981 results about "Methyl acrylate" patented technology

The invention discloses a repulpable and degradable PHA heat-seal barrier coating and a composition thereof, and belongs to the field of water-based functional coatings and cellulose-based packaging materials. The coating composition is prepared from the following components in percentage by non-volatile solids: 30 to 85 weight percent of polyhydroxyalkanoate emulsion, 5 to 60 weight percent of flaky natural inorganic matters, a water-based cross-linking agent and an auxiliary agent, and 1 to 20 weight percent of ethylene-acrylic acid or ethylene-methyl acrylate dispersion can be selected. The pH value of the composition is 6.5-9.0, and organic fluorine is not artificially added. When the dry weight is 6-20 g / m, the coating meets at least one of the following four items: the water vapor transmission rate (38 DEG C, 90% RH) is less than or equal to 80 g / m.d, Cobb60 is less than or equal to 15 g / m, the oil resistance grade is greater than or equal to 11, and the laboratory repulping rate is greater than or equal to 98%; and the heat-sealing peel strength is greater than or equal to 2.5 N / 15mm under the conditions of 150 DEG C, 0.2 MPa and 0.5 s. And the coating and the stripping film thereof meet the industrial composting standard.

The invention relates to the technical field of textiles, and discloses a cool and washable bio-based nylon 56 fabric and a preparation method thereof. The preparation method of the cool and washable bio-based nylon 56 fabric comprises the following steps: loading modified nano aluminum oxide on modified aluminum nitride microchips to obtain a composite cool material; nylon 56, an ethylene-methyl acrylate-glycidyl methacrylate terpolymer, polypentamethylene guanidine hydrochloride and a composite cool feeling material are subjected to blending extrusion and melt spinning, and then the bio-based nylon 56 fabric is woven. Mixing the composite modified boron nitride and ethanol to obtain finishing liquid; spraying the finishing liquid on one side of the bio-based nylon 56 fabric, and drying to obtain the cool washable bio-based nylon 56 fabric. The cool and washable bio-based nylon 56 fabric disclosed by the invention has excellent cool feeling, antibacterial property, washable property, moisture absorption property and unidirectional perspiration property.

The invention relates to the technical field of blocking medicine bottles, and particularly discloses a blocking medicine bottle and a preparation method thereof, aiming at the problems that the upper limit of the blocking performance of the existing blocking medicine bottle is low and the blocking performance is difficult to break through due to the fact that the blocking performance of the existing blocking medicine bottle is mostly realized through structural design. A bottle body of the blocking medicine bottle comprises an inner layer, a secondary inner layer, a middle layer, a secondary outer layer and an outer layer which are sequentially arranged in a covering mode. The inner layer comprises polyethylene; the secondary inner layer comprises an ethylene-methyl acrylate copolymer; the middle layer comprises an ethylene-vinyl alcohol copolymer, cyclic polyolefin and modified montmorillonite; the secondary outer layer comprises an ethylene-methyl acrylate copolymer; the outer layer comprises polyethylene, cyclic polyolefin and modified montmorillonite. The barrier medicine bottle is formed by compositing five layers of materials, the oxygen and water transmittance is low, the barrier property is high, and the barrier medicine bottle has great application value in packaging of medicine or food and the like.

The invention discloses a high-RAP-doping-amount cold-mixed asphalt regenerant, and particularly relates to the technical field of asphalt regenerant, the high-RAP-doping-amount cold-mixed asphalt regenerant comprises the following raw materials: hydrogenated extract oil, acetyl tributyl citrate, a low-temperature penetrant, pre-swelling SEBS master batch, a crosslinking catalyst and a microcapsule antioxidant. Molecular-level branched-chain alkyl sodium sulfonate can be wedged into aged asphalt microcracks at the temperature of 65 DEG C, lost light components are balanced and supplemented through hydrogenated extract oil, an SEBS micro-crosslinking network forms an in-situ reinforcement effect at the temperature of 90 DEG C, the triple regeneration effect of regenerated asphalt is achieved, and the service life of the regenerated asphalt is prolonged. Nano-zinc oxide is treated by a silane coupling agent and then is modified by using methyl methacrylate and potassium persulfate, so that the nano-zinc oxide is coated with polymethyl methacrylate, the compatibility of the microcapsule antioxidant and the recycled asphalt can be improved, and the anti-aging performance of the recycled asphalt is improved.

The invention provides transparent high-impact-resistance heat-resistant MBS (methyl methacrylate-butadiene-styrene) resin and a preparation method thereof, and relates to the field of high polymer material preparation methods, the transparent high-impact-resistance heat-resistant MBS resin is prepared from the following raw materials: water, ethanol, maleic anhydride, an emulsifier, MBS resin grafted latex, potassium persulfate and an antioxidant; the MBS resin grafted latex is prepared from the following raw materials: water, modified styrene-butadiene latex, sodium hydrogen sulfite, potassium persulfate, methyl methacrylate and styrene, the modified styrene-butadiene latex is prepared from the following raw materials: a pre-emulsion, glycidyl methacrylate, ammonium persulfate, divinyl benzene and potassium persulfate; the pre-emulsion is prepared from the following raw materials: water, an emulsifier, butadiene and styrene. The product is good in heat resistance and good in PVC modification effect, and the modified PVC composite material is high in light transmittance, high in cantilever beam impact strength and resistant to aging.

The invention discloses a hydrogel dressing with a double-slow-release effect as well as a preparation method and application of the hydrogel dressing. The preparation method of the hydrogel dressing comprises the following steps: firstly, preparing methyl acrylate modified hyaluronic acid capable of being photo-crosslinked, then preparing carboxymethyl chitosan nanoparticles loaded with chlorogenic acid, and finally, mixing the methyl acrylate modified hyaluronic acid and the carboxymethyl chitosan nanoparticles loaded with chlorogenic acid to obtain the hydrogel dressing. The hydrogel dressing embedded with the nanoparticles is obtained in a photo-crosslinking mode. The hydrogel dressing provided by the invention not only has good biocompatibility and mechanical properties, but also plays an anti-oxidation role by removing free radicals in a body, and can effectively kill bacteria such as escherichia coli and staphylococcus aureus to play an antibacterial role. The hydrogel dressing can also reduce excessive inflammatory response in the wound healing process by influencing macrophage polarization, promote chronic wound healing and relieve pain of patients.

The invention relates to the technical field of cables, and provides a tensile new energy charging pile cable which comprises a conductor, an insulating layer, a shielding layer and a sheath layer which are sequentially arranged from inside to outside. The sheath layer comprises the following components in parts by weight: 60-70 parts of chlorinated polyethylene, 15-20 parts of polyisoprene, 5-10 parts of an ethylene-methyl methacrylate copolymer, 8-18 parts of an acrylonitrile-butadiene-styrene copolymer, 20-30 parts of modified hydroxyapatite, 1-5 parts of a lubricant, 3-6 parts of a plasticizer, 30-40 parts of a flame retardant and 1-3 parts of an antioxidant; the raw materials of the modified hydroxyapatite comprise hydroxyapatite and a modifier; the modifier comprises maleic acid-acrylic acid copolymer sodium salt; the weight ratio of the hydroxyapatite to the modifier is 45: (1-7). According to the technical scheme, the problem that the cable sheath layer of the new energy charging pile is poor in tensile property and corrosion resistance in the prior art is solved.

The invention relates to an epoxy core-shell polymer particle and resin, a preparation method of the epoxy core-shell polymer particle and resin and application of the epoxy core-shell polymer particle and resin to epoxy resin. The preparation method of the epoxy core-shell polymer particle comprises the following steps: heating and mixing a polybutadiene seed emulsion, a reducing agent, an emulsifier and the like; adding methyl methacrylate and an initiator, and glycidyl methacrylate and an initiator, and heating to react; compared with the prior art, the core-shell particle with the outer layer of the synthesized shell containing the epoxy group can be used for toughening the epoxy resin, so that the toughness of the epoxy resin is effectively improved while the excellent heat resistance and mechanical properties of the epoxy resin are maintained.

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 discloses a biodegradable polylactic acid composite material and a preparation method thereof, and relates to the technical field of polylactic acid materials. The method comprises the steps that firstly, chitosan activated through hydrochloric acid is subjected to graft modification through a KH550 silane coupling agent, meanwhile, nano-zinc oxide is subjected to surface modification through stearic acid, the chitosan and the nano-zinc oxide are mixed, spray drying is conducted, and antibacterial composite powder is prepared; the preparation method comprises the following steps: performing hydrochloric acid activation and KH570 silane coupling agent modification on nano silicon dioxide, performing hydroxypropylation modification on alkali lignin, and performing reflux crosslinking reaction on the modified alkali lignin, KH570 modified nano silicon dioxide, polycaprolactone, methyl methacrylate and azodiisobutyronitrile to prepare a heat-resistant reinforcer; uniformly mixing polylactic acid, poly (butylene succinate), the antibacterial composite powder, the heat-resistant reinforcer, tributyl citrate, polyethylene glycol and talcum powder, and extruding and granulating by using a twin-screw extruder to obtain the heat-resistant antibacterial material. The composite material prepared by the invention has excellent antibacterial property, heat resistance and biodegradability.

The present invention relates to the technical field of modification of lithium battery current collector materials, and provides a coating material and a preparation method for preventing PET film degradation. The coating material is a film-forming substance made of vinyl pyrrolidone / methyl acrylate / fluorinated ethylene copolymer and a graphene nanosheet as a filler. The main component of the film-forming substance is a polyvinyl pyrrolidone segment, and the relative content of the methyl acrylate segment and the fluorinated ethylene segment is small. In addition, the vinyl pyrrolidone / methyl acrylate / fluorinated ethylene copolymer forms a three-dimensional network structure through cross-linking, and the graphene nanosheet forms a chemical connection with the polymer network through a surface active group. The coating can effectively prevent the lithium battery electrolyte and the catalyst alkoxy lithium from contacting with the PET substrate, thereby preventing the PET substrate from degrading.

The invention relates to an in-situ curing gel structure electrolyte as well as a preparation method and application thereof. The preparation method comprises the following steps: (1) mixing a resin matrix with a pore-forming agent, then adding a curing agent for mixing to obtain a mixed solution, and pouring the mixed solution into a closed mold for curing to obtain a resin film; soaking and drying the resin film to obtain porous resin; and (2) mixing 4-styrene sulfonyl (phenylsulfonyl) imide lithium salt, polyethylene glycol methyl ether acrylate, polyethylene glycol dimethacrylate, ethylene carbonate and azodiisobutyronitrile to prepare a mixed solution, and soaking the porous resin in the mixed solution to react and cure, thereby obtaining the in-situ curing gel structure electrolyte. The preparation method is simple, and the prepared in-situ curing gel structure electrolyte can improve the mechanical property, the battery capacity and the cycle performance of the in-situ curing gel structure electrolyte.

The invention relates to the technical field of oilfield chemistry, in particular to an aminoethanesulfonic acid type surfactant and a preparation method and application thereof.The preparation method of the aminoethanesulfonic acid type surfactant comprises the steps that firstly, fatty amine is dissolved in a first solvent, a sodium chloroethanesulfonate aqueous solution is added, and N-long-chain alkyl-2-sodium aminoethanesulfonate is obtained through a reaction; and 2, dissolving a required amount of N-long-chain alkyl-2-sodium aminoethanesulfonate in a second solvent, adding a required amount of methyl acrylate, and reacting to obtain the aminoethanesulfonic acid type surfactant. The aminoethanesulfonic acid type surfactant disclosed by the invention contains long-chain alkyl, amino, ester groups and sulfonic acid groups, so that the aminoethanesulfonic acid type surfactant has good surface activity and can meet the development requirements of oil and gas fields. The microemulsion cleanup additive prepared from the aminoethanesulfonic acid type surfactant can effectively reduce the surface tension and the interfacial tension of an aqueous solution, and the preparation method is easy and convenient to operate, mild in condition and suitable for industrial production.

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 discloses a high-toughness biaxially oriented nylon film and a production method thereof. Comprising the following raw materials in parts by weight: 40-50 parts of copolymerized nylon resin, 10-20 parts of nylon 12, 15-25 parts of thermoplastic polyamide elastomer, 3-6 parts of nanofiller, 1-3 parts of coupling agent, 10-20 parts of reinforced fiber, 5-8 parts of additive, 3-7 parts of ethylene-methyl acrylate-glycidyl methacrylate terpolymer and 6-10 parts of modified cellulose nanocrystal. The invention relates to a flame-retardant polyamide resin, which is prepared from the following components in parts by weight: 2-4 parts of amino-terminated hyperbranched polyamide and 1-3 parts of 3, 3 '-diamino-4, 4'-difluorodiphenyl sulfone. The film is high in tensile strength, good in tear resistance and excellent in barrier property and low-temperature impact resistance.

The invention relates to the technical field of coatings, in particular to an associative emulsion thickener for latex paint and a preparation method of the associative emulsion thickener. The associative emulsion thickener for the latex paint is formed by polymerizing a monomer A, a monomer B and a monomer C, the monomer A is prepared from tridecyl methacrylate, diethyl itaconate and isobornyl acrylate; the monomer B comprises methyl acrylate, acrylic acid and acrylic acid-2-hydroxyethyl ester; the monomer C is prepared from diacetone acrylamide, N-isopropyl acrylamide, N-dodecyl acrylamide and ethylene glycol dimethacrylate. The thickening agent has the advantages of environmental protection, high biocompatibility and good thickening effect, solves the problem of poor stability of latex paint at low temperature and high temperature, and improves the glossiness.

The invention discloses a preparation process of an early-warning anti-loosening bolt, and relates to the technical field of bolts, the outer side of a bolt base body is coated with a layer of anti-corrosion sheath containing a polyamide composite material through an injection molding process, so that the effect of improving the corrosion resistance of the bolt is achieved. Furan-2, 5-diketone is used for modifying aminated graphene oxide, maleimide modified graphene oxide is obtained, maleimide has the characteristic of being sensitive to ultraviolet light, and can react with styrene and methyl methacrylate under ultraviolet irradiation, so that vinyl graphene oxide is obtained; and then polyamide modified glass fibers are added, so that the corrosion resistance of the bolt is further improved.

The invention discloses an artificial SEI film coated graphite negative electrode material and a preparation method and application thereof, and belongs to the technical field of lithium ion battery negative electrode materials. The preparation method comprises the following steps: heating and oxidizing graphite in mixed gas of air and nitrogen, and cooling to obtain oxidized and etched graphite; then dispersing the oxidized and etched graphite in a solvent, adding methyl methacrylate and graphene, stirring and initiating an in-situ polymerization reaction, and forming a doped coating layer on the oxidized and etched graphite; and finally, carrying out vacuum drying on the coated oxidized and etched graphite, and cooling to obtain the artificial SEI film coated graphite negative electrode material. The specific surface area of graphite is increased through oxidation etching, the ion diffusivity is improved, the combination effect of the organic polymer is improved, the first efficiency of the negative electrode material is remarkably improved by combining the synergistic effect of the conductive polymerized organic matter and graphene, and the conductivity, the structural stability and the interface compatibility are enhanced.

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 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.

The invention discloses a preparation method and application of an nNi / Rh (x)-La2O3 catalyst, and belongs to the technical field of catalysts. According to the technical scheme, the preparation method comprises the following steps: 1) preparing La2O3 carrier particles: screening lanthanum nitrate, dropwise adding a nitric acid solution into the lanthanum nitrate, mixing, drying and calcining; 2) preparation of Rh (x)-La2O3: adding the La2O3 carrier particles and Rh (NO3) 3.2 H2O into water, and stirring for reaction; drying and calcining to obtain an Rh (x)-La2O3 carrier; and 3) preparation of the nNi / Rh (x)-La2O3 catalyst: dispersing the Rh (x)-La2O3 carrier in water, adding Ni (NO3) 2.6 H2O into the Rh (x)-La2O3 carrier, stirring, adjusting the pH value, carrying out a reaction, cleaning and drying the precipitate, and calcining to obtain the nNi / Rh (x)-La2O3 catalyst. The nNi / Rh (x)-La2O3 catalyst has very high catalytic activity, and has a good application prospect in photocatalytic degradation of methyl acrylate.

The invention relates to the technical field of preparation of surface micro-nano structures, and discloses a method for generating a micro-bulge structure based on a controllable gas phase microreactor, which comprises the following steps: preparing an organic mixed solution, mixing a driving solution methyl methacrylate into an initiator di-tert-butyl peroxide solution, then adding a solvent dimethyl sulfoxide solution, and stirring to obtain a mixed solution; meanwhile, ultrasonic oscillation is carried out for 10 minutes; according to the method for generating the micro-bulge structure based on the controllable gas-phase microreactor, the preparation of the micro-bulge structure can be realized only by directly dropwise adding a precursor organic mixed solution of a polymer on the surface of a substrate with a photothermal effect and then controlling the irradiation position and energy of continuous wave laser; compared with a photoetching method, the method has the advantages that complicated equipment operation and tedious process steps are not needed, and compared with the photoetching method, expensive photoetching machines, masks, vacuum chambers and complicated chemical reagent treatment processes are not needed, so that the operation flow is simplified.

The invention belongs to the technical field of acrylic plates, and particularly relates to a continuous casting high-hardness acrylic plate and a preparation method thereof.The preparation method comprises the steps that siloxane modified methacrylic acid, methyl methacrylate and n-butyl methacrylate are mixed, an azo initiator is added into the mixture, and then stirring and mixing are conducted to obtain pre-polymerized slurry; the preparation method comprises the following steps: mixing hydroxyl-terminated ether polysiloxane, isophorone diisocyanate and a catalyst dibutyltin dilaurate, reacting to obtain a macromolecular prepolymer, and then adding an end-capping reagent and a photoinitiator into the macromolecular prepolymer to obtain coating slurry; and injecting the pre-polymerized slurry between two annular steel belts which operate synchronously, coating the two annular steel belts with the coating slurry, and carrying out ultraviolet curing to obtain the high-hardness acrylic plate. Through ultraviolet curing, a high-hardness layer is formed outside the acrylic plate, polyurethane is modified by hydroxyl-terminated ether polysiloxane, the rigidity of a soft chain segment is improved by a polysiloxane chain segment, and the hardness of polyurethane is improved.

The invention discloses a preparation method of ulinastatin adsorption resin, and belongs to the technical field of adsorption resin. Comprising the following steps: (1) preparing a water phase: adding pure water, gelatin, cellulose, sodium chloride and lignin into a reaction kettle until the materials are fully dissolved; (2) preparing an oil phase, wherein the oil phase contains divinylbenzene, methyl acrylate, benzoyl peroxide, tert-butyl peroxy-2-ethylhexanoate, triallyl isocyanurate, tripropanol alkyl trimethacrylate and methylbenzene, and the oil phase is uniformly stirred and mixed with the methylbenzene and the trivinylbenzene, the methyl acrylate, the benzoyl peroxide, the tert-butyl peroxy-2-ethylhexanoate, the triallyl isocyanurate, the tripropanol alkyl trimethacrylate and the methylbenzene; (3) suspension polymerization: putting the oil phase into the water phase, and carrying out staged heating reaction; (4) amination reaction; (5) alkylation reaction; and (6) acid-base alcohol treatment. Compared with the existing resin, the resin disclosed by the invention has the characteristics of high adsorption exchange rate, high desorption rate and high desorption concentration on ulinastatin, and the yield of ulinastatin is increased by 1.17 times compared with that of D215 resin.

An extreme-cold resistant low-fume halogen-free flame-retardant polyolefin sheath, a preparation method therefor, and a cable. The sheath comprises the following raw materials in parts by mass: 4-16 parts of an ethylene-vinyl acetate copolymer, 7-13 parts of a phosphate group functionalized linear low-density polyethylene, 9-15 parts of an ethylene-octene copolymer, 5-10 parts of a maleic anhydride-grafted ethylene-methyl methacrylate copolymer, 10-15 parts of magnesium hydroxide, 40-50 parts of aluminum hydroxide, etc. The preparation method for the phosphate group functionalized linear low-density polyethylene comprises: adding a catalyst to a pre-cooled ethylene monomer, adding a vinyl phosphate ester and an initiator after the reaction, and reacting for 1-2 hours at a temperature of 65-75°C and a pressure of 15-35 Mpa and then terminating the reaction, thereby obtaining the phosphate group functionalized linear low-density polyethylene. Compared with unfunctionalized polyethylene, the phosphate group functionalized polyethylene used has greatly improved low-temperature and flame-retardant performance, and can improve the overall flame-retardant and low-temperature performance of the formula.

The invention relates to the technical field of adhesives, in particular to a hot melt adhesive, a preparation method thereof and a fuel cell membrane electrode. The hot melt adhesive comprises a first bonding layer and a second bonding layer; the first bonding layer comprises polyester resin, a styrene thermoplastic elastomer, a grafted toughening agent, an epoxy chain extender and a first organic solvent; the second bonding layer comprises an ethylene-methyl acrylate copolymer, a copolyester hot melt adhesive, an ethylene-methyl acrylate-glycidyl methacrylate terpolymer, an epoxy ring-opening accelerant and a second organic solvent. The hot melt adhesive provided by the invention has a two-layer structure, can realize good bonding of PEN and PFSA, does not blister or crack after being soaked in a sulfuric acid aqueous solution with the pH value of 2 at 95 DEG C for more than 2000h, can maintain good bonding performance, and has no crystal point in a formed film.

The invention provides a bacteriostatic PET (polyethylene terephthalate) coiled material as well as a preparation method and application thereof, and belongs to the technical field of high polymer materials, the bacteriostatic PET coiled material is prepared from the following raw materials: PET, nano titanium dioxide, nano talcum powder, a compatilizer, an antioxidant, a lubricant and a modified composite bacteriostatic agent; the compatilizer is an ethylene-methyl acrylate-glycidyl methacrylate random terpolymer and / or an ethylene-acrylic ester-maleic anhydride random terpolymer, and the compatilizer is an ethylene-methyl acrylate-glycidyl methacrylate random terpolymer and / or an ethylene-acrylic ester-maleic anhydride random terpolymer; the lubricant is one or a mixture of two of pentaerythritol stearate, erucyl amide, polyethylene wax, polyvinyl alcohol and ethylene bis stearamide; the modified composite bacteriostatic agent is prepared from catechin gallate, epsilon-polylysine hydrochloride and modified porous zinc oxide. The prepared antibacterial PET coiled material can be used for packaging materials of packaging boxes, lunch boxes, cup covers, trays and the like, and has good mechanical properties such as bending strength and impact strength and excellent antibacterial performance.

The present invention relates to a matting agent for HAA powder coatings and a preparation method thereof. The matting agent is a matting polymer containing special groups such as hydroxyl and epoxy groups with significantly different activities. The matting polymer is mainly prepared from glycidyl methacrylate, methyl methacrylate, butyl acrylate, 5-norbornene-2-methanol, 2-methyl-3-butene-2-ol, dicyclopentadiene dioxide, a hydroxyl polyester resin, and an accelerator. Due to the presence of hydroxyl and epoxy groups of varying activities in its structure, supplemented by the accelerator and the physical dispersion effect during the preparation process, the product has excellent matting ability and good storage and matting stability. It can reduce the gloss of HAA system powder coatings to 3-10%.

The invention relates to the technical field of lubricating oil, and discloses a composite lubricating oil repairing additive and a preparation method thereof.The preparation method includes the steps that methyl silicone oil, sodium dodecyl benzene sulfonate, methyl acrylate, zinc dialkyl dithiophosphate and barium sulfonate are added into a stirrer and stirred, quaternary ammonium salt modified imidazoline and modified chitosan are continuously added into the stirrer and stirred, and the composite lubricating oil repairing additive is obtained; and after finishing, obtaining the composite lubricating oil repairing additive. Chitosan in the modified chitosan has a good anti-rust effect. Imidazoline in quaternary ammonium salt modified imidazoline can form a protective film on the surface of metal to effectively prevent the metal from being in contact with a corrosive medium, so that the corrosion process of the metal is slowed down, and a relatively good anti-rust effect is achieved. Wherein the quaternary ammonium salt forms a layer of protective film on the surface of metal to prevent moisture, oxygen and other corrosive substances from being in contact with the metal, so that the metal is effectively prevented from rusting.

The invention discloses a super-tough temperature-resistant self-repairing copolymer based on SBS acrylate dynamic synergistic reinforcement and a preparation method thereof, and belongs to the technical field of self-repairing materials in compositions of high-molecular compounds. The copolymer comprises SBS, an acrylate monomer, a dynamic bond functional monomer, an initiator, a cross-linking agent, a nano reinforcing agent and a temperature-resistant modifier, wherein the dynamic bond functional monomer comprises at least one of acryloyloxyethyl disulfide, acrylamide acryloyloxyethyl disulfide or anthracene methyl acrylate. The molecular structure of the dynamic bond functional monomer contains a carbon-carbon double bond and a disulfide bond, in the free radical polymerization reaction initiated by the initiator, the carbon-carbon double bond is opened and is subjected to a copolymerization reaction with an SBS chain segment or an acrylate chain segment, so that the disulfide bond enters the polymer chain segment, the dynamic disulfide bond can be reversibly broken and recombined at high temperature, and the dynamic bond functional monomer is obtained. The high-temperature viscoelasticity is maintained, the material is endowed with self-repairing capability, and the problem that the viscoelasticity of the material in the prior art is sharply reduced at high temperature (gt; 120 DEG C) is solved.