2679 results about "Vanadium(V) oxide" patented technology

The invention discloses a novel method for extracting and converting a substance containing vanadium into high-purity vanadium pentoxide by chlorination. The high-purity vanadium pentoxide process comprises batching, chlorination, dedusting, condensation, rectification, hydrolysis, filtering, drying and postprocessing. Raw materials comprise the substance containing vanadium and a carbon elementary substance and the weight ratio of the substance containing vanadium to the carbon elementary substance is 1: (0.05-0.25). The raw materials are evenly mixed, dried and put in a reactor and the high-purity vanadium pentoxide is obtained through successive chlorination, hydrolysis, postprocessing and the like. The novel method for producing high-purity vanadium pentoxide instead of a traditional method reduces industrial harmful waste water produced during a traditional hydrometallurgy process, and cyclic utilization of chlorine is achieved after the chlorine is processed. The whole production process is easy in process and basically free of produced wastes, and has certain economic benefit and social benefit. The purity of the vanadium pentoxide powder obtained by the method is 99.5%-99.99%.

The invention discloses a method for extracting tungsten, titanium and vanadium from a waste SCR (selective catalytic reduction) catalyst, which comprises the following steps: crushing the waste SCR catalyst, adding a strongly alkaline solution, and reacting; filtering, separating, then adding strong acid into the sodium tungstate and sodium vanadate mixed solution, and reacting to obtain tungstic acid and a sodium salt and vanadic acid mixed solution; regulating the pH value of the sodium salt and vanadic acid mixed solution until precipitate is separated out, thus obtaining ammonium vanadate; then adding sulfuric acid into the tungsten-and-vanadium-removed SCR catalyst, and reacting to obtain a titanyl sulfate solution and solids such as aluminum slag and the like; then adding water into the titanyl sulfate solution, and hydrolyzing to obtain titanic acid and a waste acid solution; and finally, respectively calcining the obtained ammonium vanadate, tungstic acid and titanic acid to obtain vanadium pentoxide, tungsten trioxide and titanium dioxide. According to the invention, tungsten, titanium and vanadium can be extracted from the SCR catalyst through the reaction with strong alkali and strong acid at a low temperature, the equipment requirement is low, the energy consumption is low, some products having added values can be coproduced, and no secondary pollution is generated, thereby facilitating popularization and application.

The invention discloses a process for producing vanadic anhydride by vanadium slag. The steps of the process comprise as follows: a, adding alkali metal salt in the vanadium slag, and mixing with each other uniformly, a mixture is obtained. b, laying the mixture obtained by step a into a calcining furnace to oxidize and calcine, vanadium slag grog is obtained. c, the calcined vanadium slag is discharged out of the furnace, fast cooling and performing water immersion. d, filtering the mixture obtained by step c, filter liquor is obtained. e, removing impurities in the filter liquor. f, adjusting the pH value of the filter liquor obtained by step e, adding ammonium salt to precipitate vanadium and filtering the filter liquor, then, ammonium peroxovanadate filter cake and ammonium metavanadate filter cake are obtained. g, calcining the filter cake after vanadium precipitation obtained by step f, and vanadic anhydride is obtained, wherein the content of the vanadic anhydride in the vanadium slag used in step a is 2.0%-8.0%. The invention has the advantages of simple and easy, low facility request, convenient operation and low cost, further, the residual quantity of the vanadic anhydride in waste slag is 0.55%-1.0%, which has fine economic benefit and social benefit.

The invention is a polarized sunglass lens that utilizes a multiband contrast enhancer comprised of three rare-earth oxides to provide relatively high peak transmittance in portions of the red and green spectrum, relatively lower transmittance for the blue spectrum, and very low transmittance for the UV spectrum. The lens provides enhanced perception of colors, heightened contrast, and improved visual acuity. The inclusion of vanadium pentoxide in the lens provides attenuation of the UV spectrum, thus protecting the user's eyes and the internal layers and colorants from UV-induced damage. The front lens element can be either the multiband contrast enhancer or a photochromic lens element.

The invention relates to a preparation method of a vanadium battery electrolyte solution with high purity and high concentration. The vanadium battery electrolyte solution is different from a traditional vanadium electrolyte solution with vanadium pentoxide as raw material; through the method, a qualified vanadium solution produced by a vanadium factory is adopted as raw material, steps of removing impurities, precipitating vanadium, reducing, extracting and removing oil are carried out, after carrying out processes of four-step impurity removal and one-step reduction, the impurities in the electrolyte solution are effectively removed, and the all-vanadium solution flow battery vanadyl sulfate electrolyte solution with high purity and high concentration and with the concentration of 1-4 M is obtained. The method adopts the initial vanadium solution as the raw material, has the advantages of low cost, simple preparing procedures, and mild reaction conditions, allows the obtained electrolyte solution product to have high purity, and is suitable for application in an all-vanadium solution flow battery.

The invention which relates to a method for preparing high purity vanadium pentoxide through using ammonium metavanadate belongs to the wet metallurgy field. The method comprises the following steps: heating and dissolving crude ammonium metavanadate in water, adjusting the pH value to 8-10 with an alkali after dissolving, adding an impurity removing agent to remove impurities, filtering to obtain a sodium metavanadate solution, adding ammonia water or an ammonium salt to the sodium metavanadate solution to precipitate to obtain an ammonium metavanadate precipitate, dehydrating the ammonium metavanadate precipitate, carrying out water washing on the precipitate through using a dilute ammonium salt solution, dehydrating after the wash washing, and roasting to obtain the high purity vanadium pentoxide. Vanadium pentoxide produced through adopting the method of the invention has the advantages of high purity and less impurities, and completely satisfies production requirements of high-end products; and the method of the invention has the advantages of short process flow, simple equipment, low cost and high benefit, and is suitable for the large-scale industrial production.

A frit composition useful for sealing a light emitting device is disclosed. The frit composition comprises a glass portion comprising a base component and at least one absorbing component. The glass portion of the frit comprises silica, boron oxide, optionally alumina, and (a) cupric oxide and/or a (b) combination of ferric oxide, vanadium pentoxide, and optionally titanium dioxide. Also disclosed is an article comprising a substrate and a frit, and a glass package comprising two substrates and a frit positioned between the substrates. A method for manufacturing a hermetically sealed glass package comprising the deposition of a glass frit and heating of the glass frit to form a hermetic seal is also disclosed.

A desulfurizing-denitrating catalyst contains cellular activated carbon (90-99.9 wt.%) and V2O5. It is applied through putting it on supporter in fixed-bed reactor and reacting on fume at 150-250 deg.C and 500-5000/hr of space speed. Its advantage is high transform rate of 80% for SO2 and 50-100% for NO.

The invention relates to a method for extracting vanadium pentoxide from vanadium slag, belonging to the field of vanadium metallurgy. In order to solve the technical problem, the invention provides a method for extracting vanadium pentoxide from vanadium slag with less environment pollution. The method comprises the following steps of: a. smashing the vanadium slag, and removing metal iron to obtain the refined vanadium slag; b. baking the refined vanadium slag at 800-1000 DEG C to obtain grog; c. adding the grog into alkali liquor for leaching, and filtering with hot to obtain vanadium-containing solution and tailings; d. removing impurity in the vanadium-containing solution, reducing the temperature of the impurity-removed and vanadium-containing solution to be less than 35 DEG C, crystallizing and filtering to obtain Na3VO4.5-12H2O crystalloid and filtering mother liquor thereof; and e. dissolving the Na3VO4.5-12H2O crystalloid by adding water, treating with an acid ammonium salt precipitation method to obtain ammonium poly-vanadate or ammonium metavanadate, and dehydrating, deaminizing and melting the ammonium poly-vanadate or the ammonium metavanadate to obtain the vanadium pentoxide.

The invention discloses a preparation method of high-purity vanadium pentoxide. The preparation method comprises the following steps of: returning and dissolving coarse vanadium in aqueous alkali, and filtering the solution to remove metal impurities, which are subjected to precipitation reaction with the aqueous alkali, in the coarse vanadium, thus obtaining a primary returned solution; slowly pouring the primary returned solution into a sulfuric acid solution, adjusting the pH value of the solution to be 1.0-2.0 to obtain a liquid-solid mixture, and performing solid-liquid separation on the liquid-solid mixture; filtering and washing precipitates obtained from the solid-liquid separation of the mixture, and returning and dissolving the mixture into the aqueous alkali, thus obtaining a secondary returned solution; adding ammonium sulfate into the secondary returned solution for precipitating vanadium, and filtering the solution to obtain ammonium metavanadate; and processing the ammonium metavanadate to obtain the high-purity vanadium pentoxide. The preparation method adopting multiple stages of returned dissolving can be used for effectively removing the metal canon impurities of the vanadium pentoxide, and further obtaining the high-purity vanadium pentoxide with the metal canon impurity contents of less than 0.001% and the vanadium pentoxide content of 99.99%.

The invention relates to a method for preparing vanadium pentoxide from sulfuric acid leach liquor of stone coal vanadium ore, particularly a method for preparing high-purity vanadium pentoxide from sulfuric acid leach liquor of low-impurity-content stone coal vanadium ore. The method is characterized by sequentially comprising the following steps: (1) extracting leach liquor, which is obtained by leaching stone coal vanadium ore with sulfuric acid, to remove impurities; (2) carrying out back extraction on sulfuric acid to carry an organic phase; (3) oxidizing the back extraction liquor; (4) carrying out hydrolysis to precipitate vanadium; and (5) calcining the vanadium precipitate slag to obtain the vanadium pentoxide. Compared with the traditional technique, by using oxydol, persulfuric acid and the like as oxidants in the oxidation process, the method provided by the invention can avoid introducing other impurity cations, thereby ensuring the purity of the product vanadium pentoxide. Compared with the traditional ammonium-salt vanadium-precipitation technique, the method provided by the invention saves the alkali consumption required by neutralization. The purity of the prepared vanadium pentoxide is up to 99.9%, and the recovery rate of vanadium is up to above 98%; and meanwhile, the invention can implement no pollution and cyclic utilization of the back extraction agent.

The invention relates to a low-vanadium denitration catalyst and a preparation method and application thereof, and belongs to the technical fields of environmental materials, environmental catalysis and environmental protection. The catalyst is prepared by a co-immersion method by adopting anatase titanium dioxide as a carrier, vanadium pentoxide as a main active component and tungstic oxide and cerium oxide as minor active components. Moreover, the low-vanadium denitration catalyst is characterized in that the catalyst reduces both the dosage of highly toxic vanadium and cost, and also has a conversion rate of NOx higher than 90 percent within a temperature range from 200 to 450 DEG C. The method provided for reducing nitrogen oxide comprises the following steps: putting the catalyst in a fixed bed reactor and controlling the reaction temperature between 200 and 500 DEG C; and taking NH3 as a reducing agent and controlling air speed at 28,000h and total gas flow at 300ml/min. The low-vanadium denitration catalyst still maintains high conversion rate of NOx in the presence of water and sulfur dioxide, and is suitable for treating NOx in exhaust gases discharged from thermal power plants, smelting plants, oil plants, and the like.

The invention relates to a method for preparing vanadic anhydride. It comprises following steps: employing ammonium vanadate, vanadic anhydride of technical grade or waste catalyst discharged in sulfuric acid preparation process; treating with ammonium hydroxide, sulfuric acid and ammonium chloride, washing with water; getting fine active vanadic anhydride; removing foreign matter with ammonium hydroxide, calcium hydroxide, sodium aluminate, sodium silicate, sulfuric acid and ammonium chloride; washing with water again; drying; calcing at 670 Deg. C and getting high-purity vanadic anhydride. The invention is characterized in that it makes use of current material to prepare chemical materials urgently needed by industrial production, and saves a large amount of foreigh exchange.

The invention discloses a method of preparing high-purity vanadium pentoxide from roasting-method vanadium solution. The method comprises the following steps: adding a purifying agent into the roasting-method vanadium solution, wherein the purifying agent is polyaluminium chloride, magnesium chloride or calcium chloride, or the purifying agent is polyaluminium chloride and magnesium chloride, or polyaluminium chloride and calcium chloride; uniformly stirring the roasting-method vanadium solution containing the purifying agent, standing for settling, then filtering, and adding ammonium salt into the filtrate to precipitate vanadium; and finally, calcining meta-ammonium and deaminizing to prepare vanadium pentoxide with the purity being higher than 99.5%. Polyaluminium chloride serving as the purifying agent can be used for polymerizing jellies with several molecules into large particles with several tens of thousands of molecules, even hundreds of thousands of molecules. The large-particle molecular polymer is easy to settle in the vanadium solution and can be separated from the solution. The method provided by the invention has the advantages that the consumption of polyaluminium chloride is low, the flocculation process is simple, the flocculation capacity is strong, the flocculation speed is high, pollution is hardly caused and the cost is low.

A process for preparing V2O5 from the used catalyst containing V includes such steps as removing deposited oil from said catalyst, pulverizing, immersing in water, oxidizing, adding alkali to regulate pH=8.5-9.5, extracting at 50-60 deg.C for 1-2 hr, solid-liquid separation, recovering the solution of sodium vanadate and sodium molybdate, washing filtered dregs, calcining in rotary furnace, dissolving the calcined material in water, stirring, solid-liquid separation, recovering the solution of sodium vanadate and sodium molybdate, collecting said solution, removing impurity P, adding ammonium chloride to generate ammonium metavanadate deposit, solid-liquid separation, adding ammonium metavanadate in flake-making furnace, decomposing at 800-850 deg.C to obtain fused V2O5, and preparing V2O5 flakes.

The invention discloses a preparation method for vanadium dioxide and doped powder thereof. The method comprises the following steps: 1, weighing vanadium pentoxide, hydrogen peroxide and distilled water, preparing the materials into a V<5+>-containing complex aqueous solution; 2, adding a reducing agent, a surfactant and a dopant to the complex aqueous solution, and stirring to form a clear solution; 3, transferring the resulting solution from the step 2 to a hydrothermal reaction kettle, and carrying out a reaction for 1-168 hours at a temperature of 140-220 DEG C to obtain the doped powderof the VO2(B); 4, placing the resulting doped powder of the VO2(B) from the step 3 in high pure argon atmosphere or nitrogen atmosphere, and annealing for 10-720 minutes at the temperature of 400-700DEG C to obtain the doped powder of the VO2(M). The method of the present invention has characteristics of low cost, simple process and easy control, and is suitable for the large-scale industrial production. With the method of the present invention, the doping of the VO2 powder material can be realized, and the doped atoms can be uniformly dispersed in the VO2.

The invention relates to a method for preparing high-purity vanadium from heteropolyacid impurities in an amine extraction mode. Generally an ordinary vanadium solution is doped with impurities such as chromium, silicon, phosphorus, tungsten, molybdenum and arsenic, if acid is added into the solution, heteropolyacids such as phosphorus tungsten, phosphorus vanadium tungsten, silicon tungsten, phosphorus molybdenum tungsten, silicon molybdenum tungsten, molybdenum vanadium arsenic and tungsten arsenic can be formed, the impurities in the solution are removed by carrying out compounding synergic extraction on the heteropolyacids in the ordinary vanadium solution by using amines and a synergist so as to obtain a purified vanadium-containing raffinate, subsequently the vanadium-containing raffinate is evaporated and concentrated to be the concentration that each liter of the solution contains 40g vanadium, ammonium salt is further added into the concentrated liquid to obtain ammonium metavanadate solid, vanadium pentoxide with the purity greater than 99.9% is obtained through washing in pure water, drying and calcining in an oxygen atmosphere, the organic phase after the heteropolyacid is extracted is subjected to reverse extraction by using an alkali solution so as to form a heteropolyacid water phase, and the organic phase is recycled and circulated. The method has low requirement on equipment, and is simple to operate, key extraction agents are good in thermal stability and not sensitive in acid and alkali, and a recycling and circulating method is simple and easy to be industrialized.

The present invention relates generally to the production of a vanadium electrolyte, including a mixture of trivalent and tetravalent vanadium ions in a sulphuric acid solution, by the reactive dissolution of vanadium trioxide and vanadium pentoxide powders, the surface area and particle size characteristics being controlled for complete reaction to produce the desired ratio of V(III) to V(IV) ions in the solution. The solution may be suitable for direct use in the vanadium redox battery, or the solution can provide an electrolyte concentrate or slurry which can be reconstituted by the addition of water or sulphuric acid prior to use in the vanadium redox battery.

The invention provides a boiler coal combustion-improving desulfurizing and denitrifying agent composition. The composition comprises the following raw materials in parts by weight: 2-7 parts of sodium carbonate, 1-3 parts of alumina, 2-8 parts of aluminium hydroxide, 2-5 parts of ferric trichloride, 2-6 parts of ferric oxide, 3-10 parts of potassium permanganate, 3-10 parts of potassium chlorate, 10-35 parts of activated attapulgite clay, 15-30 parts of urea, 2-4 parts of ammonium formate, 2-4 parts of ammonium chloride, 6-23 parts of ammonium acetate, 3-9 parts of manganese oxide, 9-12 parts of copper chloride, 1-3 parts of copper oxide, 2-4 parts of zinc sulfate, 1-3 parts of zinc nitrate, 7-18 parts of potassium dichromate, 1.0-1.5 parts of titanium dioxide, 0.5-1.0 part of barium molybdate, 0.5-1.5 parts of cobalt sulfate, 0.5-1.5 parts of vanadium pentoxide, 0.3-0.7 part of cerium oxide, 0.1-0.2 part of sodium dodecyl benzene sulfonate and 0.1-0.2 part of alkyl glyceryl ether. The composition is convenient to use, has stable properties, plays roles of combustion improving, desulfurization and denitrification, has coal saving rate of 8-25% and can remove fixed sulfur by 50-70%.

The invention discloses a preparation method of monodispersed M-phase vanadium dioxide nanoparticles. The preparation method comprises the following steps: mixing vanadium pentoxide, oxalate dihydrate and water according to a molar ratio of (1-2.5) : 1 : (500-800) to obtain mixed liquid, adding 4%-6% of a surfactant based on the volume of the mixed liquid into the mixed liquid, and stirring for at least 2 hours to obtain a precursor solution; reacting the precursor solution in a sealed state at 200-260 DEG C for at least 1 day to obtain reaction liquid; performing solid-liquid separation and washing on the reaction liquid in sequence to obtain orthogonal vanadium dioxide powder; annealing the orthogonal vanadium dioxide powder in a nitrogen atmosphere at 300-600 DEG C for 0.5 hour to obtain the monodispersed M-phase vanadium dioxide nanoparticles with particle sizes of 60nm-80nm. The preparation method has the advantages of environmental protection and no temperature gradient control during annealing, and can be widely used for preparing the M-phase vanadium dioxide nanoparticles with very good dispersity.

The invention relates to a method for extracting V2O5 from stone coal vanadium ores, which is characterized in that the stone coal vanadium ores are grinded, subjected to high-temperature roasting, and directly leached out by a dilute sulfuric acid; slag is washed and filtered by water; and a leached solution is extracted by extract containing an N235 extractant, and subjected to back-extraction, ammonium metavanadate precipitation, filtration, washing, deamination and roasting to obtain the V2O5. The method greatly reduces pollution of waste gas and waste water. Compared with the prior salt roasting (sodium modification) technology, the technology has a reasonable design structure, high comprehensive utilization rate of resources, proper material consumption, strong controlled ability of the process, high product quality and high automation degree of the technological flow, and is convenient for large-scale industrial production. The technology does not have exact demands on the raw ores and has good adaptability. The overall yield of the technology is high, reaches more than 85 percent, is on the advanced level in China currently, and is improved by approximately 25 percent compared with the overall yield of sodium modification roasting technology of other vanadium smelting plants in Hunan province.

The invention relates to an iron powder production method by using a tunnel kiln to reduce concentrate pellets containing carbon vanadium ferrotitanium with titanium slag and vanadium pentoxide as combined products. Concentrate pellets are made from vanadium-titanium iron concentrate through crashing and damp milling. The iron powder and tailings are obtained by putting the concentrate pellets into the tunnel kiln to be reduced, crashing, wet-grinding, magnetic separation and gravity separation. The tailings are soaked with titania waste acid to eliminate remnants magnesium and iron. Then the tailings are filtrated and dried to obtain a new material. And then the new material is added with sodium salt to do salt roast and then to be soaked by water, then titanium slag and sodium vanadate are obtained respectively after the water soaking. At last, the vanadium pentoxide is obtained by ammonium vanadate precipitating and calcination deaminase to the sodium vanadate liquid. The invention eliminates the disadvantage of high energy consumption by electric furnace smelting and bad separating effect of vanadium and titanium, difficult control of vanadium and titanium trend and low yield rate of extracting vanadium and titanium through converter blowing iron molten, etc. The invention has the advantages of high yield rate of vanadium, titanium and iron and high resources utilization rate and explores a novel practical way for comprehensive utilization of vanadium, titanium and iron concentrate ore.

The invention belongs to the chemical engineering field, in particular relates to a method for preparing ammonium polyvandata with vanadium-containing solution. The method uses the vanadium-containing solution produced with the traditional sodium roasting-water immersing technology as the raw material. First, vanadium combines with added calcium compounds and produces calcium vanadate, which reacts with ammonium bicarbonate and transfers vanadium into the solution but transforms calcium into more insoluble calcium carbonate; the ammonium polyvandata is produced with the separated solution under appropriate pH and heating conditions. After redissolution of calcium vandata, the ammonium bicarbonate containing less than 0.1percent of SUM (Na2O+K2 O) can be obtained. The ammonium bicarbonate can be used for production of vanadium trioxide and vanadium pentoxide with exceedingly low contents of potassium and sodium; and the ammonia content of vanadium-precipitation waste water is only 60percent to 75 percent of vanadium-extraction waste water in traditional technologies. The invention has very promising application prospect.

The invention discloses a selective catalyst for removing oxynitrides from tail gases of diesel vehicles and a preparation method thereof. Cordierite honeycomb ceramic serves as a carrier, and the oxides of vanadium, zirconium, tungsten and titanium form a catalytic active site. The preparation method comprises the following steps of: sequentially dissolving vanadium pentoxide, a zircon salt, tungsten trioxide and titanium dioxide into the aqueous solution of oxalic acid, adding a bonder into the mixed solution to prepare pulp, impregnating the cordierite honeycomb ceramic in the pulp, drying the cordierite honeycomb ceramic for 1 to 3 hours at 100 to 150 DEG C, and roasting the cordierite honeycomb ceramic for 2 to 4 hours at 450 to 550 DEG C. In the invention, the preparation method is improved, and a powder catalyst is improved into a honeycomb selective catalytic reduction (SCR) catalyst applied to the removal of the oxynitrides from the tail gases of the diesel vehicles, so the high-efficiency catalytic removal of the oxynitrides can be realized at the temperature of 205 to 515 DEG C; and in the presence of steam or SO2, the activity of the catalyst is kept over 80 percent.

The invention belongs to the field of non-ferrous metal recycling, and in particular relates to a method for separating and recycling vanadium pentoxide in a waste SCR (Selective Catalytic Reduction) denitration catalyst according to a reduction acid leaching method. The method provided by the invention comprises the following steps: firstly, reducing pentavalent vanadium in the catalyst by using a reducing agent in an acidic solution to tetravalent vanadium which is more soluble, then oxidizing the tetravalent vanadium in the acidic solution to the pentavalent vanadium by using an antioxidant, fully hydrolyzing the pentavalent vanadium under certain conditions for precipitation by adjusting the pH value of the solution, collecting the precipitation, roasting the precipitation and then obtaining the vanadium pentoxide with high purity. The method disclosed by the invention is simple in process, higher in operability, and suitable for large-scale production. The recovery rate of the vanadium pentoxide can be ensured to reach above 95%, and the purity of the obtained vanadium pentoxide is high (higher than 98%), so that the vanadium pentoxide can be directly used for preparing raw materials of the SCR denitration catalyst; the method disclosed by the invention can not only turn wastes into useful resources, and harm into benefits, but also solve a series of potential environmental pollution problems to bring considerable economic benefits and environmental benefits.