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31results about How to "Low commercial price" patented technology

Preparation method of ultraviolet-resistant and high-temperature-resistant methyl silicone resin

The invention relates to a preparation method of ultraviolet-resistant and high-temperature-resistant methyl silicone resin, relates to the preparation method of modified methyl silicone resin, and is used for solving the problems that the existing methyl silicone resin is poor in high temperature and ultraviolet resistance, complicated in preparation method and high in cost. The preparation method comprises the following steps of:1, dispersing ethyl orthosilicate in anhydrous ethanol and then adding a mixing solution of deionized water, the anhydrous ethanol and ammonia, thereby obtaining a silica ethanol solution; 2, dispersing tetrabutyl titanate in the anhydrous ethanol and then adding the mixing solution of the deionized water, the anhydrous ethanol and hydrochloric acid, thereby obtaining a titania ethanol solution; 3, dispersing methyl triethoxysilane and diethoxydimethylsilane in the anhydrous ethanol, thereby preparing a methyl silicone resin prepolymer; and 4, regulating the pH values of the solutions obtained in the steps 1 and 2 to be 7 and performing a refluxing operation after adding the prepolymer, thereby obtaining the methyl silicone resin. The method is conventional in raw material preparation as well as simple and easy to implement. The thermal weight loss rate of the modified methyl silicone resin at the temperature of 300 DEG C is 0.6, so that the modified methyl silicone resin is good in ultraviolet resistance.
Owner:HARBIN INST OF TECH

Method for treating high-concentration difficulty-degradable alkaline waste liquid by using iron carbon activated persulfate

The invention relates to a method for treating high-concentration difficulty-degradable alkaline waste liquid by using iron carbon activated persulfate. The method comprises the following steps: adding a certain amount of zero-valent iron (Fe0), activated carbon (AC) and persulfate (PS) into high-concentration difficulty-degradable organic matter containing alkaline waste liquid at normal temperature and pressure, uniformly stirring, and reacting for 2-3h under the condition that the initial pH is alkaline to oxidatively degrade contaminants. A synergistic activating oxidant is obtained by adding the zero-valent iron and the activated carbon into the alkaline basic waste liquid, and sulfate and hydroxyl radicals are produced to oxidize the contaminants so as to degrade the alkaline waste liquid; compared with the conventional Fenton oxidation technology, the method has the advantages as follows: the pH application range is wider, the step of adding acid for neutralizing is omitted, removal of the contaminants is facilitated, and the economic cost is reduced; in addition, with the Fe0 and the AC as a catalyst, the efficiency of producing SO4- through activation of PS is significantly improved, so that efficient treatment to the alkaline waste liquid is facilitated better.
Owner:SUZHOU UNIV OF SCI & TECH

Preparation method of 2, 3, 3, 3-tetrafloropropylene

ActiveCN103833511AReduce the probability of side effectsAvoid the production of highly toxic substance perfluoroisobutyleneHalogenated hydrocarbon preparationChemistryPyrolysis
The invention provides a preparation method of 2, 3, 3, 3-tetrafloropropylene. The method comprises the following steps: with monochlorodifluoromethane and monochloro methane which are in a molar ratio of (0.5-4):1 as reaction raw materials, preheating the reaction raw materials, then mixing with superheated steam, wherein the volume ratio of the superheated steam to the reaction raw materials is (1-20):1, the temperature of the superheated steam is 900-1100 DEG C, the temperature in the reaction section is 600-1100 DEG C, and the stay time of reactants in the reaction section is 0.01-1s; and quenching, deacidifying, drying and rectifying and separating the product mixed flow to obtain 2, 3, 3, 3-tetrafloropropylene. The method provided by the invention overcomes the deficiency that a hollow tube is prone to carbonization in pyrolysis and side reactions are complex, the equipment maintenance rate is reduced, and meanwhile, the reaction period is prolonged, and the utilization ratio of the device is improved. The method provided by the invention has the characteristics of use of easily available raw materials, simple reaction process and the like. The obtained 2, 3, 3, 3-tetrafloropropylene has the advantages of zero ODP (Ozone Depletion Potential) and low GWP (Global Warming Potential), and is used as a substituent of automotive air conditionor refrigerant.
Owner:SHANDONG DONGYUE POLYMER MATERIAL

Antibacterial low-toxicity modified pueraria starch powdery adhesive

An antibacterial and low-toxic modified pueraria starch powdery adhesive, comprising the following components in parts by weight: 120-140 parts of pueraria starch, 6-10 parts of montmorillonite, 20-30 parts of casein, 22 parts of sodium acetate ‑24 parts, 3‑5 parts of hydrochloric acid, 7‑9 parts of crosslinking agent, 1‑3 parts of coupling agent, 7‑9 parts of defoaming agent, 25‑35 parts of composite preservative, 13‑17 parts of antibacterial agent, urea 18-22 parts, 17-25 parts of cetyltrimethylammonium bromide, 4-6 parts of potassium permanganate; the present invention also discloses an antibacterial and low-toxic modified Pueraria starch powder adhesive Preparation method: first mix the oxidized kudzu starch, compound preservative and organically modified montmorillonite, then add urea and casein for heating reaction to obtain mixture B, then add dispersant, coupling agent and defoamer to obtain glue The solid C is finally spray-dried and centrifuged to obtain a powdery kudzu root starch adhesive. The invention has the characteristics of high bonding strength, water resistance, antibacterial, long environmental protection storage period, etc., effectively reduces the harm to the environment, reduces the production cost, and improves the production benefit of the enterprise.
Owner:李琛璞

A method of using natural chitin to prepare bio-based retarding high-efficiency water reducer

ActiveCN107033308BReduce agglomeration and flocculationFully dispersedSuperplasticizerPhenol
The invention relates to a method for preparing a bio-base high-efficiency delayed-coagulation water-reducing agent from natural chitin. The method comprises the following steps: degrading a natural high polymer, and carrying out functional group remolding, so as to obtain a chitosan oligosaccharide intermediate containing functional groups such as amino and hydroxymethyl; carrying out condensation reaction by virtue of phenol and formaldehyde under alkaline conditions so as to generate a phenolic aldehyde intermediate, and carrying out addition reaction by virtue of sodium hydrogen sulfite and formaldehyde so as to introduce hydrophilic sulfonic acid groups to the phenolic aldehyde intermediate; and linking the chitosan oligosaccharide intermediate with the sulfonated phenolic aldehyde intermediate by virtue of hydroxymethyl polycondensation, so as to obtain the bio-base high-efficiency delayed-coagulation water-reducing agent with good water-reducing and delayed-coagulation effects. The chitin bio-base high-efficiency delayed-coagulation water-reducing agent has the characteristics of low raw material cost, environment-friendly protection process and the like and further has relatively good water-reducing and delayed-coagulation effects. The chitin bio-base high-efficiency delayed-coagulation water-reducing agent has economic and environmental protection benefits and is a novel high-efficiency water-reducing agent with great promise.
Owner:JINLING INST OF TECH

The preparation method of 2,3,3,3-tetrafluoropropene

The invention provides a preparation method of 2, 3, 3, 3-tetrafloropropylene. The method comprises the following steps: with monochlorodifluoromethane and monochloro methane which are in a molar ratio of (0.5-4):1 as reaction raw materials, preheating the reaction raw materials, then mixing with superheated steam, wherein the volume ratio of the superheated steam to the reaction raw materials is (1-20):1, the temperature of the superheated steam is 900-1100 DEG C, the temperature in the reaction section is 600-1100 DEG C, and the stay time of reactants in the reaction section is 0.01-1s; and quenching, deacidifying, drying and rectifying and separating the product mixed flow to obtain 2, 3, 3, 3-tetrafloropropylene. The method provided by the invention overcomes the deficiency that a hollow tube is prone to carbonization in pyrolysis and side reactions are complex, the equipment maintenance rate is reduced, and meanwhile, the reaction period is prolonged, and the utilization ratio of the device is improved. The method provided by the invention has the characteristics of use of easily available raw materials, simple reaction process and the like. The obtained 2, 3, 3, 3-tetrafloropropylene has the advantages of zero ODP (Ozone Depletion Potential) and low GWP (Global Warming Potential), and is used as a substituent of automotive air conditionor refrigerant.
Owner:SHANDONG DONGYUE POLYMER MATERIAL

Preparation method of ultraviolet-resistant and high-temperature-resistant methyl silicone resin

The invention relates to a preparation method of ultraviolet-resistant and high-temperature-resistant methyl silicone resin, relates to the preparation method of modified methyl silicone resin, and is used for solving the problems that the existing methyl silicone resin is poor in high temperature and ultraviolet resistance, complicated in preparation method and high in cost. The preparation method comprises the following steps of:1, dispersing ethyl orthosilicate in anhydrous ethanol and then adding a mixing solution of deionized water, the anhydrous ethanol and ammonia, thereby obtaining a silica ethanol solution; 2, dispersing tetrabutyl titanate in the anhydrous ethanol and then adding the mixing solution of the deionized water, the anhydrous ethanol and hydrochloric acid, thereby obtaining a titania ethanol solution; 3, dispersing methyl triethoxysilane and diethoxydimethylsilane in the anhydrous ethanol, thereby preparing a methyl silicone resin prepolymer; and 4, regulating the pH values of the solutions obtained in the steps 1 and 2 to be 7 and performing a refluxing operation after adding the prepolymer, thereby obtaining the methyl silicone resin. The method is conventional in raw material preparation as well as simple and easy to implement. The thermal weight loss rate of the modified methyl silicone resin at the temperature of 300 DEG C is 0.6, so that the modified methyl silicone resin is good in ultraviolet resistance.
Owner:HARBIN INST OF TECH
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