In the present invention, nickel is selectively extracted from an acidic solution that contains a high concentration of manganese. This valuable metal extraction agent is represented by the general formula. In the formula, R.sup.1 and R.sup.2 are alkyl groups that may be the same or different, R.sup.3 is a hydrogen atom or an alkyl group, and R.sup.4 is a hydrogen atom or any group, other than an amino group, bonded to an α carbon atom of an amino acid. The general formula preferably has a glycine unit, a histidine unit, a lysine unit, an aspartic acid unit or a n-methylglycine unit. When extracting nickel by using this extraction agent, it is preferable to adjust the pH of the acidic solution to 2.3 to 5.5 inclusive.

This disclosure relates to a process for selectively extracting Fe(III) ions from an aqueous feedstock containing Fe(III) ions and non-ferric ions. The process comprises contacting the feedstock with an organic phase comprising a phosphonium salt or ammonium salt ionic liquid under liquid-liquid extraction conditions for a time sufficient to allow transfer of at least some of the Fe(III) ions from the feedstock to the organic phase to provide an Fe(III) ion laden organic phase and an Fe(III) depleted feed-stock, and separating the Fe(III) ion laden organic phase from the Fe(III) depleted feedstock.

This disclosure relates to a process for selectively extracting Fe(III) ions from an aqueous feedstock containing Fe(III) ions and non-ferric ions. The process comprises contacting the feedstock with an organic phase comprising a phosphonium salt or ammonium salt ionic liquid under liquid-liquid extraction conditions for a time sufficient to allow transfer of at least some of the Fe(III) ions from the feedstock to the organic phase to provide an Fe(III) ion laden organic phase and an Fe(III) depleted feed-stock, and separating the Fe(III) ion laden organic phase from the Fe(III) depleted feedstock.

A metallurgical method for operating an autogenous production circuit for producing metal(s), said method using one or more oxidizing agents generated electrolytically in a cell with one or more interfaces which allows anion exchange; said method comprising steps of: (a) leaching of mineral(s) or material(s) containing at least one metal of interest (LX) in a first cell (A) to produce a pregnant leach solution (2) and an acid-ferrous aqueous solution (8); (b) using solvent extraction process(es) or selection process(es) in a second cell (B) to concentrate said metal(s) of interest (SX) of said pregnant leach solution (2) to produce a rich electrolyte (5) and a raffinate solution (4), said raffinate solution (4) being recycled in said first cell (A); and (c) electrowinning (EW) in a third cell (C) of said rich electrolyte (5) received from said second cell (B) and said acid-ferrous aqueous solution (8) received from said first cell (A), for producing a metal cathode (6) and an acid-ferric acid solution (9), said acid-ferric acid solution (9) being recycled in said first cell (A), wherein said steps (a), (b) and (c) are performed in said autogenous circuit that includes said first, second and third cells (A, B, C) with one or more anionic interfaces producing anodic and cathode reactions.

A metallurgical method for operating an autogenous production circuit for producing metal(s), said method using one or more oxidizing agents generated electrolytically in a cell with one or more interfaces which allows anion exchange; said method comprising steps of: (a) leaching of mineral(s) or material(s) containing at least one metal of interest (LX) in a first cell (A) to produce a pregnant leach solution (2) and an acid-ferrous aqueous solution (8); (b) using solvent extraction process(es) or selection process(es) in a second cell (B) to concentrate said metal(s) of interest (SX) of said pregnant leach solution (2) to produce a rich electrolyte (5) and a raffinate solution (4), said raffinate solution (4) being recycled in said first cell (A); and (c) electrowinning (EW) in a third cell (C) of said rich electrolyte (5) received from said second cell (B) and said acid-ferrous aqueous solution (8) received from said first cell (A), for producing a metal cathode (6) and an acid-ferric acid solution (9), said acid-ferric acid solution (9) being recycled in said first cell (A), wherein said steps (a), (b) and (c) are performed in said autogenous circuit that includes said first, second and third cells (A, B, C) with one or more anionic interfaces producing anodic and cathode reactions.

A method for extracting a rare earth metal from a mixture of one or more rare earth metals, said method comprising contacting an acidic solution of the rare earth metal with a composition which comprises an ionic liquid to form an aqueous phase and a non-aqueous phase into which the rare earth metal has been selectively extracted.

The present invention relates to a method for the recovery of palladium from an aqueous solution, comprising the steps of: (A) providing a dispersion comprising an aqueous dispersing phase comprising palladium(II), at least one non-ionic surfactant and at least one compound bearing a beta-dithiocarbonyl group, so as to form a hydrophobic complex of palladium(II) with the compound bearing a beta-dithiocarbonyl group; (B) heating the dispersion resulting from step (A) to a temperature at least equal to its cloud point so as to obtain the phase separation between the aqueous dispersing phase and a dispersed phase rich in surfactant comprising at least a part of said hydrophobic complex; (C) separating the dispersed phase rich in surfactant from the aqueous dispersing phase resulting from step (B); and (D) recovering the hydrophobic complex of palladium(II) with the compound bearing a beta-dithiocarbonyl group.

There is a process for the selective recovery of transition metals from an organic stream containing transition metals. The organic stream and possibly a first extractor if solid, are melted up to the liquid state. The extractor consists of an ionic liquid or a mixture of two or more ionic liquids and the ionic liquid contains an ammonium salt as cation and as anion an anion with chelating properties. A melted organic stream and a first extractor, optionally melted, are fed to a first liquid-liquid extraction unit working at a temperature of at least 150° C. where the liquid-liquid extraction is carried out obtaining a liquid mixture containing an ionic liquid, or a mixture of two or more ionic liquids, and metals. After extraction, the liquid mixture is cooled at a temperature between 0° C. and 70° C. and becomes biphasic; then the cooled mixture is sent to a first separation unit, to separate a liquid phase that contains ionic liquids and metals, and a metal-depleted solid phase. After the first separation, the separated metal-depleted solid phase is optionally sent to a washing unit to which a solvent is fed, so as to eliminate the residual ionic liquid by transferring it into the solvent and obtaining a metal-depleted solid phase. Then the separate liquid phase containing ionic liquids and metals is sent into a liquid-liquid precipitation and separation unit, adding a counter-solvent, thereby obtaining a solid phase containing the metals and a liquid stream containing counter-solvent and ionic liquids.

There is a process for the selective recovery of transition metals from an organic stream containing transition metals. The organic stream and possibly a first extractor if solid, are melted up to the liquid state. The extractor consists of an ionic liquid or a mixture of two or more ionic liquids and the ionic liquid contains an ammonium salt as cation and as anion an anion with chelating properties. A melted organic stream and a first extractor, optionally melted, are fed to a first liquid-liquid extraction unit working at a temperature of at least 150° C. where the liquid-liquid extraction is carried out obtaining a liquid mixture containing an ionic liquid, or a mixture of two or more ionic liquids, and metals. After extraction, the liquid mixture is cooled at a temperature between 0° C. and 70° C. and becomes biphasic; then the cooled mixture is sent to a first separation unit, to separate a liquid phase that contains ionic liquids and metals, and a metal-depleted solid phase. After the first separation, the separated metal-depleted solid phase is optionally sent to a washing unit to which a solvent is fed, so as to eliminate the residual ionic liquid by transferring it into the solvent and obtaining a metal-depleted solid phase. Then the separate liquid phase containing ionic liquids and metals is sent into a liquid-liquid precipitation and separation unit, adding a counter-solvent, thereby obtaining a solid phase containing the metals and a liquid stream containing counter-solvent and ionic liquids.

It is provided a process for recycling lithium ion batteries comprising shredding the lithium-ion batteries and immersing residues in an organic solvent; feeding the shredded batteries residues in a dryer producing a gaseous organic phase and dried batteries residues; feeding the dried batteries residues to a magnetic separator removing magnetic particles; grinding the non-magnetic batteries residues; mixing the fine particles and an acid producing a metal oxides slurry and leaching said metal oxides slurry; filtering the leachate removing the non-leachable metals; feeding the leachate into a sulfide precipitation tank; neutralizing the leachate; mixing the leachate with an organic extraction solvent; separating cobalt and manganese from the leachate using solvent extraction and electrolysis; crystallizing sodium sulfate from the aqueous phase; adding sodium carbonate to the liquor and heating up the sodium carbonate and the liquor producing a precipitate of lithium carbonate; and drying and recuperating the lithium carbonate.