194 results about "Polypropylene glycol" patented technology

The invention provides bio-based MS base resin, bio-based MS glue and a preparation method of the bio-based MS base resin and the bio-based MS glue, and belongs to the technical field of high polymer materials. The MS base resin is isocyanate group silane terminated bio-based polyether polyol or polyether polyol subjected to chain extension. The polyether polyol is selected from one or more of bio-based polyethylene glycol, bio-based polypropylene glycol, bio-based poly (trimethylene ether glycol) and bio-based polytetrahydrofuran ether glycol. And mixing the bio-based MS base resin, the plasticizer, the filler, the catalyst III, the coupling agent and the auxiliary agent, and stirring under a vacuum condition to obtain the bio-based MS adhesive. The bio-based MS adhesive prepared by the invention is high in bio-based material content, uncomplicated in preparation process and low in energy consumption, and meanwhile, an adhesive body is good in mechanical property, high in stability and good in high temperature resistance and humidity and heat resistance.

The invention relates to a polyurethane-based composite solid polymer electrolyte film and a preparation method and application thereof, and belongs to the field of organic polymer solid electrolyte preparation. Polyethylene glycol-polypropylene glycol triblock copolymer and hydroxyl-terminated polybutadiene are used as soft segments, isophorone diisocyanate is used as a hard segment, and under the action of a catalyst, the polyurethane-based composite solid polymer electrolyte film is prepared. A chain extender containing disulfide bonds is utilized, and a polyurethane elastomer is prepared through gradual addition polymerization reaction; a polyurethane elastomer and a mixed solution of a lithium salt and a polyvinylidene fluoride-hexafluoropropylene copolymer are uniformly mixed, the polyurethane elastomer accounts for 10%-30% of the mass of the polyvinylidene fluoride-hexafluoropropylene copolymer, a precursor solution is obtained, the precursor solution is prepared into a film, and the polyurethane-based composite solid polymer electrolyte film is obtained. The polymer solid electrolyte membrane with excellent mechanical property and excellent lithium ion conductivity is constructed, and the development requirement of a high-performance lithium metal battery is met.

The application relates to the technical field of solar energy, in particular to a self-cleaning solar photovoltaic panel and a preparation process thereof. The application adds anhydrous ethanol, ammonia water, deionized water, methyl triethoxysilane, tetraethyl orthosilicate and octadecyl trimethoxysilane to prepare silica sol. Then, tetra(2-hydroxyethoxy)silane, polypropylene glycol, toluene diisocyanate, betulin, 3,4-diamino furazan, silica sol and a catalyst stannous octoate are added to prepare a polymer. Glass, ethylene-vinyl acetate copolymer, a cell piece and ethylene-vinyl acetate copolymer are sequentially laid in layers; the laminated assembly is assembled with a frame to obtain a solar photovoltaic panel. Finally, a coating is prepared by taking the polymer as a raw material, and the coating is coated on the solar photovoltaic panel to obtain a finished product. The finished product has good hydrophobicity and antibacterial property, and therefore has a wide application prospect.

The invention discloses a preparation method of a water-resistant and melting-resistant sodium silicate-based fireproof coating, and belongs to the technical field of preparation of fireproof materials and inorganic-organic hybrid coatings. The method comprises the following steps: (1) reacting isophorone diisocyanate with polypropylene glycol to prepare an isocyanate-terminated polyurethane prepolymer; (2) mixing the polyurethane prepolymer with piperazine pyrophosphate to obtain a component A; (3) mixing a sodium silicate aqueous solution with melamine to obtain a component B; and (4) mixing and curing the component A and the component B in proportion to obtain the coating. According to the invention, an isocyanate group in a polyurethane prepolymer and a sodium silicate aqueous solution are subjected to an in-situ chemical reaction, an organic hydrophobic network is constructed on the surface of an inorganic phase, and the water resistance of the coating is remarkably improved. Meanwhile, piperazine pyrophosphate and melamine form an intumescent flame-retardant system, the intumescent flame-retardant system and sodium silicate are synergistically promoted to form a compact and stable intumescent layer at high temperature, and the problems that a traditional water glass coating easily absorbs moisture and melts and flows at high temperature are effectively solved. The method is simple and controllable in process, and the prepared coating has excellent water resistance, fire resistance and heat insulation performance.

The invention discloses a surfactant with a branched structure as well as a preparation method and application of the surfactant. The preparation method comprises the following steps: carrying out Michael addition reaction on an amphiphilic branched polymer and polyfluorinated organic amine in an organic solvent in the presence of a catalyst to obtain the surfactant with the branched structure, the amphiphilic branched polymer has a hydrophilic chain segment and a hydrophobic chain segment, and the tail end of a branched molecular chain has double bonds. The amphiphilic branched polymer is obtained by copolymerization of polyethylene glycol di (methyl) acrylate and polypropylene glycol di (methyl) acrylate through active free radicals, or is prepared by Michael addition polymerization of a di (methyl) acrylate compound and a dimercapto compound or a diamine compound in an organic solvent in the presence of a catalyst. The surfactant can quickly reduce the surface tension and prolong the retention time of pesticide liquid, and is green, environment-friendly and degradable.

This invention discloses an electronic potting compound for encapsulating new energy power systems and its preparation method, belonging to the field of adhesive preparation technology. The electronic potting compound for encapsulating new energy power systems consists of component A and component B. Component A includes polypropylene glycol, dicyclohexylmethane diisocyanate, hydroxyl-terminated polydimethylsiloxane, bismuth-zinc composite catalyst, N,N-dimethylethanolamine, porous alumina supported filler, composite halogen-free flame retardant, thixotropic agent, defoamer, and surface-modified calcium sulfate whisker fibers. Component B includes polypropylene glycol and dicyclohexylmethane diisocyanate. The electronic potting compound prepared by this invention exhibits good thermal conductivity and electromagnetic shielding capabilities after curing, while also possessing high mechanical strength.

The invention relates to the field of auxiliary frame connecting bushings, in particular to a high-wear-resistance anti-aging new energy auxiliary frame connecting bush and a preparation method thereof, and aims at solving the problems that an auxiliary frame connecting bush is insufficient in wear resistance, poor in anti-aging performance and the like. The preparation method comprises the following steps: by taking a modified polyurethane solution as a matrix, sequentially adding modified nano silicon dioxide, modified multi-walled carbon nanotubes and polytetrafluoroethylene micro powder, uniformly mixing through ultrasonic dispersion and mechanical stirring, adding an anti-aging agent and polypropylene glycol dicyclohexyl acetate step by step, and sequentially stirring and uniformly mixing, so as to obtain a finished product. And adding dicumyl peroxide as a cross-linking agent, stirring until the system is uniform, injecting into a mold, carrying out thermal insulation cross-linking and vacuum drying, and demolding to obtain the high-wear-resistance anti-aging new energy auxiliary frame connecting bushing. The high-wear-resistance anti-aging new energy auxiliary frame connecting bush has the characteristics of high wear resistance and aging resistance and excellent mechanical strength and use stability.

The present application relates to the field of frother, in particular to a kind of copper flotation collector frother and preparation method thereof, by weight parts, including the following raw materials: N,N-dibutyl dithiocarbamic acid propyl cyanurate 100-120 parts, O-butyl-N-isobutyl thiopropyl carbamate 12-18 parts, xanthate 12-18 parts, phosphate ester polypropylene glycol ether 15-20 parts, modified betaine 5-8 parts, alcohol ether 3-5 parts, slime inhibitor 1-3 parts, alcohol ether carboxylate 2-5 parts, sorbitan monooleate 0.8-1.2 parts. Through the synergies of each raw material, the collector capacity, selectivity in copper flotation process can be effectively improved, and the reagent stability is good.

The invention relates to the technical field of sealants, and discloses a high-softness butyl sealant without sticking hands and softening wire harnesses and a preparation method of the high-softness butyl sealant. The butyl sealant is prepared from the following raw materials: 5-15 parts of butyl rubber; 3 to 15 parts of polyisobutene; 3-8 parts of petroleum resin; 30-60 parts of an inorganic filler; 15 to 30 parts of a flame retardant; 0.5 to 1.5 parts of a coloring agent; 5-15 parts of a polyester plasticizer; and 5-15 parts of rubber filling oil. The butyl rubber and the polyisobutene are mixed for use, and the hardness of the sealant is suitable for manual operation through a proper proportion; compared with the common plasticizer, the polyester plasticizer has the advantages that the polypropylene glycol adipate is large in molecular weight, low in volatility and low in mobility, cannot migrate to the wire harness from the sealant, and cannot soften the wire harness; the polyester plasticizer and the rubber filling oil are mixed for use, and the sealant has the effect of not sticking hands but sticking lines through a proper proportion.

The application belongs to the technical field of fine chemical industry, and discloses a method for synthesizing cyclopentanol, which comprises the following steps: (1) taking cyclopentene and water as raw materials, adding a solubilizer, and mixing to obtain a reaction liquid; (2) continuously hydrating the reaction liquid in a fixed bed reactor filled with a cation exchange resin to obtain a reaction product; and (3) distilling and separating the reaction product to obtain cyclopentanol. The synthesis method has the advantages of simple process flow, environmental protection, low energy consumption, excellent product indexes, and long operation cycle of the catalyst. Polyethylene glycol-400 or polypropylene glycol-400 is used as a single solubilizer, and a specific macroporous strong acid cation exchange resin catalyst is used to realize the efficient and high-selectivity hydration reaction of cyclopentene.

The invention discloses an antifouling elastic sofa fabric and a preparation method thereof, and relates to the technical field of fabrics. Diphenylmethane diisocyanate, polypropylene oxide glycol and modified silicon dioxide are subjected to surface reaction to prepare a nano waterproof finishing agent, and the modified silicon dioxide is prepared by modifying sodium hydroxide, so that the antistatic effect of the fabric can be improved; dL-3-fluorophenylalanine methyl ester hydrochloride is grafted to cotton fibers, fluorine-containing groups of the DL-3-fluorophenylalanine methyl ester hydrochloride are greatly enriched on the surface of the fabric, the low surface energy of the fabric is reduced, stains are prevented from being attached to the surface of the fabric, the antifouling effect is achieved, meanwhile, DL-3-fluorophenylalanine methyl ester hydrochloride can be bonded with the nano waterproof finishing agent, a net-shaped cross-linked structure is formed, and the anti-fouling effect is achieved. The nano waterproof finishing agent is adsorbed into fibers of the fabric, so that the waterproof and antifouling effects of the fabric are further improved. The fabric prepared by the invention has waterproof and antifouling effects.

The application belongs to the technical field of spraying materials, and particularly discloses a kind of corrosion-resistant spraying materials applied to railway freight cars and a preparation method thereof.The corrosion-resistant spraying material applied to railway freight cars provided by the application comprises component A and component B, component A comprises terminal isocyanate-based polyether type prepolymer and diphenylmethane-4,4'-diisocyanate;the terminal isocyanate-based polyether type prepolymer is prepared by reacting polyol compound and diphenylmethane-4,4'-diisocyanate;the polyol compound comprises polypropylene glycol, glycerol type polyether polyol and polyether polyol with a functionality of greater than or equal to 4.5.Component B comprises polyoxypropylene polyether polyol and diethyl toluene diamine.The application provides a corrosion-resistant, impact-resistant and strongly adhesive corrosion-resistant spraying material applied to railway freight cars by reasonably designing material components, which can effectively block corrosive media and protect the car body, and is suitable for complex railway freight transport scenarios.

The application discloses a GSH / pH dual-response Cu2O@Cu 2+ / ZIF-67@ZnPc core-shell structure nano drug, a preparation method and application thereof, and belongs to the technical field of metal organic framework materials as drug transportation carriers. First, Cu2O nanospheres are used as templates, sodium dodecyl sulfonate is used to change the potential of the Cu2O nanospheres, and then the Cu2O nanospheres are reacted with a cobalt nitrate hexahydrate solution and a 2-methyl imidazole methanol solution to obtain Cu2O@Cu 2+ / ZIF-67 core-shell structure nano material, and then a photosensitizer, a tetra-carboxy phthalocyanine zinc and a polypropylene glycol and ethylene oxide polyadduct are added to obtain the target nano drug. The nano drug is based on the synthesis of a uniform doped core-shell MOFs structure from a Cu2O self-template, has good product stability and high drug loading rate, and can activate chemical kinetics and photodynamic synergy treatment (CDT / PDT) in a tumor microenvironment.

The application relates to a salt-resistant oil displacement system for alkali-free binary compound flooding and a preparation method and application thereof, and belongs to the technical field of oil production. The oil displacement system is composed of the following components: 0.1-0.5 wt% of amino silane coupling agent modified xanthan gum, 0.1-0.5 wt% of a surfactant, 0.05-0.2 wt% of a high-temperature stabilizer, 0.05-0.1 wt% of chitosan quaternary ammonium salt, 0.05-0.1 wt% of silane coupling agent modified nano silicon dioxide, and the balance of water; the high-temperature stabilizer is one or more of polyvinyl alcohol, polyethylene glycol and polypropylene glycol. The oil displacement system provided by the application is compounded by taking xanthan gum as a core compound and a surfactant, is an oil displacement system for alkali-free binary compound flooding, utilizes the high-salt resistance of xanthan gum, and improves the defects of poor water solubility, easy decomposition at high temperature and easy degradation by bacteria, and has obvious improvement in profile control performance and can be used in a high-salt high-temperature environment.

An oil-in-water microemulsion comprising water; an oil selected from an ester oil, a triglyceride, or combinations thereof; a liquid non-ionic surfactant having an HLB from 7 to 13, preferably, from 9 to 13, and more preferably, from 9 to 11; and a polyethylene glycol / polypropylene glycol / polyethylene glycol triblock polymer having an HLB value from 15 to 29, preferably, 15 to 28, and more preferably, 16 to 27, wherein the microemulsion is transparent and mono-phasic, and wherein the pH of the microemulsion is from 4.5 to 7.5, preferably, from 5 to 7, and more preferably, from 5.5 to 7.

The invention discloses a high-elastic sweat-absorbent polyester yarn and a manufacturing method thereof, and belongs to the technical field of chemical fiber manufacturing, and the method comprises the following steps: preparing three copolyesters with matched intrinsic viscosity, preparing polypropylene glycol-containing hydrophilic copolyesters A and B through step-by-step esterification and copolycondensation, preparing polytetrahydrofuran-containing copolyester C through co-esterification, and preparing the high-elastic sweat-absorbent polyester yarn. And extruding through a multi-channel composite spinneret plate to form a calabash-shaped core layer and a spirally wound surface layer structure. According to the high-elasticity sweat-absorbent polyester yarn and the manufacturing method thereof, the fibers achieve moisture absorption and quick drying through the hydrophilic groups on the surface layer and the porous structure of the core layer, and the fibers and the calabash-shaped core layer cooperatively deform by means of the spiral elasticity design, so that the high-elasticity sweat-absorbent polyester yarn has high resilience and comfort.

The objective is to provide a moisture-curing hot-melt adhesive that has storage stability and excellent low-temperature adhesion, adhesion to SUS and PP, and heat retention. [Solution] The problem is solved by a moisture-curing hot-melt adhesive containing a urethane prepolymer (X) having isocyanate groups, which is a reaction product of a polyol compound (A) and a polyisocyanate (B), wherein the polyol compound (A) comprises polypropylene glycol (a1), a trifunctional or more polyether polyol (a2), and rosin polyol (a3), with the content of polypropylene glycol (a1) being 30% or more and less than 98% by mass per 100% by mass of polyol compound (A), the content of trifunctional or more polyether polyol (a2) being 1% or more and less than 5% by mass, and the content of rosin polyol (a3) ​​being 1% or more and 35% by mass or less.

This invention relates to the field of solder paste technology, and more particularly to an easily dispersible tin powder, its preparation method, and the solder paste thereof. The easily dispersible tin powder comprises, by weight, 10-20 parts tin powder, 1-2 parts N-aminoethyl-3-aminopropylmethyldimethoxysilane, 1.1-3 parts 3-aminopropyltriethoxysilane, 1-2 parts ascorbic acid, 0.5-1 parts polyvinylpyrrolidone, and 1-2 parts polyethylene glycol-polypropylene glycol-polyethylene glycol block copolymer. The solder paste comprises, by weight, 50-80 parts the easily dispersible tin powder, 10-20 parts rosin, 1-3 parts carboxylated carbon nanotubes, 1-2 parts nano-diatomaceous earth, 1-2 parts antioxidant, 1-5 parts activator, and 10-20 parts solvent. The solder paste obtained by this invention not only has good dispersibility, uniform texture, and strong stability, and is not prone to agglomeration, but also meets the requirements of ultra-fine pitch. Furthermore, due to its good fluidity during printing, it is less likely to clog the nozzle.

The title of the invention is' Controllable extension of flexible oligomeric glycols and methods thereof '. Disclosed is an extended diol composition comprising: a first component comprising a diol oligomer; and a second component comprising a bis (dimethylaminosilane) species wherein the first component is in a molar excess relative to the second component, and wherein the diol oligomer has a number average molecular weight Mn of from about 500 g / mol to about 5,000 g / mol. The diol oligomer may be alpha, omega hydroxyl terminated, or further includes an R group that is a polyether, such as a perfluoropolyether, polyoxymethylene, polyethylene glycol, polytetramethylene glycol, or poly (propylene glycol); or a polyester, such as poly (caprolactone), poly (lactic acid), or poly (glycolic acid). The bis (dimethylamino) silane species may include R1 and R2, which may include CH3, a vinyl group, and a phenyl group. A method for preparing the extended diol composition is also disclosed.

A composition comprising an oily medium system and an active ingredient, and a method of increasing the bioavailable rate of an active ingredient, where the method comprises incorporating the active ingredient into an oily medium system, and where the oily medium system contains a vegetable oil and / or a component of a vegetable oil, the liquid does not contain the following substances: a phosphate buffer solution, polyethylene glycol, dimethyl sulfoxide, ethanol, polypropylene glycol, polysorbate, ethyl acetate, 12-hydroxystearic acid hydroxyethyl ester and tocopherol polyethylene glycol succinate; the active ingredient is selected from the group consisting of compounds of formula (I) wherein T1 is a C6 cyclic hydrocarbon and R1 is a C1-C8 aliphatic hydrocarbon group, pharmaceutically acceptable salts thereof, and combinations thereof.

The invention discloses an antistatic waterborne polyurethane mortar coating and a preparation method thereof, and relates to the technical field of waterborne polyurethane, polylactic acid polyol and poly (1, 3-propylene glycol) polyol are subjected to prepolymerization, chain extension and other steps to prepare polylactic acid-based waterborne polyurethane, then the polylactic acid-based waterborne polyurethane is mixed with quartz sand, white cement, waterborne isocyanate, antistatic filler and auxiliaries, and the antistatic waterborne polyurethane mortar coating is prepared. The target coating is obtained. The anti-static chain extender and the anti-static filler cooperate with each other, hydrochloric acid acidification and hydroxylation modification are combined, the coating is endowed with excellent anti-static stability, mechanical properties and environmental friendliness, the VOC content is smaller than 5 g / L, and the anti-static coating meets the anti-static requirements of multiple scenes.

Provided is a means capable of sufficiently removing residues on a surface of an object to be polished while polishing the object to be polished at a moderate speed.Provided is a polishing composition containing: anionically-modified colloidal silica; a dispersing medium; an anionic water-soluble polymer which is a copolymer including a structural unit having a sulfonic acid group or a salt group thereof and a structural unit having a carboxy group or a salt group thereof; a polypropylene glycol having a weight average molecular weight of 200 or more and 700 or less; a nitrogen-free non-ionic polymer other than the polypropylene glycol having a weight average molecular weight of 200 or more and 700 or less; and a nitrogen-containing non-ionic polymer.

The invention relates to the technical field of building materials, and particularly discloses an anti-freezing concrete prefabricated part and a preparation method thereof, the anti-freezing concrete prefabricated part comprises the following raw materials by weight: 300-360 parts of cement, 40-60 parts of fly ash, 90-110 parts of mineral powder, 642-662 parts of natural sand, 1000-1100 parts of gravel, 7-9 parts of an additive, 150-170 parts of water, 0.5-1.5 parts of polypropylene glycol fiber, and 3-8 parts of phase change self-repairing microcapsules. The prepared anti-freezing concrete prefabricated part has the advantage of being good in anti-freezing performance.

This application relates to the field of coating technology, specifically disclosing a heat-insulating, flame-retardant, and anti-corrosion coating and its preparation method. A heat-insulating, flame-retardant, and anti-corrosion coating comprises the following raw materials in parts by weight: 50-80 parts of silicone-acrylic emulsion, 10-15 parts of epoxy resin, 30-40 parts of heat-insulating microcapsules, 15-21 parts of hollow glass microspheres, 3-5 parts of dispersant, 0.5-2 parts of polypropylene glycol diglycidyl ether, 1-5 parts of leveling agent, and 15-20 parts of water. The heat-insulating microcapsules comprise an aluminum powder core and a heat-insulating and flame-retardant capsule wall layer, the capsule wall layer material comprising acrylic resin and polyamide resin. The preparation method is as follows: hollow glass microspheres and heat-insulating microcapsules are added to silicone-acrylic emulsion and water and dispersed evenly to obtain a mixture; the dispersant, polypropylene glycol diglycidyl ether, epoxy resin, and leveling agent are added to the above mixture and mixed evenly to obtain the interior wall insulation coating. The composition of this application achieves a comprehensive improvement in heat insulation, flame retardancy, and anti-corrosion performance.

The invention discloses a preparation method of silicon-aluminum balls, and belongs to the technical field of molecular sieve carrier processing and forming. The preparation method comprises the following steps: mixing an aqueous solution containing an organic surfactant with a binder and a silicon-aluminum source to obtain spray slurry, carrying out spray drying after ball milling, and drying and roasting to obtain the silicon-aluminum balls, the binder is aluminum sol or silica sol; the organic surfactant is selected from at least one of polyethylene glycol, polypropylene glycol and polyvinylpyrrolidone. The silicon-aluminum ball preparation method provided by the invention has the advantages of simple process, low energy consumption, high purity, large specific surface area, large pore volume and large pore diameter, can be used for industrial production, and is a good molecular sieve carrier. The method provides an excellent condition for subsequent impregnation loading and ion exchange, can reduce the residual carbon accumulation rate and the risk of blocking pore channels, and greatly prolongs the service life of the final catalyst.

The invention discloses a sandal insole, a preparation method thereof and a sandal, and relates to the field of shoe materials. The sandal insole comprises a PU insole base material, and the PU insole base material is formed by reacting a material A and a material B; the material A comprises bifunctional polytetrahydrofuran ether, micromolecular straight-chain diol, branched-chain diol, a chemical foaming agent, a catalyst and polyether silicone oil; the branched chain diol is selected from at least one of 2-butyl-2-ethyl-1, 3-propylene glycol and 2, 2, 4-trimethyl-1, 3-pentanediol, and the branched chain diol is selected from at least one of 2-butyl-2-ethyl-1, 3-propylene glycol and 2, 2, 4-trimethyl-1, 3-pentanediol; the material B comprises an isocyanate component A and an isocyanate component B, the isocyanate component A is obtained by reaction of diphenylmethane diisocyanate, polypropylene oxide glycol, polypropylene oxide triol and carbodiimide modified diphenylmethane diisocyanate according to a specific ratio, and the isocyanate component B is isophorone diisocyanate. The sandal insole has the advantages of excellent seawater resistance, low compression set rate, good mechanical properties and long service life.

This application relates to the field of artificial stone technology, specifically to an artificial marble and its preparation method. The artificial marble of this application comprises the following components in parts by weight: 100 parts marble powder, 8-12 parts aliphatic polyisocyanate, 20-30 parts polypropylene glycol, 0.2-0.3 parts dibutyltin dilaurate, 10-15 parts cellulose ether modified magnesium lithium silicate, 5-7.5 parts polyvinyl acetate, and 2-3 parts flame retardant. This application uses aliphatic polyisocyanate to replace unsaturated polyester resin, reducing unsaturated double bonds in the system. Combined with cellulose ether modified magnesium lithium silicate and polyvinyl acetate, it improves the mechanical properties of the marble, thereby obtaining an artificial marble with excellent weather resistance, stain resistance, mechanical strength, and flame retardancy.

A nickel electrolyte for depositing a satin nickel layer, the nickel electrolyte comprising: (a) at least one source of nickel ions; (b) at least one chloride ion source; (c) at least one source of alkyl sulfonic acid zwitterions; (d) a primary brightener, wherein the primary brightener comprises saccharin or a salt thereof; (e) at least one sulfonic acid; (f) at least one polymer and / or copolymer based on polyethylene glycol and / or polypropylene glycol; (g) optionally, at least one wetting agent; and (h) optionally, at least one additional brightener. The invention further comprises a method for electrodepositing the satin nickel layer on the substrate.

The application discloses a self-emulsifying polyether amine curing agent and a preparation method and application thereof, and belongs to the field of high polymer materials. According to the application, components A-F are composed of polypropylene glycol or polytetrahydrofuran glycol with a molecular weight range of 800-2000, component B is selected from at least one of isophorone diamine, dicyclohexyl methane diamine or xylylenediamine, component C is at least one of epoxy derivatives containing long-chain alkyl and aromatic ring structures, component D is polyethylene glycol monomethyl ether amine with a polymerization degree range of 2-5 or an amine compound containing a sulfonic acid group, component E is a tertiary amine compound, and component F is at least one of a hindered phenol antioxidant and a phosphite antioxidant. The curing agent is reliably enhanced in reaction activity at normal temperature, the nucleophilic activity of terminal amino groups is significantly improved while excellent water dispersibility is maintained, and thus the curing rate at normal temperature is greatly accelerated.

The present invention provides a urethane (meth)acrylate and a method for producing the same, which can provide an active energy ray curable resin composition that has excellent transparency, resilience, and heat resistance and yields a low-hardness coating film (cured product), an active energy ray curable resin composition containing the urethane (meth)acrylate, a cured product of the active energy ray curable resin composition, and a laminate comprising the cured product. [Solution] A urethane (meth)acrylate having a structure derived from linear polypropylene glycol of the following formula (I), and containing a urethane bond and a (meth)acryloyl group. [Formula 1] TIFF2026115431000015.tif24170 (In formula (I), n1 represents a number between 10 and 100.)