2956 results about "Bisphenol" patented technology

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.

The invention relates to a photo-thermal super-hydrophobic multifunctional anti-icing coating as well as a preparation method and application thereof. The photo-thermal super-hydrophobic multifunctional anti-icing coating comprises primer and finish paint, the primer comprises the following raw materials in parts by weight: 20-25 parts of bisphenol A type epoxy resin and / or fluorine modified epoxy resin, 10-20 parts of fluorine modified polyacrylic resin and / or polyurethane resin, 5-10 parts of a curing agent and 40-55 parts of a solvent; the finish paint comprises the following components in parts by weight: 2-5 parts of polytetrafluoroethylene, 1-3 parts of soluble polytetrafluoroethylene, 1-5 parts of polydimethylsiloxane and 85-90 parts of fluorinated MOF dispersion liquid. Compared with the prior art, the photo-thermal super-hydrophobic multifunctional anti-icing coating provided by the invention has the characteristics of super-hydrophobicity, rapid ice melting, wear resistance, reduction of ice adhesion strength and reduction of icing amount, can effectively solve the problem of icing of an aluminum conductor of a power transmission line of a power system, and can be applied to power equipment such as the aluminum conductor of the power transmission line.

The invention relates to the technical field of biodegradable materials, and discloses a full-biodegradable bamboo fiber film material and a preparation method thereof, the full-biodegradable bamboo fiber film material comprises the following raw materials by weight: 30-50 parts of modified bamboo fiber, 20-40 parts of a biodegradable polymer, 3-8 parts of a plasticizer, and 1-5 parts of a cross-linking agent. Acrylic acid grafted hydroxyethyl methylacrylate is grafted to epoxy resin containing azobenzene side chains to form a grafting product of a latticed structure, and the grafting product and hydroxyl groups on bamboo fibers form ether bonds to modify the bamboo fibers. The latticed structure can effectively improve the mechanical property of the film, and azobenzene is grafted to the side chain of bisphenol A epoxy resin, so that the epoxy resin has better degradability.

The invention discloses an application of an electronic waste pollution human body exposure fingerprint spectrum in exposure risk prediction, and the human body exposure fingerprint spectrum is composed of more than three of exposure markers of 2, 4, 6-tribromophenol, 2, 4, 5-trichlorophenol, 4-bromophenol, 1-hydroxypyrene and bisphenol A. The invention further discloses an application of the electronic waste pollution human body exposure fingerprint spectrum in exposure risk prediction. According to the method, a systematic method of urine pollutant exposure omics is adopted for the first time, comprehensive screening and characterization of pollutant exposure markers related to specific components and by-products are achieved in electronic waste exposure worker groups, and the method is the most systematic organic pollutant exposure research known in the field at present.

The invention relates to the technical field of new materials, and mainly relates to a double-component low-viscosity ultralow-temperature adhesive as well as a preparation method and a use method thereof. The double-component low-viscosity ultralow-temperature adhesive comprises a component A and a component B. The component A comprises the following components in percentage by mass: 20-40% of bisphenol A epoxy resin, 4-8% of aromatic epoxy resin, 6-10% of polyurethane modified epoxy resin, 1-2% of a rubber toughening agent, 5-20% of a diluent and the balance of an additive. And the component B comprises the following components in percentage by mass: 10-40% of a polyether amine curing agent, 10-40% of a fatty amine curing agent, 10-40% of an aromatic amine curing agent and 10-40% of a phenolic aldehyde amine curing agent. The adhesive provided by the invention has relatively strong compressive strength and excellent toughness, can keep good toughness in a low-temperature environment, is not easy to cause brittle rupture, can bear relatively large mechanical load, and is suitable for various industrial applications.

The invention discloses a graphene nanometer heavy anti-corrosion coating and a preparation method thereof, and belongs to the technical field of anti-corrosion coatings. The coating is prepared from the following components in parts by mass: 50 to 70 parts of diallyl bisphenol A type epoxy resin, 8 to 15 parts of histidine modifier, 12 to 20 parts of graphene nano composite modified filler, 5 to 10 parts of curing agent, 0.5 to 2 parts of flatting agent and 0.3 to 1 part of defoaming agent. The preparation method of the histidine modifier comprises the following steps: carrying out a Schiff base reaction on 1-palmitoyl-2-oleoyl ethanolamine and N-formyl-L-histidine to generate an intermediate A; reacting with a spiro quaternization reagent to form a quaternary ammonium salt intermediate B; and then compounding with aminopropyltriethoxysilane and silicotungstic heteropoly acid salt to obtain the product. The graphene nano-composite modified filler is prepared by modifying the surface of a graphene oxide / bentonite mutual intercalation layer structure through allyl trimethoxy silane. The graphene nano heavy anti-corrosion coating prepared by the invention forms a high-density cross-linked network, and has excellent barrier property, strong adhesive force, impact resistance and long-acting anti-corrosion performance.

The invention discloses a glue solution for a copper-clad plate and a preparation method of the glue solution, and relates to the technical field of copper-clad plates. According to the prepared glue solution for the copper-clad plate, the composite epoxy resin, the curing agent, the accelerant, the solvent, the flexibilizer and the inorganic filler, the composite epoxy resin comprises bisphenol A epoxy resin, epoxy phenyl polysiloxane, itaconic acid polyaryletherketone and hydroxyl-terminated fluorine-containing vinyl polysiloxane, so that the interface bonding force with the copper plate is enhanced; the dielectric constant and the dielectric loss are effectively reduced, the peel strength and the toughness of the material are also remarkably improved, and the toughening agent is modified polyether sulfone microspheres; the modified polyethersulfone microspheres are prepared by coating polyethersulfone microspheres with hexamethylenediamine tetrapropionamide diamine, the hexamethylenediamine tetrapropionamide diamine is prepared by carrying out acylation condensation reaction on hexamethylenediamine tetramethyl propionate and ethylenediamine, and the polyethersulfone microspheres are prepared by carrying out electrostatic spinning on a spinning solution of polyethersulfone and vinylpyridine, so that the peel strength of the glue solution is remarkably improved.

The invention discloses a water-borne epoxy resin coating which comprises a component A and a component B, the component A is prepared from 60 to 80 parts of 50 percent modified water-borne epoxy resin emulsion, 5 to 15 parts of deionized water, 0.5 to 1 part of wetting dispersant, 0.2 to 0.8 part of defoaming agent, 5 to 10 parts of modified zinc phosphate, 3 to 5 parts of ion exchange antirust pigment, 4 to 6 parts of sericite powder, 3 to 5 parts of glass flake, 5 to 10 parts of precipitated barium sulphate, 1 to 5 parts of nano silicon dioxide and 0.5 to 1 part of rheological additive; 1 to 2 parts of modified organic bentonite slurry; 0.1 to 0.3 part of a pH conditioning agent; and 0.2 to 0.8 part of a flash rust inhibitor. The component B is prepared from 40 to 50 parts of waterborne epoxy-amine adduct, 20 to 30 parts of 50 percent modified polyamide curing agent, 5 to 15 parts of 60 percent Mannich base phenolic aldehyde amine curing agent, 0.5 to 1.5 parts of epoxy silane coupling agent, 1 to 2 parts of nonionic surfactant and 15 to 20 parts of deionized water. The emulsion stability of the waterborne epoxy resin coating is improved through a bisphenol A / F mixed epoxy emulsion and a grafted polyethylene glycol hydrophilic chain segment.

The invention relates to the technical field of optical protective materials, in particular to an anti-dazzle full-ultraviolet-proof optical protective material and a preparation method thereof.The anti-dazzle full-ultraviolet-proof optical protective material is formed by sequentially compounding a scratch-resistant hardened layer, a PET film layer a, a composite adhesive layer, a PET film layer b, an installation adhesive layer and a PET release film layer from top to bottom; the preparation method comprises the following steps: mixing organic silicon modified polyurethane acrylate, a pigment, a reactive diluent, a flatting agent, a photoinitiator, a solvent and modified nano silicon dioxide to prepare a photocurable scratch-resistant hardening coating liquid; in order to endow the optical material with excellent infrared barrier property and heat insulation property, cesium tungsten bronze is introduced into a composite adhesive layer as a filler, and in order to improve the adhesive power and water resistance of a composite adhesive solution, epoxy resin is taken as a base material, organic silicon modified polyurethane acrylate is introduced as a water-resistant component, acrylic acid is taken as tackifying resin, and a curing agent is taken as a curing agent. And bisphenol A ethoxylate dimethacrylate is used as a diluent.

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 discloses a light-moisture dual-curing underwater epoxy coating with a self-repairing function as well as a preparation method and a construction method of the light-moisture dual-curing underwater epoxy coating. The epoxy coating comprises a component A and a component B, wherein the mass ratio of the component A to the component B is (1.5-3.5): 1; the component A is prepared from the following raw materials: bisphenol F type epoxy resin, dynamic disulfide bond modified polysulfide rubber, boron nitride nanosheet and silicon carbide nanowire hybrid filler, a photoinitiator and a silane coupling agent; the component B is prepared from the following raw materials: moisture-cured polyether amine, a boric acid ester bond cross-linking agent and hydrophobic modified graphene oxide. According to the invention, a light-moisture dual-curing mechanism is adopted, ultraviolet irradiation initiates rapid surface curing, and then environmental moisture permeates to complete deep curing. The material provided by the invention has the advantages of rapid curing, excellent self-repairing function, significantly improved underwater adhesion and good thermal conductivity, and provides a new solution for rapid repairing and long-acting protection of underwater structures.

The invention relates to a sludge biochar modified layered bimetallic oxide, and a preparation method and application thereof. The modified layered bimetallic oxide is prepared from the following main raw materials: domestic sewage aeration tank sludge, NaOH, Na2CO3, FeCl3. 6H2O and MnCl2. 4H2O. The domestic sewage aeration tank sludge is used for preparing dry sludge, the ferric chloride solution and the manganese chloride solution are used for preparing sludge composite layered double hydroxides, and the final layered bimetallic oxide composite sludge biochar catalyst can be prepared by calcining the sludge composite layered double hydroxides. The modified layered bimetallic oxide prepared by the scheme of the invention can effectively degrade bisphenol A, has relatively strong reusability, and still keeps good degradation ability in a relatively wide pH environment.

To provide an epoxy resin composition that has low volume resistivity and exhibits suitable conductivity when formed as a coating film, and that makes it possible to form a coating film having excellent solder wettability and solder erosion resistance.SOLUTION: An epoxy resin composition contains the following components (A) to (D): (A) one or more epoxy resins selected from the group consisting of triphenylmethane-type epoxy resins, naphthalene-type epoxy resins, and phenol novolac-type epoxy resins; (B) one or more epoxy resins selected from the group consisting of polyether-modified epoxy resins, urethane-modified epoxy resins, mesogen-modified epoxy resins having an -O-CH2CH(OH)CH2-O- skeleton in the molecule thereof, bisphenol-type epoxy resins, and dicyclopentadiene-type epoxy resins; (C) an imidazole-based compound and / or a phenol-based compound; and (D) one or more conductive powders selected from among silver-coated copper powders, silver-based powders, nickel-based powders, conductive carbon powders, copper-based powders, and gold-based powders.SELECTED DRAWING: None

The invention discloses a high-temperature-resistant tough epoxy resin adhesive and a preparation method thereof, and relates to the technical field of epoxy resin, the high-temperature-resistant tough epoxy resin adhesive comprises the following components by mass: 30-60 parts of epoxy resin, 15-40 parts of a modified curing agent, 5-20 parts of a flexibilizer, 8-35 parts of an inorganic filler, 1-5 parts of a coupling agent, and 0.5-3 parts of an antioxidant; the epoxy resin is formed by compounding bisphenol A epoxy resin and novolac epoxy resin according to the mass ratio of (1-3): 1; the modified curing agent is prepared by modifying an imidazole curing agent with a silane coupling agent. The problem that high temperature resistance and toughness of an epoxy resin adhesive are difficult to consider at the same time can be solved.

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 technical field of PC transparent flame-retardant toughening modification, in particular to phenolic hydroxyl-terminated modified polysiloxane with a side chain containing phenyl and sulfonate groups and a preparation method of copolymerized PC. The modified polysiloxane is prepared by the following steps: performing ring opening polymerization on phenol-containing double end sockets and cyclotetrasiloxane to obtain modified polysiloxane containing double bonds and phenyl functional groups, and grafting sulfonate through a thiol-ene click chemical reaction. Diphenyl carbonate, bisphenol A and the modified polysiloxane are used as raw materials, a polysiloxane-PC block copolymer is formed through copolymerization, efficient flame retardance and high transparency are achieved, and meanwhile extremely high low-temperature impact strength is achieved.

The invention discloses an organic wastewater adsorbent as well as a preparation method and application thereof, and belongs to the technical field of sewage treatment. Comprising the following steps: carrying out nitration reaction on styrene porous microsphere resin, and then carrying out reduction reaction to obtain amino-modified porous microsphere resin; the preparation method comprises the following steps: carrying out polymerization reaction on high-nitrogen-content amino organic small molecules and aldehyde group small molecules under the action of a basic catalyst in an adsorption polymerization manner to generate a nitrogen-doped organic porous polymer, and coating the surface of amino-modified porous microsphere resin with the nitrogen-doped organic porous polymer to obtain the organic wastewater adsorbent. The porous microsphere resin adsorbent with large adsorption capacity and high organic matter removal rate is synthesized by using the carrier advantage of styrene microsphere resin and introducing a porous heteroatom polymer on the microsphere resin. When the adsorbent is used, the adsorbent is directly added into an organic wastewater solution, and the removal rate of bisphenol A, aniline and tetracycline can reach 90% or above.

The invention discloses a low-temperature polyether demulsifier for oil and gas gathering and transportation and a preparation method thereof, and relates to the technical field of petrochemical engineering, and the preparation method is characterized by comprising the following steps: compounding cardanol, pentaethylenehexamine and bisphenol F according to a specific molar ratio to obtain an initiator, and carrying out formaldehyde condensation to prepare a composite initiator; epoxypropane and ethylene oxide are grafted through staged block copolymerization to form a polyether skeleton; introducing a fluorine-containing epoxy monomer to carry out terminal fluorination modification; finally, adipic acid and epichlorohydrin are subjected to chain extension crosslinking, and the demulsifier with the molecular weight being 8000-12000 Da, the fluorine content being 5.5-6.5 wt% and the PDI being smaller than or equal to 1.3 is prepared. The low-temperature demulsifying agent has the effects of realizing efficient demulsification at low temperature, improving the demulsifying efficiency and reducing the dosage through coordination of the composite initiator, super-hydrophobic permeation of the fluorinated block and accurate regulation and control of the molecular weight, solving the problems of low-temperature failure and easiness in emulsification of a traditional demulsifying agent, and meeting the requirements of low-temperature working conditions of oil and gas gathering and transportation.

The invention discloses novel environment-friendly flame-retardant corrugated paper and a preparation method thereof, and belongs to the technical field of paperboard products. The corrugated paper is formed by bonding upper surface paper, a V-shaped flame-retardant core base layer and lower surface paper through a flame-retardant adhesive; the flame-retardant adhesive is prepared from the following components in parts by weight: 50 to 65 parts of oxidized cassava starch, 12 to 23 parts of phosphate esterified urea-formaldehyde resin, 5 to 15 parts of nitrogen-phosphorus modified isocyanate-based polyurethane and 2 to 8 parts of nano aluminum hydroxide; wherein the nitrogen and phosphorus modified isocyanate-based polyurethane is prepared by carrying out a reaction on isophorone isocyanate, bisphenol A type monophenyl phosphonate and modified montmorillonite, and the modified montmorillonite is prepared by carrying out a reaction on montmorillonite and polysiloxane. The corrugated paper provided by the invention has excellent flame retardant property, and also has good chemical stability and mechanical properties.

The invention discloses an impregnation liquid for preparing hydrogenated bisphenol A through bisphenol A hydrogenation. The impregnation liquid comprises a Ru complex, a water-soluble nonionic surfactant and water, wherein the molecular size of the Ru complex is greater than 1nm. According to the preparation method disclosed by the invention, by adopting the impregnation liquid containing the Ru complex of which the molecular size is greater than 1nm and the water-soluble nonionic surfactant, more Ru complex of which the molecular size is greater than 1nm can exist in mesoporous channels of an activated carbon carrier in an impregnation process, so that the contact probability of an active phase and a reactant bisphenol A molecule is increased; the purposes of improving the active metal utilization rate and improving the catalyst activity are achieved.

The invention discloses a halogen-free flame-retardant benzoxazine-epoxy / aramid fiber composite material and a preparation method thereof, and belongs to the technical field of polymer composite materials. The composite material is obtained by heating and curing main chain type phosphorus-containing benzoxazine, epoxy resin and aramid fiber according to the mass fraction ratio of (1%-50%): (40%-70%): (30%-70%); the main chain type phosphorus-containing benzoxazine is prepared by carrying out Mannich condensation reaction on phosphorus-containing diamine, bisphenol and paraformaldehyde according to the molar ratio of 1: 1: (4.1-4.4). According to the prepared composite material, main chain type phosphorus-containing benzoxazine modified epoxy resin serves as a matrix, the matrix and aramid fibers are subjected to heating curing to prepare the composite material, benzoxazine is crosslinked with the aramid fibers and the epoxy resin when subjected to ring opening polymerization, the interface bonding performance between the aramid fibers and the epoxy resin can be remarkably improved, and the composite material can be used for preparing the aramid fibers and the epoxy resin. The mechanical property of the composite material can be effectively improved; meanwhile, benzoxazine contains phosphorus, so that the flame retardant property of the composite material can be improved, and the application field of the aramid fiber composite material is expanded.

The invention belongs to the technical field of polyurethane, and particularly relates to a polyurethane material for coal rock mass and a preparation method of the polyurethane material. The polyurethane material for the coal rock mass is composed of a white material and a black material according to the mass ratio of 1: 1, and the white material comprises the following raw materials: mining polyether polyol, a flame retardant and a catalyst; the black material comprises the following raw materials: a prepolymer and a flame retardant. According to the polyurethane material for the coal and rock mass, hexahydroxy triphenylene with a star-shaped molecular structure is introduced into mine polyether polyol synthesis, a highly-crosslinked star-shaped structure is formed, rigidity and flexibility are balanced, and meanwhile the crosslinking density and compressive strength of a product are improved; secondly, bisphenol A with a benzene ring structure is adopted as a raw material for synthesizing the prepolymer, the toughness and strength of the material are improved through the interaction of benzene rings, and the prepared polyurethane material is high in compressive strength and low in reaction heat and meets the requirements of the polyurethane material for coal rock mass; the invention further provides a preparation method, and the preparation process is simple.

The invention discloses a preparation method and application of a synergistically modified waterborne polyurethane emulsion, and belongs to the technical field of macromolecular waterborne polyurethane. The preparation method comprises the following steps: firstly, modifying diisocyanate by using binary fluoroalcohol to obtain a fluorine-containing isocyanate emulsion, then preparing a waterborne polyurethane prepolymer emulsion by using the fluorine-containing isocyanate emulsion and dihydric alcohol, and finally, modifying the waterborne polyurethane prepolymer emulsion by using bisphenol A type epoxy resin to prepare the synergistically modified waterborne polyurethane emulsion. An adhesive film prepared from the synergistically modified waterborne polyurethane emulsion has excellent water resistance, mechanical properties and thermal stability, the salt spray resistance is particularly remarkably improved compared with that of an adhesive film prepared from a single compound modified waterborne polyurethane emulsion, the maximum salt spray resistance can reach 18 months, and the adhesive film has good practical application value and industrial production prospects.

The invention discloses a self-template synthesized linear biochar-based bimetallic material as well as a preparation method and application thereof, and belongs to the technical field of carbon materials. The method comprises the following steps: pretreating ganoderma lucidum residues, and pyrolyzing in a nitrogen atmosphere to prepare charcoal; and mixing the prepared biochar with cobalt nitrate and sodium molybdate to prepare CoMoO4 nanoparticles with in-situ growth of the biochar, and then washing and drying to obtain the BC-coated CoMoO4 linear biochar-based bimetallic material. Heterojunctions formed by binding sites of cobalt-molybdenum bimetal and biochar in the material form more defect sites, the synergistic effect of the metal and the micro-nano fibrous biochar is exerted, the degradation rate in the application of catalytic degradation of bisphenol A can reach 98.18% or above, a multiple reaction mechanism with sulfate free radicals is jointly shown, and the photocatalytic degradation of bisphenol A is realized. And the method has higher adaptability and effectiveness for complex pollutants.

The invention relates to the technical field of high-molecular compounds, and discloses an epoxy resin material for a high-pressure conduit and a preparation method of the epoxy resin material. The preparation method comprises the following steps: preparing the following raw materials in parts by mass: 65-70 parts of bisphenol A epoxy resin; 55-60 parts of a curing agent; 0.1 to 0.2 part of an imidazole accelerant; 10 to 15 parts of a reactive diluent; and 8 to 15 parts of epoxy silicon dioxide. The diluent is prepared from N, N, N ', N'-tetraepoxypropyl-4, 4 '-diaminodiphenylmethane and ethylene glycol diglycidyl ether according to the mass ratio of 1 to (4 to 5); the curing agent comprises a polybenzimidazole curing agent, a polyethylene glycol curing agent and methyl tetrahydrophthalic anhydride in a mass ratio of (2-3): (2-3): (5-6). The epoxy resin material prepared by the invention has excellent electrical properties and mechanical properties.

The invention relates to the technical field of adhesives, in particular to a bio-based polyurethane hot melt adhesive and a preparation process thereof. The bio-based polyurethane hot melt adhesive is prepared from the following raw materials in parts by weight: 30 to 40 parts of bio-based polyester glycol, 60 to 80 parts of bio-based polyether polyol, 25 to 35 parts of acrylic resin, 40 to 60 parts of isophorone diisocyanate, 3 to 5 parts of bisphenol A epoxy resin E-44, 3 to 5 parts of 1, 3-butanediol, 1, 3-butanediol and 1, 3-butanediol. The coating is prepared from the following raw materials in parts by weight: 1-2 parts of 1, 4-butanediol, 0.2-0.6 part of dibutyltin dilaurate, 0.6-1.0 part of 3-aminopropyltriethoxysilane, 3-5 parts of modified carbon nanotubes, 2-4 parts of a curing agent, 1-1.5 parts of an ultraviolet absorbent and 0.8-1.2 parts of an antioxidant. The bio-based polyurethane hot melt adhesive prepared by the invention not only has better adhesive property, but also has excellent mechanical property and aging resistance, and the quality of the bio-based polyurethane hot melt adhesive is ensured while the service life of the bio-based polyurethane hot melt adhesive is effectively prolonged.

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 discloses an energetic slurry toughening and photocuring 3D printing method, relates to a preparation method of energetic slurry, and aims to solve the problems that an existing energetic material is poor in mechanical property, poor in toughness and easy to crack; the particles are fast to settle in the light-cured resin, the stability is poor, and the printing precision is poor. The invention develops a photocuring high-energy resin for photopolymerization additive manufacturing. The composition contains a high-energy filler, an acrylate adhesive, whiskers and an inert plasticizer. The material has the characteristics of compatibility, printability and mechanical property, and the possibility of printing increasingly complicated high-energy articles is proved through experiments. The preparation method of the light-cured resin comprises the following steps: adding the low polymer bisphenol A epoxy acrylate and the six-functionality polyurethane acrylate; diluting monomers including 1, 6-hexanediol diacrylate and trimethylolpropane triacrylate; uniformly mixing an auxiliary agent, a thickening agent and a dispersing agent, and magnetically stirring for 30 minutes to obtain the light-cured resin. A preparation method of the energetic slurry comprises the following steps: mixing light-cured resin, whiskers, an inert plasticizer, energetic particles, a photoinitiator and a light absorber, and uniformly stirring to obtain the energetic slurry; after the energetic slurry is used for 3D printing, a sample piece is obtained, the yield reaches 95%-100%, the cost is low, preparation is easy, and the method can be applied to the field of energetic slurry 3D printing.