The present disclosure relates to a metal recovery process comprising a solvent extraction process. In an exemplary embodiment, the solution extraction system comprises a plant with a first and second circuit. A high-grade pregnant leach solution (“HGPLS”) is provided to the first and second circuit, and a low-grade pregnant leach solution (“LGPLS”) is provided to the second circuit. The first circuit produces a rich electrolyte, which can be forwarded to a primary metal recovery, and a low-grade raffinate, which can be forwarded to a secondary metal recovery process. The second circuit produces a rich electrolyte, which can also be forwarded to the primary metal recovery process. The first and second circuits are in fluid communication with each other.

Desirable methods for larger scale silver nanoplate synthesis are described along with methods for applying a noble metal coating onto the silver nanoplates to form coated silver nanoplates with a desirable absorption spectrum. The silver nanoplates are suitable for use in coatings for altering the hue of a transparent film. The hue adjustment can be particularly desirable for transparent conductive films.

Desirable methods for larger scale silver nanoplate synthesis are described along with methods for applying a noble metal coating onto the silver nanoplates to form coated silver nanoplates with a desirable absorption spectrum. The silver nanoplates are suitable for use in coatings for altering the hue of a transparent film. The hue adjustment can be particularly desirable for transparent conductive films.

A method for recycling lead from spent lead-acid battery paste, relating to the technical field of hydrometallurgy. In the method, firstly a reducing agent, and a lead paste are added into a zinc chloride solution for leaching in a stirring mill to cause lead in the lead paste to enter the solution, a lead cementation is performed by using zinc in the leached solution, after the lead cementation, the electrolytic zinc is produced by controlling an electrodeposition on the zinc chloride solution for a short time, the reducing agent is zinc, lead or hydrogen peroxide, a part of the electrolytic zinc is returned as the reducing agent for leaching, the step of returning the electrolytic zinc as the reducing agent can be omitted when the lead or the hydrogen peroxide is used as the reducing agent.

A process for removal of aluminium and iron in the recycling of rechargeable batteries comprising providing a leachate from black mass, adding phosphoric acid (H.sub.3PO.sub.4) to said leachate and adjusting the pH to form iron phosphate (FePO.sub.4) and aluminium phosphate (AlPO.sub.4), precipitating and removing the formed FePO.sub.4 and AlPO.sub.4, and forming a filtrate for further recovery of cathode metals, mainly NMC-metals and lithium.

A process for removal of aluminium and iron in the recycling of rechargeable batteries comprising providing a leachate from black mass, adding phosphoric acid (H.sub.3PO.sub.4) to said leachate and adjusting the pH to form iron phosphate (FePO.sub.4) and aluminium phosphate (AlPO.sub.4), precipitating and removing the formed FePO.sub.4 and AlPO.sub.4, and forming a filtrate for further recovery of cathode metals, mainly NMC-metals and lithium.

The present invention refers to an improved process for recovering zinc from primary and secondary raw materials, said process comprising a first leaching step wherein the ratio between the zinc weight contained in the raw material and the volume of the leaching solution is at least 20 kg zinc per m.sup.3 of acid aqueous solution; a neutralization step; and a solvent extraction stage in the presence of organic extractant, wherein the temperature is maintained from 47 to 52° C.

The present invention refers to an improved process for recovering zinc from primary and secondary raw materials, said process comprising a first leaching step wherein the ratio between the zinc weight contained in the raw material and the volume of the leaching solution is at least 20 kg zinc per m.sup.3 of acid aqueous solution; a neutralization step; and a solvent extraction stage in the presence of organic extractant, wherein the temperature is maintained from 47 to 52° C.

A process for leaching a mineral particulate material comprising the steps of feeding the mineral particulate material to a leaching step (10) in which at least one valuable metal in the mineral particulate material is leached into a leach solution to form a pregnant leach liquor and a solid residue containing undissolved mineral matter, the leaching step being conducted under conditions such that elemental sulphur is formed in the leaching step, wherein beads or particles that take up elemental sulphur are added to the leaching step such that elemental sulphur is taken up by or collects on the beads or particles, and separating the beads or particles from the pregnant leach liquor and the solid residue. The beads or particles may be treated to remove sulphur and the beads or particles are returned to the leaching step. Alternatively the mineral doesn't need to comprise a soluble component and can be a refractory sulphide of iron and/or arsenic containing precious metals that require oxidation before downstream conventional processes such as cyanidation.

A method for recovering lithium from a lithium-containing solution is provided. A lithium-containing solution with an adjusted pH value or an unadjusted pH value is mixed with a meta-aluminate, and the pH value is adjusted to weak acid/neutral, so that lithium can be separated from the lithium-containing solution in the form of a precipitate of Li.sub.aX.Math.2Al(OH).sub.3.Math.nH.sub.2O. Then, the precipitate is converted into a lithium adsorbent of (1-m)Li.sub.aX.Math.2Al(OH).sub.3.Math.nH.sub.2O and a Li.sub.aX-containing filtrate through desorption of lithium. High-purity Li.sub.2CO.sub.3 is obtained by performing precipitation of lithium on the Li.sub.aX-containing filtrate.