/3(1 - beta), where alpha is the fractional dehydration at time t. T
he activation energy was 35 +/- 5 kJ mol-1 between 273 and 313 K. It w
as shown that the dehydration rates of different lignite samples were
identical, and that they were the same as the rate of dehydration of a
rehydrated reactant sample which had previously been dried. It is con
cluded that the low temperature drying of lignite occurs by the evapor
ation of liquid water previously immobilized within the continuous coh
erent carbonaceous matrix. The drying rate depends on the particle siz
e, the rate of migration of the drying interface within the particles
and on the ambient pressure of water vapour which tends to rehydrate t
he matrix.