The filling behavior of a room temperature solvent,
perfluoromethylcyclohexane, in approximately 20 nm nanoporous alumina membranes
was investigated in situ with small angle x-ray scattering. Adsorption in the
pores was controlled reversibly by varying the chemical potential between the
sample and a liquid reservoir via a thermal offset, ΔT. The system
exhibited a pronounced hysteretic capillary filling transition as liquid was
condensed into the nanopores. These results are compared with Kelvin-Cohan
theory, with a modified Derjaguin approximation, as well as with predictions by
Cole and Saam.Comment: 4 pages, 3 figures, pre-proof