Adsorption of polyvinylimidazole onto kaolinite

dc.authorid0000-0001-9548-0227en_US
dc.contributor.authorTekin, Nalan
dc.contributor.authorKadıncı, Emine
dc.contributor.authorDemirbaş, Özkan
dc.contributor.authorAlkan, Mahir
dc.contributor.authorKara, Alien_US
dc.date.accessioned2019-10-17T10:18:22Z
dc.date.available2019-10-17T10:18:22Z
dc.date.issued2006en_US
dc.departmentFakülteler, Fen-Edebiyat Fakültesi, Kimya Bölümüen_US
dc.descriptionTekin, Nalan (Balıkesir Author)en_US
dc.description.abstractThe adsorption of polyvinylimidazole (PVI) onto kaolinite from aqueous solutions has been investigated systematically as a function of parameters such as calcination temperature of kaolinite, pH, ionic strength, and temperature. According to the experimental results, the adsorption of PVI increases with pH from 8.50 to 11.50, temperature from 25 to 55 degrees C, and ionic strength from 0 to 0.1 mol L-1. The kaolinite sample calcined at 600 degrees C has a maximum adsorption capacity. Adsorption isotherms of PVI onto kaolinite have been determined and correlated with common isotherm equations such as Langmuir and Freundlich isotherm models. The Langmuir isotherm model appeared to fit the isotherm data better than the Freundlich isotherm model. The physical properties of this adsorbent are consistent with the parameters obtained from the isotherm equations. Furthermore, the zeta potentials of kaolinite suspensions have been measured in aqueous solutions of different PVI concentrations and pH. From the experimental results, (i) pH strongly alters the zeta potential of kaolinite; (ii) kaolinite has an isoelectric point at about pH 2.35 in water and about pH 8.75 in 249.9 ppm PVI concentration; (iii) PVI changes the interface charge from negative to positive for kaolinite. The study of temperature effect has been quantified by calculating various thermodynamic parameters such as Gibbs free energy, enthalpy, and entropy changes. The dimensionless separation factor (R-L) has shown that kaolinite can be used for adsorption of PVI from aqueous solutions.en_US
dc.identifier.doi10.1016/j.jcis.2005.09.049
dc.identifier.endpage479en_US
dc.identifier.issn0021-9797
dc.identifier.issue2en_US
dc.identifier.scopus2-s2.0-33644973533
dc.identifier.scopusqualityQ1
dc.identifier.startpage472en_US
dc.identifier.urihttps://doi.org/10.1016/j.jcis.2005.09.049
dc.identifier.uri1095-7103
dc.identifier.urihttps://hdl.handle.net/20.500.12462/8007
dc.identifier.volume296en_US
dc.identifier.wosWOS:000236424600011
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoenen_US
dc.publisherAcademic Press Inc Elsevier Scienceen_US
dc.relation.ispartofJournal of Colloid and Interface Scienceen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectAdsorptionen_US
dc.subjectPolyelectrolyteen_US
dc.subjectPolyvinylimidazoleen_US
dc.subjectKaoliniteen_US
dc.subjectAdsorption İsothermsen_US
dc.subjectZeta Potentialen_US
dc.titleAdsorption of polyvinylimidazole onto kaoliniteen_US
dc.typeArticleen_US

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