A method for recovering metals, such as noble metals or copper, from secondary materials and other materials having organic constituents, wherein the organic components are extracted from the secondary materials and other material by thermal treatment in a process chamber and the secondary materials and other materials having organic constituents are prepared for the recovery process.

A dilute copper metal composition includes 57-85% wt Cu, ≥3.0% wt Ni, ≤0.8% wt Fe, 7-25% wt Sn and 3-15% wt Pb. A process includes the steps of partially oxidizing a black copper composition to obtain a first copper refining slag and a first enriched copper metal, partially oxidizing the first enriched copper metal to obtain a second copper refining slag, whereby at least 37.0% wt of the amount of tin and lead processed is retrieved in the first and second copper refining slags together; and partially reducing the first copper refining slag to form a first lead-tin based metal composition and a first spent slag. The process further includes the steps of adding the second copper refining slag to the first lead-tin based metal composition, thereby forming a first liquid bath; and partially oxidizing the first liquid bath, thereby obtaining the dilute copper metal composition.

A method for recovering a valuable substance is provided. The method includes a thermal treatment step of thermally treating a target containing a valuable substance using a continuous furnace configured to thermally treat the target while moving a target storing unit, in which the target is stored, such that the target storing unit is not contacted by a flame that is for thermal treatment, and a valuable substance recovering step of recovering the valuable substance from a thermally treated product of the target obtained in the thermal treatment step.

The present invention provides a method which is capable of more strictly controlling the oxygen partial pressure required during the melting of a starting material, thereby being capable of recovering a valuable metal more efficiently. A method for recovering valuable metals (Cu, Ni, Co), said method comprising the following steps: a step for preparing, as a starting material, a charge that contains at least phosphorus (P), iron (Fe) and valuable metals; a step for heating and melting the starting material into a melt, and subsequently forming the melt into a molten material that contains an alloy and slag; and a step for recovering the alloy that contains valuable metals by separating the slag from the molten material. With respect to this method for recovering valuable metals, the oxygen partial pressure in the melt is directly measured with use of an oxygen analyzer when the starting material is heated and melted.

A method for recovery of precious metals from copper anode slime may include leaching a leach liquor out of the copper anode slime by mixing the copper anode slime with a mixture of nitric acid and sulfuric acid, separating silver from the leach liquor by forming a silver chloride precipitate in the leach liquor by mixing a supersaturated sodium chloride solution with the leach liquor at room temperature and obtaining a first filtrate by filtering the silver chloride precipitate out of the leach liquor. Copper may be separated from the first filtrate by forming a copper hydroxide precipitate in the first filtrate by adjusting pH of the first filtrate at 9 and obtaining a second filtrate by filtering the copper hydroxide precipitate out of the first filtrate. Metallic selenium may be recovered from the second filtrate by reducing the metallic selenium via a chemical reduction utilizing L-ascorbic acid (LAA) as a reducing agent.

Processes for producing copper granules on a surface of a reducing metal. The process can include contacting the reducing metal with an aqueous solution comprising a copper(II) salt and a halide. The molar ratio of the halide to the copper(II) in the copper (II) salt can be at least about 3:1. The granular copper can be produced on a surface of the reducing metal, and is optionally removed from the surface of the reducing metal by shaking, washing, and/or brushing, and/or optionally with stirring and/or circulating of the aqueous solution.

The present disclosure discloses a method for impurity removal and treatment in the recycling process of scrap positive electrode materials of lithium batteries. The method includes controlling a flow rate of a leachate of scrap positive electrode materials of lithium batteries and a first alkaline solution at a first temperature higher than the room temperature and a constant first pH value to remove, by precipitation, iron ions, aluminum ions and at least part of copper ions to obtain a first filtrate; controlling the flow rate of the first filtrate, a complexing agent and a second alkaline solution at a second temperature higher than the room temperature and within a constant first pH range to obtain a target substance precipitate by separating a second filtrate containing lithium ions from the first filtrate; dissolving the target substance precipitate to obtain a first solution; and controlling the flow rate of the first solution and a fluorine-containing precipitant at a third temperature high than the room temperature and a constant concentration of fluorinion to remove, by precipitation, calcium ions, magnesium ions and at least part of lead ions to obtain a target solution. By the method of the present disclosure, a precipitate with a large particle size, high crystallinity and low water content can be obtained, which facilitates washing and improves the recycling rate of nickel-cobalt-manganese from the scrap positive electrode materials of lithium batteries.

A gas injection device for introducing a process gas into a non-ferrous metal melt and/or slag, in particular a copper melt and/or copper slag, including a hollow-cylindrical lance which is formed from a refractory material and/or graphite, preferably includes a refractory material and/or graphite. The lance has an inlet opening for the process gas and a gas injection module connected to the hollow-cylindrical lance and formed from a refractory material and/or graphite, preferably including a refractory material and/or graphite, with at least one outlet opening for the process gas. The outlet opening includes at least one throughflow element formed from a ceramic material via which the process gas can be introduced into the melt.

Disclosed are a method for removing elemental copper from ternary battery waste and its application. The method comprises the following steps: crushing and screening the ternary battery waste to obtain a powder, and then removing iron by magnetic separation to obtain an iron-removed ternary waste; Adding an alkaline solution to the iron-removed ternary waste to perform an aluminum removal reaction, filtering to obtain a filter slag and aluminum-containing wastewater, washing the filter slag with water and drying to obtain a copper-nickel-cobalt-manganese material. Adding an iron salt solution to the copper-nickel-containing material to perform a leaching process, filtering to obtain a leachate and a nickel-cobalt-manganese waste; adding iron powder to the leachate and stirring to perform a reaction, filtering to obtain a copper residue, washing the copper residue with water and drying to obtain a copper-removed liquid and a sponge copper.

In order to decrease arsenic, which is a harmful substance, in a copper concentrate, provided is a method for selectively recovering an arsenic-containing copper mineral from a mixture including the arsenic-containing copper mineral and a non-arsenic-containing copper mineral, and a flotation agent used in the same. For a collecting agent, which is a component of the flotation agent used in a flotation step for selectively recovering the arsenic-containing copper mineral from the mixture including the arsenic-containing copper mineral and the non-arsenic-containing copper mineral, a sulfide compound having an R.sub.1—S—R.sub.2 (in this expression, R.sub.1 is a C.sub.5-.sub.10 alkyl group, and R.sub.2 is a C.sub.1-.sub.10 alkyl group) structure such as methyl n-octyl sulfide or di-n-octyl sulfide is used.