We report a nitrogen adsorption isotherm study on three shale samples that
have been previously characterized by small-angle neutron scattering (SANS)
. The scattering data establish that the pore surfaces in these porous mate
rials are self-similar fractals over a range of length scales between 5 and
500 Angstrom, and the fractal dimension D varies between 2.59 and 2.83. Fo
r isothermal adsorption of multilayer liquid film on fractal surfaces, the
theoretical predictions are (i) the number of adsorbed molecules N increase
s with the vapor pressure P as N similar to[ln(P-0/P)](D-3) and (ii) the ar
ea of the liquid-vapor interface S-I decreases as S-I similar to[ln(P-0/P)]
(D-2). We find that fitting our data to these predictions results in D valu
es that are significantly lower than the SANS results. More careful examina
tion of the data reveals systematic deviations from the predicted power-law
behaviors. We discuss the assumptions and approximations made in the theor
ies that could have caused this discrepancy.