Sherritt Gordon Mines Limited

Cominco, Ltd.

Sherrit Gordon Mines Limited

Roman M Genik-Sas-Berezowsky

Donald R Weir

Godefridus M Swinkels

Edward Francis Milner

Charles Ray Kirby

Verner B Sefton

Eva A Vosahlo

Robert Arthur Furber

Ian M Masters

Ernest G Parker

Lynton S Gormely

A process for the recovery of silver from a residue essentially free of elemental sulphur obtained by acidic pressure oxidation leaching or iron-containing sulphidic material which comprises forming a slurry of the residue with lime at a temperature of at least about 80.degree. C. to raise the pH of the slurry to at least about 9. The slurry is maintained at this temperature for from about 0.5 to about 4 hours, and the resultant slurry is subjected to silver recovery treatment.

Process for the recovery of silver from a residue essentially free of

A process for recovering gold from refractory auriferous iron containing sulphidic material which comprises treating an aqueous slurry of the material in a pressure oxidation step at a temperature in the range of from about 135.degree. to about 250.degree. C. under a total pressure of from about 500 to about 5000 kPa to oxidize sulphide sulphur to sulphate form and release gold from a refractory state. The pH of the resultant oxidized slurry is adjusted to a value suitable for cyanidation. The pH adjusted slurry is subjected to a cyanidation step in which gold is dissolved in a cyanide solution. The cyanided slurry is diluted to a pulp density in the range of from about 2 to about 10% solids by weight. The diluted slurry is subjected to a liquid-solids separation step to produce a gold containing solution and a relatively high pulp density gold-containing slurry, and gold from the gold-containing solution and from the high pulp density gold-containing slurry is separately recovered.

Recovery of gold from refractory auriferous iron-containing sulphidic

A process for separately recovering gold and silver from a solution containing dissolved gold and silver by carbon adsorption which comprises passing the solution sequentially through a series of carbon adsorption stages and passing carbon sequentially through the series countercurrent to the solution to cause gold and silver to be loaded onto the carbon. A portion of the loaded carbon is removed partway along the series, and silver is recovered from the removed portion of the loaded carbon. Loaded carbon is removed from the beginning of the series, and gold is recovered from the carbon removed from the beginning of the series. Carbon from which gold and silver have been removed is returned to the end of the series for re-use.

Process for separately recovering gold and silver from solution by

A process for recovering gold from refractory auriferous iron-containing concentrate includes feeding the concentrate as an aqueous slurry to an acidic pretreatment step and treating the concentrate in the acidic pretreatment step with aqueous sulphuric acid solution to decompose carbonate and other acid consuming gangue compounds. The treated slurry is oxidized in a pressure oxidation step at a temperature in the range of from about 135.degree. to about 250.degree. C. under a pressurized oxidizing atmosphere while maintaining a free acid concentration of from about 5 to about 40 g/L sulphuric acid to cause dissolution of iron, formation of sulphuric acid and oxidation of substantially all oxidizable sulphide compounds to sulphate form with less than about 20% of oxidized sulphur being present as elemental sulphur during the oxidation step. Water is added to the oxidized slurry in a first repulping step to produce a repulped oxidized slurry with a pulp density in the range of from about 5 to about 15% solids by weight, the repulped oxidized slurry is subjected to a liquid-solids separation step to produce an acid and iron containing solution and oxidized separated solids, a portion of the acid and iron containing solution is recycled to the acidic pretreatment step, and gold is recovered from the oxidized separated solids.

A process for recovering gold from refractory auriferous iron-containing sulphidic ore which comprises feeding ground ore as an aqueous slurry to an acidic pretreatment step. The ground ore in the acidic pretreatment step is treated with aqueous sulphuric acid solution to decompose carbonate and acid consuming gangue compounds, and subjecting the treated slurry to a first liquid-solids separation step to produce a sulphate solution and separated solids. Water is added to the separated solids in a first repulping step to form a slurry having a pulp density in the range of from about 25 to about 60% by weight solids. The first repulped slurry is oxidized in a pressure oxidation step at a temperature in the range of from about 135.degree. to about 250.degree. C. under a pressurized oxidizing atmosphere while maintaining a free acid concentration of from about 5 to 40 g/L sulphuric acid to cause dissolution of iron, formation of sulphuric acid and oxidation of substantially all oxidizable sulphide compounds to sulphate form with less than about 20% of oxidized sulphur being present as elemental sulphur during the oxidation step. Water is added to the oxidized slurry in a seocnd repulping step to produce a repulped oxidized slurry with a pulp density in the range of from about 5 to 15% by weight, and subjecting the repulped oxidized slurry to a second liquid-solids separation step to produce an acid and iron containing solution and oxidized separated solids. The acid and iron containing solution is recycled to at least one of the first and second repulping steps.

Recovery of gold from refractory auriferous iron-containing sulphidic ore

A process for the recovery of uranium values from uranium-containing material which also contains iron, arsenic and siliceous matter, includes leaching the uranium-containing material in aqueous sulphuric acid solution under conditions to provide dissolved iron present in the resultant leach solution as predominantly ferrous iron rather than ferric iron and/or to provide a sulphuric acid concentration in the leach solution sufficiently high to substantially prevent the precipitation of arsenates. Uranium values are recovered from the leach solution by solvent extraction agent which has little affinity for arsenic.

Recovery of uranium from material containing iron, arsenic and siliceous

A process for recovering uranium values from a sulphate solution containing dissolved uranium and molybdenum and with a pH not exceeding about 5.5, includes reacting the solution with ammonia at a pH in the range of from about 8 to about 10, without the solution existing for any significant time at a pH of around 7, with resultant precipitation of uranium values relatively uncontaminated by molybdenum. The uranium containing precipitate is separated from the remaining solution while maintaining the pH of the remaining solution within the same range.

Removal of uranium from sulphate solutions containing molybdenum

A process for purifying copper sulfate solution by converting contained hexavalent selenium to tetravalent selenium which is amenable to removal from solution by heating and maintaining the solution at a temperature in the range of about 135.degree. to 220.degree. C. under a non-oxidizing atmosphere in the presence of bivalent iron. The converted selenium is removed from the solution either by co-precipitation with ferrous iron oxidized and hydrolyzed to ferric oxide at a temperature in the range of 135.degree. to 220.degree. C. and under an oxygen pressure of about 140 to 450 kPa or by cementation with a metal powder at a temperature in the range of about 25.degree. to 85.degree. C. at about ambient pressure under a non-oxidizing atmosphere.

Removal of selenium from sulphate solutions

A process for precipitation of iron as a jarosite compound from sulfate solution in which said solution fed sequentially through a plurality of reaction zones for oxidation and hydrolysis of ferrous sulfate in the presence of alkali-metal or ammonium ions for jarosite precipitation and simultaneous generation of sulfuric acid is subjected to a 'reverse temperature profile', i.e., higher temperature in the last reaction zone than in the first reaction zone, by injection of steam to the last reaction zone.

Process for the precipitation of iron as jarosite

A process for treating thermally activated metal sulfides containing copper, iron and zinc for separate recovery of zinc as zinc sulfide in which the metal sulfides are subjected to a two-stage countercurrent acid leach for the formation of copper sulfide containing acid leach residue and ferrous sulfate solution. The second-stage acid leach is performed in two steps; the first step is operated at a relatively high pulp density and high acid concentration for iron and zinc extraction, the resulting slurry diluted, and the second step is operated at a relatively low pulp density and low acid concentration for dissolution of precipitated ferrous sulfate and precipitation of any dissolved copper values by H.sub.2 S. The diluent solution for the slurry from the second-stage first step preferably is generated sulfuric acid solution from a jarosite precipitation and iron and zinc-containing solution from a subsequent activation leach. Zinc in solution from the acid leach and activation leach is precipitated as zinc sulfide in substantially pure form.

Process for recovery of copper and zinc from complex sulphides

A hydrometallurgical process for the separate recovery of non-ferrous, ferrous, and precious metal values and sulfur from metal sulfide ore concentrates by leaching of metal sulfides with a lixiviant containing ferric chloride, cupric chloride and chlorine, precipitating cuprous chloride from the leach solution with butadiene, separating and decomposing the formed addition compound to recover the cuprous chloride, oxidizing and hydrolyzing the cuprous chloride to precipitate cupric oxychloride, converting the cupric oxychloride to cupric oxide, and reducing the cupric oxide with hydrogen for the recovery of copper. The leach residue is treated for the recovery of elemental sulfur and gold. Brine solution resulting from the conversion of cupric oxychloride to cupric oxide is electrolyzed for the production of sodium hydroxide for the cupric oxychloride conversion, hydrogen for the cupric oxide reduction and chlorine, which is partly used in the recovery of gold and partly recycled to the concentrate leach. Silver is recovered as silver iodide from the mother liquor from the cuprous chloride precipitation with butadiene. A portion of the solution from the silver recovery is treated for recovery of Cu, Zn, Co and Ni, and the remaining portion and residual solution from Cu, Zn, Co and Ni recovery are treated with oxygen at elevated temperature and pressure for the regeneration of ferric chloride and precipitation of excess iron as anhydrous ferric oxide.

Hydrometallurgical process for recovering copper and other metal values

Gold, as well as copper, is recovered from copper bearing sulphidic material containing gold. The copper bearing sulphidic material is subjected to a main leach to provide a copper containing main leach liquor and a main residue. A secondary leach with ammonium thiosulphate solution is carried out on the copper bearing sulphidic material before the main leach, or on the residue from the main leach, to provide a gold containing secondary leach liquor and a secondary residue. Copper and gold are recovered from the respective leach liquors. Silver may also be recovered in addition to the gold.

Recovery of precious metals from metal sulphides

A process for recovery of zinc values contained in thermally activated iron containing copper and zinc sulfides in which said activated sulfides have been subjected to an acid leach in aqueous sulfuric acid to produce a solution of ferrous sulfate and a solids residue containing copper and zinc values. The solids residue containing copper and zinc values is reacted with an acidic copper sulfate solution to precipitate copper values as a simple copper sulfide with concurrent dissolution of iron and zinc values to form a solution of ferrous sulfate containing said dissolved zinc values and said solution of ferrous sulfate is separated from the simple copper sulfides and reacted with H.sub.2 S for precipitation of zinc values therefrom as zinc sulfide. Any nickel and cobalt values present in said activated sulfides is dissolved in said solution of ferrous sulfate and reacted with the H.sub.2 S at elevated temperature for selective precipitaton.

Recovery of copper and zinc as sulfides from copper-iron sulfides

An improvement in the process of producing substantially oxide free copper from copper salts by reacting an acidic aqueous solution which contains the copper salts with a reducing gas at elevated temperature and pressure to precipitate metallic copper. The improvement for producing copper in free-flowing powder form comprises providing in the aqueous solution a finite amount of an addition agent selected from the group consisting of polymeric polyamine compounds having amino groups linked by alkyl groups having 2 to 4 carbon atoms.

Production of copper by gaseous reduction

A hydrometallurgical process for treating iron containing metal sulfides for rendering iron and non-ferrous metal values active and amenable for selective extraction and separate recovery. Sulfur values can be controllably produced as elemental sulfur or as sulfuric acid to supply acid requirements of the process, while substantially obviating the discharge of sulfur-containing gases to the atmosphere. Ores and concentrates of the sulfides are thermally activated by sequentially heating and reducing said sulfides in a countercurrent flow of heating and reducing gases respectively in a reactor whereby the reaction products of the reducing gas and sulfides, together with liberated labile sulfur, are controllably combusted with oxygen to satisfy heat requirements of the thermal activation process and to convert sulfur values to SO.sub.2 gas. The activated sulfides are subjected to an acid leach in aqueous sulfuric acid for production of ferrous sulfate and evolution of H.sub.2 S gas which are separated from the solid sulfide residue containing concentrated non-ferrous metal values. The ferrous sulfate is oxidized and hydrolysed to precipitate the iron, which is removed from the system, and to regenerate sulfuric acid. At least a portion of the SO.sub.2 gas from said heating step and at least a portion of the H.sub.2 S from the acid leach are converted to sulfuric acid to satisfy the acid requirements of the process, and remaining SO.sub.2 is combined and catalytically reacted with remaining H.sub.2 S to produce elemental sulfur. The solids residue from the acid leach is subsequently subjected to further treatment for recovery of metal values.

Growing community of inventors

Edmonton, Canada

Roman M Genik-Sas-Berezowsky