Abstract
The adsorption isotherms for Kr monolayers on graphite measured by A. Thomy and X. Duval, J. chim. phys., 67, 1101 (1970) are transformed into the ‘spreading pressure’ as a function of the number density of adsorbed molecules and compared with the pressure of a two-dimensional Lennard-Jones fluid determined by the molecular dynamics technique. The comparison shows that the mobile-layer model for adsorption fails at low temperatures. The liquid-solid phase transitions in the adsorption monolayer appear at lower densities than in a two dimensional Lennard-Jones fluid and the adsorbed liquid layer is compressible in contrast to the two-dimensional Lennard-Jones liquid.