655results about "Molybdenum oxides/hydroxides" patented technology

Provided is a method of manufacturing a metal oxide film to be formed through the following processes: a coating process of forming a coating film on a substrate by using a coating liquid for forming metal oxide film containing any of various organometallic compounds; a drying process of making the coating film into a dried coating film; and a heating process of forming an inorganic film from the dried coating film under an oxygen-containing atmosphere having a dew-point temperature equal to or lower than −10° C.

A hydroprocessing catalyst has been developed. The catalyst is a unique crystalline transition metal oxy-hydroxide molybdate material. The hydroprocessing using the crystalline ammonia transition metal oxy-hydroxide molybdate material may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking.

A metal oxide powder except alpha-alumina, is disclosed comprising polyhedral particles having at least 6 planes each, a number average particle size of from 0.1 to 300 mum, and a D90/D10 ratio of 10 or less where D10 and D90 are particle sizes at 10% and 90% accumulation, respectively from the smallest particle size side in a cumulative particle size curve of the particles. This metal oxide powder contains less agglomerated particles, and has a narrow particle size distribution and a uniform particle shape.

The invention discloses a method for preparing an orthorhombic phase molybdenum trioxide nano wire, which is characterized in that molybdate, molybdic acid or molybdenum trioxide is dissolved in aqueous solution with quadrol concentration of 0.2-6 mol/L to cause the mol ratio of molybdenum atom and quadrol to be 1:1-6; and then strong acid solution with hydrogen ion concentration of 0.5-3.0 mol/L is dropwise added under the condition of stirring till the pH value is within 4 to 5; the solution is unceasingly stirred for 10 to 30 min; then the white precipitation is sucked, filtered, washed and dried to obtain white orthorhombic phase single crystal nano wires with the diameter of 100 to 400 nm and the length of 10-40 Mum. In the method, the raw materials are easily obtained; the needed device is simple; the technique is convenient; the reaction can be finished in an hour in the normal temperature and pressure; the method is safe and easy to be controlled; the productive rate reaches more than 99 percent; the mother solution can be reused; and the method is applicable to large-scale industry production.

A proton conductive solid electrolyte includes a proton conductive inorganic oxide including an oxide carrier and oxide particles supported on a surface of the oxide carrier, the oxide carrier containing an element Y consisting of at least one element selected from the group consisting of Ti, Zr, Si and Al, and the oxide particles containing an element X consisting of at least one element selected from the group consisting of W, Mo, Cr and V.

The invention relates to a quick and efficient non-template agent hydro-thermal synthesizing method. The system can synthesize an alpha-molybdenum trioxide nanometer rod and a high-density echinoid molybdenum oxide based nanometer materials. Molybdenum peroxide acid prepared from molybdenum trioxide and aqueous hydrogen peroxide solution is used as a precursor, is produced into scattered alpha-molybdenum trioxide nanometer rod by hydro-thermal synthesis at a temperature of between 80 and 180 DEG C, and is produced into the peroxide modified molybdenum oxide hydrate by hydro-thermal synthesis at a temperature of between 65 and 75 DEG C. The hydrate is a multiscale structure; a nanometer thin slice, a micron prism and a nanometer rod-shaped structure unit are divergently assembled into a micron-size high-density echinoid structure. The hydrate is roasted to obtain high-density echinoid alpha-molybdenum trioxide. Modulation of the synthesizing condition can realize fine adjustment for appearance of the nanometer rod, the micron-size echinoid structure and the structure unit thereof. The method uses raw materials with low cost, has the advantages of simple technical process, controllable conditions and the like, and can promote research and application of the molybdenum oxide in the fields of sensors, field transmission, electrode materials and so on.

Compositions and processes are disclosed for removing sulfur and sulfur compounds from hydrocarbon fuel feedstocks. The feedstock is contacted with a regenerable sorbent such as a compound of the formula Ti_xCe_yO₂ where 0<x/y≦1 and where 0<x≦1 and 0<y≦1 capable of selectively adsorbing sulfur compounds present in the hydrocarbon feedstock at about 0° C. to about 100° C. such as at about 25° C.

High purity ammonium dimolybdate or molybdenum oxide is produced by the pressure oxidation of low grade molybdenite concentrates or molybdenum intermediates. The process entails nearly complete oxidation of the sulfide minerals while optimizing the process chemistry and autoclave conditions to solubilize as little of the molybdenum values as possible. The autoclave discharge 12 is then subjected to a leaching step, either an alkaline leach 50, 400 or ammonium leach 250 process, before or after a liquid/solid separation step 20, 220, 410. The solution is then subjected to (a) filtration 60, 410, solvent extraction 70, 440, crystallization 90, 450, and calcination 120, 480 or (b) filtration 260, 280, crystallization 290, and calcination 320 to produce a product suitable for chemical-grade molybdenum oxide 125, 325, 485.

The invention relates to high purity MoO2 powder by reduction of ammonium molybdate or molybdenum trioxide using hydrogen as the reducing agent in a rotary or boat furnace. Consolidation of the powder by press/sintering, hot pressing, and/or HIP is used to make discs, slabs, or plates, which are used as sputtering targets. The MoO2 disc, slab, or plate form is sputtered on a substrate using a suitable sputtering method or other physical means to provide a thin film having a desired film thickness. The thin films have properties such as electrical, optical, surface roughness, and uniformity comparable or superior to those of indium-tin oxide (ITO) and zinc-doped ITO in terms of transparency, conductivity, work function, uniformity, and surface roughness. The MoO2 and MoO2 containing thin films can be used in organic light-emitting diodes (OLED), liquid crystal display (LCD), plasma display panel (PDP), field emission display (FED), thin film solar cell, low resistivity ohmic contacts, and other electronic and semiconductor devices.

Provided are methods for producing nanostructures and nanostructures obtained thereby. The methods include heating a certain point of a substrate dipped into a precursor solution of the nanostructures so that the nanostructures are grown in a liquid phase environment without evaporation of the precursor solution. The methods show excellent cost-effectiveness because of the lack of a need for precursor evaporation at high temperature. In addition, unlike the vapor-liquid-solid (VLS) process performed in a vapor phase, the method includes growing nanostructures in a liquid phase environment, and thus provides excellent safety and eco-friendly characteristics as well as cost-effectiveness. Further, the method includes locally heating a substrate dipped into a precursor solution merely at a point where the nanostructures are to be grown, so that the nanostructures are grown directly at a desired point of the substrate. Therefore, it is possible to grow and produce nanostructures directly in a device. As a result, unlike the conventional process, it is not necessary to assemble and integrate the nanostructures produced in a sacrificial substrate into a device.

Provided is a method for preparing transition metal oxide nano-particles from a transition metal as a reactant. The method includes dissolving the transition metal into aqueous hydrogen peroxide to provide peroxi-metallate solution, and then adding a reactive solution containing an alcohol, water and an acid thereto to perform hydrothermal reaction. More particularly, the method for preparing transition metal oxide particles includes: dissolving transition metal powder as a reactant into aqueous hydrogen peroxide to provide a peroxi-metallate solution with a molar concentration of transition metal of 0.001-0.2 M; adding a reactive solution containing an alcohol, water and an acid to the peroxi-metallate solution to provide a mixed solution; and subjecting the mixed solution to hydrothermal reaction to provide transition metal oxide nano-particles.

It is an object of the present invention to provide an organic electroluminescence element which can be easily produced and has a good light-emitting property and a good lifetime property, and a method for producing the same.

That is, the present invention provides the organic electroluminescence element comprising an anode, a light-emitting layer and a cathode, and further comprising a metal doped molybdenum oxide layer provided between the anode and the light-emitting layer; and the method for producing the organic electroluminescence element including a stacking step to obtain a metal doped molybdenum oxide layer by simultaneously depositing molybdenum oxide and a dopant metal on another layer which constitutes the element.

The invention provides a preparation method of a ball-flower-shaped molybdenum trioxide microsphere in a three-dimensional hierarchical structure and belongs to the technical field of preparation technologies of advanced inorganic nanomaterials. The preparation method particularly comprises the steps of adding citric acid at a certain mole ratio into a sodium molybdate and thiourea mixed solution with a certain concentration, intensively mixing, sealing a mixed solution in an autoclave, carrying out hydrothermal reaction for a certain time at specific temperature, washing, drying, and roasting in a muffle furnace in air to form the ball-flower-shaped molybdenum trioxide microsphere in the three-dimensional hierarchical structure. The method is low in cost, simple in production technology, high in productivity, free from environmental pollution and easy for industrial mass production. The ball-flower-shaped molybdenum oxide microsphere in the three-dimensional structure is regular in morphology, and can be used for the field of chemical catalysis, photocatalysts, gas sensors and the like.

Belonging to the technical field of molybdenum metallurgy, the invention relates to a method for microwave roasting of molybdenite concentrate to produce high-purity molybdenum oxide. The method includes: firstly conducting crushing and ball milling on molybdenite concentrate, then spreading the crushed molybdenite concentrate to a thickness of 1-4cm, and placing the product in a microwave cavity; turning on a microwave output switch, blowing in compressed air, regulating the microwave output power, and carrying out pre-oxidation on the crushed molybdenite concentrate; heating the pre-oxidized molybdenite concentrate to a sublimation temperature and performing thermal insulation for 30-60min, in the process, letting the molybdenum trioxide steam generated by oxidizing roasting overflow through a microwave reactor top, performing water-cooling and then conducting collection by a bag dust collector, thus obtaining high-purity molybdenum trioxide reaching the nonferrous metal industry grade 2 standard. The method provided by the invention has the advantages of short technological process, low energy consumption, and high product purity, etc.

This disclosure provides a unique approach for the synthesis of non-stoichiometric, mesoporous metal oxides with nano-sized crystalline wall. The as-synthesized mesoporous metal oxide is very active and stable (durability>11 h) electocatalyst in both acidic and alkaline conditions. The intrinsic mesoporous metal oxide serves as an electrocatalyst without the assistant of carbon materials, noble metals, or other materials, which are widely used in previously developed systems. The as-synthesized mesoporous metal oxide has large accessible pores (2-50 nm), which are able to facilitate mass transport and charge transfer. The as-synthesized mesoporous metal oxide requires a low overpotential and is oxygen deficient. Oxygen vacancies and mesoporosity served as key factors for excellent performance.

The invention discloses (NH4+)xMoS2 inserting compound and x is 0.2-3.0. The method includes the following steps: taking layer inserting to supramoly by using butyl lithium to gain layer inserting supramoly, making supramoly supernatant liquid, making (NH4+)xMoS2 layer inserting compound in ammonium chloride solution. The invention could be used as a good solid lubricant and could heating with alkali to gain single layer supramoly. It solves the storing problem of single layer of supramoly. It has crucial application value in mechanical, electric, aviation and spaceflight, chemical, etc.

The invention relates to a method for preparing molybdenum trioxide. The method comprises the following steps of: preparing a 15-60 percent sodium molybdate aqueous solution into which an organic matter additive is added; undergoing a high-pressure hydrothermal reaction; filtering and separating; evaporating and crystalizing a mother liquor; baking at a low temperature; circularly utilizing a mother liquor, and the like. A circular decomposing method is adopted, so that the decomposing rate of a sodium molybdate solution is increased effectively, and the purity of a prepared molybdenum trioxide product is higher than 99.5 percent; and compared with the conventional production technology, the method has the advantages of short production process flow, mild condition, simple equipment, low energy consumption and low pollution.

A method for the extraction and purification of molybdenum, the method comprising the steps of: transferring an irradiated fuel solution to an extraction system, the irradiated fuel solution comprising iodine and molybdenum and other fission products, the extraction system comprising at least one sorbent column; passing the irradiated fuel solution upwards through the at least one sorbent-containing extraction column; directing the irradiated fuel solution towards a fuel management system by means of at least one discharge alignment valve; directing the extraction column eluate towards an iodine removal system; removing the iodine from the extraction column eluate; purifying the extraction column eluate; and collecting the purified eluate. Also disclosed is an apparatus for accomplishing the aforementioned method.

The invention relates to a hexagonal-phase MoO2 nanosphere stacked micron hollow sphere and a preparation method and application thereof. The preparation method of the micron hollow sphere comprises the step of carrying out a hydrothermal synthesis on MoO3 powder and diethylenetriamine, wherein the mass ratio of MoO3 powder to diethylenetriamine is (3-10):1. According to the invention, the preparation method of the hexagonal-phase MoO2 nanosphere stacked micron hollow sphere is proposed for the first time, operation is simple and easy, and the prepared micron hollow sphere is good in property and can be massively synthesized; and the hexagonal-phase MoO2 nanosphere stacked micron hollow sphere prepared by the method in the invention has good circulation property and high specific capacity, and the specific capacity of the prepared micron hollow sphere still can reach 250mAhg<-1> after thirty-five-time circulation under the condition that current density is 0.5Ag<-1>.