A method for preparing a basic copper carbonate is provided. The method includes: mixing a copper hydroxide with water to obtain a precursor slurry; adding an accelerator to the precursor slurry and mixing the two to obtain a first mixture; introducing gaseous carbon dioxide into the first mixture for reaction whereby obtaining a crude basic copper carbonate; and purifying the crude basic copper carbonate whereby obtaining the basic copper carbonate. The accelerator is at least one selected from the group consisting of an ammonia water and an ammonium salt.

A method according to an embodiment is for recovering a valuable metal from a waste electrode material of a lithium secondary battery by using lithium carbonate. An anode-cathode mixed electrode material that has been separated by draining, crushing, screening, and sorting a waste lithium secondary battery is preprocessed. A precipitation operation performed by adding lithium carbonate (Li2CO3) to a metal melt acquired by performing sulfuric acid dissolution using sulfuric acid. A valuable metal such as nickel, cobalt, manganese, aluminum, and copper is recovered as a residue in the form of a carbonate composite, and a lithium sulfate (Li2SO4) aqueous solution including lithium is recovered as a filtrate.

The present invention relates to an antiviral material including a Cu-M-O compound, in which the Cu at least includes a monovalent-state Cu and the M is at least one element selected from the group consisting of B, Al, Sc, Ti, Co, Cr, Ni, Ga, Y, Zr, In, Rh, and a lanthanoid.

The present invention relates to a broad-spectrum biocidal composition, with fungicidal and bactericidal activity, containing metal or metal oxide nanoparticles, polymeric thickeners, plant extracts, surfactants, and additives in an aqueous solvent, as well as the method for in situ production of said metal nanoparticles under controlled operating conditions: concentration, volumetric ratio, time, agitation, temperature, and pH, using plant extracts as reducing agents.

The disclosure relates to mineral processing, and more particularly to a copper(II)-ammonia complex ion sulfidization activator, and its preparation and application. A molar ratio of NH.sub.3 to Cu.sup.2+ in the active ingredient of the copper(II)-ammonia complex ion sulfidization activator is 2:1-4:1. The preparation method includes: dropwise adding an ammonia solution to a copper salt solution; and adjusting the mixture to pH 6-7.2 with dilute sulfuric acid to obtain the copper(II)-ammonia complex ion sulfidization activator. During the sulfidization flotation for the copper oxide ore, the copper(II)-ammonia complex ion sulfidization activator is added and mixed uniformly with the ore slurry prior to the introduction of the sulfidizing agent.

The present invention concerns a method for producing a solid material according to general formula (I) as follows: Li.sub.6-.sub.x_.sub.2yCu.sub.xPS.sub.5_.sub.yX (I) wherein X is selected from the group consisting of: F, CI, I and Br; 0.005 ≤ x ≤ 5; and 0 ≤y ≤ 0.5.; comprising at least bringing at least lithium sulfide, phosphorous sulfide, halogen compound and a copper compound, optionally in one or more solvents. The invention also refers to said solid materials and their use as solid electrolytes notably for electrochemical devices.

The copper oxide nanoparticles synthesized using Rhatany root extract involves preparing the Rhatany root extract by adding powdered Rhatany roots to boiling water, allowing the mixture to soak overnight, and removing any solid residue by filtering to obtain the aqueous extract. The copper oxide nanoparticles are prepared by mixing equal volumes of the aqueous Rhatany root extract and 0.1 M aqueous copper sulfate, heating the mixture at 80° C. for 40 minutes, and adding 1 M sodium hydroxide dropwise to the mixture to precipitate CuO. The precipitate is removed by centrifuge, washed with ethanol, dried, and calcined at 400° C. for 4 hours to obtain the copper oxide nanoparticles. The resulting nanoparticles proved effective in degrading wastewater dyes, showed anticancer activity against human cervical cancer by cell viability assay, and showed antibacterial activity against various strains of bacteria by agar diffusion.

The present disclosure provides a method of preparing a chalcogen containing solution that is hydrazine free and hydrazinium free, wherein the method comprises: providing a predetermined amount of elemental chalcogen; providing a predetermined amount of elemental sulfur; providing an amine solvent; and combining the predetermined amount of elemental chalcogen and the predetermined amount of elemental sulfur in the amine solvent, thereby dissolving the elemental chalcogen and the elemental sulfur in the amine solvent. The chalcogen containing solution can advantageously be used as a precursor for the formation of a chalcogen containing layer on a substrate.

The subject matter of the present invention concerns means of storage, transport and/or biocide treatment of a liquid, paste or gel, characterized in that said means comprises a copper base powder composition, said composition: containing at least 60% by weight of copper, does not contain more than 70% by weight of powder particles whose diameter is less than 45 μm maximum, and is at least partially in contact with said liquid, paste or gel.

A superconducting bulk magnet comprising a plurality of superconducting bulk materials combined, in which breakage of superconducting bulk materials is prevented and a strong magnetic field can be generated, that is, a superconducting bulk magnet comprising a plurality of superconducting bulk materials, each comprising a single-crystal formed RE.sub.1Ba.sub.2Cu.sub.3O.sub.y (RE is one or more elements selected from Y or rare earth elements, where 6.8≦y≦7.1) in which RE.sub.2BaCuO.sub.5 is dispersed and each provided with a top surface, a bottom surface, and side surfaces, combined together, in which superconducting bulk magnet, bulk material units, each comprising a superconducting bulk material and a bulk material reinforcing member arranged so as to cover a side surface of the same, are arranged facing the same direction and contacting each other to form an assembly, a side surface of the assembly is covered by an assembly side surface reinforcing member, a top surface and bottom surface of the assembly are respectively covered by an assembly top reinforcing member and an assembly bottom reinforcing member, and the assembly side surface reinforcing member, the assembly top reinforcing member, and the assembly bottom reinforcing member are joined into an integral unit, is provided.