1994 results about "Vanadium oxide" patented technology

A catalyst system and a method for reducing nitrogen oxides in an exhaust gas by reduction with a hydrocarbon or oxygen-containing organic compound reducing agent are provided. The catalyst system contains a silver catalyst and a modifier catalyst, where the modifier catalyst contains a modifier oxide, where the modifier oxide is selected from the group consisting of iron oxide, cerium oxide, copper oxide, manganese oxide, chromium oxide, a lanthanide oxide, an actinide oxide, molybdenum oxide, tin oxide, indium oxide, rhenium oxide, tantalum oxide, osmium oxide, barium oxide, calcium oxide, strontium oxide, potassium oxide, vanadium oxide, nickel oxide, tungsten oxide, and mixtures thereof. The modifier oxide is supported on an inorganic oxide support or supports, where at least one of the inorganic oxide supports is an acidic support. The catalyst system of the silver catalyst and the modifier catalyst provides higher NO_x conversion than either the silver catalyst or the modifier catalyst alone.

A light emitting device comprises a pair of electrodes and a mixed layer provided between the pair of electrodes. The mixed layer contains an organic compound which contains no nitrogen atoms, i.e., an organic compound which dose not have an arylamine skeleton, and a metal oxide. As the organic compound, an aromatic hydrocarbon having an anthracene skeleton is preferably used. As such an aromatic hydrocarbon, t-BuDNA, DPAnth, DPPA, DNA, DMNA, t-BuDBA, and the like are listed. As the metal oxide, molybdenum oxide, vanadium oxide, ruthenium oxide, rhenium oxide, and the like are preferably used. Further, the mixed layer preferably shows absorbance per 1 μm of 1 or less or does not show a distinct absorption peak in a spectrum of 450 to 650 nm when an absorption spectrum is measured.

The invention discloses a method of vanadium slag direct entering high temperature roasting furnace calcify roasting, that is, high calcium vanadium slag or ordinary vanadium slag and lime or limestone are mixed uniformly without the gradual heating up process from low temperature to high temperature, the mixture enters into the roasting furnace of more than 600 DEG C for calcified roasting., the vanadium of the vanadium slag is changed into vanadium acid calcium, vanadium of the roasting clinker is dissolved into the solution under the leaching function of sulphuric acid solution, vanadium oxide and the like vanadium products are further made. The invention needs no gradual heating up process from low temperature to high temperature of the prior sodium treatment roasting, thereby reducing roasting time, improving productivity of unit and reducing production cost.

The invention relates to a method for cleanly producing vanadium oxide, which belongs to the field of extraction of vanadium oxide. The technical problems to be solved by the invention is to provide the method for cleanly producing the vanadium oxide which not only can obtain a high-quality vanadium product, but also can ensure that vanadium waste water can be reclaimed. The method for producing the vanadium oxide comprises the following steps: preparing roasting raw materials, calcification roasting; infiltrating, separating solid and liquid, precipitating vanadium by ammonium salt, calcining for deaminating or reducing, and the like. Waste water after vanadium extraction can be returned to a system for recycling after the waste waster is subjected to neutralizing treatment by lime cream so as to realize zero drainage of the waste water. The method also improves the reclamation rate of vanadium to be superior to that of the prior process, and reduces production cost. Through combining with other technologies, the method can change extracted slag and other waste into secondary resource to be used once again, and realize clean production.

A glass composition substantially free from lead and bismuth and containing vanadium oxide and phosphor oxide as main ingredients, wherein the sintered glass of the glass composition exhibits 10⁹ Ωcm or more at 25 ° C.

Certain example embodiments relate to seals for glass articles. Certain example embodiments relate to a composition used for sealing an insulted glass unit. In certain example embodiments the composition includes vanadium oxide, barium oxide, zinc oxide, and at least one additional additive. For instance, another additive that is a different metal oxide or different metal chloride may be provided. In certain example embodiments, a composition may be combined with a binder solution that substantially or completely burns out by the time the composition is melted. In certain example embodiments, a CTE filler is included with a frit material. In certain example embodiments, a vacuum insulated glass unit includes first and second glass substrates that are sealed together with a seal that includes the above-described composition.

A method of operating an implantable medical device containing a Lithium Silver Vanadium Oxide battery. In response to a detected need for therapy, a current flow is delivered from the battery to a charge storage device. After the battery is at least partly depleted by one or more such deliveries of current or other power consumption, the battery is recharged. The recharging may be initiated in response to a selected time threshold, a selected number of current flow delivery events, a selected voltage level, an excess charge time duration, or other operating characteristics. A limited number of recharging cycles may be provided if the charging is done under controlled conditions with respect to charge current and voltage.

One aspect of the present invention is a light emitting element having a layer including an aromatic hydrocarbon and a metal oxide between a pair of electrodes. The kind of aromatic hydrocarbon is not particularly limited; however, an aromatic hydrocarbon having hole mobility of 1×10⁻⁶ cm²/Vs or more is preferable. As such aromatic hydrocarbon, for example, 2-tert-butyl-9,10-di(2-naphthyl)anthracene, anthracene, 9,10-diphenylanthracene, tetracene, rubrene, perylene, 2,5,8,11-tetra(tert-butyl)perylene, and the like are given. As the metal oxide, a metal which shows an electron-accepting property to the aromatic hydrocarbon is preferable. As such metal oxide, for example, molybdenum oxide, vanadium oxide, ruthenium oxide, rhenium oxide, and the like are given.

The invention discloses a method for preparing a cathode material of a sodium-ion battery, namely sodium vanadium fluorophosphates. The method comprises the following steps: using a vanadium source, a phosphorus source and a carbon source as main synthetic raw materials; dissolving into deionized water according to the molar ratio 1:1:1.2 of vanadium: phosphorus: carbon, heating in water bath, and continuously stirring to obtain light green pulp; after vacuum drying, grinding, then transferring into a tube furnace, preburning in an inert atmosphere at a certain temperature rise rate, cooling and then taking out to obtain black VPO4/C precursor powder; mixing the VPO4/C with NaF according to a stoichiometric ratio, ball-milling for 3 hours, sending into the tube furnace, then roasting in the inert atmosphere at the certain temperature rise rate, and cooling along with the furnace to obtain a positive active material NaVPO4F/C. According to the invention, cheap and easily-obtained pentavalent vanadium oxide or trivalent vanadium oxide is used as the main raw materials to prepare the sodium vanadium fluorophosphates cathode material through a sol gel activated auxiliary two-step high-temperature solid phase method, and the sodium vanadium fluorophosphates cathode material has the advantages of good stability, uniform particle size and good electrochemical performance. Meanwhile, the method has the advantages of simple synthesis process, short period and low cost and is convenient for large-scale production.

The present invention is directed to an unexpected benefit in a lithium cell derived from using a combination of silver vanadium oxide prepared in a temperature range of about 450° C. to about 500° C. activated with a nonaqueous electrolyte having a passivation inhibitor additive selected from a nitrite, a nitrate, a carbonate, a dicarbonate, a phosphonate, a phosphate, a sulfate and hydrogen fluoride, and mixtures thereof. The benefits include additional battery life resulting from a reduction in voltage delay and RDC build-up. A preferred electrolyte is 1M LiAsF6 in a 50:50 mixture, by volume, of PC and DME having dibenzyl carbonate added therein.

A catalyst used directly for oxidative desulfurizing to H2S gas contained acidic gas is proportionally prepared from iron oxide, aluminum oxide, titanium oxide, zinc oxide, and vanadium oxide by co-deposition method. It has high activity, selectivity and H2s conversion rate.

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.

A microbolometer includes a micro-bridge structure for uncooling infrared or terahertz detectors. The thermistor and light absorbing materials of the micro-bridge structure are the vanadium oxide-carbon nanotube composite film formed by one-dimensional carbon nanotubes and two-dimensional vanadium oxide film. The micro-bridge is a three-layer sandwich structure consisting of a layer of amorphous silicon nitride base film as the supporting and insulating layer of the micro-bridge, a layer or multi-layer of vanadium oxide-carbon nanotube composite film in the middle of the micro-bridge as the heat sensitive and light absorbing layer of the microbolometer, and a layer of amorphous silicon nitride top film as the stress control layer and passivation of the heat sensitive film. The microbolometer and method for manufacturing the same can overcome the shortcomings of the prior art, improve the performance of the device, reduce the cost of raw materials and is suitable for large-scale industrial production.

The invention discloses a catalyst for low-temperature flue gas denitration, and a preparation method thereof. The method adopts a selective catalytic reduction (SCR) technique, takes vanadium oxide as an active component and titanium oxide as a carrier, and substitutes fluorine for partial oxygen in an oxide catalyst, so as to prepare the catalyst, wherein the vanadium oxide as the active component is loaded on the carrier by an impregnation method; the titanium oxide as the carrier is prepared by a sol-gel method; and the substitution of fluorine for oxygen can be carried out when the titanium oxide as the carrier is prepared, or when the vanadium oxide as the active component is loaded, or when the titanium oxide as the carrier is prepared and the vanadium oxide as the active component is loaded. The catalyst remarkably improves low-temperature denitration activity and catalytic capability, can reach the NO removal rate of over 90 percent at a temperature over 200 DEG C, has strong industrial application value, and can be widely applied to the NH3 selective catalytic reduction of nitrogen oxides in flue gas.

A negative active material for a rechargeable lithium battery of the present invention includes a lithium-vanadium oxide core material being capable of performing reversible electrochemical oxidation and reduction, and an inorganic oxide coating layer disposed on the surface of the core material. The negative active material can improve stability at the interface between a negative electrode and an electrolyte, charge and discharge efficiency, and cycle-life, and can be applied along with all kinds of aqueous and non-aqueous binders.

The invention belongs to the field of metallurgy and particularly relates to a method for preparing ferrovanadium by a rollover furnace through the electro-aluminothermic process. The method for preparing the ferrovanadium by the rollover furnace through the electro-aluminothermic process comprises the steps that raw materials of vanadium oxide, aluminum, iron and lime which meet the production requirement are evenly mixed and then added into the rollover type electric-arc furnace, the method combining multi-phase smelting and stepping aluminum distribution is adopted, most slag is removed after the content of vanadium in the slag is reduced to a certain level, the repeated operation of multiple phases of feeding and slag discharging is conducted, the slag and iron are discharged together when the last phase of smelting is conducted and poured into an ingot mould, and ferrovanadium alloy can be obtained after cooling is conducted. The method for preparing the ferrovanadium by the rollover furnace through the electro-aluminothermic process is convenient to operate, capable of lowering aluminum consumption and obvious in economic benefit; meanwhile, the smelting yield of the ferrovanadium is increased, and the obtained ferrovanadium product is low in content of aluminum.