1572 results about "Bisphenol" patented technology

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 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 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 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 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 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 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.

This anticorrosive coating composition comprises a main agent (I) and a curing agent (II), wherein: the main agent (I) contains an epoxy resin (a); the epoxy resin (a) contains at least one of a bisphenol A epoxy resin (a-11) and a novolac epoxy resin (a-12) each having a weight average molecular weight of 6,000-12,000; the curing agent (II) contains a polyamine (b) and an alkylphenol (c); the polyamine (b) contains an alicyclic polyamine (b-1) having a cyclic aliphatic hydrocarbon group to which an amino group is bonded and contains a non-alicyclic polyamine (b-2) having no cyclic aliphatic hydrocarbon group to which an amino group is bonded; at least one of the main agent (I) and the curing agent (II) includes a vinyl-based defoaming agent (d) that has a constituent unit derived from at least one monomer selected from the group consisting of alkyl (meth)acrylates, alkyl vinyl ethers, and olefins and that has a number average molecular weight of 30,000-100,000 or 300,000-2,000,000; the content of the alicyclic polyamine (b-1) is 30%-80% by mass of the solid content of the curing agent (II); the content of the non-alicyclic polyamine (b-2) is 2%-45% by mass of the solid content of the curing agent (II); the content of the alkylphenol (c) is 5%-60% by mass of the solid content of the curing agent (II); and the content of the vinyl-based defoaming agent (d) is 0.005-3 parts by mass with respect to 100 parts by mass of the anticorrosive coating composition.

The invention discloses a flame-retardant cable and a preparation method thereof. The cable comprises conductor wire cores, a fireproof layer, an insulating layer, a shielding layer, a filling layer and a sheath layer from inside to outside. According to the cable sheath layer, 100 parts of high density polyethylene (HDPE), 5-15 parts of ethylene-vinyl acetate rubber and 3-10 parts of fluororubber are used as main materials, triallyl isocyanurate and bisphenol A diallyl ether are introduced for synergistic crosslinking, and nano montmorillonite is used as an auxiliary material, so that a compact interpenetrating network is constructed. The tensile strength of the sheath layer composite material is greater than or equal to 26.5 MPa, the elongation at break is greater than or equal to 387%, the performance retention rate is greater than 92% after the sheath layer composite material is soaked in slurry for 28 days, the limit oxygen index is greater than 38%, the water vapor transmission coefficient is less than or equal to 1.5 * 10 <-4 > g.mm / (m < 2 >. D.Pa), and the sheath layer composite material has excellent flame retardance, barrier property and slurry resistance and is suitable for harsh outdoor environments such as rail transit.

The invention relates to the technical field of epoxy resin, in particular to self-repairing epoxy resin and a preparation method thereof. The self-repairing epoxy resin is prepared from the following raw materials in parts by mass: 80 to 120 parts of bisphenol A type epoxy resin, 20 to 40 parts of bisphenol F type epoxy resin, 5 to 15 parts of 1, 6-hexanediol diglycidyl ether, 1 to 3 parts of 3, 5-dimethylphenylboronic acid, 1 to 5 parts of furyl maleimide, 10 to 20 parts of dodecanedioic acid, 5 to 15 parts of butanetetracarboxylic acid, 1 to 3 parts of catalyst, 10 to 15 parts of nano silicon dioxide, 1 to 2 parts of boron nitride nanosheet and 1 to 2 parts of hyperbranched polyamidoamine. The curing agent is prepared from the following components in parts by weight: 20-30 parts of epoxy resin, 1-2 parts of sulfydryl-terminated polysiloxane, 20-30 parts of amine curing agent, 5-15 parts of reinforcing filler and 0.5 According to the invention, the balance among self-repairing capability, mechanical property and heat resistance is successfully realized; in the microcrack propagation process, fracture and recombination mechanisms of dynamic covalent bonds effectively prevent further propagation of cracks.

The invention discloses a high-temperature-stripping-resistant epoxy structural adhesive as well as a preparation method and application thereof, and belongs to the technical field of high-performance composite materials. The epoxy structural adhesive comprises bisphenol A type epoxy resin, novolac epoxy resin, polysiloxane-polyurethane modified epoxy resin, core-shell modified epoxy resin, PEEK ultrafine powder and other components, and through mutual cooperation of all the components, the problems that in a high-temperature service environment, the adhesive layer modulus of traditional adhesive is rapidly attenuated, and a bonding interface is prone to failure are solved; the epoxy structural adhesive provided by the invention has both rapid curing and heat resistance, is stable in interface bonding, has the highest modulus of 1.28 GPa at 80 DEG C, the highest peel strength of 7.8 N / mm at 80 DEG C, and a damage mode of cohesion or high-proportion mixed damage, and is especially suitable for structural bonding requirements of harsh scenes such as peripheral structures of automobile engines, high-temperature areas of electronic equipment and the like.

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.

The invention relates to the technical field of functional coatings, in particular to a graphene reinforced heavy-duty epoxy coating for a marine environment. The invention discloses a graphene-based epoxy resin coating which is prepared from the following raw materials in parts by weight: 60-80 parts of bisphenol A epoxy resin, 5-10 parts of aminated graphene-carbon nanotube composite powder, 3-6 parts of zinc-aluminum-cerium ternary composite phosphate, 3-6 parts of nano boron nitride / silicon dioxide core-shell particles, 15-25 parts of a polyamide-epoxy curing agent, 1-3 parts of a silane coupling agent KH-560 and 5-8 parts of cashew nut shell oil modified phenolic aldehyde amine. The anti-rust paint is prepared from the following components in parts by weight: 0.5-2 parts of carboxylated graphene quantum dots, 2-4 parts of organic montmorillonite, 0.1-0.5 part of a fluorocarbon surfactant, 8-15 parts of a composite anti-rust pigment and 10-20 parts of an organic solvent. The coating is excellent in corrosion resistance, capable of resisting marine corrosion for a long time, resistant to high temperature and resistant to cathodic disbonding, has the functions of aging tracing and biological adhesion resistance, is convenient to construct and stable in performance, and provides reliable protection for ocean engineering.

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 provides a method for preparing polyarylester by interfacial polycondensation, which comprises the following steps: dissolving a diphenol monomer in an alkali solution to prepare a bisphenol salt solution, and dissolving an interfacial catalyst in a bisphenol salt water phase to obtain a water phase; dissolving aromatic dicarboxylic acid acyl chloride in a halogenated hydrocarbon solvent to obtain an organic phase; s2, slowly adding the organic phase obtained in the step S1 into the water phase in a stirring state within 10-60 minutes, and continuously reacting for 10-120 minutes in the stirring state; the product is separated out in the form of precipitate, the precipitated precipitate absorbs the halogenated hydrocarbon solvent, so that a liquid phase main body is water, a solid phase is a muddy product containing the halogenated hydrocarbon solvent, and the obtained muddy product is filtered, washed and dried to obtain a powdery product. According to the method disclosed by the invention, the polymer is directly precipitated by controlling the solute concentration and the mixing ratio, so that the efficient in-situ removal of the solvent is realized, the solvent is directly separated from water through simple filtration, and'zero separation, zero crushing and zero distillation 'is realized.

The invention discloses a composite catalyst in a Fe3O4 nanoparticle confined carbon nanotube and application of the composite catalyst in degradation of bisphenol pollutants in water, and belongs to the technical field of environmental protection and water treatment. According to the catalyst, Fe3O4 nano-particles with the particle size of 1-5 nm are confined in inner channels of multi-walled carbon nanotubes (CNTs), stable Fe-C bonds are formed between Fe atoms and carbon atoms on the inner walls of the CNTs, a nano confinement structure is constructed, and the stability and electron transfer efficiency of the catalyst are improved. When the catalyst is used for activating peracetic acid (PAA), bisphenol pollutants in water can be quickly and efficiently removed. The catalyst can keep high-efficiency degradation performance in a wide range of pH value of 4-12, the degradation efficiency is still kept at 95% or above after the catalyst is recycled for 10 times, and the catalyst shows remarkable stability and practicability. The invention provides a novel catalyst which is excellent in performance, economical and environment-friendly and a process method for the field of actual water treatment.

The invention belongs to the technical field of automatic control, and particularly relates to an intelligent temperature control method for a bisphenol F type epoxy resin reaction kettle, which comprises the following steps: acquiring the temperature in the kettle, the frequency of a stirring motor and the flow of cooling water, and carrying out de-noising treatment; obtaining a dynamic viscosity thermal resistance operator based on the processed frequency of the stirring motor and the processed temperature in the kettle, and quantifying the heat transfer obstruction degree caused by the viscosity change of the material; obtaining a thermal inertia compensation driving operator by combining the target set temperature and the dynamic viscosity thermal resistance operator; the power of the heating actuator is obtained based on the thermal inertia compensation driving operator and the static balance power, and the input current of the heating actuator is adjusted through mapping and the cooling water flow is cooperatively adjusted. By sensing the thermal resistance dynamic state in a variable viscosity environment and performing feedforward compensation, the problem of temperature overshoot caused by large lag of the reaction kettle is solved, and the stability of the reaction process is improved.

The invention relates to the technical field of high polymer materials, and discloses a preparation method of high-dielectric-constant epoxy resin. The method comprises the following steps: (1) carrying out copolymerization reaction on bisphenol A epoxy resin and polytetrafluoroethylene at 80-100 DEG C for 2-3 hours; (2) adding a dicyandiamide curing agent into the reaction product obtained in the step (1), and carrying out gradient heating for curing; and (3) adding surface-modified barium titanate nanoparticles into the product obtained in the step (2), performing ultrasonic treatment, performing casting molding, and performing annealing treatment. According to the method, through molecular level design, the dielectric constant is remarkably improved while the excellent mechanical property of the epoxy resin is maintained, the dielectric loss (tan delta) and the thermal stability are optimized, and a high-performance base material is provided for electronic devices.

The embodiment of the invention provides a plastic-coated steel pipe and a plastic coating process thereof, and relates to the technical field of plastic-coated steel pipes. The plastic-coated steel pipe comprises a steel pipe base body, a metal transition layer, an inner anticorrosive coating, a fiber reinforced winding layer and an outer protective coating are sequentially arranged on the outer surface of the steel pipe base body from inside to outside, and the metal transition layer is a nickel-chromium-aluminum-yttrium alloy layer and is formed on the surface of the steel pipe base body through a supersonic plasma spraying process. And the inner anticorrosive coating is formed by a mixture of bisphenol F type epoxy resin and novolac epoxy resin, and is doped with silicon nitride and zirconium oxide composite nanoparticles subjected to surface treatment. By arranging a multi-stage composite structure of the metal transition layer, the high-temperature-resistant anti-corrosion coating, the fiber reinforcement layer and the self-repairing outer layer and arranging the detachable heat insulation sheath, the interface bonding strength, heat resistance, mechanical damage resistance and corrosion resistance of the plastic-coated steel pipe are improved; and the service life of the composite material in high-temperature, strong-corrosion and complex construction environments is effectively prolonged.

The invention provides a glass fiber impregnating compound composition, a glass fiber impregnating compound, a glass fiber direct yarn product and application. The glass fiber impregnating compound composition comprises effective components and water, and the effective components comprise a silane coupling agent, a film-forming agent A, a film-forming agent B, a lubricant, a flexibilizer, a wetting agent and a pH value regulator; the film-forming agent A is a water-based bisphenol A epoxy resin emulsion, and the film-forming agent B is a water-based polyether polyurethane modified aliphatic epoxy emulsion; the silane coupling agent comprises a first silane coupling agent and a second silane coupling agent, the first silane coupling agent is an epoxy silane coupling agent, the second silane coupling agent is an amino-containing silane coupling agent, and the mass ratio of the film-forming agent A to the film-forming agent B is (2-4.5): 1. The problems that in the prior art, when glass fibers are applied to winding gas cylinders, abrasion resistance is insufficient, fuzzing is prone to occurring in the winding process, and due to incomplete resin permeation, the winding gas cylinders are prone to layering, cracking and other defects in the high-pressure environment are solved.

The invention belongs to the technical field of composite processing aids, and particularly relates to a processing aid for a tensile CPVC (chlorinated polyvinyl chloride) board and a preparation process thereof, and the preparation process comprises the following steps: dispersing glass fibers in a KH-550 hydrolysate for stirring reaction, dispersing in a bisphenol A epoxy resin solution for stirring reaction after washing and drying, dispersing in an ODI (Olefin Diisocyanate) solution for stirring reaction after washing and drying, and drying to obtain the tensile CPVC board. After washing, dispersing in a GMA solution for stirring reaction, and washing and drying to obtain modified glass fibers; and dispersing the modified glass fiber in the dispersion liquid, adding an initiator and BA, heating, stirring for reaction, adding an initiator and MMA, stirring for reaction, washing and drying to obtain the processing aid. When a CPVC plate prepared by blending the processing aid and CPVC is used in a high-temperature and high-humidity environment, high tensile strength and impact strength can be kept for a long time.

The invention relates to a high-heat-resistance and high-insulation two-component epoxy resin adhesive and application thereof, and belongs to the technical field of epoxy resin. The technical problem to be solved by the invention is to provide the high-heat-resistance and high-insulation two-component epoxy resin adhesive. The adhesive comprises a component A and a component B. The component A comprises bisphenol A epoxy resin, novolac epoxy resin, silicon carbide whiskers, potassium titanate fibers, boron phenolic resin and modified nano boron nitride. The component B is prepared from methylhexahydrophthalic anhydride, methyl tetrahydrophthalic anhydride, 2-phenylimidazole, modified aluminum oxide, polyimide micro powder and modified wollastonite. Through synergism of multiple materials, balance of heat conduction, insulation, mechanical strength and thermal stability of the adhesive is realized. Under high-frequency pulse voltage, the adhesive is long in electrical aging life. A gradient curing process is adopted for curing, complete reaction in each stage is guaranteed, and internal stress is reduced. The process fault tolerance is high, the environment compatibility is high, the cost is low, and the curing time is short.

The invention discloses composite epoxy resin resistant to damp-heat aging and a preparation method and application thereof, and belongs to the technical field of electrical equipment insulating materials. The composite epoxy resin is prepared by the following steps: preparing an epoxy resin mixture from bisphenol A diglycidyl ether type epoxy resin and N, N, N ', N'-tetraepoxypropyl-4, 4 '-diaminodiphenylmethane according to a mass ratio of (1.5-4): 1, and reacting the epoxy resin mixture with a methylhexahydrophthalic anhydride curing agent with a specific molar ratio and a 2, 4, 6-tri (dimethylaminomethyl) phenol accelerant with a certain amount. Through collaborative optimization of the components and the process, the glass-transition temperature, bending strength and breakdown field strength of the epoxy resin are remarkably improved, and the dielectric loss is effectively reduced, so that the epoxy resin shows excellent thermal stability, mechanical property retention rate and insulation reliability in a high-temperature and high-humidity environment; the method is especially suitable for manufacturing insulation parts of electrical equipment in coastal and other high-humidity areas.

The invention belongs to the technical field of high polymer materials, and particularly relates to a polyolefin composite material as well as a preparation method and application thereof. The polyolefin composite material is prepared from the following raw materials: polyethylene, a polyolefin toughening agent, a compound flame retardant and a filler, the melt index of the polyethylene at 190 DEG C / 2.16 kg is greater than or equal to 18 g / 10 min, and the bending modulus is less than or equal to 160 MPa; the polyolefin toughening agent is selected from at least one of an ethylene-propylene copolymer, an ethylene-butylene copolymer and an ethylene-vinyl acetate copolymer, and the melt index at 230 DEG C / 2.16 kg is greater than or equal to 9 g / 10 min; the compound flame retardant comprises tetrabromobisphenol S bis (2, 3-dibromopropyl) ether, antimony trioxide and hydroquinone bis (diphenyl phosphate), and the filler is at least one of talcum powder, barium sulfate and wollastonite. Through specific types of polyethylene, the polyolefin flexibilizer, the compound flame retardant and the filler, excellent flame retardance and toughness can be obtained.

The invention relates to a high-toughness anti-crack magnetic decorative film and a preparation method thereof. The decorative film is prepared from the following raw materials in parts by weight: 40 to 60 parts of poly (dihydrothiophene-vinyl ether) copolymer, 10 to 25 parts of shell layer self-assembly modified Fe3O4 nanosheets, 5 to 15 parts of polyether ester block elastomer, 0.5 to 2 parts of sodium dodecyl benzene sulfonate, 0.5 to 1.5 parts of fluorosilane coupling agent, 0.1 to 1.0 part of 2-hydroxybenzotriazole ultraviolet absorbent, 3 to 6 parts of bisphenol A type epoxy curing agent and 0.05 to 0.5 part of imidazole catalyst. The flexible copolymer is synthesized through copolymerization of dihydrothiophene and vinyl ether, the modified Fe3O4 nanosheets form a Fe3O4 structure through coprecipitation of ferric chloride and ferrous chloride and regulation and control of ammonia water, and shell self-assembly coating is carried out through tetraethoxysilane and a block micromolecule interface agent. The material has excellent tensile strength, elongation at break, magnetic adsorption force and cycling stability, and is suitable for the application fields of flexible magnetic films and high-adhesion decorations.

The invention relates to a high-solid-content epoxy glass flake heavy anti-corrosion coating for an offshore wind power foundation, which consists of a component A and a component B, the component A is prepared from raw materials in percentage by weight as follows: 10%-20% of bisphenol A epoxy resin, 20%-40% of modified hydrogenated epoxy resin, 5%-10% of liquid petroleum resin, 1%-2% of a rheological aid, 0.1%-1% of a dispersant, 0.1%-1% of a defoaming agent, 1%-3% of a silane coupling agent, 5%-10% of modified glass flakes, 20%-40% of functional filler and 0-10% of a composite environment-friendly solvent; and the component B is a mixed amine epoxy curing agent. The epoxy glass flake coating disclosed by the invention can be thickly coated at one time, has excellent adhesive force, hardness, wear resistance and impact resistance, is high in drying speed, excellent in chemical corrosion resistance, seawater soaking resistance and cathodic disbonding resistance, and meets the performance requirements of NORSOK M-501: 2022 (edition VII) Surface Treatment and Protective Coating.

The application discloses a method for inhibiting the migration of toxic small molecules in plastics based on a protein-based phase transition composite coating, which is characterized by the following steps: inducing the rapid phase transition of proteins on the surface of plastics by a disulfide bond reducing agent to form a nanofilm, and adsorbing polysaccharides on the surface of the nanofilm to form a protein-based phase transition composite coating on the surface of the plastics, which can inhibit the migration of toxic small molecules in the plastics. The preparation method of the protein-based phase transition composite coating is simple, the cost is low, the inhibition effect on the migration of phthalate plasticizers and bisphenol A in plastics (such as PVC, PP, PE, PS and PET) is good, the adsorption of drugs on the surface of medical plastics can be prevented at the same time, the protein-based phase transition composite coating has good biocompatibility, is suitable for temperature-sensitive plastics, has universality, can be safely used on the surface of food and medical plastic products, and has a good popularization and application prospect on the surface of plastics.

The invention discloses an adhesive tape with high stripping stability and a preparation process thereof. The adhesive tape comprises a PET (Polyethylene Terephthalate) base material subjected to corona treatment, an acrylic acid pressure-sensitive adhesive layer, a release layer and an antistatic liquid coating. The acrylic pressure-sensitive adhesive layer is composed of acrylate monomers, saturated polyester resin, bisphenol F, bisphenol A epoxy resin and amino resin. The preparation process comprises the steps of corona pretreatment of the polyethylene glycol terephthalate base material, coating of the antistatic liquid, coating of the pressure-sensitive adhesive, compounding of the release layer and curing treatment. The stripping force change rate of the adhesive tape after damp-heat aging and low-temperature aging is smaller than 5% and is far lower than the industrial standard, and the adhesive tape has excellent stripping stability, antistatic property and weather resistance and is suitable for the fields of electronic product protection, automobile paint spraying shielding and the like.

To provide a liquid spray head that has a low environmental impact, is acid-resistant, and is highly reliable. [Solution] A liquid spray head that sprays liquid from a nozzle comprises a first member, a second member, and a cured product of a one-component adhesive that adheres the first member and the second member, wherein the one-component adhesive comprises a bisphenol-free epoxy resin, a curing agent containing an aromatic amine polymer, and an alkylphenol, wherein the alkylphenol is (a) an alkylphenol having at least one ethyl group, or (b) an alkylphenol having 1 to 3 carbon atoms in the alkyl group and at least one methyl group and one isopropyl group.

The invention relates to a 1D / 2D dual-heterojunction catalyst, a preparation method thereof and application of the 1D / 2D dual-heterojunction catalyst in photo-assisted periodate activated degradation of bisphenol A. The preparation method comprises the following steps: mixing a concentrated hydrochloric acid solution with LiF, adding Ti3AlC2, carrying out a heating reaction, carrying out solid-liquid separation to obtain a solid phase, washing the solid phase to be neutral, and dispersing the solid phase in ethanol to obtain an MXene ethanol solution; adding a cerium source aqueous solution into an MXene ethanol solution, mixing, and placing in liquid nitrogen to obtain a mixed solution; mixing an organic ligand, ethanol and pure water to obtain a mixed solution, carrying out a mixed heating reaction on the mixed solution and the mixed solution, carrying out solid-liquid separation to obtain a precipitate, and freeze-drying to obtain powder; and heating and calcining the obtained powder in an inert atmosphere to obtain the 1D / 2D dual-heterojunction catalyst. According to the invention, photogenerated electron-hole recombination is effectively inhibited by constructing double heterojunctions, and ultrafast electron transfer is realized at the same time, so that the oxidation effect is enhanced, and the efficient photocatalytic activity of '1 + 1gt, 2' is realized.