Adsorption behavior of propylamine on activated carbon fiber surfaces as induced by oxygen functional complexes
In this study, the surfaces of activated carbon fibers (ACFs) were modified by nitric acid to introduce surface oxygen complexes and to observe the influence of those complexes on the propylamine adsorption of the ACFs. It was found that the oxygen complexes including carboxylic and phenolic groups...
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Veröffentlicht in: | Journal of colloid and interface science 2006-10, Vol.302 (2), p.695-697 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | In this study, the surfaces of activated carbon fibers (ACFs) were modified by nitric acid to introduce surface oxygen complexes and to observe the influence of those complexes on the propylamine adsorption of the ACFs. It was found that the oxygen complexes including carboxylic and phenolic groups were predominantly increased, resulting in the increase of total surface acidity. However, the specific surface areas and the total pore volumes of the modified ACFs were decreased by 5–8% due to the increased blocking (or demolition) of micropores in the presence of newly introduced complexes. Despite the decrease of textural properties, it was found that the amount of propylamine adsorbed by the modified ACFs was increased by approximately 17%. From the XPS results, it was observed that propylamine reacted with strong or weak acidic groups, such as COOH or OH, on the ACF surfaces, resulting in the formation of pyrrolic-, pyridonic-, or pyridine-like structures.
The figure above illustrates the adsorption isotherms of PA on the V-ACFs at 298 K. It was found that the amount of adsorbed PA rapidly increased as a result of the micropore filling effects under 0.1 relative pressure, and then reached a plateau at 1.0 of relative pressure, as representative of a typical Type I isotherm. |
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ISSN: | 0021-9797 1095-7103 |
DOI: | 10.1016/j.jcis.2006.07.028 |