Abstract: A bacterially assisted heap leach characterized by the steps of: providing an ore heap to oxidize sulphide minerals therein; providing a biological contactor inoculated with ferrous iron oxidizing bacteria; providing at least one leach solution pond to feed solution to, and receive leach solution from both the heaps; and bleeding a portion of the leach solution and passing same to a means for metals recovery.

Abstract: A method of recovering metal and/or oxide thereof from a slurry is described. The method involves magnetically separating at least a portion of any magnetic impurities from the slurry and then leaching or dissolving at least a portion of any remaining magnetic impurities in a slurry. At least one chelating agent can then be added to the slurry and the solids can be recovered from the slurry by various separation techniques. The methods of the present invention are particularly useful in the recovery of tantalum and/or oxide thereof especially tantalum and/or oxide thereof having a very fine size.

Abstract: The present invention involves a system and method of making ferric chloride with reduced amounts of hydrochloric acid for water treatment. The method comprises preparing a reactant batch comprising ferric oxide and hydrochloric acid at a predetermined molar ratio. The method further includes mixing the reactant batch with an impeller rotating between about 60 and 150 revolutions per minute. The method further includes maintaining the reactant batch at a temperature between about 70° Fahrenheit and 180° Fahrenheit. The method forms a reaction product including ferric chloride and a reduced amount of hydrochloric acid.

Abstract: An anode of a cell for the electrowinning of aluminium comprises a nickel-iron alloy substrate having an openly porous nickel metal rich outer portion whose surface is electrochemically active. The outer portion is optionally covered with an external integral nickel-iron oxide containing surface layer which adheres to the nickel metal rich outer portion of the nickel-iron alloy and which in use is pervious to molten electrolyte. During use, the nickel metal rich outer portion contains cavities some or all of which are partly or completely filled with iron and nickel compounds, in particular oxides, fluorides and oxyfluorides.

Abstract: A process for removing chloride from chloridic iron oxide comprises mixing said chloridic iron oxide with an acid and subsequently conducting a thermal treatment at from 50 to 1300° C.

Abstract: The process chemistry during the oxidation of molybdenite concentrates in an oxygen pressure leach can be controlled by regulating the amount of ferric iron and excess sulfuric acid recycled as autoclave discharge slurry or filtrate to the autoclave feed. A computer model capable of predicting the concentration of soluble molybdenum in the autoclave discharge and based on the concentrate and recycle analyses was developed.

Abstract: An industrially excellent process for producing a poly(meth)acrylate having a reduced metal content which comprises contacting a mixture of a poly(meth)acrylate and an organic solvent with an acidic aqueous solution, such as an aqueous solution obtained by dissolving a polyprotic carboxylic acid having about 2 to 12 carbon atoms in water, is provided, and, by this invention, contents of metals such as sodium, potassium, iron and the like can be remarkably reduced.

Abstract: A hydrometallurgical process utilizing an atmospheric calcium chloride leach to selectively recover from various metal feed stocks (consisting of elemental metals, metal oxides, metal ferrite, metal hydroxide, metal carbonates, metal sulfate/sulfur compounds, and their hydrates, specifically including but not limited to EAF Dust KO61) zinc, lead, cadmium, silver, copper and other valuable metals to the exclusion of iron, magnesium, halogen salts and other unwanted elements. The process solves the problem of iron and magnesium leach solution contamination because iron is unexpectedly converted to magnetite. The heavy metals are cemented out of solution using zinc or other selected dust at a pH of 6 or greater under unique and unexpected conditions, which do not require acid.

Abstract: The invention relates to an effective and environmentally safe process for the microbial leaching of sulfidic materials, particularly of sulfide ores such as pyrite, marcasite, chalcopyrite, bornite, or covelline, which process is characterized in that the aqueous leaching fluid is added with sulfur-containing amino acids or derivatives thereof. The invention is also directed to the use of sulfur-containing amino acids or derivatives thereof in the microbial leaching of sulfidic materials, particularly in pyrite leaching.

Abstract: A process for the oxidative leaching of sulphide mineral species, the method characterised by the method steps of: leaching a slurry containing the mineral species in one or more reaction vessels; circulating a stream of leach liquor to a flash cooler; flashing the liquor in the flash cooler at a pressure less than atmospheric pressure so as to dissipate heat; and recirculating the liquor to the or each reaction vessel.

Abstract: The invention relates to a method for the hydrolytic precipitation of iron from a sulphate solution as jarosite. A sulphate-containing solution, with iron present in divalent form, is routed to an iron precipitation stage, where the iron is oxidised to the trivalent form using an oxygen-containing gas. Also present in the precipitation stage are Na, K or NH4 ions and jarosite nuclei.

Abstract: The present invention provides methods for the isolation and production of magnesium products from leaching of laterite material with acid. A magnesium compound is formed by downstream treatment of a leach stream after at least one of nickel or cobalt have been brought into solution. Magnesite is then obtained by adding at least one of alkali metal or alkaline earth metal carbonate to the leach stream. The magnesite may be converted into magnesium chloride by adding an acid, such as HCL.

Abstract: A hydrometallurgical process is provided for leaching nickeliferous laterite ores at temperatures below the boiling point of the pulp and at atmospheric pressure. The high iron fraction of the laterite, referred to as limonite, is first contacted with concentrated sulfuric acid to partially or completely dissolve the iron and nickel into solution. A reducing agent is used to keep the redox potential in solution below 1000 mV to enhance cobalt dissolution and more advantageously between 1000 and 900 mV to avoid reduction of ferric iron. Further mixing of the leach slurry in the presence of sodium, potassium, or ammonium allows formation of iron jarosite at ambient pressure. The resulting acid from iron hydrolysis is neutralized with the low iron fraction of the laterite ore (saprolite), thereby dissolving nickel into solution. The resulting final leach slurry can then be treated with conventional methods to recover nickel and cobalt from solution.

Abstract: Liquor compositions for the extraction of metallic elements from a metal-contaminated starting material such as mineral ores, recyclable wastes, contaminated soils, toxic wastes such as dusts producing through steelmaking processes by effectuating preferably prolonged contacting of such starting material with the liquor to cause the underlying structure of the starting material to be broken down. The contaminated starting materials are more susceptible to metal separation because the released metallic element are readily solubilized in the contacting liquor. Compositions of the contacting liquor comprise caustic silicate solutions containing essentially saturating levels of silica. Once the plurality of metallic elements contained in the starting material have been solubilized, they tend to remain in solution, and then may be routinely extracted and removed using conventional extraction methodologies such as precipitation of insoluble salts, electrowinning, or electrodeposition.

Abstract: A system 10 is provided to recycle a waste gas stream 32 of an autoclave 20 to re-use oxygen in the waste gas stream 32 to compliment an oxygen feed stream 19 to the autoclave 20, thereby recycling the waste gas stream 31 to avoid the necessity of having to continuously purge the waste stream 32 of contaminants, while also reducing the amount of oxygen necessary in the feed stream 19 to the autoclave 20. The waste gas stream 32 is also pressurized to be substantially similar in pressure to that of the feed stream 19 to the autoclave 20.

Abstract: A method for producing small spherical particles that are especially useful as catalysts and catalyst supports employed in chemical processes is disclosed. According to some embodiments, the method includes impregnating a porous support with a metal or metal oxide and dissolving the support to release spherical particles. In certain embodiments the support that is employed in the method comprises a number of spherical voids which determine the size of the spherical particles, and preferably have micrometer range diameters. One embodiment of an attrition resistant Fischer-Tropsch catalyst comprises a plurality of micrometer size spherical metal and/or metal oxide particles that are prepared according to the above-described method.

Abstract: A hydrometallurgical process for the recovery of nickel and cobalt values from a sulfidic flotation concentrate. The process involves forming a slurry of the sulfidic flotation concentrate in an acid solution, and subjecting the slurried flotation concentrate to a chlorine leach at atmospheric pressure followed by an oxidative pressure leach. After liquid-solids separation and purification of the concentrate resulting in the removal of copper and cobalt, the nickel-containing solution is directly treated by electrowinning to recover nickel cathode therefrom.

Abstract: Fairly pure metallic nickel may be efficiently dissolved in non-oxidizing acid. If the nickel includes individual pieces longer than 0.5 mm in any linear dimension, oxidizing agent is preferably added from the beginning of dissolution, while if the nickel is powdered so that no single piece has a linear dimension longer than 0.35 mm, oxidizing agent is preferably added only after most of the originally supplied nickel has been dissolved. After oxidizing agent is added, most or all of the remaining undissolved nickeliferous solid will then dissolve. The temperature of the reaction mixture of acid liquid and solid nickel preferably is room temperature at the beginning of dissolution but is raised in steps to a final value of at least 65° C. and maintained at that temperature for several hours.

Abstract: The present is a hydrometallurgical procedure for nickel and cobalt recovery, which involves leaching with ammonia-ammonium carbonate solution of the nickel and cobalt bearing mineral material, using a tubular reactors aid mineral material is previously submitted to processes such as selective reduction, cooling, new ammonia leaching, liquid/solid separation and/or nickel and/or cobalt extraction by solvent or ion-exchange resin, allowing the recovery of all the extractable nickel and up to the 130% cobalt extraction reported by the standard ammonia-ammonium leaching.

Abstract: A method for dissolving base metals and noble metals from ores having base metals and noble metals which comprises adding the ore to a solution of a non-acid oxidizing agent, then adding an aqueous solution of an acid forming halide and then adjusting the H+ concentration of the combined solutions to a minimum H+ concentration of 1 mol/l.

Abstract: A method of decontaminating a radioactively contaminated oxide on a surface. The radioactively contaminated oxide is contacted with a diphosphonic acid solution for a time sufficient to dissolve the oxide and subsequently produce a precipitate containing most of the radioactive values. Thereafter, the diphosphonic solution is separated from the precipitate. HEDPA is the preferred diphosphonic acid and oxidizing and reducing agents are used to initiate precipitation. SFS is the preferred reducing agent.

Abstract: A method for processing alumina-bearing ores such as bauxite to recover iron, aluminum, silicon and titanium metal values therefrom the method comprising the steps of adding the alumina-bearing ores to a digester containing an acid to provide a mixture of acid and alumina-bearing ores and heating the mixture to dissolve soluble compounds of at least one of iron, aluminum, silicon and titanium to provide a digest containing dissolved salts of the soluble compounds and to provide a gas component. Thereafter, the digest is treated with water to dissolve water soluble salts therein to provide a slurry comprised of a liquid containing water and the dissolved soluble salts and a solid component comprised of silica. The solid component is separated from the liquid and the pH of the liquid is adjusted to form an aluminate and an iron-containing precipitate.

Abstract: A method of leaching sulphidic material that contains metals and arsenic under oxidising conditions and with the aid of microorganisms is characterised by mixing the material with an acid aqueous solution to form a pulp, and in that the material is leached in a first leaching stage at a pH of below 2 and at a temperature that ranges from room temperature to about 55° C. in the presence of an active quantity of microorganisms of the mesophilic and/or moderately thermophilic type, wherewith the major part of the arsenic content of the material and possibly also part of its metal content is/are leached-out and the arsenic leached from said material is oxidised successively to a pentavalent state.

Abstract: A method of extracting active mineral liquid from a rock such as granite is described. This method comprises charging an extraction vessel with finely divided granite at ambient temperature and pressure; introducing an aqueous ammonia solution with agitating and then diluted sulfuric acid into the vessel; introducing 98% ethyl alcohol at below 80° C. into the vessel to elevate the inner pressure of the vessel to 2-3 kg/cm2 for facilitating the formation of complexes; and agitating the resulting reaction mixture for 20-160 minutes at 80° C. to 85° C. while maintaining the internal pressure of the vessel. The active mineral liquid is advantageously used as a mineral source for soils, animals, plants, the human body and so forth, and as an agent for the purification of waterworks as well as for the treatment of wastewater.

Abstract: A process for the extraction of alumina, iron oxide and titanium dioxide from bauxite ore and clays, and other ore bodies and feedstocks. The process starts by sulfuric acid leaching of the feedstocks in pressure autoclaves at about 200° C. and appropriate pressure. A leach liquor of sulfate salts of aluminum, iron and titanium is obtained. Any iron values are converted to a ferrous state. A recycled potassium sulfate helps produce double aluminum alkali sulfate crystals in the reduced leach liquor. The crystals are removed at about 20°-60° C. with the help of SO2 gases that reduce the ferric. Such double salt is hydrolyzed into a basic aluminum alkali precipitated sulfate salt. This is then dried and calcined at about 950° C. Any alkali sulfate is washed out and recycled. The remainder is alumina. The ferrous sulfate is crystallized out at about 10° C. It is dried and calcined at about 450° C. to produce an iron oxide mixed with other sulfate salts that can be washed out and recycled.

Abstract: A hydrometallurgical process for the recovery of nickel and cobalt values from a sulfidic flotation concentrate. The process involves forming a slurry of the sulfidic flotation concentrate in an acid solution, and subjecting the slurried flotation concentrate to a chlorine leach at atmospheric pressure followed by an oxidative pressure leach. After liquid-solids separation and purification of the concentrate resulting in the removal of copper and cobalt, the nickel-containing solution is directly treated by electrowinning to recover nickel cathode therefrom.

Abstract: A process for removing impurities contained in the crystal lattice of minerals, comprising the steps of forming a mixture of a mineral capable of structurally reorganizing its crystal lattice which contains an impurity in its crystal lattice and a halogen anion, and water; heating the mixture to the mineral's structural reorganization transition temperature; holding the mixture at the structural reorganization transition temperature for a sufficient period of time to allow the impurity to freely migrate from the lattice to combine with the halogen anion; and separating the combined impurity and anion from the mixture to render the mineral essentially free of the impurity. The process is applicable to numerous minerals and impurities, but is especially useful to remove arsenic from fluorspar. Numerous halogen anions can be employed, such as chlorides, fluorides, bromides and iodides, but the preferred halogen anion is a metal chloride such as calcium chloride.

Abstract: The present invention relates to an apparatus and a process for producing zinc oxide from a zinc-bearing material. The process according to the present invention comprises the steps of leaching the complex sulfide material with hydrochloric acid and oxygen; precipitating iron from the leach solution using magnesium oxide and oxygen; removing copper, silver, cadmium, cobalt and lead from the leach solution by cementation with zinc dust; precipitating zinc oxide from the leach solution using magnesium oxide; and spray roasting the remaining magnesium chloride leach solution to regenerate hydrochloric acid and magnesium oxide. The present invention further relates to processes for recovering copper, silver, lead, and iron from complex sulfide materials.

Abstract: A process for the recovery of nickel and/or cobalt values from a concentrate containing nickel or cobalt hydroxide comprises the steps of subjecting the concentrate to a leaching stage with an ammonium solution to produce a leach solution containing nickel and/or cobalt values and a residue. The nickel concentration in the leach solution is controlled to a maximum value of about 3 to 25 g/l, preferably 8 to 15 g/l and more preferably 10 g/l.

Abstract: A process is provided for the leaching of both the “limonite” (Fe approx. ≧25% and Mg approx. ≧6%) and “saprolite” (Fe approx. ≦20% and Mg approx. ≧10%) fractions of typical nickel and cobalt bearing laterite ore. The low magnesium fraction of the laterite ore is leached with sulfuric acid at high pressure and temperature to solubilize the metal values while precipitating most of the solubilized iron as hematite or other iron compounds and a portion of the dissolved aluminum as alunite or other aluminum compounds. After reducing the pressure of the leach slurry to approximately atmospheric pressure, the pregnant leach slurry or solution is contacted with the high magnesium fraction of the ore to solubilize most of the nickel contained in the high-magnesium ore fraction while dissolving only a small portion of the iron content of the high magnesium ore fraction.

Abstract: The present invention provides an atmospheric acid leaching process for leaching nickel and cobalt from highly-serpentinized saprolitic fractions of nickel laterite deposits that are generally too low in nickel to support economical extraction of their nickel contents by pyrometallurgical processing except under special circumstances, and generally too high in magnesium to be suitable for processing by modern high pressure acid leaching processes employed for treating predominantly limonitic nickel laterites. The process involves leaching the highly-serpentinized saprolitic portion of the nickel laterite ore profile in strong sulphuric acid solutions at atmospheric pressure and temperatures between 80° C. and 100° C., essentially autogenously, to extract at least 90% of its contained nickel content and a large proportion of its cobalt content after leaching reaction times of about one hour or less.

Abstract: A method for precipitating nickel and cobalt from an acid aqueous solution containing at least dissolved nickel, cobalt and manganese, the method including: adding solid caustic calcined magnesium oxide or freshly slurried caustic calcined magnesium oxide to the solution, the magnesium oxide being added in an amount sufficient to precipitate a substantial proportion of the nickel and cobalt in solution and to precipitate a minor proportion of the manganese in solution, maintaining the magnesium oxide in contact with the solution for a period of about 1 hour to about 9 hours to thereby achieve precipitation of a substantial proportion of the nickel and cobalt in solution and precipitation of a minor proportion of the manganese in solution; and separating solids precipitated in step (b) above from the aqueous solution. Preferably, about 80% to 100% of the Ni and Co in solution is precipitated and about 5% to 15% of the Mn in solution is precipitated. The precipitated material separates early from the solution.

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: A process for the recovery of nickel and/or cobalt values from a concentrate containing nickel or cobalt hydroxide comprises the steps of subjecting the concentrate to a leaching stage with an ammonium solution to produce a leach solution containing nickel and/or cobalt values and a residue. The nickel concentration in the leach solution is controlled to a maximum value of about 3 to 25 g/l, preferably 8 to 15 g/l and more preferably 10 g/l.

Abstract: A process is provided for the leaching of both the “limonite” (Fe approx. ≧25% and Mg approx. ≦6%) and “saprolite” (Fe approx. <20% and Mg approx. ≧10%) fractions of typical nickel and cobalt bearing laterite ore. The low magnesium fraction of the laterite ore is leached with sulfuric acid at high pressure and temperature to solubilize the metal values while precipitating most of the solubilized iron as hematite or other iron compounds and a portion of the dissolved aluminum as alunite or other aluminum compounds. After reducing the pressure of the leach slurry to approximately atmospheric pressure, the pregnant leach slurry or solution is contacted with the high magnesium fraction of the ore to solubilize most of the nickel contained in the high-magnesium ore fraction while dissolving only a small portion of the iron content of the high magnesium ore fraction.

Abstract: High yields of vanadium containing virtually no nickel or magnesium are obtained from natural bitumen ash consisting of up to 5% carbon, more than 95% of water-soluble compounds of vanadium, nickel and magnesium by mixing the ash with water to produce a 20% solids slurry of pH below 6.5 and temperature of 80-85° C. oxidizing any reduced vanadium in the slurry and then separating and removing the resulting polyvanadate precipitate from the liquid phase containing substantially all the nickel and magnesium values of the ash.

Abstract: A process for recovering a base metal from a material, the base metal being selected from cobalt, copper, nickel and zinc, the process comprising the steps of reacting the host material with a ferric ion species in a leach solution, at conditions sufficient to cause at least a portion of the base metal to be oxidized by the ferric ion species, thereby causing the ferric ion species to be converted to a ferrous ion species, and oxidizing the ferrous ion species with an oxidation mixture of SO2 and oxygen to form the ferric ion species for subsequent reaction with the material.

Abstract: A process for producing cobalt metal powder from nickel-cobalt sulphides wherein said nickel-cobalt sulphides are leached in an ammoniacal ammonium sulphate solution under an elevated pressure of an oxygen bearing gas, at a temperature of at least 80° C., with an effective ammonia to metals mole ratio in the range of 5:1 to 6.5:1 to oxidize the nickel and cobalt sulphides to sulphates, and to produce an ammoniacal leach liquor in which dissolved cobalt is predominantly in the (III) oxidation state, and an ammoniacal ammonium sulphate leach residue containing a cobalt (III) hexammine sulphate-calcium sulphate double salt.

Abstract: There is provided a process for the recovery of cobalt as cobalt (III) hexammine sulphate, comprising adding an effective amount of a calcium sulphate slurry to an ammoniacal ammonium sulphate solution containing cobalt (III) hexammine sulphate to thereby selectively precipitate a cobalt (III) hexammine sulphate-calcium sulphate double salt. The solution containing other base metal impurities is separated from the cobalt (III) hexammine sulphate-calcium sulphate double salt precipitate. An effective amount of an ammonium carbonate containing solution is added to the double salt precipitate to thereby redissolve cobalt (III) hexammine sulphate and precipitate calcium carbonate.

Abstract: A process is provided for leaching nickeliferous laterite ores by hydrometallurgical methods at temperatures below the boiling point of the pulp and at atmospheric pressure from which high overall nickel and cobalt extractions are obtained. The high iron fraction of the laterite, referred to as limonite, is first contacted with a concentrated mineral acid to partially or completely dissolve the iron and nickel in solution. During this process, a reducing agent is used to keep the redox potential in solution below 1000 mV to enhance cobalt dissolution and more advantageously between 1000 and 900 mV to avoid reduction of ferric iron. Further mixing of the leach slurry in the presence of sodium, potassium, or ammonium will allow the formation of iron jarosite at ambient pressure. The resulting acid from iron hydrolysis is neutralized with the low iron fraction of the laterite ore (saprolite) dissolving nickel into solution.

Abstract: A process for the recovery of nickel from a nickel containing ore in which the ore, particularly a laterite ore, is initially leached with an aqueous acid solution, after which the nickel is precipitated as nickel hydroxide by adding a hydroxide to the aqueous acid leach solution containing the nickel, followed by a re-leaching of the nickel with an aqueous ammoniacal solution and recovery of the nickel by a solvent extraction of the nickel from the aqueous ammoniacal solution with an organic phase of a water insoluble oxime extractant comprising a ketoxime containing less than 10% phenols dissolved in a water-immiscible hydrocarbon solvent and the nickel recovered by electrowinning the nickel from the aqueous acid stripping solution employed to strip the nickel from the organic phase.

Abstract: Hafnium is recovered from irradiated tantalum by: (a) contacting the irradiated tantalum with at least one acid to obtain a solution of dissolved tantalum; (b) combining an aqueous solution of a calcium compound with the solution of dissolved tantalum to obtain a third combined solution; (c) precipitating hafnium, lanthanide, and insoluble calcium complexes from the third combined solution to obtain a first precipitate; (d) contacting the first precipitate of hafnium, lanthanide and calcium complexes with at least one fluoride ion complexing agent to form a fourth solution; (e) selectively adsorbing lanthanides and calcium from the fourth solution by cationic exchange; (f) separating fluoride ion complexing agent product from hafnium in the fourth solution by adding an aqueous solution of ferric chloride to obtain a second precipitate containing the hafnium and iron; (g) dissolving the second precipitate containing the hafnium and iron in acid to obtain an acid solution of hafnium and iron; (h) selectively ad

Abstract: A method is disclosed for recovering a metal from a metal containing material by autoclaving with an autoclave which includes an agitator that includes a first inlet for a recycled oxygen-containing gas, a second inlet for a fresh oxygen-containing gas, an impeller having a plurality of outlets to recirculate or introduce the oxygen-containing gases into the slurry and a set of mixing blades located below the outlets to radially disperse gas bubbles substantially uniformly throughout the slurry. The outlets for the gas can be located in an intermediate set of blades for thorough dispersion of the gas bubbles in the slurry.

Abstract: A process for the extraction of metal from an ore or concentrate which contains nickel and/or cobalt values and other metals, comprises subjecting the ore or concentrate to acid leaching under pressure at pH≦2 to obtain a liquor containing nickel and/or cobalt values, subjecting the liquor to a first precipitation stage at pH of about 5 to 6 to produce a solid containing non nickel and non cobalt metals and a resultant solution containing the nickel and/or cobalt values and subjecting the resultant solution to a second precipitation stage at a pH of about 7 to 8 to produce a solid containing nickel and/or cobalt.