302 results about "Molybdenum oxide" patented technology

The invention relates to superfine molybdenum powder and a converter reduction preparation method thereof, belongs to the technical field of rare metal powder metallurgy, and solves the problems that the existing molybdenum powder preparation process is easy to cause hardening and agglomeration, the appearance granularity of the molybdenum powder cannot be controlled, the reduction process is complicated, the efficiency is low, the energy consumption is high and the cost is high. The method comprises the following steps: (1) preparing molybdenum oxide powder; (2) adding the molybdenum oxide into a converter, and introducing hydrogen for reduction; wherein the molybdenum oxide powder is nanoscale molybdenum oxide. The contact area between the adopted nanoscale molybdenum oxide powder raw material and the reducing gas is large, the converter rotates to drive the raw material powder to flow, full contact between the raw material powder and the reducing gas is promoted, hardening and agglomeration are inhibited, the reduction efficiency is improved, one-step reduction is achieved, the morphology is easy to control, and no waste gas is generated; compared with a traditional static pusher furnace, the closed dynamic converter has the advantages that reduction hydrogen escape is greatly reduced, safety is improved, energy consumption is reduced, and the use amount of hydrogen is greatly reduced.

The invention relates to the technical field of alloy processing, and discloses a high-performance corrosion-resistant nickel-based alloy plate and a preparation method thereof, and the method comprises the following steps: raw material preparation, smelting treatment, casting treatment, hot rolling treatment, solution treatment, aging treatment and surface passivation treatment. According to the invention, when a composite acid system is adopted for passivation treatment, the concentration of chromium / molybdenum atoms in a passivation film is optimized and balanced due to the specific ratio of nitric acid to chromic acid, a chromium oxide provides a compact passivation barrier, and a molybdenum oxide endows the film layer with a self-repairing characteristic to synergistically inhibit pitting nucleation; meanwhile, nano titanium dioxide particles pretreated by silane are embedded into the passivation film in situ under the action of ultrasonic oscillation, organic pollutants adsorbed on a film layer can be decomposed by the photocatalytic characteristic of the nano titanium dioxide particles, the local corrosion effect of a battery caused by dirt coverage is avoided, and the performance of the battery is improved through double upgrading of components and the structure of the passivation film. And the alloy plate has excellent pitting corrosion resistance and fouling resistance in a chloride ion-containing medium.

The invention relates to the technical field of superfine molybdenum powder preparation, in particular to a preparation device and method for low-oxygen superfine molybdenum powder. The specific preparation device comprises a sublimation bin, a reaction area and a gas-solid separation bin which are sequentially connected, the reaction zone comprises a preheating zone, a reduction zone and a conversion zone; a part of the hydrogen pipeline and a part of the carbon monoxide pipeline are arranged in the preheating area; one end of the hydrogen pipeline extends to the reduction area and is used for providing preheated hydrogen and carrying out gas-phase reduction reaction on the preheated hydrogen and the gas-phase MoO3 subjected to heat preservation; one end of the carbon monoxide pipeline extends to the conversion area and is used for providing preheated carbon monoxide and reacting with water vapor to complete primary water vapor conversion; meanwhile, partial carbon monoxide is subjected to a disproportionation reaction to generate micro carbon powder, and the micro carbon powder and water vapor are subjected to a water gas reaction to complete secondary water vapor conversion. The problem that the oxygen content of existing superfine molybdenum powder prepared through gas-phase molybdenum trioxide reduction is too high is solved.

The invention discloses a molybdenum oxide nanorod material, a preparation method of the molybdenum oxide nanorod material and application of the molybdenum oxide nanorod material to improvement of corn nutrient utilization, growth promotion and lodging resistance, and belongs to the technical field of corn nutrient utilization and agricultural nano material application. The morphology and dispersity of the nanorod are optimized by combining molecular composition characteristics of key enzymes (such as nitrate reductase and glutamine synthetase) in a corn nutrient utilization process, and finally the functional nanorod with targeting property and biocompatibility is obtained and can be widely applied to nutrient regulation and control scenes of corn water culture and field planting. After the material is applied, the activity of nitrate reductase and glutamine synthetase of a corn root system can be activated in a targeted manner, the nutrient utilization efficiency is accurately improved, and sufficient nutrition support is provided for plant growth. After the fertilizer is applied to plants, the root system is promoted to be developed, the stalks are thick and strong, the lodging resistance is remarkably enhanced, the protein content of the plants and grains can be increased, and the synergistic effects of efficient nutrient utilization, robust plant growth, lodging resistance and yield increase are achieved.

The invention belongs to the technical field of polymer composite materials, and particularly relates to an efficient flame-retardant low-toxic-gas-release silicone rubber composite material and a preparation method thereof. The high-efficiency flame-retardant low-toxic-gas-release silicone rubber composite material comprises the following components in parts by weight: 100 parts of methyl vinyl silicone rubber; 10 to 20 parts of ZIF-67 modified by polysiloxane; 5-10 parts of modified nano molybdenum oxide; 5 to 10 parts of melamine cyanurate; 40 to 50 parts of mesoporous SiO2 aerogel; 1-3 parts of hydroxyl silicone oil; 0.5 to 1.5 parts of a vulcanizing agent; and 0-5 parts of an auxiliary agent. The flame-retardant and smoke-suppression performance of the silicone rubber composite material is remarkably improved through material technology innovation, and meanwhile, the mechanical property and the high temperature resistance are improved.

Provided herein are methods of depositing molybdenum (Mo) films. The methods involve depositing a thin layer of a molybdenum (Mo)-containing film such a molybdenum oxide, a molybdenum nitride, or a molybdenum oxynitride. The Mo-containing film is then converted to an elemental Mo film. A bulk Mo film may then be deposited on the elemental Mo film. In some embodiments, the process is performed at relatively low temperatures.

A production process of electronic grade molybdenum dichloride dioxide comprises the following steps: S1, pretreatment: contacting molybdenum trioxide with a dilute acid solution at a low temperature for pickling to remove alkaline impurities and soluble metal impurities adsorbed on the surface, and drying for later use after washing; s2, wet synthesis: in an inert gas atmosphere, reacting the molybdenum trioxide subjected to acid pickling in the step S1 with concentrated hydrochloric acid of which the mass is 4-5 times of that of the molybdenum trioxide at 80-100 DEG C, and after the reaction is finished, evaporating and concentrating in a high-temperature chlorine atmosphere to generate a crude product of dichloromolybdenum dioxide; s3, primary sublimation purification; s4, complexing and decomplexing purification; and S5, secondary sublimation purification: using a quartz sublimation tower to carry out vacuum sublimation on the secondary decomplexed molybdenum dichloride obtained in the step S34, and collecting sublimation condensate to obtain the electronic grade molybdenum dichloride. The final product purity of the production process is greater than or equal to 6N, and the process can be used for large-scale production.

Provided herein are methods of depositing molybdenum (Mo) films. The methods involve depositing a thin layer of a molybdenum (Mo)-containing film such a molybdenum oxide, a molybdenum nitride, or a molybdenum oxynitride. The Mo-containing film is then converted to an elemental Mo film. A bulk Mo film may then be deposited on the elemental Mo film. In some embodiments, the process is performed at relatively low temperatures.

The invention discloses a method for improving the molybdenum yield in the direct alloying process of molybdenum oxide, which comprises the following steps of: 1, adjusting the lance position of an oxygen lance, and detecting a sonar slagging curve and a CO curve: judging the foaming performance of slag by combining sonar slagging and a furnace gas CO curve in the smelting process; step 2, molybdenum oxide is added, bottom blowing is enhanced, and the lance position of an oxygen lance is reduced; and step 3, the lance position is further reduced, the lance position is reduced to 0.1-0.3 m below the basic lance position, the decarburization speed is increased to 0.3% / min or above, volatilization of molybdenum oxide is inhibited through slag foaming and high CaO content, and the yield of molybdenum is increased. The slag composition and foaming performance are controlled by adjusting the lance position of the oxygen lance, the slag foaming performance is judged by combining sonar slagging and a furnace gas CO curve, a molybdenum oxide raw material is added when the slag foaming performance is good, and meanwhile volatilization of molybdenum oxide is inhibited through slag foaming and high CaO content. The sublimation of molybdenum oxide is effectively prevented, the yield of metal molybdenum can reach 95% or above, and the production cost of the molybdenum-containing steel grade is reduced.

The invention relates to the technical field of hydrodesulfurization catalysts, and discloses a molecular sieve hydrodesulfurization catalyst and a preparation method thereof.Active Si-Cl bonds of maleate methyl dichlorosilane react with hydroxyl in an MCM-41 molecular sieve, then hydrolysis is conducted through sodium hydroxide, and therefore a large number of carboxyl groups are grafted in the molecular sieve; carboxyl can form a strong coordination effect with metal ions such as nickel and the like, so that nickel and molybdenum are uniformly adsorbed into a matrix of the molecular sieve, a nickel-molybdenum oxide catalytic active center is uniformly generated in the molecular sieve through high-temperature roasting, catalytic sites are not easy to agglomerate, the dispersity is good, and the catalytic activity is stable. The catalyst can effectively perform hydrogenation reaction on sulfur-containing substances such as thiophenes in straight-run diesel oil, and has higher desulfurization rate. The catalyst has good practical application in the aspects of oil hydrodesulfurization catalysis and the like.

The invention provides a self-supporting molybdenum oxycarbide catalyst as well as a preparation method and application thereof. The preparation method mainly comprises the following steps: 1) heating a stainless steel mesh; 2) performing quenching reaction on the stainless steel mesh in urea and a solution containing molybdenum salt to introduce a molybdenum source and a carbon source; 3) alternately heating the stainless steel mesh and quenching to obtain a carbon-containing molybdenum oxide nanosheet as a precursor; and 4) carrying out rapid instantaneous heating treatment on the carbon-containing molybdenum oxide nanosheet precursor through a flash evaporation Joule technology under the protection of an inert atmosphere to obtain the self-supporting molybdenum oxycarbide catalyst. The self-supporting molybdenum oxycarbide catalyst provided by the invention is of a two-dimensional ultrathin nanosheet structure, and the nanosheet is rich in oxygen defects and has super-hydrophilic capacity, so that the adsorption of water molecules can be effectively enhanced, and the energy potential barrier of conversion of a hydrogen evolution reaction intermediate can be reduced. The method is short in technological process, high in preparation efficiency and suitable for large-scale industrial production, and has huge development potential in the field of hydrogen production through water electrolysis.

Provided are an oxide sintered body mainly containing a molybdenum oxide, a sputtering target containing the sintered body, and an oxide thin film formed by the sintered body. In the present invention, by adding a specific (pseudo) metal oxide in a prescribed range to a molybdenum oxide and a niobium oxide which are difficult to sinter, the sinterability can be improved and high-density characteristics can be ensured even if pressureless sintering is performed.

This invention discloses a machine learning-based method for parameter prediction and fabrication of compound silicon heterojunction solar cells, belonging to the field of silicon heterojunction solar cells. The J-V parameters of the solar cell are used as input features, and fabrication and performance parameters are used as target labels. A variational autoencoder is used to learn the latent representation of the data, and adversarial examples are generated by calculating the gradient of the input features relative to the model loss. A multilayer perceptron network incorporating a multi-head self-attention mechanism and L2 regularization is constructed, and adversarial training is performed using an enhanced training set to accurately predict the optimal UV / ozone treatment time and cell performance parameters. The intrinsic hydrogenated amorphous silicon / silicon oxide composite passivation layer is fabricated using the optimal UV / O3 treatment time. This invention, driven by machine learning, effectively captures the complex nonlinear relationships between parameters, improves the prediction accuracy of process parameters, and shortens the R&D cycle. It also effectively suppresses atomic diffusion between intrinsic hydrogenated amorphous silicon and the molybdenum oxide transport layer, improving cell performance.

An apparatus for producing molybdenum oxyhalides according to one aspect of the invention includes a reaction zone to which a halogen-containing gas is supplied, wherein a raw material containing molybdenum oxide is conveyed through the reaction zone to produce molybdenum oxyhalides.

The invention relates to the field of catalysts. The invention relates to a catalyst for catalytic oxidation of carbon monoxide in industrial sulfur-containing flue gas. A carrier is a cordierite honeycomb ceramic carrier coated with activated aluminum oxide (Al2O3), silicon oxide (SiO2) or titanium oxide (TiO2), or a honeycomb carrier with titanium oxide as a skeleton; the noble metal active component is selected from one or a combination of more of palladium (Pd), platinum (Pt) and rhodium (Rh), the total loading capacity accounts for 0.05-0.4 wt% of the mass of the carrier, and the noble metal component is loaded on the surface layer of the carrier at the depth of 10-300 microns and is of an eggshell type distribution structure; the cocatalyst component is selected from one or a combination of more of vanadium oxide (VO), tungsten oxide (WO), cerium oxide (CeO), molybdenum oxide (MoO) and lanthanum oxide (La2O3) and is uniformly distributed on the carrier. Unification of activity, stability and economical efficiency of the catalyst is achieved, the problems that a catalytic oxidation catalyst is prone to inactivation, low in activity and high in cost in complex sulfur-containing flue gas are solved, and the industrial application value is remarkable.

The application discloses a method for removing organic pollutants by using molybdenum dioxide to promote activated periodate, and comprises the following steps: adding molybdenum dioxide, ferric salt and periodate into wastewater containing organic pollutants, and then performing catalytic degradation reaction to remove the organic pollutants in the wastewater. In the method, molybdenum dioxide is introduced into the homogeneous ferric / periodate system, and serves as an electron donor and mediator of a Fenton-like reaction. The molybdenum dioxide can not only accelerate the Fe 3+ / Fe 2+ cycle rate and promote the activation of the periodate, but also promote the generation of high-valence iron (Fe(IV)) in the system, form a non-radical pathway dominated oxidation mechanism, promote the degradation reaction to be more rapid and intense, and finally realize the efficient degradation of the organic pollutants. The method has the advantages of rapid degradation rate, good reusability, simple process, convenient operation and environmental friendliness, and can be widely used in the treatment of organic pollutant wastewater.

The invention discloses a method for preparing monophenol compounds from lignin. The method comprises the following steps: mixing a raw material lignin with a solvent, and carrying out a one-step hydrogenation reaction in a hydrogen atmosphere under the action of a nickel-molybdenum-based catalyst to prepare the monophenol compound, the nickel-molybdenum-based catalyst comprises metal nickel and nickel oxide, molybdenum oxide and silicon oxide. The method provided by the invention has the characteristics of low production cost, simple separation, high monophenol compound yield and the like.

This invention discloses a method for hydrotreating catalytic cracking slurry. A fixed-bed hydrotreating process is employed, comprising: in the presence of hydrogen, the catalytic cracking slurry sequentially contacts a hydrotreating protectant, a hydrotreating transition catalyst, and a hydrodesulfurization catalyst to undergo a hydrotreating reaction, yielding hydrotreated oil. The hydrotreating protectant comprises an alumina support with a most probable pore size of 40–100 nm, molybdenum oxide, and cobalt oxide. The hydrotreating transition catalyst comprises an alumina support containing additives and MoO3 and CoO. The support has a bimodal pore size distribution, with smaller pores concentrated in the 10–40 nm range and larger pores concentrated in the 150–400 nm range. This method eliminates the diffusion resistance during the adsorption and reaction of large molecules on the catalyst surface during the hydrotreating of catalytic cracking slurry, increases the capacity for more deposits such as coke, extends the operating cycle of the unit, and facilitates hydrodesulfurization and other reactions. It also increases the content of tricyclic and tetracyclic aromatics in the hydrotreated oil, making it a high-quality feedstock for needle coke production.

The invention relates to the technical field of beneficiation, and particularly provides a beneficiation process for tungsten-molybdenum ore with calcium and magnesium ions easy to separate out. According to the beneficiation process disclosed by the invention, the iron ore concentrate, the molybdenum sulfide concentrate and the tungsten molybdenum oxide concentrate can be comprehensively obtained by improving the magnetic separation process, the flotation reagent combination, the desliming, the ore washing and other operation procedures; the problem of loss of tungsten and molybdenum metal along with magnetic concentrate due to the existence of a large amount of magnetite-molybdenite and magnetite-tungsten-molybdenum oxide ore intergrowth of the ore is effectively solved, and the problem of low molybdenum sulfide flotation index due to mismatching of a sulfuration flotation process is solved; the core problem that a large number of calcium and magnesium ions are separated out and react with a fatty acid collecting agent to cause heating flotation failure is solved, the technical bottleneck troubling the type of mine for more than ten years is successfully overcome, and the tungsten and molybdenum resource comprehensive recovery competitiveness of related enterprises can be remarkably improved.

The invention belongs to the technical field of water electrolysis hydrogen production energy conversion, and particularly relates to a molybdenum oxide-nickel molybdenum based compound water electrolysis hydrogen production catalyst material and a preparation method thereof. The method comprises the following steps: preparing a molybdenum oxide nanofiber substrate by adopting an electrostatic spinning technology in combination with pre-oxidation treatment; introducing a mixed valence state and oxygen vacancy defect into the substrate through a double-temperature-zone molybdenum vapor doping technology; performing bombardment treatment on the doped substrate by using argon-hydrogen low-temperature plasma to activate the surface; a nickel-molybdenum-based compound grows in situ on an activated substrate through a soaking crystallization method, and a final catalyst material is obtained through reductive heat treatment. The material has a unique three-dimensional hierarchical structure, a large specific surface area and abundant active sites. When being applied to a water electrolysis hydrogen evolution reaction, the catalyst shows excellent catalytic activity and stability under an alkaline condition, hydrogen evolution overpotential and electrolysis energy consumption can be remarkably reduced, the preparation process is controllable, the raw material cost is low, and the catalyst has a good application prospect.

The present application relates to the technical field of steelmaking auxiliary materials, in particular to a method for improving the balling rate of molybdenum oxide composite briquetting, in which process, in order to control the material temperature and overcome the problem of reaction heat release in the material, raw dolomite or limestone particles which are not easy to react with water are used to replace the traditional inhibitor lime, and the chemical reaction heat production is effectively controlled; the briquetting process provided by the present application adjusts the conventional one-time stirring and mixing to twice stirring, dry ice is added for cooling during the stirring process, and each time after stirring, standing is carried out, and through the above measures, the problem of material heating caused by the heat generated by material stirring and chemical reaction and then causing the problem of cracked briquetting after briquetting can be effectively solved. The balling rate of the molybdenum oxide composite briquetting for steelmaking produced by the process reaches more than 90%, the breaking strength is greater than 600N, and the falling strength is more than 15 times / (0.5m).

The invention relates to a graphene-coated molybdenum dioxide nanorod composite material as well as a preparation method and application thereof. The composite material is of a core-shell structure and takes a molybdenum dioxide nanorod as a core and a graphene layer as a shell; the graphene layer is formed by high-temperature carbonization of polyaniline, and the thickness of the graphene layer is 10-80 nm. The preparation method comprises the following steps: dissolving a molybdenum source in a nitric acid aqueous solution for hydrothermal reaction to prepare a molybdenum trioxide nanorod precursor; dispersing the molybdenum trioxide nanorod precursor in an acidic solution, sequentially adding aniline and ammonium persulfate under a stirring condition, and reacting to obtain a polyaniline / molybdenum trioxide composite precursor; and drying the composite precursor, and carrying out high-temperature calcination to obtain the graphene-coated molybdenum dioxide nanorod composite material. Compared with the prior art, the composite material has the high conductivity of graphene and the chemical activity of molybdenum dioxide, and shows excellent removal efficiency and cycling stability on lead ions in the capacitive deionization process.

The application provides a molybdenum trioxide extraction method, and belongs to the field of extraction metallurgy. The molybdenum trioxide extraction method provided by the application comprises the following steps: vacuum smelting a molybdenum-containing material to obtain sublimates, and cooling the sublimates to obtain the molybdenum trioxide; the molybdenum content in the molybdenum-containing material is 37.42-46.31 wt%, and the oxygen content is 30.74-38.13 wt%; the temperature of the vacuum smelting is 880-1200 DEG C, and the vacuum degree is 0.47-10 Pa; and the cooling rate of the cooling is 5-10 DEG C / min. The molybdenum trioxide is obtained by decomposing molybdate in the molybdenum-containing material through vacuum smelting, and the original molybdenum trioxide in the molybdenum-containing material sublimates under high-temperature conditions to obtain high-purity molybdenum trioxide, thereby effectively improving the extraction efficiency of the molybdenum trioxide; and the extraction method is simple, the low-grade molybdenum-containing material is used as the raw material, the extraction cost is lower, and the environment is not polluted.

A molybdenum trioxide powder, which contains an aggregate of primary particles comprising a crystal structure of molybdenum trioxide, the crystal structure comprising α-crystals having an average crystallite size of 50 nm or less. The median particle diameter D50 of the primary particles, which is obtained by a dynamic light scattering method, is 2000 nm or less. 50 is 2000 nm or less.

The present invention developed a composite having a novel structure containing, in a high content, a powder having a radiation-shielding function.　Provided is a composite having a radiation-shielding function and a method for producing the same. The composite comprises a preform made from a mixture containing a liquid silica-based binder and one or more radiation-shielding powders selected from gadolinium oxide, boron carbide, boron oxide, boron, barium sulfate, strontium oxide, tungsten, tungsten oxide, tungsten carbide, molybdenum, molybdenum oxide, iron powder, iron oxide powder, and ferrite powder, the radiation-shielding powder(s) being contained in the range from 3% to 85% in total. All of the voids in the preform are impregnated and filled with molten aluminum and solidification is allowed to occur to form a composite, or 25% or more of the voids in the preform are impregnated with a liquid organic / inorganic sealing agent and solidification is allowed to occur to form a composite. The liquid silica-based binder has properties that allow the preform to be formed at a temperature at which the radiation-shielding powder(s) does not decompose.

Systems and method for upgrading pyrolysis oil to produce greater value aromatic compounds includes combining heavy pyrolysis oil and a diluent to produce the pyrolysis oil feed. The systems and methods include passing the pyrolysis oil feed to a fixed bed reactor having a hydrocracking catalyst where the hydrocracking catalyst is a supported metal oxide catalyst that includes molybdenum oxide and nickel oxide supported on a catalyst support material comprising a large-pore alumina. The methods may further include contacting the pyrolysis oil feed with the hydrogen in the presence of the hydrocracking catalyst at reaction conditions in the fixed bed reactor to produce a reaction effluent.

Various embodiments herein relate to electrochromic devices and electrochromic device precursors, as well as methods and apparatus for fabricating such electrochromic devices and electrochromic device precursors. In certain embodiments, the electrochromic device or precursor may include one or more particular materials such as a particular electrochromic material and / or a particular counter electrode material. In various implementations, the electrochromic material includes tungsten molybdenum oxide. In these or other implementation, the counter electrode material may include nickel tungsten oxide, nickel tungsten tantalum oxide, nickel tungsten niobium oxide, nickel tungsten tin oxide, or another material.

The present application relates to a kind of low sulfur high performance fuel oil production device, it relates to fuel oil production technical field.Low sulfur modified residual oil, hydrogenation low sulfur raffinate are used as main raw material, auxiliary agent A, auxiliary agent B prepared by special oil device are matched, reaction conditions are accurately controlled through DCS system, low sulfur high performance marine fuel oil is prepared in low temperature mild environment;Device integrates vacuum deep pull and viscosity reduction cracking combined process, light fraction can be deep-processed into three kinds of base oil, etc.Additional value products, heavy fraction is reduced in viscosity by viscosity reduction cracking, and low-temperature fluidity is improved;Auxiliary agent B is prepared by dithiophosphoric acid, molybdenum trioxide, epoxy succinic acid polymer, 2,6-naphthalene dicarboxylic acid, anhydrous toluene, phosphorous acid;Fuel oil prepared by the present application, sulfur content is lower, environmental protection is better, low-temperature fluidity is improved, and combustion efficiency is better.

This invention provides a molybdenum alloy and its preparation method, relating to the field of powder metallurgy materials technology. The molybdenum alloy, by mass percentage, comprises the following components: rare earth element (RE): 0.045wt%-0.1wt%, zirconium salt: 0.15wt%-0.20wt%, with the balance being Mo. The preparation method of the molybdenum alloy includes: heating and stirring rare earth salts, zirconium salts, and water to obtain a mixed solution; continuously spraying the mixed solution onto the surface of stirred molybdenum oxide powder using a high-pressure spraying device to obtain a spray-coated mixed powder; drying and calcining the spray-coated mixed powder to obtain rare earth-doped molybdenum oxide powder; and reducing and sintering the rare earth-doped molybdenum oxide powder to obtain the molybdenum alloy. This invention improves the strength and plasticity of sintered molybdenum alloys, eliminating the need for subsequent plastic processing steps.

A molybdenum trioxide powder contains an aggregate of primary particles having a β crystal structure of molybdenum trioxide. The molybdenum trioxide powder has a MoO3 content ratio of 99.6% or more measured by X-ray fluorescence (XRF), and has an average particle diameter of the primary particles of 1 μm or less. A method for producing the above molybdenum trioxide powder includes vaporizing a molybdenum oxide precursor compound to form molybdenum trioxide vapor, and cooling the molybdenum trioxide vapor.