Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/40489
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSarkar, Jaya-
dc.contributor.authorBag, Saswati P-
dc.date.accessioned2017-02-17T09:09:43Z-
dc.date.available2017-02-17T09:09:43Z-
dc.date.issued1997-03-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/40489-
dc.description244-246en_US
dc.description.abstractN-cinnamoyl-o-tolylbhydroxylamine (CT0HA.HL) forms extractable binary complex with uranium. The extracted complex, UO2L2(0) when shaken with tri-n-octylphosphine oxide (TOPO R) in chloroform, is gradually back-extracted into aqueous phase due to formation of the cationic complex, UO2LR +. The gradual substitution has been followed spectrophotometrically by the decrease in absorbance of UO2L2(0) Uranium(VI) can be extracted into the chloroform phase by formation of ion-pair [UO2LR + .PF)0 of UO2LR + with the anion hexafluorophosphate. Extraction of the ion-pair complex is followed by enhanced absorbance values. The substitution constant. Ka and ion-pair constant, KI, have been evaluated to be 0.075 and 2.05 x 103 respectively.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.36A(03) [March 1997]en_US
dc.titleIon-pair extraction of uranium(VI) using N-cinnamoyl-o-tolyl hydroxylamine in presence of tri-n-octyl phosphine oxide in chloroform and hexafluorophosphoric aciden_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.36A(03) [March 1997]

Files in This Item:
File Description SizeFormat 
IJCA 36A(3) 244-246.pdf306.42 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.