Ljm. Schlangen et al., THIN HYDROCARBON AND WATER FILMS ON BARE AND METHYLATED SILICA - VAPOR ADSORPTION, WETTABILITY, ADHESION, AND SURFACE FORCES, Langmuir, 11(5), 1995, pp. 1701-1710
The vapor adsorption of different n-alkanes, cyclohexane, toluene, and
water on bare and methylated pyrogenic silica (Aerosil OX-50) has bee
n studied gravimetrically. Linear adsorption isotherms of the n-alkane
s and of cyclohexane on both substrates are found up to high relative
vapor pressures; the same holds true for toluene on methylated silica.
The linearity of the isotherms indicates relatively weak lateral inte
ractions. On bare silica, the adsorption, expressed in mol/m(2), of th
e n-alkanes studied (C7-C9) is independent of chain length. The adsorp
tion strongly increases after the coverage, corresponding to a monolay
er of alkanes oriented perpendicular to the surface has been reached.
Methylation of the silica is found to decrease the adsorption of all t
he adsorptives studied. On methylated silica the octane isotherm lies
below the coverage of a monolayer parallel to the surface until just b
efore saturation. From the adsorption data, surface pressure isotherms
are constructed, and the work of adhesion is obtained. The work of ad
hesion reveals that the Lifshits-van der Waals part of the silica surf
ace tension is reduced from 44 mJ/m(2) for bare (pyrogenic) silica to
30 mJ/m(2) for methylated silica. The adsorption data are also convert
ed to disjoining pressure isotherms. At small film thicknesses, the di
sjoining pressure can be described by an exponential short-range inter
action.