Scandium recovery method
US-2016340757-A1 · Nov 24, 2016 · US
US10450631B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10450631-B2 |
| Application number | US-201615542852-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 20, 2016 |
| Priority date | Jan 22, 2015 |
| Publication date | Oct 22, 2019 |
| Grant date | Oct 22, 2019 |
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This invention relates to a process for the recovery of cobalt ions and tungstic acid and/or its derivatives from aqueous solutions, such as in particular the spent catalytic waters deriving from processes for the oxidative cleavage of vegetable oils. In particular this invention relates to a process for the recovery of cobalt ions and tungstic acid and/or its derivatives which provides for the use of cation-exchange resins.
Opening claim text (preview).
The invention claimed is: 1. A process for recovering Cobalt ions and tungstic acid and/or its derivatives from an aqueous solution, which comprises the following steps: a) removing Cobalt ions by contacting said aqueous solution with a cationic exchange resin; b) separating said aqueous solution from the cationic exchange resin; c) concentrating said aqueous solution obtained from step b), obtaining a concentrated aqueous solution containing tungstic acid and/or its derivatives; d) eluting the Cobalt ions from the cationic exchange resin of step b) with an acid aqueous solution. 2. The process according to claim 1 , in which said aqueous solution comes from exhausted catalytic waters deriving from oxidative cleavage processes of vegetable oils. 3. The process according to claim 2 , comprising before step a) a preliminary purification step for separating an organic phase from said aqueous solution. 4. The process according to claim 2 , in which said cationic exchange resin is crosslinked. 5. The process according to claim 2 , in which said cationic exchange resin is of the strong acid type. 6. The process according to claim 1 , comprising before step a) a preliminary purification step for separating an organic phase from said aqueous solution. 7. The process according to claim 6 , in which said separation of the organic phase is performed by decantation. 8. The process according to claim 7 , in which said decantation is performed in presence of an organic solvent. 9. The process according to claim 8 , in which said organic solvent is selected from the group consisting of n-hexane, n-heptane, n-octane, n-nonanoic acid and mixtures thereof. 10. The process according to claim 9 , in which said organic solvent is n-octane, nonanoic acid or mixtures thereof. 11. The process according to claim 9 , in which said cationic exchange resin is crosslinked. 12. The process according to claim 8 , in which said cationic exchange resin is crosslinked. 13. The process according to claim 7 , in which said cationic exchange resin is crosslinked. 14. The process according to claim 6 , in which said cationic exchange resin is crosslinked. 15. The process according to claim 1 , in which said cationic exchange resin is crosslinked. 16. The process according to claim 1 , in which said cationic exchange resin is of the strong acid type. 17. The process according to claim 16 , in which the functional group of said cationic exchange resin of the strong acid type is constituted by sulphonic groups. 18. The process according to claim 1 , in which said acid aqueous solution of the d) step is constituted by an aqueous solution of an acid selected from the group consisting of hydrochloric acid, sulphonic acid, phosphoric acid, hydrobromic acid, acetic acid. 19. The process according to claim 1 , in which said step a) is performed with an ionic exchange column. 20. The process according to claim 19 , in which said aqueous solution is fed to step a) with a flow rate between 1 and 50 BV*/h (LHSV).
by extraction · CPC title
Hydrocarbons, e.g. oil · CPC title
from vegetable oil production, e.g. olive oil production · CPC title
from spent catalysts · CPC title
Heavy metals or heavy metal compounds · CPC title
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