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dc.contributor.authorDeligöz H.
dc.contributor.authorErdem E.
dc.contributor.authorKocaokutgen H.
dc.date.accessioned2020-06-21T09:15:28Z
dc.date.available2020-06-21T09:15:28Z
dc.date.issued2000
dc.identifier.issn1300-0527
dc.identifier.urihttps://hdl.handle.net/20.500.12712/2725
dc.description.abstractThe solvent extraction of Fe3+ cations from the aqueous to the organic (chloroform) phase was carried out using p-tert-butyl calix[4]arene(1), calix[4]arene(2), diazo-coupling calix[4]arenes [p-(4-n-butyl-phenylazo)calix[4]arene (3), p-(4-phenylazophenylazo)calix[4]arene(4), p-(4-acetanilidazo)calix[4]arene(5), p-(N'-2-thyazol-2ylsulphanylazo)calix[4]arene(6) and p-(2-thyazolazo)calix[4]arene(8) and the derivatives of phenol [2-(5-bromo-2-pyridylazo)-5-diethylaminophenol(8) (Bromo-PADAP) and 2-hydroxy-5-methyl-phenylazonapthol(9) (HMPAN)]. It was found that the compounds (1-9) showed the highest extractability toward Fe3+ at pH 4.5-5.4 Compound 5 shows strong binding ability to Fe3+ ion. Based on the method of continuous variation, calixarene 5 formed a 1:1 complex with Fe3+ ion.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleSolvent extraction of Fe3+ cation by diazo-coupling calix[4]arenesen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume24en_US
dc.identifier.issue2en_US
dc.identifier.startpage157en_US
dc.identifier.endpage163en_US
dc.relation.journalTurkish Journal of Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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