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dc.contributor.authorDonmez, Merve
dc.contributor.authorCamci, Selva
dc.contributor.authorAkbal, Feryal
dc.contributor.authorYagan, Mehtap
dc.date.accessioned2020-06-21T13:46:12Z
dc.date.available2020-06-21T13:46:12Z
dc.date.issued2015
dc.identifier.issn1944-3994
dc.identifier.issn1944-3986
dc.identifier.urihttps://doi.org/10.1080/19443994.2014.905972
dc.identifier.urihttps://hdl.handle.net/20.500.12712/14259
dc.descriptionWOS: 000353715700022en_US
dc.description.abstractThe adsorptive properties of natural sepiolite in the removal of copper (Cu2+) from aqueous solution were investigated. The results show that the amount of adsorption of copper ion increases with initial copper concentration, contact time, and solution pH. The pseudo-first-order, pseudo-second-order, and Elovich models were used to describe the kinetic data and the rate constants were evaluated. The adsorption of the copper onto natural sepiolite at different operating conditions followed the pseudo-second-order model. The equilibrium data were analyzed using the Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich (D-R) isotherm models. The equilibrium adsorption results are fitted better with Langmuir isotherm compared to the other models. The Langmuir monolayer adsorption capacity of sepiolite was estimated as 9.64 mg/g at pH 6.0 and temperature of 20 degrees C. An increase in temperature was found to induce a positive effect on the sorption process. Sorption of Cu2+ onto sepiolite was spontaneous and endothermic. The values of the enthalpy (Delta H) and entropy of activation (Delta S) were 14.892 kJ/mol and 96.342 J/mol K, respectively, at pH 5.0.en_US
dc.language.isoengen_US
dc.publisherDesalination Publen_US
dc.relation.isversionof10.1080/19443994.2014.905972en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectRegenerationen_US
dc.subjectKineticsen_US
dc.subjectIsothermsen_US
dc.subjectSepioliteen_US
dc.subjectThermodynamicsen_US
dc.subjectAdsorptionen_US
dc.titleAdsorption of copper from aqueous solution onto natural sepiolite: equilibrium, kinetics, thermodynamics, and regeneration studiesen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume54en_US
dc.identifier.issue10en_US
dc.identifier.startpage2868en_US
dc.identifier.endpage2882en_US
dc.relation.journalDesalination and Water Treatmenten_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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