2123 results about "Phenol" patented technology

The invention relates to the technical field of organic chemical synthesis, in particular to a preparation method of 3, 4 '-diaminodiphenyl ether.The preparation method comprises the steps that S1, under inert gas and in a first solvent, m-dinitrobenzene and p-acetamidophenol are subjected to a heating reaction under the condition of a weak base catalyst, and 3-nitro-4-acetamido diphenyl ether is prepared; s2, in a second solvent, the 3-nitro-4-acetamido diphenyl ether is subjected to a hydrogenation reduction reaction, and 3-amino-4-acetamido diphenyl ether is prepared; and S3, dissolving the 3-amino-4-acetaminodiphenyl ether in an alcohol solvent system, adding an aqueous solution of alkali, controlling the reaction temperature, carrying out a hydrolysis reaction, and after the reaction is finished, carrying out post-treatment to obtain the 3, 4 '-diaminodiphenyl ether. The preparation method provided by the invention has the advantages of easily available raw materials, low price, good selectivity and high product yield, and is more suitable for industrial production by comprehensively considering economical efficiency and safety.

The invention discloses a method for preparing calcium hydroxide slurry with high specific surface area and high pore volume, which comprises the following steps: S1, adding an alcohol reagent into water to obtain a solution A; s2, adding an inorganic salt solution into the solution A, and uniformly mixing to obtain a solution B; s3, a reagent X is added into the solution B, ultrasonic mixing is performed to obtain a solution C, and the reagent X is a mixture of phenol or triethanolamine, ethidene diamine and ethylamine; and S4, adding calcium oxide powder into the solution C, continuously stirring, and reacting to obtain calcium hydroxide slurry. The invention provides a method for preparing calcium hydroxide slurry with high specific surface area and high pore volume, the calcium hydroxide slurry prepared by the method can form calcium hydroxide with high specific surface area and high pore volume when in use, and the method aims to solve the problems of low specific surface area and low pore volume of the existing calcium hydroxide. Therefore, the problem of desulfurization performance inactivation caused by blockage of calcium hydroxide (desulfurizer) pores by generated CaSO3 and CaSO4 in the desulfurization process is avoided.

The invention discloses a catalyst for hydrogen production through tar steam reforming and a preparation method and application thereof. The catalyst comprises a cobalt-magnesium-aluminum composite spinel carrier and an active component loaded on the cobalt-magnesium-aluminum composite spinel carrier, the active component comprises nickel and at least one metal additive selected from iron, zirconium and ruthenium. The preparation method mainly comprises the following steps: preparing the carrier by adopting a coprecipitation method, loading the active component by adopting an impregnation method, and drying and reducing to obtain the final catalyst. The catalyst is used for tar component steam reforming hydrogen production reaction, especially for treating raw materials containing phenol and water vapor at 600-700 DEG C, tar conversion can be efficiently catalyzed, product gas rich in hydrogen can be generated, hydrogen selectivity is high, and almost no methane is generated. The catalyst has the advantages of high activity, good stability, strong carbon deposition resistance and the like, and is suitable for purification and high-value utilization of biomass pyrolysis tar.

The invention relates to the technical field of high polymer materials, and particularly discloses a fluoride-free halogen-free flame-retardant polycarbonate material and a preparation method and application thereof.The fluoride-free halogen-free flame-retardant polycarbonate material is prepared from, by weight, 70-90 parts of polycarbonate resin, 8-15 parts of phosphorus-nitrogen flame retardant and 3-8 parts of silicon flame-retardant synergist, the composite material is prepared from the following raw materials in parts by weight: 20-30 parts of polypropylene, 2-5 parts of nano reinforcing filler, 0.1-0.5 part of hindered phenol antioxidant, 0.1-0.5 part of phosphite ester antioxidant and 0.1-0.5 part of pentaerythritol stearate. Through the synergistic effect of the composite flame-retardant system and the nanofiller, high flame retardance (UL94 V-0 level, 1.5 mm thickness), high heat resistance (the heat distortion temperature is greater than or equal to 130 DEG C) and excellent mechanical property are realized, the control is easy, the processing is stable, good balance of flame retardance and mechanical property is achieved on the premise of environmental protection, and the composite flame-retardant material is suitable for the fields of high-end household appliances and consumer electronics.

The invention relates to the technical field of transfer films, in particular to a graphene-containing far-infrared warm-keeping polyurethane transfer film and a preparation method thereof. The far-infrared warm-keeping polyurethane transfer film containing graphene comprises a three-layer structure including a supporting layer, a polyurethane transfer layer and a bonding layer, the polyurethane transfer layer is located on one side of the supporting layer, and the bonding layer is located on the other side of the polyurethane transfer layer; the polyurethane transfer layer is prepared from polyurethane resin, an organic solvent, an organic pigment and a composite modifier, the composite modifier is prepared from alkenyl modified graphene oxide, chloropropenyl modified hindered phenol and 4-allyloxy-2-hydroxybenzophenone, and the composite modifier is added, so that the polyurethane transfer layer is formed. The polyurethane transfer film has far infrared thermal insulation performance and good oxidation resistance and hydrolysis resistance.

The invention discloses a fluorescent covalent organic framework material for hydrogen sulfide detection as well as a preparation method and application thereof, relates to a covalent organic framework material as well as a preparation method and application thereof, and aims to solve the technical problems that an existing porous material for H2S detection is few in structure type, unstable in COFs (Covalent Organic Frameworks) structure, high in detection limit and harsh in detection environment. The periodic structure fragment of the fluorescent covalent organic framework material for hydrogen sulfide detection is shown in the specification. 3-(5, 10-diamino-1H-phenanthrene) [9, 10-d] imidazole-2-yl) phenol and 2, 4, 6-tri (4-formylphenoxy)-1, 3, 5-triazine are subjected to a reaction to obtain a hydroxyl intermediate, the hydroxyl intermediate is modified with 2, 4-dinitrofluorobenzene, and the fluorescent material is used for qualitative detection of H2S. The method is not interfered by amino acids and anions in the environment, and is not influenced by an acid-base environment. The method can be used in the field of H2S detection.

The invention relates to the technical field of coatings, in particular to a corrosion-resistant coating material and a preparation method thereof. The corrosion-resistant coating material comprises the following components in parts by mass: 80-100 parts of epoxy resin, 5-20 parts of a modified phenolic aldehyde amine curing agent, 2-5 parts of a waterproof agent, 5-10 parts of a corrosion inhibitor and 40-55 parts of a lubricant. The modified phenolic aldehyde amine curing agent is obtained by carrying out Mannich reaction on phenol, thymol, aliphatic polyamine and formaldehyde. The phenol provides a rigid benzene ring structure, and endows a cured product with good heat resistance and chemical resistance. Thymol improves the flexibility and adhesive force of the cured product and enhances the hydrophobicity of the cured product at the same time. The epoxy resin and the modified phenolic aldehyde amine curing agent are polymerized, the waterproof agent, the corrosion inhibitor and the lubricant are wrapped, and the obtained coating material has good adhesive force and corrosion resistance.

The invention relates to the technical field of fine chemical engineering and flame retardant preparation, and discloses a preparation method of bromo-triazine capable of improving thermal stability, and the preparation method comprises the following steps: mixing phenol, water and dichloromethane, controlling the temperature, and carrying out oxidative bromination reaction to prepare an organic phase containing tribromophenol; then, under the action of an organic amine catalyst, carrying out condensation reaction on the organic phase, liquid caustic soda and cyanuric chloride; after the reaction, washing with water to remove impurities; and in the presence of process water, firstly controlling the temperature at 38-42 DEG C for azeotropic desolvation, then raising the temperature to 85-95 DEG C for high-temperature crystallization and crystal growing, and finally cooling, filtering and drying to obtain the bromo-triazine product. By utilizing the high selectivity of the organic amine catalyst and a two-stage azeotropic crystallization process, the side reaction is effectively reduced, the solvent wrapped in the crystal is eliminated, the prepared product is high in main content and extremely low in volatile component, the temperature can reach 370 DEG C or above when the thermal weight loss is 2%, and the thermal stability is remarkably improved.

The invention discloses an antistatic agent for polyolefin film material production and a preparation method thereof. According to the invention, through reasonable molecular structure design, raw material selection and synthesis process optimization, the antistatic agent has multiple functions of high-efficiency antistatic property, oxidation resistance, antibacterial property, mechanical property enhancement and the like. The polyolefin material added with the multifunctional antistatic agent has good antistatic performance under different environmental conditions, and the oxidation resistance, the antibacterial property and the mechanical property are also remarkably improved. The antistatic agent has good adaptability with processing of a polyolefin film material and has wide application prospects and market competitive advantages, and the comprehensive performance of the polyolefin film material is remarkably improved through multi-component collaborative design. The composite system of the polyolefin quaternary ammonium salt and the graphene quantum dots strengthens the long-term effect of the antistatic effect, and meanwhile, the synergistic effect of the hindered phenol and the phosphite strengthens the antioxidant stability of the material in the processing and using processes.

The invention provides a preparation method for preparing porous carbon based on an aerogel method, the porous carbon and application of the porous carbon, and belongs to the technical field of porous carbon material preparation. The preparation method comprises the following steps: mixing polyhydroxy phenol, aromatic aldehyde, acrylamide, graphene oxide and lithium salt according to a mass ratio of 100: (50-200): (5-30): (1-5): (1-5), carrying out hydrothermal reaction at 100-200 DEG C for 1-6 hours, and freeze-drying at-40 DEG C to obtain a hydrogel precursor; and carbonizing the precursor in organic heteroatom gas at 500-800 DEG C, mixing the intermediate with alkali according to the ratio of 100: (100-500), activating at 900-1100 DEG C, pickling and drying to obtain the porous carbon. The conductivity of the product is improved by means of graphene, lithium salt and heteroatoms, and the aerogel method obtains large aperture, has the characteristics of low impedance, high first efficiency and small charge-discharge expansion, and can be efficiently applied to silicon-carbon materials.

The invention discloses a lignin-based epoxy anticorrosive paint and a preparation method thereof. The anticorrosive paint is prepared by mixing a lignin-based epoxy anticorrosive paint component, a lignin-based phenolic amine curing agent and a diluent. According to the lignin-based epoxy anticorrosive paint disclosed by the invention, on one hand, a lignin epoxy resin acetylation modification method based on lipase is introduced, and the content of hydrophilic groups is reduced, so that formation of a compact lignin cross-linked network structure is promoted, and the barrier ability, heat resistance and aging resistance of an anticorrosive coating on a chemical medium are improved on the resin level; on the other hand, lignin and furfural are respectively used for partially replacing phenol and paraformaldehyde to prepare a lignin-based phenolic aldehyde amine curing agent with high chemical inertness, so that the protection effect of a coating in an extreme corrosion environment and the adhesive force to a metal base material are improved on the curing agent level. The lignin-based epoxy anticorrosive paint prepared by the invention has good corrosion resistance, aging resistance, thixotropy and adhesive force.

The invention belongs to the technical field of sulfonamide synthesis, and particularly relates to a green and environment-friendly sulfonamide amidation preparation method. Comprising the following steps: adding chlorosulfonic acid into a reactor, stirring, heating, adding o-nitrochlorobenzene, carrying out staged heat preservation, cooling, and adding thionyl chloride to obtain 2-nitro-4-chlorine sulfonate-chlorobenzene; the method comprises the following steps: separating and filtering 2-nitro-4-chlorine sulfonate-chlorobenzene, adding ammonia water, stirring, preserving heat, and carrying out filter pressing to obtain 2-nitro-4-amine sulfonate-chlorobenzene; the preparation method comprises the following steps: adding liquid caustic soda into 2-nitro-4-amine sulfonate-chlorobenzene, stirring, heating, and adjusting the pH value to obtain 2-nitro-4-amine sulfonate-phenol; the method comprises the following steps: adding water, a catalyst and hydrazine hydrate into 2-nitro-4-amine sulfonate-phenol, heating, stirring, and carrying out filter pressing to obtain 4-sulfonamide-2-amino-phenol. According to the preparation method of sulfonamide, generated tail gas is subjected to falling film absorption treatment, and the product prepared by the preparation method is high in purity.

The invention relates to the technical field of adhesives, and discloses an anti-aging polyurethane sealant and a preparation method thereof.The polyurethane sealant is prepared by the steps that polyether polyol and binary isocyanate serve as raw materials and react under the action of a catalyst to form a polyurethane prepolymer, then a functional chain extender is used for conducting chain extension on the prepolymer to form polyurethane latex, and then the polyurethane latex is subjected to heat preservation to form the anti-aging polyurethane sealant. The structure of the functional chain extender contains a hindered phenol antioxidant group, and the hindered phenol antioxidant group is introduced into a polyurethane molecular chain by adopting a chemical grafting mode, so that the aging resistance of the polyurethane sealant can be effectively improved, the aging resistance durability of the polyurethane sealant is guaranteed, and the service life of the polyurethane sealant is prolonged. Therefore, the service life and the application value of the polyurethane sealant are effectively improved.

The invention relates to a composite resin material for 3D printing and a preparation method thereof. The material is prepared from the following raw materials in parts by weight: 60-90 parts of polylactic acid, 5-15 parts of a toughening agent, 5-15 parts of a flame retardant, 5-10 parts of modified carbon nanotubes, 0.3-1 part of an anti-hydrolysis agent and 0.3-0.5 part of a lubricant. The flame retardant is added, a phosphate structure, a benzene ring and a hindered phenol structure are introduced into 5, 5 '-dibromo-[2, 2'-bipyridyl]-3, 3 '-diamine, and efficient flame retardance is achieved and the anti-aging performance of the composite resin material is enhanced through multiple synergistic effects of hindered phenol-phosphorus heterocycle-bipyridyl. The modified carbon nanotube is added as a reinforcing agent, so that the mechanical property of the composite resin material is remarkably improved, and the composite resin material is endowed with antibacterial property.

The invention discloses a method for preparing a porous carbon material by recycling coal gasification slag and semi-coke wastewater, which comprises the following steps: by taking coal gasification fine slag as a carrier and semi-coke wastewater as a phenol source, carrying out flotation-acid leaching modification on the fine slag to purify a carbon-rich component and optimize the surface adsorption activity of the carbon-rich component; then fully adsorbing phenolic substances in the wastewater by utilizing the modified slag body; introducing a composite aldehyde cross-linking agent, and initiating an in-situ phenolic aldehyde polymerization reaction to generate a composite precursor; the precursor is subjected to high-temperature carbonization and alkali activation pore forming, and finally the porous carbon material with the characteristics of high specific surface area, rich graded pores and low ash content is prepared. According to the process, full-amount collaborative recycling of the two wastes is achieved, and the process is green and free of secondary pollution. The obtained material is high in carbon content and rich in defect structure and surface functional groups, shows excellent adsorption capacity and catalytic carrier performance, can be widely applied to the fields of deep purification of water pollutants, adsorption of volatile organic compounds, energy catalysis and the like, and has remarkable environmental protection benefits and resource economic values.

The invention relates to the technical field of coatings, in particular to a graphene modified epoxy anticorrosive coating and a preparation method thereof. The coating is prepared from epoxy resin, graphene-hyperbranched epoxy resin, a reactive diluent and an auxiliary agent, wherein the graphene-hyperbranched epoxy resin is prepared by a three-step method comprising the following steps: firstly, performing dual modification on graphene oxide by adopting 11-aminoundecyltriethoxysilane and 3-aminopropyltriethoxysilane; then reacting with 2-formyl-5-phenylphenol, and finally carrying out condensation polymerization with trimethylolpropane triglycidyl ether to form a hyperbranched structure. According to the invention, collaborative optimization of mechanical strength and corrosion resistance is realized, and the coating has excellent adhesive force, hardness and long-acting corrosion resistance, and is suitable for severe corrosion environments such as ocean engineering and the like.

According to the cell fixing liquid, phenol oxidase is used for catalyzing phenol to be oxidized into a quinone structure, the quinone structure reacts with protein amido to form light covalent immobilization, cell immobilization is achieved, a stable hydration environment and membrane protection are provided through the ionic liquid solvent choline dihydrogen phosphate, a phosphate-free buffer system is provided, and cell immobilization is achieved. Therefore, a novel cell fixing liquid is obtained, the cell structure integrity required by cell imaging analysis is effectively reserved, meanwhile, cell staining fluorescence signal interference is avoided, and therefore the accuracy of cell counting and cell imaging analysis is ensured.

The invention discloses a modified microfiltration membrane for enriching biological particles and a preparation method and application thereof, and belongs to the technical field of biological separation.The preparation method of the modified microfiltration membrane comprises the following steps that a mixed cellulose ester microfiltration membrane is provided and subjected to alkali liquor activating treatment; placing the activated membrane in a weakly alkaline buffer solution for balancing; the preparation method comprises the following steps: in a weakly alkaline buffer solution, firstly contacting the surface of the membrane with a tannic acid solution to carry out a first reaction, and then directly adding a polyethyleneimine solution to carry out a second reaction under the condition of not replacing a system, so as to form a phenol-amine cross-linked network on the surface of the membrane in situ; sodium cyanoborohydride is continuously added for reduction stabilization treatment, and the modified microporous filter membrane is obtained. The modified microporous filter membrane prepared by modifying the microporous filter membrane with tannic acid and polyethyleneimine can realize one-step synchronous enrichment of all negatively charged targets, and the problems of target loss, efficiency loss and the like caused by a multi-step process are avoided from the source.

A preparation method of the cardanol-based phosphorus-containing side group novolac epoxy resin comprises the following steps: (1) in the presence of a catalyst A, carrying out a stirring reaction on cardanol and an aldehyde compound at 80-110 DEG C for 3-10 h to prepare an intermediate A; (2) stirring the intermediate A and a phosphorus-containing compound at 50-150 DEG C to react for 10-24 hours to prepare an intermediate B; and (3) in the presence of a catalyst B, stirring and reacting the intermediate B and epichlorohydrin at 70-110 DEG C for 2-6 hours, and in the presence of a catalyst C, stirring and reacting at 30-65 DEG C for 1-4 hours to prepare the cardanol-based phosphorus-containing side group novolac epoxy resin. Through a rigid structure on a main chain of the novolac epoxy resin, a phosphorus-containing structure on a side chain of the novolac epoxy resin and an epoxy group, the toughness and flame retardance of an epoxy cured product can be improved on the premise that the thermal stability is not reduced, and the novolac epoxy resin has an extremely good application research prospect.

The invention discloses a strong acid and alkali resistant plastic material for fume hood surface decoration and a preparation method of the strong acid and alkali resistant plastic material, belongs to the technical field of plastic material processing, and aims at solving the technical problem that in the prior art, the acid and alkali resistance and the bending modulus of a plastic material for fume hood surface decoration need to be further improved. The preparation method specifically comprises the following steps: stirring amino-modified fluorosilicone resin, paraformaldehyde and 1, 4-dioxane in a reaction kettle, dropwise adding an anacardol solution, heating the reaction kettle to 85-95 DEG C, carrying out heat preservation reaction for 6-8 hours, and carrying out post-treatment to obtain the anacardol-based benzoxazine resin. Perfluoro-modified polysiloxane benzoxazine is prepared, naphthalene-containing epoxy resin and imidazole-modified silicon carbide microspheres are compounded, in-situ catalysis synergistic curing is carried out by using filler interface imidazole, a compact organic-inorganic hybrid interpenetrating network is constructed, and the strong acid and alkali corrosion resistance and bending modulus of the material are remarkably improved.

The invention discloses a preparation method of reactive antioxidant grafted modified nylon 6 and a film thereof, and belongs to the technical field of nylon modification. A reactive antioxidant containing a hindered phenol structure and nylon 6 are subjected to melt chemical grafting to form a covalent bond combined nylon 6-antioxidant system, and hindered phenol provides hydrogen atoms and can be combined with free radicals generated in the aging process, so that the chain reaction of the hindered phenol is terminated, and phenoxy free radicals with low activity are formed by the hindered phenol. According to the invention, the reactive antioxidant grafted modified nylon 6 is further processed into a film product, and the nylon 6 film product prepared by the method has the advantages of less antioxidant migration, aging resistance, high mechanical property retention rate and the like.

The invention discloses a method for preparing phenol by utilizing a biomass raw material, which comprises the following steps: 1) crushing biomass, adding the crushed biomass into a caustic alkali solution to carry out hemicellulose removal treatment, and carrying out solid-liquid separation to take a solid substance, so as to obtain hemicellulose-removed biomass; 2) adding the hemicellulose-removed biomass into an ethylene glycol-ferric chloride eutectic solvent for lignin extraction, then adding an acetone-water mixed solution, then carrying out solid-liquid separation, taking a liquid substance, adding water to precipitate the lignin, then carrying out solid-liquid separation, and taking a solid substance to obtain the lignin; and 3) pyrolyzing the lignin in a protective atmosphere to obtain lignin oil containing phenol. The method for preparing phenol from biomass raw materials has the advantages of simple operation, high phenol yield, high product purity, low energy consumption, safety, environmental protection and the like, and is suitable for large-scale industrial application.

Provided are chemically modified silk fibroin and a use thereof in cell and organoid culture. The chemically modified silk fibroin is a product obtained by sequentially carboxylating silk fibroin and modifying same by an organic amine having a phenol group. Also provided is a hydrogel based on the chemically modified silk fibroin. A hydrogel system has a hierarchical structure and mechanical properties similar to those of an extracellular matrix, and exhibits characteristics such as definite composition, controllable physicochemical properties, low cytotoxicity, good biocompatibility, and biodegradability, can support the growth and differentiation of cells and organoids, and is suitable as a matrigel for cell and organoid culture.

The invention discloses a hindered phenol monomer containing organic phosphorus heterocyclic rings as well as a preparation method and application of the hindered phenol monomer. The hindered phenol monomer has any one of the following structures: R is selected from-(CH2) b-or an aromatic ring, b is 3 or 4, and the aromatic ring comprises a benzene ring and / or a furan ring. The intrinsic flame-retardant anti-droplet polymer provided by the invention has the characteristics of excellent flame retardance and no droplet, and meanwhile, the intrinsic flame retardant is copolymerized into a molecular chain, so that the intrinsic flame-retardant anti-droplet polymer is not easy to migrate, does not permeate into the surrounding environment, is stable in property, can be used for injection molding and spinning, and can be used for preparing flame-retardant blocky products and fabrics; the composite material is used for interiors of electric appliances, switches, firefighter uniform, military uniform, automobiles, high-speed rails and other limited spaces.

The invention relates to a corrosion-resistant polypropylene modified plastic and a preparation method thereof, and belongs to the technical field of polypropylene plastic modification. The modified plastic is prepared from isotactic polypropylene, exfoliated montmorillonite, polyvinylidene fluoride powder, anhydride grafted polypropylene, a beta-crystal nucleating agent, diethyl aluminum chloride, peroxide, hindered phenol, phosphite ester and N, N-distearoyl hydroxylamine. The preparation method comprises the steps of low-shear melting and blending, high-shear supercritical COviscosity reduction, vacuum exhaust, bidirectional orientation, infrared local crosslinking, co-extrusion cooling and the like. The obtained material is excellent in tensile strength, elongation at break, low-temperature impact strength, strong acid corrosion resistance and the like.

The invention relates to the technical field of preparation of polyurethane plastic materials, in particular to an environment-friendly high-elasticity foaming material as well as a preparation method and application thereof. The preparation method of the foaming material comprises the following steps: perfluorooctyl sulfonyl fluoride and diaminopropyl polydimethylsiloxane are subjected to a reaction, and fluorine-containing polydimethylsiloxane is obtained; the preparation method comprises the following steps: reacting 3-(3, 5-di-tert-butyl-4-hydroxyphenyl) propanohydrazide with terephthalic diisothiocyanate to obtain isothiocyanate modified hindered phenol; the isothiocyanate modified hindered phenol reacts with primary amine at the terminal position of a fluorine-containing polydimethylsiloxane molecule through an isothiocyanate group to obtain an intermediate, and the intermediate is subjected to a desulfurization reaction to obtain a modifier; the preparation method comprises the following steps: reacting diisocyanate with polyether polyol, polyester polyol and natural polyol to obtain a component A, and stirring and mixing polyether polyol, a bio-based chain extender, a modifier, a catalyst and a foaming agent to obtain a component B; stirring and mixing the component A and the component B, and foaming to obtain the environment-friendly high-elasticity foaming material.

The invention discloses a preparation method of a hydrophobic modified copper-based monatomic catalyst. The preparation method comprises the following steps: S1, dissolving Cu (NO3) 2 and L-alanine in deionized water; dissolving trimesic acid in an ethanol solution; s2, mixing the two solutions, and stirring at regular time at normal temperature to obtain a Cu-BTC precursor; s3, grinding and uniformly mixing the Cu-BTC precursor and dicyandiamide, and then putting the mixture into a tubular furnace for high-temperature pyrolysis treatment to obtain Cu-N-C-Pre powder; s4, the Cu-N-C-Pre powder is subjected to acid leaching impurity removal treatment in an acid solution, and the copper-based monatomic catalyst is obtained; and S5, dissolving the Cu-N-C catalyst and triacetylene benzene in an organic solvent, adding pyridine, uniformly stirring, and carrying out a hydrothermal reaction to obtain the hydrophobic modified copper-based monatomic catalyst. Hydrophobic modification is performed on the surface of the Cu-N-C monatomic catalyst, so that the hydrophobicity of the surface of the catalyst is enhanced, the catalytic activity of the catalyst in a reaction for preparing phenol by activating a benzene C-H bond by taking H2O2 as an oxidizing agent is improved, and the yield of phenol is increased.

The invention relates to the technical field of adhesives, and discloses a preparation method of an epoxy resin adhesive, which comprises the following steps: reacting p-aminophenol with diphenyl dichlorosilane under the catalysis of triethanolamine to obtain di (p-aminophenoxy) diphenyl silane; the preparation method comprises the following steps: carrying out Mannich reaction on amino in di (p-aminophenoxy) diphenyl silane, amino in polyether amine, formaldehyde and phenol to obtain the silane-containing polyether amine type benzoxazine intermediate. And finally, uniformly mixing the silane-containing polyether amine type benzoxazine intermediate and epoxy resin, and curing to obtain the epoxy resin adhesive. The prepared silane-containing polyether amine benzoxazine intermediate contains a silane structure and a benzoxazine structure, both the silane structure and the benzoxazine structure have excellent heat resistance, and the epoxy resin adhesive prepared by adding the silane-containing polyether amine benzoxazine intermediate into epoxy resin has excellent heat resistance.

The application discloses a method for realizing resource utilization of phenol pollutants in water by using a nickel-ruthenium hybrid electrocatalyst, and belongs to the technical field of environmental electrocatalytic water treatment. The nickel-ruthenium hybrid electrocatalyst loaded on carbon cloth is prepared by using a simple two-step electrodeposition method, aiming at problems such as high energy consumption, high material consumption and high carbon emission of a traditional wastewater treatment mode. The catalyst has high stability and high selectivity, and can realize directional conversion of phenol pollutants in water into high-value p-benzoquinone under mild conditions, so as to simultaneously realize removal of the phenol pollutants in water and recovery of high-value-added chemicals. The application provides a new method for treatment and resource utilization of high-concentration phenol wastewater.

The present disclosure relates to an improved, efficient, scalable process to prepare intermediate compounds, such as 2,2′,2″-(1,3,5,2,4,6-trioxatriborinane-2,4,6-triyl)tris (3-fluorophenol), useful for the synthesis of compounds, such as Compound 9, for the treatment of KRAS G12C mutated cancers.