Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/2183
Title: Para-substituted 1-phenyl-3-emethyl-4-aroyl-5-pyrazolones as selective extractants for vanadium(V) from acidic chloride solutions
Authors: Remya, P N
Ambili Raj, D B
Reddy, M L P
Keywords: Solvent extraction
Vanadium(V)
Para-substituted 1-phenyl-3-methyl-4-aroyl-5-pyrazolones
Neutral organophosphorus extractants
Solvent extraction
Separation
Titanium (iv)
Complexes
Cyanex-923
Iron(iii)
Issue Date: 2006
Publisher: Taylor & Francis
Citation: Solvent Extraction and Ion Exchange 24(6):877-892;Nov-Dec 2006
Abstract: Para-substituted 4-aroyl derivatives of 1-phenyl-3-methyl-5-pyrazolones (HX), namely, 1-phenyl-3-methyl-4-(4-fluorobenzoyl)-5-pyrazolone (HPMFBP) and 1-phenyl-3-methyl-4-(4-toluoyl)-5-pyrazolone (HPMTP) were synthesized and examined with regard to the extraction behavior of multivalent metal ions such as magnesium(II), aluminum(III), titanium(IV), vanadium( V), chromium( III), manganese( II), iron( II), and iron( III) that are present in titania waste chloride liquors. For comparison, studies have also been carried out with 1-phenyl-3-methyl-4-benzoyl- 5-pyrazolone (HPMBP). The results demonstrate that vanadium( V) and iron( III) are extracted into chloroform with 4-aroyl-5-pyrazolones as VO2X. HX and FeX3, respectively. On the other hand, magnesium( II), aluminum( III), titanium( IV), chromium( III), manganese( II), and iron( II) were not found to be extracted into the organic phase. The equilibrium constants of vanadium( V) and iron( III) with various 4-aroyl-5-pyrazolones follow the order HPMFBP. HPMBP. HPMTP, which is in accordance with their pKa values. The selectivity between vanadium( V) and iron( III) increases with increasing hydrochloric acid concentration. Further, it is clear from the results that iron( III) is not getting extracted above 1.0 mol dm(-3) hydrochloric acid solution. The electronic and IR spectra of the extracted complexes of vanadium( V) and iron( III) were used to further clarify the nature of the extracted complexes. The potential of these reagents for the selective extraction and separation of vanadium( V) from titania waste chloride liquors has also been discussed.
URI: http://ir.niist.res.in:8080/jspui/handle/123456789/2183
ISSN: 0736-6299
Appears in Collections:2006

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