3031 results about "Polyacrylic acid" patented technology

The invention relates to a photo-thermal super-hydrophobic multifunctional anti-icing coating as well as a preparation method and application thereof. The photo-thermal super-hydrophobic multifunctional anti-icing coating comprises primer and finish paint, the primer comprises the following raw materials in parts by weight: 20-25 parts of bisphenol A type epoxy resin and / or fluorine modified epoxy resin, 10-20 parts of fluorine modified polyacrylic resin and / or polyurethane resin, 5-10 parts of a curing agent and 40-55 parts of a solvent; the finish paint comprises the following components in parts by weight: 2-5 parts of polytetrafluoroethylene, 1-3 parts of soluble polytetrafluoroethylene, 1-5 parts of polydimethylsiloxane and 85-90 parts of fluorinated MOF dispersion liquid. Compared with the prior art, the photo-thermal super-hydrophobic multifunctional anti-icing coating provided by the invention has the characteristics of super-hydrophobicity, rapid ice melting, wear resistance, reduction of ice adhesion strength and reduction of icing amount, can effectively solve the problem of icing of an aluminum conductor of a power transmission line of a power system, and can be applied to power equipment such as the aluminum conductor of the power transmission line.

The invention relates to an insulating weather-resistant powder coating and a preparation method thereof, and belongs to the technical field of coatings, and the powder coating comprises composite modified resin, a dual curing agent, a functional filler, a polyacrylate leveling agent, fumed silica, a benzotriazole ultraviolet light absorber, polytetrafluoroethylene wax powder and the like. A core-shell structure of the composite modified resin is designed, high insulativity is kept through a silane modified epoxy core layer, a weather-proof barrier is provided through an acrylic acid shell layer, and the phase separation problem is solved through interface chemical bonding; a dual-curing mechanism is designed, and isocyanate and acrylic hydroxyl react to form an interpenetrating network while an epoxy core layer is cured by anhydride; a filler synergistic effect is designed, silane coupling agent modified nano boron nitride forms a three-dimensional heat-conducting insulating network, and rutile type titanium dioxide is coated with silicon dioxide, so that ultraviolet aging is resisted. All the components cooperate with one another, so that the coating has excellent insulativity, weather resistance, adhesiveness and the like at the same time.

The invention discloses a hydrophilic polyacrylate / epoxy silica sol composite coating and a preparation method thereof. The composite coating is prepared from a polyacrylate epoxy silica sol solution containing carboxyl and a polyethylene glycol side chain through blending, coating, drying and heating crosslinking. The polyacrylate is synthesized by taking methyl methacrylate, methacrylic acid, hydroxyethyl methylacrylate and allyl polyethylene glycol as comonomers through a solution free radical copolymerization method, and the epoxy silica sol solution is prepared by taking tetraethoxysilane and gamma-glycidoxypropyltrimethoxysilane as raw materials through a solution polymerization method. The composite material is prepared through a sol-gel and core-shell preparation process. The preparation method comprises the following steps: carrying out solution blending on polyacrylate and epoxy silica sol, and carrying out coating, drying and other processes to generate the cross-linked polyacrylate / epoxy silica sol composite coating through a cross-linking reaction between carboxyl and epoxy. The prepared composite coating has the characteristics of long durability, wear resistance, hydrophilicity, antifogging, protein adsorption resistance and the like.

The invention belongs to the technical field of cement manufacturing, and particularly relates to high-strength weather-resistant environment-friendly cement and a preparation method thereof. The environment-friendly cement is prepared from the following raw materials in parts by mass: 40 to 55 parts of Portland cement, 15 to 25 parts of fly ash, 10 to 15 parts of slag powder, 6 to 12 parts of biomass reinforced composite mineral material, 2 to 4 parts of nano silicon dioxide, 1 to 4 parts of modified polymer emulsion and 1 to 3 parts of additive. The biomass reinforced composite mineral material is prepared from zeolite, bentonite, sepiolite and chitosan; the modified polymer emulsion comprises a modified polyacrylate emulsion and a modified polystyrene-butadiene emulsion in a mass ratio of (1-3): 1; the additive is prepared from basalt fiber, sodium lignin sulfonate, a rosin thermopolymer and sodium gluconate. The environment-friendly cement prepared by the invention not only has high strength and good weather resistance, but also remarkably reduces carbon footprint and saves natural resources.

A biodegradable polymer composite, a method of making the same and use for same are provided. The biodegradable polymer composite has about 30 to 99.5% by weight of a polymer selected from a group consisting of polybutylene adipate terephthalate (PBAT), polybutylene succinate (PBS), polyhydroxyalkanoates (PHA), and polycaprolactone (PCL) grafted with a compatibilizer selected from a group consisting of maleic anhydride, glycidyl methacrylate, pyromellitic anhydride, acrylic acid, polyacrylic acid, methylene diphenyl diisocyanate, poly(glycidyl methacrylate, copolymer(s) of glycidyl methacrylate; and about 0.5 to 50 % by weight a nano-filler or a micro-filler. The biodegradable polymer composite does not contain polylactic acid. Surfaces of the nano-filler or the micro-filler may be modified using a grafting agent so that the biodegradable polymer composite has enhanced mechanical properties, increased heat resistance, compostablity and / or improved processability. The biodegradable polymer composite may be used to make flexible articles, such as a freezer wrap and a farming sheet.

The invention provides a solid electrolyte slurry, an electrode slurry, a solid electrolyte sheet, an electrode sheet, a solid battery monomer, a battery device and a power utilization device.The solid electrolyte slurry comprises a sulfide solid electrolyte material, a solvent and a binder dissolved in the solvent, and the solvent is a non-polar solvent, a weak-polar solvent or a mixed solvent of the non-polar solvent and the weak-polar solvent; the binding agent comprises a polyacrylate binding agent and a non-polar polyolefin binding agent. The slurry disclosed by the invention has high dispersity, high suspension property and good cohesiveness, and can enable the solid-state battery monomer to have high initial coulombic efficiency when being used in the solid-state battery monomer.

The invention provides a high-temperature-resistant magnesia-carbon composite refractory brick and a preparation method thereof, and belongs to the technical field of magnesium oxide refractory wall bricks, the refractory brick comprises the following raw materials: double-layer modified magnesium oxide, modified crystalline flake graphite, zircon powder, modified liquid phenolic resin and a benzoxazine cross-linking agent; the double-layer modified magnesium oxide is obtained by firstly coating magnesium oxide with powder phenolic resin, aluminum oxide and zirconium oxide and then coating magnesium oxide with asphalt, micron magnesium oxide, zirconium oxide and calcium oxide; the modified crystalline flake graphite is obtained by coating crystalline flake graphite with strontium hydroxide, asphalt and boron carbide; the modified liquid phenolic resin is formed by mixing liquid phenolic resin with a silane coupling agent and a polyacrylate cross-linked polymer. Double-layer modified magnesium oxide, modified crystalline flake graphite and modified liquid phenolic resin are prepared by adopting special components and a method and are matched with zircon powder and a benzoxazine cross-linking agent for use, and a reasonable forming and sintering process is designed, so that the refractory brick has good high-temperature stability, oxidation resistance, thermal shock resistance and the like.

The invention relates to the technical field of high polymer material chemistry, and discloses a high and low temperature resistant anti-yellowing optical adhesive and a preparation process thereof, the high and low temperature resistant anti-yellowing optical adhesive comprises the following components by weight: 40-60% of modified organic silicon resin, 20-30% of urethane acrylate, 10-15% of alicyclic epoxy resin, 0.5-5% of a nano inorganic filler, 0.8-2.5% of an anti-yellowing composite reagent, and the balance of a solvent. The coating is prepared from the following components in percentage by weight: 0.5 to 1.5 percent of 2-hydroxy-2-methyl-1-phenyl-1-acetone, 0.1 to 0.3 percent of fluorine modified polyacrylate flatting agent and 0.3 to 1.0 percent of chloroplatinic acid-divinyl tetramethyl disiloxane complex catalyst. The preparation method comprises the following steps: mixing alpha, omega-dihydroxy polydimethylsiloxane and phenyltrimethoxysilane according to a mass ratio of 8: 2-7: 3, adding 0.3-1.0% of a chloroplatinic acid-divinyl tetramethyl disiloxane complex catalyst, and raising the temperature by stages under the protection of nitrogen, so that the glass transition temperature of the adhesive can reach 120 DEG C below zero and 125 DEG C, and the temperature of the adhesive can reach 120 DEG C below zero and 125 DEG C below zero. And the long-term service requirement of the optical device in an extreme temperature environment is met.

The invention is applicable to the technical field of daily cleaning chemicals, and provides a double-shell probiotic microcapsule which comprises probiotics, a fat-soluble plant extract, cellulose nanocrystals, a polyacrylic acid-chitosan compound, a surfactant, diisocyanate, polyethylene glycol and ethyl acetate. A wall material of the microcapsule is formed by compounding a polyacrylic acid-chitosan compound and a fat-soluble plant extract, the particle size D50 is smaller than or equal to 5 microns, the microcapsule is stable in an environment with the pH being 8-10, and the microcapsule is broken to release probiotics when the pH is smaller than or equal to 6. The outer layer is polyacrylic acid / chitosan compound / polyurethane crosslinking (pH response), the inner layer is coconut oil and soybean oil (fat-soluble core), meanwhile, the material preparation process is simple, the controllable degree is high, and the material is suitable for batch preparation.

The invention relates to a preparation method of a core-shell fluorine-free super-hydrophobic emulsion based on acrylate pressure-sensitive adhesive viscosity. According to the method, a polyacrylate pressure-sensitive adhesive is adopted, an acrylate soft monomer and a functional monomer are copolymerized on the surface layer of the polyacrylate pressure-sensitive adhesive, and a polyacrylate copolymer with pressure-sensitive adhesiveness and reaction activity is coated to obtain a pressure-sensitive adhesive'rigid core at flexible shell 'core-shell polymer microsphere emulsion with a core-shell structure; the production process is simplified (two steps are combined into one step), and chromatic aberration is eliminated; the silane coupling agent can be used for replacing a silane coupling agent, and the problem of insufficient durability is further solved. According to the invention, the simplification and batch production of the production process can be effectively realized, and meanwhile, the requirements of modern industry on economic and green production can be met.

The invention discloses a silicon negative electrode binder as well as a preparation method and application thereof. The silicon negative electrode binder is a graft copolymer with a comb-shaped structure; the grafted copolymer comprises a polyurethane chain segment forming a main chain of the comb-shaped structure, a polyacrylic acid chain segment serving as a branch chain and connected to the main chain through a covalent bond, and a fluorine-containing chain segment. According to the preparation method, a graft copolymerization method is adopted, the preparation method is carried out in a water-based system, the silicon negative electrode binder with hardness and softness is obtained, and the silicon negative electrode binder is applied to a lithium battery through the synergistic effect of mechanical property, interface stability and electrochemical performance. And a solution of a key material is provided for a high-capacity and long-cycle lithium battery which takes an active material with high silicon content as a negative electrode.

The invention discloses a polyurethane protective adhesive tape for aviation and a preparation method thereof, and relates to the technical field of adhesives. When the polyurethane protective adhesive tape for aviation is prepared, polyester glycol, an ultraviolet absorption monomer, 3-(4-pyridyl) pentane-1, 5-diol, 1, 4-butanediol and isophorone diisocyanate are polymerized to prepare polyurethane; the preparation method comprises the following steps: carrying out a reaction on polyurethane and 2-bromoethyl acrylate to prepare modified polyurethane; enabling the pretreated magnesium hydroxide to react with 3-epoxypropoxy-1, 1, 3, 3-tetramethyldisiloxane and ammonia water in sequence, so as to obtain modified magnesium hydroxide; the modified polyurethane and the modified magnesium hydroxide are mixed and then subjected to compression molding to prepare a polyurethane film; and coating a polyurethane film with the polyacrylate glue solution, and drying to obtain the polyurethane protective adhesive tape for aviation. The polyurethane protective adhesive tape for aviation prepared by the invention has excellent flame-retardant, anti-aging, antibacterial and self-repairing properties.

The invention belongs to the technical field of printing materials, and provides a thermal printing material with a cleaning function and a preparation method and application thereof. The thermal printing material comprises a base material, a thermal imaging layer and a protective layer which are sequentially stacked, the protective layer is prepared from a first film forming material, a second film forming material and a cleaning function material, and the cleaning function material comprises rare earth oxide. The first film-forming material is at least one of modified polyvinyl alcohol, styrene acrylic resin, polyurethane resin, polyacrylic resin, styrene maleic anhydride copolymer and waterborne epoxy resin, and the second film-forming material is a carbonyl compound and / or an amino compound. The thermal printing material provided by the invention can clean a thermal printing head while printing, the thermal printing head is kept clean for a long time, the service life is long, the printing effect of an output information image is not influenced, and the thermal printing material has the characteristics of high-transparency appearance, clear image, high density and no scratch.

The invention discloses a high-strength silicon carbide ceramic material and a preparation method thereof, and relates to the technical field of ceramic material preparation. The silicon carbide ceramic material is prepared from the following raw materials in parts by weight: 70-85 parts of silicon carbide powder, 5-15 parts of B4Cw-coated BN, 3-5 parts of a sintering aid, 0.5-1 part of a dispersing agent and 0.5-2 parts of carbon black, the B4Cw-coated BN is prepared by the following steps: pretreating a boron carbide whisker with a silane coupling agent, adding the pretreated boron carbide whisker into a precursor solution containing boric acid and urea, and reacting to obtain the boron carbide whisker with a BN coating; the sintering aid is formed by mixing Y2O3 and Al2O3; the dispersing agent is ammonium polyacrylate. The preparation method of the high-strength silicon carbide ceramic material comprises the following steps: pretreating boron carbide whiskers, synthesizing B4Cw-coated BN, preparing composite powder, and preparing the silicon carbide ceramic material. The high-strength silicon carbide ceramic material disclosed by the invention has relatively high bending strength and elasticity modulus.

The invention provides a secondary battery, a preparation method of the secondary battery and an electronic device, the secondary battery comprises a positive electrode plate, a negative electrode plate, a diaphragm and an electrolyte, the negative electrode plate comprises a negative electrode current collector and a negative electrode material layer located on at least one surface of the negative electrode current collector, and the negative electrode material layer comprises hydrophobic modified polyacrylic acid; powder of the negative electrode material layer is dissolved in deionized water to obtain first slurry with the solid content of 45 wt%-50 wt%, the shear rate is 0.1 S <-1 >, the shear viscosity eta of the first slurry is 1 mPa.s, and eta is larger than or equal to 1000 and smaller than or equal to 30000. When the negative electrode material layer comprises the hydrophobic modified polyacrylic acid, in the preparation process of the negative electrode plate, the negative electrode slurry containing the hydrophobic modified polyacrylic acid has the characteristic of high viscosity under low shear, so that the risk of edge thinning after coating is reduced, and the electrode assembly interface in the later period of circulation is improved.

The invention discloses a method for synthesizing electronic-grade ethyl acetate through catalytic esterification of acidic ion exchange resin, and belongs to the technical field of ethyl acetate preparation. The method comprises the following steps: mixing crosslinked polystyrene white balls and a swelling agent, and dropwise adding concentrated sulfuric acid for reaction to obtain S-PS resin; mixing an EDTA disodium salt saturated solution and a polyacrylic acid solution, adding a cross-linking agent and an emulsifier, and carrying out a cross-linking curing reaction to obtain EDTA microcapsules; the preparation method comprises the following steps: dispersing S-PS resin in a solvent, adding EDTA microcapsules, a dehydration condensation agent and a catalyst, reacting under the protection of inert gas, and filtering and recovering after the reaction is finished to obtain S-PS-EDTA resin; mixing glacial acetic acid, absolute ethyl alcohol and S-PS (at) EDTA resin for reaction, and filtering and collecting liquid after the reaction is finished; and rectifying the collected liquid to obtain the product. According to the method provided by the invention, metal impurities can be chelated in the synthesis process, and the electronic-grade ethyl acetate with high purity and low impurity content is produced.

The invention relates to environment-friendly hydrophobic ink and a preparation method thereof, and belongs to the technical field of water-based ink. A copolymerization modifier capable of being combined in a water-based polyacrylate emulsion in an initiation polymerization mode in the stage of preparing the modified water-based polyacrylate emulsion is prepared, and an o-hydroxy aromatic ketone structure in the copolymerization modifier can endow water-based ink with lasting ultraviolet absorption performance; the trifluoromethyl structure can reduce the surface energy of the water-based ink, and the benzimidazole ring structure can form stable coordinate bonds with metal ions, so that the bonding performance of the water-based ink and a metal substrate is enhanced; when the copolymerization modifier is used for modifying the water-based polyacrylate emulsion, the long-term performance, the hydrophobic and oil-resistant performance and the adhesion performance on the surface of a metal base material of the finished water-based ink can be effectively improved.

The invention belongs to the field of conductive paste preparation, and particularly discloses conductive paste containing ruthenium oxide and a preparation method of the conductive paste. The conductive paste is prepared from the following components in percentage by mass: 40 percent to 50 percent of ruthenium oxide, 3.8 percent to 5 percent of carbon nano tubes, 5 percent to 10 percent of PbO-B2O3-SiO2, 3 percent to 8 percent of ethyl cellulose, 21 percent to 28 percent of terpilenol, 9 percent to 12 percent of butyl carbitol, 0.7 percent to 1 percent of ammonium polyacrylate and 1 percent to 2 percent of dibutyl phthalate. According to the preparation method, ruthenium oxide is activated in vacuum, a mixed solvent is combined after dispersion, and a ball milling and ultrasonic dispersion synergistic process is adopted, so that the slurry is uniformly dispersed and has excellent stability. According to the invention, a ruthenium oxide-carbon nanotube-frit ternary synergistic system is constructed, and terpilenol and butyl carbitol in a specific mass ratio are taken as a mixed solvent, so that the problems of insufficient conductivity and easy agglomeration of traditional paste are effectively solved, and the method can be widely applied to manufacturing of high-precision electronic devices.

The invention relates to the field of zipper processing, in particular to a processing method of a fluoride-free DWR waterproof zipper, which sequentially adopts four steps of pretreatment, padding treatment, drying treatment and heat treatment to carry out waterproof processing on the zipper, the fluorine-free DWR waterproof zipper prepared by matching paraffin, polyether modified silicone oil, carbodiimide, nano silicon dioxide dispersion liquid, fatty alcohol-polyoxyethylene ether and diethylene glycol monobutyl ether has the following advantages that 1, the fluorine-free DWR waterproof zipper meets the limitation requirements of Europe and America regulations and various standards on fluorine element, 2, the waterproof grade meets the grade 4.5 or above of standards such as AATCC / ISO / GB / T and the like, and the fluorine-free DWR waterproof zipper has a good waterproof effect. 3, the washing resistance can reach more than 20 times of washing and drying tests; 4, the phenomenon of white grasping in the market is avoided; and 5, the anti-siphon performance can reach 10H without climbing.

The invention discloses an optical-grade PET release film and a preparation method and application thereof, and belongs to the technical field of PET release liners.The preparation method comprises the steps that organic silicon resin, polyacrylate and functional silicone oil serve as raw materials, hexadecafluorophthalocyanine copper serves as a catalyst, sodium hydroxide provides hydroxyl anions, and hydroxyl-containing fluorinated hydroxyaniline is obtained; amino groups on the surface of fluorinated hydroxyaniline react with carboxyl groups of graphene oxide and are grafted on the surface of graphene oxide, then hydroxyl groups in the fluorinated hydroxyaniline and carboxyl groups of acrylic acid are subjected to esterification reaction under the action of a catalyst, so that acrylic acid is grafted on fluorinated modified graphene oxide, and the fluorinated modified graphene oxide is obtained. Therefore, hydroxyl and epoxy functional groups on the surface of the graphene oxide are consumed, hindering of electron transmission is reduced, the conductivity of the release film is improved, and the antistatic requirement of the release film is met.

The invention discloses a starch-based full-biodegradable mulching film capable of being rapidly degraded and a preparation method of the starch-based full-biodegradable mulching film, and belongs to the technical field of degradable materials.The preparation method comprises the steps of tea polyphenol calcium salt preparation, filler preparation, thermal plasticization and film preparation. The preparation of the filler comprises the following steps: adding silicon dioxide into a polyacrylic acid aqueous solution, stirring and centrifuging at room temperature, taking a precipitate, adding the precipitate into a polyvinylpyrrolidone aqueous solution, adjusting the pH value to 3-3.5, stirring and centrifuging at room temperature, taking the precipitate, adding the precipitate into the polyacrylic acid aqueous solution, adjusting the pH value to 3-3.5, stirring and centrifuging at room temperature, taking the precipitate, and freeze-drying to obtain the filler. The starch-based full-biodegradable mulching film prepared by the preparation method disclosed by the invention is good in processability, waterproofness and heat resistance and high in mechanical strength, the problem of phase separation does not occur in preparation, the problem of plasticizer precipitation does not easily occur in long-term use, and rapid degradation can be realized.

The invention discloses a dispersing agent for water-based nano pigment color paste, and relates to the technical field of water-based paint preparation, the dispersing agent comprises 50-150 parts of a polyether modified polyol compound, 30-80 parts of modified polyacrylate, 10-50 parts of a nonionic surfactant, 5-30 parts of a thickener, 700-850 parts of an environment-friendly solvent and 5-20 parts of a surface modifier; the invention further discloses a preparation method of the dispersing agent for the water-based nano pigment color paste. The preparation method comprises the following steps: preparing materials; adding the polyether modified polyol compound into the stirring container; adding modified polyacrylate into the polyether modified polyol compound solution; a nonionic surfactant is added; adding a thickening agent from a natural plant source; adding an environment-friendly solvent; and adding a surface modifier. The dispersing agent disclosed by the invention not only can effectively disperse pigment particles and prevent agglomeration of the pigment, but also can maintain good flowability and proper viscosity of the pigment and ensure high stability of color paste.

The invention discloses a dynamic borate bond-based self-healing polyacrylic acid binder and a preparation method thereof. The dynamic borate bond-based self-healing polyacrylic acid binder comprises a polymer main chain and a dynamic cross-linking agent, the dynamic cross-linking agent is a polyol compound containing at least two pairs of ortho-hydroxyl groups; the polymer main chain is formed by copolymerizing the following monomers: an acrylic structural monomer, the molar fraction of which accounts for 85-94% of the total monomer; a functional monomer containing a boric acid group, wherein the molar fraction of the functional monomer accounts for 3-8% of the total monomer; the mole fraction of the flexible monomer containing the acrylate group accounts for 3-8% of the total monomer. Various stresses generated by different negative electrode materials in circulation can be effectively adapted and buffered through a network formed by dynamic boric acid ester bonds and reversible fracture and combination of the boric acid ester bonds, so that the service life of the battery is generally prolonged, the working temperature range of the battery can be remarkably widened, the low-temperature discharge capacity can be remarkably increased, and the high-temperature cycle life can be prolonged.

The invention discloses a high-dispersion graphene conductive adhesive solution for a battery and a preparation method of the high-dispersion graphene conductive adhesive solution, and belongs to the technical field of conductive adhesive solutions. The high-dispersion graphene conductive adhesive solution for the battery prepared by the invention is prepared from the following raw material components in parts by mass: 6 to 8 parts of high-dispersion graphene, 4.5 to 13.5 parts of an adhesive and 60 to 90 parts of a solvent, the preparation method comprises the following steps: ultrasonically dispersing graphene in a mixed solution of hexadecyl triyl ammonium bromide and deionized water, sequentially adding hexadecyl triyl ammonium bromide, sodium molybdate dehydrate, bismuth nitrate pentahydrate and cerium nitrate hexahydrate, uniformly stirring and dispersing, performing hydrothermal reaction, washing, drying, grinding and sieving to obtain the high-dispersion graphene. The adhesive is prepared from an amphiphilic polyethylene glycol-polycaprolactone block copolymer and amphiphilic polyacrylate.

The invention provides high-strength retarded magnesium phosphate cement as well as a preparation method and application thereof, and belongs to the technical field of magnesium phosphate cement. The high-strength retarded magnesium phosphate cement provided by the invention is prepared from the following raw materials in parts by mass: 60 to 95 parts of dead burned magnesia powder, 20 to 50 parts of phosphate, 3 to 15 parts of a composite retarder, 5 to 20 parts of an admixture, 8 to 14 parts of fly ash microspheres, 1 to 2 parts of carbon nanotubes, 1 to 5 parts of carbon fibers and 5 to 30 parts of water, the composite retarder comprises sodium tripolyphosphate, zinc acetate, EDTA (Ethylene Diamine Tetraacetic Acid) disodium and polyacrylic acid; the admixture comprises phosphorus slag powder and silica fume. The result of the embodiment shows that the setting time of the high-strength delayed-setting magnesium phosphate cement provided by the invention is controllable between dozens of minutes and dozens of hours, meanwhile, the compressive strength of the magnesium phosphate cement 28d is greater than 90MPa, and the magnesium phosphate cement has excellent mechanical properties.

The invention provides a polyacrylic acid inverse emulsion thickener and a preparation method thereof. The polyacrylic inverse emulsion thickener is prepared from the following components in parts by mass: 1 to 10 parts of modified attapulgite, 0.1 to 5 parts of hyperbranched acrylate, 30 to 60 parts of acrylic acid, 1 to 5 parts of a hydrophobic long-chain acrylate monomer, 5 to 20 parts of solvent oil, 0.5 to 5 parts of an emulsifier, 0.01 to 1 part of an initiator and 0.5 to 2.5 parts of a phase inversion agent. The preparation method comprises the following steps: firstly, introducing an isocyanate chain segment and a double-bond active group to the surface of acid-activated attapulgite to improve dispersity and reaction activity; then trimethylolpropane is used as a core, hyperbranched acrylate with multiple double bonds and a hyperbranched structure is constructed, and then the polyacrylic acid inverse emulsion thickener is prepared through an inverse emulsion method. Through the synergistic effect of the hyperbranched acrylate, the modified attapulgite and the hydrophobic long-chain monomer, the thickening performance, the electrolyte resistance and the long-term stability are remarkably improved.

The invention discloses a preparation method of a metal organic framework modified fluorine-free super-amphiphobic coating, and belongs to the technical field of super-amphiphobic coatings. According to the technical scheme, the method comprises the steps of preparation and modification of a metal organic framework and formation of a fluoride-free super-amphiphobic coating. Adding a metal oxide and nano silicon dioxide particles into a polyacrylic acid solution to form spherical particles; enabling the spherical particles to react with imidazole ligands to obtain metal organic framework particles with porous spherical structures, and wrapping nano silicon dioxide particles in the metal organic framework particles; modifying the metal organic framework particles by using a silane coupling agent; the preparation method comprises the following steps: firstly, attaching modified metal organic framework particles to the surface of a metal matrix, then attaching fluorine-free alkyl silane to the surface of the metal matrix, and heating and curing to obtain the fluorine-free super-amphiphobic coating. The fluorine-free super-amphiphobic coating is applied to the aspect of a metal surface super-amphiphobic coating, and the problems that an existing fluorine-free super-amphiphobic coating is poor in oleophobic and hydrophobic performance and poor in durability are solved.

The invention provides a battery positive plate and a battery. The battery positive plate comprises a positive active material and a binder, and the binder is a product obtained by crosslinking a phenylboronic acid compound modified polyacrylic acid compound and a hydroxylated carbon nanotube. According to the battery positive plate, a three-dimensional conductive network binder based on crosslinking of a phenylboronic acid compound modified polyacrylic acid compound and a hydroxylated carbon nanotube is adopted, and the binder utilizes a multi-crosslinking mechanism between a phenylboronic acid group and the hydroxylated carbon nanotube (OHCNT) and between the phenylboronic acid group and positive active particles; a boroxane structure is formed through self-crosslinking of the boron oxide and the phenylboronic acid, and a special three-dimensional conductive network structure is formed, so that the mechanical strength and the conductivity of the binder and the cycle performance and the stability of the battery are improved; the discharge performance and the rapid charge-discharge capability of the battery can be improved, and the consumption of electrolyte can be reduced, so that the cycle life of the battery is prolonged.

The invention discloses a preparation method and application of a ceramic glaze layer protecting and repairing material, and belongs to the technical field of cultural relic protection. The preparation method comprises preparation of a core-shell self-repairing nanocapsule, and the preparation of the core-shell self-repairing nanocapsule comprises the following steps: reacting a calcium chloride solution with a sodium hydroxide solution, then adding sodium polyacrylate and nano ZnO, and carrying out dispersion, centrifugation, washing and other operations to prepare the nano Ca (OH) 2-ZnO composite material. The nano Ca (OH) 2-ZnO composite material of the core-shell self-repairing nanocapsule can be rapidly released through the 3.5 nm aperture of the mesoporous SiO2 shell, glaze layer cracks are physically filled and react with CO2 in air to generate CaCO3 crystals, crack plugging is achieved, meanwhile, dynamic disulfide bonds of a PU layer are broken and recombined under stress stimulation, a crack interface is repaired through chemical bonding, and the performance of the core-shell self-repairing nanocapsule is improved. The 24-hour crack repair rate is greater than or equal to 96%, and the limitation of'one-time repair 'of a traditional material is solved.

The invention discloses a modified thermal insulation coating and a preparation method and application thereof, and belongs to the field of building energy-saving materials. One modified compound is a thermo-sensitive polyelectrolyte layer-by-layer self-assembled alumina microsphere formed by alternately depositing polyethyleneimine and polyacrylic acid through electrostatic interaction, and the polyelectrolyte layer can dynamically swell or shrink along with the temperature to adjust the heat conductivity coefficient; and the other is magnesium silicate nanofiber coated with silicon dioxide and then grafted with fluorosilane, the hydrophobicity is improved by utilizing the low surface energy of the fluorosilane, and meanwhile, the binding force with a polymer interface is enhanced. The coating further comprises fumed silica, a dispersing agent, a defoaming agent and other auxiliaries. The preparation method comprises the following steps: sequentially adding the components into a high-speed dispersion machine, mixing, adjusting the viscosity, filtering and packaging. The coating has the advantages of intelligent temperature-sensitive adjustment, low heat conductivity, strong adhesion and weather resistance; the material is suitable for long-acting heat preservation in the fields of buildings, industrial equipment and cold chains.