1787 results about "Furan" patented technology

The application discloses a method for selectively preparing furan amine or tetrahydrofuran amine from furan aldehyde substances, which comprises the following steps: in an aqueous solution with the volume percentage concentration of ammonia water being greater than 70%, furan aldehyde substances are subjected to a reductive amination reaction in the presence of H2 and under the action of a catalyst to prepare furan amine; and in an aqueous solution with the volume percentage concentration of ammonia water being less than 20%, furan aldehyde substances are subjected to a reductive amination reaction in the presence of H2 and under the action of a catalyst to prepare tetrahydrofuran amine. The method can realize the selectivity of products by changing the addition amount of ammonia water in the aqueous solution, and is simple, easy to control, and suitable for industrial production and market promotion and application.

The invention relates to the technical field of aerogel, in particular to flexible flame-retardant aerogel and a preparation method thereof.The flexible flame-retardant aerogel is prepared from modified graphene, modified polyvinyl alcohol, silver nanowires, phytic acid and epoxy resin E-51; the furan group is introduced into the aerogel through the modified graphene, the furan group and the maleimide group are subjected to a D-A reaction, an adhesive is prevented from being used when the aerogel is bonded with a screen backboard, the D-A reaction is reversible, and lossless reworking can be realized. PVA and epoxy resin E-51 are added together, so that the heat resistance and mechanical strength of the material are improved. PVA is grafted with a large-steric-hindrance amine group, weak interaction with a furan group is generated, side reaction with an epoxy group of epoxy resin E-51 is avoided, and when aerogel is bonded to an OLED screen backboard, the protective layer is reversibly released, so that D-A reaction can be smoothly carried out. The hydrophobic treatment of the modified graphene and the modified grafting of the polyethylene to the mPEG can effectively improve the agglomeration of the modified graphene and ensure the uniform dispersion of the modified graphene.

The invention discloses a large-current-carrying-capacity flexible power cable, which belongs to the technical field of cable preparation, is used for solving the technical problem that the flame retardant property and the mechanical property of the power cable need to be further improved in the prior art, and specifically comprises a cable core, a wrapping layer, an insulating layer and a sheath layer which are sequentially arranged from inside to outside. The preparation method comprises the following steps: preparing alkoxy silane containing a benzocyclobutene group, preparing flame-retardant particles by using a sol-gel method, preparing modified polyurethane by using modified polysiloxane and 2, 5-furandimethanol as soft segments, naphthalene diisocyanate as a hard segment and trimethylolpropane as a chain extender, and preparing the flame-retardant flame-retardant polyurethane. The linear low-density polyethylene, the MAH-g-PE, the modified polyurethane, the flame-retardant particles and the auxiliary additive are melted and extruded outside the wire core to form the insulating layer, so that the power cable is obtained, the flame-retardant property of the power cable is effectively improved, and the mechanical property and the current-carrying stability of the power cable are also improved.

The invention discloses a cobalt-copper bimetallic nitrogen-doped carbon catalyst, which is characterized in that CoCu-coated LNC, Co and Cu nanoparticles are anchored on a nitrogen-doped carbon carrier derived from lignin. Accordingly, the inventor also establishes a corresponding preparation method, and the catalyst is prepared by taking lignin as a carrier, cobalt-copper bimetal as an active component and dicyandiamide as a nitrogen source through one-pot pyrolysis. The method has the characteristics of simple and efficient process, high catalyst stability and activity, economy, high efficiency, environmental friendliness and the like. The method is used for preparing 2, 5-furandicarboxylic acid through thermal catalytic oxidation of 5-hydroxymethylfurfural, the yield of the target product FDCA almost reaches 100%, and the application prospect is wide.

The invention discloses a high-oxidation-resistance long-life polyethylene cable sheath material and a preparation method thereof, and relates to the technical field of high polymer materials. Comprising the following components: high-molecular-weight high-density polyethylene, surface-modified nano-dioxide, furan-maleimide grafted polyethylene, a Schiff base dynamic cross-linking agent, tea polyphenol grafted polyethylene, a temperature-responsive oxygen-blocking microcapsule, a main antioxidant, an auxiliary antioxidant, an emergency antioxidant, a light stabilizer, a halogen-free flame retardant, a processing aid and an acid absorbent. According to the invention, the main antioxidant, the auxiliary antioxidant and the tea polyphenol grafted polyethylene form a chemically synthesized and naturally modified composite antioxidant system, the designed service life of the material is greatly prolonged, the temperature-responsive oxygen-blocking microcapsule automatically cracks to release the core material when the operating temperature of the cable is greater than or equal to 90 DEG C, a dynamic oxygen-blocking layer is formed, and the service life of the cable is prolonged. The defect that the effect of traditional physical oxygen barrier is attenuated at high temperature is overcome, and the oxygen permeability at high temperature is reduced compared with that of a single nano barrier scheme.

The invention relates to the technical field of multi-layer copolyester films, and discloses a high-temperature-resistant antistatic multi-layer copolyester film and a preparation method and application thereof, and the multi-layer copolyester film comprises an ABA three-layer structure obtained through melt co-extrusion; the layer A is prepared from the following raw materials in percentage by mass: 5 to 30 percent of anti-blocking agent master batch and the balance of modified copolyester; the raw material of the layer B is modified copolyester; the modified copolyester is prepared from a binary acid mixture, a dihydric alcohol mixture and a catalyst through an esterification reaction and a condensation polymerization reaction; the binary acid mixture comprises furandicarboxylic acid and 2, 2 '-bifuran-5, 5'-dicarboxylic acid, and the dihydric alcohol mixture comprises ethylene glycol, 2, 2, 4, 4-tetramethyl-1, 3-cyclobutanediol and 1, 4-cyclohexanedimethanol. According to the invention, the modified copolyester is used as a main raw material, and the film is endowed with good temperature resistance in a copolymerization modification manner, and has stable and lasting antistatic performance.

The invention discloses a full bio-based copolymer based on a citric acid bicyclic monomer, a preparation method and an application, and belongs to the technical field of material synthesis, citric acid-derived bicyclic OPD diol and OPBMC diester are synthesized through oxidation reduction and transesterification, and then 1, 4-butanediol is partially replaced with OPD or 2, 4-butanediol is partially replaced with OPBMC through melt phase polycondensation reaction. Two series of random copolyester PBxOyF copolymer and PBOmFn copolymer of the PBF are prepared by adding 2, 5-dimethyl furandicarboxylate into the PBF, and then adding the PBxOyF copolymer and the PBOmFn copolymer into the PBF. According to the full-bio-based copolymer based on the citric acid bicyclic monomer, the preparation method and the application, the citric acid bicyclic monomer obviously improves the glass transition temperature and shows good mechanical properties; therefore, the bicyclic monomer based on citric acid has huge potential in the aspect of synthesizing novel bio-based copolyester with expected thermodynamic properties, and is expected to further expand the application range of the 2.5 furandicarboxylic acid-based polyester.

The application provides a crosslinked polyethylene insulating material with intrinsic self-repairing and recyclable characteristics, a preparation method and application thereof, and relates to the technical field of cable materials.The crosslinked polyethylene insulating material with intrinsic self-repairing and recyclable characteristics is prepared from the following components in parts by weight: 99.7 parts by weight of low-density polyethylene, 1.0-2.6 parts by weight of peroxide, 0.1-0.5 parts by weight of antioxidant, 5-20 parts by weight of maleimide monomer, 0.35-0.7 parts by weight of catalyst, 0.5-3.0 parts by weight of ligand and 0.5-3.0 parts by weight of furan-based small molecule.The low-density polyethylene is functionally modified through catalytic amination reaction, so that the chain breaking and crosslinking in the modification process are avoided, and the mechanical properties, insulating properties and dielectric properties of the crosslinked polyethylene are enhanced through the post-absorption of the introduced peroxide.Meanwhile, the dynamic reversible Diels-Alder reaction introduced by the post-absorption of the furan-based small molecule enables the polyethylene insulating material to have good intrinsic self-repairing effect on mechanical damage and electrical damage.

Disclosed in the present invention are a branched-chain-containing long-carbon-chain polyester elastomer based on biomass-based 2,5-furandicarboxylic acid, and a preparation method therefor. Monomers for preparing the polyester elastomer comprise 2,5-furandicarboxylic acid or 2,5-furandicarboxylic acid ester, a dihydric alcohol and a branched-chain-containing long-carbon-chain dibasic acid. The preparation method comprises: (1) performing a melting reaction on furandicarboxylic acid or an ester thereof, a branched-chain-containing long-carbon-chain dibasic acid and a dihydric alcohol to prepare an oligomer; and (2) performing melt polycondensation on the oligomer to synthesize a furandicarboxylic acid-based branched-chain-containing long-carbon-chain polyester elastomer. By means of the branched-chain-containing long-carbon-chain polyester elastomer of the present invention, the molecular structure can be effectively designed, and the molecular weight can be regulated, thereby optimizing mechanical properties, thermal properties, barrier properties, etc. The preparation process thereof is simple, convenient and safe, and the equipment requirements and catalysis cost are relatively low. The raw material 2,5-furandicarboxylic acid used in the present invention is a potential substitute for terephthalic acid, is derived from biomass, has a wide range of sources and is environmentally friendly.

The invention discloses a production method of a PET composite current collector base film with high mechanical property. The base film comprises an outer surface layer, a middle core layer and an inner surface layer, the outer surface layer is composed of PET, fumaric acid, hydroxyl-terminated polybutadiene and an antioxidant; the middle core layer consists of PET (Polyethylene Terephthalate), furandicarboxylic acid, an antioxidant and a stabilizer; the inner surface layer is composed of dimethyl terephthalate, ethylene glycol, spiro diol, ethylene glycol antimony and zinc acetate. The PET composite current collector base film prepared by the preparation method disclosed by the invention has relatively high mechanical properties.

The invention relates to the technical field of high polymer materials, and discloses a high-chemical-resistance TPO material which comprises the following components in parts by mass: 55-65 parts of polypropylene; 35 to 45 parts of a styrene-ethylene / butylene-styrene block copolymer; 0.4 to 0.6 part of a furan end-capping reagent; 0.2 to 0.4 part of a maleimide cross-linking agent; 4-6 parts of modified shell powder; 8 to 12 parts of epoxidized cardanol; 2-4 parts of a heat-sensitive microcapsule, wherein the heat-sensitive microcapsule comprises a shell layer and an inner core; and 0.5 to 1.5 parts of a nano cellulose surface treating agent. Through the synergistic effect of a dynamic cross-linked network and fluorocarbon chain surface modification, when the material is in contact with acid, alkali and an organic solvent, reversible cross-linked bonds release local stress through a fracture-reconstruction mechanism, and microcrack propagation is inhibited; and the compact fluorocarbon layer on the surface forms a chemical inert barrier, so that the permeation rate of a corrosive medium is remarkably reduced, and the structural stability and long-term durability of the material in a complex chemical environment are guaranteed.

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

The invention provides a semiconductive shielding material, a preparation method and application thereof and a high-voltage cable, and belongs to the technical field of high-voltage cable materials. The semiconductive shielding material is prepared from the following components in parts by weight: 60 to 70 parts of matrix resin, 20 to 30 parts of carbon black, 5 to 10 parts of Diels-Alder cross-linking agent, 1 to 3 parts of antioxidant and 2 to 5 parts of dispersing agent, the Diels-Alder cross-linking agent is prepared from a furan compound and a maleic acid derivative. A Diels-Alder type dynamic covalent cross-linking structure is introduced by adopting a Diels-Alder cross-linking agent consisting of a furan compound and a maleic acid derivative in certain parts by mass to construct a reversible cross-linking network, so that the scorching phenomenon can be remarkably inhibited, the conductivity and the mechanical property are improved, the material processing window is improved, the industrial applicability is excellent, and the application prospect is wide. And the operation stability of the high-voltage cable can be improved when the cable is used.

The invention discloses a DA bond polymer with antibacterial and self-repairing functions for a wood surface as well as a preparation method and a use method of the DA bond polymer. Chitosan serves as a wall material, cinnamon essential oil serves as a core material, the cinnamon essential oil and chitosan antibacterial microcapsules are prepared through emulsification, crosslinking and spray drying, and essential oil controlled release is achieved. Then bisphenol A diglycidyl ether DGEBA and furfuryl alcohol FA are used as raw materials, furyl functional epoxy resin FER is prepared under the catalysis of triethylamine TEA, bismaleimide BMI is added, and a DA bond self-repairing polymer is prepared through a DA reaction; and adding 4, 4-diaminodiphenylmethane DDM into the system, reacting with redundant DGEBA to generate a cross-linked polymer network, and adding the microcapsules into a DA bond semi-interpenetrating self-repairing network solution to obtain the DA bond polymer. A thin film formed by brushing and curing wood has antibacterial and self-repairing functions, scratches and microcracks on the surface of the wood can be repaired, and microbial erosion is inhibited.

The invention discloses a synthesis method of special bio-based unsaturated polyester resin for zero-crystalline silicon quartz stone, which comprises the following steps: firstly, putting bio-based dihydric alcohol, 2, 5-furandicarboxylic acid, itaconic acid, an antioxidant and a polymerization inhibitor into a reaction kettle, heating to 205-210 DEG C, carrying out polymerization reaction for 2-4 hours, then vacuumizing for 2-3 hours, and cooling to room temperature to obtain the special bio-based unsaturated polyester resin for zero-crystalline silicon quartz stone. When the reaction acid value is tested to be smaller than 25 mgKOH / g and the cone plate viscosity at 125 DEG C is 500-900 mpa.s, the reaction endpoint is reached, finally, a bio-based crosslinking monomer is added for dilution, and the bio-based unsaturated polyester resin special for the zero-crystallization silicon quartz stone is obtained. The bio-based unsaturated polyester resin special for the zero-crystalline silicon quartz stone synthesized by the method can meet the requirements of a zero-crystalline silicon quartz stone production process, and solves the problems that a zero-crystalline silicon quartz stone plate is easy to generate surface pulverization corrosion, glass explosion and the like.

The invention provides high-transparency bio-based polyimide as well as a preparation method and application thereof. The high-transparency bio-based polyimide comprises a polymerization product of a diamine monomer and a dicarboxylic anhydride monomer, and the diamine monomer is selected from 2, 5-bis (aminomethyl) furan and / or 2, 5-furandiamine. The high-transparency bio-based polyimide disclosed by the invention has high transparency, good heat resistance, film forming performance and the like, and can replace a traditional optical thin film material.

The invention discloses a high-strength and high-resilience TPE (thermoplastic elastomer) and a preparation method thereof in the technical field of high polymer materials, and the elastomer is prepared by taking a hydrogenated styrene block copolymer as a matrix and matching with a polyolefin rigid phase, plasticizing oil and a specific additive. The method is characterized in that two self-made reaction type modifiers are introduced, wherein one self-made reaction type modifier is a core-shell nano reinforcing agent containing an epoxy functional group and polyhedral oligomeric siloxane, and the other self-made reaction type modifier is a furan maleimide bifunctional dynamic cross-linking agent. The nano reinforcing agent is prepared through silane hydrolysis and amination reaction, and can react with a matrix for grafting, so that the strength and creep resistance of the material are remarkably improved; the dynamic cross-linking agent is synthesized through step-by-step isocyanate addition reaction, a cross-linked network can be reversibly formed in the processing process, and the material is endowed with extremely high rebound resilience and low permanent deformation. The obtained product has high strength, high resilience and excellent processability, and is especially suitable for high-end fitness equipment.

The present invention provides an epoxy resin material and a preparation method thereof. The epoxy resin material is prepared from the following raw materials in parts by weight: 63-82 parts of epoxy resin, 13-29 parts of curing agent, 1.8-4.3 parts of toughening agent, and 1.8-6 parts of reactive diluent. The epoxy resin is an epoxy resin having a benzene ring in the main chain, and the reactive diluent is an aliphatic chain segment containing a terminal amine group, wherein the aliphatic chain segment contains a furan ring or a benzene ring. The addition of the reactive diluent to the epoxy resin material prepared by the present invention not only reduces the viscosity of the epoxy resin system before the reaction, but also improves the modulus and toughness of the epoxy resin material obtained after curing, and increases the gel time of the epoxy system.

The invention relates to polyethylene wax with a reversible crosslinking characteristic and a preparation method and application thereof, and relates to the field of polymer functional aids and processing and application thereof. The polyethylene wax with the reversible cross-linking characteristic is prepared from three monomers of furyl ethylene, maleimide ethylene and ethylene through double-bond addition copolymerization, and the number-average molecular weight is 1000-100000. The polyethylene wax provided by the invention can be used as a flow modifier during polyethylene material processing and a cross-linking modifier during use. The low molecular weight polyethylene wax can reduce the energy consumption of processing equipment and increase the flatness of the product. And meanwhile, the reversible crosslinking of furan and maleimide groups on the chain segment can endow the resin with thermoset property in use and thermoplastic cycle processability after use.

The invention discloses a gold nanocluster and application thereof in electro-catalysis of carbon dioxide reaction. The synthesis method comprises the following synthesis steps: firstly, adding a gold source into a tetrahydrofuran solution, stirring for five minutes, then adding tetra-n-octyl ammonium bromide, stirring until the solution is dark red, adding cyclohexanol, stirring until the solution is transparent, then adding a reducing agent, stirring overnight, then washing with methanol for multiple times, dissolving a crude product into a small amount of methylbenzene, and drying to obtain a target product. And adding a certain amount of cyclohexanol and 3 (2-furyl) phosphorus again, slowly stirring at 60 DEG C for 12 hours to obtain a crude product, washing with methanol for several times again, and purifying and separating to obtain the gold nanocluster. The gold nanocluster provided by the invention has the characteristics of novel structure, good stability, easy synthesis and high yield, and has excellent catalytic performance in electrocatalytic carbon dioxide reaction.

The invention discloses a self-repairing composite floor for a clean room and a preparation method of the self-repairing composite floor, and the preparation method comprises the following steps: carrying out amination treatment on nano silicon dioxide and carbon quantum dots by using a silane coupling agent, and sulfonating polyethersulfone ketone by using concentrated sulfuric acid; the preparation method comprises the following steps: carrying out curing treatment on epoxy resin, an amine curing agent, N-hydroxyethyl maleimide and tetrakis (3-mercaptopropionic acid) pentaerythritol ester to obtain epoxy-mercaptan resin; the preparation method comprises the following steps: carrying out prepolymerization reaction on vacuum dehydrated polyester polyol, tetrahydroxyethyl ethylenediamine, furanpropanol, diisocyanate, a catalyst, 2, 2 '-thiodiethanol and hydroxyl silicone oil to obtain a star-shaped polyurethane prepolymer, adding epoxy-thiol resin, glyceryl borate, sulfonated polyethersulfone ketone, aminated silicon dioxide, aminated carbon quantum dots and an auxiliary agent, carrying out ultrasonic treatment, and carrying out drying to obtain the star-shaped polyurethane resin. The self-repairing coating material is obtained; and coating the self-repairing coating material on the surface of a base plate, and performing hot-pressing curing molding to obtain the self-repairing composite floor for the clean room.

The invention relates to the technical field of intermediate membranes, in particular to a heat insulation type ionic intermediate membrane and a preparation method thereof.The heat insulation type ionic intermediate membrane is characterized in that hollow silicon dioxide nanotubes serve as filler, epoxy resin modified polyurethane emulsion serves as a base material, auxiliaries are added to prepare a heat insulation coating, and the ionic intermediate membrane layer is coated with the heat insulation coating to form a heat insulation layer; the preparation method comprises the following steps: carrying out amination on a hollow silicon dioxide nanotube by using 3-aminopropyltriethoxysilane, carrying out dehydration condensation on furan-2, 5-diketone and an amino group to synthesize maleimide so as to obtain a maleimide modified hollow silicon dioxide nanotube, and grafting furan carboxylic acid imidazolium salt polyionic liquid by using a Diels-Alder reaction so as to obtain a composite hollow silicon dioxide nanotube; aminated glass fibers, composite hollow silicon dioxide nanotubes, epoxy resin modified polyurethane emulsion and auxiliaries are mixed, and a reinforcing layer coating is obtained; and coating the lower surface of the ionic intermediate film layer with a reinforcing layer coating to form the reinforcing layer.

The invention belongs to the technical field of chemical synthesis, and particularly relates to a method for preparing 5-methylfurfural by using 2-methylfuran. The special solid acid catalyst is used for replacing traditional phosphorus oxychloride, hydrogen chloride and phosphorus-containing wastewater are eliminated from the source, and the sulfolane is used for replacing DMF (Dimethyl Formamide), so that solvent residues in the product are reduced. The solid catalyst SO4 < 2-> is modified to form a strong Bronsted acid site (-SO3H) which cooperates with Ce < 3 + > / Ce < 4 + > redox to inhibit carbon deposition, selectively activate 2-methylfuran alpha-C and inhibit side reactions, so that the selectivity and yield of a target product are improved. Na2CO3 neutralization is replaced by electrochemical neutralization, salt slag solid waste is eliminated, and environmental pollution is reduced. After the organic phase is dried and dewatered through a molecular sieve, most of the solvent is removed through rotary evaporation, and the residual crude product is subjected to centrifugal molecular distillation, so that unreacted raw materials and trace impurities are effectively removed, and the product purity is remarkably improved.

The invention discloses a self-repairing type phase change microcapsule and application thereof in a wood-based energy storage wall, the self-repairing type phase change microcapsule is characterized in that an inner core layer is composed of composite paraffin and butyl stearate composite phase change materials, gradient refractive index silicon dioxide microspheres are arranged on the surface of the inner core layer, and a middle shell layer is a composite film formed by polyurea and furan-epoxy monomer copolymer; the reinforced shell layer is of a three-dimensional network structure which is formed by nano SiO2 through a sol-gel method, has the porosity of 20-25% and is in gradient distribution; according to the invention, a three-dimensional network structure formed by a Diels-Alder dynamic bonding network of a middle shell layer and nano SiO2 of an enhanced shell layer is used for synergistically constructing a self-repairing system of the microcapsule, so that the self-repairing function of the phase change microcapsule material is realized, the defect of failure caused by physical damage of the microcapsule is avoided, and the service life of the phase change microcapsule material is prolonged. And meanwhile, through gradient packaging preparation of the inner core layer and the enhanced shell layer, the problem of thermal stress concentration is effectively solved.

The synthesis method comprises the following steps: S1, adding furandicarboxylic acid into a reaction container, adding a certain amount of methanol, adding a double-acid-site strong acid solid catalyst, starting stirring, controlling the reaction temperature to carry out esterification reaction, and after the reaction is finished, filtering, washing and drying to obtain furandihydrazide; separating out the double-acid-site strong acid solid catalyst to obtain clear liquid, namely dimethyl furandicarboxylate; s2, transferring dimethyl furandicarboxylate serving as a raw material into another reaction container, adding a certain amount of sodium formate serving as a catalyst, then adding a proper amount of hydrazine hydrate, controlling the reaction temperature, keeping a reflux state, reacting for a period of time, cooling to room temperature after the reaction is finished, and performing centrifugal separation to obtain white solid furandihydrazide. The synthesis method has the advantages of simple reaction steps, no need of toxic and harmful catalysts, mild reaction conditions, high conversion rate and high yield, and can realize efficient, green and low-cost production of furandihydrazide.

The invention discloses a bone cement composition and application thereof, and relates to the technical field of bone cement. The bone cement composition comprises a solid phase component and a liquid phase component, wherein the solid phase component comprises 60-75 parts of composite calcium phosphate, 10-20 parts of strontium glass powder, 8-12 parts of a reinforcing agent and 3-7 parts of a solidification reaction regulator; the liquid phase component comprises 20-30 parts of a phosphate buffer solution, 3-8 parts of a sodium citrate solution, 5-15 parts of an anti-inflammatory agent and 1-5 parts of a hyaluronic acid solution. The preparation method comprises the following steps: reacting 1, 10-phenanthrene-2, 9-dicarboxylic acid with 2-aminomethyl furan to obtain an intermediate 1, and reacting the intermediate 1 with poly (ethylene glycol) maleimide to prepare the reinforcing agent. The prepared bone cement composition has good mechanical properties, self-repairing performance and anti-inflammatory performance, and has a good application prospect in the field of bone repairing.

A method for catalyzing selective oxidation of 5-hydroxymethylfurfural by ion-doped birnessite belongs to the field of chemical engineering, and comprises the following steps: adding an ion-doped birnessite type catalyst into a solvent, and catalyzing 5-hydroxymethylfurfural to prepare 2, 5-furandicarboxaldehyde and 2, 5-furandicarboxylic acid in the atmosphere of air or oxygen at the temperature of 25-240 DEG C, wherein the solvent is water, methanol, ethanol, acetonitrile, dichloromethane, N, N-dimethylformamide, N, N-dimethylacetamide and the like. The method is simple, few in by-products and environmentally friendly. By adopting ion-doped birnessite as the catalyst, the method has the advantages of economy, environmental protection, mild conditions, high selectivity, easiness in recovery of the catalyst and the like; the ion-doped birnessite catalyst can efficiently and highly selectively catalyze oxidation of 5-hydroxymethylfurfural to prepare 2, 5-furandicarboxaldehyde, catalytic materials are easy to separate, the production cost is low, and the ion-doped birnessite catalyst has remarkable technical and economic effects and application prospects.

The invention provides a graphene dispersion liquid, a preparation method thereof and a water-based paint, aiming at solving the problem that the performance of graphene is influenced due to insufficient dispersion force and poor dispersion stability when a conventional dispersing agent is used for dispersing graphene in water in the prior art. The graphene dispersion liquid comprises a first solvent and modified graphene oxide, and the modified graphene oxide is dispersed in the first solvent; the modified graphene oxide comprises an inner core and a shell layer, the inner core is graphene oxide, the shell layer is a diene modified polymer, and the diene modified polymer is grafted on the inner core; the diene modified polymer comprises one or more of a cyclopentadiene modified polymer and a furan modified polymer. According to the graphene dispersion liquid provided by the invention, the diene modified polymer is grafted on the graphene oxide, and the graphene oxide is uniformly dispersed in the solvent by utilizing the hydrophilicity of the diene modified polymer, so that the graphene dispersion liquid with stable dispersion performance can be obtained.

The embodiment of the invention provides a self-repairing UV (Ultraviolet) excimer skin-touch coating as well as a preparation method and application thereof. The self-repairing UV excimer skin-touch coating comprises 50-60 parts of bio-based aliphatic polyurethane acrylate; 25 to 36 parts of a UV reactive diluent; 5 to 8 parts of a maleimide derivative; 0.1 to 0.3 part of a polymerization inhibitor; 1-3 parts of organic silicon micro powder; 3.5 to 6 parts of a photoinitiator; 0.2 to 0.3 part of a defoaming agent; 0.2 to 0.5 part of a leveling agent; wherein the content of bio-based carbon in the bio-based aliphatic polyurethane acrylate is 72%-75%. According to the self-repairing UV quasi-molecular skin-touch coating and the preparation method and application thereof provided by the embodiment of the invention, reversible covalent crosslinking is realized through DA reaction of the maleimide derivative and the 2, 5-furandimethanol grafted to the bio-based aliphatic polyurethane acrylate, so that the coating is endowed with self-repairing capability within the range of 60-100 DEG C, and the self-repairing UV quasi-molecular skin-touch coating has the advantages that the self-repairing UV quasi-molecular skin-touch coating has a good skin-touch effect; and the organic silicon micro powder is compounded with the components, so that the scratch resistance and the skin feeling effect of a coating film are improved.

The invention belongs to the technical field of drug development, and particularly relates to application of (E)-N-benzyl-2-((5-(thiophenyl) furan-2-yl) methylene) hydrazine-1-thioformamide in preparation of drugs for treating nervous system diseases. The invention aims to provide a medicine which has small toxic and side effects and can target SLC11A2 to treat or improve nerve cell injury. According to the technical scheme, the invention relates to application of (E)-N-benzyl-2-((5-(thiophenyl) furan-2-yl) methylene) hydrazine-1-thioformamide in preparation of a medicine for treating nervous system diseases, in particular to application of (E)-N-benzyl-2-((5-(thiophenyl) furan-2-yl) methylene) hydrazine-1-thioformamide. It is proved that the compound (E)-N-benzyl-2-((5-(thiophenyl) furan-2-yl) methylene) hydrazine-1-thioformamide is small in toxic and side effect, and nerve cell damage can be protected or improved by targeting SLC11A2; and a new choice is provided for treating or improving nerve cell injury.