1569 results about "Butyl acrylate" patented technology

Provided are a water-resistant wood-plastic reinforced composite flooring and a manufacturing method therefor. Wood flour is boiled in boiling water for 3-4 hours, filtered and dried, to obtain dried wood flour; polypropylene, butyl acrylate, methyl methacrylate, maleic anhydride and dicumyl peroxide are mixed evenly, extruded and granulated, and dried to obtain a compatibilizer; the dried wood flour and polypropylene are mixed evenly, the compatibilizer is added and mixed evenly, then extrusion and granulation, and injection molded, are performed, to obtain a wood-plastic flooring blank; a composite resin emulsion and a photoinitiator are ultrasonically mixed evenly, and the wood-plastic flooring blank is immersed therein, then taken out and dried at room temperature, and then vacuum dried and UV cured, to obtain water-resistant wood-plastic reinforced composite flooring.

The invention relates to the technical field of wood corrosion prevention and corrosion resistance treatment, in particular to a preparation process of a coating for improving the antibacterial and corrosion-resistant performance of wood. In order to improve the antibacterial and corrosion-resistant capabilities of the prepared coating, a corrosion-resistant antibacterial agent is prepared and added into the raw materials of the coating, and quaternary ammonium salt, guanidyl and other group structures are introduced into the corrosion-resistant antibacterial agent, so that the antibacterial performance on microorganisms such as fungi is realized; the introduction of fluorine can effectively improve the hydrophobicity of a coating of the paint and reduce the influence of water vapor on antibacterial components in the coating, and the introduction of allyl can enable the corrosion-resistant antibacterial agent to react with butyl acrylate and other raw materials under the action of an initiator to achieve the cross-linking ability, so that the loss of the corrosion-resistant antibacterial agent is effectively avoided, and the service life of the coating is prolonged. The antibacterial activity is kept for a long time.

The invention discloses a single-ion conductor polymer, a ternary composite binder solution, high-solid-content sulfide electrolyte slurry and a wet film forming method and application thereof, and belongs to the technical field of all-solid-state lithium batteries. The key technical problems in the wet membrane preparation of the sulfide electrolyte are solved through an innovative solvent-binder synergistic system, and the method specifically comprises the steps that 1, through the synergistic effect of a non-polar solvent and a weak-polar solvent, low-viscosity coating of high-solid-content slurry is achieved while the chemical stability of the sulfide electrolyte is guaranteed; 2, a poly (lithium styrenesulfonate-butyl acrylate), styrene butadiene rubber and polyisobutene ternary composite binder is designed, a lithium ion transmission channel is provided through a lithium sulfonate group, a benzene ring structure in the styrene butadiene rubber enhances the mechanical strength, long-chain alkane in the polyisobutene improves the interface adhesive force, and the mechanical strength is improved; the three components cooperate to realize balance of mechanical and electrochemical properties of the electrolyte membrane, so that the prepared electrolyte membrane has low porosity, high ionic conductivity and mechanical strength.

Disclosed in the present invention are a fluorosilicone-modified low-surface-energy antifouling coating and a preparation method therefor. The coating comprises the following components in parts by weight: 11-15 parts of butyl acrylate, 3-4 parts of dodecafluoroheptyl methacrylate, 3-4 parts of vinyl-terminated polydimethylsiloxane, 3-4 parts of 2-hydroxy-4-acryloyloxybenzophenone, 30-38 parts of methyl isobutyl ketone, 0.15-0.25 parts of azobisisobutyronitrile, 0.1-0.2 parts of sodium hydroxide, 2-3 parts of modified titanium dioxide nanoparticles, and 0.5-1.5 parts of 3-aminopropyltriethoxysilane. In the present invention, vinylpentamethyldisiloxane reacts with decamethylcyclopentasiloxane to prepare vinyl-terminated polydimethylsiloxane; a titanium dioxide precursor is mixed with polydopamine nanoparticles for modification to prepare modified titanium dioxide nanoparticles; and then the components above are mixed to prepare the fluorosilicone-modified low-surface-energy antifouling coating. The coating has low surface energy and good adhesion and ultraviolet resistance.

The invention belongs to the technical field of sewage treatment, and particularly relates to a demulsifier for eliminating an oil-water interface emulsion layer in oilfield produced liquid treatment and a preparation method of the demulsifier. The preparation method comprises the following steps: adding acrylamide, 1-allyl-3-methylimidazolium bis (trifluoromethanesulfonyl) imine salt, allyl tributyl phosphonium chloride and deionized water into a first reactor, and heating and dissolving the acrylamide, the 1-allyl-3-methylimidazolium bis (trifluoromethanesulfonyl) imine salt, the allyl tributyl phosphonium chloride and the deionized water; adding allyl (diisopropylamino) dimethylsilane, butyl acrylate, deionized water, octylphenol polyoxyethylene ether-10, lauryl sodium sulfate and monopotassium phosphate into the second reactor, and stirring to obtain an emulsion; adding an initiator and sodium hydrogen sulfite into a second reactor, carrying out heating and heat preservation reaction, pouring the mixed solution in the first reactor, and continuously carrying out reaction, heating and heat preservation to obtain a viscous liquid; and drying and granulating the viscous liquid to obtain the demulsifier. The demulsifier provided by the invention has the characteristics of simple synthesis process and high demulsification rate.

The invention belongs to the field of modified self-repairing calcium aluminate cement 3D printing, and particularly relates to a phosphate modified self-repairing calcium aluminate cement 3D printing material and a preparation method thereof. The phosphate modified self-repairing calcium aluminate cement 3D printing material prepared by the invention is prepared from the following raw materials in parts by mass: 60 to 70 parts of calcium aluminate cement, 3 to 7 parts of silica fume, 2 to 4 parts of metakaolin, 0.5 to 3.5 parts of double-template modified calcium bentonite, 0.8 to 1.5 parts of amino modified sodium polyphosphate and 0.15 to 0.8 part of basalt fiber. The invention relates to a concrete anti-microbial agent, which is prepared from the following raw materials in parts by weight: 20-30 parts of water, 20-30 parts of water, 20-30 parts of water, 20-30 parts of nano calcium carbonate, 20-30 parts of nano calcium carbonate, 20-30 parts of magnesium phosphate cement coated bacteria-loaded porous microspheres, 20-30 parts of a polycarboxylate superplasticizer, 20-30 parts of an organic silicon defoaming agent and 25-35 parts of mixing water. The technical-economic cooperation requirement of building 3D printing under complex working conditions is met, and various indexes of phosphate modified calcium aluminate cement applied to the 3D printing technology are met.

The invention relates to the technical field of plugging agents, and discloses a viscoelastic polymer type self-assembly plugging agent and a preparation method thereof. The preparation method comprises the following steps: adding acrylamide, butyl acrylate, 2-acrylamide-2-methylpropanesulfonic acid, quaternized cyclodextrin, gamma-glycidyl ether oxypropyl trimethoxy silane modified bentonite, Schiff base styrene, a sodium dodecyl benzene sulfonate emulsifier and octadecyl dimethyl allyl ammonium chloride into a reaction kettle; and adding an azodiisobutyronitrile initiator into the deionized water, uniformly mixing, and reacting for 4-5 hours at 50-65 DEG C to obtain the viscoelastic polymer type self-assembled plugging agent after the reaction is finished. The plugging agent disclosed by the invention has a relatively good plugging effect, and effectively solves the problem that the gel strength is weakened or the gelling is not thorough due to the formation shearing effect in a continuous gel migration process.

The invention discloses a super-hydrophobic anti-icing coating for a power transmission line and a preparation method, and belongs to the technical field of preparation of anti-icing coatings. The super-hydrophobic anti-icing coating for the power transmission line is composed of a coating wrapping the surface of the power transmission line, and the coating is composed of the following components in parts by weight: 34-45 parts of composite resin, 8-14 parts of a composite ice melting agent, 10-18 parts of deionized water, 1-3 parts of hexadecyl trimethoxy silane and 50-58 parts of tetrahydrofuran, the composite resin is prepared from carboxyl multi-walled carbon nanotubes, isopropanol, tetraethoxysilane, a silane coupling agent KH-550, perfluorodecyl trimethoxysilane, butyl acrylate, methyl methacrylate and dodecafluoroheptyl methacrylate, and the composite ice melting agent is prepared from pyridine-2, 6-dicarboxylic acid, thionyl chloride and nicotinic acid hydrazide. The coating prepared by the method has excellent hydrophobicity, wear resistance and anti-icing effect.

A carbon-coated current collector. The carbon-coated current collector comprises a foil and a conductive coating arranged on the surface of the foil. The conductive coating comprises a combination of a modified conductive carbon material and a binder. The binder is prepared from the following raw materials in parts by weight: 40-60 parts of methyl isobutyl ketone, 25-30 parts of a solvent, 20-25 parts of isobornyl methacrylate, 20-25 parts of methyl methacrylate, 20-25 parts of n-butyl acrylate, 20-25 parts of hydroxyethyl acrylate, 18-22 parts of silicone oil, and 50-55 parts of an initiator. The modified conductive carbon material is a fluorosilane-modified carbon material. The modified conductive carbon material and the binder can form silanols by means of hydrolysis reaction of respective alkoxy groups, then the silanols form new hydrogen bonds with OH groups, and covalent bonds are formed on the surface of the carbon material, thereby forming a highly cross-linked network structure, which further enhances water resistance, allowing for the ability to withstand 200 or more wiping operations.

The invention relates to the technical field of dispersing agents, and particularly discloses a high-concentration water-based graphene dispersing agent. The high-concentration water-based graphene dispersing agent is prepared from the following raw materials in parts by weight: 25 to 30 parts of a modified nonionic surfactant, 8 to 12 parts of sodium lignin sulfonate, 0.4 to 0.8 part of a de-foaming agent and 90 to 100 parts of de-ionized water, the modified nonionic surfactant is prepared by the following steps: carrying out dehydration esterification reaction on 1-pyrene butyric acid and N-hydroxysuccinimide, carrying out nucleophilic substitution reaction on the obtained product and polyethylene glycol monododecyl ether to obtain modified 1-pyrene butyric acid, and finally polymerizing the modified 1-pyrene butyric acid and n-butyl acrylate. The method is easy to operate, graphene does not need to be subjected to oxidation reduction, the integrity of a graphene sheet layer can be completely kept, and the performance of the graphene can be fully exerted; the prepared graphene dispersing agent realizes efficient dispersing effect, excellent stability and environment-friendly safety characteristics, and provides solid technical support for wide application of graphene in multiple fields.

The invention discloses quick-dry water-based ink and a preparation method thereof, and relates to the technical field of ink. The preparation method comprises the following steps: firstly, enabling 4, 6-bis (allyloxy)-n-butyl-1, 3, 5-thiazine-2-amine and vinyl sulfonamide to participate in a polymerization reaction of acrylic acid and butyl acrylate, and preparing 4, 6-bis (allyloxy)-n-butyl-1, 3, 5-thiazine-2-amine and vinyl sulfonamide through a two-step emulsion polymerization method; the core-shell structure modified polyester emulsion with 2, 5-thiazine-2-amine and vinyl sulfonamide as soft shells and acrylic acid and butyl acrylate as hard cores improves the wear resistance and durability of the ink. Then allyl polyether reacts with 2-(p-chlorphenyl) ethylene oxide, so that the drying time is shortened, and the wear resistance of the ink is improved; then through addition reaction of reactants, bis (2-ethoxyl) dimethyl ammonium chloride and hydrogen-containing silicone oil, the epoxy-amino-polyether combined modified silicone oil flatting agent is formed, the flatting agent has hydrophilicity and hydrophobicity, the drying speed is increased, and the wear-resistant effect is improved.

The invention relates to a biodegradable composite material as well as a preparation method and application thereof, and belongs to the technical field of compositions of high-molecular compounds. The biodegradable composite material is prepared from the following components in parts by weight: 46 to 87 parts of PBAT resin, 2 to 10 parts of PLA resin, 10 to 40 parts of calcium carbonate, 0.5 to 2 parts of a slipping aid and 0.5 to 2 parts of an edge sealing aid, the molar content of D-lactic acid in the PLA resin is greater than or equal to 2%; the particle size D50 of the calcium carbonate is less than 1.8 microns; the edge sealing auxiliary agent is an ethylene-acrylic acid copolymer, an ethylene-vinyl acetate copolymer, an ethylene-methyl acrylate copolymer, an ethylene-methyl acrylate-glycidyl methacrylate terpolymer, an ethylene-butyl acrylate copolymer, an ethylene-butyl acrylate-glycidyl methacrylate terpolymer, an ethylene-vinyl acetate copolymer, an ethylene-vinyl acetate copolymer, an ethylene-vinyl acetate copolymer, an ethylene-vinyl acetate copolymer, an ethylene-vinyl acetate copolymer, an ethylene-vinyl acetate copolymer, an ethylene-vinyl acetate copolymer and an ethylene-vinyl acetate copolymer. And at least one of epoxy resin. The biodegradable composite material has excellent long-acting edge sealing performance.

The invention relates to a degradable acrylic pressure-sensitive adhesive and a preparation method thereof, and belongs to the technical field of acrylic pressure-sensitive adhesives. The degradable acrylic pressure-sensitive adhesive provided by the invention is prepared from the following raw materials: polylactic acid, butyl acrylate, 2-ethylhexyl acrylate, benzoyl peroxide, ethyl acetate, temperature-sensitive microcapsules, a tackifier, an antioxidant and a stabilizer. The degradable acrylic pressure-sensitive adhesive disclosed by the invention is prepared from a plurality of components, and the polylactic acid not only endows the pressure-sensitive adhesive with good biodegradability, but also provides proper mechanical strength and flexibility; butyl acrylate and 2-ethylhexyl acrylate are combined, so that the pressure-sensitive adhesive has excellent adhesion and weather resistance; due to the introduction of the temperature-sensitive microcapsules, the tackifier, the antioxidant and the stabilizer, the performance of the pressure-sensitive adhesive is further improved, and the degradability of the pressure-sensitive adhesive is improved.

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 discloses an OCA (Optical Clear Adhesive) solution for a folding screen protective film, the OCA solution comprises an optical raw adhesive, a curing agent and a first solvent, the raw adhesive is prepared from the following raw materials in parts by mass: 270-283 parts of 2-ethylhexyl acrylate, 50-62 parts of butyl acrylate, 318-330 parts of methyl acrylate, 40-55 parts of acrylic acid, 1-2 parts of gamma-acryloyloxypropyltrimethoxysilane, 2.1-2.3 parts of an initiator and 1250-1350 parts of a second solvent; the second solvent comprises methylbenzene and ethyl acetate. According to the OCA optical glue solution for the folding screen protection film, raw glue is prepared from the isooctyl acrylate, the butyl acrylate, the methyl acrylate, the acrylic acid, the gamma-acryloyloxy propyl trimethoxy silane and the initiator in a toluene and ethyl acetate compounded solvent system, and an OCA glue layer with excellent stripping force, light transmittance, holding power and bending resistance is obtained after curing; and the cost of the raw materials is optimized, and the method is more economical.

The invention relates to the technical field of fabric waterproofing agents, in particular to a polyurethane modified organic silicon fluoride-free waterproofing agent and a preparation method thereof. The polyurethane modified organic silicon fluoride-free waterproof agent is prepared from the following raw materials in parts by mass: 5 to 15 parts of hexamethylene diisocyanate, 5 to 15 parts of butyl acrylate, 1 to 5 parts of methyl methacrylate, 40 to 60 parts of octamethylcyclotetrasiloxane, 10 to 30 parts of alpha, omega-dihydroxy polydimethylsiloxane and 5 to 10 parts of gamma-aminopropyl methyl diethoxy silane. The invention relates to a silane coupling agent, which is prepared from the following raw materials in parts by weight: 1 to 5 parts of glycidyl ether oxypropyl trimethoxy silane, 0.1 to 1 part of tetramethylammonium hydroxide, 0.1 to 1 part of triethylamine, 2 to 5 parts of tetraethoxysilane, 0.2 to 0.75 part of ammonia, 0.1 to 1 part of silane coupling agent KH-570, 0.01 to 0.1 part of dibutyltin dilaurate, 1 to 5 parts of epsilon-caprolactam, 1 to 2 parts of emulsifier and 0.1 to 1 part of initiator. The fabric treated by the method has good softness and excellent hydrophobic effect.

The invention relates to the technical field of chemical adhesives, and discloses a polyurethane modified acrylate aqueous emulsion and a preparation method thereof. The polyurethane modified acrylate aqueous emulsion is prepared from a polyurethane dispersion and polyacrylate; the polyurethane dispersoid is formed by polymerizing isophorone diisocyanate, polycaprolactone polyol, 2, 2-bis (hydroxymethyl) propionic acid and trimethylolpropane; the polyacrylate is formed by polymerizing methyl methacrylate, butyl acrylate and N-methylacryloyl glycine. According to the polyurethane modified acrylate aqueous emulsion and the preparation method thereof disclosed by the invention, the prepared aqueous emulsion is nanoscale, and after the aqueous emulsion is prepared into a film, the tensile strength of the film is increased along with the increase of the addition amount of N-methylacryloylglycine, and the elongation at break of the film is reduced along with the increase of the addition amount of N-methylacryloylglycine; when the addition amount of the N-methylacryloyl glycine is 1.96% and 3.85% of the total amount of the monomer, the optimal tensile strength and elongation at break are achieved, and the N-methylacryloyl glycine copolymer can be used for preparing chemical adhesives.

The present invention relates to the field of food packaging, and in particular to a mixed coating liquid and a fluorine-free oil-proof barrier paper and a preparation method thereof, which are prepared by uniformly mixing the following raw materials in percentage by mass: component A: 1-5% silica gel; component B: 1-5% methylhydrogensiloxane / polysiloxane; component C: 5-15% styrene; component D: 3-10% acrylic acid; component E: 5-20% butyl acrylate; component F: 20-70% water; the sum of the mass percentages of the above components is 100%. At the same time, a fluorine-free oil-proof barrier paper is provided, which is formed by coating a mixed coating liquid on at least one surface of a paper substrate. This scheme completely excludes the use of fluoride-containing materials, realizes green packaging product materials that are harmless to the human body, and conforms to the concept of environmental protection and health. At the same time, through a specific silicon nano-modified material mixed coating liquid, this scheme reaches the oil-proof level of 6 and above (up to 12) required by the market, effectively preventing grease penetration and keeping the outer surface of the package clean.

The invention provides an environment-friendly water-based acrylic emulsion adhesive without containing an organic solvent. The environment-friendly water-based acrylic emulsion adhesive is prepared from the following raw materials: 55-60 wt% of eleostearic acid hydroxyethyl acrylate (TMA), 15-25 wt% of butyl acrylate (BA), 3-10 wt% of acrylic acid (AA), 2-5 wt% of a cross-linking agent, 3-8 wt% of modified soil and 0.5-1 wt% of an initiator as a solid phase; the liquid phase is deionized water, and the environment-friendly water-based acrylic emulsion adhesive is prepared through semi-continuous emulsion polymerization. The prepared environment-friendly water-based acrylic emulsion adhesive is high in biodegradability and low in VOC content, has the mechanical property matched with that of a traditional acrylic emulsion adhesive and also has the self-repairing capacity, waste materials can be treated by changing the temperature or pH condition, the environment-friendly water-based acrylic emulsion adhesive can be recycled for multiple times, and the recycling cost is reduced.

The invention relates to a preparation method of an active oxygen responsive microneedle with a separable base, which comprises the following steps: mixing 3-(acrylamide) phenylboronic acid, epigallocatechin gallate and N-vinyl pyrrolidone, and standing to obtain an E-A compound solution; dissolving cyclosporine and an initiator in the E-A compound solution to obtain a microneedle precursor solution; placing the microneedle precursor solution on the surface of a microneedle mold, and performing in-situ polymerization to form a microneedle body; paving a mixed aqueous solution of poly (N-isopropylacrylamide-n-butyl acrylate) and polyvinyl alcohol on the microneedle mold substrate forming the microneedle body, and drying to form a microneedle substrate; and stripping the microneedle body with the microneedle substrate from the microneedle mold to obtain the active oxygen responsive microneedle with the separable base. According to the product prepared by the preparation method, drug release can be adjusted by sensing ROS of an inflammation part, deep penetration of the drug is realized, controllable separation between a backing layer and a needle head can be realized, and discomfort of a patient is reduced.

The invention discloses an acrylate finishing emulsion and a preparation method thereof, and the acrylate finishing emulsion comprises the following components in parts by mass: 18-30 parts of styrene, 5-15 parts of methyl methacrylate, 1-5 parts of 2-ethylhexyl acrylate, 5-14 parts of butyl acrylate, 0.5-1 part of acrylic acid, 0.6-1.2 parts of acrylamide, 0.8-2 parts of a high-density crosslinking monomer, 0.2-0.5 part of an initiator, 0.7-1 part of an emulsifier and 50-60 parts of water. 0.1-0.5 part of an oxidant, 0.1-0.5 part of a reducing agent, 1-5 parts of a pH regulator and 10-20 parts of an inorganic material; after the emulsion is coated to form a film, the hardness, the water resistance, the stain resistance, the low-temperature stability and the temperature change resistance are remarkably improved, and the acrylate emulsion with high hardness, high water resistance and high stain resistance can be prepared.

The invention relates to the technical field of cables, and provides a wear-resistant cable and a preparation method thereof. The wear-resistant cable sequentially comprises an outer protective layer, an insulating layer and a conductor from outside to inside, and the outer protective layer comprises the following components in parts by weight: 80 parts of polyurethane, 18-24 parts of high-density polyethylene, 4-6 parts of an ethylene-butyl acrylate copolymer, 5-8 parts of an ethylene-vinyl acetate copolymer, 10-20 parts of sillimanite, 4-8 parts of a lubricating component, 20-30 parts of a flame retardant, 1-3 parts of an antioxidant and 2-4 parts of a plasticizer; the lubricating component comprises N, N-di (hydroxyethyl) cocamide and aluminum dihydroxy stearate in a weight ratio of (1: 9)-(9: 1). According to the technical scheme, the problem of poor wear resistance of the outer sheath of the cable in the prior art is solved.

The invention discloses a high-toughness polyethylene composite film and a preparation method thereof, and belongs to the field of high polymer materials. The outer layer is prepared from linear low-density polyethylene, an ethylene-butyl acrylate copolymer, an antioxidant 1010 and an ultraviolet light absorber UV-531; the middle layer is prepared from linear low-density polyethylene, a polyolefin elastomer, an ethylene-butyl acrylate copolymer, stearic acid modified calcium carbonate, an antioxidant and an ultraviolet light absorber; and the inner layer is composed of linear low-density polyethylene, an ethylene-butyl acrylate copolymer, an antioxidant 1010 and an ultraviolet light absorber UV-531. Drying the raw materials; mixing heavy calcium carbonate with stearic acid; each layer is mixed at a low speed according to a ratio; and carrying out three-layer co-extrusion film blowing, two-way stretching, corona and annealing. The surface tension of the composite film reaches 40 mN / m, the maximum longitudinal and transverse tensile strength is 23 MPa, the tearing strength is 120 kN / m, the elongation at break is 700%, and the performance of the composite film is superior to that of traditional casting and blow molding process products.

The invention discloses a high-flexibility anti-cracking coating and a preparation method thereof, and belongs to the technical field of building coatings. The coating is prepared from the following components in parts by mass: 50 to 70 parts of acrylic acid-organic silicon copolymer elastic emulsion with a core-shell structure, 3 to 8 parts of nano cellulose and polyester staple fiber composite fiber reinforced system, 20 to 30 parts of modified mica powder and fumed silica functional filler with a high radius-thickness ratio, 5 to 10 parts of auxiliaries and 10 to 15 parts of deionized water. A core layer of the elastic emulsion is a butyl acrylate-styrene elastomer, a shell layer of the elastic emulsion is a methyl methacrylate-organosiloxane copolymer, and a coating is endowed with high elongation at break and low-temperature crack resistance through the synergistic effect of a flexible network of the core layer and a rigid-flexible gradient structure of the shell layer. The nano cellulose and the polyester staple fiber form a dual-scale reinforcing system, so that cracks are bridged, and stress is dispersed; and the modified mica powder and fumed silica are compounded to improve the compactness and wear resistance of the coating.

The invention belongs to the technical field of oil exploitation, and relates to a comb-shaped demulsifier for demulsifying high-solid-phase crude oil and a preparation method of the comb-shaped demulsifier. The preparation method comprises the following steps: adding 2-methallyl alcohol and a catalyst into a high-pressure reaction kettle, adding epoxypropane, heating, carrying out a thermal insulation reaction, cooling, introducing ethylene oxide, heating, carrying out a thermal insulation reaction, cooling, and adjusting the pH value to 7-8 to obtain an intermediate; transferring the intermediate into a reaction kettle, sequentially adding (3-acrylamidopropyl) trimethyl ammonium chloride, benzyl methacrylate, butyl acrylate, nonylphenol polyoxyethylene ether, buffer salt and deionized water, stirring at a high speed to form a uniform emulsion, and adjusting the pH value to 7-8; dropwise adding an initiator, heating, carrying out heat preservation reaction, continuously heating, carrying out heat preservation reaction, and cooling to obtain a viscous liquid; and granulating the viscous liquid to obtain a final product. The demulsifying agent has the characteristics of wide raw material source, simple synthesis process, no by-product and good demulsifying effect.

The invention discloses an anti-aging and anti-corrosion coating and a preparation method thereof, and relates to the technical field of coatings. When the anti-aging and anti-corrosion coating is prepared, firstly, tetramethyl tetravinyl cyclotetrasiloxane, n-butyllithium and dimethyl-3-chloropropyl chlorosilane react to obtain modified polysiloxane, then 4-vinylpyridine, methyl methacrylate and n-butyl acrylate are copolymerized and then react with the modified polysiloxane, and then bis (4-chlorphenyl) phosphine is grafted to obtain the anti-aging and anti-corrosion coating. Finally, reacting with p-aminodiphenylamine to obtain modified acrylic resin; secondly, enabling the titanium dioxide nanosheet pretreated by 3-aminopropyltrimethoxysilane to react with ester phthalocyanine, and then hydrolyzing to obtain a modified titanium dioxide nanosheet; finally, mixing the modified acrylic resin, the modified titanium dioxide nanosheet, a solvent, a dispersing agent and a defoaming agent to obtain the anti-aging and anti-corrosion coating. The anti-aging and anti-corrosion coating prepared by the invention has excellent anti-aging, anti-corrosion, flame-retardant and antibacterial properties.

The invention relates to the technical field of high polymer materials, and discloses a high-durability pressure-sensitive adhesive with low VOCs release and a preparation method thereof.The high-durability pressure-sensitive adhesive is prepared from, by weight, 50-80 parts of acrylate copolymer, 0.5-5 parts of cross-linking agent, 10-30 parts of tackifying resin, 1-10 parts of inorganic filler, 0.1-2 parts of antioxidant and 20-50 parts of solvent. Wherein the tackifying resin is at least one of hydrogenated petroleum resin and glycerol ester of rosin, and the inorganic filler is one of nanoscale silicon dioxide and calcium carbonate. Butyl acrylate is used as a main monomer, 2-ethylhexyl acrylate is used as a comonomer, acrylic acid is used as a functional monomer, benzoyl peroxide is used as an initiator, free radical polymerization is carried out at the temperature of 60-85 DEG C under the protection of nitrogen for 4-8 hours, and a copolymer chain with the molecular weight distribution index (PDI) smaller than or equal to 2.5 is formed, so that the viscosity and elasticity of colloid can be balanced; the peeling strength and the weather resistance are improved, and the colloid is prevented from being too soft or embrittled.

The invention provides an acrylate assistant for PVC (polyvinyl chloride) and a preparation method of the acrylate assistant, and belongs to the technical field of acrylate assistants. The preparation method comprises the steps of nano montmorillonite functionalization, synthesis of a core layer, synthesis of a middle layer and synthesis of a shell layer. The synthesis step of the core layer comprises the following steps: adding a core layer emulsion into a reaction kettle, adding an ammonium persulfate solution for the first time, heating to 64-68 DEG C, adding an ammonium persulfate solution for the second time, and reacting for 48-55 minutes to obtain a functionalized core emulsion; the core layer emulsion is prepared from deionized water, functionalized nano montmorillonite, sodium allyloxy hydroxypropyl sulfonate, butyl acrylate, 2-ethylhexyl acrylate, hydroxyethyl methylacrylate and gamma-methacryloyloxypropyltrimethoxysilane through ultrasonic treatment, and the core layer emulsion is prepared from the deionized water, the functionalized nano montmorillonite, the sodium allyloxy hydroxypropyl sulfonate, the butyl acrylate, the 2-ethylhexyl acrylate, the hydroxyethyl methylacrylate and the gamma-methacryloyloxypropyltrimethoxysilane through ultrasonic treatment; the prepared acrylate auxiliary agent is used in PVC, the fluidity can be improved, and meanwhile the impact resistance, the strength performance and the high-temperature stability performance are enhanced.

The present application provides a modified conductive carbon material, and a preparation method therefor and a use thereof. The modified conductive carbon material is prepared from the following raw materials in parts by weight: 60-80 parts of methyl methacrylate, 10-20 parts of butyl acrylate, 1-5 parts of a polymerizable silane coupling agent, 5-10 parts of a conductive carbon material, 0.1-0.2 parts of a first initiator, 0.1-0.3 parts of a second initiator, 1-10 parts of a first solvent and 0.1-1 part of a second solvent. A methyl methacrylate-butyl acrylate-polymerizable silane coupling agent copolymer is used to carry out surface modification on the conductive carbon material, and physical action and chemical bonding are carried out on the conductive carbon material by means of a polar bond, thereby reducing the surface free energy of carbon material powder, increasing the affinity with styrene-butadiene rubber latex, enabling the styrene-butadiene rubber latex tend to be stable in a slurry, solving the problem of coating film surface stripes caused by instability of the styrene-butadiene rubber latex in the slurry, and enhancing water resistance.

The invention discloses a high-temperature-resistant flame-retardant CPVC power cable protection pipe and a preparation method thereof, and relates to the technical field of cable protection pipes. The high-temperature-resistant flame-retardant CPVC power cable protection pipe at least comprises the following raw materials in parts by mass: 100 parts of chlorinated polyvinyl chloride; 15 to 25 parts of high impact resistance type MCS resin; 8 to 12 parts of poly (1, 2-propylene glycol adipate); 12 to 20 parts of a sepiolite-methyl methacrylate-butyl acrylate compound; 8-15 parts of aluminum-titanium composite coupling agent modified magnesium-aluminum-lanthanum hydrotalcite; 3-6 parts of a rare earth composite heat stabilizer; 2-4 parts of a processing aid; 0.5 to 1.5 parts of an antioxidant; and 1-2 parts of a lubricant. The prepared high-temperature-resistant flame-retardant CPVC power cable protection pipe has high heat resistance, high flame retardance and high impact resistance, and is excellent in comprehensive performance, high in safety and reliability and long in service life.