A two-stage mechanism of adsorption, including nucleation and condensation,
was proposed to describe the formation of the water liquid phase in carbon
adsorbents. Adsorption is assumed to occur in cylindrical pores. Nucleatio
n is described by a modified BET model, and condensation is treated by the
model of a stretched liquid film on a bent surface. The onset of formation
of the liquid phase (OFLP) is determined from the intersection of the adsor
ption isotherms for these stages. The theoretical value of the relative pre
ssure of OFLP varies over a wide range, decreasing with a decrease in the p
ore radius and reaching the relative vapor pressure of 0.178 for the spinod
al state of water. The comparison method using isotherms of graphitized car
bon black as the reference isotherms was applied for the determination of O
FLP of water in real active carbons. This resulted in good agreement betwee
n theory and experiment.