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Separation and recovery of rare earths by in situ selective electrochemical oxidation and extraction from spent fluid catalytic cracking (FCC) catalysts.
- Source :
-
Hydrometallurgy . Jun2020, Vol. 194, pN.PAG-N.PAG. 1p. - Publication Year :
- 2020
-
Abstract
- An efficient method for recovering and separating Ce3+ and La3+ rare earth elements from spent fluid catalytic cracking (FCC) catalyst is described. Initially, the spent FCC catalyst was leached with 2 M HNO 3 at 80 °C then removal of iron from the leach solution was carried out by solvent extraction with 25% (v/v) diisooctyl phosphinic acid (DiOAP) in n -octane. Extraction of the above rare earths was then undertaken from the nitric acid leach solution using an organic phase consisting of 25% (v/v) di(2-ethylhexyl) phosphoric acid (D2EHPA) and 25% (v/v) tri- n -butyl phosphate (TBP) in n -octane. Both rare earths were stripped form the organic phase using H 2 SO 4. Separation of the Ce3+ from La3+ was then achieved by means of an in situ electrochemical oxidation coupled with a simultaneous solvent extraction process. In this, the Ce3+ was electrochemically oxidized to Ce4+ and removed from the aqueous phase by solvent extraction employing 100 mM D2EHPA in n -octane. This led to efficient separation of the above rare earths, giving rise to La3+ in high purity of up to 99.5% and Ce4+ up to 100%. The separation occurs via a single extraction step without the need for pH adjustment or for the use of additional reagents. Unlabelled Image • Development of an in situ electrolysis/extraction process for La/Ce separation. • Optimized separation of rare earths in a single extraction step. • Application of a process for rare earth recovery from spent FCC catalyst. • Recovery of La and Ce in very high purity (> 99.5%). [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 0304386X
- Volume :
- 194
- Database :
- Academic Search Index
- Journal :
- Hydrometallurgy
- Publication Type :
- Academic Journal
- Accession number :
- 143552320
- Full Text :
- https://doi.org/10.1016/j.hydromet.2020.105300