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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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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