798 results about "Glycerol Ethers" patented technology

The invention discloses an electrolytic adhesive, an electrolytic cotton adhesive tape and a preparation method of the electrolytic adhesive. The electrolytic cotton adhesive tape comprises the following components in parts by weight: 5-10 parts of 1, 1 '-ferrocene diformyl chloride, 10-15 parts of acrylic acid beta-cyclodextrin ester, 3-8 parts of polyethylene glycol diglycidyl ether, 10-20 parts of ionic liquid, 1.5-3 parts of a cross-linking agent, 10-15 parts of tackifying resin and 0.5-1.5 parts of an initiator, and a polymer matrix comprises an acrylic acid-hydroxypropyl acrylate copolymer and acrylic acid-2-ethylhexyl ester. Comprising an adhesive layer and an adhesive tape base layer, the adhesive layer is prepared from the electrolytic adhesive, and the adhesive tape base layer is prepared from acrylic foam; the obtained electrolytic cotton adhesive tape has high initial adhesion and viscosity strength after power-on and power-off re-adhesion.

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

The invention relates to the field of packaging materials, and discloses low-temperature heat-sealing water-based coated paper and a preparation method and application thereof.The water-based coated paper comprises a base paper layer and a water-based coating, and the water-based coating comprises water-based ethylene-acrylic acid copolymer emulsion, modified nano-silica, a coalescing agent and water; a cardanol derivative is introduced into the water-based ethylene-acrylic acid copolymer emulsion as a functional component; the cardanol derivative is prepared by reacting epoxidized cardanol with 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide and then grafting with acryloyl chloride. The preparation method comprises the following steps: reacting epoxidized cardanol with 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide; the modified nano silicon dioxide is prepared by mixing aminated nano silicon dioxide and chitosan and adding a cross-linking agent prepared by grafting phytic acid and ethylene glycol diglycidyl ether. The water-based coating paper prepared by the invention overcomes the defects that the existing BOPP film is not environment-friendly, and the conventional coating paper is high in heat sealing temperature and easy to stick; meanwhile, good mechanical properties, water resistance and flame retardance are achieved.

The invention belongs to the technical field of nanocrystal nucleus early strength agents, and provides a damp and hot nanocrystal nucleus early strength agent, a tailing solidification filling material and a preparation method and application of the damp and hot nanocrystal nucleus early strength agent and the tailing solidification filling material. The invention discloses a molybdenum ore tailing slurry which is prepared from the following raw materials in parts by weight: 1 part of Portland cement, 4 to 6 parts of molybdenum ore tailings, 0.06 to 0.1 part of zeolite powder, 0.07 to 0.1 part of nanoscale attapulgite powder, 0.06 to 0.1 part of gamma-glycidyl ether oxypropyl trimethoxy silane, 0.03 to 0.1 part of potassium silicate, 0.04 to 0.1 part of sodium hydroxide, 0.06 to 0.1 part of calcium formate, 0.04 to 0.1 part of lithium metaaluminate and 1.25 to 1.75 parts of water. According to the technical scheme, the problem that a filling body prepared from an early strength agent in the prior art is low in early and later strength is solved, and meanwhile, the early strength agent is simple and convenient in preparation mode, low in cost and wide in application range.

The invention relates to the field of coatings, and discloses a biomass-based oil-resistant coating and a preparation method thereof, the coating comprises an additive solution, a paraffin solution and gallic acid; the paraffin solution is obtained by dissolving paraffin in absolute ethyl alcohol; a preparation method of the additive solution comprises the following steps: mixing chitosan powder and an acetic acid aqueous solution to prepare a chitosan solution, ultrasonically dispersing functionalized montmorillonite in deionized water to prepare a suspension, then uniformly mixing the chitosan solution and the suspension, adding modified phytic acid prepared by grafting phytic acid and ethylene glycol diglycidyl ether, and stirring to react; the functional montmorillonite is prepared by modifying modified montmorillonite with titanium dioxide and zinc oxide, then activating the modified montmorillonite with 3-aminopropyltriethoxysilane and succinic anhydride, and then carrying out a ring-opening reaction with glycidyl neodecanoate. The coating prepared by the invention has high water resistance, the Kit oil-proof grade is kept at grade 12, and the oil-proof performance of the coating is greatly improved. Meanwhile, the antibacterial performance, the tensile index and the ultraviolet aging resistance are relatively high.

The invention discloses a polyurethane modified epoxy resin adhesive as well as a preparation method and application thereof, and the polyurethane modified epoxy resin adhesive is prepared from the following components in parts by mass: 7-10 parts of E51 type bisphenol A diglycidyl ether, 3.5 parts of a phenolic aldehyde amine T31 curing agent and 1-3 parts of synthetic polyurethane, the synthetic polyurethane is prepared from polyether triol, polyether amine, isophorone diisocyanate and glycerol carbonate, and a blending system of the synthetic polyurethane and bisphenol A diglycidyl ether is adopted to be subjected to covalent crosslinking with phenolic aldehyde amine T31, so that the adhesive has high toughness and strength guarantee; the synthetic polyurethane prepared by the method is obtained through simple, green and efficient solvent-free synthesis, and the synthesized product has certain fluidity at room temperature, so that the subsequent stirring preparation process of an adhesive is facilitated. And a solvent-free synthesis method is adopted, so that the use of a toxic organic solvent in the traditional polyurethane synthesis process is avoided, and the synthesis process is greener.

The invention relates to the technical field of epoxy resin, in particular to self-repairing epoxy resin and a preparation method thereof. The self-repairing epoxy resin is prepared from the following raw materials in parts by mass: 80 to 120 parts of bisphenol A type epoxy resin, 20 to 40 parts of bisphenol F type epoxy resin, 5 to 15 parts of 1, 6-hexanediol diglycidyl ether, 1 to 3 parts of 3, 5-dimethylphenylboronic acid, 1 to 5 parts of furyl maleimide, 10 to 20 parts of dodecanedioic acid, 5 to 15 parts of butanetetracarboxylic acid, 1 to 3 parts of catalyst, 10 to 15 parts of nano silicon dioxide, 1 to 2 parts of boron nitride nanosheet and 1 to 2 parts of hyperbranched polyamidoamine. The curing agent is prepared from the following components in parts by weight: 20-30 parts of epoxy resin, 1-2 parts of sulfydryl-terminated polysiloxane, 20-30 parts of amine curing agent, 5-15 parts of reinforcing filler and 0.5 According to the invention, the balance among self-repairing capability, mechanical property and heat resistance is successfully realized; in the microcrack propagation process, fracture and recombination mechanisms of dynamic covalent bonds effectively prevent further propagation of cracks.

A photocurable resin composition for nails or artificial nails, contains the following components (A) to (D): a component (A): a urethane (meth)acrylate oligomer, a component (B): a monomer selected from the group consisting of a (meth)acrylate monomer, a (meth)acrylamide monomer, and (meth)acrylic acid (excluding the component (A)), a component (C): polyglycerol having no (meth)acryloyl group and / or a compound having a polyglyceryl ether skeleton having no (meth)acryloyl group, a component (D): a photoinitiator. A molecular weight of the component (C) is 200 or more.

The invention belongs to the technical field of high polymer materials, and particularly relates to a PET decorative film and a preparation method thereof. The preparation method comprises the following steps: synthesizing hydroxyl-terminated hyperbranched polyester by taking pentaerythritol and 2, 2-dimethylolpropionic acid as raw materials, and reacting with polyol glycidyl ether to prepare an epoxy-terminated organic modifier; silver-loaded nano silicon dioxide subjected to surface treatment by an amino silane coupling agent is used as inorganic functional particles; pET resin, an organic modifier and inorganic functional particles are subjected to melt blending and extrusion granulation, and modified PET is prepared; the modified PET is prepared into the film through a two-way stretching process. Epoxy groups of the organic modifier chemically react with amino groups at the tail end of a PET molecular chain and on the surfaces of inorganic particles respectively, a stable organic-inorganic hybrid network is constructed, synergistic improvement of reinforcement, toughening and long-acting antibiosis is achieved, and the technical problems that functional particles are not uniform in dispersion, interface bonding is weak, and antibacterial components are prone to migration are effectively solved.

The invention provides a nylon modified material as well as a preparation method and application thereof, and relates to the technical field of nylon compositing, the nylon modified material comprises the following components: nylon 66, low-viscosity nylon 6, a toughening agent, a compatilizer and a flow crystallization accelerant; wherein the toughening agent comprises a block copolymer containing a polyethylene glycol chain segment and a polydimethylsiloxane chain segment; the compatilizer comprises a compound containing a diglycidyl ether group. According to the nylon modified material provided by the invention, under the condition that the modulus of nylon 66 is slightly reduced, the impact strength is improved, so that the nylon modified material has the characteristics of high flowability, high toughness, self-lubrication and the like, and can meet the requirements of occasions such as automobile parts and industrial production.

The invention relates to an aliphatic copolyester elastomer and a preparation method thereof, and belongs to the field of high polymer materials. The elastomer is prepared through a series ring-opening copolymerization reaction of epoxide and cyclic anhydride, and the method comprises the following steps: under the action of a metal-free catalyst (a phosphazene ligand P1-tert-octyl / triethyl boron system) and an initiator (terephthalyl alcohol), carrying out a series ring-opening copolymerization reaction on epoxide and cyclic anhydride, the preparation method comprises the following steps: reacting epoxide (such as epoxypropane and allyl glycidyl ether) with aliphatic anhydride (such as glutaric anhydride) in a xylene solvent to generate a polyester prepolymer retaining an active end; adding a second group of epoxide (such as cyclohexene oxide) and anhydride (such as tetrahydrophthalic anhydride and norbornene dianhydride), continuously reacting to form a block copolymer, and then crosslinking. The material performance can be regulated by changing the monomer combination, the atom economy is high, and the raw materials can be produced on a large scale. The process is simple and environment-friendly, and a new choice is provided for application of the degradable elastomer in the fields of medical treatment, environmental protection and the like.

The application discloses a light anti-impact PC / ABS and application thereof in a robot shell and belongs to the technical field of plastic alloys. The light anti-impact PC / ABS provided by the application comprises the following components in parts by weight: polycarbonate 70-90 parts, ABS 10-30 parts, PMMA 10-20 parts, toughening and compatibilizing agent 8-10 parts, modified hollow glass microbead 8-10 parts, flame retardant 5-15 parts, lubricant 1-3 parts and antioxidant 0.1-2 parts. The toughening and compatibilizing agent is a copolymer of branched polysiloxane, methyl methacrylate, 3-methoxystyrene, glycidyl methacrylate and N-phenylmaleimide. The light anti-impact PC / ABS provided by the application reduces the density of PC / ABS and improves the anti-impact performance of PC / ABS by adding the modified hollow glass microbead and the toughening and compatibilizing agent, and is especially suitable for being used in a robot shell material.

The invention relates to the technical field of coatings, in particular to a graphene modified epoxy anticorrosive coating and a preparation method thereof. The coating is prepared from epoxy resin, graphene-hyperbranched epoxy resin, a reactive diluent and an auxiliary agent, wherein the graphene-hyperbranched epoxy resin is prepared by a three-step method comprising the following steps: firstly, performing dual modification on graphene oxide by adopting 11-aminoundecyltriethoxysilane and 3-aminopropyltriethoxysilane; then reacting with 2-formyl-5-phenylphenol, and finally carrying out condensation polymerization with trimethylolpropane triglycidyl ether to form a hyperbranched structure. According to the invention, collaborative optimization of mechanical strength and corrosion resistance is realized, and the coating has excellent adhesive force, hardness and long-acting corrosion resistance, and is suitable for severe corrosion environments such as ocean engineering and the like.

The invention discloses composite epoxy resin resistant to damp-heat aging and a preparation method and application thereof, and belongs to the technical field of electrical equipment insulating materials. The composite epoxy resin is prepared by the following steps: preparing an epoxy resin mixture from bisphenol A diglycidyl ether type epoxy resin and N, N, N ', N'-tetraepoxypropyl-4, 4 '-diaminodiphenylmethane according to a mass ratio of (1.5-4): 1, and reacting the epoxy resin mixture with a methylhexahydrophthalic anhydride curing agent with a specific molar ratio and a 2, 4, 6-tri (dimethylaminomethyl) phenol accelerant with a certain amount. Through collaborative optimization of the components and the process, the glass-transition temperature, bending strength and breakdown field strength of the epoxy resin are remarkably improved, and the dielectric loss is effectively reduced, so that the epoxy resin shows excellent thermal stability, mechanical property retention rate and insulation reliability in a high-temperature and high-humidity environment; the method is especially suitable for manufacturing insulation parts of electrical equipment in coastal and other high-humidity areas.

The invention discloses polymer-based anti-crack concrete and a preparation method thereof, and relates to the technical field of concrete. When the polymer-based anti-crack concrete is prepared, acrylic acid is grafted on the surfaces of pretreated polypropylene particles to prepare modified polypropylene particles; coating sodium metasilicate with sodium alginate to prepare a self-repairing microcapsule; the preparation method comprises the following steps: hydrolyzing 3-glycidyl ether oxypropyl trimethoxy silane, and grafting the hydrolyzed 3-glycidyl ether oxypropyl trimethoxy silane on the surface of silicon dioxide to prepare modified silicon dioxide; mixing the modified polypropylene particles, basalt fibers and polyacrylonitrile fibers to obtain a solid functional component; cement, slag powder, silica fume, an expanding agent, a solid functional component, modified silicon dioxide, a water reducing agent, an air entraining agent, deionized water, river sand, gravel and the pre-wetted self-repairing microcapsule are mixed, and the polymer-based anti-crack concrete is prepared. The polymer-based anti-crack concrete prepared by the invention has excellent anti-crack, freeze-thaw-resistant and self-repairing properties.

The present invention relates to the technical field of polyurethane coatings, and in particular to a polyurethane coating with sufficient tack-free dryness and a preparation method therefor. In the present invention, ethylene glycol, potassium methoxide, and glycidol are used to prepare a branched polyglycidyl ether and silicon dioxide is modified using the branched polyglycidyl ether. The addition of the branched polyglycidyl ether improves the compatibility of the modified silicon dioxide in a modified polyurethane emulsion, thereby enhancing the hydrophobicity and corrosion resistance of the coating. The backbone of the branched polyglycidyl ether has a high molecular weight, providing a large number of crosslinking sites, and by adding the branched polyglycidyl ether-modified silicon dioxide to the polyurethane coating, the water resistance of the polyurethane coating is enhanced. In the present invention, benzotriazole is also loaded on the silicon dioxide as a corrosion inhibitor, thereby imparting a corrosion-resistant effect to the coating.

A conductive epoxy composition is disclosed comprising an epoxy resin, a low-viscosity hydrocarbon diluent, silver, and graphene. The one-part formulation provides enhanced electrical conductivity, mechanical strength, and process stability. The epoxy resin may include resorcinol diglycidyl ether, diglycidyl ether of Bisphenol A, or Bisphenol F. The hydrocarbon diluent may include glycidyl-ether-family resins having defined carbon-chain characteristics and molecular weights. Silver may be present in particulate, flake, nanoparticle, or coated forms at about 55-90 wt. %, while graphene may be present at 0.03-0.3 wt. % with dimensions of 1-10 μm and surface areas of 400-2,000 m2 / g. Optional additives include solvents, ionic liquids, latent curing agents, and strength enhancers to optimize curing and adhesion.

The invention relates to organosilicone modified acrylic resin, a UV-thermal dual-curing adhesive and a preparation method of the organosilicone modified acrylic resin. The organosilicone modified acrylic resin is obtained by reacting a bifunctional acrylate monomer and modified polysiloxane under the action of a polymerization inhibitor 1 and a catalyst 1; the modified polysiloxane is obtained by reacting hydrogen-containing silicone oil, allyl glycidyl ether and 1, 4-cyclohexanedimethanol divinyl ether under the action of a polymerization inhibitor 2 and a catalyst 2. The adhesive prepared by matching the organic silicon modified acrylic resin with auxiliaries such as a monomer and an initiator can be subjected to UV-heat dual curing, the surface is dry and comfortable after curing, the sticky'oxygen inhibition 'phenomenon is avoided, and the adhesive has good hardness; the adhesive force with various base materials including PC, aluminum materials, glass and PET is good; the shear strength retention rate of each base material after double 85 1000 hours of aging is 70% or above; the appearance is not obviously changed in a high-temperature aging test, and better heat resistance is shown.

The invention provides an elastic polyaspartic acid ester polyurea floor coating and a preparation method thereof, the floor coating comprises a main agent and a curing agent, the main agent comprises first polyaspartic acid ester resin, second polyaspartic acid ester resin, a functional auxiliary agent, and a pigment filler; the curing agent comprises first isocyanate and second diisocyanate; the first polyaspartic acid ester resin is selected from PAE0760, and the second polyaspartic acid ester resin is selected from F520; the first isocyanate is selected from a glycidyl ether compound modified HDI (Hexamethylene Diisocyanate) tripolymer; and the second diisocyanate is selected from HDI (hexamethylene diisocyanate) uretdione. The polyaspartic acid ester polyurea floor coating disclosed by the invention can be used for obviously improving the tensile strength and the scratch resistance of the polyaspartic acid ester polyurea floor coating and improving the leveling property of the polyaspartic acid ester polyurea floor coating while keeping good elastic property, and is a solvent-free polyaspartic acid ester polyurea floor coating with excellent comprehensive performance.

The invention relates to the technical field of automobile essence preparation, and particularly discloses automobile essence capable of removing formaldehyde and releasing anions and a preparation method of the automobile essence. Comprising the following raw materials in parts by weight: 500-600 parts of deionized water, 18-24 parts of a negative ion release enhancing component, 12-20 parts of an aldehyde removing component, 30-40 parts of absolute ethyl alcohol, 8-14 parts of a dispersing agent, 14-18 parts of phenoxyethanol, 22-26 parts of an initiator solution and 6-10 parts of citral. A negative ion release enhancing component and a formaldehyde removal component are added, the negative ion release enhancing component is prepared by modifying core-shell particles with a silane coupling agent, the outer layer of each core-shell particle is of a porous titanium dioxide structure, the inner core of each core-shell particle is modified electrical powder, and the formaldehyde removal component is prepared by carrying out a ring-opening esterification reaction on sodium alginate and allyl glycidyl ether, so that the formaldehyde removal effect is improved. And then carrying out chemical cross-linking with hydroxypropyl acrylate and methacrylic acid, thereby coordinating and enhancing the formaldehyde removal capability, the anion release capability and the antibacterial effect.

The invention provides epoxy resin for halogen-free flame-retardant self-leveling powder coating and a preparation method of the epoxy resin, and belongs to the technical field of powder coating. The flame retardant is mainly prepared from anhydrous piperazine, bisphenol A diglycidyl ether, trihydroxymethyl phosphorus oxide, triethyl phosphite, epoxy chloropropane, sodium hydroxide, N-methyl iminodiacetic acid, ethylene glycol diglycidyl ether and other main raw materials through polymerization. The prepared epoxy resin and 2-phenylimidazoline are subjected to low-temperature curing (135 DEG C / 20 min) on the premise that an additional flatting agent does not need to be used, the flexibility of a coating film is good, the impact resistance grade is high, the impact performance reaches the condition that no cracking phenomenon exists in the front and back 60cm, the leveling grade reaches the grade 7 or above, the gloss is high and reaches 95% or above, the oxygen index reaches 34% or above, and the halogen-free flame retardant performance is excellent.

The invention provides a special fiber material and a preparation method thereof, and belongs to the technical field of polymer composites.The preparation method comprises the following steps that cellulose and an ethanol solution are mixed, polyvinyl alcohol and a 3-glycidoxypropyltrimethoxysilane solution are added, the pH is adjusted to be acidic, heating, suction filtration and drying are conducted, and modified cellulose is obtained; mixing expanded graphite, deionized water, ammonium persulfate and dilute sulphuric acid, heating, cooling, dropwise adding amino polyethylene glycol silane, heating, washing and drying to obtain modified expanded graphite; the preparation method comprises the following steps: mixing modified cellulose, modified expanded graphite, phosphate montmorillonite, 3-(methacryloyloxy) propyltrimethoxysilane, bisphenol A diglycidyl ether and 2-methylimidazole, stirring, heating, defoaming, and carrying out two-stage constant-temperature treatment to obtain the special fiber material. The special fiber material disclosed by the invention has good flame retardance, mechanical strength, water resistance and filtering performance, and can be applied to various organic composite boards, filter membranes and the like with high quality requirements.

The invention provides a pipeline anticorrosive coating and a preparation method thereof, and relates to the technical field of material science and engineering. The pipeline anticorrosive paint is prepared from GMA (glycidyl methacrylate) grafted PTFE (polytetrafluoroethylene) powder, novolac epoxy resin and an epoxy resin curing agent, the GMA grafted PTFE powder is activated and then grafted with GMA, and AIBN (azodiisobutyronitrile) is used for removing residual free radicals. The novolac epoxy resin is composed of novolac epoxy resin, polyethylene glycol diglycidyl ether, GMA grafted PTFE powder, silicon dioxide powder, a solvent and an auxiliary agent, and the epoxy resin curing agent is composed of polyamide, DMP-30 and a solvent. The pipeline anticorrosive paint provided by the invention has the advantages of excellent corrosion resistance, excellent temperature resistance and low frictional resistance.

This invention discloses a method for preparing a fluorine-free superhydrophobic nano-silica cotton fabric, belonging to the field of superhydrophobic textile technology. The invention utilizes trichlorooctadecylsilane (OTS), γ-glycidyl etheroxypropyltrimethoxysilane (KH-560), and hexadecyltrimethoxysilane (HDTMS) to modify silica, obtaining a fluorine-free superhydrophobic coating. This coating, applied to the surface of the cotton fabric, results in a fabric with both low surface energy and a rough surface structure, exhibiting excellent superhydrophobic properties. Furthermore, it also imparts durability, self-cleaning, and stain-resistant capabilities to the hydrophobic coating.

The invention relates to a bi-component epoxy coating, a wire winding, a preparation method of the wire winding and an electric reactor. The bi-component epoxy coating comprises an epoxy prepolymer, an epoxy curing agent and a self-repairing microcapsule, wherein the self-repairing microcapsule contains an epoxy microcapsule and an amine microcapsule; wherein the amine microcapsule and the capsule wall of the epoxy microcapsule comprise polyurea, so that core liquid of the epoxy microcapsule and the amine microcapsule can be effectively preserved during primary thermocuring, and is not easy to flow out in advance. When the coating has cracks, bisphenol F diglycidyl ether in the amine microcapsules and aliphatic polyamine in the epoxy microcapsules can flow out and are gradually mixed, due to the high reaction activity of the aliphatic polyamine, secondary curing can be achieved without high temperature, microcracks can be repaired, further spreading of defects is prevented, and the service life of the coating is prolonged. And the long-term service capability of the self-repairing resin layer is effectively improved.

The invention relates to degradable self-repairing epoxy resin based on adjustable performance of dual dynamic covalent bonds and preparation and application of the degradable self-repairing epoxy resin. Firstly, two dynamic bond curing agents (a hindered urea bond and an imine bond) are prepared respectively, and an epoxy monomer bisphenol A diglycidyl ether, the two curing agents and a cross-linking agent 4, 4 '-diphenyl-1, 3-pentanediol diglycidyl ether are mixed to prepare a mixture; the preparation method comprises the following steps: mixing 4, 4 '-diaminodiphenylmethane according to the proportion of each dynamic bond, stirring and reacting at 70-80 DEG C for 30-60 minutes, and carrying out vacuum defoaming; and finally, pouring the mixture into a mold, and molding through a gradient curing process. Compared with the prior art, two different dynamic bond curing agents are utilized to construct a double-dynamic epoxy cross-linked network, so that the obtained material has excellent performance and degradable self-repairing capability, and a high-performance solution capable of repairing, degrading and prolonging the service cycle is provided for the field of electrical insulation.

The invention discloses a chlorphenesin coupling crystallization-adsorption purification method based on a deep eutectic solvent, and belongs to the technical field of chemical purification. According to the technical scheme, the method comprises the following steps: S1, mixing crude chlorphenesin with supercritical CO2, and extracting to obtain pretreated chlorphenesin; s2, dissolving the pretreated chlorphenesin in a choline chloride-glycerol DES system, adding an adsorbent after sufficient dissolution, cooling, and separating out chlorphenesin. The technical problems that an organic solvent is used in an existing chlorphenesin purification method, and the solvent is inflammable, toxic, large in dosage, long in purification time and high in energy consumption are solved, and the chlorphenesin coupling crystallization-adsorption purification method based on the eutectic solvent is safe, environmentally friendly, capable of improving production efficiency and high in product purity and yield.

The invention relates to a low-temperature-bending-resistant data line and a preparation method thereof. The low-temperature-bending-resistant data line comprises the following components in parts by weight: 45-65 parts of TPU, 8-12 parts of polypropylene, 15-25 parts of ethylene propylene diene monomer, 10-12 parts of a plasticizer, 10-16 parts of a modified flame retardant, 1-2 parts of a modified anti-aging agent, 1-2 parts of a lubricant and 1-2 parts of a coupling agent. The modified flame retardant achieves efficient environment-friendly flame retardance through phosphorus-oxygen-silicon synergism, gamma-glycidyl ether oxypropyl trimethoxy silane promotes surface char formation, delays combustion and reduces smoke generation, hydroxybenzophenone in the modified anti-aging agent resists ultraviolet rays through electron transition and converts the ultraviolet rays into heat energy, a maleimide group improves the glass transition temperature of the material, and the flame-retardant performance of the material is improved. A six-membered ring structure and N-phenylmaleimide are cooperated, so that high-temperature yellowing is reduced; the low-temperature-bending-resistant data line prepared by the invention not only has a good flame-retardant effect, but also has an excellent anti-aging effect.

The application belongs to the technical field of surfactants, and discloses a kind of organic counterion quaternary ammonium salt gemini surfactants without chlorine and a preparation method and application thereof.The organic counterion quaternary ammonium salt gemini surfactants without chlorine are obtained by adding a certain amount of alkyl diamine compound acidified by organic acid into C1-C 18 The alkyl glycidyl ether is subjected to quaternary ammonium reaction by adding a certain amount of alkyl diamine compound acidified by organic acid.The obtained organic counterion quaternary ammonium salt gemini surfactants without chlorine contain two organic counterions and two hydroxyl groups, the synthesis process is simple, the conditions are mild, and no toxic and harmful by-products are produced, which can avoid the corrosion of halogen ions to equipment and environmental pollution during preparation.

This invention discloses a bio-based flame-retardant thermally expanding powder coating and its preparation method, relating to the field of coatings. It comprises the following components: bio-based epoxy resin, phenolic epoxy curing agent, ammonium polyphosphate, nano-titanium dioxide, zinc borate, expanded graphene, 8-12 parts of imidazole, benzoin, and a leveling agent. The bio-based epoxy resin is prepared by ring-opening copolymerization of cashew phenol glycidyl ether and linoleic acid prepolymer, followed by epoxy end-capping, with an epoxy equivalent of 900-1200 g / eq; the phenolic epoxy curing agent has an epoxy equivalent of 200-250 g / eq; and the expanded graphene has an initial expansion ratio of 200-300 times. The preparation method employs a two-step, staged mixing process. This invention, while maintaining zero VOC in powder coatings and the same film thickness, achieves for the first time the outstanding performance of 6H hardness, UL94V-0 flame retardancy, and 120 times expansion ratio through the systematic synergy of high epoxy equivalent bio-based resin, four-component complete flame retardant system, specific EG:APP ratio, and two-step process.