1806 results about "Zirconium" patented technology

The invention discloses a matte glaze and a preparation method thereof. The matte glaze comprises the following components by weight: 1-5 parts of zinc oxide, 5-15 parts of barium carbonate, 0-15 parts of zirconium silicate, 10-25 parts of potassium feldspar, 10-20 parts of kaolin, 5-15 parts of calcite, 5-15 parts of calcined talcum powder, 20-35 parts of a matte frit and 0.5-1 part of an additive. Specifically, the matte frit comprises the following components by weight: 30-50 parts of SiO2, 15-20 parts of Al2O3, 0.01-0.5 part of Fe2O3, 3-10 parts of CaO, 0.5-5 parts of MgO, 1-5 parts of K2O, 3-10 parts of Na2O, 3-10 parts of ZnO, 0.1-1 part of B2O3 and 10-25 parts of BaO. By introducing the matte frit, the melting temperature of the formula is lowered, the firing range of the formula isbroadened, and the glaze texture achieves a fine matte effect.

The invention discloses a fluoride salt-free nitrate-free cast iron enamel semitransparent glaze as well as a preparation method and application thereof, and belongs to the technical field of enamel. The semitransparent glaze is prepared from quartz, anhydrous borax, sodium carbonate, potassium carbonate, calcium carbonate, potassium feldspar, zinc oxide, lithium carbonate, zirconium silicate, titanium dioxide, aluminum oxide, trisodium phosphate, antimony oxide, magnesium carbonate and barium carbonate according to a specific mass ratio. The preparation method comprises the steps of raw material mixing, high-temperature melting under a pure oxygen condition, wiredrawing detection, quenching and the like. The semitransparent glaze is completely free of fluoride salt and nitrate, the problems of fluoride emission and environmental protection equipment blockage are avoided from the source, the fluorine content of the product is not detected through detection, the product meets the requirements of European Union REACH regulations, meanwhile, the product has good porcelain surface, luster and low-temperature firing adaptability, and is suitable for cast iron matrixes, the firing temperature is 740-760 DEG C, and the firing time is 2-3 hours. The method can be used for producing green and environment-friendly enamel products.

The invention provides a high-stability lithium-rich manganese-based positive electrode material and a preparation method thereof, and relates to the technical field of lithium-rich manganese-based positive electrode materials, and the method comprises three steps of preparation of a homogeneous precursor, solid-state mechanical fusion doping and coating, and high-temperature sintering; a lithium-rich manganese-based precursor is prepared by adopting a homogeneous coprecipitation process, uniform distribution of metal ions is ensured, then an aluminum source, a zirconium source and a fluorine source are introduced as doping agents, phosphate and a titanate coating agent are combined, doping and coating integrated treatment is realized through mechanical ball milling, and the lithium-rich manganese-based composite material is obtained. And finally, mixing with a lithium source in an argon atmosphere, and carrying out high-temperature sintering of temperature programming and staged heat preservation to form a stable composite coating layer in situ. Therefore, manganese ion migration is effectively inhibited through lattice doping, a layered structure is prevented from being converted into spinel or rock salt phase, meanwhile, a nanoscale ion / electron transmission channel is constructed, interface impedance is reduced, and the charging and discharging efficiency under high voltage is improved.

The invention relates to the technical field of rare earth metal electrolysis cathode protection coatings, in particular to a high-temperature-corrosion-resistant yttrium-stabilized zirconia gradient coating on the surface of a tungsten cathode. A metallurgically bonded strong bonding bottom layer is constructed on a tungsten substrate through surface pretreatment and reactive sintering, then an atmosphere plasma technology is adopted to spray a creep-resistant gradient layer with continuous components to buffer thermal stress, and finally a sol-gel technology is utilized to construct an extremely compact corrosion-resistant surface layer in a superposition mode. The high-temperature-corrosion-resistant yttrium-stabilized zirconia gradient coating is constructed through a multi-scale and multi-mechanism synergistic effect, the problems that a tungsten cathode coating is insufficient in binding force and poor in thermal shock resistance are fundamentally solved, molten salt permeation can be blocked, and the service life of a tungsten cathode in a severe environment is remarkably prolonged.

The invention provides a low-cost high-specific-surface-area cerium-aluminum composite oxide, a preparation method and application thereof, and relates to the technical field of catalysts, the preparation method comprises the following steps: step S1, adding 10-40% of cerium salt, 50-90% of aluminum salt and 0-10% of lanthanum source or zirconium source into deionized water, stirring and mixing, filtering, and washing to be neutral to obtain a cerium-containing solution; step S2, impregnating an alumina carrier in the cerium-containing solution prepared in the step S1, and standing to enable the cerium-containing solution to be impregnated on the alumina carrier, so as to obtain impregnated slurry; and S3, drying the dipping slurry, and then roasting in an inert atmosphere to obtain the cerium-aluminum composite oxide. The stable cerium-aluminum composite material is formed by doping one of lanthanum and zirconium with different masses into aluminum oxide or cerium oxide, the problem that the adsorption capacity of a traditional ammonia trapping method is limited is effectively solved, and the adsorption capacity of the material to ammonia is remarkably improved.

The invention discloses double-layer fancy glaze with chapped ground texture and a preparation method of the double-layer fancy glaze, and relates to the technical field of ceramic glaze. The double-layer fancy glaze is composed of a ground glaze layer and a cover glaze layer. The ground glaze raw materials comprise potassium feldspar, kaolin, calcite, quartz, dolomite, zinc oxide and pigment; the cover glaze raw materials comprise potassium feldspar, waste porcelain powder, blank powder, chinastone, limestone, sepiolite, quartz, zirconium silicate with the particle size D50 being less than or equal to 1.0 mu m and pigment. The preparation method comprises the following steps: respectively carrying out ball milling to prepare ground glaze slip (32-40 baume degrees) and cover glaze slip (51-53 baume degrees); spraying ground glaze on the green body, drying, and then soaking with cover glaze; and finally, sintering at the temperature of 1250-1270 DEG C in a reducing atmosphere. Through the synergistic effect of the sepiolite and other components, the cover glaze has high surface tension, forms a microcrack network during drying, generates controllable glaze shrinkage during firing, forms a three-dimensional chap texture with crack width of 1-5mm and strong curled and raised crack edges, and meanwhile, the ground glaze completely covers a green body, so that the product practicability is ensured.

The invention discloses a catalyst for hydrogen production through tar steam reforming and a preparation method and application thereof. The catalyst comprises a cobalt-magnesium-aluminum composite spinel carrier and an active component loaded on the cobalt-magnesium-aluminum composite spinel carrier, the active component comprises nickel and at least one metal additive selected from iron, zirconium and ruthenium. The preparation method mainly comprises the following steps: preparing the carrier by adopting a coprecipitation method, loading the active component by adopting an impregnation method, and drying and reducing to obtain the final catalyst. The catalyst is used for tar component steam reforming hydrogen production reaction, especially for treating raw materials containing phenol and water vapor at 600-700 DEG C, tar conversion can be efficiently catalyzed, product gas rich in hydrogen can be generated, hydrogen selectivity is high, and almost no methane is generated. The catalyst has the advantages of high activity, good stability, strong carbon deposition resistance and the like, and is suitable for purification and high-value utilization of biomass pyrolysis tar.

The invention relates to a preparation process optimization method of a zirconium alloy material with high fretting wear resistance, which comprises the following steps: setting a chemical component optimization range of a zirconium alloy, including specific proportions of tin, iron, niobium, chromium and oxygen elements; establishing a computer simulation model, and predicting the wear volume, tribological stability and microstructure evolution of the material under the fretting wear condition; then, a complete optimization scheme is output based on the model optimization homogenization treatment temperature interval, the hot working deformation range, the cold working cumulative deformation degree and the annealing system; and finally, a preparation process sequence including smelting, homogenization treatment, hot working deformation, cold working deformation and final heat treatment is implemented, the zirconium alloy material with the equiaxed grain structure is prepared, and the wear resistance of the zirconium alloy material is verified through an experimental fretting wear performance test. Compared with the prior art, the method has the advantages that through systematic component design and process parameter simulation optimization, the material performance is remarkably improved, and the application reliability is enhanced.

The invention discloses fluoride salt-free and nitrate-free low-temperature matte glaze for steel plate enamel as well as a preparation method and application of the low-temperature matte glaze, and belongs to the technical field of enamel. The matte glaze is prepared from quartz, borax pentahydrate, sodium carbonate, titanium dioxide, magnesium oxide, monopotassium phosphate, calcium carbonate, zinc oxide, magnesium carbonate, lithium carbonate, aluminum oxide and zirconium silicate according to a specific mass ratio. The preparation method comprises the following steps: mixing the raw materials, melting at 1300 + / -10 DEG C in a pure oxygen environment, and quenching after wiredrawing to detect a molten state. The matte glaze completely avoids the use of fluoride salt and nitrate, the problems of fluoride emission and environmental protection equipment blockage are eliminated from the source, the fluorine content of the product is not detected through detection, and the limit value requirements of European Union REACH regulations are met. Zinc oxide and ZnO / TiO2 are added, so that the liquid phase viscosity is reduced, ion diffusion is accelerated, and the opacity (opacification performance) and gloss of the porcelain glaze are enhanced.

The invention discloses a fluoride-salt-free and nitrate-free cast iron enamel zirconium white glaze as well as a preparation method and application thereof, and belongs to the technical field of enamel. The zirconium white glaze is prepared from quartz, borax pentahydrate, magnesium carbonate, potassium carbonate, potassium feldspar, zinc oxide, aluminum hydroxide, calcium carbonate, zirconium silicate, sodium tripolyphosphate and lithium carbonate according to a specific mass ratio. The preparation method comprises the steps of raw material mixing, high-temperature melting under a pure oxygen condition, wiredrawing detection, quenching and the like. The zirconium white glaze is completely free of fluoride salt and nitrate, the problems of fluoride emission and environmental protection equipment blockage are avoided from the source, the fluorine content of the product is not detected through detection, the product meets the requirements of European Union REACH regulations, and meanwhile, the zirconium white glaze has good porcelain surface, luster and firing adaptability, is suitable for cast iron matrixes, has the firing temperature of 740-760 DEG C and the firing time of 87-87 hours, and can be widely applied to cast iron substrates. The method can be used for producing green and environment-friendly enamel products.

The invention discloses a titanium-based-iridium tantalum oxidation coating anode and a preparation method and application thereof, and belongs to the technical field of anode preparation, and the preparation process of the titanium-based-iridium tantalum oxidation coating anode comprises the steps that a titanium substrate is brushed with a solution containing a tantalum source A, then sintering is conducted, brushing-sintering is repeated, and a tantalum-coated titanium substrate is obtained; the tantalum-coated titanium substrate is brushed with the iridium-tantalum oxidation coating liquid, then sintering is carried out, and brushing-sintering is repeated, so that the tantalum-coated titanium substrate is obtained; the iridium-tantalum oxidation coating liquid contains a tantalum source B, an iridium source and a zirconium source; in the iridium tantalum oxidation coating liquid, the mass ratio of tantalum to iridium is (6-7): (4-5), according to the preparation method provided by the invention, through two times of brushing, the tantalum content in the titanium-based-iridium tantalum oxidation coating anode is more than 5% greater than the iridium content, and when the titanium-based-iridium tantalum oxidation coating anode is used for an alkaline citric acid electroplating system, the decomposition of a complexing agent can be effectively inhibited, the components of the electroplating liquid are maintained to be stable, so that the quality of a plating layer is ensured, and the service life of the plating layer is prolonged. The maintenance cost of the plating solution is reduced and the service life is prolonged.

The invention relates to the field of refractory castable, in particular to mullite-based modified high-strength refractory castable and a preparation process thereof. The refractory castable is used for solving the problems of low strength and poor wear resistance of the existing refractory castable. The niobium-zirconium alloy and the benzoxazine-PAMAM copolymer are added into the refractory castable, the benzoxazine-PAMAM copolymer wraps a matrix in a three-dimensional network structure, so that the cohesive force is improved, a carbon layer is formed among matrix particles after sintering to improve the overall compactness of the material, micropores in the matrix of the refractory castable can be filled with the niobium-zirconium alloy, the porosity is reduced, and the porosity of the refractory castable is improved. The refractory castable disclosed by the invention can be used for reducing stress concentration, remarkably improving normal-temperature compression resistance and breaking strength, maintaining long-term high-temperature strength and ensuring that the refractory castable can still be kept stable in severe environments such as high temperature, high pressure and corrosion, so that the service life is prolonged, and the production safety is improved.

The invention relates to the technical field of welding materials, and particularly discloses a high-temperature-resistant flux-cored wire containing rare earth elements and a preparation method of the high-temperature-resistant flux-cored wire. The high-temperature-resistant flux-cored wire containing the rare earth elements comprises a welding wire skin and a flux core. The flux core comprises the following raw materials of dehydrated rutile, dehydrated potassium feldspar, zircon sand, metal chromium powder, metal nickel powder, electrolytic manganese, ferrotitanium, ferro-aluminum, potassium cryolite, potassium titanate, sodium titanate, fine iron powder, yttrium-based iron alloy powder, atomized ferrosilicon, nitrided ferrochrome, bismuth oxide, auxiliaries and the balance reduced iron powder. The auxiliary agent is a mixture of a zirconium-iron alloy, a titanium-iron alloy and an aluminum-magnesium alloy. A specific alloy auxiliary is introduced into the flux core to protect stable transition of rare earth yttrium, yttrium and multiple components synergistically optimize the weld joint performance, 253MA heat-resistant steel is matched, slag and electric arc regulation and control components and a reasonable process are matched, and the welding quality of the welding wire is improved.

The invention discloses a method for prolonging the service life of a resistance spot-welding electrode, a manufactured resistance spot-welding electrode cap and application, and the method comprises the following steps: taking a chromium-zirconium-copper electrode cap as a base body, grinding the working surface of the base body step by step by adopting abrasive paper, and then sequentially polishing, ultrasonically cleaning and drying to obtain a pretreated base body; performing vacuum zirconium permeation treatment on the pretreated matrix by adopting a permeation agent so as to form a zirconium-rich solid solution diffusion layer in the pretreated matrix, thereby obtaining the matrix subjected to zirconium permeation reinforcement; physical vapor deposition treatment is adopted, and a metal transition layer is deposited on the surface of the solid solution diffusion layer of the matrix subjected to zirconium permeation strengthening; wherein the metal transition layer is a Cr transition layer or a Ti transition layer; and a graphite target and titanium target co-sputtering mode is adopted, and a composite gradient functional layer is sputtered and deposited on the surface of the metal transition layer of the matrix treated in the step S3. The electrode service life of the method is improved by magnitude order, and the effect is extremely remarkable.

The invention provides a method for preparing a zirconium boride ceramic material through pressureless sintering, and belongs to the technical field of zirconium boride ceramics. The method comprises the steps of preparing zirconium boride composite powder, modifying silicon carbide nanowires and mixing and sintering. The method for modifying the silicon carbide nanowire comprises the steps of acid treatment and modification, the modification step comprises the following steps: adding aluminum isopropoxide into absolute ethyl alcohol, adding a nitric acid solution, stirring for 1.5-2.0 hours at the temperature of 60-63 DEG C, adding the acid-treated silicon carbide nanowire, carrying out ultrasonic dispersion and water bath evaporation, then drying, putting into a muffle furnace, and carrying out heat preservation for 2.0-2.2 hours at the temperature of 490-500 DEG C to obtain a modified silicon carbide nanowire; the ceramic material prepared by adopting the method disclosed by the invention is high in density, good in mechanical property and excellent in high-temperature oxidation resistance and stability in a complex environment.

The invention belongs to the technical field of zirconite porous ceramics, and discloses a method for preparing high-strength zirconite porous ceramics by a foaming injection-coagulation method, which is characterized in that zirconite powder, yttrium oxide powder and manganese oxide powder are used as raw materials, and the foaming injection-coagulation method is adopted to prepare the zirconite porous ceramics. The zirconite porous ceramic is obtained through the steps of syrup solution preparation, ceramic powder premixing, ceramic slurry preparation, injection molding gelling, sintering treatment and the like. The foaming gel casting method is adopted, so that the porosity of the zirconite porous ceramic can be effectively increased, and the heat radiation transmission efficiency is reduced; saccharide is used as a solution medium instead of water, so that the sintering surface is increased and the strength of the porous ceramic is improved; the manganese oxide and the yttrium oxide are added, so that the merging and growing process among zirconite crystal grains is accelerated, the crystal form of zirconium oxide is stabilized at high temperature, cracks caused by crystal form transformation are avoided, the strength of the zirconite porous ceramic is further improved, and the prepared zirconite porous ceramic is stable in high-temperature performance, high in strength and low in heat conductivity coefficient.

The invention discloses a high-aluminum wear-resistant ceramic grinding ball and a preparation method thereof. The grinding ball comprises the following raw materials in percentage by weight: 85%-95% of aluminum oxide, 2%-10% of silicon dioxide, 1%-3% of calcium carbonate, 0.2%-0.5% of magnesium carbonate, 0.03%-0.05% of titanium dioxide, 0.01%-0.03% of sodium oxide and 1%-5% of modified zirconium dioxide. The preparation method of the modified zirconium dioxide comprises the following steps: adding hydrogen peroxide into a mixed solution of soluble cerium salt and soluble zirconium salt to obtain a reaction system; adding the reaction system into an alkaline solution for reaction, and collecting an insoluble substance after the reaction is finished; and calcining the insoluble substance to obtain the modified zirconium dioxide. The ceramic ball is simple in formula, rich in raw materials, low in price and low in production cost, the operation stability of the ceramic ball is improved, and the service life is prolonged.

The invention relates to the technical field of solid-state batteries, and discloses an optimized preparation method of a solid-state battery electrolyte, a composition comprises a lithium source, a lanthanum source and a zirconium source, and the molar ratio of lithium to lanthanum to zirconium is (7.0-8.0): 3.0: 2.0; the use amount of the photoacid generator accounts for 0.5-5.0 mol% of the total molar weight of the metal ions; and an organic solvent. The method comprises the following steps: S1, placing a substrate in a high-pressure reaction kettle, and injecting the precursor composition in a supercritical carbon dioxide (scCO2) environment; s2, irradiating the surface of the substrate with ultraviolet rays, performing photolysis on the photoacid generator to generate acid, and catalyzing the metal precursor to be decomposed and deposited into an amorphous film; and S3, taking out the substrate after pressure relief, and carrying out low-temperature heat treatment at 400-700 DEG C to obtain the solid electrolyte film. Through combination of photochemical deposition and a supercritical fluid technology, the problem of decomposition of a positive electrode material caused by high temperature in a traditional process is solved.

The invention relates to chemical-corrosion-resistant full-polished glaze as well as a preparation method and application thereof, and belongs to the technical field of ceramic production and manufacturing. The chemical-corrosion-resistant fully-polished glaze comprises the following mineral components in percentage by mass: 5%-10% of quartz, 5%-10% of kaolin, 1%-10% of calcined talc, 20%-25% of wollastonite, 10%-20% of calcined kaolin, 1%-5% of calcined alumina, 1%-5% of calcined zinc oxide, 1%-5% of barium carbonate, 1%-3% of titanium oxide, 1%-5% of zirconium silicate and 10%-20% of boron frit. By specially designing a full-polishing glaze formula of the ceramic tile, adjusting the firing temperature and discharging or reducing defects such as air holes in a glaze layer as much as possible, the glaze layer forms a stable inert surface, and chemical substances cannot react with the glaze layer or only slightly react with the glaze layer, so that the transparency, integrity and glossiness of the surface are kept.

The invention discloses super duplex stainless steel powder for laser cladding of a nuclear power pump shaft. The super duplex stainless steel powder comprises chemical components in percentage by weight as follows: 25.0%-26.0% of Cr, 7.4%-8.0% of Ni, 3.5%-4.0% of Mo, 0.22%-0.32% of N, 0.002%-0.010% of B, 0.01%-0.05% of Zr, 0.8%-1.0% of Cu, 0.5%-0.8% of W and the balance of Fe and inevitable impurities. The impurities comprise less than or equal to 100 ppm of C, less than or equal to 50 ppm of S, less than or equal to 50 ppm of P, less than or equal to 150 ppm of O and less than or equal to 5 ppm of H. According to the F55 super duplex stainless steel, trace boron (B) and zirconium (Zr) elements are synergistically added into an existing F55 super duplex stainless steel component system, so that the high-temperature thermoplasticity of the alloy is remarkably improved, and the process window of laser cladding is widened. Meanwhile, the invention further provides a preparation method and application of the super duplex stainless steel powder.

The invention relates to the technical field of radionuclide separation, in particular to an Eu (III) / An (III) separation method based on a zirconium phosphonate-based metal organic framework adsorbent, which comprises the following steps: adding the zirconium phosphonate-based metal organic framework adsorbent into an Eu (III) and / or An (III) nuclide-containing aqueous solution with the acid concentration of 0.001-3M to carry out adsorption reaction, and then carrying out solid-liquid separation, wherein the zirconium phosphonate-based metal organic framework adsorbent is a zirconium phosphonate-based metal organic framework material exchanged by metal cations M; the metal cation M is selected from one of alkali metal ions, alkaline earth metal ions or divalent transition metal ions. According to the invention, the interlayer chemical properties of the material are regulated and controlled through ion exchange, so that the adsorbent has ultrahigh selectivity, rapid adsorption kinetics, high adsorption capacity and excellent structural stability on trivalent actinide / simulated nuclides in extremely high-acid, high-salt and intense-radiation environments; the key problems of low separation efficiency and poor stability in a high-acid complex system in the prior art are solved, and the method is suitable for treating high-level liquid waste.

A nuclear fuel cell cladding that includes a zirconium-carbon covetic material. The zirconium-carbon covetic material has a carbon component associated with the surface of zirconium particles. The amount of carbon present in the zirconium-carbon covetic material is in a range of greater than 0.1 wt % to about 25 wt % of the zirconium-carbon covetic material. The carbon component may include carbon nanotubes, carbon nanomaterials, graphene, or graphene nanoplatelets. The carbon component may be uniformly distributed within the zirconium matrix. The zirconium-carbon covetic material may be formed from a zirconium alloy. The zirconium-carbon covetic material may be configured for use in various types of nuclear reactors. The synthesis of the cladding involves a process of plasma-enhanced chemical vapor deposition. The resulting nuclear fuel cell cladding offers improved performance and reliability for nuclear reactor applications.

The invention belongs to the field of metal additive manufacturing, and particularly relates to a high-strength and high-toughness electric arc fuse wire additive rare earth magnesium alloy component and a preparation method thereof. The high-strength and high-toughness electric arc fuse wire additive rare earth magnesium alloy component is prepared from, by mass, 7.0%-7.4% of gadolinium, 0.6%-1.0% of yttrium, 0.4%-0.5% of zirconium and the balance Mg, wherein inevitable impurities are smaller than or equal to 0.03%. The preparation method comprises the steps of wire material preparation, electric arc fuse wire additive manufacturing, solid solution, water quenching and aging treatment, tissue refinement, texture regulation and control and strengthening phase uniform precipitation are achieved, and the comprehensive mechanical property of a component is remarkably improved. According to the obtained high-strength and high-toughness electric arc fuse wire additive rare earth magnesium alloy component, the yield strength and the tensile strength are larger than 230 MPa and 340 MPa correspondingly, the ductility is larger than 19%, and the application requirements of light-weight structural parts for high specific strength and high ductility can be met.

The invention provides a polysilicate aluminum zirconium coagulant as well as a preparation method and application thereof, and relates to the technical field of solid waste recycling. The preparation method of the polysilicate aluminum zirconium coagulant comprises the following steps: S1, activation preparation of a polysilicate solution; S2, introduction and pre-complexation of a metal salt solution; and S3, alkalization induced polymerization and curing. According to the invention, the efficient charge neutralization capability of zirconium and aluminum metal ions and the long-chain network structure characteristic of polysilicic acid are organically combined through a copolymerization reaction by molecular design, the developed polysilicate aluminum zirconium coagulant can maintain a good coagulation effect in a wide pH range, is suitable for treating residual sludge with different sources and properties, and has a good coagulation effect under the dosage of 7.5%. The CST value is reduced to 35.4 s from 190.7 s, the water content of a filter cake is reduced to 77.4%, and the Zeta potential is-8.2 mV, so that the polysilicate aluminum ferric coagulant is obviously superior to a traditional polysilicate aluminum ferric coagulant, and has the advantages of high operation flexibility, good process stability and good application prospect.

The invention discloses an anti-oxidation coating and a manufacturing method thereof, and belongs to the field of coatings. The anti-oxidation coating is arranged on the surface of a zirconium alloy matrix, the anti-oxidation coating is a pure Cr coating, the hardness of the anti-oxidation coating is in gradient distribution in the thickness direction, the hardness of a surface layer is larger than that of a bottom layer, and the hardness gt of the bottom layer of the anti-oxidation coating is larger than that of gt; the hardness gt at the 1 / 2 thickness is 4GPa; the hardness of the surface layer is gt; and 6 GPa. Good bonding strength is achieved between the anti-oxidation coating and the zirconium alloy matrix, cracks are not prone to being generated on a bonding interface when the anti-oxidation coating serves in a long-term high-temperature and high-pressure corrosion environment, the service life of the zirconium alloy matrix can be effectively prolonged, and the reliability of the zirconium alloy matrix can be effectively improved.

The invention discloses a method for refining a rare earth magnesium alloy structure through combination of composite Zr salt and an ultrasonic field, the composite Zr salt is added as a chemical refiner in the magnesium alloy smelting process, and low-temperature ultrasonic treatment is carried out before pouring. Low-temperature chemical refinement and physical refinement are combined, the composite Zr salt is adopted to replace a traditional Mg-Zr intermediate alloy to serve as a chemical refiner, the refinement cost is reduced, magnesium element oxidation burning loss is avoided, on the basis, an ultrasonic physical field is introduced before melt pouring, Zr element sedimentation and decline effects are effectively avoided, and the mechanical property of the alloy is improved. The yield of Zr particles and the nucleation rate of crystal grains are increased, the Zr particles can play a nucleation role, and the effects of refining the solidification structure of the rare earth magnesium alloy and purifying the melt are achieved, so that the comprehensive mechanical property of the rare earth magnesium alloy is improved, and the rare earth magnesium alloy is suitable for the aerospace field with strict requirements for light weight, high specific strength and high temperature resistance.

The invention relates to a battery material preparation technology, in particular to a method for preparing high-purity cobaltous sulfate from crude cobaltous hydroxide, which comprises the following steps: S1, reacting the crude cobaltous hydroxide with sulfuric acid to generate magnesium sulfate; s2, washing to remove magnesium; s3, adding sulfuric acid and hydrogen peroxide into the crude cobalt hydroxide after magnesium washing; adding crude cobalt hydroxide to adjust the pH value to obtain a purified solution; s4, adding sodium fluoride into the purified liquid, and filtering after reaction to obtain filtrate; s5, saponifying with sodium hydroxide by using an acidic extractant, then performing soap conversion by using a cobalt sulfate solution, extracting manganese in the filtrate by using an obtained organic phase, and then performing reverse extraction on the organic phase by using sulfuric acid to obtain a manganese sulfate solution; s6, the raffinate obtained after manganese extraction is introduced into an adsorption tower loaded with a zirconium-based composite fluorine adsorbent; and S7, concentrating and crystallizing the defluorinated solution. According to the method, the zirconium-based composite fluorine adsorbent is introduced to be coupled with the process, fluorine ions can be removed, and cobalt loss caused by cobalt fluoride precipitation and the influence of the fluorine ions on the quality of a cobalt sulfate product are avoided.

The invention relates to the technical field of electrophoretic display, in particular to a preparation method of black electrophoretic particles with low reflectivity and high charge quantity. The method comprises the following steps: S1, mixing pre-dried black electrophoretic particles with ethanol, water and zirconium beads, adjusting the pH value by using ammonia water, and carrying out ball milling; transferring to a four-neck flask, adding a silane coupling agent, adjusting the pH value again, reacting at 80 DEG C, washing, centrifuging and drying to obtain modified particles; s2, carrying out ball milling on the modified particles, a monomer 1, a monomer 2 and a solvent, transferring into a four-neck flask, heating to 50 DEG C under the protection of nitrogen, adding an initiator, and reacting at 70-85 DEG C; after cooling, adding 3-5 parts of monomers and a solvent, repeatedly heating, adding an initiator, and reacting at 70-85 DEG C; and cooling again, supplementing the monomer 2 or 3, reacting under the same condition, and finally centrifuging, washing and drying to obtain the modified electrophoretic particle with the controllable shell structure. According to the invention, controllable regulation and control of low reflectivity and high charge quantity of the black electrophoretic particles are realized.

The invention provides a refractory ceramic-based material for a smelting furnace lining and a preparation method of the refractory ceramic-based material, and belongs to the technical field of ceramic refractory materials. The material comprises coated modified fused magnesite main aggregate, ceramic sand main aggregate, surface coated magnesium oxide fine powder, gamma-phase aluminum oxide micro powder, an aluminum dihydrogen phosphate solution, alkaline silica sol, a pre-reaction spinel precursor and zirconium boride micro powder. The coated modified fused magnesite main aggregate is prepared by mixing and sintering fused magnesite, silicon carbide composite powder, chromium sesquioxide powder and phenolic resin powder. And mixing the silicon carbide powder and the magnesium oxide powder, and depositing a silicon nitride layer on the particle surface to prepare the silicon carbide composite powder. The surface-coated magnesium oxide fine powder is formed by coating the surfaces of magnesium oxide fine powder particles with aluminum oxide. The pre-reaction spinel precursor is prepared by the following steps: preparing a mixed salt solution from magnesium nitrate hexahydrate and aluminum nitrate nonahydrate by using deionized water, reacting, aging and carrying out heat treatment. And the ceramic sand main aggregate is made of zirconium oxide. And all the layers are matched for use to realize balanced improvement of performance.

The invention discloses a copper-based catalyst for catalyzing partial hydrogenation of nitrocyclohexane to prepare cyclohexanone-oxime as well as a preparation method and application of the copper-based catalyst. The catalyst comprises a main active component and an auxiliary active component, the main active component is copper, the auxiliary active component is selected from one or more of titanium, vanadium, chromium, molybdenum, zirconium, cadmium, indium, tin, antimony, niobium, silver, iron, zinc, magnesium, aluminum, bismuth, manganese, lanthanum, gold or lead, the total molar ratio of the copper to the auxiliary active component is (100-1): 1, and the catalyst is prepared by adopting a coprecipitation method or a supported impregnation-coprecipitation method. And the process is simple and green. Under mild conditions, the catalyst can realize the conversion rate gt of nitrocyclohexane; the selectivity of cyclohexanone-oxime is greater than or equal to 99%, and the method is obviously superior to the existing non-noble metal system, and is low in cost, good in stability and suitable for industrial production of green synthesis of caprolactam.