Three samples of activated carbons of various origins were used in this stu
dy. The initial samples were oxidized with nitric acid to introduce oxygen-
containing groups. The surface of sorbents was characterized using sorption
of nitrogen, Boehm and potentiometric titrations, DRIFTS, and thermal anal
ysis. Then adsorption of acetaldehyde was studied by means of inverse gas c
hromatography at infinite dilution. From the retention volumes the heats of
acetaldehyde adsorption were calculated. The results showed that the heats
differ depending on the pore structure and surface chemistry of materials.
On materials with very small pores and surface groups incorporated into th
e carbon matrix, interactions of acetaldehyde are strongest. This is due to
the contribution of hydrogen bonding to dispersive interactions of hydroca
rbon moiety with the activated carbon pore walls. After oxidation, for the
carbons with unaltered or decreased surface area the isosteric heat of acet
aldehyde adsorption decreased due to an increase in the density of oxygen-c
ontaining groups resulting in a decrease in dispersive interactions and blo
cking of the pore entrances. Oxidation of carbon surfaces results also in a
n increase in the amount of acetaldehyde adsorbed under saturation conditio
ns. (C) 2001 Academic Press.