Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/2191
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dc.contributor.authorAgrawal, Y K-
dc.contributor.authorSharma, C R-
dc.date.accessioned2008-10-10T11:26:07Z-
dc.date.available2008-10-10T11:26:07Z-
dc.date.issued2007-11-
dc.identifier.issn0376-4710-
dc.identifier.urihttp://hdl.handle.net/123456789/2191-
dc.description1772-1777en_US
dc.description.abstractA new reagent, [2] rotaxane hydroxamic acid, is reported for extraction and trace determination of vanadium(V) in nutritional and biological substrates. The extraction mechanism of vanadium from 6 M HCl media is investigated. Optimum conditions like solvent, influence of reagent and diverse ions etc on the extraction of vanadium have been examined. The overall stability constant (log β₂Ke) and extraction constant (Kex) in chloroform are 2.50 ± 0.02 and 4.0 ± 0.02  10⁻⁸ respectively. The system obeys Beer’s law in the range of 0.815-3.26 μg mL⁻¹ of vanadium(V). The molar absorptivity is 6.66  10³ L mol⁻¹ cm⁻¹ at 525 nm. The vanadium(V) complex chloroform extract has been directly inserted into plasma for ICP-AES measurements, which increases the sensitivity by 50 folds. The method is applied for determination of vanadium(V) in standard samples, sea water and environment samples.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt. Cl. ⁸ B01D11/00en_US
dc.sourceIJCA Vol.46A(11) [November 2007]en_US
dc.titleA novel [2] rotaxane hydroxamic acid for the liquid-liquid extraction and determination of vanadium(V)en_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.46A(11) [November 2007]

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