293 results about "Glyceryl Ethers" patented technology

The invention relates to the technical field of ink, and discloses a preparation method of bio-based degradable water-based ink, which comprises the following steps: carrying out esterification polymerization on vanillin-based spiro acetal diglycidyl ether and diacid to obtain bio-based polyester resin, mixing and dispersing the bio-based polyester resin, petroleum-based resin, pigment, auxiliary agent and the like to obtain the bio-based degradable water-based ink. The bio-based degradable water-based ink is prepared. The bio-based resin contains a plurality of hydrophilic hydroxyl groups, has good solubility and dispersibility in the water-based ink, and generates denser hydrogen bonds and other cross-linking effects with the acrylic resin, so that the hardness of the ink is improved. Meanwhile, the polar hydroxyl groups also greatly enhance the hydrogen bond bonding and anchoring effect between the paint film and the base material, so that the adhesive force is improved. In addition, easily-hydrolyzed spiral acetal bonds, polyester structural units and other degradable chemical bonds in molecular chains of the bio-based resin provide more attack sites for water and microorganisms, the degradation rate is increased, and the degradable function is achieved.

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 agricultural fertilizers, in particular to an organic-inorganic composite silicon-calcium-magnesium fertilizer and a preparation method and application of the organic-inorganic composite silicon-calcium-magnesium fertilizer. The high-temperature activated silicon-calcium-magnesium mineral powder is composed of calcined wollastonite powder, calcined serpentine powder, dolomite powder and zeolite powder; 2%-5% of an organosilane modifier, wherein the organosilane modifier is composed of gamma-aminopropyl triethoxy silane and gamma-glycidyl ether oxypropyl trimethoxy silane, and the organic silane modifier is composed of gamma-aminopropyl triethoxy silane and gamma-glycidyl ether oxypropyl trimethoxy silane; 18%-35% of a functional organic matter complex, wherein the functional organic matter complex is composed of mineral source sodium humate, bioactive small peptide, sodium alginate and polyglutamic acid; and 3%-8% of auxiliary functional components, so that the solubility and the bioavailability of silicon, calcium and magnesium elements in minerals are remarkably improved.

The invention relates to a marine epoxy resin composite material. The marine epoxy resin composite material is characterized by comprising the following components in parts by mass: 100 parts of epoxy resin, 20-30 parts of a curing agent, 100-120 parts of a reinforcing material, 2050 parts of hollow microsphere filler and 5-15 parts of a flame retardant, the epoxy resin is one or a mixture of two of bisphenol A type epoxy resin, bisphenol F type epoxy resin, polyphenol type glycidyl ether epoxy resin or aliphatic glycidyl ether epoxy resin. When in use, the marine epoxy resin composite material disclosed by the invention has the advantages of excellent comprehensive performance, corrosion resistance, flame retardance, water resistance, high strength, light weight and the like, still has excellent performance retention rate after being soaked in water for several days, and is more suitable for complex and severe working conditions on a ship.

The invention discloses a DA bond polymer with antibacterial and self-repairing functions for a wood surface as well as a preparation method and a use method of the DA bond polymer. Chitosan serves as a wall material, cinnamon essential oil serves as a core material, the cinnamon essential oil and chitosan antibacterial microcapsules are prepared through emulsification, crosslinking and spray drying, and essential oil controlled release is achieved. Then bisphenol A diglycidyl ether DGEBA and furfuryl alcohol FA are used as raw materials, furyl functional epoxy resin FER is prepared under the catalysis of triethylamine TEA, bismaleimide BMI is added, and a DA bond self-repairing polymer is prepared through a DA reaction; and adding 4, 4-diaminodiphenylmethane DDM into the system, reacting with redundant DGEBA to generate a cross-linked polymer network, and adding the microcapsules into a DA bond semi-interpenetrating self-repairing network solution to obtain the DA bond polymer. A thin film formed by brushing and curing wood has antibacterial and self-repairing functions, scratches and microcracks on the surface of the wood can be repaired, and microbial erosion is inhibited.

A photoelectric composite cable for an underwater buoy, and a preparation process therefor. A polyurethane, a self-repairing polyurethane prepolymer, and a composite nano zinc oxide are selected as an outer sheath base material. A modified polysiloxane having a B-O six-membered ring dynamic cross-linked network and a long-chain alkane group and an amino is introduced into the self-repairing polyurethane prepolymer; 5,5'-methylenedisalicylaldehyde and isophorone diisocyanate are together subjected to stepwise polymerization with the modified polysiloxane, and the 5,5'-methylenedisalicylaldehyde is cross-linked with diphenylmethane diisocyanate to obtain a self-repairing polyurethane prepolymer; and nano zinc oxide is subjected to a modification treatment, wherein dodecyltrimethoxysilane and 3-glycidoxypropyltrimethoxysilane are used for dual modification, such that super-hydrophobic nano zinc oxide having good thermal stability and high dispersity is prepared in a toluene system.

The invention discloses a single-component high-heat-resistance type epoxy adhesive and a preparation method of the single-component high-heat-resistance type epoxy adhesive. The adhesive is prepared from the following components in parts by weight: 30 to 40 parts of N, N-4, 4 '-diphenylmethane bismaleimide; 50 parts of bisphenol F epoxy resin; 36.47 parts of 4, 4 '-diaminodiphenyl sulfone; 20 to 40 phr of phenyl glycidyl ether; 1 to 2 phr of two terminal type epoxy silicone oil; 4 to 6 phr of hydroxyl-terminated polyether sulfone; 10 to 20 phr of boron nitride, the surface of which is modified by gamma-glycidyl ether oxypropyl trimethoxy silane; and 1 to 3 phr of an adhesion promoter. According to the adhesive disclosed by the invention, the heat resistance, the mechanical property, the dimensional stability, the process adaptability and the like are synergistically improved, the use requirements of an aviation structural part on long-term service at 150-180 DEG C and an electronic packaging device on the condition of short-time reflow soldering at about 200 DEG C can be met, and the reliability of the adhesive in a high-temperature environment is remarkably improved.

The invention discloses a peracetylated polysaccharide derivative mixing accelerator as well as a preparation method and application thereof, and relates to the technical field of polysaccharide derivatives. Alkyl polyglucoside and glycidyl ether are subjected to etherification reaction to obtain polysaccharide derivatives; and adding acetic anhydride and an organic weak base catalyst into the polysaccharide derivative, and carrying out esterification reaction to obtain the peracetylated polysaccharide derivative. The obtained peracetylated polysaccharide derivative can be used for reducing the minimum miscible pressure of CO2 in an offshore oilfield. The polysaccharide derivative provided by the invention is simple in synthesis process, and the molecular activity of the polysaccharide derivative can be regulated and controlled by changing the number of carbon dioxide-philic groups and the length of oleophylic unsaturated hydrocarbon chains, so that the polysaccharide derivative can be used in the CO2 oil displacement process of oilfield exploitation, and the minimum miscible pressure in the CO2 oil displacement process is effectively reduced.

The present invention provides an epoxy resin adhesive and a preparation method thereof, and relates to the technical field of building structure adhesives, the epoxy resin adhesive is prepared from a component A and a component B, the component A comprises the following raw materials by weight: 90-110 parts of epoxy resin, 15-25 parts of a toughening agent, 40-50 parts of a filler I and 15-20 parts of benzyl alcohol, and the toughening agent comprises polycarbonate, polyamide and polypropylene glycol diglycidyl ether; the component B is prepared from the following raw materials in parts by weight: 40 to 60 parts of curing agent, 10 to 20 parts of filler II, 1.5 to 3 parts of polyvinylpyrrolidone and 5 to 10 parts of benzyl alcohol. The preparation method comprises the following steps: S1, preparing A glue; s2, preparing B glue; and S3, mixing glue. The toughening agent is added in the component A, polycarbonate, polyamide and polypropylene glycol diglycidyl ether are selected as the toughening agent, the three raw materials are compounded and cooperated, the processability and flowing property of the epoxy resin adhesive can be effectively improved, and the problems that a cured finished product is high in brittleness and poor in impact resistance are solved.

The present invention discloses a monodisperse lignin colloidal sphere, a preparation method, and an application as a structural color material. The method comprises the following steps: first, lignin is steamed under alkaline conditions, and then ultrafiltration is performed to remove low-molecular-weight and high-molecular-weight lignin to obtain a uniform medium-molecular-weight lignin, which is then reacted with a glycidyl ether compound to further regulate polar groups such as hydroxyl groups, and then short-chain alcohols are used to separate alcohol-insoluble lignin. The alcohol-insoluble lignin is dissolved in an organic solvent-water mixed solvent, water is added dropwise to cause phase separation, and finally, centrifugal sedimentation is performed to obtain monodisperse lignin colloidal spheres. The preparation process of the method of the present invention is green and environmentally friendly, the organic solvents used can be recycled and reused, and the product yield reaches more than 70%. The obtained monodisperse lignin colloidal spheres can be used as a structural color material.

The invention discloses fluorine-containing bio-based epoxy resin as well as a preparation method and application thereof, and relates to the technical field of high polymer materials. The preparation method of the fluorine-containing bio-based epoxy resin comprises the following steps: enabling octafluoropentyloxy glycidyl ether as a fluorine unit to react with dihydric alcohol to obtain fluorine-terminated side chain butanediol, enabling the fluorine-terminated side chain butanediol to react with isocyanate to obtain a polyurethane prepolymer, and performing boric acid end capping on the polyurethane prepolymer by using 3-aminophenylboronic acid to obtain the fluorine-containing bio-based epoxy resin. The fluorine-containing bio-based epoxy resin (FBPU-ER) is prepared by the following steps: adding fluorine-containing polyurethane resin and phenylboronic acid into epoxidized soybean oil to obtain phenylboronic acid modified fluorine-containing polyurethane resin (FBPU), carrying out boric acid treatment on the epoxidized soybean oil by using 3-aminophenylboronic acid to obtain phenylboronic acid modified epoxy resin (BER), and finally, mixing the phenylboronic acid modified fluorine-containing polyurethane resin and the phenylboronic acid modified epoxy resin to obtain the fluorine-containing bio-based epoxy resin (FBPU-ER). The fluorine-containing bio-based epoxy resin prepared through fluorine-containing modification and toughening design has good mechanical properties, stability and self-repairing performance.

The invention provides a cationic waterborne epoxy hardener without containing free amine and a preparation method thereof, and relates to the technical field of epoxy hardeners, the method comprises the following steps: 1) mixing small molecular aldehyde and hydroxyethyl diethylenetriamine for reaction to obtain oxazolidine and aldimine terminated modified amine; (2) carrying out reaction on the modified amine and polyfunctional epoxy resin to obtain modified oxazolidine and aldimine-terminated modified resin amine; 3) mixing the modified oxazolidine and aldimine terminated modified resin amine, monofunctional glycidyl ether and water for reaction to obtain terminated modified resin amine; and 4) adding small molecular acid to neutralize the terminated modified amine, and transferring water to obtain the cationic waterborne epoxy curing agent without free amine. The paint film can be endowed with excellent boiling water resistance, acid and alkali resistance, neutral salt mist resistance and the like, the preparation process is simple, the production cost is low, and the paint is suitable for large-scale industrial application.

The invention discloses a hyperbranched polyether branching agent with an adjustable structure and a preparation method and application thereof.According to the branching agent, 3-butene-1-alcohol serves as an initiator, a hyperbranched skeleton is constructed through anion ring-opening polymerization reaction and diglycidyl ether, then esterification and end capping are conducted through anhydride, and the hyperbranched polyether branching agent with the adjustable structure is obtained. The tail end of the hyperbranched polyether contains vinyl double bonds, and the ester group structure of the hyperbranched polyether can be regulated and controlled. Different diepoxy compounds are selected to control a main chain structure, and different anhydrides are used for regulating and controlling the chemical composition of branched chains, so that accurate design of molecular weight, polarity and number of functional groups of the branching agent is realized. The branching agent has excellent dissolvability in common organic solvents, and solves the problem of poor dissolvability of the traditional polydiene branching agent. When the star-shaped branched butyl rubber is applied to the synthesis of star-shaped branched butyl rubber, the distribution and number of branched points can be accurately regulated and controlled, the weight-average molecular weight and molecular weight distribution index of the rubber are remarkably improved, and the side reaction of gel is avoided.

The invention discloses a temperature-resistant and salt-resistant tackifier and a preparation method thereof, and relates to the technical field of fracturing fluids. The preparation method of the temperature-resistant and salt-resistant tackifier comprises the following steps: taking a first monomer and diethanol amine to carry out epoxy ring-opening reaction, and after the reaction is finished, separating and purifying to obtain an intermediate; taking the intermediate, adding a quaternization reagent for quaternization reaction, and then separating and purifying to obtain an active monomer; the first monomer is one of allyl alcohol glycidyl ether, acrylic acid glycidyl ether and methacrylic acid glycidyl ether, and the quaternization reagent is one of halogenated carboxylate or halogenated sulfonate; the preparation method comprises the following steps: dissolving acrylamide, an active monomer and unsaturated phosphate, and carrying out free radical polymerization under the action of an initiator. The tackifier provided by the invention has good temperature-resistant and salt-resistant effects, and can tolerate salt water with mineralization degree of 120,000 mg / L and high temperature of 150 DEG C.

The invention relates to the technical field of sound insulation materials, in particular to flame-retardant epoxy resin composite diatomite sound insulation cotton and a preparation method thereof. The flame-retardant epoxy resin composite diatomite sound insulation cotton is prepared from epoxy resin, diatomite, a composite flame retardant, a coupling agent, a curing agent, a diluent, a foaming agent and a charring agent. The composite flame retardant at least comprises ammonium polyphosphate and melamine; the coupling agent is a silane coupling agent or a titanate coupling agent; the curing agent is methyl tetrahydrophthalic anhydride; the diluent is n-butyl glycidyl ether; the foaming agent is azodicarbonamide; the charring agent is pentaerythritol. By optimizing the diatomite modification process and combining physical dispersion and chemical modification means, the compatibility of the diatomite and the epoxy resin is greatly improved, the pain point of filler agglomeration in the traditional process is thoroughly solved, the porous sound insulation potential of the diatomite is fully released, and the sound absorption and sound insulation performance of the material is qualitatively improved.

The invention relates to low-viscosity high-strength two-component epoxy winding resin and a preparation method and application thereof, the resin comprises a component A and a component B, and the mass ratio of the component A to the component B is 100: (80-110); the component A consists of the following raw materials in percentage by mass: 70-85% of modified epoxy resin, 14-20% of a functional reactive diluent and 1-10% of an impregnating compound; the modified epoxy resin is formed by compounding bisphenol A epoxy resin and polyether modified epoxy resin, and the functional active diluent is formed by compounding 1, 6-hexanediol diglycidyl ether and phenyl glycidyl ether; the component B is prepared from the following raw materials in percentage by mass: 85-96% of a composite anhydride curing agent, 2.5-10% of a high-efficiency accelerant and 1.5-5% of a defoaming agent; the composite anhydride curing agent is compounded by methyl tetrahydrophthalic anhydride and succinic anhydride, the efficient accelerant is compounded by imidazole and phosphine, and the defoaming agent is an organic silicon defoaming agent.

The invention provides a super wear-resistant polyurethane floor coating and a preparation method thereof, the super wear-resistant polyurethane floor coating comprises a component A, a component B and a component C. The component A comprises glycidyl ether compound modified polyisocyanate; the component B comprises a latent imine curing agent, a diluent, a functional auxiliary agent and a pigment filler; the component C comprises aggregate; the mass ratio of the component A to the component B to the component C is (4-6): (2-4): (1-3). By optimizing and modifying the components in the super wear-resistant polyurethane coating, the properties such as high hardness, excellent wear resistance and the like of the super wear-resistant polyurethane finish paint are maintained; the interlayer adhesive force between the super-wear-resistant polyurethane floor finish paint material and various epoxy floating coatings can be obviously improved, and the construction matching property in a high-humidity environment and the wear resistance of a whole floor coating system are improved.

The invention relates to the technical field of adhesives, and particularly discloses an adhesive for repairing a glass fiber reinforced plastic pipeline and a preparation process. The invention relates to an adhesive for repairing a glass fiber reinforced plastic pipeline. The adhesive is prepared from the following raw materials: modified bisphenol A epoxy resin, a curing agent, a glass fiber reinforced filler, a silane coupling agent, phenyl glycidyl ether, hydroxyl-terminated nitrile rubber and an antioxidant 1076, the modified bisphenol A type epoxy resin is prepared by grafting and modifying bisphenol A type epoxy resin through amino-terminated polyether; the glass fiber reinforced filler is prepared from hydroxylated glass fibers and a graphene-carbon nanotube compound through covalent grafting. The adhesive can be used for emergency repair of glass fiber reinforced plastic pipelines, has the advantages of high low-temperature curing speed, high bonding strength and good durability, can effectively avoid cracking and leakage of repaired parts, and is adaptive to low-temperature and high-pressure complex repair working conditions. The preparation process is simple and convenient to operate and high in controllability, the adhesive with uniform performance can be stably prepared, and the repair efficiency and repair quality are guaranteed.

The invention discloses a halogen-free flame-retardant epoxy resin system composition and application, the epoxy resin system composition is composed of an epoxy resin part and a curing agent part, the epoxy resin part is composed of dihydroxydiphenylmethane glycidyl ether, 2, 2 '-[(1-methylethylene) bis (4, 1-phenylene formaldehyde)] dioxirane, 2, 2'-dihydroxydiphenylmethane glycidyl ether, 2, 2 '-[(1-methylethylene) bis (4, 1-phenylene formaldehyde)] dioxirane, 2, 2'-dihydroxydiphenylmethane, 2, 2 '-dihydroxydiphenylmethane, the halogen-free flame retardant is composed of hydroxyl-terminated polysiloxane modified bisphenol A glycidyl ether, an organophosphorus flame retardant, an active diluent and an auxiliary agent. And the curing agent part consists of an alicyclic amine curing agent, amine-terminated polyether and an accelerant. The epoxy resin system composition provided by the invention is low in mixing viscosity and strong in operability, a cured product has excellent toughness and heat resistance while ensuring that the flame retardant grade meets UL94V0, and the problems that a halogen-free flame-retardant system is poor in process operability, the performance of the cured product is reduced, halogen elements can release harmful gas at high temperature, and the service life of the cured product is prolonged can be effectively solved. And harm to human health and environment is caused.

The invention discloses a solvent-free epoxy anticorrosive coating and a preparation method thereof, and relates to the technical field of coatings. The invention discloses a solvent-free epoxy anticorrosive coating. The coating comprises the following raw materials in parts by weight: 40-60 parts of modified epoxy resin, 5-10 parts of modified nano zinc oxide, 15-25 parts of a polyamide curing agent, 5-10 parts of butyl glycidyl ether, 10-15 parts of titanium dioxide, 8-12 parts of talcum powder, 5-8 parts of barium sulfate, 0.5-1 part of an organic silicon defoaming agent, 0.5-1 part of an acrylate flatting agent, 1-2 parts of a silane coupling agent KH-550 and 3-5 parts of carboxyl-terminated nitrile rubber. And 1-2 parts of fumed silica. The solvent-free epoxy anticorrosive paint adopts a solvent-free formula, and is environment-friendly and low in volatility. The modified epoxy resin and the modified nano-zinc oxide have a synergistic effect, a chain is accurately controlled through'water diversion-viscosity feedback ', and molecular weight distribution is narrow. The pigment filler is uniformly dispersed at a high speed after being pretreated by the silane coupling agent, and is matched with the defoaming agent and the leveling agent, so that the coating has good leveling property, few bubbles, accurate viscosity regulation and control and stable and reliable comprehensive performance.

The invention discloses a water-based composite coating with a hybrid structure, which comprises a modified acrylate emulsion which can form an organic-inorganic hybrid structure and contains an epoxy group and a furan group, a reinforced phase dispersion liquid containing a maleimide group, a water-based polyurethane emulsion, deionized water and other functional aids. Wherein the modified acrylate emulsion is obtained by carrying out emulsion free radical copolymerization on glycidyl methacrylate and furfuryl methacrylate, namely other acrylate substances; the reinforced phase dispersion liquid is obtained through maleimide addition and substitution reaction and grafting with the modified nano silicon dioxide. The invention further discloses a preparation method of the hybrid-structure water-based composite coating. The preparation method comprises the steps of preparation of the organic-inorganic hybrid emulsion, preparation of the wax-containing composite emulsion and preparation of the hybrid-structure water-based composite coating. According to the preparation method, a Diels-Alder reaction is taken as a core, and the hybrid-structure water-based composite material which is good in physical property, repairable and convenient in process method is prepared.

A composition includes at least one of: (a) an amino acid isocyanate adduct of Formula I:and salts thereof, and (b) an amino acid epoxide adduct of Formula II:and salts thereof. R1 is a moiety of a monomer or prepolymer including two —NCO functional groups, which have reacted to form urea linkages; R2 is a moiety of a monomer or prepolymer including two glycidyl ether epoxide functional groups, which have reacted to form amino alcohol groups; R6, R7, R20 and R21 are independently (CH2)n, n is 1-6; R8, R9, R10 and R11 are independently hydrogen or CH2X; R12, R13, R14 and R15 are independently hydrogen, alkali metal cation, or X; R16 and R17 are independently hydrogen or X; R18 and R19 are independently hydrogen, SiO3 or X; and each X is independently hydrogen or a substituent. Controlled release particles, consumer products and methods including the composition are also disclosed.

This application belongs to the technical field of grouting materials for tunnel engineering, specifically relating to a grouting material suitable for tunnel rock strata reinforcement and its preparation method. It includes component A and component B; by weight, component A comprises: 75-85 parts of a first base material, 10-20 parts of a coupling agent, and 2-5 parts of a catalyst; component B comprises: 70-80 parts of a second base material and 15-25 parts of a modifying accelerator; wherein, the first base material is a water glass solution, and the physicochemical properties of the water glass solution meet the following conditions: modulus > 2.5, Baume degree < 40°Bé; the second base material is composed of isocyanate compounds and glycidyl etheroxypropyl cage-like polysilsesquioxane in a weight ratio of 100:(11-23); the modifying accelerator includes polyvinylpyrrolidone and dicarboxylic acid alkyl ester compounds. The two base materials synergistically cure at low temperature to form a highly cross-linked organic-inorganic composite network, thereby significantly improving the compressive strength of the solidified body.

The application belongs to the technical field of soft capsules, and discloses a starch-based soft capsule material and a preparation method thereof. The preparation method comprises the following steps: mixing wheat starch and deionized water, adding a sodium periodate solution to react, so as to obtain dialdehyde starch; reacting the dialdehyde starch with glycidyl methacrylate and triethylamine, so as to obtain grafted modified starch; mixing the grafted modified starch with modified nano-silicon dioxide, and reacting after ultrasonic oscillation, so as to obtain nano-silicon dioxide composite modified starch; mixing the composite modified starch with polyvinyl alcohol and polyvinylpyrrolidone, so as to obtain a film forming solution; and after the film forming solution is cast and dried, hot pressing is performed, so that the starch-based soft capsule material is finally obtained. The starch is subjected to multiple hydrophobic modifications, so that the hydrophilic performance is reduced, and the stability of the soft capsule is improved.

The invention belongs to the technical field of insulating materials, and particularly provides a high-strength insulating material, a preparation method and a disc insulator. The invention relates to a high-strength insulating material, which is prepared from the following components: epoxy resin, a maleic anhydride-1-octene copolymer, SiO2 (at) COF-NH2, butyl glycidyl ether and 4, 4 '-diaminodiphenyl-methane. The high-strength insulating material prepared by the preparation method disclosed by the invention is excellent in mechanical property, and can keep excellent insulating property at room temperature and high temperature.

This invention relates to the field of polyurethane foam materials, specifically, to a preparation process for an aging-resistant and flame-retardant polyurethane foam material. The preparation process includes the preparation of a composite flame retardant, the preparation of component A, and the preparation of the polyurethane foam material. This invention integrates the composite flame retardant into the cross-linked network of the polyurethane foam material via chemical bonds. The composite flame retardant is prepared by grafting a phosphorus-containing flame-retardant structure onto the cage-like polysilsesquioxane structure after a ring-opening reaction between the epoxy groups in glycidyl etheroxypropyl cage-like polysilsesquioxane or octacyclooxycyclohexylethyl cage-like polysilsesquioxane and the acidic hydroxyl groups in diphenyl phosphate. The composite flame retardant of this invention is less prone to migration, precipitation, or loss, and improves the rigidity and aging resistance of the polyurethane matrix through its rigid cage structure and benzene rings, thereby improving flame retardant performance while reducing adverse effects on the mechanical properties of the foam material.

The application belongs to the technical field of sand consolidation agent preparation, and particularly relates to a sand consolidation agent and a preparation method thereof. The sand consolidation agent is composed of component A and component B. The component A is composed of the following raw materials: a diphenyl phenolic epoxy resin, hexakis(4-hydroxymethylphenoxy)cyclotriphosphazene, modified nano calcium zirconate, cage octakis(aminophenyl)silsesquioxane, n-butyl glycidyl ether, KH-550 silane coupling agent, polyether amine, fumed silica and defoaming agent. The component B is composed of the following raw materials: polyborosilazane and 2-ethyl-4-methyl imidazole. The cage octakis(aminophenyl)silsesquioxane in the raw material of the sand consolidation agent strengthens the network structure stability through chemical bonding, the hexakis(4-hydroxymethylphenoxy)cyclotriphosphazene realizes thermal stabilization through chemical bonding and physical dispersion, and the modified nano calcium zirconate provides physical support. The three components synergistically improve the heat resistance of the system.

The present application belongs to the technical field of coating, and particularly relates to an epoxy asphalt coating, a preparation method and application thereof. The epoxy asphalt coating comprises component A and component B; the component A comprises epoxy resin, asphalt, active diluent and additive; the active diluent comprises glycidyl ether containing two epoxy groups; the component B comprises modified amine curing agent. The components jointly act to make the epoxy asphalt coating have high solid content, easy construction, fast drying speed, and good waterproof performance and anticorrosion performance. The active diluent prepared by the reaction of p-xylyl alcohol and diglycidyl ether can greatly reduce the viscosity of the system, facilitating construction; meanwhile, the active diluent has a double epoxy group structure, can participate in the reaction of the system, accelerate the drying speed, and the rigid benzene ring structure can improve the mechanical properties.

The present disclosure relates to a composite material for application to a bone defect site to promote new bone growth at the site comprising: a combination of freeze-dried mineralized bone allograft particles; and a monophasic gel comprising cross-linked hyaluronic acid; wherein the hyaluronic acid is cross-linked by a cross-linking agent, the cross-linking agent being a diglycidyl ether. The present disclosure also relates to a method to obtain a composite material for application to a bone defect site to promote new bone growth at the site comprising mixing freeze-dried mineralized bone allograft particles with a monophasic gel comprising hyaluronic acid; and to a bone regenerative material comprising the composite material as defined herein for use in a method of treating a patient suffering from a degenerative bone condition, bone loss, bone deficiency or bone atrophy.

The application discloses an end hexaazido nitrate polyether adhesive and a synthesis method thereof. The method first takes triazido neopentyl alcohol and glycidyl ether nitrate as raw materials, boron trifluoride-ether complex as a catalyst, and obtains triazido neopentyl polyglycidyl ether nitrate alcohol through cation ring-opening polymerization reaction; then takes triazido neopentyl polyglycidyl ether nitrate alcohol and hexamethylene diisocyanate as raw materials, dibutyl tin dilaurylate as a catalyst, and obtains end hexaazido polyglycidyl ether nitrate through addition reaction, namely the end hexaazido nitrate polyether adhesive. The application is mainly used for solid propellants, is used for synthesizing polytriazole elastomers, improves the content and crosslinking density of hard segments, promotes microphase separation of the elastomers, and thus improves mechanical properties.