An integrated pressure leaching, heap leaching process for recovering copper from sulphidic feed containing iron, arsenic, and copper. Aqueous feed slurry of the sulphidic feed is pressure oxidized to form a liquid phase containing free sulphuric acid and aqueous copper sulphate, and to precipitate arsenic as solid iron arsenic compounds. Treated slurry is withdrawn from the pressure vessel and the liquid phase is separated from the solids. Copper is recovered from the separated liquid phase and generates a solution enriched in acid and depleted in copper. At least a portion of this solution is neutralized in a copper heap leach to produce a PLS containing copper and reduced in acid. At least a portion of the heap leach PLS is neutralized to produce a solution further reduced in acid, and solids containing copper precipitates, followed by a liquid solid separation.

An integrated pressure leaching, heap leaching process for recovering copper from sulphidic feed containing iron, arsenic, and copper. Aqueous feed slurry of the sulphidic feed is pressure oxidized to form a liquid phase containing free sulphuric acid and aqueous copper sulphate, and to precipitate arsenic as solid iron arsenic compounds. Treated slurry is withdrawn from the pressure vessel and the liquid phase is separated from the solids. Copper is recovered from the separated liquid phase and generates a solution enriched in acid and depleted in copper. At least a portion of this solution is neutralized in a copper heap leach to produce a PLS containing copper and reduced in acid. At least a portion of the heap leach PLS is neutralized to produce a solution further reduced in acid, and solids containing copper precipitates, followed by a liquid solid separation.

A method for extracting base and precious metals, all contained in refractory minerals, using aqueous media. The method includes mixing the mineral (Cu2S, CuS, CuFeS2, Cu5FeS4, FeS2, FeAsS.NiS, (Ni,Fe)xSy), ground to an appropriate size (2.5 centimetres), with a specific dose of solid reagent in a rotary agglomeration drum and then adding slightly acidified water to obtain a defined water content (5-8%) depending on the type of gangue contained in the metal-containing solid, thereby forming an agglomerate that will form a heap, which is subsequently allowed to stand for a period of several days (20-60 days), during which the conditions required to transform the refractory matrix into a highly soluble solid will be generated. Finally, appropriately regulated irrigation is applied, thus resulting in extraction of the metal by simple aqueous washing.

A method for extracting base and precious metals, all contained in refractory minerals, using aqueous media. The method includes mixing the mineral (Cu2S, CuS, CuFeS2, Cu5FeS4, FeS2, FeAsS.NiS, (Ni,Fe)xSy), ground to an appropriate size (2.5 centimetres), with a specific dose of solid reagent in a rotary agglomeration drum and then adding slightly acidified water to obtain a defined water content (5-8%) depending on the type of gangue contained in the metal-containing solid, thereby forming an agglomerate that will form a heap, which is subsequently allowed to stand for a period of several days (20-60 days), during which the conditions required to transform the refractory matrix into a highly soluble solid will be generated. Finally, appropriately regulated irrigation is applied, thus resulting in extraction of the metal by simple aqueous washing.

Cathode material from exhausted lithium ion batteries are dissolved in a solution for extracting the useful elements Co (cobalt), Ni (nickel), Al (Aluminum) and Mn (manganese) to produce active cathode materials for new batteries. The solution includes compounds of desirable materials such as cobalt, nickel, aluminum and manganese dissolved as compounds from the exhausted cathode material of spent cells. Depending on a desired proportion, or ratio, of the desired materials, raw materials are added to the solution to achieve the desired ratio of the commingled compounds for the recycled cathode material for new cells. The desired materials precipitate out of solution without extensive heating or separation of the desired materials into individual compounds or elements. The resulting active cathode material has the predetermined ratio for use in new cells, and avoids high heat typically required to separate the useful elements because the desired materials remain commingled in solution.

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.

Disclosed herein are methods for the recovery of lithium from lithium-bearing materials. More specifically, disclosed herein are methods comprising heating the lithium-bearing material with a solid roasting agent, forming a water suspension to allow to leach at least a portion of lithium into the water, separating a liquid and solid phase, and then exposing the collected solid phase to acid to allow acid leaching of the remaining amount of lithium.

Disclosed herein are methods for the recovery of lithium from lithium-bearing materials. More specifically, disclosed herein are methods comprising heating the lithium-bearing material with a solid roasting agent, forming a water suspension to allow to leach at least a portion of lithium into the water, separating a liquid and solid phase, and then exposing the collected solid phase to acid to allow acid leaching of the remaining amount of lithium.