Recovery of yttrium and europium from spent fluorescent lamps using pure levulinic acid and the deep eutectic solvent levulinic acid-choline chloride

A solvometallurgical approach for the recovery of rare-earth elements from lamp phosphor waste was developed. The solubility of individual phosphors in different deep-eutectic solvents (DESs) was measured. The DES levulinic acid-choline chloride ( x ChCl = 0.33) showed high solubility of the YOX pho...

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Published inRSC advances Vol. 1; no. 48; pp. 28879 - 2889
Main Authors Pateli, Ioanna M, Abbott, Andrew P, Binnemans, Koen, Rodriguez Rodriguez, Nerea
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 04.08.2020
The Royal Society of Chemistry
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Summary:A solvometallurgical approach for the recovery of rare-earth elements from lamp phosphor waste was developed. The solubility of individual phosphors in different deep-eutectic solvents (DESs) was measured. The DES levulinic acid-choline chloride ( x ChCl = 0.33) showed high solubility of the YOX phosphor (Y 2 O 3 :Eu 3+ ) and low solubility of the HALO phosphor (Sr,Ca) 10 (PO 4 )(Cl,F) 2 :Sb 3+ ,Mn 2+ , which does not contain any rare-earth element. This DES was selected for further investigation. When the DES was compared to pure levulinic acid, very similar leaching behaviour was observed, showing that the proton activity is more important than the chloride as a metal ligand. The leaching of YOX and HALO using levulinic acid-choline chloride ( x ChCl = 0.33) or pure levulinic acid was optimised in terms of water content, temperature and leaching time. The optimised parameters were validated in a synthetic mixture of phosphors and in real lamp phosphor waste. The co-dissolution of HALO is higher in the real waste than in the synthetic mixture. The real waste was also leached with an aqueous solution of hydrochloric acid, which was non-selective against dissolution of YOX, and with the functionalised ionic liquid betainium bis(trifluoromethylsulfonyl)imide. The ionic liquid gave a similar selectivity as levulinic acid, but is much more expensive. The recovery of the metals from the pregnant leach solution was tested via precipitation with oxalic acid and solvent extraction. Oxalic acid precipitation was not suitable for the DES system. The metals could be extracted via solvent extraction with the acidic extractant bis(2-ethylhexyl)phosphoric acid (D2EHPA) and stripped by an aqueous hydrochloric acid solution. Pure levulinic acid was found to be more suitable than the corresponding ChCl-based DES for the selective recovery of YOX. Yttrium and europium are selectively recovered from spent fluorescent lamps using levulinic acid-based solvents.
Bibliography:1
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H NMR spectra of the lixiviant and the extractant phases after solvent extraction experiments. See DOI
Electronic supplementary information (ESI) available
H NMR spectra of LevA-ChCl before and after a leaching. Composition of the leaching residue.
C NMR spectra of OxaA-ChCl before and after the leaching.
10.1039/d0ra05508e
H NMR of LevA-ChCl PLS before and after oxalic acid addition.
H NMR spectra of GlyA-ChCl before and after a leaching.
C NMR of LevA-ChCl before and after oxalic acid addition.
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ISSN:2046-2069
2046-2069
DOI:10.1039/d0ra05508e