dc.contributor.author | Deligöz H. | |
dc.contributor.author | Erdem E. | |
dc.contributor.author | Kocaokutgen H. | |
dc.date.accessioned | 2020-06-21T09:15:28Z | |
dc.date.available | 2020-06-21T09:15:28Z | |
dc.date.issued | 2000 | |
dc.identifier.issn | 1300-0527 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12712/2725 | |
dc.description.abstract | The 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.iso | eng | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.title | Solvent extraction of Fe3+ cation by diazo-coupling calix[4]arenes | en_US |
dc.type | article | en_US |
dc.contributor.department | OMÜ | en_US |
dc.identifier.volume | 24 | en_US |
dc.identifier.issue | 2 | en_US |
dc.identifier.startpage | 157 | en_US |
dc.identifier.endpage | 163 | en_US |
dc.relation.journal | Turkish Journal of Chemistry | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |