1577 results about "Glycerol Ethers" patented technology

The invention belongs to the technical field of recoverable epoxy resin, and relates to a degradable epoxy resin system material and application thereof, a body, a composite material and a recovery method thereof. The degradable epoxy resin system material comprises a first component and a second component, the first component comprises first epoxy resin and second epoxy resin, and the second component comprises a first curing agent, a second curing agent and an accelerant; the first epoxy resin is a mixture of one or more of glycidyl ether epoxy resin and glycidyl amine epoxy resin and accounts for 15-35% of the first component by mass, the second epoxy resin is selected from one or more of epoxy resin with the structure containing # imgabs0 #, and the second epoxy resin accounts for 60-80% of the first component by mass; the first curing agent is one or a mixture of more of alicyclic amines and accounts for 40%-60% of the second component by mass, the second curing agent is one or a mixture of more of polyether amines and accounts for 40%-60% of the second component by mass, and the accelerant accounts for 0.5%-3% of the second component by mass. The requirement for vacuum infusion of the wind power blade can be met.

The invention discloses a toughened epoxy resin and a curing method thereof, and relates to the technical field of epoxy resins, the toughened epoxy resin comprises the following components: 100 parts of an epoxy resin matrix, specifically a mixture of bisphenol A epoxy resin and alicyclic epoxy resin, 5-35 parts of a composite amine curing agent, and 5-20 parts of a nano toughening agent, in particular to core-shell rubber particles grafted with epoxy groups on the surfaces, the core layer of each core-shell rubber particle is cross-linked polybutadiene, the shell layer of each core-shell rubber particle is polymethyl methacrylate, 0.5-3 parts of an accelerant comprising a bi-component synergistic accelerant, 1-5 parts of an interface enhancer, and a mixture of gamma-glycidyl ether oxypropyl trimethoxy silane and a titanate coupling agent, a bisphenol A type epoxy resin and a specific proportion of alicyclic epoxy resin are combined to construct an epoxy resin matrix according to a mass ratio of 2: 1, the epoxy resin matrix is matched with a composite amine curing agent prepared by carrying out a special three-step reaction on long-chain polyether diamine, aromatic diamine and anhydride, and key parameters such as molecular weight, functionality and molar ratio of the components are accurately regulated and controlled.

A fireproof magnesium oxide board is prepared by mixing the following raw materials, the raw material names and weight parts are as follows: 80-100 parts of magnesium oxide; 20-30 parts of anhydrous magnesium chloride; 10-20 parts of modified expanded vermiculite foaming agent; 20-30 parts of aluminum silicate fiber; 5-10 parts of sawdust; 10-15 parts of fly ash; 8-12 parts of glass magnesium board crushed powder; 1.5-5 parts of non-woven fabric; 10-20 parts of water; wherein the modified expanded vermiculite is prepared by the following steps: (1) Vermiculite is incompletely expanded and calcined; (2) acrylic acid monomer, sodium hydroxide, acrylamide monomer, initiator potassium persulfate, crosslinking aid pentaerythritol polyglycidyl ether, incompletely expanded vermiculite, and water are taken, stirred evenly and ultrasonically dispersed to obtain a first reaction solution, which is placed in a reactor for reaction to obtain a gel material; (3) the gel material is preliminarily crushed and dried, and then further crushed in a ball mill to obtain a fire-resistant expanded vermiculite with water absorption performance.

The invention relates to the technical field of macromolecules, and discloses a preparation method of modified polyurethane toughened epoxy resin, which comprises the following steps: by taking 4-(Boc-amino) phenylboronic acid, diethanol amine, 1, 3-bis (3-glycidyl ether oxypropyl) tetramethyldisiloxane and the like as raw materials, carrying out a series of chemical reactions to obtain a borate siloxane chain extender; the method comprises the following steps: adding a polyurethane prepolymer into the epoxy resin, participating in chain extension of polyurethane, and modifying the epoxy resin by using the polyurethane prepolymer to obtain the modified polyurethane toughened epoxy resin. A'soft segment 'and an Si-O structure in the modified polyurethane can also improve the flexibility of a curing network, effectively change the fracture mechanism of the resin, absorb a large amount of energy when the resin is fractured, and contribute to improving the toughness of the epoxy resin; on the basis of ensuring the strength of the epoxy resin, the toughness and flame retardant property of the epoxy resin are improved, and the epoxy resin can be applied to the fields of composite materials, coatings, adhesives and the like with higher toughness and flame retardant requirements, and has wide applicability.

The invention relates to the field of adhesives, and particularly discloses an OCA optical adhesive for a folding screen and a preparation method of the OCA optical adhesive. The OCA optical adhesive for the folding screen is prepared from the following raw materials in parts by weight: 60 to 80 parts of urethane acrylate, 15 to 25 parts of organic silicon grafted glycidyl ether, 20 to 30 parts of a diluent, 5 to 10 parts of a photoinitiator and 1 to 2 parts of an antioxidant, the organic silicon grafted glycidyl ether is prepared by reacting vinyl siloxane, pentaerythritol triallyl ether, allyl glycidyl ether and a catalyst. The OCA optical cement for the folding screen prepared by the invention is applied to the folding screen, and can keep relatively good elasticity, bending resistance and bonding strength in the long-term repeated folding use process, and wrinkles and bubbles are not easy to appear.

The invention discloses a waterborne epoxy resin coating, a preparation method and application in bridge protection, and belongs to the technical field of coatings. The water-borne epoxy resin coating comprises the following raw material components in parts by weight: 15-25 parts of epoxy composite resin emulsion, 100 parts of emulsified asphalt, 3-5 parts of a curing agent and 6-10 parts of water, wherein the epoxy composite resin emulsion is obtained by carrying out a composite reaction on 30-60 parts by mass of epoxy resin, 2-3 parts by mass of an emulsifier, 6-9 parts by mass of an acrylate composition and 1.4-1.6 parts by mass of a co-stabilizer; the acrylate composition is prepared by prepolymerizing 15 to 16 parts by mass of butyl methacrylate, 10 to 12 parts by mass of 2-isopropenyl aniline, 5 to 7 parts by mass of allyl glycidyl ether and 1 to 1.2 parts by mass of allyl polyhedral oligomeric silsesquioxane and then combining the prepolymerized materials with 1 to 3 parts by mass of acrylic acid.

The invention relates to the technical field of petrochemical engineering, and discloses a temperature-resistant anti-swelling agent for fracturing and a preparation process thereof.The preparation method comprises the steps that glycerol triglycidyl ether and diethanol amine are subjected to a ring-opening reaction, a polyhydroxy tertiary amine monomer is obtained, then the polyhydroxy tertiary amine monomer and chloromethylated polystyrene are subjected to a quaternization reaction, and the temperature-resistant anti-swelling agent for fracturing is obtained. Quaternary ammonium salt groups of the anti-swelling agent and negative charges on the surface of clay form electrostatic interaction, and hydroxyl groups and the surface of the clay form hydrogen-bond interaction, so that the anti-swelling agent can be firmly adsorbed on the surface of the clay to form a layer of polymer film, the clay is prevented from being in contact with water, the phenomenon that the clay swells when encountering water is effectively inhibited, and the anti-swelling rate is very high. And the anti-swelling agent contains a heat-resistant polystyrene molecular chain, has excellent high temperature resistance, can maintain good structural stability at high temperature, still maintains high anti-swelling rate, and is suitable for a fracturing fluid system for high-temperature oil reservoir exploitation.

The invention discloses a flexible PI heat-conducting insulating film pad and a preparation method thereof, and relates to the field of film pads. The preparation method comprises the following steps: preparing Fe3O4 magnetic heat-conducting core and SiO2 insulating shell composite nanoparticles by a sol-gel method, treating and grafting epoxy groups by a silane coupling agent, performing ring-opening addition with one end amino group of amino-terminated polydimethylsiloxane, and reacting the other end amino group with polyethylene glycol diglycidyl ether, so that two flexible long chains are grafted on SiO2. Due to the modified composite nanoparticles and the flexible long-chain structure, the flexibility of the film pad is remarkably improved; thermal vibration of silicon-oxygen bonds and ether bonds promotes heat transfer, a hydrogen bond network is formed with a PI substrate to improve dispersion stability, particles are orderly arranged under the action of a high-frequency magnetic field to construct a three-dimensional heat conduction network, and heat conduction efficiency is enhanced; the SiO2 isolates the inner core from conducting and improves the insulating property of the film pad by virtue of good insulativity and no free charge in the flexible long-chain polymer. The flexible PI heat-conducting insulating film pad prepared by the invention has the effects of flexibility, heat conduction and insulation.

The invention discloses an anti-scale cross-linked polymer fracturing fluid and a preparation method thereof, and relates to the technical field of petroleum fracturing fluids. When the anti-scale cross-linked polymer fracturing fluid is prepared, allylamine hydrochloride and epoxy chloropropane react to prepare a double-bond chlorinated intermediate; reacting the double-bond chlorinated intermediate with lauramidopropyl dimethylamine to prepare a cationic monomer; copolymerizing a cationic monomer and acrylamide to prepare a cationic polymer; the preparation method comprises the following steps: reacting L-lysine with formaldehyde and phosphorous acid to prepare phosphoric acid modified lysine; reacting the phosphoric acid modified lysine with allyl glycidyl ether to prepare a phosphoric acid modified monomer; acrylamide and an anionic monomer are copolymerized to prepare an anionic polymer; the anionic polymer and the cationic polymer are dissolved in water to prepare the anti-scale cross-linked polymer fracturing fluid. The anti-scale cross-linked polymer fracturing fluid prepared by the invention has the advantages of scale prevention, good temperature resistance, good shear resistance and self-crosslinking.

The invention relates to the technical field of plugging agents, and discloses a viscoelastic polymer type self-assembly plugging agent and a preparation method thereof. The preparation method comprises the following steps: adding acrylamide, butyl acrylate, 2-acrylamide-2-methylpropanesulfonic acid, quaternized cyclodextrin, gamma-glycidyl ether oxypropyl trimethoxy silane modified bentonite, Schiff base styrene, a sodium dodecyl benzene sulfonate emulsifier and octadecyl dimethyl allyl ammonium chloride into a reaction kettle; and adding an azodiisobutyronitrile initiator into the deionized water, uniformly mixing, and reacting for 4-5 hours at 50-65 DEG C to obtain the viscoelastic polymer type self-assembled plugging agent after the reaction is finished. The plugging agent disclosed by the invention has a relatively good plugging effect, and effectively solves the problem that the gel strength is weakened or the gelling is not thorough due to the formation shearing effect in a continuous gel migration process.

The invention relates to a degradable epoxy resin composite material with an adjustable curing speed, and a preparation method and a mild total recycling method thereof. Existing degradable epoxy resin has the problems of high cost, harsh degradation conditions and the like, and is difficult to meet the requirements of different application scenes on curing speed and temperature at the same time. The invention provides an epoxy resin composite material which comprises curing agent components (an epoxy resin amine curing agent and an ester-containing polythiol curing agent) and epoxy resin components (glycidyl ether epoxy resin, glycidyl amine epoxy resin and glycidyl ester epoxy resin). The cured composite material can be fully recycled through catalytic degradation under mild conditions by using a lewis acid and an amino group breaking ester bond mechanism, and the degradation product can be directly used as a curing agent, a toughening agent and a chain extender. The epoxy resin composite material disclosed by the invention not only has adjustable curing speed and high use performance, but also realizes environmental friendliness and resource recycling, and provides a new solution for sustainable development of epoxy resin.

The invention belongs to the technical field of high polymer chemical materials, and particularly relates to a self-repairing composite waterproof board and a preparation method thereof. The invention relates to a high-temperature-resistant graphene coating which is prepared from the following raw materials: bisphenol A diglycidyl ether, fluorosilane modified nano SiO2, graphene slurry, polydimethylsiloxane, epoxy-terminated polydimethylsiloxane, a urea-formaldehyde prepolymer, a silane coupling agent, sodium dodecyl benzene sulfonate, an FSO-100 fluorocarbon surfactant, a CTBN adhesive, a curing agent, an epoxy accelerator DMP-30 and a diluent. Through the collaborative design of the gradient structure of the hard framework and the soft coating, low-surface-energy filler chemical anchoring, microcapsule local material supplementing and thermal triggering dynamic bond rearrangement, the board obtains balance among the bearing strength, long-term hydrophobicity, weather-proof barrier and repeatable thermal self-repairing; and meanwhile, the common defects that room-temperature self-repairing is difficult to realize, hydrophobic particles are easy to agglomerate, a coating is easy to layer and the like are avoided.

The invention relates to the technical field of electric wire materials, in particular to a preparation process of a high-strength halogen-free flame-retardant electric wire. According to the preparation method, the polyolefin flame-retardant microspheres are obtained by adding propenylated cyclotriphosphazene, propenylated phosphaphenanthrene, methyl methacrylate, lauroyl peroxide, polyvinyl alcohol and deionized water. The flame-retardant modified boron nitride nanosheet is prepared by the following steps: firstly, preparing a flame-retardant modified boron nitride nanosheet, and then adding hydroxylated boron nitride, gamma-glycidyl ether oxypropyl trimethoxy silane and 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide, so as to obtain the flame-retardant modified boron nitride nanosheet. An ethylene-vinyl acetate copolymer, polyolefin flame-retardant microspheres, flame-retardant modified boron nitride nanosheets, an antioxidant and a lubricant are mixed and react, and the high-strength halogen-free flame-retardant protective sleeve is obtained. And wrapping the periphery of the copper core wire with the high-strength halogen-free flame-retardant protective sleeve to obtain a finished product. The finished product prepared by the invention has excellent flame retardant property and high strength, thereby having a wide application prospect in the technical field of electric wire materials.

The invention provides a modified amine curing agent, a preparation method, epoxy resin anticorrosive paint and application, and belongs to the technical field of paint. The modified amine curing agent provided by the invention is prepared from preparation raw materials including alicyclic diamine, m-xylylenediamine, a first glycidyl ether reagent, a second glycidyl ether reagent and a glycidyl ester reagent through amination reaction, the alicyclic diamine contains at least one primary amine group; the first glycidyl ether reagent is ethylene glycol diglycidyl ether and / or bisphenol A type diglycidyl ether; and the second glycidyl ether reagent is 1, 4-butanediol diglycidyl ether and / or C12-14 glycidyl ether. The modified amine curing agent is combined with the curing characteristics of amide and phenolic aldehyde amine, the epoxy resin anticorrosive paint prepared from the modified amine curing agent has a proper curing speed, the adhesive force of a cured coating is high, the anticorrosive effect is good, and the epoxy resin anticorrosive paint is particularly suitable for a high-humidity environment and an underwater environment.

The invention discloses a preparation method of two-component microcapsule self-repairing insulation paper based on epoxy resin and polymercaptan. The preparation method comprises the following steps: (1) preparing a repairing agent microcapsule and a curing agent microcapsule by an emulsion polymerization method; (2) mixing the prepared repairing agent microcapsule and curing agent capsule to obtain a bi-component microcapsule solution, and adding the bi-component microcapsule solution into the treated paper pulp; and (3) performing papermaking, drying and calendaring on the paper pulp added with the bi-component microcapsule solution to obtain the insulation paper. According to the invention, diglycerol ether type bisphenol F epoxy resin (DGEBF) stabilized by an emulsifier is adopted as a core of a repairing agent, polythiol (PETMP) stabilized by the emulsifier is adopted as a core of a curing agent, and the emulsifier is cellulose nanofiber, so that the insulating paper with self-repairing performance is prepared. The dielectric constant, the breakdown field strength, the tensile strength, the elongation at break and the thermal stability of the insulation paper are superior to those of traditional cellulose insulation paper, and the overall performance and the service life of the insulation paper can be effectively improved.

The invention relates to the field of plastic bags, and discloses a biodegradable plastic bag and a preparation method thereof, the biodegradable plastic bag comprises polylactic acid, poly (butylene adipate-co-terephthalate), a functional additive, modified starch, a lubricant and an antioxidant; the functional additive is prepared by grafting hydroxylated modified castor oil and isocyanated montmorillonite loaded titanium dioxide; the hydroxylation modified castor oil is prepared by modifying castor oil with chloroethyl isocyanate, then reacting with N-allylimidazole, and then reacting with 6-mercaptohexyl-1-alcohol; the isocyanated montmorillonite loaded titanium dioxide is prepared by reacting montmorillonite loaded titanium dioxide obtained by a sol-gel method with isophorone diisocyanate; the modified starch is prepared by reacting octadecanoyl chloride and acryloyl chloride with starch, then carrying out graft copolymerization with ethyl acrylate and further introducing glycidyl methacrylate, so that the plastic bag is endowed with excellent mechanical properties, biodegradability and antibacterial property.

The invention relates to the field of copper-clad plates, and discloses a low-dielectric-constant high-performance copper-clad plate and a preparation method thereof.The preparation method comprises the specific steps that epoxy resin, phenolic resin, polyphenyl ether modified resin, modified nano silicon dioxide and the like are taken and mixed to obtain a resin glue solution; impregnating glass fabric in the resin glue solution to obtain a prepreg; laminating prepregs, and covering copper foil for hot pressing; the polyphenyl ether modified resin comprises epoxy resin, diallyl cyanate and fluorine-containing polyphenyl ether resin prepared by reaction of polyphenyl ether, bisphenol AF and benzoyl peroxide; the modified nano silicon dioxide is prepared by reacting allyl glycidyl ether, vinyltriethoxysilane and phenyltris (dimethylsiloxane) silane, then grafting with a phosphorus-containing intermediate to prepare a modified additive, and grafting with nano silicon dioxide, and the phosphorus-containing intermediate is prepared by reacting phenylphosphoryl dichloride and eugenol. The copper-clad plate with high flame retardance, high peel strength, heat resistance and low dielectric constant is prepared.

The invention relates to the technical field of toughening agents, in particular to a hyperbranched epoxy resin modified MBS toughening agent and a preparation method thereof.The preparation method comprises the following steps that (S1) a cyclotriazine compound, polyglycidyl ether and a catalyst are added into an organic solvent to be mixed, a reaction is conducted for 8-72 h at the temperature of 30-150 DEG C under the protection of nitrogen, and after the reaction is completed, alcohol precipitation and drying are conducted to obtain a hyperbranched epoxy resin modified MBS toughening agent; the hyperbranched epoxy resin is obtained; (S2) adding the hyperbranched epoxy resin into the solvent A, uniformly mixing, then adding MBS resin, stirring for 0.5-1 hour at a high speed under the condition of room temperature, then heating to 70-110 DEG C, stirring for 0.5-1 hour, and removing the residual solvent to obtain the hyperbranched epoxy resin modified MBS toughening agent, and by utilizing the hyperbranched characteristic of the resin, enabling the modified MBS toughening agent to be used for preparing the hyperbranched epoxy resin modified MBS toughening agent. The toughening effect can be achieved by adding a small amount of the toughening agent into common epoxy resin.

The invention relates to the technical field of polyurethane acrylate, and particularly discloses dual-curing polyurethane acrylate resin and a preparation method thereof. Wherein the dual-curing polyurethane acrylate resin is prepared from the following raw materials: polyester polyol, polyether polyol, diisocyanate, hydroxyl acrylate, a chain extender, a photoinitiator, cardanol glycidyl ether, a polymerization inhibitor and modified nanoparticles. Wherein the citric acid and the polyethyleneimine are adopted to carry out synergistic modification on the nano particles, the dispersion stability of the nano particles is improved, so that the mechanical property of the resin is improved, the cardanol glycidyl ether and the photoinitiator generate a synergistic effect, and the resin can be quickly shaped through photocuring promoted by the photoinitiator; the cardanol glycidyl ether participates in the subsequent thermocuring reaction, so that the curing effect is improved, and the adhesive force between the film layer and the base material is enhanced.

The invention discloses an electrolytic adhesive, an electrolytic cotton adhesive tape and a preparation method of the electrolytic adhesive. The electrolytic cotton adhesive tape comprises the following components in parts by weight: 5-10 parts of 1, 1 '-ferrocene diformyl chloride, 10-15 parts of acrylic acid beta-cyclodextrin ester, 3-8 parts of polyethylene glycol diglycidyl ether, 10-20 parts of ionic liquid, 1.5-3 parts of a cross-linking agent, 10-15 parts of tackifying resin and 0.5-1.5 parts of an initiator, and a polymer matrix comprises an acrylic acid-hydroxypropyl acrylate copolymer and acrylic acid-2-ethylhexyl ester. Comprising an adhesive layer and an adhesive tape base layer, the adhesive layer is prepared from the electrolytic adhesive, and the adhesive tape base layer is prepared from acrylic foam; the obtained electrolytic cotton adhesive tape has high initial adhesion and viscosity strength after power-on and power-off re-adhesion.

The invention discloses a quick-curing polyurethane seamless expansion joint material for roads and a preparation method, and belongs to the technical field of road engineering materials. The material is prepared from polyether polyol, polycaprolactone glycol, a bisphenol A epoxy-polyether block isocyanate terminated prepolymer, a methyl phenyl silicon-boron hybrid hydroxyl chain extender, diphenylmethane diisocyanate, calcium carbonate, wollastonite, a hindered amine anti-aging agent and dioctyl phthalate. Wherein the bisphenol A epoxy-polyether block isocyanate terminated prepolymer is prepared by the following steps: reacting bisphenol A with epoxy chloropropane to generate epoxy resin, reacting with polytetramethylene ether glycol, and introducing isophorone diisocyanate; the methyl phenyl silicon-boron hybrid hydroxyl chain extender is prepared by carrying out hydrosilylation and ethylene glycol reaction on methyl trimethoxy silane, 3-glycidyl ether oxypropyl trimethoxy silane and allylboronic acid pinacol ester; and the methyl phenyl silicon-boron hybrid hydroxyl chain extender is prepared by carrying out hydrosilylation on methyl trimethoxy silane, 3-glycidyl ether oxypropyl trimethoxy silane and allylboronic acid pinacol ester. The material has the advantages of quick curing property, weather resistance and high-temperature stability, and is suitable for road seamless expansion joint scenes.

The invention relates to the field of packaging materials, and discloses low-temperature heat-sealing water-based coated paper and a preparation method and application thereof.The water-based coated paper comprises a base paper layer and a water-based coating, and the water-based coating comprises water-based ethylene-acrylic acid copolymer emulsion, modified nano-silica, a coalescing agent and water; a cardanol derivative is introduced into the water-based ethylene-acrylic acid copolymer emulsion as a functional component; the cardanol derivative is prepared by reacting epoxidized cardanol with 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide and then grafting with acryloyl chloride. The preparation method comprises the following steps: reacting epoxidized cardanol with 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide; the modified nano silicon dioxide is prepared by mixing aminated nano silicon dioxide and chitosan and adding a cross-linking agent prepared by grafting phytic acid and ethylene glycol diglycidyl ether. The water-based coating paper prepared by the invention overcomes the defects that the existing BOPP film is not environment-friendly, and the conventional coating paper is high in heat sealing temperature and easy to stick; meanwhile, good mechanical properties, water resistance and flame retardance are achieved.

The invention relates to a heat dissipation coating composition, a preparation method thereof and application of the heat dissipation coating composition in a battery protection plate, and belongs to the technical field of new energy heat dissipation coatings. According to the preparation method, methyl methacrylate, 2-vinylpyridine, methacrylamide, dipropylene glycol diacrylate, azodiisobutyronitrile and tetradecane are taken as raw materials, a coating dispersion liquid is prepared firstly, then hydroxylated graphene is subjected to polymerization coating by utilizing the coating dispersion liquid based on an in-situ polymerization method, a coating layer with amino and pyridine rings is constructed, and the coating layer with amino and pyridine rings is prepared. The preparation method comprises the following steps: coating a coating particle with amino boron nitride to obtain a coated particle, compounding the amino boron nitride onto the coated particle through addition of amino and epoxy groups by taking ethylene glycol diglycidyl ether containing double-terminal epoxy groups as a bridging agent to prepare a modified composite particle, and blending the modified composite particle with water-borne epoxy resin and other components to obtain the heat-dissipating coating composition. The coating has excellent heat dissipation performance, can still keep a good heat dissipation effect even after being heated and cooled for multiple times, and is suitable for being applied to the battery protection plate.

The invention discloses compression-resistant glass and a preparation method thereof, and relates to the technical field of special glass. When the compression-resistant glass is prepared, an anorthite crystal phase is used as a main material, a wollastonite crystal phase is used as an auxiliary material, and zinc, barium, boron, sodium, antimony and titanium elements are added, so that the compression-resistant glass ceramic is prepared; the preparation method comprises the following steps: mixing tetraethoxysilane, zirconium oxychloride octahydrate and 3-glycidyl ether oxypropyl trimethoxy silane, adding hydrochloric acid, and stirring to obtain modified sol; the preparation method comprises the following steps: mixing hydroxyl-terminated polysiloxane, trimethyl ethyoxyl silane, methyl triethyoxyl silane and octadecyl triethyoxyl silane, adding a hydrochloric acid solution, and reacting to prepare an organosilane modified solution; mixing the modified sol and the organosilane modified solution, coating the surface of the compression-resistant microcrystalline glass with the mixture, and curing to obtain the compression-resistant glass. The compressive glass prepared by the invention has the advantages of high compressive strength, hydrophobicity, wear resistance and high surface hardness.

The invention provides a composite diaphragm, a preparation method thereof and a lithium ion battery. The composite diaphragm comprises a base diaphragm and a solid electrolyte-water-soluble gel electrolyte composite coating, wherein the surface of the base diaphragm is coated with the solid electrolyte-water-soluble gel electrolyte composite coating by utilizing a roller coating process; the water-soluble gel electrolyte is obtained by co-polymerizing an intermediate I prepared from methyl methacrylate and N-isopropylacrylamide and neopentyl glycol diglycidyl ether. In the composite diaphragm provided by the invention, the water-soluble gel electrolyte can effectively improve the adhesion of the solid electrolyte on the base membrane, and ensure that the solid electrolyte can be effectively adhered to the surface of the base membrane; lithium titanium aluminum phosphate and the like can effectively promote transmission of lithium ions through the solid electrolyte, the hexagonal boron nitride composite coating can prevent direct contact between the lithium titanium aluminum phosphate solid electrolyte and the like and lithium, and the solid electrolyte is protected. And the interface stability of the composite diaphragm is relatively good, and a compact phase formed in the circulation process can effectively inhibit the permeation of lithium dendrites, so that the safety of the battery is improved.

The invention discloses a thermal interface material based on elastomer glass and a preparation method thereof. The thermal interface material is prepared from the following raw materials: a diglycidyl ether-terminated liquid polythioether prepolymer, methyl tetrahydrophthalic anhydride, ethylene glycol diglycidyl ether, a catalyst and a heat-conducting filler. According to the invention, the highly vertical orientation of the heat-conducting filler is realized through a process of combining hot pressing and stack welding, and the heat-conducting filler has an extremely high heat conductivity coefficient in the vertical direction. The Rc of the thermal interface material is much lower than that of a commercial thermal interface material adopting a traditional silicon matrix, and the thermal interface material has a spontaneous contact behavior on the surface of the substrate.

The invention discloses weather-resistant water-based two-component epoxy paint and a preparation method thereof, and belongs to the technical field of paint. The weather-resistant water-based two-component epoxy paint comprises a component A and a component B, the component A comprises 50-70 parts by mass of a modified waterborne epoxy emulsion, 3-6 parts by mass of a pigment, 7-13 parts by mass of a modified filler, 0.3-1.5 parts by mass of a wetting dispersant, 2-4 parts by mass of a coalescing agent, 0.1-0.5 part by mass of a defoaming agent, 0.5-5 parts by mass of water and 0.5-1 part by mass of a leveling agent; the component B comprises 35-65 parts by mass of a modified curing agent, 10-20 parts by mass of ethanol and 30-40 parts by mass of water; the component A and the component B are mixed according to the mass ratio of 100: (20-30); the modified curing agent is obtained by reacting polyethylene glycol diglycidyl ether, epoxy resin, triethylene tetramine, functional organic silicon and phenyl glycidyl ether; the modified filler is obtained by modifying nano silicon dioxide with poly (m-xylylenediamine) and a silane coupling agent KH560; the modified water-based epoxy emulsion is a phytic acid modified water-based epoxy emulsion.

The invention belongs to the technical field of nanocrystal nucleus early strength agents, and provides a damp and hot nanocrystal nucleus early strength agent, a tailing solidification filling material and a preparation method and application of the damp and hot nanocrystal nucleus early strength agent and the tailing solidification filling material. The invention discloses a molybdenum ore tailing slurry which is prepared from the following raw materials in parts by weight: 1 part of Portland cement, 4 to 6 parts of molybdenum ore tailings, 0.06 to 0.1 part of zeolite powder, 0.07 to 0.1 part of nanoscale attapulgite powder, 0.06 to 0.1 part of gamma-glycidyl ether oxypropyl trimethoxy silane, 0.03 to 0.1 part of potassium silicate, 0.04 to 0.1 part of sodium hydroxide, 0.06 to 0.1 part of calcium formate, 0.04 to 0.1 part of lithium metaaluminate and 1.25 to 1.75 parts of water. According to the technical scheme, the problem that a filling body prepared from an early strength agent in the prior art is low in early and later strength is solved, and meanwhile, the early strength agent is simple and convenient in preparation mode, low in cost and wide in application range.

The invention relates to the technical field of fabric waterproofing agents, in particular to a polyurethane modified organic silicon fluoride-free waterproofing agent and a preparation method thereof. The polyurethane modified organic silicon fluoride-free waterproof agent is prepared from the following raw materials in parts by mass: 5 to 15 parts of hexamethylene diisocyanate, 5 to 15 parts of butyl acrylate, 1 to 5 parts of methyl methacrylate, 40 to 60 parts of octamethylcyclotetrasiloxane, 10 to 30 parts of alpha, omega-dihydroxy polydimethylsiloxane and 5 to 10 parts of gamma-aminopropyl methyl diethoxy silane. The invention relates to a silane coupling agent, which is prepared from the following raw materials in parts by weight: 1 to 5 parts of glycidyl ether oxypropyl trimethoxy silane, 0.1 to 1 part of tetramethylammonium hydroxide, 0.1 to 1 part of triethylamine, 2 to 5 parts of tetraethoxysilane, 0.2 to 0.75 part of ammonia, 0.1 to 1 part of silane coupling agent KH-570, 0.01 to 0.1 part of dibutyltin dilaurate, 1 to 5 parts of epsilon-caprolactam, 1 to 2 parts of emulsifier and 0.1 to 1 part of initiator. The fabric treated by the method has good softness and excellent hydrophobic effect.

The invention relates to the field of coatings, and discloses a biomass-based oil-resistant coating and a preparation method thereof, the coating comprises an additive solution, a paraffin solution and gallic acid; the paraffin solution is obtained by dissolving paraffin in absolute ethyl alcohol; a preparation method of the additive solution comprises the following steps: mixing chitosan powder and an acetic acid aqueous solution to prepare a chitosan solution, ultrasonically dispersing functionalized montmorillonite in deionized water to prepare a suspension, then uniformly mixing the chitosan solution and the suspension, adding modified phytic acid prepared by grafting phytic acid and ethylene glycol diglycidyl ether, and stirring to react; the functional montmorillonite is prepared by modifying modified montmorillonite with titanium dioxide and zinc oxide, then activating the modified montmorillonite with 3-aminopropyltriethoxysilane and succinic anhydride, and then carrying out a ring-opening reaction with glycidyl neodecanoate. The coating prepared by the invention has high water resistance, the Kit oil-proof grade is kept at grade 12, and the oil-proof performance of the coating is greatly improved. Meanwhile, the antibacterial performance, the tensile index and the ultraviolet aging resistance are relatively high.