Abstract: A molybdenum oxychloride or a tungsten oxychloride, wherein the molybdenum oxychloride or the tungsten oxychloride has a moisture content of less than 1 wt %. A method of producing a molybdenum oxychloride or a tungsten oxychloride, wherein a molybdenum oxide or a tungsten oxide as a raw material is subject to dehydration treatment at 400° C. or higher and 800° C. or less, and the raw material that underwent dehydration treatment is thereafter reacted with a chlorine gas to synthesize a molybdenum oxychloride or a tungsten oxychloride. An object of the present invention is to provide a molybdenum oxychloride or a tungsten oxychloride having a low moisture content, as well as a production method thereof.

Abstract: The present disclosure provides a phosphate framework electrode material for sodium ion battery and a method for synthesizing such electrode material. A surfactant and precursors including a sodium precursor, a phosphate precursor, a transition metal precursor are dissolved in a solvent and stirred for sufficient mixing and reaction. The precursors are reacted to yield a precipitate of particles of NaxAbMy(PO4)zXn compound and with the surfactant attached to the particles. The solvent is then removed and the remaining precipitate is sintered to crystallize the particles. During sintering, the surfactant is decomposed to form a carbon network between the crystallized particles and the crystallized particles and the carbon matrix are integrated to form the electrode material.

Abstract: A process for producing a homogenous multi compound system which is hydroxide- and/or oxide-based includes a first alternative process comprising providing a first and a second refractory metal in respective hydrofluoric solutions, and mixing the first and second hydrofluoric solutions to provide a mixed hydrofluoric solution comprising a dissolved first and second refractory metal. A second alternative process comprises dissolving the first and the second refractory metal in an alternative mixed hydrofluoric solution. The mixed hydrofluoric solution or the alternative mixed hydrofluoric solution is precipitated with a precipitant to provide a solids mixture in a suspension. The first and second refractory metal is from the group consisting of Mo, W, Nb, Re, Zr, Hf, V, Sb, Si, Al, and Ta. The first and second refractory metal are different. At least one of the first and second refractory metal is provided as a fluoro and/or as an oxyfluoro complex.

Abstract: A looping method for production of MoO2, the method including reacting molybdenite feed with a substantially stoichiometric mixture comprising MoO3 and oxygen in a first furnace to produce MoO2 and SO2, removing a first portion of the MoO2 from the first furnace, transferring a second portion of the MoO2 from the first furnace to a second furnace, reoxidizing of the transferred portion of the MoO2 in the second furnace to MoO3; and looping the MoO3 from the second furnace to the first furnace for use as an oxidizing agent.

Abstract: [Object] To provide a composition for forming a tungsten oxide film from an aqueous solution, and also to provide a pattern formation method employing that composition. [Means] The present invention provides a tungsten oxide film-forming composition comprising: water, a water-soluble metatungstate, and at least one additive selected from the group consisting of anionic polymers, nonionic polymers, anionic surfactants, and tertiary amino group-containing nonionic surfactants. For forming a pattern, this composition can be employed in place of a silicon dioxide film-forming composition in a pattern formation process using an image reversal trilayer structure, a resist undercoat layer or a resist top protective film.

Abstract: The present invention provides a method for the preparation of low-dimensional materials, comprising mixing a pristine material to be abraded with an organic solvent to form a mixture, abrading the material to be abraded by bead-milling, obtaining a suspension comprising the material of low dimension and the organic solvent, and removing the organic solvent from the suspension to obtain the low-dimensional material.

Abstract: A heat shielding material and method for manufacturing thereof is provided. The method for manufacturing the heat shielding material, includes: providing a tungsten oxide precursor solution containing a group VIII B metal element; drying the tungsten oxide precursor solution to form a dried tungsten oxide precursor; and subjecting the dried tungsten oxide precursor to a reducing gas at a temperature of 100° C. to 500° C. to form a composite tungsten oxide. The heat shielding material includes composite tungsten oxide doped with a group I A or II A metal and halogen, represented by MxWOy or MxWOyAz, wherein M refers to at least one of a group I A or II A metal, W refers to tungsten, O refers to oxygen, and A refers to a halogen element. The heat shielding material also includes a group VIII B metal element.

Abstract: An object of the present invention is to provide an infrared-shielding nanoparticle dispersion that has a property whereby visible light is adequately transmitted, and light in the near-infrared region is adequately shielded; an infrared-shielding body manufactured using the infrared-shielding nanoparticle dispersion; a method for manufacturing infrared-shielding nanoparticles that are used in the infrared-shielding nanoparticle dispersion; and infrared-shielding nanoparticles manufactured using the method for manufacturing infrared-shielding nanoparticles.

Abstract: A method for producing an ammonium tungstate aqueous solution includes the steps of: adding sulfuric acid to a solution containing tungstate ions; bringing the solution having the sulfuric acid added therein, into contact with an anion exchange resin; and bringing the anion exchange resin into contact with an aqueous solution containing ammonium ions.

Abstract: The present invention provides an electrode material for batteries made from tungsten oxide powder, wherein the tungsten oxide powder has a first peak present within a wavenumber range of 268 to 274 cm?1, a second peak present within a wavenumber range of 630 to 720 cm?1, and a third peak present within a wavenumber range of 800 to 810 cm?1, when a Raman spectroscopic analysis method is performed on the electrode material.

Abstract: A method of preparing an organic light-emitting device having excellent sealing characteristics against external environment and flexibility.

Abstract: 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.

Abstract: A process for preparing a mesoporous metal oxide, i.e., transition metal oxide, Lanthanide metal oxide, a post-transition metal oxide and metalloid oxide. The process comprises providing a micellar solution comprising a metal precursor, an interface modifier, a hydrotropic ion precursor, and a surfactant; and heating the micellar solution at a temperature and for a period of time sufficient to form the mesoporous metal oxide. A mesoporous metal oxide prepared by the above process. A method of controlling nano-sized wall crystallinity and mesoporosity in mesoporous metal oxides. The method comprises providing a micellar solution comprising a metal precursor, an interface modifier, a hydrotropic ion precursor, and a surfactant; and heating the micellar solution at a temperature and for a period of time sufficient to control nano-sized wall crystallinity and mesoporosity in the mesoporous metal oxides. Mesoporous metal oxides and a method of tuning structural properties of mesoporous metal oxides.

Abstract: According to one embodiment, there is provided a method for producing highly crystallized particles having a specific surface area of 5 m2/g or more. The raw material composition contains a resin and at least partially amorphous precursor particles. The composition is heat-treated to carbonize the resin and improve the crystallinity of the precursor particles. A mixture of highly crystallized particles and carbon is prepared. Then, a solution containing an acid is contacted with the mixture to react the acid with the carbon. The carbon is removed and a slurry containing reaction product is prepared. The highly crystallized particles include a first portion having a smaller diameter and a second portion having a larger diameter.

Abstract: A process comprises (a) combining (1) at least one base and (2) at least one metal carboxylate salt comprising (i) a metal cation selected from metal cations that form amphoteric metal oxides or oxyhydroxides and (ii) a lactate or thiolactate anion, or metal carboxylate salt precursors comprising (i) at least one metal salt comprising the metal cation and a non-interfering anion and (ii) lactic or thiolactic acid, a lactate or thiolactate salt of a non-interfering, non-metal cation, or a mixture thereof; and (b) allowing the base and the metal carboxylate salt or metal carboxylate salt precursors to react.

Abstract: A molybdenum disulfide powder product produced by jet milling a molybdenum disulfide precursor material and substantially continuously combining newly sized-reduced particles with oil to produce said molybdenum disulfide powder product, said molybdenum disulfide powder product having a D50 particle size of less than 4 ?m and an acid number that is less than about 0.5 mg KOH/g. A method for producing powder product includes the steps of: Providing a supply of a precursor powder material; accelerating particles of the precursor powder material by combining them with a flow of gas; confining the accelerated particles in a milling chamber so that they collide with one another to effect a size reduction; and coating newly exposed surfaces of size-reduced particles with oil.

Abstract: A lithographic process includes the use of a silicon-containing polymer or a compound that includes at least one element selected from the group consisting of: Ta, W, Re, Os, Ir, Ni, Cu or Zn in a resist material for an EUV lithographic process. The wavelength of the EUV light used in the process is less than 11 nm, for example 6.5-6.9 nm. The invention further relates to novel silicon-containing polymers.

Abstract: Molybdic oxide is recovered from molybdenite by a multistep process in which (A) the molybdenite is converted to soluble and insoluble molybdic oxide by pressure oxidation, (B) the insoluble molybdic oxide is converted to soluble molybdic oxide by alkaline digestion and then combined with the soluble molybdic oxide, and (C) the molybdenum values of the combined streams are extracted into an organic phase using a nonprimary amine. The extracted molybdenum values are recovered from the organic phase using aqueous ammonia to form ammonium dimolybdate (ADM) which is recovered as refined crystals from a two-step calcination process.

Abstract: A looping method for production of MoO2, the method including reacting molybdenite feed with a substantially stoichiometric mixture comprising MoO3 and oxygen in a first furnace to produce MoO2 and SO2, removing a first portion of the MoO2 from the first furnace, transferring a second portion of the MoO2 from the first furnace to a second furnace, reoxidizing of the transferred portion of the MoO2 in the second furnace to MoO3; and looping the MoO3 from the second furnace to the first furnace for use as an oxidizing agent.

Abstract: Tungsten trioxide (WO3) nanoparticles are synthesized via a sol-gel route using metallic tungsten as precursor and printed on a flexible electrode using inkjet printing in order to build solid-state electrochromic cells. A method for separate control of different spectral regions of the electrochromic device (near infrared and visible) is disclosed.

Abstract: Embodiments may pertain to methods for preparing a transition metal oxide.

Abstract: The present invention relates to a method for producing a tungsten oxide photocatalyst having titanium oxide and copper ion supported thereon, comprising dissolving urea in a solution in which copper-ion supporting tungsten oxide particles are uniformly dispersed in a titanium oxide sol, thermally decomposing the urea to thereby allow the titanium oxide to precipitate on the surface of copper ion-supporting tungsten oxide and to be supported thereon; and a tungsten oxide photocatalyst modified by both titanium oxide and copper ion obtained by the method, wherein the rate of change of diffuse reflectivity (at wavelength of 700 nm) is less than 3% before and after the irradiation of ultraviolet and the titanium oxide is supported on the tungsten oxide in an island shape of 1 to 100 nm in size. The tungsten oxide photocatalyst having titanium oxide and copper ion supported thereon of the present invention exhibits high catalyst activity under visible light irradiation.

Abstract: Porous metal oxides are provided. The porous metal oxides are prepared by heat treating a coordination polymer. A method of preparing the porous metal oxide is also provided. According to the method, the shape of the particles of the metal oxide can be easily controlled, and the shape and distribution of pores of the porous metal oxide can be adjusted.

Abstract: The present disclosure generally relates to processes, apparatuses and custom catalysts designed to depolymerize a polymer. In one embodiment, the present invention relates to a de-polymerizing apparatus, catalysts and reaction schemes to obtain useful monomers including fuel products by “in situ” reactions using coupled electromagnetic induction.

Abstract: Molybdic oxide is recovered from molybdenite by a multistep process in which (A) the molybdenite is converted to soluble and insoluble molybdic oxide by pressure oxidation, (B) the insoluble molybdic oxide is converted to soluble molybdic oxide by alkaline digestion and then combined with the soluble molybdic oxide, and (C) the molybdenum values of the combined streams are extracted into an organic phase using a nonprimary amine. The extracted molybdenum values are recovered from the organic phase using aqueous ammonia to form ammonium dimolybdate (ADM) which is recovered as refined crystals from a two-step calcination process.

Abstract: The present disclosure relates to insulation components and their use, e.g., in regenerative reactors. Specifically, a process and apparatus for managing temperatures from oxidation and pyrolysis reactions in a reactor, e.g., a thermally regeneratating reactor, such as a regenerative, reverse-flow reactor is described in relation to the various reactor components.

Abstract: Process for the production of doped metal oxide particles, wherein the doping component is present on the surface in the form of domains, wherein in a first reaction zone, an oxidizable and/or —hydrolysable metal compound as dopant together with an atomization gas is atomized into a flow of metal oxide particles in a carrier gas, wherein the mass flow of the metal oxide particles und —the mass flow of the dopant are selected such that the doped metal oxide particles contain 10 ppm to 10 wt.

Abstract: The present application provides a heterojunction nano material, a negative pole piece of a lithium ion battery, and a lithium ion battery, where the heterojunction nano material includes a MoO3 nanobelt and a metal oxide in the alloy lithium intercalation mechanism coated on the surface of the MoO3 nanobelt. The negative pole piece of the lithium ion battery uses the heterojunction nano material as an active material, and the lithium ion battery using the negative pole piece of the lithium ion battery has a large reversible specific capacity and a high cycle stability.

Abstract: The object of the invention is the synthesis of threadlike tungsten oxide W5O14, in the presence of nickel at a temperature lower than 1000° C. Represented is a procedure for the synthesis of a highly homogeneous phase of the W5O14 compound from the vapor phase, in the presence of nickel, by means of a chemical transport method in a closed quartz ampoule. As an alternative example, a procedure is represented for the synthesis of the W5O14 compound in a through-flow reaction vessel. Both procedures yield electrically conductive threadlike crystals of the W5O14 compound. The synthesis is performed in vapor phase. Tungsten enters the reaction as a pure phase or via WS2±x, x?4, previously synthesized from the elements, and/or the source of tungsten may also be tungsten oxides WO3?Y, 0?y?1. Nickel may enter the reaction via NiI2, Ni(OH)2 and/or atomic nickel.

Abstract: Disclosed herein are photocatalyst powder and a production method thereof, and by having photocatalyst particles corn binded without reduction of a specific surface area, the reduction of the specific surface area is nearly none while the pores are developed, as well as the absorption rate with respect to light is superior, the method of producing photocatalyst powder includes forming initial photocatalyst powder by molding nanoparticles of photocatalyst substance into a certain shape through extrusion, and splitting the initial photocatalyst powder into a plurality of photocatalyst powder by injecting the initial photocatalyst powder into a predetermined splitting solution, the initial photocatalyst powder being split into the plurality of photocatalyst powder by the predetermined spliting solution.

Abstract: There is provided infrared shielding nanoparticles having excellent water-resistant property and excellent infrared shielding property, which is the infrared shielding nanoparticles of composite tungsten oxide expressed by a general formula WyOz and/or a general formula MxWyOz, with an average primary particle size of the nanoparticle being 1 nm or more and 800 nm or less, and a surface of the nanoparticle being coated with tetrafunctional silane compound or its hydrolysis product and/or an organic metal compound.

Abstract: Process for the production of a powdered spherical tungstic acid by acidification of an aqueous alkaline tungstate solution with mineral acid at elevated temperature, preferably in a continuous stirred tank or a cascade of at least 2 continuous stirred tanks, and tungstic acid obtainable in this way, which is characterized by a high bulk density and spherical morphology.

Abstract: The present invention includes a method of producing a crystalline metal oxide nanostructure. The method comprises providing a metal salt solution and providing a basic solution; placing a porous membrane between the metal salt solution and the basic solution, wherein metal cations of the metal salt solution and hydroxide ions of the basic solution react, thereby producing a crystalline metal oxide nanostructure.

Abstract: The present invention relates to (i) a plant growth-improving agent containing a growth-improving component that increases a concentration of an oxoanion in an area around a plant, the oxoanion being heavier than a sulfate ion and containing four oxygen atoms, (ii) a seed to which such a plant growth-improving agent has been applied, and (iii) a plant growth-improving method including a cultivating step of growing a plant in the presence of such a growth-improving component.

Abstract: The present invention provides a non-toxic yellow inorganic pigment consist of samarium and molybdenum oxides which may be used as additives to plastics, glasses, ceramics and paints. The samarium molybdenum yellow pigment preferably comprise Sm6MoO12 having a cubic crystal structure. Inorganic pigments according to the invention are formed by mixing stoichiometric amounts of (NH4)6Mo7O24.4H2O and Sm2O3; ball milled and calcined 1500-1650 C for 10-12 h in air atmosphere. The well ground calcined powders were used for characterization of the pigments. The phase purity and optical properties of the prepared pigments were investigated. A further aspect of the present invention is to provide of colouring a substrate. The method includes the steps of providing a substrate, and adding a samarium molybdate yellow pigment to the substrate. The samarium molybdate yellow pigment may be dispersed in the substrate or coated on the substrate.

Abstract: Disclosed herein is a method for preparing a near infrared absorbing agent. The method includes admixing tungsten trioxide and a reducing agent in water and allowing for a partial reduction of the tungsten trioxides to yield the near infrared absorbing agent.

Abstract: In one embodiment, an aqueous dispersion liquid contains at least one particles selected from tungsten oxide particles and tungsten oxide composite particles. A mean primary particle diameter (D50) of the particles is in the range of 1 nm to 400 nm. In the aqueous dispersion liquid, concentration of the particles is in the range of 0.1 mass % to 40 mass %, and pH is in the range of 1.5 to 6.5. The aqueous dispersion liquid excels in dispersibility of particles and capable of maintaining good liquidity for a long period.

Abstract: An object of the present invention is to provide a metal salt-containing composition which is applicable to many metal source materials, and can be used for forming a compact and uniform metal oxide film comparable to those formed according to a sputtering method, as well as to provide a substrate having a metal complex film on the surface thereof obtained using the metal salt-containing composition, and a substrate having a metal complex film on the surface thereof obtained by further heating the substrate. Moreover, another object of the present invention is to provide a method for manufacturing a substrate having such a metal complex film on the surface thereof. According to the present invention, a metal salt-containing composition containing a metal salt, a polyvalent carboxylic acid having a cis-form structure, and a solvent, in which: the molar ratio of the polyvalent carboxylic acid to the metal salt is not less than 0.5 and not more than 4.

Abstract: In one embodiment, an antiviral material includes at least one microparticles selected from tungsten oxide microparticles and tungsten oxide composite microparticles. The microparticles have an inactivation effect R of 1 or more expressed by [R=logC?logA], when there is evaluated a virus titer by inoculating on a specimen to which the microparticles are adhered, at least one virus selected from a low pathogenic avian influenza virus (H9N2), a high pathogenic avian influenza virus (H5N1) and a swine influenza virus, and irradiating the specimen with visible light having a wavelength of 380 nm or more and illuminance of 6000 1× for 24 hours.

Abstract: The object of the invention is the synthesis of threadlike tungsten oxide W5O14, in the presence of nickel at a temperature lower than 1000° C. Represented is a procedure for the synthesis of a highly homogeneous phase of the W5O14 compound from the vapor phase, in the presence of nickel, by means of a chemical transport method in a closed quartz ampoule. As an alternative example, a procedure is represented for the synthesis of the W5O14 compound in a through-flow reaction vessel. Both procedures yield electrically conductive threadlike crystals of the W5O14 compound. The synthesis is performed in vapor phase. Tungsten enters the reaction as a pure phase or via WS2±x, x?0, previously synthesized from the elements, and/or the source of tungsten may also be tungsten oxides WO3?y, 0?y?1. Nickel may enter the reaction via NiI2, Ni(OH)2 and/or atomic nickel.

Abstract: A heat shielding material and method for manufacturing thereof is provided. The method for manufacturing the heat shielding material, includes: providing a tungsten oxide precursor solution containing a group VIII B metal element; drying the tungsten oxide precursor solution to form a dried tungsten oxide precursor; and subjecting the dried tungsten oxide precursor to a reducing gas at a temperature of 100° C. to 500° C. to form a composite tungsten oxide. The heat shielding material includes composite tungsten oxide doped with a group I A or II A metal and halogen, represented by MxWOy or MxWOyAz, wherein M refers to at least one of a group I A or II A metal, W refers to tungsten, O refers to oxygen, and A refers to a halogen element. The heat shielding material also includes a group VIII B metal element.

Abstract: Single crystal MoO3 nanowires were produced using an electrospinning technique. High resolution transmission electron microscopy (HRTEM) revealed that the 1-D nanostructures are from 10-20 nm in diameter, on the order of 1-2 ?m in length, and have the orthorhombic MoO3 structure. The structure, crystallinity, and sensoric character of these electrostatically processed nanowires are discussed. It has been demonstrated that the non-woven-network of MoO3 nanowires exhibits higher sensitivity and an n-type response to NH3 as compared to the response of a sol-gel based sensor.

Abstract: Provided is a roasting method capable of reducing both C and S components in minerals down to 0.5% or less, respectively, and securing a yield ratio of 90% or more for the Mo component. In a rotary kiln 7, a V, Mo and Ni containing material containing C and S components is subjected to oxidizing roasting to remove the C and S components from the material before reducing the material by means of a reducing agent in order to recover valuable metals composed of V, Mo and Ni. The rotary kiln is equipped with a burner 11 disposed on a material charge side 8a of the roasting furnace 8 to which the material is charged. In the roasting furnace, a direction along which the material moves and a flow of oxygen-containing gas introduced into the roasting furnace 8 are set to be parallel with each other.

Abstract: Process for the production of a powdered spherical tungstic acid by acidification of an aqueous alkaline tungstate solution with mineral acid at elevated temperature, preferably in a continuous stirred tank or a cascade of at least 2 continuous stirred tanks, and tungstic acid obtainable in this way, which is characterised by a high bulk density and spherical morphology.

Abstract: Disclosed is a method and device for detection of H. Pylori in breath emissions utilizing an unlabelled urea, in which a patient ingests a safe quantity of unlabelled urea. After ingestion, expired breath of the patient is analyzed for ammonia, with a detection based on levels of ammonia lower than 50 parts per billion to 500 ppm to detect helicobacter pylori.

Abstract: An optical element is disclosed which includes transparent superconductor material.

Abstract: Process for the production of a powdered spherical tungstic acid by acidification of an aqueous alkaline tungstate solution with mineral acid at elevated temperature, preferably in a continuous stirred tank or a cascade of at least 2 continuous stirred tanks, and tungstic acid obtainable in this way, which is characterized by a high bulk density and spherical morphology.

Abstract: A hydrogen gas detecting material, which changes in light absorption characteristics when exposed to an atmosphere containing hydrogen, and the coating method are characterized in that (1) the principal component of the hydrogen gas detecting material is tungsten oxide, (2) palladium is deposited on the surface of the tungsten oxide, (3) the tungsten oxide is coated on a substrate by a sputtering method involving a controlled oxygen pressure, and (4) the temperature of the substrate during coating with the tungsten oxide is room temperature (20° C.).

Abstract: Process for preparing a mixed metal oxide powder, in which oxidizable starting materials are evaporated and oxidized, the reaction mixture is cooled after the reaction and the pulverulent solids are removed from gaseous substances, wherein as starting materials, at least one pulverulent metal and at least one metal compound, the metal and the metal component of the metal compound being different and the proportion of metal being at least 80% by weight based on the sum of metal and metal component from metal compound, together with one or more combustion gases, are fed to an evaporation zone of a reactor, where metal and metal compound are evaporated completely under nonoxidizing conditions, subsequently, the mixture flowing out of the evaporation zone is reacted in the oxidation zone of this reactor with a stream of a supplied oxygen-containing gas whose oxygen content is at least sufficient to oxidize the starting materials and combustion gases completely.

Abstract: The present invention relates to a method of recovering rhenium (Re) and other metals from Re-bearing materials.