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293results about How to "Can be produced industrially" patented technology

Preparation method of friction type silicon dioxide

The invention discloses a preparation method of friction type silicon dioxide. The preparation method comprises the following steps of: preparation of a first tank of materials: adding sodium sulfate solution into a reaction tank, heating, and then adding hexadecyl trimethyl ammonium bromide, then adding sodium silicate solution and sulfuric acid, controlling PH value, and after addition of the sodium silicate solution, adding the sulfuric acid till the final PH value is 4.4-5.0; preparation of a second tank of materials: adding sodium sulfate solution into another reaction tank, heating, and then adding hexadecyl trimethyl ammonium bromide, then adding sodium silicate solution and sulfuric acid, controlling PH value, and after addition of the sodium silicate solution, adding the sulfuric acid till the final PH value is 4.4-5.0; while stirring, adding a half of the material of the first tank into the material of the second tank, stirring, carrying out pressing filtration, washing and crushing on the formed silicon dioxide to prepare the friction type silicon dioxide. In the silicon dioxide, the RDA (Relative Dentine Attrition) value is 120-140, the PCR (Pellicular Cleaning Ratio) value is 100-130, and the PCR / RDA is equal to 0.80-1. The friction type silicon dioxide has the advantages of low wear, high cleanness and good thickening property.
Owner:GUANGZHOU FEIXUE MATERIAL TECH

Method for preparing mixed-valent-state iron doped zeolite imidazate skeleton nano-material

InactiveCN110724272AUniform and controllable particle sizeHigh ROS Generation EfficiencyIron saltsMeth-
The invention relates to a method for preparing a mixed-valent-state iron doped zeolite imidazate skeleton nano-material. The method comprises the steps of simultaneously dispersing bivalent and trivalent iron salts and zinc nitrate into a methanol solvent to form an iron-zinc precursor solution, mixing a 2-methylimidazole methanol solution with the precursor solution, placing the mixture in an oil bath with the temperature of 40 DEG C to 100 DEG C, carrying out a sustained magnetic stirring reaction, and then, subjecting a product to centrifugation, washing and drying treatment, thereby obtaining the mixed-valent-state iron doped zeolite imidazate skeleton nano-material. The mixed-valent-state iron doped zeolite imidazate skeleton nano-material with relatively high yield and uniform and controllable particle size is obtained. According to the method disclosed by the invention, the total iron doped amount can reach 50% to the maximum through adjusting a ratio of bivalent iron salts totrivalent iron salts, and conversion ratios of zinc ions and iron ions can separately reach up to 78% and 60%. The method is simple and economical, and reacted mother liquor can be reused. The obtained nano-material has a relatively high active oxygen generating efficiency under ultrasonic induction, has a tremendous application value in degradation of environmental pollutants and sonodynamic therapy of tumors and can be applied to preparation of high-concentration monoatomic iron-carbon based catalysts.
Owner:BEIJING UNIV OF CHEM TECH

Preparation method of low-specific-surface-area high-oil-absorption-value friction type silicon dioxide

The invention belongs to the technical field of silicon dioxide, and particularly relates to a preparation method of low-specific-surface-area high-oil-absorption-value friction type silicon dioxide.The preparation method comprises the steps that S1, 8-12 m<3> of ethanol aqueous solution is injected and heated to 60-70 DEG C, and stirring starts; S2, water glass and sulfuric acid are added dropwise to carry out a parallel flow reaction, the pH value in the reaction process is controlled to be 6.0-6.8, meanwhile, absolute ethyl alcohol is added every 5-10 minutes in the reaction process to keep the volume ratio of ethyl alcohol to water in a reaction system to be 1:(3-7), after the water glass is dropwise added, dropwise addition of sulfuric acid is stopped, and stirring continues; S3, stirring and heating are stopped, aging is conducted for one hour, and pressure filtration, washing, drying and crushing are conducted on the on formed silicon dioxide to prepare silicon dioxide. The silicon dioxide has the advantages of a low in specific surface area, a high oil absorption value, a high water absorption amount, the friction property and the like; toothpaste has good friction and cleaning performance after the silicon dioxide is used, and meanwhile, the problem of expansion of the viscosity of the toothpaste is well solved.
Owner:GUANGZHOU FEIXUE MATERIAL TECH

Functional resin containing 4,6-dimercapto-1,3,5-triazine alkali metal salt and preparation method thereof

The invention discloses functional resin containing 4,6-dimercapto-1,3,5-triazine alkali metal salt and a preparation method thereof. The method comprises the steps of dripping ethanediamine into chloromethylated bead mixture swelled by a solvent to carry out nucleophilic substitution to obtain the resin containing active amino; carrying out substituted grafting reaction on the obtained resin containing the active amino and cyanuric chloride to obtain the resin grafted with the cyanuric chloride; carrying out sulfhydrylation reaction on the prepared resin grafted with the cyanuric chloride in water solution of Na2S and/or NaSH, and then alkalifying with aqueous alkali after the sulfhydrylation reaction is finished. The method is simple in processing equipment, and convenient and simple to operate; and the sulfydryl resin prepared by the method is high in sulfydryl content, large in adsorbing capacity on heavy metal ions, strong in adsorption capacity, strong in regeneration capacity, good in repeated use effect, free of pollution, and low in cost, can remove and gather metal ions of heavy metals such as copper, lead, nickel, chromium, mercury and the like in waste water at the same time, and especially has good absorption efficiency when the concentration of the heavy metals in the waste water is low.
Owner:JIENTE NEW MATERIAL TECH CO LTD

Bacterial cellulose-based antibacterial dry film for acute trauma and preparation method and application thereof

The invention relates to a bacterial cellulose-based antibacterial dry film for acute trauma, which comprises a bacterial cellulose-based dry film and an inorganic antibacterial agent. The drug loading quantity of the bacterial cellulose-based antibacterial dry film is 1.00*10<-5>-4.0mg / cm<2>. The preparation method of the bacterial cellulose-based antibacterial dry film comprises the following steps: cutting a bacterial cellulose-based wet film into a diaphragm; drying; then, soaking the diaphragm into an inorganic antibacterial agent solution which is prepared in advance; and drying for the second time to obtain the bacterial cellulose-based antibacterial dry film. The bacterial cellulose-based antibacterial dry film provided by the invention has the advantages of light and soft texture, good biocompatibility, high hygroscopicity, good air permeability, lasting antibacterial property and the like; and the preparation method is simple, convenient and easy to implement and is low in cost. In the practical application process, the bacterial cellulose-based antibacterial dry film can be cut into pieces in arbitrary shapes, can not adhere to the skin, can not irritate the skin, can be quickly degraded in the environment after being discarded, and can be used as an environment-friendly functional antibacterial dressing.
Owner:DONGHUA UNIV

Preparation method of porous nanocrystalline Cu2S counter electrode of quantum-dot-sensitized solar cell

The invention belongs to the technical field of solar cells and energies, and particularly relates to a preparation method of a porous nanocrystalline Cu2S counter electrode of a quantum-dot-sensitized solar cell. The preparation method comprises the steps of: regarding copper acetate and thioacetamide as precursors; obtaining 20-100 nm cuprous sulfide (Cu2S) nanometer particles through solvothermal reaction; preparing the cuprous sulfide (Cu2S) nanometer particles and ethanol into a thick liquid; forming 5-10 microns Cu2S nanocrystalline porous film on a conductive base body by utilizing a knife coating method, a silk screen print method or a spin-coating method; sintering at 300-500 DEG C in an inert atmosphere or vacuum for 10-60 min to obtain a battery electrode. The prepared Cu2S nanometer porous counter electrode extremely increases contact area of the counter electrode and electrolyte, further increases catalytic reaction site of the Cu2S and the electrolyte, and improves performance of the solar cell. In addition, the preparation method of the porous nanocrystalline Cu2S counter electrode of the quantum-dot-sensitized solar cell is simple in preparation technology, relatively low in cost and has wide application foreground and wide research values.
Owner:UNIV OF SCI & TECH BEIJING

Organic luminous material and preparation method thereof

The invention provides an organic luminous material and a preparation method thereof, and relates to an organic silicon polymer. Raw materials of the organic luminous material comprise metallic organic substance and polycarbosilane. The preparation method comprises the following steps of: putting polydimethylsiloxane into a reaction kettle, heating the polydimethylsiloxane under the protection ofargon, inflating the argon to the reaction kettle, adding n-hexane into the reaction kettle to dissolve the product after the temperature in the reaction kettle is naturally cooled to room temperature, filtering the product, removing the n-hexane in vacuum to obtain the polycarbosilane, soaking the ground polycarbosilane into ethanol, flushing the insoluble substances by using the ethanol and then drying the insoluble substances in vacuum; and pouring the polycarbosilane powder and the metallic organic substance powder into a three-necked bottle, heating the mixed powder to between 150 and 160 DEG C under the protective atmosphere of argon, preserving the heat for 1 to 1.5 hours, heating the mixed powder to between 260 and 270 DEG C, preserving the heat for 1 to 1.5 hours, dissolving the product by using the dry n-hexane after the reaction is finished and the product is cooled, filtering the product to remove the insoluble substances, and finally distilling the product with reduced pressure to obtain the powdery solid organic luminous material.
Owner:XIAMEN UNIV
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