1448 results about "Thiokol" patented technology

The invention discloses a self-repairing polymer electrolyte, a preparation method and application thereof, and a polymer lithium battery, the self-repairing polymer electrolyte comprises the following preparation raw materials by mass: 50-100 parts of polysiloxane diacrylate, 1-10 parts of disulfide diacrylate, 10-40 parts of a cross-linking agent, 60-120 parts of a plasticizer, 60-120 parts of a lithium salt, and 1-10 parts of a photoinitiator. According to the self-repairing polymer electrolyte disclosed by the invention, a thiol-ene click reaction can be carried out between carbon-carbon double bonds in polysiloxane diacrylate and disulfide diacrylate and sulfydryl of the cross-linking agent, so that a dynamic disulfide bond and hydrogen bond network structure is endowed to the self-repairing polymer electrolyte; and the dynamic disulfide bond and the hydrogen bond can enable the electrolyte membrane to realize self-healing at room temperature without external stimulation.

The invention discloses a transparent composition photoresist with low shrinkage and low vacuum deflation. Comprising the following raw materials in percentage by mass: 1-5% of modified polyhedral oligomeric silsesquioxane (POSS), 1-5% of an expanding monomer, 1-5% of modified acrylic resin, 1-5% of epoxy resin, 1-5% of a thiol cross-linking agent, 1-5% of an initiator, 0.1-3% of a curing accelerator, 0.2-0.5% of a flatting agent, 0.1-5% of a silane coupling agent, 0.01-0.2% of an antioxidant and 80-90% of an electronic-grade organic solvent. The invention also provides a preparation method of a cured coating prepared from the transparent composition photoresist with low shrinkage and low vacuum deflation. The product provided by the invention not only can maintain the properties of high hardness, high thermal stability, high planarization ability, high barrier property, low hygroscopicity, low dielectric constant and the like of the transparent composition photoresist coating, but also can enable the transparent composition photoresist coating to have excellent low shrinkage and low outgassing, thereby achieving the purposes of saving energy, reducing emission, reducing cost and improving efficiency; the low shrinkage of the transparent composition photoresist coating also widens the development of the material in the fields of other panel production processes such as OLED (Organic Light Emitting Diode) and the like.

The invention provides a novel polynorbornene anion exchange ionomer containing a polar functional group as well as a preparation method and application of the novel polynorbornene anion exchange ionomer. The polynorbornene has excellent thermal stability and chemical stability. Meanwhile, the AEI main chain of the polynorbornene has no aryl group, so that the adsorption influence caused by the aryl group is avoided. The synthesized addition polynorbornene AEI in the form of quaternary ammonium salt can be dissolved in a low-boiling-point solvent, and it is ensured that a membrane electrode can be prepared through a solvent casting method. Besides the solubility of the AEI, the addition polynorbornene-based AEI in the form of quaternary ammonium salt is modified by utilizing a thiol-ene click reaction, an anion exchange ionomer containing a polar functional group can be prepared, the interaction between the AEI and an electrolytic catalyst is improved, the reaction is simple and easy to operate, the universality is high, and the method is suitable for industrial production. And the current density in the AEMWE system containing the AEI can be effectively improved.

The invention relates to a degradable epoxy resin composite material with an adjustable curing speed, and a preparation method and a mild total recycling method thereof. Existing degradable epoxy resin has the problems of high cost, harsh degradation conditions and the like, and is difficult to meet the requirements of different application scenes on curing speed and temperature at the same time. The invention provides an epoxy resin composite material which comprises curing agent components (an epoxy resin amine curing agent and an ester-containing polythiol curing agent) and epoxy resin components (glycidyl ether epoxy resin, glycidyl amine epoxy resin and glycidyl ester epoxy resin). The cured composite material can be fully recycled through catalytic degradation under mild conditions by using a lewis acid and an amino group breaking ester bond mechanism, and the degradation product can be directly used as a curing agent, a toughening agent and a chain extender. The epoxy resin composite material disclosed by the invention not only has adjustable curing speed and high use performance, but also realizes environmental friendliness and resource recycling, and provides a new solution for sustainable development of epoxy resin.

The preparation method comprises the following steps: mixing 20-40 parts by mass of substituted hydroxymethyl glycoluril, 45-85 parts by mass of mercaptocarboxylic acid and 0.5-3 parts by mass of an acidic catalyst, stirring and reacting for 1-10 hours at the temperature of 50-150 DEG C under the pressure condition of-0.01 to-0.1 MPa, adding 300-800 parts by mass of an organic solvent for diluting after the reaction is finished, washing and purifying with deionized water, and collecting an organic layer, thereby obtaining the mercaptan curing agent. Concentrating and drying to obtain the mercaptan curing agent. According to the thiol curing agent, the rigid glycoluril group is introduced, so that the rigidity of a cured product structure is improved, and the mechanical property, the adhesive property, the heat resistance and the damp-heat aging resistance of a cured product are improved; four tertiary amine groups in the substituted glycoluril have a certain self-promotion effect on a thiol curing epoxy reaction, and the curing reaction temperature is reduced under the condition that an accelerant is not added; the glycoluril-containing thiol epoxy resin curing agent disclosed by the invention has good application value and development prospect.

The invention relates to the technical field of waterproof agents for fabrics, and particularly discloses a fluoride-free waterproof agent for fabrics and a preparation method of the fluoride-free waterproof agent. The preparation method specifically comprises the following steps: dehydrating polyol / ester, adding isocyanate, heating to 80-90 DEG C, reacting for 2-3 hours, cooling, dropwise adding a chain extender, reacting for 0.5-1 hour at 45-48 DEG C, adding POSS, stirring for 1-2 hours at 45-48 DEG C, adding an acrylic monomer A for blocking, cooling, dropwise adding acid, stirring and neutralizing to obtain a prepolymer; pouring the prepolymer into water, stirring and emulsifying to obtain a POSS-PU emulsion; quickly stirring the POSS-PU emulsion, an acrylic monomer B, an emulsifier, water, a co-emulsifier, a pH regulator and the like to obtain a composite emulsion; homogenizing the composite emulsion until the composite emulsion has obvious blue light; and adding dodecanethiol and an azo amidine initiator, reacting at 68-70 DEG C for 3-7 hours, cooling, filtering and taking out to obtain the fluoride-free waterproof agent.

A flame-retardant laminated solid wood composite floor and a manufacturing method therefor. The manufacturing method comprising: first reacting dopamine hydrochloride with acryloyl chloride to generate a dopamine acrylamide monomer; by means of a double bond in the dopamine acrylamide monomer, carrying out a click reaction with a phosphate monomer containing a sulfydryl group, so as to introduce a catechol group into a side chain of the phosphate monomer and obtain a flame-retardant monomer containing the double bond; and then mixing pentaerythritol tetra(3-mercaptopropionate), pentaerythritol triacrylate, perfluorodecanethiol and the flame-retardant monomer containing the double bond to obtain a photocurable coating material. The coating material is photocured after being coated on the surface of a wood veneer, thus effectively improving the flame-retardant performance of the wood veneer; moreover, the adhesion between the coating layer and the wood veneer is excellent. The wood veneers are laminated in multiple layers, are glued and assembled into a layered structure, and then hot-pressed to form the solid wood composite floor, thus improving the comprehensive performance.

The invention provides a preparation method of a self-repairing waterborne polyurethane coating based on a synergistic effect of a dynamic disulfide bond and a pH response microcapsule. The preparation method comprises the following steps: step 1, preparing a dynamic disulfide bond-containing waterborne polyurethane (D-WPU) emulsion; step 2, preparing a pH response microcapsule; step 3, preparing a self-repairing waterborne polyurethane coating; a dynamic disulfide bond of the self-repairing waterborne polyurethane coating rapidly repairs macrocracks at 50-60 DEG C through mercaptan catalysis, and pH < lt > is caused by local corrosion of a pH response microcapsule; when the pH value is 4.0, cysteine is released, sulfydryl accelerates recombination of dynamic bonds, and amino enhances cohesive force of the coating and neutralizes H < + >. And in combination with a hydrogen bond network of the nanocellulose, the coating has low-temperature repair (the mechanical strength recovery rate is greater than or equal to 90%), high toughness (the water absorption rate is less than or equal to 2.1%) and long-acting corrosion resistance (the salt spray resistance life is greater than or equal to 600 hours), and is suitable for severe environments such as ocean engineering and new energy equipment.

The invention belongs to the technical field of polyurethane coatings and coatings, and particularly relates to an anti-doodling polyurethane coating, a coating as well as a preparation method and application of the anti-doodling polyurethane coating, and the anti-doodling polyurethane coating comprises the following components in parts by weight: 15-30 parts of dimercaptomercaptan, 5-30 parts of polymercaptan, 0.20-0.6 part of a catalyst and 20-55 parts of isocyanate. The molecular weight of the dimercapto mercaptan is 154.32; and the molecular weight of the polymercaptan is 260.53. Polyurethane is prepared through reaction of dimercaptomercaptan, polymercaptan and isocyanate, the adhesion performance and anti-doodling performance of polyurethane on the surface of synthetic leather / leather are remarkably improved, industrial production is easy, and wide application prospects and market value are achieved.

The invention relates to an automobile paint surface protective film agent and a preparation method thereof, and belongs to the technical field of automobile beauty. The automobile paint surface protective film agent is prepared from the following raw materials: amino functional polysiloxane, fluorine modified acrylic resin, epoxy modified organic silicon emulsion, functional filler, a surfactant, hydrophobic modified silicone oil, a brightening agent, a penetrating agent, a cosolvent and deionized water, and the raw materials are blended to prepare the automobile paint surface protective film agent. The functional filler is prepared by firstly carrying out surface modification on a polymer and then carrying out click chemistry on dodecanethiol on hydroxylated nano silicon dioxide, and the polymer is prepared by carrying out nucleophilic addition on poly (ethylene glycol) methacrylate Mn360, poly (ethylene glycol) methacrylate Mn500 and isophorone diisocyanate. The automobile paint surface protective film agent is high in film forming speed, a formed film layer has the characteristic of multiple effects, and meanwhile, the wear resistance is also very good.

The invention discloses a high-reliability PbS quantum dot film, a preparation method thereof and a photoelectric device. The preparation method comprises the following steps: 1) obtaining a first quantum dot solution; 2) adding medium-chain and long-chain amine; 3) adding an anti-solvent; 4) obtaining medium-chain and long-chain amine modified PbS quantum dot solids; 5) obtaining a second quantum dot solution; (6) forming a PbS quantum dot coating; 7) forming a mercaptan solution; 8) coating the PbS quantum dot coating with a mercaptan solution; (9) annealing treatment; 10) forming a new PbS quantum dot coating, and coating the new PbS quantum dot coating with a mercaptan solution; according to the PbS quantum dot thin film and the preparation method thereof, through the induction and synergistic effect of halogen atoms, the binding capacity of halogenated mercaptan ligands and the surface of the PbS quantum dot thin film is enhanced, the surface defect state of the PbS quantum dots is effectively inhibited, and the reliability of the PbS quantum dot thin film and a photoelectric device under the conditions of high temperature, high humidity and long-time illumination is remarkably improved.

The invention relates to the technical field of polyurethane adhesives, and provides a heat-conducting polyurethane structural adhesive and a preparation and use method thereof.The heat-conducting polyurethane structural adhesive comprises a first component and a second component, and the first component comprises modified bio-based polyol, polythiol, heat-conducting filler, a first water removal agent, a thixotropic agent, a first catalyst and a second catalyst; the second component comprises epoxy resin, diisocyanate, polyisocyanate, a heat-conducting filler, a coupling agent, a second dewatering agent, a dispersing agent and a retarder; the modified bio-based polyol is selected from at least one of modified castor oil polyol, modified grease polyol and modified cashew nut shell oil polyol; the polythiol is selected from at least one of trimethylolpropane tri (3-mercaptopropionic acid ester), pentaerythritol tetra (3-mercaptopropionic acid ester), butanediol mercaptopropionic acid ester and polythiol. Through the arrangement, the heat-conducting polyurethane structural adhesive has relatively long openable time, and is rapidly cured at room temperature within a short time to generate relatively high initial curing strength.

The invention belongs to the technical field of optical materials, and particularly relates to an environment-friendly mercaptan optical resin material and a preparation method thereof. Comprising the following steps: (1) uniformly mixing a catalyst, a release agent and a polyisocyanate compound to prepare a mixture; (2) adding titanium dioxide nanoparticles with different particle sizes, which are modified by a polythiol compound and a sulfydryl silane coupling agent, into the mixture; and (3) heating and curing to prepare the environment-friendly mercaptan optical resin material. On the basis of small-particle-size titanium dioxide, a small amount of large-particle-size titanium dioxide is added. The large-particle-size titanium dioxide is not prone to agglomeration and good in dispersity, in the blending process, the granular large-particle-size titanium dioxide is easier to disperse, and agglomeration of small-particle-size titanium dioxide is prevented. Due to the addition of the small-particle-size titanium dioxide and the large-particle-size titanium dioxide, the mechanical strength of the mercaptan optical resin is further improved on the basis of maintaining the high refractive index of the mercaptan optical resin.

The invention discloses a medical washable high-temperature-resistant modified polyester fiber fabric and a preparation method thereof, and relates to the technical field of fabrics. The medical washable high-temperature-resistant modified polyester fiber fabric prepared by the invention is obtained by blending, spinning and weaving modified polyester and modified mica and activating with sodium hypochlorite; the modified polyester is obtained by grafting organic silicon modified polyester with n-dodecanethiol and then reacting with bromooctylhydantoin; the modified mica is prepared by polymerizing diethyl phosphite and bisphenol S on the surface of the pretreated mica, grafting a vinyl monomer and then reducing; the vinyl monomer is obtained by carrying out a reaction on 1-allyl-3-cyano-6-hydroxy-4-methyl-2-pyridone and an azo salt, and the vinyl monomer is obtained by carrying out a reaction on 1-allyl-3-cyano-6-hydroxy-4-methyl-2-pyridone and an azo salt; the medical washable high-temperature-resistant modified polyester fiber fabric prepared by the invention has good antibacterial, anti-aging and flame-retardant properties.

The invention discloses a method for preparing 12-mercaptan through solid organic acid catalysis, belongs to the technical field of 12-mercaptan preparation, and aims to solve the problems of low catalyst activity, harsh reaction conditions, serious pollution, high cost and dependence on import in the prior art. N-dodecanol and hydrogen sulfide are used as raw materials and are mixed according to the molar ratio of 1: 1.2-1: 1.3; the method comprises the following steps: gasifying n-dodecanol, mixing with purified hydrogen sulfide, preheating to 210-240 DEG C, introducing into a fixed bed reactor filled with a solid organic acid catalyst, and reacting at-0.08-3.0 MPa for 3.5-4 hours; and cooling and condensing the reaction product, carrying out gas-liquid separation, rectifying and purifying the liquid product to obtain 12-mercaptan with the purity of more than or equal to 99.5%, and recycling unreacted hydrogen sulfide. The solid organic acid can be a catalyst of p-toluenesulfonic acid and the like or mesoporous silica loaded nickel, cobalt and molybdenum metal oxides. The method has the advantages of high catalytic activity, mild reaction conditions, high product yield (the conversion rate of n-dodecanol is greater than or equal to 94.5%), environmental protection and low cost, can realize the domestic mass production of 12-mercaptan, and meets the market demand.

The invention discloses a preparation method of a polymer dispersed liquid crystal holographic grating with s polarization high diffraction characteristics, and belongs to the technical field of holographic optics. Raw materials comprise 60-90% of a thiol-ene monomer, 10-40% of liquid crystals, a photoinitiator accounting for 1.25% of the mass of the monomer, and a coinitiator accounting for 1.56% of the mass of the monomer. Light with the wavelength of 532 nm and the light intensity of 5-30 mW / cm < 2 > is used for carrying out double-interference photoetching to generate photochemical reaction so as to generate the polymer grating film, and the light is s polarized light. Under the optimal recording condition, delta n under s polarization can reach 1.93 * 10, and delta n under p polarization can reach 1.21 * 10. In combination with morphology analysis, it is found that refractive index modulation strongly depends on the proportion of a liquid crystal-rich phase to a polymer-rich phase in the grating. It is proved that the size of liquid crystal microdroplets formed by holographic recording is larger due to low recording intensity, and therefore the threshold driving voltage of the HPDLC grating is reduced.

The invention relates to the technical field of silicon dioxide surface modification, in particular to a silicon dioxide hollow sphere with an MOF composite layer, a manufacturing method and a dielectric loss prediction method. The silicon dioxide hollow sphere comprises a hollow spherical structure formed by silicon dioxide, an amino silane layer grafted on the surface of an inner core layer through a covalent bond, a ZIF-8 crystal layer growing in situ by taking amino as a nucleation site, and thiol groups distributed on the outer surface of an MOF crystal. According to the silicon dioxide hollow sphere with the MOF composite layer, the manufacturing method and the dielectric loss prediction method, the silicon dioxide hollow sphere with the MOF composite layer has good compatibility and stability in an LCP matrix, the dielectric loss is small, and the performance of a high-frequency FPC is effectively improved.

The invention discloses a phosphorus-sulfur synergistic flame retardant with high gas phase activity, a durable flame-retardant nylon fabric and a preparation method of the flame-retardant nylon fabric, and relates to the technical field of flame-retardant nylon fabric preparation.The preparation method of the phosphorus-sulfur synergistic flame retardant comprises the steps that 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide and polyepoxide are mixed and heated to be molten for a reaction, and the phosphorus-sulfur synergistic flame retardant is obtained; obtaining an intermediate after the reaction is finished; the intermediate and a thiophenethiol derivative are subjected to a click chemical reaction, and a 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide derivative containing phosphorus and sulfur is obtained; the preparation method comprises the following steps: dissolving a 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide derivative containing phosphorus and sulfur into a mixed solvent of ethanol and water, so as to obtain the phosphorus-sulfur synergistic flame retardant with high gas phase activity. The raw materials are safe and environmentally friendly, the preparation method is simple, and the prepared flame-retardant nylon fabric is excellent in flame retardance and washing resistance and free of pollution in the using process.

The invention discloses an impact-resistant industrial coating and a manufacturing method thereof, and relates to the technical field of industrial coatings. The impact-resistant industrial coating comprises the following raw materials in parts by weight: 80-100 parts of epoxy resin, 2-5 parts of graphene oxide, 3-5 parts of an antistatic agent, 5-8 parts of a modified thickener, 1-3 parts of a dispersant, 0.5-1.5 parts of a leveling agent, 2-3 parts of an antioxidant, 8-12 parts of a curing agent and 100-140 parts of deionized water. The preparation method comprises the following steps: reacting polyethylene glycol diethylene oxide methyl ether with 2-(methacrylic acid) ethyl ester 3, 5-diaminobenzoic acid to generate a polymer; reacting the polymer with 3-(dimethylamino)-1-propanethiol to generate a tertiary amine-terminated polymer; and carrying out quaternization reaction on the tertiary amine-terminated polymer and bromododecane to obtain the antistatic agent. The impact-resistant industrial coating prepared by the invention has excellent antistatic property and rheological property.

The invention provides a method 100 for separating different polymeric spectacle lens materials in a mixture comprising at least two different polymeric spectacle lens materials by separating at least one polymeric spectacle lens material of the at least two different polymeric spectacle lens materials by using their different physical behavior and / or chemical behavior, wherein the at least two different polymeric spectacle lens materials are selected from the group consisting of polyallyl carbonate, polyurea, polyurethane, polyurethane / polyurea, polycarbonate, polyepisulfide and polythiourethane. The invention further provides a method for separating at least one polythiourethane from a mixture comprising at least two different polythiourethanes by thiolysis.

The invention belongs to the technical field of adhesives, and particularly relates to a polyurethane super-strong adhesive as well as a preparation method and application thereof. The preparation method comprises the following steps: mixing branched-chain multi-mercapto mercaptan with an epoxy compound, adding a catalyst for reaction, and then adding a neutralizer for terminating the reaction to prepare an epoxy prepolymer; the preparation method comprises the following steps: mixing an epoxy prepolymer with branched chain multi-mercapto mercaptan to prepare a mixture; and mixing the mixture with isocyanate, reacting to obtain a product, and defoaming the product to obtain the polyurethane super-strong adhesive. The sulfur element is introduced into a polymer molecular chain, so that the bonding performance between the base cloth (base cloth) and the coating is remarkably improved, meanwhile, the water resistance, solvent resistance and low temperature resistance are also greatly improved, the method is suitable for humid, low-temperature and organic solvent environments, no solvent participates in the preparation process, and the environment-friendly requirement is met.

A thiol masterbatch composition for preparing a UV curable composition is provided, the thiol masterbatch composition comprising at least 70% by weight of a thiol compound, and at least one stabilizer. A kit for providing an ultraviolet curable composition includes: a first portion including a thiol masterbatch composition therein; and a second portion separate from the first portion and including a (meth) acrylate composition therein. A method of making a UV curable composition includes combining a thiol masterbatch composition and a (meth) acrylate composition.

The invention discloses a bio-based super-hydrophobic ultraviolet curing coating which is prepared from the following raw materials in parts by weight: 33-66 parts of plant oil-based active monomers, 20-45 parts of polythiol, 1-40 parts of modified cellulose, 15-150 parts of an organic solvent and 1-5 parts of a photoinitiator, wherein the plant oil-based active monomer is prepared from epoxidized plant oil, unsaturated organic matters and a Lewis acid catalyst, and the unsaturated organic matters contain hydroxyl and carbon-carbon double bonds located at the tail end of a molecular chain. According to the bio-based super-hydrophobic ultraviolet curing coating disclosed by the invention, a three-dimensional interpenetrating network structure is obtained by cross-linking the plant oil-based active monomer, the polythiol and the cellulose in an ultraviolet curing process, a chemical bonding type surface microstructure super-hydrophobic material with excellent wear resistance is constructed, and the preparation method is simple. The invention further discloses application of the bio-based super-hydrophobic ultraviolet curing coating in surface treatment of a base material.

The invention discloses a high-performance modified resin material and a preparation method thereof, and belongs to the technical field of resin composite material preparation. The high-performance modified resin material is prepared from a main agent, a curing agent and nano filler, the main agent is prepared from 70 to 100 parts of bisphenol epoxy resin, 20 to 40 parts of dopamine modified epoxy resin, 5 to 15 parts of diglycidyl ether, 3 to 15 parts of flame retardant, 0.3 to 1 part of anti-settling agent, 0.05 to 0.3 part of defoaming agent and 0.1 to 0.5 part of pigment; the curing agent is prepared from the following components in parts by weight: 15-35 parts of a rapid curing agent, 10-30 parts of a toughening curing agent, 5-15 parts of a dopamine modified amine curing agent, 0.5-3 parts of an accelerant and 0.1-0.5 part of an antioxidant; and the nano filler is nano-particle coated PDA (potato dextrose agar). Amino of dopamine reacts with epoxy group, catechol is oxidized to generate a quinoneform structure, thiol-epoxy click reaction is catalyzed, and the material can be rapidly cured at low temperature; a flexible chain (-S-CH-CH-) of polymercaptan and a polyether chain of amine-terminated polyether are synergistically toughened, so that the toughness and impact resistance of the material can be improved.

The invention relates to a method for constructing a composite super-hydrophobic coating through double bonding. The preparation method comprises the following steps: taking a clean copper sheet which is not pretreated as a substrate, dipping the copper sheet in a suspension consisting of nanoparticles and sulfydryl-containing siloxane ethanol, taking out, washing, drying, dipping in a perfluoromercaptan ethanol solution, taking out, washing, and drying to obtain the copper-based super-hydrophobic surface coating. The coating prepared by the method has excellent super-hydrophobicity, icing resistance and stability. Different from an existing conventional preparation method, the method has the advantages that pretreatment operation such as abrasive paper polishing, strong acid etching or anodic oxidation does not need to be carried out on a copper sheet, and micro-nano roughening and low-surface-energy self-assembly can be completed on the copper surface only through two-step normal-temperature dipping. The method is simple in preparation process, mild in condition, free of expensive equipment, thin in coating thickness and small in influence on electric conduction and heat conduction of the copper substrate, intrinsic performance of copper can be reserved, the electric conduction / heat conduction characteristic of the copper substrate is considered, and the method has wide application value and prospects.

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 discloses an anti-ultraviolet automobile window film and a preparation method thereof, and relates to the field of high polymer materials. When the anti-ultraviolet automobile window film is prepared, methylcyclotetrasiloxane, octamethylcyclotetrasiloxane, 3-glycidyl propyl (dimethoxy) methylsilane and 1, 3-bis (3-aminopropyl)-1, 1, 3, 3-tetramethyldisiloxane are subjected to a reaction, and modified polysiloxane is prepared; the preparation method comprises the following steps: reacting benzo [1, 2-d: 5, 4-d '] bis (oxazole)-2, 6-dithiol with 4-aminobenzoyl chloride to prepare a modified ultraviolet absorbent; isophorone diisocyanate, polytetrahydrofuran ether glycol, the modified polypyrrole particles, the modified polysiloxane and the modified ultraviolet absorbent are subjected to a reaction, and the reaction product is spread in a mold. The anti-ultraviolet automobile window film prepared by the invention has good anti-ultraviolet, heat-insulating, flame-retardant and anti-aging properties and good mechanical properties.

The invention discloses a negative electrode interface self-repairing material, a negative electrode plate, a positive electrode interface material, a positive electrode plate, a solid electrolyte, a solid-state battery and an electric device, and relates to the technical field of batteries, the negative electrode interface self-repairing material comprises a porous material and a self-repairing material, the self-repairing material comprises a core layer material and a shell layer material at least partially coating the surface of the core layer material, the material of the core layer comprises a thiol-olefin repairing agent and a photoinitiator; the material of the shell layer comprises a self-repairing polymer. Silicon expansion can be inhibited through the porous electrolyte, meanwhile, an ion guide channel is constructed, interface impedance is reduced, meanwhile, the porous electrolyte is stable in chemical performance and compatible with a silicon-based material, and side reactions can be reduced. A three-dimensional network is formed through a mercaptan-olefin click chemical reaction of the self-repairing polymer, in-situ crosslinking can be triggered when cracks are generated, interface cracks can be rapidly and dynamically repaired, fracture of a conductive ion channel is reduced, and therefore interface impedance is reduced.

The present invention provides a polymer production method comprising: (1) a step in which a monomer starting material including a prescribed monomer is polymerized by living radical polymerization using a radical initiator and a RAFT agent to obtain a polymer P-1 having a terminal structure that includes, at a terminal of the main chain thereof, a sulfur atom derived from the RAFT agent; (2) a step in which, subsequent to step (1), a radical generator and a thiol compound are added to a solution including the polymer P-1 and the same is heated to remove the terminal structure from the main chain of the polymer P-1; and (3) a step in which, subsequent to step (2), the solution including the polymer P-1 with the terminal structure removed therefrom is mixed with a poor solvent to precipitate the polymer as a solid and purify the same.

The invention discloses a preparation method of a waterborne polyurethane dispersion with excellent corrosion resistance, which comprises the following steps: (1) firstly carrying out vacuum dehydration on polyol, a micromolecular polyhydroxy chain extender and a hydrophilic chain extender, and then adding polyisocyanate to carry out polymerization reaction; the preparation method comprises the following steps: firstly, adding an alkynyl silane coupling agent into a reaction kettle, then adding micromolecular diol, diol containing an alkynyl side chain and a micromolecular diamine chain extender, carrying out a chain extension reaction, and finally, adding a monoamino silane coupling agent, and carrying out an end capping reaction, so as to prepare a polyurethane polymer; (2) dispersing the polyurethane polymer solution into water to obtain a polymer emulsion; and (3) adding a dithiol compound and an initiator into the polymer emulsion, so that an alkyne group on a polymer side chain and a sulfydryl of thiol are subjected to a click coupling reaction, and the waterborne polyurethane dispersion with the side chain containing free sulfydryl is obtained. According to the invention, the micromolecular mercaptan corrosion inhibitor is grafted to a side chain of a waterborne polyurethane molecule, and the obtained waterborne polyurethane has significantly improved corrosion resistance.