Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/7122
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dc.contributor.authorDeligöz, H.-
dc.contributor.authorErdem, Emin-
dc.date.accessioned2019-08-16T12:16:04Z
dc.date.available2019-08-16T12:16:04Z
dc.date.issued2008-
dc.identifier.issn0304-3894-
dc.identifier.urihttps://hdl.handle.net/11499/7122-
dc.identifier.urihttps://doi.org/10.1016/j.jhazmat.2007.09.096-
dc.description.abstractThe ionophore solvent extraction of various alkali metal and transition metal cations from the aqueous phase to the organic phase was carried out by using diazo-coupling calix[n]arenes [p-(4-phenylazophenylazo)calix[4]arene (L1) and p-phenylazocalix[6]arene (L2)], phenol derivatives [2,6-dimethyl-3-phenylazophenol (L3), 2-(5-bromo-2-pyridylazo)-5-diethylamino phenol (L4), 2-chloro-4-nitro(phenylazo)-5-sec-butyl-2-phenol (L5) and 2-chloro-4-nitro(phenylazo)-5-tert-butyl-2-phenol (L6)], and ester derivatives [quinoline-8-benzoate (L7), phenyl-1,4-dibenzoate (L8), p-tolyltiobenzoate (L9)]. It was found that, all the compounds (L1-L9) examined showed selectivity for transition metal cations such as Ag+, Hg+ Hg2+, and poor efficiency for alkali metal cations (Na+ and K+). The best extraction efficiency was obtained with L1 and L4. © 2007 Elsevier B.V. All rights reserved.en_US
dc.language.isoenen_US
dc.relation.ispartofJournal of Hazardous Materialsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAlkali metal ionsen_US
dc.subjectDiazo compoundsen_US
dc.subjectDiazo-coupling calyx[n]arenes (n = 4, 6)en_US
dc.subjectSolvent extractionen_US
dc.subjectTransition metal ionsen_US
dc.subjectEstersen_US
dc.subjectPhenolsen_US
dc.subjectPositive ionsen_US
dc.subjectMetal ionsen_US
dc.subject2 (5 bromo 2 pyridylazo) 5 diethylamino phenolen_US
dc.subject2 chloro 4 nitro(phenylazo) 5 sec butyl 2 phenolen_US
dc.subject2 chloro 4 nitro(phenylazo) 5 tert butyl 2 phenolen_US
dc.subject2,6 dimethyl 3 phenylazophenolen_US
dc.subject4 (4 phenylazophenylazo)calix[4]areneen_US
dc.subject4 phenylazocalix[6]areneen_US
dc.subject4 tolyltiobenzoateen_US
dc.subjectalkali metalen_US
dc.subjectcalixareneen_US
dc.subjectester derivativeen_US
dc.subjectphenol derivativeen_US
dc.subjectphenyl 1,4 dibenzoateen_US
dc.subjectpolycyclic aromatic hydrocarbon derivativeen_US
dc.subjectquinoline 8 benzoateen_US
dc.subjecttransition elementen_US
dc.subjectcationen_US
dc.subjectcomparative studyen_US
dc.subjectesteren_US
dc.subjectextraction methoden_US
dc.subjectnitrogen compounden_US
dc.subjectphenolen_US
dc.subjectpolymeren_US
dc.subjectsolventen_US
dc.subjectarticleen_US
dc.subjectcoupling factoren_US
dc.subjectencapsulationen_US
dc.subjecthydrogen bonden_US
dc.subjectsolvent extractionen_US
dc.subjectCalixarenesen_US
dc.subjectLigandsen_US
dc.subjectMetalsen_US
dc.subjectPicratesen_US
dc.subjectSolventsen_US
dc.titleComparative studies on the solvent extraction of transition metal cations by calixarene, phenol and ester derivativesen_US
dc.typeArticleen_US
dc.identifier.volume154en_US
dc.identifier.issue1-3en_US
dc.identifier.startpage29
dc.identifier.startpage29en_US
dc.identifier.endpage32en_US
dc.authorid0000-0003-3442-332X-
dc.identifier.doi10.1016/j.jhazmat.2007.09.096-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid17980958en_US
dc.identifier.scopus2-s2.0-43049101693en_US
dc.identifier.wosWOS:000256111200004en_US
dc.identifier.scopusqualityQ1-
dc.ownerPamukkale University-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.dept17.01. Chemistry-
Appears in Collections:Fen-Edebiyat Fakültesi Koleksiyonu
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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