411 results about "Germanium dioxide" patented technology

The present invention relates to a method of fabricating an improved lithium silicate glass ceramic and to that material for the manufacture of blocks for dental appliances using a CAD/CAM process and hot pressing system. The lithium silicate material has a chemical composition that is different from those reported in the prior art with 1 to 10% of germanium dioxide in final composition. The softening points are close to the crystallization final temperature of 800° C. indicating that the samples will support the temperature process without shape deformation.

The invention discloses an ion nutritional liquid fertilizer and a preparation method thereof. The fertilizer comprises the following components by weight parts: 15-35 parts of potassium hydroxide, 5-15 parts of germanium dioxide, 1-5 parts of sodium selenite or sodium selenate, 5-15 parts of zinc acetate or zinc sulfate, 1-5 parts of chromic chloride, 2-8 parts of ammonium metavanadate, 15-40 parts of organic acid, 20-50 parts of amino acid, 10-20 parts of boric acid, 2-10 parts of urea and 500-900 parts of water, wherein the organic acid is citric acid or acetic acid and the amino acid is compound amino acid or monomer amino acid. The preparation method comprises the following steps of: taking the components of the fertilizer by weight parts; dissolving germanium dioxide into the potassium hydroxide; adding the organic acid, and then performing acidizing chelation reaction for 5-10 hours; adding the sodium selenite, zinc acetate, amino acid, boric acid, chromic chloride, ammonium metavanadate, urea and water; reacting for 5-10 hours; and filtering and removing slag, thereby obtaining the ion nutritional liquid fertilizer.

The invention relates to a method for recovering germanium from flyash by a wet process, belonging to the technical field of wet-process metallurgy. The method comprises the following steps of: (1) crushing flyash to more than 200 meshes by a wet process; (2) carrying out oxidizing leaching twice on wet flyash by using a sulfuric acid solution, sodium chlorate and ammonium fluoride; (3) crushing the flyash to 200-400 meshes for a second time; (4) leaching 3 or 4 times by using the same condition as that of the first leaching; (5) regulating the pH value of the first leached liquid to 2-2.5 by using ammonia water, and then precipitating and leaching out germanium in the liquid by using tannin with a weight percentage content of 80-99 percent; (6) drying and roasting the germanium precipitate to prepare a germanium concentrate; distilling the germanium concentrate with hydrochloric acid by using a conventional method to obtain germanium tetrachloride; and redistilling, rectifying, purifying and hydrolyzing to obtain high-purity germanium dioxide. The invention is used for flyash after recovering germanium by a fire process, sufficiently utilizes rare germanium metal, reduces the pollution of tailings to the environment, and has the advantages of low cost and high recovery rate.

The invention provides a method for preparing germanium dioxide (GeO2). According to the embodiment of the invention, the method comprises the following steps: hydrolyzing the germanium tetrachloride(GeCl4) in a fully-closed hydrolysis reactor to obtain the hydrolysis product of the GeCl4, centrifuging and filtering the hydrolysis product of the GeCl4 to obtain the GeO2 and the filtrate, and cleaning the GeO2 by high-purity water to obtain the high-purity GeO2 and the cleaning solution. According to the embodiment of the invention, the GeO2 hydrolyzing, filtrating and washing method and device have the advantages of high degree of automation, high GeO2 hydrolysis yield, good solid-liquid centrifugal separation effect, low production costs, less metal loss and environment friendliness.

The invention relates to a low cost method for rapidly synthesizing an ITQ-13 molecular sieve. The method comprises the steps of dissolving a template in deionized water; adding a promoter, an alkali source, germanium dioxide, an aluminium source and crystal seeds; adding a silicon source and a fluorine source successively when the above materials are dissolved; stirring to form a uniform gel; crystallizing for 0.5-8 days under self-generated pressure and at a crystallization temperature of 100-220 DEG C; shock cooling with cold water; fully washing a crystallization product with the deionized water; and drying to obtain molecular sieve raw powder. The synthetic method has the advantages of simpleness, rapidity, easiness and low cost.

The invention relates to the field of hydrometallurgy, in particular to a preparation method of low-chloride high-purity germanium dioxide. According to the process, coarse germanium tetrachloride is subject to repeated steaming and rectification to obtain high-purity germanium tetrachloride, and a brand new method is adopted in the hydrolysis section of the high-purity germanium tetrachloride, wherein high-purity nitrogen is adopted for gasifying the high-purity germanium tetrachloride into germanium tetrachloride gas, then the germanium tetrachloride gas is led into a special hydrolysis device, vacuum filtration and germanium dioxide washing are carried out after hydrolysis is finished, then germanium dioxide is dried, the germanium dioxide is dried secondly, and drying is carried out secondly. The low-chloride high-purity germanium dioxide obtained through the process method has the beneficial effects that the purity can reach 99.9999% or above, the chlorine content is lower than 0.0030%, and the germanium dioxide direct recovery rate reaches 92.0% or above.

An ytterbium-doped optical fiber includes: a core which contains at least ytterbium, aluminum, and phosphorus; and a cladding which encircles the core, wherein an aluminum oxide equivalent concentration of the aluminum in the core is 0.2 mol % or more, a diphosphorus pentaoxide equivalent concentration of the phosphorus is higher than the aluminum oxide equivalent concentration, and the core either does not contain germanium or contains less than 1.1 mol % of germanium in a germanium dioxide equivalent concentration.

The invention belongs to the technical field of display of fully-organic perovskite quantum dots, and discloses a CsPbBr3 (cesium-lead-bromide) perovskite quantum dot fluorescent glass for display ofwide color gamut and a preparation method and application thereof. The CsPbBr3 perovskite quantum dot fluorescent glass comprises the following components in percentage by mole: 0 to 45% of SiO2 (silicon dioxide), 0 to 45% of GeO2 (germanium dioxide), 30 to 40% of B2O3 (boron oxide), 2 to 8% of Al2O3 (aluminum oxide), 3 to 7% of MCO3 (metal carbonate), 1 to 5% of ZnO (zinc oxide), 5 to 15% of CsBr(cesium bromide) or Cs2CO3 (cesium carbonate), 2 to 10% of PbBr2 (lead bromide) or PbO (lead oxide), and 3 to 15% of NaBr (sodium bromide) or KBr (potassium-bromide), wherein M is Ca (calcium) or Sr(strontium); the sum of the components in percentage by mole is 100%. The CsPbBr3 perovskite quantum dot fluorescent glass has the advantages that the technology is simple, and the operation is easy;after in-situ crystallization, the quantum efficiency is higher, the light emitting stability is obviously improved, and the broad application prospect is realized.

The present invention discloses one kind of bright red underglaze color, one kind of overglaze and their preparation process. The bright red underglaze color consists of stabilizer, 0.02-34 wt%, silica 11.3-56 wt%, lead oxide 2.4-27 wt%, cadmium sulfoselenide 2-20 wt%, Al2O3 1.7-27 wt%, B2O3 1.5-27 wt%, CrO2 0.3-32 wt%, GeO2 0.08-33 wt%, MgO 1.4-13 wt%, CaO 0.7-15 wt%, Li2O 0.7-13.2 wt%, K2O 1-7 wt% and NaO 1-5.3 wt%; and the overglaze consists of clinker 5-55 wt%, ZnO 3-12 wt%, albite 5-30 wt%, potash feldspar 7-35 wt%, baked talc 2-16 wt%, silica 2-18 wt%, and kaolin 2-26 wt%. The bright red underglaze color and the overglaze have pure color and very low Pb and Cd leaching amount.

In one embodiment, the present application discloses a cell culture medium for culturing cell lines suitable for producing a therapeutic protein, comprising an amino acid selected from a group consisting of L-arginine, L-asparagine, L-proline, L leucine and L hydroxyproline and a mixture thereof; a vitamin selected from a group consisting of ascorbic acid Mg²⁺ salt, biotin, pyridoxine HCL, folic acid, riboflavin and D-calcium pantothenate, and a mixture thereof; an element selected from a group consisting of ammonium meta vanadate, sodium meta vanadate, germanium dioxide, barium acetate, aluminum chloride, rubidium chloride, cadmium chloride, ammonium molybedate, stannous chloride, cobalt chloride, chromium sulfate, silver nitrate, sodium metasilicate, zinc sulfate, manganese sulfate H₂O, manganous chloride, ferric nitrate 9H₂O, ferrous sulfate 7H₂O, ferric ammonium citrate, magnesium chloride anhydrous, and magnesium sulfate anhydrous, and a mixture thereof; a nucleoside selected from a group consisting of uridine and cystidine; a sugar selected from a group consisting of galactose, mannose and N-Acetyl-D-Mannosamine; and a triple buffering system comprising sodium carbonate, sodium bicarbonate and HEPES; wherein the cell culture medium is animal component-free, plant component-free, serum-free, growth factors-free, recombinant protein-free, lipid-free, steroid-free, and free of plant or animal hydrolysates and/or extracts.

A method is disclosed for depositing a dielectric film on a substrate having a plurality of gaps formed between adjacent raised surfaces disposed in a high density plasma substrate processing chamber substrate. In one embodiment the method comprises flowing a process gas comprising a germanium source, a silicon source and an oxidizing agent into the substrate processing chamber; forming a high density plasma that has simultaneous deposition and sputtering components from the process gas to deposit a dielectric film comprising silicon, germanium and oxygen; and during the step of forming a high density plasma, maintaining a pressure within the substrate processing chamber of less than 100 mTorr while allowing the dielectric film to be heated above its glass transition temperature.

A method for synthesis of germanium nanoparticles in thin SiO₂ films comprising: preparing a solution comprising silicon esters, germaniumtetrachloride (GeCl₄) or germanium esters, methyl- or higher alcohols, and water; applying the solution to a surface of a substrate; consolidating the solution on the surface of the substrate, thereby obtaining a glass comprising silicon dioxide and germanium dioxide; selectively reducing the germanium dioxide to form germanium nanoparticles.

The invention relates to a method for recovering germanium from germanium-containing materials, particularly relates to a method for recovering germanium from germanium-containing materials of non-ferrous smelting industry, and belongs to the technical field of hydrometallurgy. The method comprises the steps of leaching germanium-containing materials as raw materials of which the particle sizes are 100 meshes with inorganic strong acid as an leaching agent of which the concentration is 50-120g/L and an aid-leaching agent at 35-95 DEG C and filtering to obtain a germanium-containing leaching solution, adjusting the pH value of the germanium-containing leaching solution to be 6-9, stirring and carrying out liquid-solid separation to obtain germanium residues, and calcining the germanium residues at 350-500 DEG C to obtain a crude germanium dioxide product, wherein the aid-leaching agent is one of tartaric acid, water-soluble tartrate, citric acid, water-soluble citrate, oxalic acid and water-soluble oxalate. The method disclosed by the invention has the advantages of simple process, easiness in operation, high recovery ratio of germanium, large enrichment ratio, and convenience in industrial production and application.

The invention relates to a method for comprehensively recovering various valuable metals from a germanium-containing material by a wet process, belonging to the field of metallurgy of rare metals. The method comprises the following steps: leaching and separating lead slag in the circulation process, recovering germanium dioxide by tannin extract germanium participation, and recovering copper slag and zinc slag from the germanium participation waste liquor. The method provided by the invention can comprehensively and effectively recover valuable elements, such as lead, zinc, copper and germanium, and the technological process is stable and convenient to control; the invention effectively solves the problem of environmental pollution, and the recovery rate of germanium is up to 90% or above.

The invention discloses a preparation method of rare earth ion doped tungsten oxygen fluoride silicate up-converted luminescent glass. The preparation method comprises the steps of: firstly, uniformly mixing silicon dioxide, germanium dioxide, aluminum oxide, tungsten oxide, calcium fluoride, titanium dioxide and rare earth oxide in a mortar; and then preparing the Er<3+>-Yb<3+> rare earth ions doped tungsten oxygen fluoride silicate up-converted luminescent glass by adopting a high-temperature melting annealing method. The method disclosed by the invention is simple in preparation method, low in raw material cost and simple in required device without a special device; and the overall preparation process is carried out in air atmosphere. According to the invention, tungsten oxide is introduced into an oxygen fluoride silicate glass substrate for the first time, and the further solution of the problems that the oxygen fluoride silicate glass is poor in chemical stability and mechanical strength after tungsten oxide is introduced is facilitated, so that the glass product has the advantages of low phonon energy of fluoride and good crystallization stability of oxide, thereby obtaining strong up-converted red and green light output visible to naked eyes.

The invention discloses a germanium-graphene composite cathode material for a lithium ion battery and a preparation method of the germanium-graphene composite cathode material. The composite cathode material is prepared from germanium particles and grapheme through compounding, wherein the nano germanium particles are uniformly distributed in a grapheme sheet layer to form a grapheme network cladded three-dimensional net structure. The preparation method comprises the following steps: (1) stirring and dispersing; (2) carrying out microwave hydrothermal; and (3) washing, drying and collecting. According to the germanium-graphene composite cathode material for the lithium ion battery and the preparation method of the germanium-graphene composite cathode material, germanium and germanium dioxide are re-crystallized and grow on the graphene in situ, the bonding strength of the germanium and the grapheme is higher than that of germanium-graphene composite material obtained through mixing simply, the electrical conductivity of the grapheme network is fully exerted, and the volume effect of the germanium is effectively inhibited. The germanium-graphene composite cathode material for the lithium ion battery has the characteristics of high capacity, high magnification and excellent cycling stability, the preparation process adopts simple and effective microwave hydrothermal reaction, the process is simple, the energy consumption is low, the yield is high, no pollution is caused, the germanium-graphene composite cathode material can be promoted and applied conveniently and is suitable for large-scale production.

The invention provides a preparation method of a germanium nano-particle/multi-layer graphite compound-based high-performance anode material for a lithium-ion battery. By a common water solution method, germanium nano-particles are formed by reducing germanium dioxide, and are compounded with a multi-layer graphite material to prepare a nontoxic nano germanium/multi-layer graphite composite material, so that the nontoxic nano germanium/multi-layer graphite composite material is applied to the anode material for the lithium-ion battery and demonstrates excellent electrochemical properties. According to the preparation method provided by the invention, a high-quality germanium nano-particle/multi-layer graphite compound is obtained for the first time. Compared with other physical or chemical methods, the experimental operation is simpler and more convenient; a fussy chemical preparation process is not needed; meanwhile, the prepared composite material is high in purity and free of an oxidation layer; and the electric capacity of the lithium-ion battery can be greatly improved.

The invention discloses a germanium/carbon composite negative electrode material and a preparation method thereof. The preparation method comprises the steps of carrying out ball milling and mixing on germanium dioxide and polyvinylpyrrolidone, annealing at a hydrogen atmosphere in the presence of argon, so as to prepare the germanium/carbon composite negative electrode material. When being used as a negative electrode material of a lithium ion battery, the germanium/carbon composite negative electrode material has the characteristics of good cycling stability and high multiplying power capacity.

The invention specifically discloses a preparation method of a polyester substance, the polyester substance, a polyester chip and a polyester film. The preparation method comprises the following operation steps of: a) mixing an acid component with an alcohol component, and performing esterification reaction or transesterification to obtain an ester; b) performing condensation polymerization to the ester obtained in the step a) under the effect of a catalytic system; and c) obtaining the polyester substance from the step b), wherein the catalytic system adopts a germanium dioxide catalyst, and the germanium dioxide is in form of a tetragonal crystal or a hexagonal crystal or is in an amorphous state. The polyester substance, polyester chip and polyester film prepared by the preparation method have low chromatic value b, high degree of purity and other outstanding characteristics, and are specifically suitable for being used for preparing an optical thin-film with high performance requirement.

The invention discloses a germanium-carbon-graphene composite material which is compounded from nano germanium. germanium dioxide, flocculent carbon and reduction-oxidation graphene, wherein the germanium dioxide is coated on the surface layer of the germanium to form a core shell, thereby forming nano core-shell particles; and the nano core-shell particles are uniformly dispersed and distributed in the flocculent carbon, and coated by the reduction-oxidation graphene network. The invention also discloses a preparation method and application of the germanium-carbon-graphene composite material. The germanium-carbon-graphene composite material disclosed by the invention has the characteristics of high capacity, high ratio and high loop stability, and has the advantages of simple preparation technique, low energy consumption, high yield and no pollution.