Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10611371 | Carbon | 2005 | 9 Pages |
Abstract
Wood-based activated carbon was ground and mixed with 10% bentonite binders containing either iron, zinc or copper cations adsorbed within the interlayer space and/or on the external surface of bentonite flakes. To better understand the role of transition metals, carbon was also impregnated with iron, zinc and copper salts. The structure of materials after modification was determined using nitrogen adsorption. The modification resulted in a decrease in porosity, especially in micropore volume, as a result of combined mass dilution effect and adsorption/re-adsorption of metals in small pores. Introduction of bentonite binders containing adsorbed metal increased the capacity of carbon for hydrogen sulfide only in the case of material containing copper. Copper also significantly increases the performance of carbon as an H2S adsorbent when impregnation is applied whereas the effects of other metals used in this study are much less pronounced. It is likely that copper present in the small pores acts as a catalyst for oxygen activation causing hydrogen sulfide oxidation. As a result of this process, elemental sulfur is formed which, when present in small pores, is oxidized to weakly adsorbed SO2. The SO2 is removed from the surface when continuous reaction with hydrogen sulfide occurs. Thus, even though binding carbon with spent bentonites after copper adsorption increases the capacity of carbon toward H2S removal, the formation of SO2, another undesirable pollutant, does detract somewhat from the procedure.
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Authors
Danh Nguyen-Thanh, Teresa J. Bandosz,