1200 results about "Glycidyl ether" patented technology

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 present invention relates to the field of biomedicine technology, specifically a preparation method of a silk fibroin hyaluronic acid filler for injection. The present invention concentrates a silk fibroin solution to obtain a concentrated silk fibroin solution, and then dilutes it to obtain a diluted silk fibroin solution; the diluted silk fibroin solution is heated to form a silk fibroin gel, granulated to obtain silk fibroin gel particles; 1,4-butanediol diglycidyl ether and a sodium hydroxide solution are mixed uniformly, hyaluronic acid and 1 / 3 of the mass fraction of hydroxyapatite are added, after stirring uniformly, swelling, purification and granulation are carried out, and the remaining mass fraction of hydroxyapatite is added to obtain composite gel particles; the composite gel particles and the silk fibroin gel particles are mixed uniformly, added to the gel to mix, and a silk fibroin hyaluronic acid filler is obtained, which effectively prolongs its degradation time.

The invention discloses a hydrophilic polyacrylate / epoxy silica sol composite coating and a preparation method thereof. The composite coating is prepared from a polyacrylate epoxy silica sol solution containing carboxyl and a polyethylene glycol side chain through blending, coating, drying and heating crosslinking. The polyacrylate is synthesized by taking methyl methacrylate, methacrylic acid, hydroxyethyl methylacrylate and allyl polyethylene glycol as comonomers through a solution free radical copolymerization method, and the epoxy silica sol solution is prepared by taking tetraethoxysilane and gamma-glycidoxypropyltrimethoxysilane as raw materials through a solution polymerization method. The composite material is prepared through a sol-gel and core-shell preparation process. The preparation method comprises the following steps: carrying out solution blending on polyacrylate and epoxy silica sol, and carrying out coating, drying and other processes to generate the cross-linked polyacrylate / epoxy silica sol composite coating through a cross-linking reaction between carboxyl and epoxy. The prepared composite coating has the characteristics of long durability, wear resistance, hydrophilicity, antifogging, protein adsorption resistance and the like.

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 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 crosslinked polyethylene reinforced high-strength insulating aerial cable, and belongs to the technical field of crosslinked polyethylene cable materials.The crosslinked polyethylene reinforced high-strength insulating aerial cable is prepared by the steps that hydroxyl is introduced to nano boron nitride powder, then amino is grafted through KH-550, nano alpha-Al2O3 powder is modified through gamma-glycidyl ether oxypropyl trimethoxy silane, and the cross-linked polyethylene reinforced high-strength insulating aerial cable is obtained; the preparation method comprises the following steps: preparing low-density polyethylene, compounding the low-density polyethylene with aminated nano boron nitride powder to form nano composite powder, improving the interface bonding force between the low-density polyethylene and the nano composite powder, carrying out melt blending on the low-density polyethylene and the nano composite powder to improve the dispersity of the nano composite powder in the low-density polyethylene, and carrying out nucleophilic acyl substitution reaction to obtain a fluorine-containing modified monomer. The nano boron nitride powder and the nano alpha-Al2O3 powder are subjected to a cross-linking reaction under the initiation action of an initiator and then coat the exterior of the thermal insulation layer, and the nano boron nitride powder and the nano alpha-Al2O3 powder are bridged through siloxane bonds to form a three-dimensional heat-conducting network, so that the heat resistance of the outer insulating layer is improved.

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 a poly-(2-oxazoline) epoxy derivative and application thereof, and belongs to the technical field of crosslinking. The invention provides a poly-(2-oxazoline) epoxy derivative, which is completely different from existing cross-linking agents such as 1, 4-butanediol diglycidyl ether (BDDE), divinyl sulfone, glycidyl methacrylate and the like in structure, and has the advantages that the structure is simple; the polymer can be used as a cross-linking agent for cross-linking natural high-molecular polymers such as polysaccharide (such as hyaluronic acid) and protein and synthetic high-molecular polymers such as polyethylene glycol and polyvinyl alcohol. Compared with an existing cross-linking agent, the poly-(2-oxazoline) epoxy derivative has the advantages that the poly-(2-oxazoline) epoxy derivative can be easily subjected to a cross-linking reaction with high-molecular polymers such as hyaluronic acid, the prepared cross-linked substances such as sodium hyaluronate gel are more stable and uniform, the performance of the prepared cross-linked substances is easier to regulate and control and the like, and the poly-(2-oxazoline) epoxy derivative has a great application prospect.

The invention relates to the technical field of lithium battery diaphragms, and discloses a water-soluble gel electrolyte, a preparation method thereof, water-based slurry and application. The preparation method of the water-soluble gel electrolyte comprises the following steps: in the presence of an initiator, carrying out first polymerization reaction on methyl methacrylate and N-isopropylacrylamide to obtain an intermediate I; carrying out second polymerization reaction on the polymer solution A and the polymer solution B to obtain an intermediate I; the polymer solution A contains an intermediate I with the concentration of 8-12wt%; the polymer solution B contains neopentyl glycol diglycidyl ether with the concentration of 0.5 to 1.2 weight percent; and carrying out heating treatment on the intermediate I to obtain the water-soluble gel electrolyte. When the water-soluble gel electrolyte is applied to the battery diaphragm, the addition amount of the electrolyte can be reduced during electrolyte injection in a battery cell, and the cost is effectively reduced; battery leakage is reduced, and the safety performance of the battery cell is improved; and the internal resistance can be reduced, and the cycle performance of the battery cell can be improved.

The invention discloses a preparation method of sandwich type immunomagnetic beads with high thermal stability, which comprises the following steps: by taking polystyrene microspheres as a template, introducing oil-phase Fe3O4 nanoparticles into the polystyrene microspheres through a swelling method, and then carrying out hydrolytic condensation reaction on the surface of a microsphere assembly by utilizing n-octyltrimethoxysilane OTMS to obtain the sandwich type immunomagnetic beads with high thermal stability. The preparation method comprises the following steps: carrying out surface amination modification on a silicon dioxide thin layer which is grown by hydrolysis of tetraethoxysilane TEOS to realize coating of an outermost organic shell layer, carrying out surface amination modification, and carrying out cross-linking on 1, 4-butanediol diglycidyl ether and erythritol on the surface to form an epoxy polymer layer so as to obtain the sandwich-type immunomagnetic bead with a cross-linked epoxy polymer layer introduced to the outer layer. According to the epoxy group modification process on the surface of the magnetic bead, a direct cross-linking modification process is adopted, so that the operation steps are simplified, and the obtained epoxy group magnetic bead is ensured to show excellent biocompatibility. In addition, the method omits the tedious process of functional group activation, and allows direct coupling with the antibody, thereby greatly improving the efficiency and convenience of the experiment.

The invention discloses a corrosion-resistant polypropylene edge band material and a preparation method thereof, and belongs to the technical field of preparation of edge band materials. The corrosion-resistant polypropylene edge sealing strip material is prepared from, by weight, 50-75 parts of polypropylene, 2-5 parts of an antioxidant, 3-6 parts of a corrosion-resistant agent, 2-4 parts of a composite flame retardant, 8-15 parts of calcium carbonate and 2-4 parts of dye, the corrosion-resistant agent is prepared from 2, 6-dichlorobenzonitrile, 1, 2, 4-triazole, a sulfuric acid solution, sodium nitrite and parachloroaniline, and the corrosion-resistant agent is prepared from 2, 6-dichlorobenzonitrile, 1, 2, 4-triazole, a sulfuric acid solution, sodium nitrite and parachloroaniline. The composite flame retardant is prepared from 3-glycidyl ether oxypropyl trimethoxy silane, diphenyl silanediol, barium hydroxide and boric acid. The edge band material prepared by the method has excellent corrosion resistance, flame retardance, heat resistance and mechanical properties.

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 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 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 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 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 biology, and discloses a halohydrin dehalogenase mutant, a coding gene, a recombinant vector, a recombinant strain, an enzyme preparation and application of the halohydrin dehalogenase mutant, the coding gene, the recombinant vector, the recombinant strain and the enzyme preparation in synthesis of chiral (S)-5-phenoxymethyl-2-oxazolidinone compounds. The halohydrin dehalogenase mutant is obtained by performing combined mutation on an enzyme with an amino acid sequence as shown in SEQ ID NO.1 at the 15th site, the 137th site and the 179th site. The mutant can obviously improve the ee value of a chiral (S)-5-phenoxymethyl-2-oxazolidinone compound synthesized by catalyzing phenyl glycidyl ether, the purity of catalytic synthesis and resolution is higher, and industrial production is facilitated.

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.

An organic silicon resin toughening agent, a single-component high-strength epoxy structural adhesive, and preparation methods for both. The organic silicon resin toughening agent is prepared by reacting epoxy modified hydrogen-containing silicone oil and vinyl six-membered cyclic oligomeric silsesquioxane; and the epoxy modified hydrogen-containing silicone oil is prepared by reacting allyl alcohol glycidyl ether and hydrogen-containing silicone oil which contains hydrogen at both ends. Compared with toughening agents such as nitrile rubber and core-shell structured rubber, the synthesized organic silicon resin toughening agent having a cyclic mesh structure unit in the present invention has better high and low temperature resistance, and can significantly improve the high and low temperature resistance of the single-component high-strength epoxy structural adhesive while improving the toughness of the single-component high-strength epoxy structural adhesive.

The invention relates to the field of polyurethane film materials for batteries, and discloses a TPU composite material for a new energy battery and a preparation method of the TPU composite material. A TPU composite material for a new energy battery is composed of a cloth film layer, an adhesive film layer and a TPU film layer, the TPU film layer is prepared by melting and casting TPU hot melt adhesive, and the TPU hot melt adhesive is prepared from the following raw materials in parts by weight: 60-80 parts of polyurethane elastomer, 20-30 parts of a toughening aid, 15-25 parts of a flame retardant, 8-15 parts of a heat conducting agent, 2-4 parts of a lubricant and 1-3 parts of an antioxidant; the toughening auxiliary agent is prepared from a POE (Polyolefin Elastomer), long carbon chain alkyl glycidyl ether, dibutyl itaconate and a vinyl dimethyl terminated dimethyl-methyl trifluoropropyl polysiloxane copolymer. The TPU composite material disclosed by the invention is applied to a new energy battery, has relatively good buffering and damping effects and puncture resistance, and is good in flame retardance and thermal conductivity.

The invention discloses a polyurethane modified epoxy resin adhesive as well as a preparation method and application thereof, and the polyurethane modified epoxy resin adhesive is prepared from the following components in parts by mass: 7-10 parts of E51 type bisphenol A diglycidyl ether, 3.5 parts of a phenolic aldehyde amine T31 curing agent and 1-3 parts of synthetic polyurethane, the synthetic polyurethane is prepared from polyether triol, polyether amine, isophorone diisocyanate and glycerol carbonate, and a blending system of the synthetic polyurethane and bisphenol A diglycidyl ether is adopted to be subjected to covalent crosslinking with phenolic aldehyde amine T31, so that the adhesive has high toughness and strength guarantee; the synthetic polyurethane prepared by the method is obtained through simple, green and efficient solvent-free synthesis, and the synthesized product has certain fluidity at room temperature, so that the subsequent stirring preparation process of an adhesive is facilitated. And a solvent-free synthesis method is adopted, so that the use of a toxic organic solvent in the traditional polyurethane synthesis process is avoided, and the synthesis process is greener.

The invention relates to the technical field of coating materials, in particular to a high-scratch-resistant and wear-resistant coating material and a preparation method thereof.The high-scratch-resistant and wear-resistant coating material is prepared from, by weight, 20-30 parts of tetraphenol ethane tetraglycidyl ether epoxy resin, 15-25 parts of polyurethane modified polytetrafluoroethylene, 15-25 parts of acrylate modified polysilazane and 5-15 parts of modified nano tungsten carbide. 2-5 parts of a curing agent, 1-3 parts of a dispersing agent and 0.5-1 part of an antioxidant; the preparation method comprises the steps of raw material mixing, stirring, coating, drying, heat treatment and the like. Through matching of specific raw materials, the prepared coating paint not only can improve the scratch resistance and wear resistance of a metal matrix, but also has good high temperature resistance, high humidity resistance and corrosion resistance, and the performance is not affected when the coating paint is used in different environments.

The invention belongs to the technical field of plastic processing, and particularly relates to a hydrophobic solvent-resistant biodegradable polyester material as well as a preparation method and application thereof in plastic bottles. The preparation method of the hydrophobic solvent-resistant biodegradable polyester material comprises the following steps: reacting polyol glycidyl ether with acrylic acid to prepare polyol glycidyl ether acrylate; the preparation method comprises the following steps: reacting isophthalic dihydrazide with polyol glycidyl ether acrylate to prepare a modifier; pBAT reacts with a modifier and an acrylic acid fluorine monomer to obtain the hydrophobic solvent-resistant biodegradable polyester material. The hydrophobic solvent-resistant biodegradable polyester material adopts PBAT as matrix resin, has biodegradability, has good hydrophobicity and solvent resistance through modification treatment of the modifier and the acrylic acid fluorine monomer, and can be applied to manufacturing of plastic bottles.

The invention relates to the field of electronic packaging materials, and discloses an epoxy molding compound as well as a preparation method and application thereof. Based on the total weight of the epoxy molding compound, the epoxy molding compound contains 13 to 20 weight percent of epoxy resin, 6 to 14 weight percent of a curing agent, 0.05 to 0.2 weight percent of a curing accelerator, 70 to 78 weight percent of filler, 0.1 to 1 weight percent of a coupling agent, 0.1 to 4 weight percent of a stress modifier, 0.1 to 2 weight percent of a release agent, 3 to 8 weight percent of a flame retardant, 0.01 to 0.3 weight percent of an ion trapping agent and 0.3 to 0.6 weight percent of a coloring agent, wherein the curing accelerator is 2-undecylimidazole, and the curing accelerator is 2-undecylimidazole; and the coupling agent is gamma-mercaptopropyl trimethoxy silane and / or gamma-glycidyl ether oxypropyl trimethoxy silane. The invention further discloses a preparation method of the silane coupling agent. The epoxy molding compound is simple to prepare, shows relatively high bonding performance and demolding performance when being used for packaging semiconductor components, and has relatively high operability and reliability.

The invention discloses a low-shrinkage creep-resistant plastic-wood product and a preparation method thereof, and belongs to the technical field of plastic-wood composite materials. The composite material is prepared from the following raw materials in parts by weight: 10 to 18 parts of polypropylene, 22 to 35 parts of high-density polyethylene, 58 to 83 parts of eucalyptus / walnut shell / montmorillonite composite modified powder, 10 to 15 parts of hydroxyl-terminated polybutadiene and graphene / ZnO2 / CaO, 7 to 15 parts of basic magnesium sulfate whisker, 3 to 4.6 parts of gamma-glycidyl ether oxypropyl trimethoxy silane and 0.3 to 1 part of antioxidant. In this way, the plastic-wood product is high in low-temperature impact strength, good in creep resistance, small in linear thermal expansion coefficient and high in thermal deformation temperature. Specifically, the impact strength of the plastic-wood product is 6.96-7.27 KJ / m < 2 >; the tensile creep modulus is 18.8 to 21.6 Mpa; the linear thermal expansion coefficient is 2.5-3.1 * 10 <-5 > / DEG C; the thermal deformation temperature is 163.2 to 178.5 DEG C;

The invention discloses a high-temperature-resistant and weather-resistant epoxy resin adhesive and a preparation method thereof, and belongs to the field of epoxy resin adhesives, the adhesive can keep stable bonding strength for a long time at high temperature through the synergistic effect of hydrogenated bisphenol F type epoxy resin, silicon-containing phenyl glycidyl ether epoxy resin and a dicyandiamide-imidazole composite curing agent, and the adhesive has high temperature resistance and weather resistance. According to the present invention, the graphene aerogel is added to the silicon-containing phenyl glycidyl ether epoxy resin to meet the high temperature environment use requirement, and the silica bond in the silicon-containing phenyl glycidyl ether epoxy resin and the aging resistance of the graphene aerogel enable the adhesive to have characteristics of excellent ultraviolet aging resistance, excellent thermal cycling resistance and excellent moisture resistance, solve the performance defects of the traditional product, and be suitable for the application in the high temperature and severe environment, the method has an important practical value.

The invention relates to the technical field of water treatment, and particularly discloses a crystal nucleus granulation induced hardness removal integrated water treatment process which comprises the following steps: firstly, ultrasonically dispersing nano-hydroxyapatite in deionized water, adding gamma-glycidoxypropyltrimethoxysilane for reaction, and treating to obtain a silanized hydroxyapatite crystal nucleus; the sodium polyacrylate reacts with aluminum sulfate and the like in an ethylene glycol solution to prepare the composite inducer. The preparation method comprises the following steps: reacting the two components in a phosphate buffer solution in proportion to obtain inducer-loaded crystal nucleus particles, carrying out multi-step reaction and treatment on the inducer-loaded crystal nucleus particles with calcium chloride and the like to obtain surface-coated crystal nucleus granulation bodies, and mixing the surface-coated crystal nucleus granulation bodies with cationic polyacrylamide and nano-zinc oxide to prepare the reinforced hardness removal agent. When to-be-treated water is treated, the reinforced hardness removal agent is added, stirring and precipitation are performed, supernate sequentially passes through the activated carbon filter column to adsorb impurities and is sterilized by the ultraviolet disinfection device, and finally effluent is collected, so that the hardness in the water can be efficiently removed, the process integration level is high, and the effect is good.

The invention provides an ultraviolet curing coating, a strippable coating and a preparation method of the ultraviolet curing coating and the strippable coating, and belongs to the technical field of coatings. The ultraviolet curing coating provided by the invention is prepared from the following components in parts by weight: 50 to 60 parts of light-cured resin oligomer, 15 to 25 parts of reactive diluent, 2 to 5 parts of glycidyl methacrylate, 5 to 8 parts of photoinitiator, 1 to 3 parts of glycidyl ether oxypropyl cyclotetrasiloxane, 1 to 3 parts of ultraviolet absorbent, 3 to 5 parts of filler and 1 to 3 parts of aluminum chelate. According to the invention, glycidyl methacrylate is added, so that more uniform photocuring can be promoted, and the comprehensive performance of a photocuring coating is improved; according to the invention, glycidyl ether oxypropyl cyclotetrasiloxane is added, so that a light-cured coating has excellent salt mist resistance, weather resistance and impact resistance; by adding the aluminum chelate, the peelability of the photocuring coating can be improved.

The invention discloses a strong-hydrophobicity chromatographic stationary phase modified by a covalent triazine skeleton containing an octyl chain as well as a preparation method and application of the strong-hydrophobicity chromatographic stationary phase. Activated silica gel is modified by utilizing a silane coupling agent, so that gamma-glycidyl ether oxypropyl trimethoxy is introduced into the surface of the silica gel; and performing in-situ growth of a covalent triazine skeleton layer containing an octyl chain through a Schiff base condensation reaction to prepare the strong-hydrophobicity chromatographic stationary phase. A covalent triazine skeleton containing a hydrophobic octyl chain in the structure is used for modifying the surface of silica gel, and a bonding phase contains a triazine ring, a benzene ring, an octyl chain and an amino group. According to the stationary phase, a hydrophobic long octyl chain is introduced into a bonding unit of CTF, so that the structure, morphology and performance of the CTF are changed, a'flower-on-sphere 'morphology is formed, and the stationary phase has a rigid porous structure, adjustable hydrophilicity / hydrophobicity, a rich pi electron system, strong hydrophobicity and good separation selectivity for non-polar compounds, and can be widely applied to separation of various samples.