A three-phase model for adsorption in zeolite cavities is proposed. Th
e adsorbed molecules are taken to be distributed between a surface lay
er and a dense phase filling the rest of the cavity volume. This model
is a more realistic representation of molecules in zeolite cages espe
cially at high pressures. The equation for the adsorption isotherm, ba
sed on this model, has two contributions: a surface term and a dense p
hase term. The dense phase contribution was estimated from a simple eq
uation that obeys the limiting values at low and high pressures. The s
urface contribution can be estimated from the existing surface adsorpt
ion models. When all model parameters are estimated from molecular and
literature data, the combination of the two terms was found to be an
improvement over traditional treatment of adsorption data of a number
of gases in zeolite-A for a wide range of pressures. However, new mode
ls for the adsorbed phase that account for sorbate-sorbate repulsive f
orces correctly are needed for accurate prediction of adsorption data.