1950 results about "Triethoxysilane" patented technology

The invention relates to the field of membrane materials, and discloses an epoxy modified starch-based degradable membrane and a preparation method thereof, the epoxy modified starch-based degradable membrane comprises epoxidized starch, modified nanocellulose and a plasticizer; the modified nano cellulose is prepared by mixing a modified composite filler, a nano cellulose dispersion liquid and a zinc acetate dihydrate aqueous solution; the nano-cellulose dispersion liquid is prepared by adhering polytannic acid formed by oxidation and self-polymerization of tannic acid to the surface of nano-cellulose; the modified composite filler is prepared by performing carboxylation modification on nano titanium dioxide coated fumed silica nanoparticles by using succinic anhydride and gamma-aminopropyltriethoxysilane, then reacting with polyethyleneimine to obtain an aminated composite filler, and finally grafting glycidyl dodecyl dimethyl ammonium chloride to the surface of the aminated composite filler. The prepared film material is high in tensile strength, has certain hydrophobicity, and has good heat resistance, antibacterial property and flame retardant property.

The invention relates to the field of textile materials, and particularly discloses a graphene enhanced polyester yarn and a preparation method thereof.The preparation method comprises the following steps that silicon dioxide aerogel serves as a porous carrier to be loaded with graphene, and a graphene-porous carrier composite material is prepared; the graphene-porous carrier composite material is subjected to modification treatment through vinyl trimethoxy silane and 3-amino propyl triethoxy silane, and then a modified graphene composite material is prepared; reacting the modified graphene composite material, a styrene monomer, an acrylate monomer and an initiator to prepare modified graphene; mixing the prepared modified graphene with polyester chips, and then carrying out melt spinning to prepare graphene enhanced polyester yarns; the invention further discloses the graphene enhanced polyester yarn prepared by adopting the preparation method. The preparation method has the characteristics that the dispersion of the graphene in the polyester is improved, and the direct interface compatibility of the graphene and the polyester fiber is improved, so that the mechanical property of the polyester yarn is improved.

The invention relates to the field of textile materials, and provides an antibacterial breathable yarn obtained by blended spinning of polyester fibers, polyamide fibers, cotton fibers and elastic fibers. The polyester fiber is prepared through melt blending and spinning processes and comprises polyethylene glycol terephthalate slices, modified chitosan zinc oxide, an antioxidant 1010, a POE elastomer, polyether modified silicone oil and polyethylene glycol 200, and the modified chitosan zinc oxide is prepared by compounding chitosan cinnamyl aldehyde Schiff base and silane modified zinc oxide. The chitosan cinnamyl aldehyde Schiff base is prepared through a Schiff base condensation reaction of chitosan and cinnamyl aldehyde, and the silane modified zinc oxide is prepared from nano rod-shaped zinc oxide particles modified by isocyanate propyl triethoxy silane. The yarn has excellent antibacterial property, air permeability and flexibility and is further used for knitting antibacterial breathable socks, the knitting density of the sock bottom part is reduced to enhance the air permeability, the knitting density of the sock opening part is improved to improve the elasticity and the fitting degree, and the yarn has wide application value.

The invention relates to the technical field of catalyst carriers, and relates to a modified alpha-alumina carrier, a preparation method thereof, a supported silver catalyst and application. The modified alpha-alumina carrier is an alpha-alumina carrier with a silane coupling structure on the surface, and silane is at least one of silane compounds containing 1-3-Si-O-C-structures and containing vinyl or amino. Preferably, the silane compound is selected from at least one of vinylmethoxysilane, 3-aminopropyltriethoxysilane and methylvinyldimethoxysilane. According to the modified alpha-alumina carrier, the silane solution is adopted to treat the alpha-alumina carrier, silane contains a-Si-O-C-structure, the group can form a relatively stable structure on the surface of the carrier after hydrolysis or dehydration condensation, and influence is generated for a long time in the use process of a silver catalyst, so that the performance of the catalyst is improved.

The invention relates to the technical field of environmental materials and water treatment, in particular to a graphene amino silica gel composite adsorbent for heavy metal wastewater treatment and a preparation method thereof.The graphene amino silica gel composite adsorbent is prepared from # imgabs0 nanoparticles, an amino-functionalized silicon dioxide coating layer, carboxylated reduced graphene oxide, a polydopamine modification layer and tetraethyl orthosilicate; the coating is prepared from the following raw materials: 3-aminopropyltriethoxysilane, 3-mercaptopropyltrimethoxysilane, N-((4-vinyl benzyl) amino) diacetic acid, chitosan, beta-cyclodextrin, hexadecyl trimethyl ammonium bromide, polyethylene glycol, L-ascorbic acid, 1-ethyl-3-(3-dimethyl aminopropyl) carbodiimide hydrochloride and N-hydroxysuccinimide. The composite adsorbent shows excellent adsorption performance on various heavy metal ions, and the adsorption performance is far higher than that of traditional adsorption materials and existing composite adsorbents.

The invention relates to the technical field of heavy anti-corrosion coatings, in particular to a graphene enhanced epoxy modified organic silicon resin heavy anti-corrosion powder coating. The coating is prepared from the following components in parts by weight: 42 to 58 parts of epoxidized epoxy modified organic silicon resin, 0.8 to 2.5 parts of hydroxylated graphene, 6 to 11 parts of nano zirconium dioxide coated boron nitride, 2.5 to 5.5 parts of lanthanum iso-octoate-titanate composite coupling agent, 1.5 to 3.5 parts of bis (3-triethoxysilylpropyl) disulfide, 4 to 7 parts of polyhedral oligomeric silsesquioxane, 5 to 8 parts of curing agent, 0.8 to 1.8 parts of flatting agent and 0.4 to 0.9 part of defoaming agent. 2.5 to 4.5 parts of polyether-ether-ketone micro powder and 1.2 to 2.8 parts of fluorine-containing phosphate ester. According to the invention, the resin is modified through chemical bridging, the modified graphene and the nano-coated powder are matched to construct a synergistic enhancement system, and the interface bonding is optimized by the composite coupling agent. The coating is excellent in adhesive force, corrosion resistance and mechanical property, good in processing fluidity and high in aging resistance and thermal stability, solves the problem that a traditional product is short in performance, and meets the industrial requirement.

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

The invention discloses a flame-retardant corrosion-resistant coating and a preparation method thereof, and relates to the technical field of coatings. When the flame-retardant and corrosion-resistant coating is prepared, hexaaryl biimidazole and epoxy chloropropane are subjected to a reaction, and epoxidized hexaaryl biimidazole is prepared; the pre-modified mica sheet and 3-aminopropyltriethoxysilane are subjected to a reaction, and a modified mica sheet is prepared; the preparation method comprises the following steps: reacting allyl amine with 4 '-[4-(bromomethyl) phenyl]-2, 2': 6 ', 2' '-terpyridyl to obtain allyl terpyridyl; the preparation method comprises the following steps: reacting epoxy resin with allyl terpyridyl to obtain modified epoxy resin; and uniformly mixing the modified epoxy resin, epoxidized hexaaryl biimidazole, the modified mica sheet, isophorone diamine and acetone to prepare the flame-retardant corrosion-resistant coating. The flame-retardant corrosion-resistant coating prepared by the invention has excellent corrosion resistance, flame retardance and self-repairing performance.

The preparation method comprises the following steps: obtaining a ZnO nano-particle seed crystal layer by a dip-coating-calcining method, and growing the ZnO nano-particle seed crystal layer on a porous ceramic membrane; inducing growth of ZnO nano-clusters on the surface of the ceramic membrane on which the ZnO nano-particles grow and in pore channels of the ceramic membrane through a hydrothermal reaction; and finally, soaking the ceramic membrane on which the ZnO nano-cluster grows in an n-octyltriethoxysilane-absolute ethyl alcohol solution, and carrying out silane chemical grafting treatment. A firm micro-nano composite multilevel structure is obtained on the surface and in pore channels of the ceramic membrane after modification through the method, meanwhile, the surface free energy of the surface and pore channels of the ceramic membrane is reduced through n-octyltriethoxysilane, the surface and the pore channels of the ceramic membrane have super-hydrophobic performance, and the preparation method is simple in preparation process, short in period and suitable for industrial production. And the universality is high.

The invention discloses a UV photocureable coating as well as a preparation method and application thereof in automobiles, and relates to the technical field of coatings. When the UV photocureable coating is prepared, 4-aminophenylboronic acid is dehydrated to prepare aminated boron oxygen six-ring; carrying out a reaction on the aminated boroxane and diallyl chlorophosphate to prepare functionalized boroxane; the preparation method comprises the following steps: sequentially reacting graphene oxide with 3-chloropropyltriethoxysilane and 1, 3-diallyl-1, 3, 5-triazine-2, 4, 6-triketone, so as to obtain modified graphene; the preparation method comprises the following steps: reacting epoxy resin with 2-butenal thiosemicarbazone to prepare modified epoxy resin; and uniformly mixing the modified epoxy resin, the epoxy acrylate resin, the modified graphene, the functionalized boroxane, the 1, 6-hexanediol diacrylate and the 1-hydroxycyclohexyl phenyl ketone, so as to obtain the UV photocureable coating. The UV photocureable coating prepared by the invention has excellent flame retardant, self-repairing and mechanical properties.

The invention relates to the field of coatings, and discloses an outer wall light radiation heat preservation and heat insulation decorative sheet and a preparation method thereof.A radiation refrigeration layer on the surface of the outer wall light radiation heat preservation and heat insulation decorative sheet comprises modified acrylate resin, silicon dioxide, ground calcium carbonate, talcum powder, modified hollow glass beads and auxiliaries; the modified acrylate resin is prepared by copolymerizing perfluorooctyl ethyl acrylate, methyl methacrylate, modified isocyano ethyl methacrylate and vinyltriethoxysilane, and the modified isocyano ethyl methacrylate is prepared by using salicylaldehyde and benzothiazole-2-formaldehyde as well as 1, 2, 4-trimethyl-1, 3-pentanediol monoisobutyrate as an initiator and using 2, 3, 4-trimethyl-1, 3-pentanediol monoisobutyrate as an initiator. The preparation method comprises the following steps: reacting amino groups at two ends of 1, 5-naphthylenediamine with DOPO, carrying out nucleophilic addition reaction with DOPO, and grafting with isocyano ethyl methacrylate. The modified hollow glass beads are prepared by using tetrabutyl titanate as a titanium source through a sol-gel method, and the prepared radiation refrigeration layer has the super-amphiphobic self-cleaning effect, the radiation refrigeration effect is good, and meanwhile the flame retardant property and the antibacterial effect are excellent.

The invention discloses a graphene nanometer heavy anti-corrosion coating and a preparation method thereof, and belongs to the technical field of anti-corrosion coatings. The coating is prepared from the following components in parts by mass: 50 to 70 parts of diallyl bisphenol A type epoxy resin, 8 to 15 parts of histidine modifier, 12 to 20 parts of graphene nano composite modified filler, 5 to 10 parts of curing agent, 0.5 to 2 parts of flatting agent and 0.3 to 1 part of defoaming agent. The preparation method of the histidine modifier comprises the following steps: carrying out a Schiff base reaction on 1-palmitoyl-2-oleoyl ethanolamine and N-formyl-L-histidine to generate an intermediate A; reacting with a spiro quaternization reagent to form a quaternary ammonium salt intermediate B; and then compounding with aminopropyltriethoxysilane and silicotungstic heteropoly acid salt to obtain the product. The graphene nano-composite modified filler is prepared by modifying the surface of a graphene oxide / bentonite mutual intercalation layer structure through allyl trimethoxy silane. The graphene nano heavy anti-corrosion coating prepared by the invention forms a high-density cross-linked network, and has excellent barrier property, strong adhesive force, impact resistance and long-acting anti-corrosion performance.

The invention relates to the technical field of biodegradable materials, and particularly discloses a BBM-added bamboo powder biodegradable material and application thereof in beer bottles. The BBM-added bamboo powder biodegradable material is prepared from the following raw materials in parts by mass: 10 to 20 parts of poly (butylene succinate), 10 to 30 parts of poly (butylene adipate-co-terephthalate), 10 to 20 parts of bamboo powder, 1 to 3 parts of dopamine hydrochloride, 0.1 to 0.5 part of n-butylamine, 1 to 2 parts of hexadecyl trimethyl ammonium bromide, 1 to 5 parts of tetraethyl orthosilicate and 1 to 2 parts of tetrabutyl titanate. 1-2 parts of 3-aminopropyltriethoxysilane, 1-2 parts of an antioxidant and 1-2 parts of a plasticizer. The BBM obtained by the invention has excellent mechanical properties, improves the anti-ultraviolet intensity of a degradable material to a certain extent, and has very good biodegradability.

The invention relates to the technical field of corrosion resistance, in particular to a corrosion-resistant and wear-resistant copper insert and a preparation method thereof.The copper insert is subjected to plating treatment in an ionic liquid electroplating mode, then the surface of a plating layer is subjected to hole sealing treatment, and a nickel-copper-composite halloysite nanotube layer is electrically deposited on the surface of the formed copper insert; the preparation method comprises the following steps: taking a halloysite nanotube as a nano loader of a corrosion inhibitor, and coating with dopamine to obtain a composite halloysite nanotube; in the hole sealing liquid, the composite halloysite nanotube is used as a filler, silane modified polyurethane is used as a base material, the silane modified polyurethane is a prepolymer synthesized by using isophorone diisocyanate and polytetramethylene ether glycol as raw materials, octylamine ring-opened 3-(2, 3-epoxypropoxy) propyltrimethoxysilane is used as a chain extender, and the silane modified polyurethane is used as the base material. And 2-(perfluorodecyl) ethanol and aminopropyltriethoxysilane are used as end-capping reagents, so as to prepare the high-temperature-resistant coating.

The invention discloses quick-hardening cement mortar and an application method thereof, and relates to the technical field of building materials, the quick-hardening cement mortar is composed of the following components: quick-hardening sulphoaluminate cement, common Portland cement, aggregate, an additive and a fiber composition; the fiber composition comprises galvanized steel fibers and polymer fibers, and the polymer fibers comprise PVA fibers; a film layer modified by a silane coupling agent is formed on the surfaces of the galvanized steel fiber and the polymer fiber, and the silane coupling agent is selected from at least one of aminopropyltriethoxysilane and diamino type functional group silane. The galvanized steel fibers and the polymer fibers are adopted in the cement mortar, the polymer fibers generate pressure stress in a cement block by utilizing an environment that the cement is severely hydrated in a short time, and the polymer fibers and the galvanized steel fibers generate a synergistic effect, so that the overall anti-dry-crack effect of the cement block is achieved; through a silane coupling agent surface modification scheme, the anti-cracking effect is enhanced, and the effect of common long fibers is achieved through short fibers.

The invention relates to the field of wear-resistant fabrics, and discloses a high-strength wear-resistant fabric and a preparation method thereof.The high-strength wear-resistant fabric comprises a surface coating and a base cloth layer, the surface coating and the base cloth layer are formed by coating and drying modified waterborne polyurethane emulsion, and the modified waterborne polyurethane emulsion comprises isophorone diisocyanate, ethylene glycol terephthalate, 2, 3, 4-trimethyl-1, 3-pentanediol monoisobutyrate, polyisobutylene glycol monoisobutyrate, according to the present invention, 2, 2-dimethylolpropionic acid, a modified additive, a flame retardant modifier, 1, 4-butanediol, trimethylolpropane and the like are adopted to prepare the modified additive, dopamine is subjected to in-situ auto-polymerization on the surface of a titanium dioxide nanotube, nano-silica is grown on the surface in situ, and modification is performed through a polysiloxane solution to prepare the modified titanium dioxide nanotube flame retardant; the polysiloxane solution is prepared by carrying out a reaction on methyl triethoxysilane and dihydroxyl-terminated polydimethylsiloxane; the flame-retardant modifier is prepared by reacting 2-chloro-4, 6-diamino-1, 3, 5-triazine, 5-hydroxymethylfurfural and phosphorous acid, so that the fabric is endowed with good mechanical properties and wear resistance, and the fabric has a hydrophobic surface and is excellent in flame retardance and durability.

The invention relates to the field of coatings, and discloses a solvent-resistant antirust anticorrosive biological resin coating and a preparation method thereof, the biological resin coating comprises modified bio-based epoxy resin, modified graphene oxide, modified nano titanium dioxide, a curing agent and a diluent; the modified bio-based epoxy resin is prepared by modifying epoxidized polysiloxane formed by self-polymerization of siloxane; the modified nano titanium dioxide is prepared by modifying a fluorine-containing group; the modified graphene oxide is prepared by grafting a flame-retardant modifier on the surface of graphene oxide, the flame-retardant modifier is prepared by reacting 3-amino-1, 2, 4-triazole with phosphonitrilic chloride trimer to prepare a flame-retardant intermediate, then grafting the flame-retardant intermediate and gamma-aminopropyltriethoxysilane by taking terephthalaldehyde as a bridging agent, and further reacting with DOPO (9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide). The prepared biological resin coating is high in adhesive force, high in pencil hardness and good in corrosion resistance, solvent resistance and flame retardant effect.

The invention relates to the technical field of composite materials, in particular to a nano-montmorillonite reinforced unsaturated polyester resin based composite material and a preparation method thereof. Comprising the following raw materials in parts by weight: 60-85 parts of orthophthalic unsaturated polyester resin, 3-15 parts of nano montmorillonite, 1-5 parts of a polyfunctional group intercalator, 1-4 parts of an initiator, 0.5-2 parts of dimethylaniline and 0.5-3 parts of gamma-aminopropyltriethoxysilane. The polyfunctional intercalator interacts with interlayer ions and surface groups of the nano-montmorillonite through multiple functional groups of the polyfunctional intercalator, and is effectively inserted into the interlayer of the nano-montmorillonite, so that the interlayer spacing is obviously increased, and favorable conditions are provided for subsequent insertion and compounding of resin; the functional groups not only can chemically react with active groups of unsaturated polyester resin to form stronger chemical bonding, but also can enhance the interface bonding force between two phases through physical entanglement, so that the overall performance of the composite material is remarkably improved.

The invention discloses room-temperature end-capped silicone rubber based on 107 glue and a preparation method of the room-temperature end-capped silicone rubber, and relates to the technical field of silicone rubber. The preparation method comprises the following steps: step 1, uniformly mixing 107 glue, isobornyl silane and a catalyst in a nitrogen atmosphere; stirring at room temperature for 1-1.5 hours to obtain room-temperature end-capping base glue; and 2, uniformly stirring and mixing the room-temperature end-capped base rubber, dimethyl silicone oil, the modified filler, methyltrimethoxysilane, gamma-aminopropyltriethoxysilane and an organic tin catalyst in a nitrogen atmosphere, and finally vacuumizing and stirring to obtain the room-temperature end-capped silicone rubber. According to the invention, the prepared room-temperature end-capped silicone rubber has excellent mechanical properties and stability.

The invention provides a wear-resistant, transparent, flexible and fluoride-free super-hydrophobic composite coating and a preparation method thereof. The preparation method comprises the following steps: mixing hydroxyl-terminated polydimethylsiloxane, gamma-aminopropyltriethoxysilane and dibutyltin dilaurate for reaction to obtain a modified precursor solution, adding swelled epoxy resin into the modified precursor solution, and heating for reaction to obtain siloxane modified epoxy resin; the preparation method comprises the following steps: dispersing nano silicon dioxide in an ethyl acetate solution to form a SiO2 suspension; and uniformly mixing the modified epoxy resin with a SiO2 suspension, adding polyether amine as a curing agent, stirring and mixing, and constructing the epoxy resin / hydroxyl-terminated polydimethylsiloxane / nano-silica super-hydrophobic coating on a substrate by adopting an air spraying mode. According to the preparation method disclosed by the invention, the super-hydrophobic coating with excellent transparency and flexibility and good adhesive force and wear resistance can be prepared, and the super-hydrophobic coating has a wide application prospect in the fields of wearable electronic equipment, photoelectric devices and the like.

The invention relates to a preparation method of a hydrophobic and oleophobic PTFE membrane, and belongs to the technical field of PTFE membrane preparation. Aiming at the problems that an existing PTFE membrane is difficult to construct a micro-nano multi-stage coarse structure and has a synergistic effect with low chemical surface energy, the hydrophobic and oleophobic properties are insufficient and the structural stability is poor, the key points of the technical scheme provided by the invention are as follows: firstly, carrying out ethanol ultrasonic cleaning on a PTFE base membrane of 20-30 microns, and carrying out vacuum plasma treatment to form a nano coarse structure and oxygen-containing polar group active sites; then, under the protection of nitrogen, immersing into an ethanol solution containing perfluorodecyltriethoxysilane, dibutyltin dilaurate and nano cellulose whiskers, carrying out hot-pressing compounding with PET non-woven fabric, carrying out heat treatment, and finally, coating with a fluorine-containing polymer nano fiber layer through an electrostatic spinning process; the composite hydrophobic layer with the synergistic effect of a micro-nano multistage coarse structure and chemical low surface energy is formed, the water contact angle is larger than or equal to 155 degrees, and the oil contact angle is larger than or equal to 130 degrees. The PTFE film prepared by the preparation method can be used in the fields of waterproof breathable materials, self-cleaning surfaces, oil-resistant packaging and the like.

The invention relates to the field of drain pipes, and discloses an antibacterial polypropylene noise-reduction drain pipe and a preparation method thereof, the antibacterial polypropylene noise-reduction drain pipe comprises polypropylene, modified glass fiber, an antibacterial additive, a compatilizer and a stabilizer; the modified glass fiber is prepared by performing formylation modification on glass fiber by using 3-aminopropyltriethoxysilane and glutaraldehyde, grafting triethylene tetramine and DOPO into a glass fiber structure, and then grafting a hindered phenol antioxidant; the antibacterial additive is prepared by compounding chitosan Schiff base and modified nano titanium dioxide, the chitosan Schiff base is prepared by utilizing a Schiff base reaction between chitosan and vanillin, and the modified nano titanium dioxide is prepared by utilizing isocyanate propyl triethoxy silane and ethyl glycolate to modify nano titanium dioxide. By adding the modified glass fiber and the antibacterial additive, the pipe is endowed with excellent heat resistance, aging resistance, flame retardance and antibacterial performance.

The invention provides weather-resistant anti-freezing road concrete and a preparation method thereof, and belongs to the technical field of concrete. The concrete comprises the following components: sulphoaluminate cement, Portland cement, silica fume, fly ash, modified granite gravel coarse aggregate, medium sand fine aggregate, silica fume blended fiber, silica fume blended polyacrylonitrile fiber, a composite air entraining agent, a functional modifier, a composite antifreeze agent, pre-absorbent zeolite powder and the like. The preparation method comprises the following steps: modifying granite macadam with Al (H2PO4) 3, SiO2 and methoxypolyethylene glycol triethoxysilane, and modifying with a lithium silicate aqueous solution to obtain the modified granite macadam coarse aggregate. The composite air entraining agent comprises a JRY-Q air entraining agent and sodium alpha-olefin sulfonate. The functional modifier is prepared from gas phase method spherical nano silicon dioxide and nano alpha-Al2O3. The composite antifreeze agent comprises ethylene glycol butyl ether acetate and modified calcium carbonate. The modified calcium carbonate is obtained by sequentially modifying nano calcium carbonate with calcium chloride, a KH-550 silane coupling agent and stearic acid.

The invention relates to the technical field of conductive materials, in particular to a high-concentration dispersion system and a preparation method thereof. The high-concentration dispersion system comprises a conductive agent, a dispersing agent, a solvent and a viscosity reduction auxiliary agent, the conductive agent is modified carbon nanotubes, the dispersing agent is modified polyvinylpyrrolidone, the solvent is N-methyl pyrrolidone or deionized water, and the viscosity reduction auxiliary agent is piperazine anhydrous; wherein the modified carbon nano tube is obtained by mixing and heating a carbon nano tube and a mixed acid solution of nitric acid and sulfuric acid, then cooling, filtering, washing, drying, then dispersing in 75% ethanol, and finally adding 3-[3-carboxyl allylamido] propyltriethoxysilane for modification; the modified polyvinylpyrrolidone is obtained by heating polyvinylpyrrolidone at 310-330 DEG C and then oxidizing the polyvinylpyrrolidone. The conductive agent content of the high-concentration dispersion system is high, the conductive agent accounts for 15%-20% of the high-concentration dispersion system by mass, and the high-concentration dispersion system is low in viscosity, high in dispersity and good in conductivity.

The invention discloses a corrosion-resistant polysilsesquioxane modified polyurethane emulsion and a preparation method thereof, and belongs to the technical field of emulsions.The preparation method comprises the steps that gamma-aminopropyltriethoxysilane, namely APTES, is subjected to hydrolytic condensation under the catalysis of tetraethylammonium hydroxide, and POSS is prepared; the preparation method comprises the following steps: carrying out hydrolytic condensation reaction on APTES, synchronously adding phenyltrimethoxysilane in the hydrolytic condensation reaction, forming phenyl-amino difunctional POSS (Polyhedral Oligomeric Silsesquioxane) according to a molar ratio of phenyltrimethoxysilane to APTES of 1: 4, and grafting POSS and graphene oxide GO in dimethyl sulfoxide through amidation reaction to prepare a POSS / GO composite material; dispersing POSS / GO / Zn in the polyurethane prepolymer, adding a curing agent and a solvent, and stirring to form a homogeneous emulsion; through phenyl trapezoid polysilsesquioxane modification and dynamic reversible self-repairing network design, the wear resistance of the coating is improved, microcracks can be closed at the temperature of 60 DEG C, and the maintenance requirement is reduced; laser micro-nano structured base material treatment is combined, the adhesive force is increased to be larger than or equal to 20 MPa, and meanwhile a gamma-butyrolactone low-VOC solvent is adopted.

The invention discloses a load type regenerated asphalt mixture composite regenerant, which is composed of a porous carrier and a regenerant loaded in the pore channel of the carrier, and the mass ratio of the porous carrier to the regenerant is 5: 1. The regenerant is prepared from the following raw materials in parts by weight: 90 to 110 parts of furfural extract oil, 5 to 10 parts of triallyl isocyanurate, 2 to 6 parts of triethoxysilane, 4 to 10 parts of a three-dimensional porous material, 3 to 8 parts of a penetrant, 20 to 30 parts of toluene-2, 4-diisocyanate, 10 to 20 parts of hydroxyl-terminated polybutadiene, 5 to 12 parts of a plasticizer and 5 to 10 parts of a tackifier. The regenerant is loaded in pores of the porous carrier, so that the deformation resistance of asphalt mortar can be improved, the aging resistance of asphalt can be effectively improved, and the regenerant can improve the high-temperature stability, low-temperature stability and water stability of the thermally-regenerated asphalt mixture and can improve the skid resistance and sound absorption performance of the thermally-regenerated asphalt mixture. Meanwhile, the economic cost is saved.

The invention provides a diaphragm and a preparation method thereof and a lithium ion battery, the diaphragm comprises a base membrane layer and a composite functional layer, the composite functional layer comprises hydrophobic SiO2 aerogel modified by a hydrophobic agent, a conductive ion polymer and a solid electrolyte, and the composite functional layer respectively accounts for 3-12wt%, 0.5-1.0 wt% and 0.5-1.5 wt% of the total mass of the diaphragm; the hydrophobic agent comprises trimethylchlorosilane, hexamethyldisilazane, perfluorooctyltriethoxysilane, polyvinylidene fluoride, polydimethylsiloxane and the like, the conductive ionic polymer comprises polyvinylpyrrolidone, lithium polymethacrylate, lithium polystyrene sulfonate, polyacrylamide and the like, and the solid electrolyte comprises lithium lanthanum titanium oxide, lithium lanthanum zirconium oxide, lithium lanthanum zirconium tantalum oxide and the like. The wettability is improved by the high porosity of the hydrophobic SiO2 aerogel, the stability and strong conductivity of a physical conductive network of the solid electrolyte and the ion affinity and amphoteric binding capacity of the conductive ion polymer are optimized, the electrochemical performance and thermal stability of the interface are optimized, and comprehensive optimization of the thermal-electric-interface performance of the diaphragm is realized through combination.

The invention discloses a self-adaptive light-dimming temperature-control polyurethane protective film and a preparation method thereof, and relates to the technical field of high polymer materials. When the self-adaptive light-dimming temperature-control polyurethane protective film is prepared, castor oil reacts with sulfhydrylated thiosemicarbazone to prepare modified castor oil; the preparation method comprises the following steps: carrying out ring opening polymerization on flame-retardant cyclotetrasiloxane and tetramethyl cyclotetrasiloxane to prepare a siloxane oligomer; enabling vanadium pentoxide, oxalic acid and tungstic acid to react to prepare tungsten-doped vanadium dioxide; the preparation method comprises the following steps: carrying out a reaction on tungsten-doped vanadium dioxide and allyltriethoxysilane to prepare modified vanadium dioxide; uniformly mixing castor oil, modified castor oil, siloxane oligomer, isophorone diisocyanate and copper chloride, pouring the mixture into a mold, and performing curing molding, so as to obtain the self-adaptive light-dimming temperature-control polyurethane protective film. The self-adaptive light-dimming temperature-control polyurethane protective film prepared by the invention has excellent flame retardance, tensile strength and self-adaptive light-dimming temperature-control performance.

The invention provides a preparation method of a Janus material for simultaneous screening of protein phosphorylation and palmitoylation modification, and belongs to the technical field of magnetic material synthesis. The method comprises the following steps: firstly, preparing MCeO2; the preparation method comprises the following steps: mixing MCeO2, hexadecyl trimethyl ammonium bromide and ammonia water to obtain a mixed solution, adding 1, 2-bis (triethoxysilane) ethane into the mixed solution for reaction to obtain a product, and dispersing the product into an NH4NO3 solution for reflux reaction to obtain Janus MCP; the preparation method comprises the following steps: reacting Janus MCP with a silane coupling agent, dissolving aminated Janus MCP and 4-ethylene sulfonyl benzoic acid in a buffer solution containing EDC and NHS, and reacting to obtain the Janus material. The preparation method is reliable, the material performance is stable, and the enrichment efficiency of the magnetic Janus on target peptide fragments (phosphorylated peptide fragments and palmitoylated peptide fragments) is remarkably improved.

The invention relates to the technical field of polyethylene cables, in particular to a high-strength flame-retardant polyethylene cable and a preparation method thereof.The high-strength flame-retardant polyethylene cable is composed of a copper stranded wire core and a flame-retardant protective layer on the surface of the copper stranded wire core; the flame-retardant protective sleeve is made of a high-strength flame-retardant material; the high-strength flame-retardant material comprises the following components in parts by weight: 80-100 parts of low-density polyethylene, 5-10 parts of a flame retardant, 3-5 parts of a performance additive, 1-1.5 parts of filler, 0.1-0.2 part of a voltage stabilizer, 0.1-0.5 part of an antioxidant, 0.5-1 part of an initiator and 1-5 parts of a lubricant. The amino group on the surface of the silicon dioxide carrier treated by 3-aminopropyltriethoxysilane in the modification additive can be subjected to acid-base interaction with the phosphate group of APP to form chemical bridging; the interface bonding enables the APP and the modification additive to synchronously migrate to the surface of the material during combustion to cooperatively construct a protection layer, so that the problem of protection failure caused by migration rate difference of different flame retardants in a traditional flame-retardant system is solved, and the flame-retardant performance of the cable can be greatly improved.