3466 results about "Prepolymer" patented technology

The invention relates to a flexible aqueous binder for a lithium battery negative electrode and a preparation method thereof. The preparation method comprises the following steps: firstly, preparing a flexible polyurethane prepolymer containing vinyl by taking hydroxyl-terminated polybutadiene, isocyanate and hydroxyl acrylate as main raw materials; vinyl-containing compounds such as water-soluble acrylic acid (salt) or acrylamide, oil-soluble acrylic ester or acrylonitrile and the like are used as monomers and are combined with a flexible polyurethane prepolymer to prepare the negative water-based binder with flexible cross-linking points through free radical polymerization. The aqueous binder prepared by the technical method provided by the invention can realize point-to-point and point-to-line bonding modes with a pole piece active substance on a microstructure, so that the bonding strength of the active layer material and a copper foil is improved on the premise of not influencing the electrolyte resistance of the binder; and the flexibility of the negative pole piece and the subsequent processing stability are obviously improved.

The invention discloses an uvioresistant acrylic resin coating and a preparation method thereof, and belongs to the technical field of acrylic resin paints.The uvioresistant acrylic resin coating is characterized in that step-by-step functional design is adopted, a functional polyurethane prepolymer is constructed through prepolymerization reaction and double-bond end capping, fluorosilicone modified acrylate emulsion is prepared through a core-shell emulsion polymerization process, and the uvioresistant acrylic resin coating is obtained. Then carrying out surface silane modification on hexagonal boron nitride and carrying out composite coating to obtain a modified boron nitride auxiliary agent; and finally, carrying out composite emulsification and dispersion compounding on all the components to obtain the anti-ultraviolet acrylic resin coating. Through the synergistic enhancement effect of the fluorosilicone modified core-shell structure and the surface modified boron nitride, the ultraviolet aging resistance and the insulation reliability of the coating are remarkably improved on the basis of keeping high adhesive force, excellent flexibility and impact resistance of the coating; the problems that a traditional acrylic coating is prone to yellowing and pulverization under long-term ultraviolet radiation, and the mechanical property is reduced are effectively solved, and the acrylic coating is suitable for the field of electronic equipment protective coatings with high requirements for weather resistance, mechanical strength and electrical insulating property.

The invention provides a preparation method of a self-repairing resin-based composite material based on dynamic bonds. The self-repairing epoxy resin comprises one covalent dynamic bond of a Diels-Alder bond, a disulfide bond or a borate bond, and the preparation method of the self-repairing epoxy resin comprises the following steps: heating epoxy resin to a molten state, adding a curing agent component while stirring, and carrying out a prepolymerization reaction to obtain a prepolymer; the curing agent comprises a rigid diamine curing agent, a dynamic diamine monomer and a flexible chain segment regulator, and the dynamic diamine monomer contains a dynamic covalent bond; and carrying out curing molding on the prepolymer to obtain the self-repairing epoxy resin. And impregnating reinforced fibers or fabrics thereof with the prepared prepolymer, and heating and curing to obtain the self-repairing resin-based composite material. The invention provides a chemical molecule design, dynamic reversible chemical bonds are introduced into a resin matrix, and by constructing the dynamic bonds, the composite material has high performance of a traditional composite material and also has life-like self-healing ability.

The invention discloses a quick-curing polyurethane seamless expansion joint material for roads and a preparation method, and belongs to the technical field of road engineering materials. The material is prepared from polyether polyol, polycaprolactone glycol, a bisphenol A epoxy-polyether block isocyanate terminated prepolymer, a methyl phenyl silicon-boron hybrid hydroxyl chain extender, diphenylmethane diisocyanate, calcium carbonate, wollastonite, a hindered amine anti-aging agent and dioctyl phthalate. Wherein the bisphenol A epoxy-polyether block isocyanate terminated prepolymer is prepared by the following steps: reacting bisphenol A with epoxy chloropropane to generate epoxy resin, reacting with polytetramethylene ether glycol, and introducing isophorone diisocyanate; the methyl phenyl silicon-boron hybrid hydroxyl chain extender is prepared by carrying out hydrosilylation and ethylene glycol reaction on methyl trimethoxy silane, 3-glycidyl ether oxypropyl trimethoxy silane and allylboronic acid pinacol ester; and the methyl phenyl silicon-boron hybrid hydroxyl chain extender is prepared by carrying out hydrosilylation on methyl trimethoxy silane, 3-glycidyl ether oxypropyl trimethoxy silane and allylboronic acid pinacol ester. The material has the advantages of quick curing property, weather resistance and high-temperature stability, and is suitable for road seamless expansion joint scenes.

The invention discloses a reprocessable solid-solid phase change material based on dynamic borate bonds and a preparation method of the reprocessable solid-solid phase change material. Based on the mechanism that boric acid ester is subjected to ester exchange during thermal stimulation, a dynamic cross-linking agent containing boric acid ester is adopted for cross-linking a polyurethane prepolymer, polyethylene glycol is cross-linked through chemical bonds, the tensile strength and the elongation at break of the phase change material are improved, and the problem that the phase change material is prone to leakage in the phase change process is solved; besides, borate bonds belong to associated dynamic covalent bonds and can keep the crosslinking density of the material unchanged when ester exchange occurs under thermal stimulation, so that the thermal stability of the material is relatively good; the solid-solid phase change material disclosed by the invention is excellent in mechanical property, has a relatively high enthalpy value, can be reprocessed, and has an application prospect in the fields of thermal management, energy storage, infrared stealth and the like.

The invention belongs to the technical field of high polymer materials, and particularly relates to bio-based light-cured polyurethane acrylate resin as well as a preparation method and application thereof. The preparation method of the bio-based light-cured polyurethane acrylate resin comprises the following steps: (1) mixing a catalyst, a first polymerization inhibitor, first hydroxyl acrylate and itaconic acid, stirring and reacting at 90-120 DEG C for 6-9 hours to obtain a reaction product, then adding epoxidized soybean oil, and stirring at 90-120 DEG C for 3-5 hours to obtain a prepolymer; and (2) cooling the prepolymer obtained in the step (1) to room temperature, dropwise adding second acrylic hydroxyl ester and diisocyanate, and then stirring and reacting at 30-60 DEG C for 1.5-4 hours until an NCO infrared peak value disappears, thereby obtaining the polyurethane acrylate. The resin is high in bio-based content, moderate in viscosity, good in flexibility, high in hardness, strong in adhesive force, high in glossiness, small in smell and good in storage stability, and is suitable for being applied to preparation of UV curing coatings, UV curing printing ink, UV curing adhesives, 3D printing materials and nail polish glue.

The invention relates to the technical field of coatings, in particular to an acrylate-epoxy resin composite coating and a preparation method thereof. According to the technical scheme, the coating is prepared from 25 to 35 parts of methyl methacrylate, 15 to 25 parts of butyl acrylate, 10 to 20 parts of epoxy resin E-5110, 8 to 15 parts of organic silicon modified acrylate prepolymer, 5 to 12 parts of fluorocarbon modified epoxy resin, 4 to 8 parts of core-shell structure corrosion inhibition nano container, 1 to 3 parts of functionalized graphene quantum dots and 4 to 10 parts of polyhedral oligomeric silsesquioxane maleimide modified amine curing agent. And 1-3 parts of a hindered amine light stabilizer. By integrating the core-shell structure corrosion inhibition nano container, the functionalized graphene quantum dots and the photo-thermal dual responsive curing agent component, the sensing, response and self-repairing of the coating on damage are realized, and long-acting corrosion resistance, weather resistance, bacteria resistance, mechanical property balance and intelligent maintenance are considered; and efficient and economical full-period protection is provided for equipment in an extreme environment.

The invention relates to the technical field of polyurethane impermeable materials, and particularly discloses a high-molecular impermeable material with oil resistance and impermeability as well as a preparation method and application thereof, and the high-molecular impermeable material comprises the following components in parts by weight: 120 parts of a polyurethane prepolymer, 20-45 parts of a diluent, 10-30 parts of an auxiliary agent, 15-20 parts of a micro-powder filler, 10-15 parts of carboxymethyl cellulose and 3-8 parts of dibasic hydrogen phosphate; wherein the polyurethane prepolymer is prepared from a diisocyanate compound and polyether polyol through a reaction; wherein the micro powder filler is a mixture of sodium acrylate hydrogel micro powder and sodium alginate hydrogel micro powder; wherein the dibasic hydrogen phosphate is monovalent ion salt. The high-molecular anti-seepage material has excellent anti-seepage performance in an oil storage environment, has relatively high adhesive force, and can be suitable for grouting in a humid environment; and water resistance and oil resistance of an underground water-sealed stone cavern oil depot environment can be better realized.

The invention relates to a high-temperature-resistant and high-salt-resistant carbon dot-hydrogel blocking agent and a preparation method and application thereof.The preparation method comprises the following steps that a reaction monomer, an initiator, an organic cross-linking agent and an inorganic cross-linking agent are added into water to be evenly mixed, and a precursor mixed solution is obtained; adding a polysaccharide polymer into the precursor mixed solution, and stirring and dissolving to obtain a hydrogel prepolymer; polymerizing and partially hydrolyzing the hydrogel prepolymer to obtain partially hydrolyzed interpenetrating network hydrogel; the partially hydrolyzed interpenetrating network hydrogel is carbonized at the constant temperature of 50-70 DEG C to form carbon dots, and the carbon dot-hydrogel blocking agent is obtained. The prepared carbon dot-hydrogel has the advantages that synthesis is green, raw materials are easy to obtain, and toxic reagents do not need to be introduced; the nano enhancement effect of the carbon dots and the physical entanglement effect of the polysaccharide polymer enable the obtained hydrogel to have high toughness and compression strength after high salinity and high-temperature aging, and the hydrogel can be used for profile control and water shutoff of high-temperature and high-salinity oil reservoirs so as to improve the recovery rate of crude oil.

The invention relates to the technical field of semiconductors, and discloses a preparation method of a heat-conducting polyurethane polishing pad, which comprises the following steps: coupling a silane coupling agent with a hydroxylated inorganic heat-conducting material, and carrying out condensation reaction on silanol groups in the silane coupling agent and hydroxyl groups in the hydroxylated inorganic heat-conducting material to form Si-O-Si covalent bonds; bridging a hydroxylated inorganic heat-conducting material at one end of a silane coupling agent to obtain an intermediate; the intermediate is an inorganic heat-conducting material modified by a silane coupling agent; mixing the polyurethane prepolymer with the intermediate to form a mixed prepolymer, and curing the mixed prepolymer at a first temperature to obtain heat-conducting polyurethane; or curing the polyurethane prepolymer to obtain polyurethane, carrying out melt blending on the polyurethane and the intermediate at a second temperature, and curing at a first temperature to obtain heat-conducting polyurethane, in the heat-conducting polyurethane, polyurethane is bridged at the other end of the silane coupling agent. Compared with the prior art, the heat transfer and heat conduction performance of the polishing pad is effectively improved.

The invention relates to a long-life room-temperature phosphorescent material and a preparation method and application thereof.According to the phosphorescent material, epoxy resin is doped with an epoxy prepolymer containing a fluorine-containing chain segment to serve as a host matrix, F-pi and pi-pi non-covalent synergistic interaction is formed between the host matrix and aromatic fluorescent guest molecules, the energy level difference of the excited state is adjusted, and the phosphorescent material is obtained. Intersystem crossing (ISC) and radiative transition rates are optimized, so that the phosphorescence lifetime and environmental adaptability are improved; a fluorine-containing chain segment introduced into a polymer system can be enriched on the surface of a material to form a needle-shaped structure, so that the surface energy of the material is remarkably reduced, the antifouling property is excellent, and additional functions of lyophobicity, transparency, chemical stability and the like are also realized while ultra-long room-temperature phosphorescence is realized; and cooperative enhancement and multifunctional integration of optical performance and surface performance are realized.

The invention belongs to the technical field of functional finishing of textiles, and particularly relates to microcapsule emulsion with a pH indicating function, preparation of the microcapsule emulsion and application of the microcapsule emulsion in a textile finishing agent. The invention provides a preparation method of a microcapsule emulsion with a pH indication function, which comprises the following steps: reacting isocyanate with polyol to obtain a polyurethane prepolymer, mixing and dissolving the polyurethane prepolymer with a pH indicator solution, an acrylate monomer and an initiator to obtain an oil phase, and taking an aqueous solution of a polymer emulsifier as a water phase; then mixing and emulsifying the oil phase and the water phase, adding a chain extender, heating to carry out chain extension reaction, cross-linking to a certain degree to form a polyurethane-polyurea-polyacrylate hybrid shell layer on an oil-water interface, and coating a core material pH indicator to obtain the microcapsule emulsion with the pH indication function. According to the invention, the pH indicator is coated in the form of microcapsules for the first time, and industrial production and processing can be carried out.

The application discloses a kind of imitated plant leaf hydrogel composite material and preparation method thereof, belong to bionic composite material field.The application first by colorant compounding preparation printing paste, and fabric is printed, obtain the green fabric that can realize to plant leaf " green peak " and " red edge " spectral characteristic simulation, and with green fabric simulation leaf structure in fence organization and skeleton;Then with biomaterial polyvinyl alcohol (PVA) as base material, join with strong hygroscopic monomer and crosslinking agent, initiator blend preparation hydrogel prepolymer solution;Finally, hydrogel prepolymer solution is poured into the mold containing green fabric and copolymerization, it directly forms hydrogel in fabric surface and pore interior, obtains imitated plant leaf hydrogel composite material.The material gets rid of the dependence on hygroscopic salt, has water absorption and simulation effect stable, durability is good and the like advantages.

The invention discloses high-temperature-resistant fluorine-modified estersil and a preparation method thereof, and relates to the technical field of organosilicon materials.The high-temperature-resistant fluorine-modified estersil comprises a group A and a group B. The group A serves as a main base material and functional filler and is used for providing a film-forming framework and the high-temperature-resistant characteristic; the group B is a cross-linking curing unit and is used for regulating and controlling the reaction rate and the final cross-linking density; the component A comprises the following raw materials: a fluorine-terminated vinyl estersil prepolymer, a vinyl estersil diluent, surface fluorinated nano silicon dioxide, spherical aluminum oxide, an antioxidant and a defoaming agent; the component B comprises the following raw materials: a hydrogen-containing silyl ester cross-linking agent, a platinum catalyst and an inhibitor. A fluorine-terminated structure is introduced into a vinyl estersil prepolymer, and surface fluorinated nano silicon dioxide and spherical aluminum oxide are adopted for synergistic filling, so that the thermal stability and interface bonding force of the material are improved; the obtained high-temperature-resistant fluorine-modified estersil can still keep excellent mechanical strength and electrical insulation performance under the condition of 250-300 DEG C, and has the characteristics of low surface energy and pollution resistance at the same time.

The invention relates to the technical field of preparation of water-based functional polymer materials, in particular to a preparation method of water-based polyurethane slurry for sports shoe leather, which comprises the following steps: mixing polycarbonate diol, core-shell structure graphene oxide-polycaprolactone hybrid nanoparticles and dimethylolpropionic acid, and carrying out vacuum dehydration treatment, isophorone diisocyanate is added for a reaction, and a polyurethane prepolymer is obtained; after the polyurethane prepolymer is cooled, triethylamine is added for a neutralization reaction; under violent stirring, adding a mixture composed of 1, 4-butanediol and a hyperbranched organosilicon amino chain extender serving as a flexible functional core into the neutralized prepolymer to carry out chain extension reaction, and adding deionized water to carry out reversed-phase emulsification, so as to obtain a waterborne polyurethane emulsion; standing and curing the waterborne polyurethane emulsion at a preset temperature to obtain waterborne polyurethane slurry; the finally prepared shoe leather material has excellent wear resistance and excellent low-temperature bending durability.

The invention relates to a self-repairing hydrogen barrier composite coating for a hydrogen storage or transportation device as well as a preparation method and application of the self-repairing hydrogen barrier composite coating, and belongs to the technical field of hydrogen energy storage and transportation materials. The coating is of a double-layer structure and is composed of a bottom coating and a humidity response microcapsule self-repairing barrier layer. The humidity response microcapsule is composed of a capsule core containing a polyurethane prepolymer and a hybrid capsule shell formed by polyurethane and siloxane, and has good hydrogen barrier performance and environmental response characteristics. In a certain humidity environment, the microcapsule is stimulated to release the capsule core material, and in-situ self-repairing is achieved. The problem that a traditional hydrogen-resistant coating is short of repairing capacity is solved, and the hydrogen-resistant coating has a wide application prospect in the aspect of improving the safety of a hydrogen conveying and storage system.

The invention relates to high-strength all-water-blown polyurethane foam and a preparation method thereof. The high-strength all-water-blown polyurethane foam comprises the following components in parts by weight: a polyol composite material: 100 parts of polyether polyol, 2-8 parts of water, 0.5-3 parts of an amine catalyst, 0.2-2 parts of a gel catalyst, 1-5 parts of an organosilicon surfactant, 3-8 parts of a composite filler and 0-10 parts of an auxiliary agent; wherein the composite filler is formed by coating the surfaces of glass beads with porous nano silicon dioxide; the isocyanate material is an MDI (Diphenyl Diisocyanate) or TDI (Toluene Diisocyanate) prepolymer, and the isocyanate index of the MDI or TDI prepolymer is 100 to 120 percent. The surface of the glass bead is coated with a nano silicon dioxide porous shell layer in situ to form a unique'hard core-soft shell 'gradient interface structure, so that the interface bonding force between the filler and a polyurethane matrix is improved, stress transfer is optimized, and the foam material is endowed with excellent comprehensive mechanical properties, especially compressive strength and structural stability.

The invention relates to the technical field of films, in particular to a high-surface tension aluminized base film and a preparation method thereof. The method comprises the following steps: grafting modified fumed silica with a silane coupling agent KH-570, and grafting a ternary polymerization shell layer composed of 2-acrylamide-2-methylpropanesulfonic acid, lauryl methacrylate and glycidyl methacrylate on the surface of the modified fumed silica to obtain organic anti-sticking silica; secondly, synthesizing an aromatic sulfonated polyester prepolymer, loading nano titanium dioxide, and carrying out melt blending extrusion with polypropylene to form polar cluster polypropylene master batches; and finally, blending polypropylene resin, the master batch and maleic anhydride grafted polypropylene, and carrying out melt extrusion, air cooling and slow cooling and two-way stretching molding. The obtained base film is high in surface tension, high in aluminized layer adhesive force, excellent in oxygen and water vapor barrier property, good in thermal stability and suitable for the field of high-end packaging.

The invention discloses a UV curing adhesive for coating a low-refractive-index optical fiber and a processing method thereof, belongs to the technical field of adhesive preparation, and is used for solving the technical problem that the refractive index and the damp-heat resistance of the UV curing adhesive for coating the optical fiber in the prior art need to be further improved. The preparation method comprises the following steps: introducing a low-refractive-index hybrid siloxane prepolymer, a multi-component interface bonding prepolymer and a modified branched polyester prepolymer into a system together, and constructing a compact and uniform organic-inorganic three-dimensional network in a curing process by utilizing silica condensation, interface chemical bonding and a flexible chain segment cross-linking reaction, the low-refractive-index hybrid siloxane prepolymer endows a film layer with a stable refractive index, the multi-component interface bonding prepolymer enhances the binding force of a base material, the modified branched polyester prepolymer improves stress buffering and toughness, and the obtained cured film is low in refractive index, firm in interface bonding and small in mass change in a humid and hot environment and shows excellent optical stability and long-term reliability.

The invention provides a polyurethane composite material and application thereof, and relates to the technical field of polyurethane materials. The polyurethane composite material consists of a component A and a component B, the component A comprises the following raw material components in parts by weight: 100 parts of polymer dihydric alcohol, 1-8 parts of a chain extender, 1-3 parts of a catalyst, 0-5 parts of a cross-linking agent, 0.1-2 parts of a carbon-based material, 1-10 parts of an anthraquinone compound and 0.5-2 parts of water; and the component B is an isocyanate curing agent and comprises a prepolymer with a plurality of ester bonds and urea bonds. The polyurethane composite material disclosed by the invention has relatively high mechanical strength, wear resistance and the like, and is suitable for treating nitrogen-containing sewage.

The invention discloses a high-performance conductive adhesive doped with conductive nanoparticles, and belongs to the technical field of conductive adhesives. The high-performance conductive adhesive provided by the invention is prepared from the following raw materials in parts by weight: 50 to 100 parts of vinyl liquid silicone rubber, 100 to 400 parts of modified silver coated copper powder, 1 to 10 parts of nano silver powder I, 1 to 10 parts of epoxy silane modified prepolymer, 3 to 30 parts of hydrogen-containing silicone oil, 0.1 to 5 parts of platinum catalyst and 0.05 to 1 part of inhibitor. The silver-coated copper powder and the epoxy silane are modified, so that the conductivity and the binding power of the conductive adhesive are greatly improved, and the epoxy silane modified prepolymer can form strong covalent bond combination with the surface of an adhered object through a high-density epoxy group of the epoxy silane modified prepolymer; the nano-silver bulges on the surface of the modified silver coated copper powder increase the effective contact area and the number of contact points among the conductive filler particles, so that the conductive adhesive has the characteristics of high conductivity, low resistance, high adhesive strength and strong toughness.

The invention relates to the technical field of polyurethane material preparation, in particular to a polyurethane structural adhesive prepolymer online monitoring and quality control method and system.The method comprises the steps that raw material moisture content and feeding quality data are obtained, a raw material feeding threshold value is set, and whether a prepolymerization reaction is conducted or not is judged; collecting temperature data, viscosity data, isocyanate content, pressure data and stirring power data in real time to obtain real-time data flow; inputting the real-time data flow into a preset prepolymerization reaction prediction model for fusion analysis to obtain a reaction prediction result; generating a regulation and control instruction to optimize the prepolymerization reaction; and after the prepolymerization reaction, carrying out quality detection on the polyurethane prepolymer according to a release quality standard, and executing an automatic release decision. According to the invention, the problems of hysteresis quality, dependence on experience and data islanding of production quality control of the polyurethane prepolymer are effectively solved, and full-flow online monitoring and intelligent quality control from raw material feeding judgment to automatic release of product quality are realized.

The invention relates to the field of ink, in particular to bio-based elastomer heat transfer printing ink and a low-temperature microwave curing method thereof. The bio-based elastomer heat transfer printing ink at least comprises the following raw materials in parts by mass: 50-75 parts of a bio-based prepolymer, 5-10 parts of a cross-linking agent, 15-30 parts of an anti-pinhole agent, 0.5-1.5 parts of a curing catalyst, 5-15 parts of a pigment and 15-30 parts of a solvent. The bio-based elastomer thermal transfer printing ink finally prepared by the invention not only has an excellent transfer printing effect, but also can greatly improve the bio-based carbon content in the printing ink, and avoids the problems of environmental pollution and discontinuity; and on the other hand, compared with the traditional petroleum-based TPU ink, the required energy consumption is lower, the flexibility and the washability are also obviously improved, the pinhole defect is reduced, and the probability of secondary printing blooming caused by solvent migration is greatly reduced.

The invention relates to the technical field of shield tunnel construction, and discloses a shield tunnel segment joint waterproof material and a waterproof structure, the shield tunnel segment joint waterproof material comprises a component A and a component B; the component A comprises the following component: 30-40 parts of liquid polysulfide rubber; 5 to 10 parts of a fluorinated polyurethane prepolymer; 1-5 parts of a silane coupling agent; 3-5 parts of fumed silica; 8-15 parts of hollow glass beads; 10 to 15 parts of nano calcium carbonate; 0.5 to 2 parts of polytetrafluoroethylene micro powder; 0.1 to 1 part of ettringite; the component B comprises the following component: 1-5 parts of manganese dioxide; and 5 to 10 parts of dioctyl phthalate. By utilizing the characteristics that the sealing gasket has excellent fluidity during injection and can be automatically cured into a high elastomer within a set time, a pre-installed sealing gasket can be replaced by adopting an innovative injection process, and the construction difficulty faced by high-precision shield segment assembly in a high-water-pressure environment is effectively solved.

The invention belongs to the technical field of carbon fiber composite materials, and particularly relates to a carbon fiber reinforced composite material for an aerospace low-temperature storage tank and a preparation method of the carbon fiber reinforced composite material. The preparation method of the carbon fiber reinforced composite material for the aerospace low-temperature storage tank comprises the following steps: (1) preparing a polyamide acid prepolymer solution; (2) adding the polyamide acid prepolymer solution, a phosphorus-containing flame-retardant monomer and nano nitrile rubber into a solvent for reaction to prepare a sizing agent; (3) carbon fibers are soaked in the sizing agent, taken out and dried, and sized carbon fibers are obtained; and (4) mixing nano nitrile rubber with a resin matrix, and then carrying out prepolymerization and thermal imidization curing molding on the mixture and the sized carbon fibers to obtain the carbon fiber composite material. The carbon fiber reinforced composite material obtained by the invention not only has excellent liquid oxygen compatibility, but also can maintain excellent leakage resistance and mechanical properties in an extremely high and low temperature cycle environment, and provides technical support for application of aerospace low-temperature storage tanks.

The invention discloses a nanoimprint adhesive and a preparation method thereof, the nanoimprint adhesive is prepared from the following raw materials: an optical monomer, an acrylate prepolymer, a modified acrylate prepolymer, nanoparticles, a photoinitiator, a coupling agent and a diluent, the structural general formula of the optical monomer is shown in the specification, R1 is methyl or hydrogen, R2 is methyl or hydrogen, and R3 is methyl or hydrogen. And the difference between the refractive index of the nanoparticles and the refractive index of the optical monomer is greater than 0.4. According to the nanoimprint adhesive provided by the invention, the optical monomer and the nanoparticles have a synergistic effect, so that the refractive index of the cured nanoimprint adhesive can reach 1.7-1.8. The optical monomer can participate in curing together with other components to form a macromolecular or cross-linked network, so that the cured colloid can realize higher structural strength, nanoimprint demoulding is facilitated, the micro-nano structure is kept intact during demoulding, and the colloid is not easy to remain; and when a reliability test is carried out, the micro-nano structure on the cured colloid can be kept relatively complete, so that the production yield can be improved.

The invention is directed to a biodegradable, thermoplastic multiblock copolymer, to a process for preparing a biodegradable, thermoplastic multiblock copolymer, to the use of a biodegradable thermoplastic multiblock copolymer, to a composition for the delivery of at least one pharmacologically active compound to a host, and a medical device comprising a biodegradable, thermoplastic multiblock copolymer. The biodegradable, thermoplastic multiblock copolymers of the invention comprise at least one prepolymer (A) segment and at least one hydrolysable amorphous prepolymer (B) segment, wherein the segments are linked by a multifunctional chain extender, wherein the at least one prepolymer (A) segment comprises: a) one or more hydrolysable linkages, b) a water-soluble polyoxazoline-based polymer, and c) reaction products of one or more cyclic monomers and / or one or more non-cyclic monomers, wherein the water-soluble polyoxazoline-based polymer is a polymer containing a repeating unit of structure −[N(COR1)CH2CH2]n− where R1 is independently selected for each repeating unit from an alkyl group and n is 3-100, and wherein the multiblock copolymer is amorphous.

The invention belongs to the technical field of polyurethane, and provides polyurethane resin, polyurethane gloves and a preparation method and application thereof. The polyurethane resin is prepared from the following raw materials in percentage by mass: 5%-12.5% of modified organic silicon polyol, 5%-12.5% of bio-based polyol, 5%-8% of isocyanate, 0.01%-0.02% of an antioxidant, 0.001%-0.002% of a catalyst, 1%-2% of a chain extender, 0.1%-0.7% of polyether polyol, 0.02%-0.05% of a terminating agent and 71%-75% of a solvent, the preparation raw materials of the modified organic silicon polyol comprise a dihydroxyl-terminated organic silicon prepolymer and binary acid. The polyurethane glove prepared by compounding two specific polyhydric alcohol modified organic silicon polyhydric alcohol and bio-based polyhydric alcohol as well as other substances has good wear resistance and fingerprint-free characteristic, is easy to demould, and is suitable for the field of automobile film and chip manufacturing.

The present invention relates to the technical field of polymer compositions, particularly to a polyurethane toughened vinyl resin preparation method, which comprises: mixing a polyurethane prepolymer, a vinyl resin, a catalyst and a polymerization inhibitor to obtain an initial system, and stirring; the light transmittance of the initial system is detected, a phase separation starting point is determined according to the light transmittance change rate value and the light transmittance change acceleration value, and a homogeneous system is obtained; determining polymerization parameters according to the phase separation characteristic parameters; adjusting the homogeneous system to an initial polymerization temperature and an initial polymerization shear rate, and adding an initiator in batches according to the adding times of the initiator; and after the initiator is completely added, detecting the viscosity and temperature distribution of the homogeneous system to obtain a polymerization state index, and adjusting the polymerization temperature and the polymerization shear rate to obtain the high-toughness vinyl resin. According to the method, the problems that a phase separation point is difficult to accurately judge and the polymerization process is uncontrollable in the preparation of the polyurethane toughened vinyl resin, so that a network structure defect is caused are solved.

The invention relates to the technical field of chemical coatings, and discloses a paint formula containing an epoxy modified organic silicon resin liquid, which comprises the following raw materials by weight: 50-70 parts of an epoxy modified organic silicon resin liquid, 15-30 parts of a pigment filler, 5-15 parts of a functional auxiliary agent, 10-25 parts of a solvent, and 8-20 parts of a curing agent. Through graft copolymerization of an organosilicon prepolymer and epoxy resin, an organosilicon chain segment and an epoxy chain segment form stable chemical bonding on a molecular level, the organosilicon chain segment endows a paint film with excellent flexibility, heat resistance and hydrophobicity, and the epoxy chain segment provides strong adhesive force and chemical stability. The two components cooperate with each other to construct a composite three-dimensional network structure with rigid supporting and elastic buffering functions, so that the adhesion fastness of a paint film to a base material is enhanced, and the deformation recovery capability of the paint film under the action of thermal stress or mechanical stress is also improved, thereby realizing cooperative reinforcement of physical and mechanical properties of the paint film.