A series of activated carbon fibers (ACFs) and ammonia-treated ACFs prepare
d from phenolic fiber precursors have been studied to elucidate the role of
pore size, pore volume, and pore surface chemistry on adsorption of sulfur
dioxide and its catalytic conversion to sulfuric acid. As expected, the in
corporation of basic functional groups into the ACFs was shown as an effect
ive method for increasing adsorption of sulfur dioxide. The adsorption capa
city for dry SO2 did not follow specific trends; however the adsorption ene
rgies calculated from the DR equation were found to increase linearly with
nitrogen content for each series of ACFs. Much higher adsorption capacities
were achieved for SO2 in the presence of oxygen and water due to its catal
ytic conversion to H2SO4. The dominant factor for increasing adsorption of
SO2 from simulated flue aas for each series of fibers studied was the weigh
t percent of basic nitrogen groups present. In addition, the adsorption ene
rgies calculated for dry SO2 were shown to be linearly related to the adsor
ption capacity of H2SO4 from this flue g-as for all fibers. It was shown th
at optimization of this parameter along with the pore volume results in hig
her adsorption capacities for removal of SO2 from flue gases. (C) 2001 Else
vier Science Ltd. All rights reserved.