Abstract:In order to apply ionic liquids (ILs) to the separation of rare earth metals, liquid-liquid extraction of a series of rare earth elements into the ILs was investigated mainly using 1-octyl-3-methylimidazolium bis(trifluoromethyl sulfonyl) imide, [C 8
mim][Tf 2 N], withN,N-dioctyldiglycol amic acid (DODGAA) as the extractant. A higher selectivity was exhibited for the heavier rare earth elements as in the n-dodecane system, and the order of the extractability of Y(III) in the IL system, situated in the heavy … Show more
“…As for the middle rare earth, Eu, the extraction efficiency in both systems was similar. Similar behavior wherein the selectivity between light and heavy rare-earth ions was increased in the ILs compared to that in the organic solvent was observed for other extractants such as PC-88A and recently developed DODGAA (N, N-dioctyldiglycol amic acid) [8,18].…”
Section: Extraction Of Rare-earth Ions With Ho8qsupporting
The extraction behavior of rare-earth ions with an 8-hydroxyquinoline derivative, HO8Q (5-octyloxymethyl-8-quinolinol), was studied using an ionic liquid,(1-octyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide), as the extracting phase. Compared with a conventional organic solvent, n-dodecane, the ionic liquid system showed a higher extraction ability for a heavy rare earth, Dy, and a better selectivity between Dy and Nd (separation factor β Dy/Nd : 108). In the liquid-liquid extraction system, the color of the extracting phase changed from colorless to light yellow along with the extraction of rare-earth ions. Furthermore, the extraction efficiency was enhanced by the addition of TOPO (tri-n-octylphosphine oxide) as a co-extractant.
“…As for the middle rare earth, Eu, the extraction efficiency in both systems was similar. Similar behavior wherein the selectivity between light and heavy rare-earth ions was increased in the ILs compared to that in the organic solvent was observed for other extractants such as PC-88A and recently developed DODGAA (N, N-dioctyldiglycol amic acid) [8,18].…”
Section: Extraction Of Rare-earth Ions With Ho8qsupporting
The extraction behavior of rare-earth ions with an 8-hydroxyquinoline derivative, HO8Q (5-octyloxymethyl-8-quinolinol), was studied using an ionic liquid,(1-octyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide), as the extracting phase. Compared with a conventional organic solvent, n-dodecane, the ionic liquid system showed a higher extraction ability for a heavy rare earth, Dy, and a better selectivity between Dy and Nd (separation factor β Dy/Nd : 108). In the liquid-liquid extraction system, the color of the extracting phase changed from colorless to light yellow along with the extraction of rare-earth ions. Furthermore, the extraction efficiency was enhanced by the addition of TOPO (tri-n-octylphosphine oxide) as a co-extractant.
“…The liquid-liquid extraction and liquid-membrane transfer of rare-earth metal ions from aqueous solutions containing base metal ions were performed using DODGAA, which indicated that DODGAA has higher selectivity for rare-earth metal ions than for base metal ions. [28][29][30][31] In the present study, we comprehensively investigated the extraction behavior of all Ln 3+ ions, except Pm 3+ , with DODGAA, and investigated the extraction mechanism using slope analysis, loading tests, and electrospray ionization mass spectrometry (ESI-MS) measurements. The mutual separation of individual Ln 3+ ions using DODGAA was compared with mutual separation using D2EHPA (Fig.…”
Liquid-liquid extraction of lanthanide ions (Ln 3+ ) using N,N-dioctyldiglycolamic acid (DODGAA) was comprehensively investigated, together with fluorescence spectroscopic characterization of the resulting extracted complexes in the organic phase. DODGAA enables the quantitative partitioning of all Ln 3+ ions from moderately acidic solutions, while showing selectivity for heavier lanthanides, and provides remarkably high extraction separation performance for Ln 3+ compared with typical carboxylic acid extractants. Furthermore, the mutual separation abilities of DODGAA for light lanthanides are higher than those of organophosphorus extractants. Slope analysis, loading tests, and electrospray ionization mass spectrometry measurements demonstrated that the transfer of Ln 3+ with DODGAA proceeded through a proton-exchange reaction, forming a 1:3 complex, Ln(DODGAA)3. The stripping of Ln 3+ from the extracting phase was successfully achieved under acidic conditions. Time-resolved laser-induced fluorescence spectroscopy revealed that the extracted Eu 3+ ions were completely dehydrated by complexation with DODGAA.
“…DODGAA is expected to be useful for the separation of rare-earth metal ions from foreign metal ions 9,10 as well as the mutual separation of individual rare-earth metal ions from each other. 7,8,12,23 The extractability of Sc(III) gradually increased compared with that of the other rare-earth metal ions. In fact, the slopes of the logarithmic distribution ratio versus the pH were approximately 3 for all rare-earth metal ions, except for Sc(III), and the slope for Sc(III) was 1.08, which is not equivalent to the valence of Sc(III).…”
We report on the acid dissociation constants (Ka) of diglycolamic acid-type ligands together with comprehensive data on the extraction performance of N,N-dioctyldiglycolamic acid (DODGAA) for 54 metal ions. The pKa of the diglycolamic acid framework was determined to be 3.54 ± 0.03 in water (0.1 M LiCl, 25 C) by potentiometric titration, indicating that DODGAA is strongly acidic compared with acetic acid. DODGAA can quantitatively transfer various metal ions among the 54 metal ions through a proton-exchange reaction, and provides excellent extraction performance and separation ability for rare-earth metal ions, In(III), Fe(III), Hg(II), and Pb(II) among the 54 metal ions.
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