A series of activated carbon fibers (ACFs) and heat-treated oxidized A
CFs prepared from phenolic fiber precursors have been studied to eluci
date the role of pore size, pore surface chemistry and pore volume for
the adsorption of SO(2)and its catalytic conversion to H2SO4. For unt
reated ACFs, the initial rate of SO2 adsorption from flue gas was show
n to be inversely related to pore size. Ar longer times, the amount of
SO2 adsorbed from flue gas was dependent on both the pore size and po
re volume. Oxidation of the ACFs, using an aqueous oxidant, decreased
their adsorption capacity for SO2 from flue gas due to a decrease in p
ore volume and repulsion of the SO2 from acidic surface groups. IT the
se samples were heat-treated to desorb the oxygen containing function
groups, the amount of SO2 adsorption increased. This increase in adsor
ption capacity was directly correlated to the amount of CO2 evolved du
ring heat-treatment of the oxidized ACFs. The amount of SO2 adsorbed f
or these samples was related to the pore size, pore surface chemistry
and pore volume. This analysis is explained in more derail in this pap
er. (C) 1997 Elsevier Science Ltd.