The Removal of Phenol and Its Derivatives from Aqueous Solutions by Adsorption on Petroleum Asphaltene

This research describes the adsorption of phenol and o-substituted phenols and xylenol isomers on petroleum asphaltenes from aqueous solution. The results revealed that the adsorption equilibrium data were best fitted with the generalized and Freundlich isotherms. For o-substituted phenols, it was f...

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Main Authors: Omer El-Amin Ahmed Adam, Ammar Hani Al-Dujaili
Format: Article
Language:English
Published: Hindawi Limited 2013-01-01
Series:Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2013/694029
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spelling doaj-3720baf70eb640dc81f8fcb9c0ab81f62020-11-25T00:14:04ZengHindawi LimitedJournal of Chemistry2090-90632090-90712013-01-01201310.1155/2013/694029694029The Removal of Phenol and Its Derivatives from Aqueous Solutions by Adsorption on Petroleum AsphalteneOmer El-Amin Ahmed Adam0Ammar Hani Al-Dujaili1Department of Chemistry, Faculty of Education for Pure Science/Ibn Al-Haitham, University of Baghdad, P.O. Box 4150, Baghdad, IraqDepartment of Chemistry, Faculty of Education for Pure Science/Ibn Al-Haitham, University of Baghdad, P.O. Box 4150, Baghdad, IraqThis research describes the adsorption of phenol and o-substituted phenols and xylenol isomers on petroleum asphaltenes from aqueous solution. The results revealed that the adsorption equilibrium data were best fitted with the generalized and Freundlich isotherms. For o-substituted phenols, it was found that electron-withdrawing groups increase the adsorption capacity. The uptake of these phenols decreases in the order: o-nitrophenol > o-chlorophenol > o-aminophenol > o-cresol > phenol, while the adsorption of xylenol isomers decreases in the order: 2,6-xylenol > 2,5-xylenol > 3,5-xylenol > 3,4-xylenol. Batch equilibrium results at different temperatures suggest that the adsorption of 2,6-xylenol and 3,5-xylenol onto asphaltene is an endothermic process, values obtained were positive indicating a nonspontaneous process with increasing randomness at the solid-solution interface. The influence of solution pH on the adsorption of 3,5-xylenol on asphaltenes was also investigated. The adsorption process was found to be independent on the solution pH. The adsorption capacity of 3,5-xylenol was found to increase with the decrease in particle size of the adsorbent.http://dx.doi.org/10.1155/2013/694029
collection DOAJ
language English
format Article
sources DOAJ
author Omer El-Amin Ahmed Adam
Ammar Hani Al-Dujaili
spellingShingle Omer El-Amin Ahmed Adam
Ammar Hani Al-Dujaili
The Removal of Phenol and Its Derivatives from Aqueous Solutions by Adsorption on Petroleum Asphaltene
Journal of Chemistry
author_facet Omer El-Amin Ahmed Adam
Ammar Hani Al-Dujaili
author_sort Omer El-Amin Ahmed Adam
title The Removal of Phenol and Its Derivatives from Aqueous Solutions by Adsorption on Petroleum Asphaltene
title_short The Removal of Phenol and Its Derivatives from Aqueous Solutions by Adsorption on Petroleum Asphaltene
title_full The Removal of Phenol and Its Derivatives from Aqueous Solutions by Adsorption on Petroleum Asphaltene
title_fullStr The Removal of Phenol and Its Derivatives from Aqueous Solutions by Adsorption on Petroleum Asphaltene
title_full_unstemmed The Removal of Phenol and Its Derivatives from Aqueous Solutions by Adsorption on Petroleum Asphaltene
title_sort removal of phenol and its derivatives from aqueous solutions by adsorption on petroleum asphaltene
publisher Hindawi Limited
series Journal of Chemistry
issn 2090-9063
2090-9071
publishDate 2013-01-01
description This research describes the adsorption of phenol and o-substituted phenols and xylenol isomers on petroleum asphaltenes from aqueous solution. The results revealed that the adsorption equilibrium data were best fitted with the generalized and Freundlich isotherms. For o-substituted phenols, it was found that electron-withdrawing groups increase the adsorption capacity. The uptake of these phenols decreases in the order: o-nitrophenol > o-chlorophenol > o-aminophenol > o-cresol > phenol, while the adsorption of xylenol isomers decreases in the order: 2,6-xylenol > 2,5-xylenol > 3,5-xylenol > 3,4-xylenol. Batch equilibrium results at different temperatures suggest that the adsorption of 2,6-xylenol and 3,5-xylenol onto asphaltene is an endothermic process, values obtained were positive indicating a nonspontaneous process with increasing randomness at the solid-solution interface. The influence of solution pH on the adsorption of 3,5-xylenol on asphaltenes was also investigated. The adsorption process was found to be independent on the solution pH. The adsorption capacity of 3,5-xylenol was found to increase with the decrease in particle size of the adsorbent.
url http://dx.doi.org/10.1155/2013/694029
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