1384 results about "Bisphenol A" 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 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 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 low-temperature curing high-throwing-power cathode electrophoretic coating and a preparation method and application thereof, and belongs to the field of automobile coating materials, the coating is composed of epoxy resin, a fluorosilicone copolymerization type epoxy modifier, a polyamino siloxane-acrylic acid hybrid and other components, and performance improvement is achieved through the synergistic effect of the two brand-new modifiers. Wherein the fluorine-silicon copolymerization type epoxy modifier is prepared by taking bisphenol A epoxy resin as a framework, introducing fluorine-containing alkyl and siloxane groups and carrying out ultraviolet reaction, so that the surface energy is reduced, and low-temperature crosslinking is promoted; the polyamido siloxane-acrylic acid hybrid takes siloxane as a core, and acrylic acid and polyamido are bridged through isocyanate, so that the crosslinking density and the water solubility are enhanced. When the coating is prepared, the two modifiers are mixed with epoxy resin, a solvent and the like, and the coating is prepared through dispersion and dilution. The coating can be cured at low temperature, so that a uniform thick film is obtained in an inner cavity of a complex workpiece, and meanwhile, the coating has excellent corrosion resistance and adhesive force and is suitable for efficient and environment-friendly coating of an automobile body and parts.

The invention relates to the technical field of materials and advanced oxidation, and discloses a covalent organic framework catalyst with a benzothiadiazole structure, a preparation method of the covalent organic framework catalyst and application of the covalent organic framework catalyst in peroxymonosulfate (PMS) activation and organic pollutant degradation. The preparation method of the covalent organic framework catalyst comprises the following steps: adding precursors 1, 3, 6, 8-tetra-(p-aminophenyl)-pyrene and 2, 7-dibenzaldehyde-benzothiadiazole into a mixed solvent composed of o-dichlorobenzene and n-butyl alcohol, carrying out a reaction by using acetic acid as a catalyst through a solvothermal method, and after the reaction, carrying out multiple times of centrifugal washing and drying to obtain the covalent organic framework catalyst. The catalyst shows excellent performance in the aspect of activating PMS to degrade organic pollutants, the degradation rate constant of bisphenol A reaches 1.68 min <-1 >, and 100% removal can be achieved within 5 minutes. Meanwhile, the catalyst has the advantages of no secondary pollution, strong anti-interference performance, reusability and the like. Compared with a traditional method, the catalyst has high PMS activation efficiency, the catalysis process is energy-saving and environment-friendly, the operation is simple and convenient, the preparation process is simple and feasible, and a new solution is provided for efficient degradation of organic pollutants in water.

The invention discloses a protective coating for an aluminum alloy heat exchange tube and a preparation method of the protective coating, and relates to the technical field of coating materials. The protective coating for the aluminum alloy heat exchange tube at least comprises the following raw materials in parts by mass: 100 parts of bisphenol A epoxy resin; 28 to 32 parts of polyether amine D230; 8 to 12 parts of a modified MgAlCe-BTC-LDH filling material; 4 to 6 parts of polydopamine modified hexagonal boron nitride; 35 to 45 parts of propylene glycol methyl ether acetate; and 1-2 parts of a dispersant. The modified MgAlCe-BTC-LDH filler prepared by the invention realizes triple functions of Ce element oxidation resistance, BTC corrosion inhibition and layered barrier, and the polydopamine modified hexagonal boron nitride prepared by the invention effectively improves the heat-conducting property, solves the contradiction between insulation and heat conduction, and adapts to the protection requirement of an aluminum alloy heat exchange tube.

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 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.

Disclosed are a two-component low-density PU structural adhesive, a preparation method therefor and an application thereof. The two-component low-density PU structural adhesive is composed of Component A and Component B, where a volume ratio of Component A to Component B is 1:0.8-1.2, Component A includes polyether carbonate polyol, castor oil or / and modified castor oil, bisphenol A polyether polyol, a chain extender, hollow glass beads, molecular sieve, fumed silica, a silane coupling agent and catalysts, specifically, the polyether carbonate polyol and the castor oil or / and the modified castor oil cannot be zero at the same time; and Component B includes isocyanate prepolymer, polyisocyanate, hollow glass beads, fumed silica, and a dehydrating agent, the present disclosure solves the problems of poor storage stability, low bonding strength and low elongation at break of the low-density structural adhesive in the prior art.

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 belongs to the technical field of inclusion type composite catalysts, and particularly relates to a preparation method of a spherical sulfur-doped carbon-based catalyst based on cyclodextrin and application of the spherical sulfur-doped carbon-based catalyst in bisphenol A sewage treatment. Cyclodextrin, elemental sulfur and polyether F127 are subjected to supercritical carbon dioxide reaction and high-temperature roasting to obtain the spherical sulfur-doped carbon-based catalyst, the spherical sulfur-doped carbon-based catalyst has excellent degradation and adsorption functions on bisphenol A (BPA) pollutants in sewage, the adsorption rate of 0.005 g of the catalyst to 50 mL of 0.02 g / L BPA is 46% in 10 min and reaches 90% in 90 min, 0.03 g of PMS is added for catalytic degradation, and the adsorption rate reaches 90% in 90 min. The degradation rate of 50 mL of 0.02 g / L BPA can reach 100% in 20 min, and the adsorption efficiency is remarkably improved. After three times of recycling, the adsorption rate is still kept at 85% or above, and the adsorbent has excellent regeneration cyclicity. The preparation method is simple, environment-friendly and low in cost.

The invention discloses nano UV light-cured printing ink and a preparation method thereof, and relates to the technical field of printing ink preparation. The nano UV light-cured printing ink is prepared from nano UV light, the invention discloses a UV (ultraviolet) photoinitiator, which is prepared from the following raw materials in parts by weight: 20 to 40 parts of polyurethane acrylate oligomer, 15 to 30 parts of modified bisphenol A type epoxy acrylate, 10 to 15 parts of tripropylene glycol diacrylate, 5 to 10 parts of ethoxylated trimethylolpropane triacrylate, 5 to 15 parts of modified nano titanium dioxide, 3 to 8 parts of nano silver wire, 2 to 5 parts of photoinitiator 1173 and 1 to 3 parts of benzoin dimethyl ether. The invention relates to a silver-loaded zirconium phosphate composite material which is prepared from the following components in parts by weight: 0.5-2 parts of polyether modified polydimethylsiloxane, 0.3-1 part of a defoaming agent, 1-3 parts of a dispersing agent, 1-5 parts of silver-loaded zirconium phosphate, 0.5-2 parts of an antioxidant 1010, 0.5-2 parts of a coupling agent KH-550 and 10-25 parts of propylene glycol methyl ether acetate. The raw materials are scientifically proportioned and contain various modified components, and parameters of each step are clear. The preparation method is reasonable in process, the performance of the ink is improved through multi-step modification, and the obtained ink is good in dispersity and compatibility, high in curing efficiency and excellent in comprehensive performance and has good practicability and innovativeness.

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 invention relates to the technical field of coatings, and discloses a composition for a polyurethane waterproof coating, the polyurethane waterproof coating as well as a preparation method and application of the polyurethane waterproof coating. The composition contains a main agent and an auxiliary agent, the main agent is formed by polymerizing raw material components including polyol, diisocyanate A, bisphenol A epoxy acrylate and a prepolymer; the prepolymer is prepared by a method comprising the following steps: in the presence of a polymerization catalyst, carrying out contact reaction on bisphenol A epoxy resin, polyaspartic acid ester, diisocyanate B and an isocyanate tripolymer to obtain the prepolymer, the use amount molar ratio of the bisphenol A epoxy resin to the polyaspartic acid ester to the diisocyanate B to the isocyanate tripolymer is 1: (0.6 to 1.5): (0.5 to 1): (0.05 to 0.5). The coating provided by the invention is high in modulus, and has higher tensile strength, hardness and waterproof performance.

The invention relates to the technical field of epoxy resin modification, in particular to low-dielectric modified epoxy resin as well as a preparation method and application thereof. The preparation method comprises the following steps: mixing epoxy resin, a curing agent, polyhedral oligomeric silsesquioxane-octa-epoxy group and a catalyst to obtain a resin mixed system, and curing the resin mixed system to obtain the low-dielectric modified epoxy resin. According to the invention, a cage type polysilsesquioxane-octa-epoxy space structure and a group effect are utilized, after anhydride is used as a curing agent, epoxy group ring-opening cross-linking curing is simultaneously carried out with bisphenol A type epoxy resin, a hybrid system is obtained, and the overall dielectric property of the modified epoxy resin is promoted to be improved. Test results show that when the mass ratio of the POSS-101 is 10%, the modified epoxy resin shows a relatively low dielectric constant of about 2.87 under the condition of 1GHz, and the dielectric loss tangent value can reach (0.02). The whole modification scheme is simple in process step, high in operation feasibility and easy for practical production.

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 discloses an anti-ultraviolet epoxy resin coating and a preparation method thereof, and belongs to the technical field of epoxy resin coatings. Comprising a component A and a component B, wherein the component A comprises the following raw materials in parts by weight: 80-90 parts of bisphenol A epoxy resin, 5-8 parts of a reactive diluent, 10-15 parts of modified titanium dioxide, 2-6 parts of an anti-ultraviolet agent, 0.2-0.5 part of a defoaming agent and 0.2-0.5 part of a flatting agent. And the component B is a curing agent. The modified titanium dioxide and the self-made anti-ultraviolet agent are introduced, and the modified titanium dioxide and the self-made anti-ultraviolet agent can achieve a synergistic effect, so that the anti-ultraviolet performance of the coating is remarkably improved; wherein the modified titanium dioxide has better compatibility with an epoxy resin matrix, the dispersion is more uniform, and the problem that traditional inorganic nanoparticles are easy to agglomerate is avoided; in conclusion, the prepared coating has stable and efficient anti-ultraviolet performance and has important application value in the field of epoxy resin coatings.

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 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.

A plugging material is prepared from the following raw materials in terms of mass fractions, which include: 1 to 3.6 parts of PETA-modified bisphenol A epoxy resin, 1.5 to 2.4 parts of addition product of m-phenylenediamine and methacrylic acid, 0.12 to 0.17 parts of nanosilica dispersion liquid, with the remainder being water, such that the sum of the mass fractions of the aforementioned raw materials totals 100 parts. The preparation method includes: pouring a water phase mixture into a continuously stirred oil-phase mixture to form a gel-forming liquid through continued stirring; transferring the gel-forming liquid to be mixed with dibenzoyl peroxide, and stirring and reacting at a temperature of 50° C. to 120° C. to obtain the plugging material. The plugging material is resistant to high temperatures and high salinity, and exhibits strong plugging performance.

The invention provides a method for preparing hydrogenated bisphenol A by continuous catalytic hydrogenation of a fixed bed. The method comprises the following steps: step A, mixing and preheating a bisphenol A solution, a low-carbon amine additive and hydrogen in a gas-liquid mixing preheater to prepare a reaction material; step B, enabling the preheated reaction material to flow through a fixed bed reactor preloaded with a Ru-based catalyst, and carrying out catalytic hydrogenation reaction in the fixed bed reactor to generate a product material; step C, separating the product material through a gas-liquid separator to obtain a hydrogenated bisphenol A solution and hydrogen, and recycling the hydrogen; and rectifying the hydrogenated bisphenol A solution to obtain hydrogenated bisphenol A. The method provided by the invention effectively overcomes the defect that the single-batch reaction time of the existing catalytic hydrogenation process reaches 4-12 hours, and greatly shortens the continuous catalytic hydrogenation reaction time; by adding the low-carbon amine auxiliary agent, the reaction activity is promoted, and the generation of dehydroxylation byproducts is reduced; the selectivity of the product can be effectively guaranteed, the product is easy to separate, the safety is good, the cost is obviously reduced, and industrial application is easy.

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 provides a multi-walled carbon nanotube paste electrode based on gold nanoparticles and C60 modification as well as a preparation method and application thereof, and belongs to the technical field of electrochemical sensors. The preparation method comprises the following steps: firstly, modifying fullerene C60 on the surface of a carbon nanotube paste electrode (MWCNTPE) to form C60 / MWCNTPE, then loading gold nanoparticles on the surface of the C60 / MWCNTPE, and finally constructing the AuNPs / C60 / MWCNTPE composite electrode. The prepared composite electrode is used for environmental estrogen detection, especially for simultaneous detection of hydroquinone, catechol and bisphenol A. The method has the advantages of high sensitivity and low detection limit, can solve the problem that hydroquinone and catechol isomeride are difficult to separate through the detection capability, has the advantages of simplicity and convenience in operation and low cost, and has good practical applicability, stability and reproducibility.

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.

The invention discloses a wear-resistant stone-impact-resistant powder coating and a preparation method thereof, and belongs to the technical field of paints.The wear-resistant stone-impact-resistant powder coating has the advantages that epoxy resin, a polyurethane prepolymer mixture and a high-temperature-resistant and low-temperature-resistant elastomer modifier are compounded to form an epoxy-polyurethane-elastomer chemical bonding effect, and the wear-resistant stone-impact-resistant powder coating is excellent in compatibility and better in crosslinking density, flexibility and elasticity; the stone impact resistance is greater than or equal to 4B grade, and the problem of poor stone impact resistance of a powder coating in the prior art is effectively solved; the epoxy resin is compounded by bisphenol A epoxy resin and hydrogenated bisphenol A epoxy resin, and forms a coating system with a composite antirust system, a gradient wear-resistant filler (compounded by nano ZrO and emery powder), a composite antirust system and a composite flame retardant, and interacts with each other, so that the wear resistance, the impact resistance, the flame retardance and the corrosion resistance of the coating are further enhanced, and the service life of the coating is prolonged. And the coating is durable, so that the frequent maintenance or replacement requirement of the chassis is reduced, and the coating is also suitable for protecting high-value parts of the new energy automobile.