Adsorption of SO2 on Bituminous Coal Char and Activated Carbon Fiber
J.A. DeBarr, A.A. Lizzio, Michael A. Daley
Abstract
J.A. DeBarr, A.A. Lizzio, Michael A. Daley
Abstract
The SO 2 adsorption behaviors of activated carbons produced from Illinois coal and of commercially prepared activated carbon fibers (ACFs) were compared. There was no relation between surface area of coal-based carbons and SO 2 adsorption, whereas adsorption of SO 2 on the series of ACFs was inversely proportional to N 2 BET surface area. Higher surface area ACFs had wider pores and adsorbed less SO 2; thus, pore size distribution is thought to play a significant role in SO 2 adsorption for these materials. Oxidation with HNO 3 and/or H 2 SO 4, followed by heat treatment at 700−925 °C to remove carbon−oxygen complexes, resulted in increased SO 2 adsorption for both coal chars and ACFs. This behavior was explained by an increase in the available number of free sites, previously occupied by oxygen and now available for SO 2 adsorption. The use of nitrogen-containing functional groups on ACFs of proper pore size shows promise for further increasing SO 2 adsorption capacities. Knowledge of the relationship among the number of free sites, pore size, and surface chemistry on corresponding SO 2 adsorption should lead to the development of more efficient adsorbents prepared from either coal or ACFs.
OpenAlex reports 52 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
The SO 2 adsorption behaviors of activated carbons produced from Illinois coal and of commercially prepared activated carbon fibers (ACFs) were compared. There was no relation between surface area of coal-based carbons and SO 2 adsorption, whereas adsorption of SO 2 on the series of ACFs was inversely proportional to N 2 BET surface area. Higher surface area ACFs had wider pores and adsorbed less SO 2; thus, pore size distribution is thought to play a significant role in SO 2 adsorption for these materials. Oxidation with HNO 3 and/or H 2 SO 4, followed by heat treatment at 700−925 °C to remove carbon−oxygen complexes, resulted in increased SO 2 adsorption for both coal chars and ACFs. This behavior was explained by an increase in the available number of free sites, previously occupied by oxygen and now available for SO 2 adsorption. The use of nitrogen-containing functional groups on ACFs of proper pore size shows promise for further increasing SO 2 adsorption capacities. Knowledge of the relationship among the number of free sites, pore size, and surface chemistry on corresponding SO 2 adsorption should lead to the development of more efficient adsorbents prepared from either coal or ACFs.
Key concepts: Adsorption, Coal, Activated carbon, Char, Bituminous coal, Specific surface area, BET theory, Chemical engineering