Abstract
A series of activated carbon fibers (ACFs) and heat-treated oxidized ACFs prepared from phenolic fiber precursors have been studied to elucidate the role of pore size, pore surface chemistry and pore volume for the adsorption of SO 2 and its catalytic conversion to H 2SO 4. For untreated ACFs, the initial rate of SO 2 adsorption from flue gas was shown to be inversely related to pore size. At longer times, the amount of SO 2 adsorbed from flue gas was dependent on both the pore size and pore volume. Oxidation of the ACFs, using an aqueous oxidant, decreased their adsorption capacity for SO 2 from flue gas due to a decrease in pore volume and repulsion of the SO 2 from acidic surface groups. If these samples were heat-treated to desorb the oxygen containing function groups, the amount of SO 2 adsorption increased. This increase in adsorption capacity was directly correlated to the amount of CO 2 evolved during heat-treatment of the oxidized ACFs. The amount of SO 2 adsorbed for these samples was related to the pore size, pore surface chemistry and pore volume. This analysis is explained in more detail in this paper.
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