Patent classifications
C01G53/11
Flotation reagents and flotation processes utilizing same
Methods of enhancing recovery of value sulfide and/or precious metal-bearing minerals from an ore containing such minerals as well as Mg-silicate, slime forming minerals, and/or clay by adding a froth phase modifier agent to the ore, and subjecting the ore to a froth flotation process performed under acidic conditions, are provided herein.
Preparation method and application for metal sulfide hollow microspheres with enriched sulfur vacancies
Disclosed is a hollow sulfide microsphere with enriched sulfur vacancies, which is prepared by a method comprising the steps of: dissolving cobalt nitrate and nickel nitrate in a mixed solution of N, N-dimethylformamide and acetone with an equal volume; then adding a chelating agent thereto, subjecting a resulting mixture to a solvothermal reaction to obtain a coordination polymer microsphere; dissolving the coordination polymer microsphere and a sulfurization agent in an organic solvent, and reacting to obtain a hollow sulfide microsphere; and subjecting the hollow sulfide microsphere to reduction treatment with sodium borohydride, centrifuging, washing and drying to obtain the hollow sulfide microsphere with enriched sulfur vacancies having a particle size of 1-2.5 ?m, a shell thickness of 15-30 nm and a specific capacity of the material of 763.4 C g.sup.?1 (current density is 1 A g.sup.?1).
Preparation method and application for metal sulfide hollow microspheres with enriched sulfur vacancies
Disclosed is a hollow sulfide microsphere with enriched sulfur vacancies, which is prepared by a method comprising the steps of: dissolving cobalt nitrate and nickel nitrate in a mixed solution of N, N-dimethylformamide and acetone with an equal volume; then adding a chelating agent thereto, subjecting a resulting mixture to a solvothermal reaction to obtain a coordination polymer microsphere; dissolving the coordination polymer microsphere and a sulfurization agent in an organic solvent, and reacting to obtain a hollow sulfide microsphere; and subjecting the hollow sulfide microsphere to reduction treatment with sodium borohydride, centrifuging, washing and drying to obtain the hollow sulfide microsphere with enriched sulfur vacancies having a particle size of 1-2.5 ?m, a shell thickness of 15-30 nm and a specific capacity of the material of 763.4 C g.sup.?1 (current density is 1 A g.sup.?1).
Moisture governed growth method of atomic layer ribbons and nanoribbons of transition metal dichalcogenides
A method of making an atomic layer nanoribbon that includes forming a double atomic layer ribbon having a first monolayer and a second monolayer on a surface of the first monolayer, wherein the first monolayer and the second monolayer each contains a transition metal dichalcogenide material, oxidizing at least a portion of the first monolayer to provide an oxidized portion, and removing the oxidized portion to provide an atomic layer nanoribbon of the transition metal dichalcogenide material. Also provided are double atomic layer ribbons, double atomic layer nanoribbons, and single atomic layer nanoribbons prepared according to the method.
Moisture governed growth method of atomic layer ribbons and nanoribbons of transition metal dichalcogenides
A method of making an atomic layer nanoribbon that includes forming a double atomic layer ribbon having a first monolayer and a second monolayer on a surface of the first monolayer, wherein the first monolayer and the second monolayer each contains a transition metal dichalcogenide material, oxidizing at least a portion of the first monolayer to provide an oxidized portion, and removing the oxidized portion to provide an atomic layer nanoribbon of the transition metal dichalcogenide material. Also provided are double atomic layer ribbons, double atomic layer nanoribbons, and single atomic layer nanoribbons prepared according to the method.
Catalyst for the gas phase production of carboxylic acids
Carboxylic acids are prepared by a one-step gas phase process comprising the step of contacting under halogen-free hydroxycarbonylation conditions an alkene, carbon monoxide, water, and a solid sulfide-containing catalyst.
Catalyst for the gas phase production of carboxylic acids
Carboxylic acids are prepared by a one-step gas phase process comprising the step of contacting under halogen-free hydroxycarbonylation conditions an alkene, carbon monoxide, water, and a solid sulfide-containing catalyst.
Flotation reagents and flotation processes utilizing same
Methods of enhancing recovery of value sulfide and/or precious-metal minerals from an ore containing said minerals and a Mg-silicate, slime forming mineral, and/or clay, and which is subjected to a froth flotation process, by adding to one or more stage of the froth flotation process a froth phase modifier having a polymer containing one or more functional groups, and optionally a monovalent ion modifier enhancing agent, thereby enhancing recovery of a value sulfide mineral and/or a precious metal-bearing mineral.
Flotation reagents and flotation processes utilizing same
Methods of enhancing recovery of value sulfide and/or precious-metal minerals from an ore containing said minerals and a Mg-silicate, slime forming mineral, and/or clay, and which is subjected to a froth flotation process, by adding to one or more stage of the froth flotation process a froth phase modifier having a polymer containing one or more functional groups, and optionally a monovalent ion modifier enhancing agent, thereby enhancing recovery of a value sulfide mineral and/or a precious metal-bearing mineral.
Method for producing nickel sulfide and hydrometallurgical method for nickel oxide ore
Provided is a method for producing nickel sulfide from an acidic sulfuric acid solution containing nickel, which is capable of suppressing particle diameters of nickel sulfide obtained thereby. The present invention is a method for producing nickel sulfide by causing a sulfurization reaction by blowing a hydrogen sulfide gas into an acidic sulfuric acid solution containing nickel, wherein: nickel sulfide having particle diameters of 5-20 m and serving as seed crystals is added into an acidic sulfuric acid solution having a nickel concentration of 0.5-5.0 g/L in an amount of 40-500% by mass relative to the amount of nickel contained in the acidic sulfuric acid solution; and a hydrogen sulfide gas is blown into the acidic sulfuric acid solution, into which the seed crystals have been added, while setting the amount of the hydrogen sulfide gas blown in to be within the range of 0.30-0.85 Nm.sup.3/kg-Ni.