Abstract: The recovery of noble metal(s) from noble-metal-containing material is generally described. The noble metal(s) can be recovered selectively, in some cases, such that noble metal(s) is at least partially separated from non-noble-metal material within the material. Noble metal(s) may be recovered from noble-metal-containing material using mixtures of acids, in some instances. In some cases, the mixture can comprise nitric acid and/or another source of nitrate ions and at least one supplemental acid, such as sulfuric acid, phosphoric acid, and/or a sulfonic acid. The amount of nitrate ions within the mixture can be, in some instances, relatively small compared to the amount of supplemental acid within the mixture. In some cases, the recovery of noble metal(s) using the acid mixtures described herein can be enhanced by transporting an electric current between an electrode and the noble metal(s) of the noble-metal-containing material.

Abstract: This invention provides a fine particle composite comprising fine powder of a sulfide or sulfide complex comprising a given element. The fine particle composite is obtained by a method for producing a fine particle composite comprising fine powder of a sulfide or sulfide complex comprising at least one element selected from the group consisting of molybdenum (Mo), rhodium (Rh), ruthenium (Ru), and rhenium (Re). Such method comprises steps of: preparing a solvent mixture from at least one compound containing an element selected from among molybdenum (Mo), rhodium (Rh), ruthenium (Ru), rhenium (Re), and sulfur (S); and subjecting the solvent mixture to a hydrothermal or solvothermal reaction. The resulting fine particle composite comprises fine particles of a sulfide or sulfide complex comprising at least one element selected from the group consisting of molybdenum (Mo), rhodium (Rh), ruthenium (Ru), and rhenium (Re).

Abstract: A process for slurry hydrocracking catalyst recovery is described. In one embodiment, the process includes separating effluent from a slurry hydrocracking zone into a first portion comprising solvent and clarified pitch and a second portion comprising pitch and catalyst. The second portion is contacted with an acid to leach the catalyst out of the pitch forming an aqueous solution and pitch residue. The aqueous solution is contacted with an anion to form an insoluble salt which is the catalyst.

Abstract: The present invention relates to methods for recovering precious metals including silver and gold, rare metals including indium and gallium, base metals including copper, lead and zinc or a combination of precious, rare and base metals from complex oxide ores, sulfide ores or oxide and sulphide ores using an acid chloride oxidizing leach.

Abstract: A process for producing a Group II metal sulfide phosphor precursor, comprising adding to an organic solvent an aqueous solution containing at least one of a Group II element compound, a sulfurizing agent, and a compound containing any of copper, silver, manganese, gold, and rare-earth elements to obtain a reaction mixture, heating the reaction mixture to produce an azeotrope of the water and the organic solvent, and removing water from the reaction mixture to produce a desired Group II metal sulfide in the reaction mixture, wherein the removal of water from the reaction mixture occurs by recovering only the water condensed from a vapor produced by the azeotropic distillation.

Abstract: The present invention relates to a method for the treatment of copper-bearing materials, such as copper concentrates, so that the impurities and gangue minerals in the materials, such as silicates, are in effect removed completely.

Abstract: The invention relates to a method for the treatment of material containing at least one valuable metal and arsenic to form a valuable metal-depleted scorodite sediment and a pure aqueous solution to be discharged from the process. According to the method, the valuable metals are first removed from the material to be treated and then arsenic precipitation from the solution is performed in two stages. By means of the method, the aim is to obtain as low a valuable metal content as possible in the scorodite sediment that will be formed. Likewise, the arsenic and valuable metal content of the aqueous solution that is formed during arsenic precipitation also remains so low that the water can be released into the environment.

Abstract: Processes are provided for recovering precious metals from refractory materials using thiosulfate lixiviants. The processes can employ heap leaching or lixiviants that include one or more blinding agents.

Abstract: A process for recovering nickel and cobalt values from nickel- and cobalt-containing laterite ores as an enriched mixed nickel and cobalt sulphide intermediate and for producing nickel and cobalt metal from the nickel and cobalt sulphide intermediate. The laterite ore is leached as a slurry in a pressure acid leach containing an excess of aqueous sulphuric acid at high pressure and temperature, excess free acid in the leach slurry is partially neutralized to a range of 5 to 10 g/L residual free H2SO4 and washed to yield a nickel- and cobalt-containing product liquor, the product liquor is subjected to a reductant to reduce any Cr(VI) in solution to Cr(III), the reduced product liquor is neutralized to precipitate ferric iron and silicon at a pH of about 3.5 to 4.0, and the neutralized and reduced product liquor is contacted with hydrogen sulphide gas to precipitate nickel and cobalt sulphides.

Abstract: A key-operating device includes a shell confining a chamber therein and connected to a video game apparatus with depressible keys, a lever pivotally mounted in the chamber and having protrusions projecting toward the keys, a wheel surrounding and connected to the shell and rotatable relative to the shell, and an actuating member projecting from the wheel and engageable with the lever in such a manner that rotation of the wheel results in engagement between the actuating member and the lever so as to permit fulcrum movement of the lever and pressing of the keys by the protrusions.

Abstract: The present invention relates generally to a process and an apparatus for flotation of sulphide minerals, such as sulphide minerals hosted in ores rich in magnesium minerals. The process involves grinding of the nickel ore rich in magnesium minerals and thereafter separation of the ground material into a coarse and fine stream of particles coarser than about 30 microns and finer than about 30 microns, respectively. Optionally, the fines stream may be further separated into a slimes fraction. The coarse and fine flotation streams are then fit to separate parallel flotation circuits. Acid and/or activator is added during flotation of the coarse stream only. Signficantly improved recoveries and grades were obtained with reduced acid consumption.

Abstract: A method of recovering precious metals from metal alloys produced aluminothermically from base metal smelter slag, includes treating the metal alloy with aqueous sulphuric acid solution having a pH of not greater than about 2 to cause dissolution of nickel and/or cobalt and iron and to cause formation of hydrogen sulfide which reacts with copper in the metal alloy to form a copper sulfide precipitate containing at least one precious metal, and separating the copper sulphide precipitate containing at least one precious metal from the remaining solution containing cobalt sulphate and/or nickel sulphate and ferrous sulphate.

Abstract: A technique is presented for the sequential extraction of nearly pure metal sulfides from solutions containing a mixture of metals, such as acid mine drainage. The technique is based on analysis of naturally occurring biofilms that selectively concentrate zinc, in zinc-sulfide, from a complex natural groundwater solution associated with a subsurface metal-sulfide mine. It was predicted and shown experimentally that release of sulfide ions, due to the activity of sulfate reducing bacteria, leads to sequential precipitation of pure metal sulfide phases from a solution of mixed metal ions, so long as the rate of production of sulfide ions does not exceed the rate of supply of the metal ions. This observation makes possible the design of biochemical processes to harness sulfate-reducing bacteria to separate and recover metals from mixed-metal waste streams.

Abstract: A process is provided for the direct recovery of nickel and cobalt from a nickeliferous oxide ore leach slurry by ion exchange. A nickeliferous ore is leached with mineral acid to solubilize the metals. The resulting leach slurry is contacted with ion exchange resin, which selectively loads the nickel and cobalt from the pulp. The resin is separated from the leach slurry by screening and then stripped with an acidic solution. After stripping, the resin is returned to the loading cycle. Nickel and/or cobalt can be recovered in substantially pure form from the eluate by known processes. The metal-depleted slurry proceeds to waste treatment and disposal. This process eliminates the difficult solid/liquid separation, which would otherwise be required to recover metals values from the pregnant leach slurry.

Abstract: The invention relates to a method for recovering non-ferrous metals, particularly nickel, cobalt, copper, zinc, manganese and magnesium, from materials containing said metals by converting said non-ferrous metals into sulphates by means of melt and melt coating sulphation, i.e. by a thermal treatment under oxidizing conditions within a temperature range of 400 to 800° C., during which a reaction mixture is formed containing at least one said non-ferrous metal, iron(III)sulphate and alkali metal sulphate, and appropriate reaction conditions are selected to substantially prevent iron(III)sulphate from thermally decomposing to hematite, and finally, said non-ferrous metals are recovered as metallic compounds. In the method of the invention, a process is formed around the melt and melt coating sulphation, which comprises nine steps.

Abstract: The invention relates to a method for the treatment of fluoboric electrolyte resulting from the processes of electro-extraction of metals such as copper and lead comprising a leaching stage with fluoboric acid, in order to recycle said fluoboric acid to be recirculated to said leaching stage devoid of impurities of metals such as Me=Fe, Zn, Ca, Mg, Cd, characterized in that it comprises the stages of: a) treating said fluoboric electrolyte comprising Cu(BF4)2 or Pb(BF4)2 with H2S in order to precipitate CuS or PbS respectively in accordance with the reactions Cu(BF4)2+H2S=>CuS+2HBF4  (1) Pb(BF4)2+H2S=>PbS+2HBF4  (2) thus obtaining a solution of HBF4 containing the fluoborates of said metals Me, said solution being separated, b) treating said Me fluoborates with H2SO4 in accordance with the reaction 2 Me(BF4)n+n H2SO4=>Me(SO4)n+2n HBF4  (3) (where Me=Fe, Zn, Ca, Mg, Cd) it being possible for said sulp

Abstract: In a process for separating tin as well as, if required, copper from scrap melts, in particular, tinplate melts or metallic melts as formed in the working up of waste or metal-oxide-containing combustion residues, the carbon content of the melt is adjusted to 3 to 4.2% by weight and hot wind, oxygen or air enriched with oxygen is locally blown on partial regions of the surface of the melt bath, whereby SnO is discharged, via the gaseous phase, from the redox-gradient-exhibiting zone formed between the carbon-rich bath and the iron oxides produced by top-blowing.

Abstract: There is disclosed a process for separating and recovering nickel and copper values from a nickel-copper matte which may contain iron and arsenic. Finely divided nickel-copper matte undergoes one or more steps of sulphuric acid leaching at atmospheric pressure to produce a nickel sulphate solution and an iron and/or arsenic containing copper-rich sulphide residue. The copper-rich sulphide residue is repulped in sulphuric acid solution to selectively redissolve most of the iron and arsenic and the iron and arsenic containing solution is separated from the copper-rich residue. The iron and arsenic are largely precipitated from the leach solution in a pressure hydrolysis step and the iron and arsenic containing precipitate is separated and discarded. The iron and arsenic-depleted solution is recombined with the copper-rich sulphide residue from the acid repulp step and the resulting slurry is treated in a non-oxidizing pressure leach in which nickel arsenic and iron are extracted.

Abstract: A process for removing H2S and mercaptans from gas streams. The process comprises contacting such gas streams with an aqueous solution of copper complex of a water soluble amine to form water insoluble copper sulfide and regenerate free water soluble amine. The copper sulfide is removed from the system and recovered. Lastly, additional copper complex of the water soluble amine is formed by reacting the regenerated water soluble amine with a copper compound.

Abstract: By using a method of removing silver in the form of sparingly soluble silver salt, especially silver sulfide, from a solution containing another silver compound, such as a silver thiosulfate complex in a photographic fix or rinsing fluid by precipitation, the solution is subjected to electromagnetic irradiation with a wavelength below 375 nm. The irradiated liquid is led through a filter-like means 33 which binds the silver sulfide to its surface as crystalline silver sulfide. As a result, the silver sulfide is precipitated and deposited on the surface of the means as solid silver sulfide which in its turns acts as a catalyst for further precipitation and depositing of solid silver sulfide on the surface of the means. By binding the solid silver sulfide to the surface of the means, the required capacity of a possible subsequent filter is reduced.

Abstract: Disclosed herein is a method for treating a spent copper-refining electrolyte to remove impurities such as copper (Cu), arsenic (As), antimony (Sb), bismuth (Bi), nickel (Ni) and the like by using a hydrogen sulfide gas. The method comprises the steps of: (a) blowing a hydrogen sulfide gas into the spent electrolyte to precipitate copper sulfide (CuS); (b) blowing air into the coprecipitates solution obtained in the above step (a) to oxidize arsenic, bismuth and antimony thereby redissolving them into the solution, and the solution is subjected to solid-liquid separation to separate copper sulfide from the liquid; (c) blowing a sulfur dioxide gas into the copper-depleted liquid to reduce arsenic, bismuth and antimony and blowing a nitrogen gas to purge the remaining sulfur dioxide gas; (d) blowing a hydrogen sulfide gas to precipitate arsenic, bismuth and antimony in the form of sulfides and blowing a nitrogen gas to purge the remaining hydrogen sulfide gas and separating arsenic sulfide (As.sub.2 S.sub.

Abstract: A process is disclosed for recovering zinc, lead, copper and precious metals from zinc plant residue, said process comprising leaching the residue with return zinc spent electrolyte, neutralizing residual acid and reducing ferric iron in the solution by addition of zinc sulphide concentrate in the presence of a limited quantity of oxygen, flotation of the resulting slurry to separate unreacted zinc sulphide, treatment of flotation tailings with sulphur dioxide and elemental sulphur to further leach iron, zinc and impurity elements and precipitate copper, flotation of the resulting slurry to separate a copper sulphide concentrate, thickening, filtering and washing of the flotation tailings followed by addition of lime and sodium sulphide to activate lead sulphate and flotation of a lead concentrate from the residue.

Abstract: A process for selectively recovering dissolved heavy metals from a solution is disclosed that involves selectively reacting a xanthate with such dissolved heavy metals. Selective reaction of a xanthate with selected dissolved heavy metals is accomplished by conducting the reaction under conditions such that only some of the heavy metals react with the xanthate, to the exclusion of reaction with other dissolved heavy metals. Selectivity of the reaction is particularly influenced by the pH at which the reaction occurs. Typically, the reaction should occur at a pH below about 4.0. Xanthates, once reacted, can be separated from the heavy metal xanthate reaction product and recycled for use within the process. Purified heavy metal product can be produced if desired.

Abstract: A method of increasing the extraction of tellurium from copper electrorefining slime comprises leaching the slime with dilute sulphuric acid in a reactor under a partial oxygen pressure of up to 150 psi and at an elevated temperature between about 100.degree. and 200.degree. C. until copper, nickel and substantially all of the tellurium is dissolved, thereby forming a leach slurry, and contacting the slurry with an appropriate reducing agent immediately after the leaching operation has been halted and the leaching reactor brough back to atmospheric pressure to reprecipitate any excessive quantities of silver and selenium solubilized during the leaching operation.

Abstract: According to the method of the invention, at least one or several of the metals nickel, cobalt and copper can be selectively precipitated as sulphide by aid of elemental sulphur from aqueous solutions containing other metals such as zinc. The temperature of the reaction is above the melting point of sulphur. The precipitation is carried out with a pH value below 2. The metals to be precipitated can be present in the solution either as oxides or sulphates. If the metals are sulphates, the sulphide of at least one of the metals is prepared to crystal seeds in the solution before precipitation.

Abstract: A process is disclosed for recovering silver sulfide from a spent photographic fixer solution, which contains silver. The process is particularly suited for treating the fixer solution in a manner which enables recycling of the solution giving rise to considerable reduction in cost of fixer solution and reduced environmental pollution. The process comprises introducing a hydrosulfide reagent into the fixer solution, which contains silver, to precipitate silver sulfide while maintaining pH and thiosulfate levels in the fixer to allow for reuse. The precipitate is isolated from the fixer solution to remove silver thereby and hence enable recycling of the fixer solution.

Abstract: A process for removing at least a portion of any iron, copper, nickel and chromium ions that are chelated by a alkylenepolyamine polyacetic acid or salt in an aqueous liquid waste. The process comprises the steps of (a) adjusting the pH of the liquid to above about 10; (b) adding sufficient sodium sulfide to react with at least a portion of the copper ions; (c) separating precipitated iron and copper compounds; (d) adding nitric acid to adjust the pH to the range of about 6 to 8; (e) adding sufficient sodium nitrite to the liquid to react with at least a portion of the nickel and chromium present; (f) heating the liquid to above about 575.degree. F. for at least about 15 minutes to facilitate precipitation of nickel and chromium; and (g) separating precipitated solids to leave a non-hazardous filtrate.

Abstract: A process for recovering gold from refractory gold-bearing ores uses sulfurous acid as the leaching agent to form a gold-sulfite complex. The ore is ground, slurried blended with a chelating agent and then subjected to a simultaneous dissolved SO.sub.2 leaching and anion exchange resin adsorption step in the presence of dissolved oxygen. The gold transfers to the resin which is later separated from the resin by chemical stripping.

Abstract: A process for recovering gold from gold-bearing ores includes the steps of forming a slurry of ground ore and treating the ore with an oxidizing and complexing agent such as hydrogen sulfide or a sulfide salt. A chelating agent, SO.sub.2, air, and an anion exchange resin are added to the slurry to subject the ore to a simultaneous sulfurous acid leaching and anion exchange resin adsorption step in the presence of dissolved oxygen. The gold transfers to the resin which is then removed from the slurry. The gold is then separted from the resin by chemical stripping. Alternately, the ground ore is blended with an oxidizing agent such as calcium hypochlorite and then with a gold-complexing agent. The ore blend is slurried in water, with the addition of a chelating agent, SO.sub.2, air and an anion exchange resin to effect the leaching and adsorption of gold values.

Abstract: A process is provided for working up dusts which have been precipitated electrostatically from the gas mixture composed essentially of carbon monoxide and phosphorus vapor produced in the electrothermal production of yellow phosphorus, which process comprises converting the dusts into a calcinate at 300.degree. to 800.degree. C. under oxidizing conditions in a first step, leaching the calcinate with phosphoric acid in a second step, adjusting the pH of the solution in phosphoric acid to 0 to 1.5 with sodium hydroxide solution in a third step, precipitating the sulfides of lead, copper and cadmium from the partially neutralized solution in phosphoric acid by adding sulfide and filtering them off in a fourth step, adjusting the pH of the filtered, partially neutralized solution in phosphoric acid to about 1.5 to 5.

Abstract: This invention is a process for removing mercury from the desorption or cyanide liquor of a precious metal recovery, cyanide leach system. A sulfide ion-producing compound and a flocculating agent are added to the desorption liquor to form and flocculate mercuric sulfide. The desorption liquor typically has a cyanide concentration of between about 0.5 percent and about 2.0 percent by weight. The flocculated mercuric sulfide is separated from a substantially mercury-free precious metal-containing, cyanide solution.

Abstract: A process for the extraction of silver and gold from refractory ore is disclosed. The process includes first grinding the refractory ore. This ground refractory ore is subsequently treated with an alkali solution of a stoichiometric excess amount of sulphide in relation to the amount of gold and silver contained in the refractory ore, to thus form a pulp containing a gold and silver sulfide. The pulp and alkaline solution ore are aerated to oxidize the excess sulfide to sulfate and then a mixture of the pulp and cyanide liquor are formed. Finally this mixture is aerated to obtain a final gold and silver product.

Abstract: The invention relates to a process for recovering silver in sulfuric solutions. Its characterizing feature is that the silver solution is contacted with a quantity of zinc sulfide which is at least equal to the stoichiometric quantity and the surface area of which is at least equal to K Ag.sup.2/3 x V, K being a constant, Ag being the silver concentration in the solution expressed in kilograms per cubic meter, and V the volume of the solution in cubic meters, the surface area being expressed in square meters and the value of K being greater than or equal to approximately 10. Application to the recovery of silver in zinc plant residues.

Abstract: A process for the treatment of a complex manganese ore, wherein it comprises the following stages:(a) crushing the ore,(b) subdividing the crushed ore into a first part and a second part,(c) preparing the first pulp from the first part of the crushed ore,(d) reacting the first pulp with a reducing agent to obtain a manganous sulphate solution,(e) separating the liquid phase constituted by the thus obtained manganous sulphate solution from the solid phase of the thus treated first pulp,(f) preparing a second pulp from the second part of the crushed ore,(g) subjecting the second pulp to a solubilization treatment of the nickel, copper and cobalt by reacting it hot with sulphuric acid and the manganous sulphate solution obtained in stage (e),(h) separating the liquid phase and the solid phase of the thus treated second pulp, and(i) recovering the nickel, copper and cobalt from the liquid phase separated in stage (h).

Abstract: A process is described by which copper and optionally silver and gold are recovered from sulfide and oxide ores, concentrates or slag, which contain the metals. The particulate materials are treated with an aqueous solution of an alkali cyanide or alkaline earth cyanide, the laden solution is filtered, if desired, a water-soluble sulfide compound is added to the laden solution or filtered laden solution, the laden solution is subsequently adjusted to a pH value below 5 by an addition of acid to precipitate the metal sulfide, which is filtered off, and the resulting hydrocyanic acid is recovered. The process steps of precipitation and filtration of the metal sulfide and the recovery of the free hydrocyanic acid contained in the filtrate are carried out under superatmospheric pressure of 1.5 to 15 bars. The precipitation is preferably effected at a pH value of 1.5 to 2.0. The free hydrocyanic acid is recovered as alkali cyanide or alkaline earth cyanide and is recirculated to the leaching stage.

Abstract: A process for separating precious metals from a roaster calcine leach residue from a process wherein copper or zinc sulfides are roasted to produce a copper or zinc calcine; the calcine is leached with an aqueous sulfuric acid leaching solution to produce a copper or zinc-containing leaching solution and a roaster calcine leach residue and the copper or zinc-containing leaching solution is separated from the roaster calcine leach residue wherein the process comprises:(a) intimately contacting the roaster calcine leach residue with an aqueous sulfuric acid leach solution containing from about 5 to about 200 grams per liter of sulfuric acid to produce a slurry of leach solution and roaster calcine leach residue and to dissolve precious metal from roaster calcine leach residue;(b) adding copper or zinc sulfide solids to the mixture of leach solution and said roaster calcine each residue;(c) agitating the copper or zinc sulfide solids in intimate contact with the mixture of leach solution and roaster calcine leac

Abstract: There is disclosed a novel method of recovering valuable metals from an industrial by-product containing copper and arsenic and at least one metal selected from among lead, zinc, iron, silver and cadmium, said method comprising leaching the by-product with sulfuric acid in an SO.sub.2 gas atmosphere at a temperature of 70.degree. C. or higher in the presence of a solid sulfide to thereby precipitate copper selectively as copper sulfide while dissolving other metal or metals in the leach solution and then separating the copper containing precipitate from the leach solution, said leach solution containing substantially no copper.

Abstract: Process for treating oxidized ores with a manganiferous matrix to recover the small quantities of copper, nickel and cobalt, which consists of attacking the aforementioned ore by means of an aqueous solution of H.sub.2 SO.sub.4 with the simultaneous injection of sulfur dioxide, at a temperature which does not exceed boiling point of the medium, at a pH less than 1.5; introducing an alkaline sulfide to precipitate the copper, nickel and cobalt sulfides in the suspension resulting from the attack; and separating by sulfides and the residue by flotation. The process is applicable to attacks on manganiferous nodules obtained from ocean beds as well as to attacks on land manganiferous matrix oxidized ores.

Abstract: A Bayer process solution is filtered through a bed of particles of a granular substance containing Fe.sub.2 O.sub.3 to remove copper and zinc species from the solution. The particles preferably have an Fe.sub.2 O.sub.3 content of about 40 to 100% by weight. For more effective removal of zinc, the particles are coated with a metal sulfide, preferably zinc sulfide.

Abstract: This invention relates to environmentally sound hydrometallurgical methods and processes for extraction of cobalt, nickel and silver from complex concentrates. The finely ground minerals are converted during an oxidative caustic leach at elevated pressures and temperatures to insoluble metal hydroxides and are separated from soluble sodium arsenate and sodium sulphate. Cobalt and nickel are extracted from the caustic cake during a two-stage sulphuric acid leach. Solution purification for cobalt and nickel recovery proceeds on the basis that only one waste residue and one liquid effluent are generated which meet strict environmental standards. A small amount of cyanidation residue is generated after silver extraction by cyanidation from the acid leach residue. Metal values extraction reaches +99.0%. Arsenic and sulphur can be recovered in an innovative recycle system as sodium, zinc or copper arsenate chemicals and as anhydrous sodium sulphate.

Abstract: The metal content of nickel-cobalt mixed sulfide slurries is recovered by atmospheric oxidation leaching, thereafter removing dissolved copper by metathesis with further mixed sulfide feed, treating the filtrate after liquid-solids separation with ammonia to selectively precipitate cobalt, separating the cobalt precipitate and working up the resulting filtrate to recover nickel.

Abstract: A process for leaching copper and arsenic from copper dross containing copper arsenide and separated from molten lead bullion comprises leaching the dross with an aqueous ammoniacal solution containing arsenate as the predominant anion under oxidizing conditions to obtain a leachate, removing copper from the leachate to obtain a raffinate and re-cycling raffinate to the leaching stage, and removing a bleed of raffinate from the circuit and precipitating a substantially insoluble arsenic compound from the raffinate bleed to remove arsenic from the circuit.

Abstract: A process is provided by which dissolved metals may be recovered from aqueous waste solutions and converted to a particulate material, which may in turn be used as a filler for products such as asphalt. The process involves effecting reaction in the solution to produce a sludge comprised of metal hydroxides and sulfides, and admixing lime with a concentrate thereof to ultimately produce the filler.

Abstract: A process for the recovery of silver values from silver-containing material which also contains iron and arsenic includes leaching the material under oxidizing conditions at elevated temperature and pressure in aqueous nitric acid solution to dissolve a substantial amount of silver together with substantial amounts of arsenic, iron and other metals if present. The resultant leach solution is separated from undissolved leach residue and treated with a solution containing chloride ions to selectively precipitate substantially all dissolved silver as silver chloride without significant co-precipitation of other dissolved metals. The silver chloride precipitate is then separated from the remaining solution.

Abstract: A finely-ground nickel-copper matte is leached using an acid at a minimum temperature of approx. 80.degree. C. and under oxidizing conditions in order to produce a nickel sulfate solution and a nickel-cooper sulfide residue, which is separated from the solution and thereafter the nickel-copper sulfide residue is leached using acid in an autoclave at a minimum temperature of 110.degree. C. and under oxidizing conditions in order to produce an additional quantity of nickel sulfate solution and a copper sulfide precipitate.

Abstract: A process for the recovery of copper and zinc values from copper and zinc containing sulphidic ore includes subjecting ground ore to a flotation operation. An initial copper concentrate is floated in a first flotation step, and the initial copper concentrate is fed to a second flotation step to float a relatively zinc free copper concentrate. Remaining ore from the first flotation step is fed to a third flotation step to float an initial zinc concentrate, and remaining ore from the third flotation step is fed to a fourth flotation step to float a copper and zinc containing material. An intermediate concentrate containing from about 5 to about 25% copper and from about 2 to about 25% zinc, with a total of at least about 12% copper and zinc, is produced by selecting at least the remaining ore from the second flotation step, and a zinc concentrate containing at least about 20% zinc is produced by at least selecting a portion of the initial zinc concentrate.

Abstract: A process for the production of a sulphidic copper concentrate from a complex sulphidic concentrate containing as its main constituents copper, iron and at least one non-ferrous metal selected from the group consisting of zinc, lead, nickel and cobalt, comprising mixing the complex sulphidic concentrate with a copper-containing predominantly chloridic solution thereby to form a suspension, and treating the suspension thus obtained at elevated temperature and pressure at a pH-value of below 3, thereby to form a sulphidic copper concentrate, thereby the non-ferrous metals being extracted from the concentrate without formation of significant amount of acid. Precious metals may also be present. Advantageously the ratio by weight of the complex concentrate added to the copper-containing predominantly chloridic solution to the copper content of the solution is such that the predominantly chloridic solution after being at least partly freed from copper by an exchange reaction has a potential at 60.degree. C.

Abstract: A multi-step process for recovering metal values from lead smelter matte. The matte is mixed with sulfuric acid and manganese oxide and leaching is effected at atmospheric pressure to form an aqueous solution including dissolved metal sulfates and a residue containing sulfur and lead sulfate. The sulfur is removable by conventional means and the lead sulfate may be returned to the smelter. The pH of the aqueous sulfate solution is adjusted to 3.5 to 4.5 to precipitate ferric iron and arsenic and pH is readjusted to about 3.0 to redissolve coprecipitated copper. After separation from the precipitate, the aqueous solution is mixed with a sulfiding agent, such as sodium sulfide at a pH of not more than 3 to selectively precipitate copper sulfide. After separating the copper sulfide, the aqueous solution is mixed with further sulfiding agent at a pH of 3 to 4.5 to form a cobalt-nickel sulfide precipitate in which the weight ratio of copper-nickel to sulfur is 1.8.

Abstract: A process for thermal activation of chalcopyrite-pyrite ore concentrates for activation of iron values in both chalcopyrite and pyrite constituents whereby said iron values can be selectively removed in a subsequent acid leach. Controlled oxidizing conditions are maintained in an oxidizing heating zone for removal of up to about 90% of total sulfur to be removed for conversion of pyrite and chalcopyrite to their acid-leachable forms, measured by a preferable oxidation of 10 to 15% of iron in the concentrate to ferromagnetic oxides, whereby remaining total sulfur to be removed is removed in a reducing zone with the assistance of a low H.sub.2 S/(H.sub.2 +H.sub.2 S) ratio by scavenging of H.sub.2 S by said oxides.

Abstract: Alkali metal sulfides are regenerated from alkali metal hydrosulfides which are produced as a result of the hydroconversion of heavy carbonaceous feeds. The regeneration is effected by contacting the alkali metal hydrosulfide with a metal oxide at elevated temperatures.