Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/13303
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dc.contributor.authorYıldız, Esra-
dc.contributor.authorLalikoğlu, Melisa-
dc.contributor.authorAşçı, Yavuz Selim-
dc.contributor.authorSırma Tarım, Burcu-
dc.date.accessioned2023-04-19T12:36:43Z-
dc.date.available2023-04-19T12:36:43Z-
dc.date.issued2023-
dc.identifier.issn0149-6395-
dc.identifier.issn1520-5754-
dc.identifier.urihttps://doi.org/10.1080/01496395.2023.2192382-
dc.identifier.urihttps://hdl.handle.net/11147/13303-
dc.description.abstractThe growing demand for producing organic acids by fermentative techniques has increased the significance of separating carboxylic acids from their fermentation broth with the reactive extraction process. Considering the environmental impacts, deep eutectic solvents can be considered as a potential green alternative for the replacement of volatile organic solvents commonly used in the extraction process. In this study, a new type of green solvent named hydrophobic deep eutectic solvent (HDES) based on decanoic acid as a hydrogen bond acceptor and menthol as a hydrogen bond donor was utilized for the reactive extraction of formic, acetic, and propionic acids from their aqueous solutions. The effect of initial acid concentration, HDES molar ratio, and tri-n-octyl amine (TOA) concentration on extraction efficiency was investigated. Modeling of the reactive extraction process was performed via a response surface methodology with a central composite design. Herein, the effect of the parameters of TOA concentration, HDES molar ratio, and initial acid concentration on the distribution coefficient was investigated. According to the results, it was reported that the most effective parameter on the extraction efficiency (%E) was the amount of extractant. The results of the experimental studies showed that the highest separation efficiency was obtained for 5% initial concentrations of formic, acetic, and propionic acids by using a mixture of 0.5 HDES molar ratio solvent and 1.9 mol/L TOA. The extraction efficiencies of these acids were found to be 88.71, 92.52, and 95.90 with +/- 0.1 standard deviation, respectively.en_US
dc.description.sponsorshipScientific Research Projects Coordination Unit of Istanbul University-Cerrahpasa [FYL-2020-35043]en_US
dc.description.sponsorshipThis study was funded by Scientific Research Projects Coordination Unit of Istanbul University-Cerrahpasa. Project number: FYL-2020-35043.en_US
dc.language.isoenen_US
dc.publisherTaylor & Francis Incen_US
dc.relation.ispartofSeparation Science and Technologyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDeep eutectic solventen_US
dc.subjectreactive extractionen_US
dc.subjectmonocarboxylic aciden_US
dc.subjectresponse surface method (RSM)en_US
dc.subjectAqueous-Solutionen_US
dc.subjectRegenerationen_US
dc.subjectGreenen_US
dc.titleInvestigation of reactive extraction of monocarboxylic acids with menthol-based hydrophobic deep eutectic solvent by response surface methodologyen_US
dc.typeArticleen_US
dc.institutionauthorSırma Tarım, Burcu-
dc.departmentİzmir Institute of Technology. Chemical Engineeringen_US
dc.identifier.volume58en_US
dc.identifier.issue8en_US
dc.identifier.startpage1450en_US
dc.identifier.endpage1459en_US
dc.identifier.wosWOS:000950946000001en_US
dc.identifier.scopus2-s2.0-85150879945en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1080/01496395.2023.2192382-
dc.authorscopusid58157618200-
dc.authorscopusid56107176200-
dc.authorscopusid25633800700-
dc.authorscopusid57343509000-
dc.identifier.scopusqualityQ2-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.cerifentitytypePublications-
crisitem.author.dept03.02. Department of Chemical Engineering-
Appears in Collections:Chemical Engineering / Kimya Mühendisliği
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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