2702 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 catalytically oxidizing lignin to depolymerize into an aviation oil intermediate by using a cellulose carbon aerogel supported copper nano-catalyst. Comprising the following steps: (1) dissolving cellulose powder into a mixed alkali solution of NaOH and urea, and stirring at low temperature to obtain a clear and transparent cellulose solution; and washing to be neutral to obtain well dispersed cellulose suspension. And (2) carrying out suction filtration molding, and freeze-drying for a period of time to obtain the cellulose aerogel. And (3) immersing in an ethanol solution of copper nitrate for ultrasonic treatment, and drying in a vacuum drying oven. And (4) carrying out high-temperature calcination in an N2 atmosphere to obtain a catalyst which is marked as Cu / CA. And (5) the catalyst can efficiently catalyze a Fenton-like reaction to oxidize a dimer model compound of lignin in acidic, neutral and alkaline environments to obtain products including benzoic acid, acetophenone, benzyl alcohol, phenol and the like, the required hydrogen peroxide concentration is low, and the catalyst has the advantages of simple process, high catalytic activity, low cost and the like, can be used for effectively degrading lignin to prepare aviation oil intermediates, and has wide application prospects. And repeated cyclic utilization is realized.

The invention relates to a composition comprising at least one oxidation coupler chosen from 6-hydroxybenzomorpholine of formula (I), one of its addition salts, its solvates and / or the solvates of its salts, at least one oxidation coupler chosen from 2-amino-5-ethylphenol of formula (II), one of its addition salts, its solvates and / or the solvates of its salts, and at least one compound chosen from N, N-dicarboxymethyl glutamic acid, one of its salts, and mixtures thereof. The invention also relates to a process for dyeing keratin fibres, preferably the hair, comprising the application of the composition to said keratin fibres.

The invention relates to the technical field of industrial wastewater deep purification, and discloses an industrial wastewater deep purification system based on nano catalytic membrane separation, which comprises a pretreatment module, a catalytic degradation module, a membrane separation module, an intelligent control module and a regeneration maintenance module which are sequentially connected according to a treatment flow, the pretreatment module adjusts the water quality of inlet water to a range suitable for subsequent treatment through pH adjustment and suspended matter interception, that is, the pH is 2-11, and the turbidity is less than or equal to 50NTU; the catalytic degradation module is used for decomposing organic pollutants and mineralizing refractory substances under the excitation of ultraviolet / visible light by utilizing the photocatalytic characteristic of a nano catalytic membrane. The TiO2 / WO3 heterojunction nano catalytic membrane is adopted, so that deep oxidation of refractory pollutants such as phenol and sulfonamide antibiotics is realized, finally, the COD removal rate of 98.7% is achieved, and compared with a traditional photocatalytic process, the energy consumption is reduced by 54%.

The invention relates to the field of cables, and discloses a modified polyvinyl chloride composite material for cables and a preparation method thereof.The composite material comprises low-density polyethylene, polyvinyl chloride, ethylene-vinyl acetate copolymer, nitrile rubber, modified graphene oxide, modified nano calcium carbonate and auxiliaries; the modified graphene oxide is prepared by reacting acylating chlorination of graphene oxide with an anti-aging derivative, the anti-aging derivative is prepared by reducing a benzoxazole-containing intermediate generated by a reaction of 2-amino-4-bromophenol and 4-cyanobenzaldehyde to obtain an aminated benzoxazole-containing intermediate, then the aminated benzoxazole-containing intermediate reacts with p-phenylenediamine, and then the product reacts with 3-(3, 4-dichlorophenyl)-1, 2, 3-triazole-3-one to obtain the anti-aging graphene oxide. 2, 5-di-tert-butyl-4-hydroxyphenyl) propionyl chloride is subjected to a reaction to prepare the product. And the modified nano calcium carbonate is prepared by reacting phosphonitrilic chloride trimer with an amino silane coupling agent and 2-amino benzoxazole-5-borate and then grafting on the surface of the nano calcium carbonate. The composite material prepared by the invention has excellent flame retardance, heat resistance and long-acting oxidation resistance.

The invention belongs to the technical field of enzyme engineering, and particularly relates to a P450 peroxygenase mutant and application of the P450 peroxygenase mutant in degradation of phenol environmental pollutants. The mutant is formed by mutating phenylalanine into alanine from the 46th amino acid of P450 peroxygenase with an amino acid sequence as shown in a sequence table SEQ ID NO.1, and the amino acid sequence of the P450 peroxygenase is as shown in a sequence table SEQ ID NO.2. The P450 peroxygenase mutant provided by the invention has the advantages of high catalytic efficiency, high protein expression quantity, low industrial cost and the like. The operation process for degrading the phenol environmental pollutants is simple, the process is mature, the cost is low, harmful impurities are not contained, and the method is non-toxic and environment-friendly.

The invention discloses a synthesis method of bromo-triazine, which belongs to the technical field of organic synthesis, and comprises the following steps: preparing an alumina-loaded N, N-dimethylaminopyridine catalyst, filling the alumina-loaded N, N-dimethylaminopyridine catalyst in a fixed bed reactor, introducing tribromophenol and metal oxide mixed slurry and cyanuric chloride slurry, carrying out a reaction for 2-4 hours, and carrying out a reaction for 2-4 hours to obtain the bromo-triazine. Raising the temperature for reaction to obtain a crude product solution; and performing post-treatment to obtain a bromo-triazine product. According to the invention, the aluminum oxide loaded N, N-dimethylaminopyridine catalyst is synthesized, and the N, N-dimethylaminopyridine enables the reaction speed to be higher and the yield to be higher; nano aluminum oxide is adopted for loading, so that on one hand, dealkalization synthesis of bromotriazine is realized, and on the other hand, the reaction efficiency is accelerated; the continuous process realizes non-aqueous medium and low-temperature short-time reaction, so that hydrolysis is further avoided; the aluminum oxide loaded N, N-dimethylaminopyridine catalyst is high in activity and stability, the synthesis method is simplified, and the aluminum oxide loaded N, N-dimethylaminopyridine catalyst is suitable for industrial large-scale production.

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 provides a binder, negative electrode slurry, a negative electrode plate and a battery. The adhesive comprises a polymer, the polymer comprises an acrylic acid structural unit, a structural unit containing quaternary ammonium salt, a phenolic ether structural unit and a flexible structural unit, and the mass ratio of the acrylic acid structural unit to the structural unit containing quaternary ammonium salt to the phenolic ether structural unit to the flexible structural unit is (30-70): (1-10): (0.5-5): (5-20); the phenolic ether structural unit comprises at least one of an aromatic phenol structural unit and an aromatic ether structural unit. The binder provided by the invention synergistically provides a triple dispersion mechanism of electrostatic stability, surface adsorption and hydrophobic anchoring through the acrylic acid structural unit, the structural unit containing quaternary ammonium salt and the phenolic ether structural unit, so that the negative electrode slurry can form a long-term stable aqueous slurry system without depending on an additional dispersant. The binder forms a bactericidal and bacteriostatic barrier in the slurry, has a stable anticorrosion structure network, and is stable in electrochemical performance.

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 discloses a degradation reagent of an anhydride cured epoxy resin composite material, a degradation method and application of a degradation product, and relates to the field of solid waste material recovery. The degradation reagent comprises a catalyst and a solvent, and the solvent is a strong alkali aqueous solution; the structure of the catalyst is p-hydroxybiphenyl of which a benzene ring is connected with a hydrogen group or a cyano group; the degradation method comprises the following steps: heating the anhydride cured epoxy resin composite material and the degradation reagent to react, neutralizing, concentrating under reduced pressure, and drying the precipitate to obtain a degradation product. Phenolic hydroxyl groups of the catalyst are deprotonated under the alkaline condition to form phenoxy anions, the phenoxy anions react with anhydride groups in the anhydride cured epoxy resin composite material, the anhydride groups are broken, high-efficiency degradation is achieved, and the degradation method is easy and convenient to operate, environmentally friendly and suitable for industrial production. After the degradation product and the anhydride curing agent are cured and regenerated, the comprehensive performance is good, and the recycling value is improved.

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 thermoplastic epoxy polymer with a micro-cross-linked structure and a preparation method thereof.The preparation method comprises the steps that in the step-by-step polymerization reaction process of thermoplastic epoxy resin, firstly, epoxy or amino or hydroxyl-terminated thermoplastic epoxy resin is obtained by controlling the group molar ratio and the reaction time of raw materials; when the molecular weight of a reaction product reaches a certain degree, polyfunctional epoxy compounds, amines, acid anhydrides, phenols and other compounds are introduced, and the thermoplastic epoxy resin with a micro-crosslinking structure is obtained through chain extension. The glass transition temperature of the thermoplastic epoxy polymer with the micro-crosslinking structure is obviously higher than that of a linear thermoplastic epoxy polymer of the same type. Compared with thermoplastic epoxy polymers of the same type, the thermoplastic epoxy polymer with the micro-crosslinking structure prepared by the invention still has the characteristics of thermoplasticity, capability of being melted by heating, capability of being dissolved by a solvent and the like.

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 viscosity-controllable and low-toxicity polysaccharide-based antibacterial detergent and a preparation method thereof, and belongs to the technical field of daily chemical sterilization. The detergent comprises the following raw materials in percentage by mass: 0.5-6% of a polysaccharide thickener, 10% of a bacteriostatic agent, 10% of a glycoside nonionic surfactant and the balance of water, the polysaccharide thickening agent is a mixture of chitosan, chitosan hydrochloride and quaternized chitosan. The polysaccharide is applied to viscosity regulation and control of a surfactant system without a petroleum-based thickening agent for the first time, application of the polysaccharide in the field of daily chemical washing is expanded, and compared with other antibacterial hand sanitizer competitive products containing benzene rings and phenol bacteriostatic agents and 6501 thickening agents, the antibacterial hand sanitizer competitive products have the remarkable advantages of high biocompatibility, high antibacterial property, easiness in degradability and the like.

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 utility model discloses a phenol water recovery system of a two-section type gas producer. The phenol water recovery system comprises a gas producer, a phenol water superheater, a phenol water boiler and a gas cooler. According to the phenol water recovery system of the gas producer at the two ends, the phenol water in the gas can be recovered, the sensible heat of the gas at the lower section is used for heating the phenol water to form phenol water vapor, the phenol water vapor and a gasifying agent are heated together, and the phenol water vapor is introduced into the gas producer through the first gasifying agent inlet and the second gasifying agent inlet; the superheat degree of water vapor in the gasifying agent is high, so that phenol is prevented from being brought into ash slag through condensation of the water vapor, the ash slag is prevented from being changed into hazardous waste, the problem of wastewater treatment is thoroughly solved, sensible heat of lower-section coal gas is fully utilized, energy waste is avoided, and the heat efficiency is improved.

The invention relates to the technical field of cables, in particular to a high-flexibility ethylene-propylene insulating rubber material for a charging pile cable and a preparation process. The composite material comprises an ethylene propylene diene monomer, a thermoplastic polyolefin elastomer, an ethylene-butylene copolymer, nanoscale magnesium hydroxide, a silane coupling agent, dicumyl peroxide, a hindered phenol antioxidant and a phosphite antioxidant. The ethylene propylene diene monomer and the ethylene-butylene copolymer form a flexible network skeleton, and the ethylene-butylene copolymer and the thermoplastic polyolefin elastomer are subjected to molecular-level blending, so that the elongation at break and the bending fatigue resistance are improved; silane coupling agent modified nano magnesium hydroxide is chemically bonded with a rubber matrix, so that the flame retardance and thermal aging resistance are enhanced, and the negative influence of filler agglomeration on flexibility is reduced; the compound antioxidant system effectively inhibits thermal oxidation degradation at high temperature, avoids insulation failure, realizes collaborative optimization of high flexibility and high heat resistance, and improves the reliability and applicability of the charging pile cable.

The invention discloses a Schiff base epoxy oligomer chain extender as well as a preparation method and application thereof. The preparation method of the Schiff base epoxy oligomer chain extender comprises the following steps: adding p-hydroxybenzaldehyde and p-hydroxyaniline into ethanol, reacting at 30-70 DEG C for 2-5 hours, and performing suction filtration to obtain a 4-((4-hydroxybenzylidene) amino) phenol intermediate; and mixing the 4-((4-hydroxybenzylidene) amino) phenol intermediate, epoxy chloropropane and a catalyst, reacting at 80-100 DEG C for 3-7 hours, cooling to 50-70 DEG C, dropwise adding a strong alkali solution, reacting for 4-8 hours after dropwise adding, washing with deionized water, retaining an organic layer, and carrying out rotary evaporation on the organic layer to obtain the product. The rigidity, toughness and heat resistance of the modified nylon 6 prepared by applying the Schiff base epoxy oligomer chain extender are improved, and the modified nylon 6 still has processability similar to that of nylon 6.

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 discloses equipment and a method for preparing an electronic-grade salicylic acid solution. The equipment comprises an acidification tank, an alkali tank, a micron filter, an anion filter, a cation adsorption column and a nano filter. The acidification tank is used for loading a salicylic acid solution and an acidic substance, and the alkali tank is used for loading an eluent. The method comprises the following steps: firstly, removing large impurities from a salicylic acid solution and acidic substances through a micron filter, then conveying the salicylic acid solution and acidic substances to an anion filter, adsorbing salicylic acid through anion adsorption resin to obtain phenol, removing the phenol, then introducing an eluent, washing off the salicylic acid solution, conveying the salicylic acid solution to a cation adsorption column to remove metal ions, and finally conveying the salicylic acid solution and the acidic substances to a nano filter to obtain the purified salicylic acid. And reducing the granularity of the salicylic acid solution to obtain the electronic-grade salicylic acid solution. The electronic-grade salicylic acid solution has the advantage of strong selective complexing ability to metals, and has a good wet etching effect in the integrated circuit manufacturing process.

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 belongs to the technical field of natural product extraction, and particularly relates to a research method for extracting polyphenol and flavonoid compounds in peony petals through an electrochemically-assisted eutectic solvent. The invention provides a research method for extracting polyphenols and flavonoids compounds in peony petals by using an electrochemically-assisted deep eutectic solvent, electrochemical wall breaking and DES regulation are combined for the first time by using a solvent design-electrochemical activation-targeted extraction method, phenol oxidation caused by traditional heating is avoided, and meanwhile, the extraction efficiency of the polyphenols and flavonoids compounds in peony petals is improved. The dissolution of target components is selectively enhanced through electrode reaction, the extraction efficiency of bioactive components in the peony petal powder is effectively improved, and the method has the advantages of greenness, high efficiency, short-time consumption reduction and the like, overcomes the defects in the prior art, and has a good application prospect.

The invention discloses a method for promoting a cobalt sulfide loaded carbon composite catalyst to activate PMS to degrade pollutants by using bicarbonate ions. According to the method, bicarbonate radical ions are added into a system for degrading organic pollutants by activating the PMS with the cobalt sulfide loaded carbon composite catalyst, so that the efficiency of removing phenol by activating the PMS with the cobalt sulfide loaded carbon composite catalyst is greatly improved, and cobalt ion leaching is reduced due to addition of the bicarbonate radical ions; the cobalt sulfide loaded carbon composite catalyst has a wide application prospect in the field of advanced oxidation treatment of organic wastewater.