327 results about "Copper nitrate" patented technology

The invention discloses a preparation method and application of amino-modified single-benzene-ring copper-based MOFs (metal organic frameworks), and the method comprises the following steps: dropwise adding a copper nitrate monohydrate solution into a diamino terephthalic acid solution, fully stirring to react, and centrifugally washing and drying the product to obtain the amino-modified single-benzene-ring copper-based MOFs. The amino-modified single-benzene-ring copper-based MOFs are used for electrocatalytic reduction of carbon dioxide. The prepared amino-modified single-benzene-ring copper-based MOFs have unique morphology, active sites can be exposed on the inner surface and the outer surface, the accessibility of the active sites is improved, and meanwhile the reaction mass transfer capacity is enhanced.

The invention discloses a high-sulfur-tolerance SCR honeycomb denitration catalyst and a preparation method thereof, and belongs to the technical field of industrial catalysts.The preparation method comprises the steps that S1, anatase type TiO2 and NH4HCO3 are mixed for pulping, pre-drying and calcination are conducted after extrusion forming, and a green body is formed; s2, carrying out nitric acid treatment on the green body, dipping the green body in a mixed solution of copper nitrate hydrate and cerium nitrate hydrate, and carrying out vacuum dipping, microwave drying and two-stage calcination to obtain a desulfurization carrier; s3, depositing an ammonium metatungstate precursor on the surface of the desulfurization carrier through CVD, and calcining to form a WO3 transition layer; and S4, dipping the transition layer in an acid solution containing NH4VO3 and ammonium metatungstate, and calcining after ultrasonic treatment to obtain a finished product. According to the method, the pore structure of the carrier is optimized through chambering treatment, and the stability and denitration efficiency of the catalyst in high-sulfur flue gas are remarkably improved by combining a multistage sulfur-resistant mechanism that the desulfurization layer preferentially captures SO2, the WO3 transition layer obstructs sulfur penetration and the denitration layer is protected by active sites.

The invention discloses a zeolite / silver / copper ternary inorganic nano antibacterial and antiviral material as well as a preparation method and application thereof. The preparation method comprises the following steps: preparing a mixed solution of a template agent and an anchoring agent, loading a metal precursor, adding a silicon source, performing hydrothermal crystallization and performing post-treatment. According to the zeolite / silver / copper ternary inorganic nano antibacterial and antiviral material disclosed by the invention, Ag-Cu bimetallic nanoparticles are formed by introducing copper nitrate and silver together, so that the catalytic activity, selectivity and stability of the zeolite / silver / copper ternary inorganic nano antibacterial and antiviral material are remarkably enhanced, and the dosage of noble metal silver can be reduced.

The invention discloses a catalyst for preparing trichlorosilane and a catalytic preparation method of trichlorosilane. The catalyst is prepared from the following components in percentage by mass: weighed copper nitrate, zinc nitrate, aluminum nitrate, lanthanum nitrate and the balance of a carrier, the preparation method comprises the following specific steps: S1, filling a catalyst; S2, purifying raw material gas; S3, reacting; and S4, separating and purifying a product, namely discharging a reacted gas product from an outlet of a reactor, and condensing through a condenser. In the prepared catalyst, the activity and selectivity of the catalyst are remarkably improved through the synergistic effect of the copper-zinc-aluminum composite oxide and the rare earth element lanthanum, the electronic structure and the surface acid-base property of the catalyst can be adjusted through doping of lanthanum, the reaction of silicon powder and hydrogen chloride is promoted, meanwhile, side reactions are inhibited, and the service life of the catalyst is prolonged. And the yield of trichlorosilane is improved.

The invention belongs to the technical field of iron ion detection, and particularly relates to a rapid detection method for ferric ions in water, which comprises the following steps: a fluorescent probe preparation step: taking trihydrate of copper nitrate and tryptamine, adding into a centrifuge tube in sequence, adding ultrapure water, performing ultrasonic dissolution, transferring into a high-pressure reaction kettle, and performing hydrothermal reaction to obtain a fluorescent probe; cooling to room temperature, centrifuging the obtained yellow green solution in a centrifugal machine, and filtering the supernate through a microfiltration membrane to obtain a copper-doped carbon quantum dot CuCDs stock solution, namely the fluorescent probe; analyzing and determining Fe < 3 + >: taking the diluent of the prepared CuCDs solution, adding the diluent into a centrifugal tube containing a Fe < 3 + > standard solution, uniformly mixing, carrying out fluorescent quantitative analysis and detection, and exploring the change rule of the fluorescence intensity ratio of CuCDs; according to the rapid detection method for Fe < 3 + > provided by the invention, the synthesized CuCDs have high sensitivity, can realize on-site rapid detection of Fe < 3 + > in a water medium, and shows a wide application prospect in the field of environmental monitoring.

The invention discloses a NiCu-based alloy catalyst for preparing high-value products through natural gas decarbonization and application of the NiCu-based alloy catalyst, and belongs to the technical field of natural gas high-value catalytic conversion. The preparation method of the NiCu-based alloy catalyst comprises the following steps: (1) adding nickel nitrate hexahydrate and urea into hot water, adding ethylene glycol, carrying out a stirring reaction at 120-150 DEG C, and calcining the obtained intermediate to obtain a nickel oxide precursor; (2) adding a copper nitrate aqueous solution and ammonia water into the nickel oxide precursor, so that copper ions are anchored on the surface of nickel oxide, drying and calcining to obtain a Ni-Cu alloy oxide precursor; and (3) adding the Ni-Cu alloy oxide precursor, bismuth trioxide and metallic tin into deionized water, adding a complexing agent, carrying out ultrasonic treatment, and carrying out H2 reduction calcination on the obtained precipitate to obtain the Ni < x > Cu < y > Bi < z > Snm alloy. The NiCu-based alloy catalyst is used in a natural gas decarburization high-value product preparation reaction, and the natural gas decarburization reaction is sufficient, and long-term efficient conversion and stable operation are achieved by combining the synergistic effect of ultrasonic waves and an alternating magnetic field.

The invention belongs to the technical field of semiconductor material detection, and particularly relates to a method for representing micro-defects of a near-perfect czochralski silicon wafer by regulating and controlling near-surface copper concentration. The invention discloses a method for representing micro-defects of a near-perfect czochralski silicon wafer by regulating and controlling the concentration of near-surface copper. The method specifically comprises the following steps: (S.1) cleaning the silicon wafer and immersing the silicon wafer into a copper nitrate solution for standing; (S.2) rinsing the silicon wafer with ionized water, taking out the silicon wafer and airing the silicon wafer; (S.3) performing high-temperature heat treatment on the silicon wafer for a period of time, and quickly cooling; (S.4) carrying out chemical polishing on the cooled silicon wafer; (S.5) horizontally placing the silicon wafer in the corrosive liquid; and (S.6) observing the surface of the silicon wafer by using an optical microscope or a scanning electron microscope so as to display the microdefects. According to the invention, copper precipitates at different depths are observed after copper is introduced at high temperature, so that the microdefect condition of the silicon wafer can be reflected. The method can clearly display the micro-defects in the nearly perfect czochralski silicon wafer, and has high detection efficiency and accuracy. The method is easy to operate, low in cost and suitable for silicon wafer microdefect detection in large-scale production.

The invention belongs to the technical field of semiconductor oxide gas sensors, and particularly relates to an rGO / CuO / Li sensitive material, a preparation method thereof and application of the rGO / CuO / Li sensitive material in H2S sensors. The preparation method comprises the following steps: firstly, preparing a graphene oxide nanosheet by using an improved Hummers method, and then preparing the rGO / CuO / Li sensitive material by using copper nitrate, lithium chloride and the prepared graphene oxide nanosheet as raw materials, polyvinylpyrrolidone as a surfactant and N, N-dimethylformamide as a solvent by using a one-step solvothermal method. Under the condition of room temperature, the sensitive material shows a relatively high response value (220.1) and a relatively low detection lower limit (1ppb) on hydrogen sulfide, has good selectivity, repeatability and stability, and has a wide application prospect in trace-level hydrogen sulfide detection in the fields of industrial safety and atmosphere detection.

The invention discloses a preparation method and application of a metal covalent organic framework material, and the prepared metal covalent organic framework material can be used for adsorption separation of elemental iodine pollutants and shows excellent iodine adsorption capacity and rate. According to the preparation method, 1H-pyrazole-4-formaldehyde and copper nitrate trihydrate are subjected to a solvothermal reaction to prepare a copper ion ring trinuclear metal complex with an aldehyde group, and the copper ion ring trinuclear metal complex and 1, 3, 5-tri (4-aminophenyl) benzene are further subjected to a Schiff base reaction to prepare the metal covalent organic framework material containing copper ions. According to the metal covalent organic framework material disclosed by the invention, copper ion active adsorption sites in a chemical structure are also retained while a developed microporous structure is maintained, and the interaction strength of pore channels to iodine is remarkably enhanced, so that the iodine adsorption rate and capacity are remarkably improved. The preparation method is simple, convenient, universal and high in controllability, and large-scale production and manufacturing of the metal covalent organic framework adsorption material can be achieved.

The invention discloses a flame-retardant cotton fiber and a preparation method thereof, and relates to the field of cotton fibers. When the flame-retardant cotton fiber is prepared, dicarboxyl phenyl porphyrin and copper nitrate react to prepare a metal organic framework nanosheet; the preparation method comprises the following steps: reacting 2, 4, 6-tri (4-formyl phenyl)-1, 3, 5-triazine, 2-aminomethyl piperazine and phosphorous acid to prepare a flame-retardant graft; the cotton balls, the metal organic framework nanosheets and the flame-retardant graft react to prepare pre-modified cotton fibers; and carrying out ring-opening reaction on the pre-modified cotton fiber and epoxy chloropropane, and then carrying out ring-closing to obtain the flame-retardant cotton fiber. The flame-retardant cotton fiber prepared by the invention has excellent antibacterial property, flame retardance, color fixation and dispersity.

The invention provides a preparation method of ultrahigh-purity copper. The preparation method comprises the following steps: providing a first anode, a first cathode and an electrolyte; the electrolyte comprises the following components: a purified copper salt solution, inorganic acid, an oxidizing agent and an additive, the purified copper salt solution comprises purified copper salt and water, the purified copper salt comprises copper sulfate and copper nitrate, and the molar ratio of nitrate to sulfate in the purified copper salt solution is (1.5-9): 1; the additive comprises any one or a combination of at least two of an alcohol compound, polyacrylamide or a tetrazole compound; and the first cathode and the first anode are immersed in the electrolyte for electrochemical deposition, and the ultra-high-purity copper is obtained. The electrolyte composed of the purified copper salt solution, the inorganic acid, the oxidizing agent and the additive is adopted, the proportion of nitrate radicals to sulfate radicals in the purified copper salt solution is controlled, the impurity content of the sulfur element and the silver element in the electrolyte can be controlled, and preparation of the ultra-pure electrolytic copper is achieved.

The application discloses a preparation method of mesoporous copper oxide and application thereof. The preparation method comprises the following steps: S1, preparing a hydroxyl copper nitrate microplate by taking calcium carbonate paper as a substrate and copper nitrate as a solvent; S2, synthesizing an ordered copper hydroxide nanowire assembly through an alkali solution reaction; and S3, performing annealing treatment in a muffle furnace to obtain the mesoporous copper oxide microplate. Under the conditions of no hard template, no soft template and no strong acid treatment, the application provides a method for synthesizing the mesoporous copper oxide microplate material with uniform pore structure on the carbonic paper by adopting copper nitrate hydrolysis, alkali etching and annealing, and the synthesis method of the mesoporous structure has the advantages of simple operation, good controllability and low cost. The application also relates to application of the mesoporous copper oxide as an electrocatalyst material in the field of glucose electrochemical sensing.

The invention relates to the technical field of supercapacitors, and particularly discloses a spherical hollow multi-layer high-entropy metal oxide and a preparation method and application thereof. The spherical hollow multi-layer high-entropy metal oxide is prepared by the following steps: cross-linking metal cation nitrate comprising iron nitrate nonahydrate, zinc nitrate hexahydrate, copper nitrate hexahydrate, cobalt nitrate hexahydrate and nickel nitrate hexahydrate with dextrose monohydrate to generate spherical high-entropy metal hydroxide FeZnCuCoNi-HO with a solid core structure, and annealing to induce the metal hydroxide. And the spherical hollow multi-layer high-entropy metal oxide is formed. Compared with the prior art, the high-entropy metal oxide is prepared through a low-energy-consumption and simple synthesis method, the problem of volume change of the high-entropy metal oxide serving as an electrode material in the circulation process is solved, more reaction active sites are provided, an ion diffusion path is improved, and the specific capacitance of the composite material is improved while the specific capacitance of the composite material is improved. And the stability of the material is maintained, so that the energy storage performance of the supercapacitor is improved.

The invention relates to the technical field of catalysts, and particularly discloses a Ni-Cu-CeO2 / ZrO catalyst for improving oxidation stability of biodiesel and a preparation method of the Ni-Cu-CeO2 / ZrO catalyst. The invention discloses a Ni-Cu-CeO2 / ZrO catalyst for improving oxidation stability of biodiesel. The Ni-Cu-CeO2 / ZrO catalyst comprises a carrier, an active component and an auxiliary agent, the carrier is a CeO2-ZrO2 composite oxide; the active components are Ni and Cu; ni accounts for 3-5 wt% of the mass of the catalyst, and Cu accounts for 1-3 wt% of the mass of the catalyst; the auxiliary agent is La2O3; the preparation method comprises the following steps: firstly preparing the CeO2-ZrO2 carrier by adopting a coprecipitation method, then impregnating nickel nitrate, copper nitrate and lanthanum nitrate in an isopyknic manner, and then carrying out stepped roasting to obtain the catalyst. The catalyst has high catalytic activity and stability, unsaturated fatty acid ester in biodiesel can be removed, the oxidation stability of the biodiesel is improved, and the cost of the catalyst is lower than that of a noble metal catalyst.

The invention discloses a two-dimensional heterostructure silver-loaded mesoporous copper nanosheet catalyst, a preparation method thereof and application of the two-dimensional heterostructure silver-loaded mesoporous copper nanosheet catalyst in electro-catalytic synthesis of alanine, amphiphilic molecules N-(2-mercaptoethyl)-N, N-dimethyldocosyl-1-ammonium chloride are dissolved in water, then metal precursors silver nitrate and copper nitrate are added, stirring is carried out, and the two-dimensional heterostructure silver-loaded mesoporous copper nanosheet catalyst is obtained. Finally, hydrazine hydrate is added for step-by-step reduction, and the two-dimensional heterostructure silver-mesoporous copper nanosheet (Ag-meso-Cu) catalyst is obtained. The Ag-meso-Cu catalyst prepared by the method disclosed by the invention has an asymmetric two-dimensional mesoporous structure and shows enhanced electro-catalysis alanine synthesis performance, the Faraday efficiency of alanine synthesis is up to 89.84%, and the yield is up to 0.23 mmol h <-1 > mg <-1 >. The preparation of the two-dimensional heterostructure nanosheet with a multilevel structure is realized by utilizing a simple liquid phase method, and a new strategy is provided for electrochemical synthesis of amino acid under a mild condition.

The invention relates to the technical field of improvement of coastal saline-alkali land, in particular to a soil conditioner for salt-control fertile soil of coastal fishery reclamation saline-alkali land and a preparation method of the soil conditioner. The invention relates to a soil conditioner for salt-control fertile soil of coastal fishery receding reclamation saline-alkali land. The soil conditioner comprises the following raw material components in parts by mass: 40-60 parts of urea, 25-45 parts of calcium superphosphate, 30-45 parts of potassium sulfate, 20-25 parts of modified oyster shell powder, 10-15 parts of humic acid, 3-5 parts of a compound microbial agent, 10-20 parts of desulfurized gypsum and 25-35 parts of a biochar composite material, the biochar composite material is prepared from the following raw material components in parts by mass: 1 to 2 parts of sodium alginate, 1 to 2 parts of chitosan, 3 to 8 parts of biochar, 1 to 5 parts of calcium chloride, 10 to 20 parts of tuff stone powder, 0.25 to 2 parts of acidified attapulgite, 0.01 to 0.08 part of graphene oxide, 1 to 5 parts of ferric nitrate, 0.6 to 3 parts of copper nitrate and 0.1 to 0.5 part of silane coupling agent. By adopting the soil conditioner prepared by the invention, the pH value of soil, the volume weight of the soil and the total amount of water-soluble salts can be remarkably reduced, meanwhile, the organic matters of the soil are increased, and the porosity of the soil is increased.

The invention discloses a preparation method of plant-based polyester fibers, and relates to the technical field of high polymer materials. When the plant-based polyester fiber is prepared, firstly, phosphorus-modified dopamine is synthesized by taking dopamine hydrochloride and sodium hypophosphite as raw materials; carrying out copolymerization on the phosphorus-modified dopamine, terephthalic acid, ricinoleic acid and 1, 3-propylene glycol to prepare modified plant-based polyester; the preparation method comprises the following steps: synthesizing 2-bornyl-4, 6-dichloro-1, 3, 5-triazine from aminated carbon nanotubes, further synthesizing 2-bornyl-4, 6-dichloro-1, 3, 5-triazine from L-borneol and 2, 4, 6-trichloro-1, 3, 5-triazine, reacting the 2-bornyl-4, 6-dichloro-1, 3, 5-triazine with the aminated carbon nanotubes, and modifying with allylamine to obtain modified carbon nanotubes; finally, the modified plant-based polyester, the modified carbon nanotubes and auxiliaries are subjected to blending extrusion, melt spinning and treatment through copper nitrate and ascorbic acid, and the plant-based polyester fiber is prepared. The plant-based polyester fiber prepared by the invention has excellent antibacterial property, flame retardant property and mechanical property.

The invention discloses a method for preparing isostearic acid by hydrogenation of a bio-based carrier catalyst, and relates to the technical field of oleochemical engineering and catalyst preparation, and the method comprises the following steps: S1, preparing a bio-based supported catalyst; s2, taking isomerized oleic acid as a raw material, and carrying out catalytic hydrogenation reaction under the action of a catalyst; s3, separating a product obtained after the hydrogenation reaction to obtain isostearic acid; according to the method for preparing isostearic acid by hydrogenation of the bio-based carrier catalyst, oyster shells are selected as a catalyst carrier, and specific pretreatment and high-temperature firing are performed, so that waste biomass resources are converted into a high-specific-surface-area calcium oxide carrier with a natural nanoscale sheet-shaped superposed three-dimensional space structure; high-value utilization of waste resources is achieved, so that the effects that the cost of raw materials of the catalyst is remarkably reduced and the carrier is environmentally friendly are achieved, and the high-activity non-noble metal hydrogenation catalyst is obtained by adopting copper nitrate solution impregnation and combining with a loading mode of subsequent hydrogen reduction.

This invention belongs to the field of catalyst technology, providing a CO purification oxygen-rich catalyst, its preparation method, and its application. The preparation method involves dispersing γ-alumina in water, then sequentially adding copper nitrate and cerium nitrate to obtain a reaction solution. The reaction solution is mixed with an inorganic base, followed by a substitution reaction and a crystallization reaction to obtain a catalyst precursor. The catalyst precursor is calcined under a reducing atmosphere to obtain the CO purification oxygen-rich catalyst; the reducing atmosphere includes hydrogen. This preparation method generates sufficient active sites through a copper-cerium binary system, and then utilizes the basic groups provided by the inorganic base to form a low-valence metal-hydroxyl composite structure under a reducing atmosphere. Through the combined action of metal atoms, hydroxyl groups, and active oxygen sites, the research goals of high efficiency, stability, high selectivity, and economy are achieved. Furthermore, this preparation method does not use precious metals, resulting in low cost.

This invention discloses a Cu-Si matrix for the synthesis of methanol / dimethyl ether from CO2. x Al 1‑x The catalyst preparation method and application are described. This catalyst can precisely control the selectivity of methanol and dimethyl ether. The catalyst is prepared from silica sol, aluminum isopropoxide, and copper nitrate trihydrate as raw materials. The precursor solution is uniformly mixed with a hexadecyltrimethylammonium chloride solution, followed by aging, evaporation, drying, and low-temperature calcination to produce a Cu-Si catalyst with defined active sites. x Al 1‑x Cluster catalyst, Cu nanoclusters encapsulated by Si with a defined composition x Al 1‑x Enclosed, but due to Si x Al 1‑x The different Si ratios and placement methods restrict the size and electronic states of Cu nanoclusters. As can be seen from the TEM images, the size of Cu nanoclusters increases with increasing Si content, thus forming Cu-Si nanoclusters with different active sites and different Cu electronic states. x Al 1‑x catalyst.

The invention provides a high-entropy nano enzyme. The chemical formula of the high-entropy nano enzyme is Mn < 0.4 > Co < 0.4 > Ni < 0.4 > Cu < 0.4 > Zn < 0.4 > Fe < 2.0 >) O. The invention also provides a preparation method of the high-entropy nano-enzyme, which comprises the following steps: dissolving manganese nitrate tetrahydrate, cobalt nitrate hexahydrate, nickel nitrate hexahydrate, copper nitrate trihydrate, zinc nitrate hexahydrate and sodium citrate in deionized water to prepare a clear solution A; dissolving potassium ferricyanide in deionized water to prepare a clear solution B; directly pouring the solution B into the solution A, stirring, standing and aging the obtained mixed solution at room temperature, and centrifugally collecting a product; and calcining the sample powder in a muffle furnace to obtain the high-entropy nano-enzyme. The invention further provides a catalyst which is composed of the high-entropy nano enzyme, 3, 3 ', 5, 5'-tetramethyl benzidine and H2O2. The invention also provides a method for detecting reduced glutathione by using the microfluidic paper chip analysis device. The invention provides a new normal form for constructing a multifunctional biosensing and environment monitoring platform.

The application discloses a kind of copper azide content trace detection method, the detection method includes: detecting copper azide content: taking the sample to be measured and inorganic acid mixed dissolution, then sequentially adding NaOH solution, buffer solution and copper nitrate solution, using ultraviolet visible spectrophotometer to measure absorbance and calculate corresponding azide radical concentration, determine the content of copper azide and cuprous azide in the sample to be measured by azide radical and copper azide content relationship model;Detect copper azide and cuprous azide: on the basis of measuring copper azide content, determine the content of copper azide and cuprous azide in the sample to be measured by azide radical and copper azide / cuprous azide content relationship model.The copper azide content trace detection method needs simple device of the application, low requirement to equipment, does not need organic solvent or color developing agent, and environmental pollution is small, and sub-milligram level copper azide used in MEMS fuze can be detected.

The invention relates to the field of biomedicine, and particularly provides bimetal MOFs with photo-thermal and anti-oxidation effects and a preparation method and application thereof.The preparation method comprises the following steps that 1, 4, 5, 8-naphthalene tetracarboxylic dianhydride and 4-amino-4H-1, 2, 4-triazole are dispersed in DMF, a reflux reaction is conducted at the temperature of 140-160 DEG C, and a DBPT organic ligand is obtained; the preparation method comprises the following steps: fully dissolving a DBPT organic ligand, anhydrous ferric chloride, anhydrous cupric nitrate and fluoboric acid in DMF at room temperature to obtain a reaction solution, carrying out ultrasonic treatment on the reaction solution, stirring until the reaction solution is completely dissolved, putting the obtained solution into a high-pressure reaction kettle, carrying out a heating reaction, and cooling to room temperature after the reaction is finished; and centrifuging the product, cleaning and drying to obtain the Fe / Cu-MOFs. The preparation method disclosed by the invention is simple to operate, and the prepared bimetallic MOFs have good photo-thermal and oxidation resistance and can be applied to multiple treatment requirements of bacterial infection and inflammation environment regulation and control.

The present application relates to the technical field of catalyst production, in particular to a preparation method of a high-selectivity and high-stability methanol synthesis catalyst, comprising the following steps: step 1: dissolving zirconium nitrate, zinc nitrate and aluminum nitrate in water to form a zirconium-zinc-aluminum mixed salt solution A, dissolving zinc nitrate, aluminum nitrate and copper nitrate in water to form a copper-zinc-aluminum mixed salt solution B, dissolving sodium carbonate in water to form alkali solution C and alkali solution D; adding a small amount of alkali solution C into deionized water to form deionized water E; step 2: using the salt solution A, the alkali solution C and the deionized water E to form a precipitate 1, then using the salt solution B, the alkali solution D and the precipitate 1 to react to form a precipitate 2, then heating the precipitate 2, and aging the precipitate 2; step 3: after aging, filtering and washing the precipitate 2, drying the filter cake obtained by filtering, and then calcining and molding to obtain the methanol synthesis catalyst.

The present invention generally relates to a method for synthesizing dysprosium-doped copper-zinc ferrite nanomaterials with enhanced structural and functional properties. The method comprises dissolving stoichiometric quantities of copper nitrate trihydrate, zinc nitrate hexahydrate, iron nitrate nonahydrate, and dysprosium nitrate hexahydrate in distilled water to prepare an oxidizer solution. A fuel mixture is separately prepared using urea and glucose in equal proportions by weight. The oxidizer and fuel mixtures are combined in 1:1 ratio, calculated based on their respective oxidizing and reducing valencies, to form a homogeneous precursor solution. This solution is stirred thoroughly for about one hour and subsequently transferred to a Pyrex dish. The dish is placed in a muffle furnace preheated to approximately 450° C., where the solution undergoes a self-sustained combustion reaction, yielding a fine, porous Cu0.5Zn0.5DyxFe2-xO4 ferrite powder within 20 minutes. The resultant powder is ground to achieve uniform particle distribution suitable for advanced applications.

The application provides an in-situ liquid gel-forming water-retaining agent and a preparation method and application thereof. The water-retaining agent is composed of A component and B component which are applied in steps. The A component contains an aqueous solution of a natural modified polymer, and the natural modified polymer is selected from one or two of carboxymethyl chitosan, carboxymethyl cellulose or a sodium salt thereof. The B component contains an aqueous solution of a cationic crosslinking agent, and the cationic crosslinking agent is selected from one or more cations of copper nitrate, iron nitrate, zinc nitrate, manganese nitrate, chitosan quaternary ammonium salt, calcium nitrate and magnesium nitrate. The water-retaining agent can realize the integrated functions of slow release of trace elements, water retention, soil improvement and precise nutrition supply. Furthermore, the water-retaining agent is applied to crop growth in combination with the "step-by-step drip irrigation and in-situ gel formation" technology, so that the agronomic characters of crops can be significantly improved.

The invention belongs to the technical field of resource recycling and metal organic framework material preparation, and particularly relates to a method for efficiently extracting a copper element from copper-indium-gallium-selenium powder and then directly synthesizing a copper-containing MOF material. The method comprises the steps that (1) the copper-indium-gallium-selenium powder and a prepared mixed solution of acid and hydrogen peroxide are subjected to contact leaching, and a solution A is obtained; (2) mixing the solution A with a first extraction agent to obtain a solution B and an organic phase A; adjusting the pH value of the solution B to 1.5, and adding a second extraction agent to obtain a solution C and an organic phase B; adding a nitric acid aqueous solution into the organic phase B for reverse extraction to obtain a copper nitrate solution and an organic phase C; (3) carrying out a hydrothermal reaction on a solution containing the organic ligand and the obtained copper nitrate solution to obtain a blue precipitate, namely a Cu-BTC material; according to the method, efficient recovery and efficient separation of the copper ions are achieved, and the Cu-BTC material with high purity is obtained in a low-cost and efficient mode.

The application relates to a CuO-ZnO-ZrO2@CeO2 core-shell catalyst and a preparation method and application thereof in preparing methanol. The preparation method is as follows: copper nitrate and zinc nitrate are dissolved in deionized water to form a mixed solution, a precipitant is added, and hydrothermal reaction is carried out to obtain copper-zinc nanoscale dispersed particles; then the particles are dispersed in deionized water, a zirconium nitrate aqueous solution is added, and hydrothermal reaction is carried out to precipitate zirconium on the outer layer of the particles; then a cerium nitrate aqueous solution and a precipitant are added to the system, and hydrothermal reaction is carried out; after the reaction, the system is subjected to filtration, washing, drying, grinding and calcination to obtain the CuO-ZnO-ZrO2@CeO2 core-shell catalyst. In the application process, CO2 and H2 are used as raw materials, cyclohexanol is used as a solvent, hydrogenation reaction is carried out under the action of the core-shell catalyst at 190-210 DEG C, and methanol is prepared. The core-shell catalyst can be applied to hydrogen transfer hydrogenation for preparing methanol, and can exhibit excellent catalytic activity and stability and higher methanol selectivity.

This invention provides a method for preparing copper powder from copper nitrate-containing wastewater. The method includes: mixing a reducing agent and a dispersant to obtain a first solution; adding copper nitrate-containing wastewater to the first solution to obtain a second solution; ultrasonically treating the second solution; and performing solid-liquid separation to obtain the copper powder. This invention utilizes ultrasound assistance to improve reaction efficiency, and through precise control of reaction conditions, achieves a copper recovery rate of over 99% from the copper nitrate-containing wastewater, obtaining copper powder with a purity of 5N.

The invention discloses a preparation method of nano silver-coated copper powder with a three-layer progressive structure, which comprises the following steps: by taking copper nitrate and silver nitrate as main raw materials, forming compact silver-coated copper powder with an inner layer as a large pure copper core, a middle layer as a copper-silver alloy gradient layer and an outer layer as a pure silver layer through various auxiliary agents and processes, and expanding to a micron level by taking nano application as a main part. The silver-coated copper is mainly used for replacing pure silver powder and silver-coated copper with a two-layer structure. In the application of electronics and other fields, the three-layer gradient compact gapless alloy structure enables multiple indexes such as structural strength, interlayer resistivity and the like to be superior to those of the two.