Method for the recovery of metallic copper

Claim 2

A process for recovering copper from a copper bearing material comprising the following steps: (a) leaching the copper bearing material in oxide form with sulfuric acid to obtain a copper sulfate containing aqueous liquor and an insoluble residue; (b) separating the copper sulfate-containing aqueous liquor from the insoluble residue; (c) contacting the separated copper sulfate-containing aqueous liquor with an organic extractant for copper of the ionic exchange type having substantially greater affinity for copper ions than other cations present in the aqueous leach liquor to extract the copper value from the aqueous leach liquor; (d) contacting the copper containing organic extractant with an aqueous solution of sulfuric acid to strip the copper in the form of copper sulfate from the copper-carrying organic extractant, thus reconstituting the organic extractant and forming a purified aqueous acidic copper sulfate solution; (e) passing the purified aqueous acidic copper sulfate solution to an amine solvent extraction step wherein an organic solution of amine salt is formed, separating the amine salt and contacting it with water whereby the amine is regenerated and sulfuric acid is recovered from the amine salt solution; (f) contacting the copper sulfate-containing solution with a sulfur dioxide type reductant whereby metallic copper is precipitated and sulfuric acid solution is produced; (g) recycling the sulfuric acid solution to the copper stripping step; and (h) recovering the precipitated copper.

Claim 3

A process according to claim 1 wherein, in step (f), the reducing gas is sulfur dioxide per se.

Claim 4

A process according to claim 1 wherein, in step (f), the sulfur dioxide is formed in situ by the action of acid on a suitable salt.

Claim 5

A process according to claim 3 wherein the salt is sodium sulfite.

Claim 6

A process according to claim 4 wherein the amine extractant comprises substantially trioctylamine.

Claim 7

A process according to claim 4 wherein the amine extractant is trioctylamine.

Claim 8

A process according to claim 1 wherein the amine extractant in step (e) is an alkyl amine.

Claim 9

A process according to claim 5 wherein the amine extractant is dissolved in a substantially water-immiscible organic diluent.

Claim 10

A process according to claim 8 wherein a modifier is present in the solution.

Claim 11

A process according to claim 9 wherein the modifier is isodecanol.

Claim 12

A process according to claim 1 wherein in step (c), the organic extractant for copper is a hydrocarbon terminating in an oxime group modified by adjacent hydroxyl groups.

Claim 13

A process for recovering copper from a copper bearing material comprising the steps of: (a) providing the copper bearing material in oxide form; (b) leaching the copper oxide with an aqueous sulfuric acid at or near ambient temperature and pressure and at a terminal pH of 1.5 to 4 to obtain a copper sulfate-containing aqueous liquor and an insoluble residue; (c) separating the copper sulfate-containing aqueous liquor from the insoluble residue; (d) contacting the copper sulfate-containing aqueous liquor with a 2% to 40% by weight solution of a selective organic ion exchange reactant dissolved in a hydrocarbon solvent; (e) contacting the solution of copper-containing organic extractant with an aqueous solution of sulfuric acid having a free acid content of 50 to 350 grams per liter of sulfuric acid to strip the copper value from the copper-carrying organic extractant, thereby forming an aqueous acidic copper sulfate solution; (f) contacting the purified aqueous acidic copper sulfate solution with a solution of 5 to 40% by volume of trioctylamine aromatic hydrocarbon solvent containing one half to twice the quantity of trioctylamine of isodecanol to form the amine sulfate and contacting the amine sulfate solution with water to regenerate the amine and recover the sulfuric acid formed; (g) contacting the copper sulfate-containing solution with sulfur dioxide in at least one stage at a temperature of 100 to 220° C. for a period of about 2 minutes to about 180 minutes, the molar ratio of sulfur dioxide to copper being about 1:1 to 1.8:1, wheregy metallic copper is precipitated and sulfuric acid solution is produced; (h) recycling the sulfuric acid solution to the copper sulfate stripping step; and (i) recovering the precipitated copper.

Claim 14

A process for recovering copper from a copper bearing material comprising the steps of: (a) providing the copper bearing material in oxide form; (b) leaching the copper oxide with an aqueous sulfuric acid at or near ambient temperature and pressure and at a terminal pH of 1.5 to 4 to obtain a copper sulfate-containing aqueous liquor and an insoluble residue; (c) separating the copper sulfate-containing aqueous liquor from the insoluble residue; (d) contacting the copper sulfate-containing aqueous liquor with a 2% to 40% by weight solution of a selective organic ion exchange reactant dissolved in a hydrocarbon solvent; (e) contacting the solution of copper-containing organic extractant with an aqueous solution of sulfuric acid having a free acid content of 50 to 350 grams per liter of sulfuric acid to strip the copper value from the copper-carrying organic extractant, thereby forming an aqueous acidic copper sulfate solution; (f) contacting the purified aqueous acidic copper sulfate solution with a solution of 5 to 40% by volume of trioctylamine aromatic hydrocarbon solvent containing one half to twice the quantity of trioctylamine of isodecanol to form the amine sulfate and contacting the amine sulfate solution with water to regenerate the amine and recover the sulfuric acid formed; (g) contacting the copper sulfate-containing solution with sulfur dioxide in at least one stage at a temperature of 100 to 220° C. for a period of about 2 minutes to about 180 minutes, the molar ratio of sulfur dioxide to copper being about 1:1 to 1.8:1, wheregy metallic copper is precipitated and sulfuric acid solution is produced; (h) recycling the sulfuric acid solution to the copper sulfate stripping step; and (i) recovering the precipitated copper.