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37results about How to "Easy to complex" patented technology

Production technology of anti-static fabric

The invention discloses a production technology of an anti-static fabric. An electric conduction wire and a polyester cotton yarn are double-twisted to obtain a conductive yarn, the conductive yarn iswoven at intervals to obtain an anti-static gray fabric, and through singeing, shape setting and dyeing, the dyed gray fabric is obtained; through anti-static after-finishing of an anti-static finishing solution, two-time soaking and two-time rolling, the anti-static gray fabric is obtained; finally, through antibacterial anti-mite finishing of an antibacterial anti-mite finishing agent, two-timesoaking and two-time rolling, the anti-static fabric is obtained. The prepared anti-static fabric has good anti-static performance, can achieve moisture absorption and air permeation, has antibacterial and anti-mite performance and is good in comfort and particularly suitable for being used as a fabric of outdoor sports wear and climbing wear. The point-to-point resistance of the anti-static fabric reaches 2.8*1,010 omega, the rate of resisting staphylococcus aureus reaches 89.7%, the rate of resisting escherichia coli reaches 86.8%, the rate of resisting candida albicans reaches 73.6%, the water absorption rate reaches 106%, and the amount of water vapor transmission reaches 8,125 g/m<2>.24 h.
Owner:保定澳森制衣股份有限公司

Preparation method of quick-drying type metal anti-corrosion coating

The invention discloses a preparation method of a quick-drying type metal anti-corrosion coating. The preparation method of the quick-drying type metal anti-corrosion coating belongs to the technicalfield of coating preparation. Although the content of epoxidized soybean oil is less in the metal anti-corrosion coating, the activity of the epoxidized soybean oil is higher when reacting with maleicanhydride, so that the curing time of the metal anti-corrosion coating is shortened; a pre-mixed solution is used as a mixed monomer of an acrylic resin so as to be doped into dissolved epoxy resin,and a composite resin emulsion is obtained through grafting reaction; when the metal anti-corrosion coating is cured, hydrophobic substances in a micelle can be gathered and arrayed on a surface of apaint film, so that surface hydrophobicity of the metal anti-corrosion coating is improved; essential oil in an essential oil microcapsule has high volatility, can be slowly released from the microcapsule, and then is micro-emulsified in water of the metal anti-corrosion coating, so that drops of water become smaller, and water is convenient to volatize; the hydrophobicity of the essential oil isalso beneficial to water volatilization in the metal anti-corrosion coating, so that when the metal anti-corrosion coating is cured, the surface drying time is shorted, the aim of quick drying is achieved, and the application prospect is broad.
Owner:唐林元

Preparation method of Astragalus polysaccharide-iron

The invention provides a preparation method of Astragalus polysaccharide-iron. The method comprises the following steps: 1, extracting and purifying Astragalus polysaccharides; and 2, preparing Astragalus polysaccharide-iron: dissolving the purified Astragalus polysaccharides obtained in step 1, sodium tartrate and sodium carbonate in distilled water according to a weight ratio of 15:3:5, adding an iron salt solution with the weight 0.8-0.9 times the weight of the pure Astragalus polysaccharides to obtain a solution A, allowing the solution A to go through an exchange column loaded with basic ion exchange resin at a flow velocity of 3-8BV / h, reacting for 0.5-1h, cooling the obtained reaction product, filtering resin, flushing the surface of the resin with deionized water 3-5 times, carrying out alcohol precipitation with ethanol with the concentration of 75-85%, and drying the obtained precipitate at 50-70DEG C to obtain the Astragalus polysaccharide-iron. An ion exchange resin technology is adopted to catalyze preparation of a complex from Astragalus polysaccharide and iron, the method is novel, and the prepared Astragalus polysaccharide-iron has high purity and high content, has an iron supplementing function, and also has a piglet immunity enhancing effect.
Owner:GUANGXI AGRI VOCATIONAL COLLEGE

Method for separating and purifying beta-end-group thio-glycoside compound

ActiveCN103342725AEasy to complexThe separation and purification method is simple and fastSugar derivativesSugar derivatives preparationOrganic solventThio-
The invention provides a method for separating and purifying a beta-end-group thio-glycoside compound. The method comprises the following steps of: dissolving a crude thio-glycoside compound containing various isomers into a first organic solvent, adding an aqueous solution containing a divalent copper salt, stirring at the temperature between minus 20 DEG C and 0 DEG C, and filtering to obtain an organic phase; drying the organic phase by distilling, dissolving the dried organic phase into a second organic solvent, and shaking ultrasonically to obtain the beta-end-group thio-glycoside compound. Because the steric hindrance of the alpha-end-group isomer is low, the alpha-end-group isomer is easy to be subjected to complexation with a cupric ion to generate a flocculent precipitate in a low-temperature aqueous phase, and because the flocculent precipitate can be removed easily by filtering, the beta-end-group isomer can be left in the organic phase. After the beta-end-group isomer is shaken ultrasonically, the beta-end-group isomer can crystallize. The method provided by the invention is simple and convenient. In addition, the experimental result shows that the purity of the beta-end-group thio-glycoside compound obtained by adopting the method can be more than 95%, and the yield can be more than 85%.
Owner:济南尚博医药股份有限公司

Barite pollution blockage remover composition of oil-gas well of oilfield and preparation method of barite pollution blockage remover composition

The invention provides a barite pollution blockage remover composition of an oil-gas well of an oilfield. The composition is prepared from the following raw materials in parts by weight: 20-25 parts of acetone semicarbazon, 16-20 parts of 5-carboxylic acid-3-amino-1,2,4-triazole, 13-16 parts of L-sodium aspartate, 3-5 parts of crown ether (18-crown-6), 7-10 parts of phenyl diethyl malonate, 11-15 parts of dimethylethanolamine, 33-37 parts of ethosuximide, 9-13 parts of iminodiacetic acid, 30-35 parts of ammonia water (40 wt%) and 70-80 parts of water. The blockage remover composition is used for removing blockage of a stratum with barite pollution in drilling mud; the blockage removal speed is high, and the blockage removal of barite pollution in the oil-gas well can be completed within 4-12 h, and therefore, the yield of the oil-gas well of the oilfield is recovered and improved; the descaling rate is 98% or higher, and the blockage removal of barite pollution in the oil-gas well of the oilfield is completed by a one-step method; the safe and non-corrosive blockage removal is achieved; no corrosion, no dead angle, no precipitation or no secondary well clogging are caused; 90% or more of barite mud pollution can be effectively removed.
Owner:兰州熙瑞化工科技有限公司

Application of sulfur/phosphorus hybrid polyether modified polycarboxylic acid

ActiveCN110280182AGood dispersionImproved dispersibility has a good effect on copper phthalocyanineTransportation and packagingOrganic dyesAdhesivePrinting ink
The invention discloses application of sulfur/phosphorus hybrid polyether modified polycarboxylic acid in the fields of paint, printing ink, ceramics, adhesives and solar cells, and particularly relates to application of the sulfur/phosphorus hybrid polyether modified polycarboxylic acid in dispersing an organic pigment in water or an aqueous solution. The sulfur/phosphorus hybrid polyether modified polycarboxylic acid is prepared in the steps that by mass, 10-30 parts of acrylic acid, 1-10 parts of polyether and 20-50 parts of water are evenly mixed and heated to 50-100 DEG C, then 0.1-10 parts by mass of an initiator solution is added, a heat preservation reaction is carried out for 2-6 hours, and 6-20 parts by mass of a chain transfer agent solution is added to stop the reaction. The preparation method is wide in raw material source, green in preparation, simple and convenient to use and environmentally friendly. The problem that the organic pigment phthalocyanine copper is difficult to disperse in water is solved, and the application range of phthalocyanine copper is widened. A phthalocyanine copper water dispersion solution can be applied to the fields of paint, printing ink, ceramics, adhesives and solar cells.
Owner:中科广化(重庆)新材料研究院有限公司 +2

A kind of preparation method of astragalus polysaccharide iron

The invention provides a preparation method of Astragalus polysaccharide-iron. The method comprises the following steps: 1, extracting and purifying Astragalus polysaccharides; and 2, preparing Astragalus polysaccharide-iron: dissolving the purified Astragalus polysaccharides obtained in step 1, sodium tartrate and sodium carbonate in distilled water according to a weight ratio of 15:3:5, adding an iron salt solution with the weight 0.8-0.9 times the weight of the pure Astragalus polysaccharides to obtain a solution A, allowing the solution A to go through an exchange column loaded with basic ion exchange resin at a flow velocity of 3-8BV / h, reacting for 0.5-1h, cooling the obtained reaction product, filtering resin, flushing the surface of the resin with deionized water 3-5 times, carrying out alcohol precipitation with ethanol with the concentration of 75-85%, and drying the obtained precipitate at 50-70DEG C to obtain the Astragalus polysaccharide-iron. An ion exchange resin technology is adopted to catalyze preparation of a complex from Astragalus polysaccharide and iron, the method is novel, and the prepared Astragalus polysaccharide-iron has high purity and high content, has an iron supplementing function, and also has a piglet immunity enhancing effect.
Owner:GUANGXI AGRI VOCATIONAL COLLEGE

High-dispersity silver powder for preparing front silver paste of solar cell and preparation method of high-dispersity silver powder

The invention provides high-dispersity silver powder for preparing front silver paste of a solar cell and a preparation method of the high-dispersity silver powder. The method comprises the steps of preparing a silver salt solution, an organic ligand solution and a reducing agent solution respectively, wherein the reducing agent solution contains ferrous sulfate; adding an acid solution into the silver salt solution, and regulating and controlling the pH value of the silver salt solution to be 5-7; and synchronously dropwise adding the organic ligand solution and the reducing agent solution into the silver salt solution according to the molar ratio of ferrous sulfate to silver salt being (1-2):1, after dropwise adding is completed, carrying out a stirring reaction for preset time, and then carrying out separation, washing and drying to obtain the high-dispersity silver powder for preparing the front silver paste of the solar cell. According to the high-dispersity silver powder for preparing the front silver paste of the solar cell and the preparation method of the high-dispersity silver powder, ferrous sulfate is adopted as a reducing agent, a small amount of organic ligands capable of being chelated with ferrous ions are added in the silver salt reducing process, the silver salt reducing rate can be effectively adjusted by regulating and controlling the adding amount and the adding speed of the organic ligands, the obtained ferrous ion chelate can further wrap the surface of the silver powder, and therefore the high-dispersity silver powder is obtained.
Owner:山东建邦胶体材料有限公司

A kind of hydroxypyridone ligand and its application

The invention relates to a hydroxy-pyridone ligand; a structural formula of the hydroxy-pyridone ligand is one of two formulas described in the description, wherein a structural formula of R is described in the description, R1 is hydrogen, alkyl of C2-C4, halogen, hydroxyl or carboxyl, m, n and p are independently selected from 1, 2 or 3, and r is 1 or 2. A preparation method of the hydroxy-pyridone ligand comprises the following steps: dissolving a compound as shown in a formula (1) into an organic solvent, and then enabling the obtained solution to react with an amino-terminated compound at the temperature of 25-35 DEG C in presence of a catalyst to obtain an intermediate compound; enabling the obtained intermediate compound to have a palladium-carbon reduction reaction in an organic solvent to obtain the hydroxy-pyridone ligand, wherein a structural formula of the compound as shown in the formula (1) is described in the description, and R1 is hydrogen, alkyl of C2-C4, halogen, hydroxyl, carboxyl or aryl. The invention also provides application of the hydroxy-pyridone ligand as chelating agents for lanthanide elements, actinide elements and / or heavy metal elements. The invention further provides application of the hydroxy-pyridone ligand as a chelating agent for the element in nuclear waste, wherein the element in the nuclear waste is Sr, Cs, Tc or I.
Owner:SUZHOU UNIV

A method for converting existing hexavalent chromium plating solution into new trivalent chromium plating solution

ActiveCN105543906BSplit smallSplitting energy is smallOrganic acidHardness
The invention discloses a method for transforming an existing hexavalent chromium plating solution into a new trivalent chromium plating solution and belongs to the technical field of electroplating. The method comprises the two steps that firstly, under the conditions that the pH value of the existing hexavalent chromium plating solution is 0.5-1.0 and the temperature is 80-90 DEG C, a specified amount of a reducing agent and a specified amount of the organic acid complexing agent are added, and heat preservation is conducted for two to four hours, so that hexavalent chromium is reduced to trivalent chromium and the trivalent chromium and an organic acid complexing agent form a trivalent chromium active ligand basic solution with the ligand structure being [CrLx.(H2O)6-x]; and secondly, the trivalent chromium active ligand basic solution is adjusted to become the new trivalent chromium plating solution by adding conducting salts and a catalyzer into the trivalent chromium active ligand basic solution formed in the first step. According to the method, the existing hexavalent chromium plating solution is effectively transformed into the environmental-friendly trivalent chromium plating solution, and the new trivalent chromium plating solution is high in electroplating speed under the standard condition; a chromium plated coating is good in brightness and uniformity, high in hardness and excellent in corrosion property, so that the chromium plated coating can be on a par with a chromium plated coating of the hexavalent chromium plating solution.
Owner:WUHAN RES INST OF MATERIALS PROTECTION

A method for separation and purification of β-terminal thioglycoside compounds

ActiveCN103342725BEasy to complexThe separation and purification method is simple and fastSugar derivativesSugar derivatives preparationOrganic solventThio-
The invention provides a method for separating and purifying a beta-end-group thio-glycoside compound. The method comprises the following steps of: dissolving a crude thio-glycoside compound containing various isomers into a first organic solvent, adding an aqueous solution containing a divalent copper salt, stirring at the temperature between minus 20 DEG C and 0 DEG C, and filtering to obtain an organic phase; drying the organic phase by distilling, dissolving the dried organic phase into a second organic solvent, and shaking ultrasonically to obtain the beta-end-group thio-glycoside compound. Because the steric hindrance of the alpha-end-group isomer is low, the alpha-end-group isomer is easy to be subjected to complexation with a cupric ion to generate a flocculent precipitate in a low-temperature aqueous phase, and because the flocculent precipitate can be removed easily by filtering, the beta-end-group isomer can be left in the organic phase. After the beta-end-group isomer is shaken ultrasonically, the beta-end-group isomer can crystallize. The method provided by the invention is simple and convenient. In addition, the experimental result shows that the purity of the beta-end-group thio-glycoside compound obtained by adopting the method can be more than 95%, and the yield can be more than 85%.
Owner:济南尚博医药股份有限公司
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