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dc.contributor.authorDeligoz, H
dc.contributor.authorErdem, E
dc.contributor.authorKocaokutgen, H
dc.date.accessioned2020-06-21T15:50:12Z
dc.date.available2020-06-21T15:50:12Z
dc.date.issued2000
dc.identifier.issn1010-7614
dc.identifier.urihttps://hdl.handle.net/20.500.12712/22375
dc.descriptiondeligoz, hasalettin/0000-0003-4238-6776; Deligoz, Hasalettin/0000-0001-8449-6901en_US
dc.descriptionWOS: 000088382300006en_US
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) under bar), calix[4]arene((2) under bar), diazo-coupling calix[4]arenes [p-(4-n-butylphenylazo)calix[4]arene ((3) under bar), p-(4-phenylazophenylazo)calix[4]arene((4) under bar), p-(4-acetanilidazo)calix[4]arene((5) under bar), p-(N'-2-thyazol-2ylsulphanylazo)calix[4]arene((6) under bar) and p-(2-thyazolazo)calix[4]arene((8) under bar) and the derivatives of phenol [2-(5-bromo-2-pyridylazo)-5-diethylaminophenol((8) under bar) (Bromo-PADAP) and 2-hydroxy-5-methylphenylazonapthol((9) under bar) (HMPAN)]. It was found that the compounds ((1) under bar-(9) under bar) showed the highest extractability toward Fe3+ at pH 4.5-5.4 Compound (5) under bar 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.publisherScientific Technical Research Council Turkeyen_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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