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Investigation of the separation of scandium and rare earth elements from red mud by use of reversed-phase HPLC

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dc.contributor.author Tsakanika, LV en
dc.contributor.author Ochsenkuhn-Petropoulou, MTh en
dc.contributor.author Mendrinos, LN en
dc.date.accessioned 2014-03-01T01:20:40Z
dc.date.available 2014-03-01T01:20:40Z
dc.date.issued 2004 en
dc.identifier.issn 1618-2642 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/16008
dc.subject Rare earth elements en
dc.subject Red mud en
dc.subject Scandium en
dc.subject Separation by reversed-phase high-performance liquid chromatography en
dc.subject.classification Biochemical Research Methods en
dc.subject.classification Chemistry, Analytical en
dc.subject.other Filtration en
dc.subject.other High performance liquid chromatography en
dc.subject.other Hydrophobicity en
dc.subject.other Ion exchange en
dc.subject.other Leaching en
dc.subject.other Negative ions en
dc.subject.other Phase separation en
dc.subject.other Rare earth elements en
dc.subject.other Hydrometallurgical treatments en
dc.subject.other Red mud (RM) en
dc.subject.other Separation by reversed-phase high-performance liquid chromatography en
dc.subject.other Supermagnetics en
dc.subject.other Scandium en
dc.title Investigation of the separation of scandium and rare earth elements from red mud by use of reversed-phase HPLC en
heal.type journalArticle en
heal.identifier.primary 10.1007/s00216-004-2667-1 en
heal.identifier.secondary http://dx.doi.org/10.1007/s00216-004-2667-1 en
heal.language English en
heal.publicationDate 2004 en
heal.abstract A chromatographic method has been developed for separation and determination of scandium (Sc) and rare earth elements (REEs) in samples from a red mud (RM)-utilization process. Reversed-phase high-performance liquid chromatography (RP-HPLC) with post-column derivatization using 4-(2-pyridylazo)-resorcinol (PAR) and UV-visible detection at 520 nm was tested using different gradient elution profiles and pH values to optimize separation and recovery, primarily for Sc but also for yttrium and the individual lanthanides, from iron present in the samples. The separation was performed in less than 20 min by use of a mobile phase gradient. The concentration of α-hydroxyisobutyric acid (α-HIBA), as eluent, was altered from 0.06 to 0.4 mol L-1 (pH 3.7) and 0.01 mol L-1 sodium salt n-octane sulfonic acid (OS) was used as modifier. Very low detection limits in the nanogram range and a good resolution for Sc and REEs except for Y/Dy were achieved. Before application of the method to the red mud samples and to the corresponding bauxites, Sc and REEs were leached from red mud with 0.6 mol L-1 HNO3 and mostly separated, as a group, from the main elements by ion exchange/selective elution (6 mol L-1 HNO 3) in accordance with a pilot-plant process developed in this laboratory. After evaporation of the eluent to dryness the extracted elements were re-dissolved in the mobile phase. By use of this chromatographic method Sc, which is the most expensive of the elements investigated and occurs in economically interesting concentrations in red mud, could be separated not only from co-existing Fe but also from Y/Dy, Yb, Er, Ho, Gd, Eu, Sm, Nd, Pr, Ce and La. All the elements investigated were individually recovered. Their recoveries were found to be nearly quantitative. © Springer-Verlag 2004. en
heal.publisher SPRINGER HEIDELBERG en
heal.journalName Analytical and Bioanalytical Chemistry en
dc.identifier.doi 10.1007/s00216-004-2667-1 en
dc.identifier.isi ISI:000223474200011 en
dc.identifier.volume 379 en
dc.identifier.issue 5-6 en
dc.identifier.spage 796 en
dc.identifier.epage 802 en


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