Abstract: A zinc production method includes a reaction step such as a leaching step (101) of bringing electric arc furnace dust (1) containing zinc oxide or the like into contact with a chlorine gas (8) to obtain a zinc oxide component in the electric arc furnace dust (1) or the like as crude zinc chloride (3), a purification step (102) of heating the crude zinc chloride (3) obtained at the reaction step to produce zinc chloride vapor, and cooling and condensing the zinc chloride vapor, thereby obtaining purified zinc chloride (6), and an electrolysis step (103) of electrolyzing the purified zinc chloride (6) obtained at the purification step (102) in a molten state to obtain a zinc melt (9) and the chlorine gas (8).

Abstract: A process for etching includes disposing an activating catalyst on a substrate; providing a vapor composition that includes an etchant oxidizer, an activatable etchant, or a combination thereof; contacting the activating catalyst with the etchant oxidizer; contacting the substrate with the activatable etchant; performing an oxidation-reduction reaction between the substrate, the activatable etchant, and the etchant oxidizer in a presence of the activating catalyst and the vapor composition; forming an etchant product that includes a plurality of atoms from the substrate; and removing the etchant product from the substrate to etch the substrate.

Abstract: An article includes a substrate; and a coating disposed on the substrate that includes a microporous layer; a gradient in a density of a volume of the microporous layer, and a plurality of dendritic veins that are anisotropically disposed in the coating. A process for forming a coating includes disposing an activating catalyst on a substrate; introducing an activatable etchant; introducing an etchant oxidizer, performing an oxidation-reduction reaction between the substrate, the activatable etchant, and the etchant oxidizer in a presence of the activating catalyst, the oxidation-reduction reaction occurring in a liquid medium including the activatable etchant; and the etchant oxidizer, forming an etchant product comprising atoms from the substrate; removing a portion of the etchant product from the substrate; and forming a dendritic vein in the substrate to form the coating, the dendritic vein being anisotropically disposed in the coating.

Abstract: An electrowinning method of metals through electrolysis of a metal chloride solution uses an anode comprising a substrate comprising titanium or titanium alloy, and a coating layer comprising a plurality of a unit layer, provided on the surface of the substrate. The unit layer comprises the first coating layer comprising a mixture of iridium oxide, ruthenium oxide and titanium oxide and the second coating layer comprising a mixture of platinum and iridium oxide. The first coating layer contacts with the surface of said substrate and an outer coating layer of the unit layer formed on the outermost layer of said coating layer is the second coating layer. The coating layer is formed by thermal decomposition baking, which followed by post-baking at a higher baking temperature.

Abstract: Processes for metal leaching/solvent extraction are described which comprise: (a) providing a first aqueous leach pulp which comprises a mixture of leached solids and an aqueous leach solution comprising a metal, a leaching agent and water; (b) subjecting the first aqueous leach pulp to a first solid-liquid separation to provide a first clarified aqueous leach solution and a second aqueous leach pulp, wherein the second aqueous leach pulp comprises the leached solids at a % solids level greater than the first pulp; (c) subjecting the first clarified aqueous leach solution to a first solvent extraction prior to any significant dilution, whereby a first aqueous raffinate is obtained; (d) subjecting the second aqueous leach pulp to a second solid-liquid separation with dilution via an aqueous stream to obtain a second clarified aqueous leach solution; and (e) subjecting the second clarified aqueous leach solution to a second solvent extraction whereby a second is aqueous raffinate is obtained.

Abstract: A process for the recovery of zinc metal from a zinc mineral includes the steps of leaching the zinc mineral in a solution including a halide species formed from two or more different halides, to leach the zinc into the solution. The zinc-bearing solution is then electrolyzed to yield zinc metal and to generate the halide species. The electrolyzed solution including the halide species is then returned to the leaching step. A portion of the electrolyzed solution can be removed as a bleed stream from a cathode compartment of an electrolytic cell of the electrolysis process and processed to remove manganese as manganese dioxide precipitate by adding thereto limestone, and the halide species from an anode compartment of the electrolysis process. In this regard, the pH and Eh of the solution can regulated in a manner that favors the formation of the manganese dioxide precipitate over the formation of a precipitate of zinc.

Abstract: A thin discontinuous layer of metal such as Au, Pt, or Au/Pd is deposited on a silicon surface. The surface is then etched in a solution including HF and an oxidant for a brief period, as little as a couple seconds to one hour. A preferred oxidant is H2O2. Morphology and light emitting properties of porous silicon can be selectively controlled as a function of the type of metal deposited, Si doping type, silicon doping level, and/or etch time. Electrical assistance is unnecessary during the chemical etching of the invention, which may be conducted in the presence or absence of illumination.

Abstract: A thin discontinuous layer of metal such as Au, Pt, or Au/Pd is deposited on a Group III-V material surface. The surface is then etched in a solution including HF and an oxidant for a preferably brief period, as little as a couple seconds to one hour. A preferred oxidant is H2O2. Morphology and light emitting properties of porous Group III-V material can be selectively controlled as a function of the type of metal deposited, doping type, doping level, metal thickness, whether emission is collected on or off the metal coated areas and/or etch time. Electrical assistance is unnecessary during the chemical etching of the invention, which may be conducted in the presence or absence of illumination.

Abstract: The process uses hydrochloric acid solutions to extract zinc from electric arc furnace dusts containing zinc oxide and zinc ferrite. To selectively leach zinc and minimize iron dissolution by precipitating as FeO.OH and Fe2O3, hot acid leaching with the aqueous solution containing 37 g/l-74 g/l HCl and 104 g/l-270 g/l ZnCl2 is used. New dust is introduced to remove iron from the filtrate of the hot acid leaching. The zinc chloride solutions purified by activated carbon and metallic zinc powder is electrolysed in electrowinning cells which had cation exchange membrane to produce high purity zinc metal and to regenerate hydrochloric acid. Electrolysing an aqueous solution of zinc chloride with Zn concentration of 50-130 g/litre below 40° C. in a cell divided by cation exchange membrane, whereby coherent zinc is yielded at the cathode with high current efficiency of exceeding 90%. HCl is directly regenerated with a very small loss below 2% and low energy consumption below 5.

Abstract: A process for recovery of zinc from sphalerite containing ores or concentrates, whereby, in a first step, these ores or concentrates are submitted to a thermal treatment consisting essentially of a heating cycle performed under non-oxidizing conditions above 900.degree. C. thereby at least partly transforming the sphalerite to wurtzite, and subsequently the wurtzite is quenched in such conditions as to retain at least partly the wurtzite after quenching. In a second step zinc is leached out of the converted ore or concentrate, and in a third step zinc is recovered from the leaching solution by electrolysis.

Abstract: The present invention is directed to a process for removing various contaminants (e.g., organic collectors, contaminant metals or spectator ions, and/or suspended and colloidal solids) from process streams in leaching processes. The contaminant removal is performed by one or more membrane filtration systems (e.g., nanofilters, ultrafilters, and/or microfilters) treating process streams including, the pregnant leaching solution, the barren raffinate, and the lean and rich electrolytes.

Abstract: A process for the extraction of precious metals from a copper sulphide ore or concentrate, by treating a leach residue of the ore or concentrate, includes the steps of removing elemental sulphur from the leach residue to obtain a low sulphur residue and subjecting the low sulphur residue to an oxidative leach at elevated temperature and pressure to oxidize sulphur and precious metal compounds present in the low sulphur residue to produce a residue for the extraction of the precious metals therefrom.

Abstract: A process for the extraction of a metal from an ore or concentrate comprises subjecting the ore or concentrate to pressure oxidation in the presence of oxygen and an acidic solution containing halogen ions and a source of bisulphate or sulphate ions, such as H.sub.2 SO.sub.4. The metals which can be extracted by the process comprises copper, as well as non-cuprous metals, such as zinc, and precious metals, such as gold and silver.

Abstract: A process for the extraction of zinc from a sulphide ore or concentrate containing copper and zinc includes subjecting the concentrate to pressure oxidation in the presence of oxygen and an acidic halide solution to obtain a resulting pressure oxidation slurry and subjecting the slurry to a liquid/solid separation step to produce a liquor containing copper and zinc in solution. The liquor containing the copper and zinc is subjected to a first solvent extraction with a copper extractant to remove copper from the solution and to produce a copper depleted raffinate. The copper depleted raffinate is subjected to a second solid extraction with a zinc extractant to produce a zinc depleted raffinate and the zinc depleted raffinate is recycled to the pressure oxidation step.

Abstract: A process for the extraction of a metal from an ore or concentrate comprises subjecting the ore or concentrate to pressure oxidation in the presence of oxygen and an acidic solution containing halogen ions and a source of bisulphate or sulphate ions, such as H.sub.2 SO.sub.4. The metals which can be extracted by the process comprises copper as well as non-cuprous metals such as zinc, nickel and cobalt. During pressure oxidation the metal may be precipitated as an insoluble basic salt, such as basic copper sulphate, or substantially completely solubilized and precipitated later as the basic metal salt.

Abstract: A process for producing one or more metals from a mineral feedstock (12) is defined. The mineral is fed to a leaching apparatus (10) wherein it is contacted with electrolyte (14). The leaching apparatus has zones of decreasing oxidation potential (17, 18, 19, 20) respectively. A stream of electrolyte (14A) is removed from zone (20) and is treated to remove impurities and unwanted metals in treatment unit (25A), prior to metal recovery by electrolysis. The electrolyte after electrolysis is then returned to the leaching unit (10). A second electrolyte stream (14B) may be removed from zone (19) for recovery of additional metals. The electrolyte (14B) is treated to remove impurities and any unwanted metals in treatment unit (25B), prior to metal recovery by electrolysis. The electrolyte after electrolysis is returned to leaching unit (10). The process enables the leaching of difficult to leach minerals, including gold, and can produce one or more metals of high purity.

Abstract: A process for the extraction of a metal from an ore or concentrate comprises subjecting the ore or concentrate to pressure oxidation in the presence of oxygen and an acidic solution containing halogen ions and a source of bisulphate or sulphate ions, such as H2SO4. The metals which can be extracted by the process comprises copper as well as non-cuprous metals such as zinc, nickel and cobalt. During pressure oxidation the metal may be precipitated as an insoluble basic salt, such as basic copper sulphate, or substantially completely solubilized and precipitated later as the basic metal salt.