The present invention discloses a method for effectively decomposing mixed wolframite and scheelite ore in an alkaline system, specifically comprising steps of: grinding mixed wolframite and scheelite ore, putting in an autoclave, adding an appropriate amount of water, and then adding sodium phosphate, sodium hydroxide and calcium fluoride for decomposition, and treating by solid-liquid separation to obtain crude sodium tungstate solution. The present invention has the advantage that the high-efficiency decomposition of the mixed wolframite and scheelite ore can be realized with low consumption of leaching agents. By this method, the mixed wolframite and scheelite ore can be directly treated by an existing tungsten smelting autoclave, with low leaching cost, high decomposition rate and easy industrial application.

The present invention relates to an ironmaking feedstock comprising a solid CaFe.sub.3O.sub.5 phase. The ironmaking feedstock may be produced by a process comprising reacting a combination of a calcium source and magnetite at elevated temperature under reducing conditions sufficient to produce the solid CaFe.sub.3O.sub.5 phase. The product may be in the form of agglomerates such as pellets, with a compressive strength such that the product is suitable for transportation.

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.

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.

A method of removing aluminum from a waste electrode. The method includes comminuting the waste electrode containing a waste current collector and an electrode active material. The method further includes screening the comminuted waste electrode to collect the electrode active material. The method further includes mixing the electrode active material and an alkaline solution to remove aluminum impurities in the electrode active material.

A method of removing aluminum from a waste electrode. The method includes comminuting the waste electrode containing a waste current collector and an electrode active material. The method further includes screening the comminuted waste electrode to collect the electrode active material. The method further includes mixing the electrode active material and an alkaline solution to remove aluminum impurities in the electrode active material.

The present invention addresses the problem, in methods for producing a metal or alloy by reducing a mixture that contains an oxide ore, of providing an oxide ore smelting method with good productivity and efficiency. The present invention is an oxide ore smelting method for producing a metal or alloy by reducing a mixture that contains an oxide ore, the method comprising at least: a mixing step S1 for mixing an oxide ore with a carbonaceous reducing agent; a mixture-molding step S2 for molding the mixture obtained to obtain a mixture-molded body; and a reducing step S3 for heating the mixture-molded body obtained at a specified reducing temperature in a reducing furnace.

Alkaline oxidation process for treating refractory sulfide ore or concentrate particles enriched in a metal to be recovered comprising stages in which refractory ore or concentrate particles are surface-oxidized in an alkaline oxidation step in alkaline liquid phase with calcium hydroxide forming an alkaline slurry, which slurry is thereafter mechanically activated to remove passivating coatings from the surface oxidized refractory ore particles.

Alkaline oxidation process for treating refractory sulfide ore or concentrate particles enriched in a metal to be recovered comprising stages in which refractory ore or concentrate particles are surface-oxidized in an alkaline oxidation step in alkaline liquid phase with calcium hydroxide forming an alkaline slurry, which slurry is thereafter mechanically activated to remove passivating coatings from the surface oxidized refractory ore particles.

The present invention relates to the recovery of metals from raw ores or concentrates, and more specifically, to the recovery of rare earth elements, or oxides or salts thereof, from ores containing bastnaesite carbonatite, and/or monazite. The ore is processed by a method that may include one or more of the following steps: (i) mechanically processing the ore; (ii) calcination and/or roasting of the ore to form a calcinated material and/or roasting of the ore to form a roasted material; (iii) leaching of the calcinated material or roasted material in an aqueous solution; (iv) solid/liquid separation to remove a solid residue from the aqueous solution to recover a rare earth element solution; and (v) precipitation of the rare earth element solution to isolate a rare earth element, or oxide or salt thereof.