A method of recovering metal compounds from solid oxide fuel cell scrap includes processing the solid oxide fuel cell scrap to form a powder, digesting the processed scrap, extracting lanthanum oxide and cerium oxide from a solution containing the digested processed scrap, extracting a zirconium compound from the solution after extracting the lanthanum oxide and cerium oxide, and extracting scandium compound from the solution extracting the zirconium compound from the solution.

High-quality noN-stoichiometric NiO.sub.x nanoparticles are synthesized by a facile chemical precipitation method. The NiO.sub.x film can function as an effective p-type semiconductor or hole transport layer (HTL) without any post-treatments, while offering wide temperature applicability from room-temperature to 150 C. For demonstrating the potential applications, high efficiency is achieved in organic solar cells using NiO.sub.x HTL. Better performance in NiO.sub.x based organic light emitting diodes is obtained as compared to devices using PEDOT:PSS. The solution-processed NiO.sub.x semiconductors at room temperature can favor a wide-range of applications of large-area and flexible optoelectronics.

Provided is a method for producing solutions, by which two solutions, namely a high-purity nickel sulfate solution and a mixed solution of nickel sulfate and cobalt sulfate are able to be obtained at the same time from a sulfuric acid solution containing nickel, cobalt and calcium. A method for producing solutions according to the present invention uses a sulfuric acid solution containing nickel, cobalt and calcium and performs a first step S1 for producing a mixed solution of nickel sulfate and cobalt sulfate from the sulfuric acid solution and a second step S2 for producing a solution of nickel sulfate from the sulfuric acid solution in parallel. In the first step, the sulfuric acid solution is subjected to solvent extraction by an extractant, thereby obtaining a first organic solvent after extraction. In the second step, the sulfuric acid solution is subjected to solvent extraction by means of an extractant.

The present description relates to a process for producing magnesium metal from magnesium-bearing ores using serpentine. The process described herein consists generally in a mineral preparation and classification followed by leaching with dilute hydrochloric acid. The slurry is filtered and the non-leached portion, containing amorphous silica is recovered. The residual solution is neutralized and purified by chemical precipitation with non activated and activated serpentine. The nickel is also recovered by precipitation at higher pH. A final neutralisation and purification step of magnesium chloride solution by precipitation allows eliminating any traces of residual impurities. The purified magnesium chloride solution is evaporated until saturation and the MgCl.sub.2.6H.sub.2O is recovered by crystallization in an acid media. The salt is dehydrated and subsequent electrolysis of anhydrous magnesium chloride produces pure magnesium metal and hydrochloric acid.

This application pertains to methods of recovering metals from metal sulfides that involve contacting the metal sulfide with an acidic sulfate solution containing ferric sulfate and a reagent that has a thiocarbonyl functional group, wherein the concentration of reagent in the acidic sulfate solution is sufficient to increase the rate of metal ion extraction relative to an acidic sulfate solution that does not contain the reagent, to produce a pregnant solution containing the metal ions.

Disclosed are a nickel-iron wet treatment method and an application thereof. The treatment method comprises: in a high-pressure oxygen environment, mixing a crushed nickel-iron material, sulphuric acid and a corrosion aid, performing an acid leaching reaction, then performing solid-liquid separation on slurry subjected to acid leaching, adding an oxidant into the obtained filtrate, performing heating, removing the corrosion aid, adding a precipitating agent into the filtrate, controlling the pH value of the filtrate, and performing solid-liquid separation to obtain a ferric hydroxide precipitate and a nickel-containing filtrate; and performing extraction and back extraction on the nickel-containing filtrate to prepare battery-grade nickel sulphate. According to the present invention, the nickel-iron is subjected to oxidation acid dissolution in cooperation with the corrosion aid under the high-pressure oxygen and acidic conditions; the nickel-iron is extremely prone to oxidation in the high-pressure oxygen environment; and a strong oxidant is added into the filtrate subsequently, so that ferrous ions in the filtrate are completely converted into ferric ions, and the corrosion aid can be oxidized to generate pollution-free carbon dioxide and water, thereby avoiding the impact of the corrosion aid on the subsequent extraction process.

Disclosed in the present invention is a method for preparing nickel sulfate from a nickel-iron-copper alloy. The method comprises: in a high-pressure oxygen environment, mixing a nickel-iron-copper alloy crushed material, aqueous ammonia, ammonium sulphate, and a corrosion assisting agent, leaching, then performing solid-liquid separation on the leached slurry, adding a precipitant into a filtrate, and performing ammonia distillation to obtain a nickel-containing leachate; then adding an extractant into the nickel-containing leachate to extract nickel so as to obtain a nickel-containing extraction organic phase; and then adding sulfuric acid into the nickel-containing extraction organic phase to perform back extraction of nickel so as to obtain a nickel sulfate solution. According to the present invention, the nickel-iron-copper alloy is separated by using different properties of nickel and iron, nickel is dissolved in a hexamine complex of nickel, iron cannot be dissolved and then continues to be remained in a solid, after the filtrate is collected, the precipitant is added and ammonia distillation is performed to remove copper, the aqueous ammonia is recycled, and the copper ions react with the precipitant to generate a copper sulfide precipitate, and thus, copper in the filtrate is removed, and the purity of nickel sulfate is further improved.

This application pertains to methods of recovering metals from metal sulfides that involve contacting the metal sulfide with an acidic sulfate solution containing ferric sulfate and a reagent that has a thiocarbonyl functional group, wherein the concentration of reagent in the acidic sulfate solution is sufficient to increase the rate of metal extraction relative to an acidic sulfate solution that does not contain the reagent, to produce a pregnant solution containing the 10 metal ions.

High-quality non-stoichiometric NiO.sub.x nanoparticles are synthesized by a facile chemical precipitation method. The NiO.sub.x film can function as an effective p-type semiconductor or hole transport layer (HTL) without any post-treatments, while offering wide temperature applicability from room-temperature to 150 C. For demonstrating the potential applications, high efficiency is achieved in organic solar cells using NiO.sub.x HTL. Better performance in NiO.sub.x based organic light emitting diodes is obtained as compared to devices using PEDOT:PSS. The solution-processed NiO.sub.x semiconductors at room temperature can favor a wide-range of applications of large-area and flexible optoelectronics.

A method of recovering metal compounds from solid oxide fuel cell scrap includes processing the solid oxide fuel cell scrap to form a powder, digesting the processed scrap, extracting lanthanum oxide and cerium oxide from a solution containing the digested processed scrap, extracting a zirconium compound from the solution after extracting the lanthanum oxide and cerium oxide, and extracting scandium compound from the solution extracting the zirconium compound from the solution.