463 results about "Propenyl" patented technology

The invention discloses an OCA optical adhesive and a preparation method thereof, and relates to the technical field of adhesives, and the OCA optical adhesive is prepared from the following raw materials in parts by weight: 35-45 parts of acrylate-terminated hyperbranched organosilicon modified polyurethane, 2-4 parts of allyl succinimido carbonate, 1-3 parts of hexafluorobisphenol A diacrylate, 1-3 parts of 1, 2, 4-trimethyl-1, 3-pentanediol monoisobutyrate, 1-3 parts of 1, 3-pentanediol monoisobutyrate, 1-3 parts of 1, 3-pentanediol monoisobutyrate, 1-3 parts of 1, 3-pentanediol The invention relates to a photocurable adhesive, which is prepared from the following components in parts by weight: 20 to 30 parts of a diluent, 0.6 to 1.2 parts of a photoinitiator, 0.5 to 1 part of an antioxidant and 0.5 to 1 part of a de-foaming agent. The photocurable adhesive is prepared from the following components in parts by weight: 1 to 5 parts of 1, 3-bis (oxiranyl methyl)-5-(2-propenyl)-1, 3, 5-triazine-2, 4, 6 (1H, 3H, 5H)-triketone, 3 to 5 parts of 2, 2 '-bis (trifluoromethyl) diaminodiphenyl, 6 to 8 parts of other polymerizable monomers, 20 to 30 parts of the diluent, 0.6 to 1.2 parts of the photoinitiator, 0.5 to 1 part of the antioxidant and 0.5 to 1 part of the de-foaming agent. The OCA optical adhesive is good in bonding performance, sufficient in weather resistance and environmental protection performance and good in oil resistance.

The invention discloses an antibacterial and deodorant blended fabric, a preparation method thereof and application of the antibacterial and deodorant blended fabric in underwear, and relates to the technical field of fabrics. When the antibacterial and deodorant blended fabric is prepared, firstly, indolyl polyester is subjected to melt spinning to be prepared into fibers; the preparation method comprises the following steps: reacting fibers, indole and indole-6-formaldehyde, reacting with 4-(aminomethyl)-2, 6-di-tert-butylphenol, and reducing to obtain modified polyester fibers; secondly, the pretreated bamboo fibers react with carbon disulfide and potassium hydroxide; the preparation method comprises the following steps: oxidizing a modified bamboo fiber precursor obtained by reacting the modified bamboo fiber with 1-(2-propenyl)-1, 3, 5-triazine-2, 4, 6 (1H, 3H, 5H)-triketone to obtain a modified bamboo fiber, and oxidizing the modified bamboo fiber precursor to obtain the modified bamboo fiber; the modified polyester fibers and the modified bamboo fibers are blended and woven to obtain fabric, and then the fabric is finished through a finishing agent to obtain the antibacterial and deodorant blended fabric. The antibacterial and deodorant blended fabric prepared by the invention has good antistatic, antibacterial and durable properties.

The invention discloses an all-solid-state composite dry conductive agent and a preparation method thereof, and belongs to the technical field of batteries. The all-solid-state composite dry conductive agent is prepared by the following steps: uniformly mixing carbon nanotubes, high-dispersion carbon black and graphene to obtain a primary mixture; then preparing a uniformly dispersed glue solution from the composite dispersant and water; and then adding the primary mixture into the glue solution, uniformly mixing, sanding, homogenizing, drying and crushing to obtain the product, the high-dispersion carbon black is obtained by oxidizing carbon black to form active groups such as carboxyl and hydroxyl on the surface of the carbon black, halogenating acyl and then reacting with lithium 2, 5-diaminobenzene sulfonate. The preparation method comprises the following steps: grafting histidine ester into carboxymethyl cellulose by using propylene glycol diglycidyl ester as a cross-linking agent, then introducing allyl-1, 3-sultone, then copolymerizing with lithium 2-acrylamido-2-methylpropanesulfonate and 3-aminobenzoic acid allyl ester protected by fluorenylmethoxycarbonyl, and then deprotecting to obtain the composite dispersant.

The invention discloses a far-infrared high-transmittance composite material, a preparation method thereof and an optical device, and the far-infrared high-transmittance composite material comprises the following components in parts by weight: 70-99 parts of a polymer matrix; 1-30 parts of an anti-reflection auxiliary agent; the polymer matrix is a sulfur-containing polymer prepared by polymerization reaction of a polymeric monomer and sulfur, and the proportion of carbon-carbon unsaturated bonds is less than 3%; the polymeric monomer is selected from at least one of a vinyl monomer, a propenyl monomer, an acrylic acid monomer, a methacrylic acid monomer, an epoxide monomer, a thiopropyl ring monomer, an alkynyl monomer, a butadiene monomer, an isoprene monomer and a norbornene monomer; the anti-reflection auxiliary agent comprises at least one of nano zinc sulfide, nano zinc selenide, nano calcium fluoride, nano magnesium fluoride and nano magnesium oxide. The composite material and the optical device thereof have high far infrared transmittance and good mechanical properties and processability, and can meet the requirements of various far infrared optical fields.

The invention discloses a process for preparing flame-retardant polyethylene plastic by recycling waste polyethylene plastic, and relates to the technical field of high polymer materials. When the flame-retardant polyethylene plastic is prepared, the waste polyethylene is extruded and granulated to prepare the polyethylene master batch; carrying out catalytic pyrolysis on the polyethylene master batch, and then reacting with potassium permanganate to prepare a hydroxylated carbon nanotube; the preparation method comprises the following steps: reacting a hydroxylated carbon nanotube with 1-(chloro-methylphosphoryl) ethylene, and then reacting with (mercaptomethyl) triethoxysilane to prepare a modified carbon nanotube; the preparation method comprises the following steps: carrying out irradiation grafting on a polyethylene master batch, 2-hydroxy-4-propenyl benzophenone and N, N-diethyl allylamine, and then reacting with chloromethyl triethoxy silane to prepare modified polyethylene; and carrying out melt extrusion on the modified carbon nanotubes and the modified polyethylene, carrying out injection molding, and carrying out water treatment to obtain the flame-retardant polyethylene plastic. The flame-retardant polyethylene plastic prepared by the invention has good flame retardant property, antibacterial property, tensile strength and anti-aging property.

The invention discloses a high-performance adhesive for automobile glass process protection, and relates to the technical field of adhesives, and the high-performance adhesive is prepared from the following raw materials: hyperbranched perfluoropolyether urethane acrylate oligomer, methyl vinyl silicone rubber, isocyano ethyl methacrylate, hexahydro-1, 3, 5-tris (hydroxyethyl)-s-triazine, 2, 4, 5-trimethyl-1, 3-pentanediol monoisobutyrate, 2, 4, 5-trimethyl-1, 3-pentanediol monoisobutyrate, 2, 4, 5-trimethyl-1, 3-pentanediol The coating is prepared from the following raw materials: 2, 6-trivinyl boroxane, methyl vinyl di (diacetylketoxime) silane, N-vinyl caprolactam, 2-(1-propylene-2-yl) benzo [D] oxazole, 3, 3 '-diamino-4, 4'-difluorodiphenyl sulfone, 3-(1, 1-difluoro-2-propylene-1-yl)-2 (1H)-quinoxalinone, a diluent, a photoinitiator, a catalyst and a defoaming agent. The adhesive is high in adhesive strength, excellent in high temperature resistance, good in adhesive removing performance and safe and environment-friendly to use.

Disclosed is a pharmaceutical composition for the treatment of tumors, the pharmaceutical composition comprising (6S, 9aS)-N-benzyl-8-({6-[3-(4-ethylpiperazin-1-yl) azetidin-1-yl] pyridin-2-yl} methyl)-6-(2-fluoro-4-hydroxybenzyl)-4, 7-dioxo-2-(propyl-2-en-1-yl) hexahydro-2H-pyrazino [2, 1-c] [1, 2, 3] triazolo [1, 2, 4] triazolo [1, 2, 4] triazolo [1, 2, 4] triazolo [1, 2, 4] triazolo [1, 2, 4] triazolo [1, 2, 4] triazolo [1, 2, 4] triazolo [1, 2, 4] triazolo [ The present invention relates to a compound of formula (I) or a pharmaceutically acceptable salt thereof and administered in combination with a MEK inhibitor.

The invention discloses a sodium-ion battery electrolyte with high cycle performance and a preparation method thereof, and the preparation method comprises the following steps: dissolving a sodium salt in an organic solvent, and mixing to obtain a sodium salt solution; the method comprises the following steps: adding a film-forming agent, a flame retardant and an additive into a sodium salt solution, and uniformly mixing to obtain the electrolyte, the additive is obtained by carrying out amino-propylene addition reaction on tri-n-butyl (1-propenyl) tin and 2, 3, 5, 6-tetra (amino) p-benzoquinone, and then carrying out sulfydryl-propylene addition reaction on the obtained product and 1, 2-disulfydryl-o-carborane. By optimizing the composition and the preparation process of the electrolyte, the obtained sodium-ion battery electrolyte shows excellent stability in multiple cycle tests, the capacity retention ratio is remarkably improved, and the capacity attenuation is lower than 5% when the cycle index reaches 1000 or above. The electrolyte also has good low-temperature performance and thermal stability, and can normally work in a wide temperature range of-20 DEG C to 60 DEG C.

The invention discloses a thermal antistatic fabric based on polyamide fibers and a preparation method thereof, and relates to the technical field of textile fibers. When the thermal antistatic fabric based on the polyamide fiber is prepared, caprolactam, a flame retardant and hexamethylenediamine react to prepare pre-modified polyamide; the pre-modified chinlon and 3-chloro-1-propanethiol are subjected to a reaction, and modified chinlon is prepared; the preparation method comprises the following steps: sequentially reacting graphene oxide with mercaptopropyltrimethoxysilane and 2-(2H-benzotriazole-2-yl)-4-methyl-6-(2-propenyl) phenol, so as to obtain modified graphene oxide; the modified chinlon and the modified graphene oxide are mixed and then subjected to melt spinning, and modified chinlon fibers are obtained; and twisting the modified polyamide fiber, spinning, and post-processing to obtain the thermal antibacterial fabric based on the polyamide fiber. The warm-keeping antistatic fabric based on the polyamide fiber has good warm-keeping, antistatic, flame-retardant, anti-aging and mechanical properties.

The invention provides a lithium battery diaphragm and a preparation method thereof, and the preparation method comprises the following steps: carrying out a reaction on melamine and terephthalaldehyde in dimethyl sulfoxide to obtain SNW-1COF; the preparation method comprises the following steps: enabling SNW-1COF to react with allyl-1, 3-sultone in acetonitrile, so as to obtain allyl SCOF; the polyarylether benzimidazole, the 2-sulfydryl-5-fluorobenzimidazole, triethylamine and allyl SCOF are subjected to a reaction in a third solvent, and a membrane casting solution is obtained; and applying the membrane casting solution to a base material, and removing the solvent in the membrane casting solution to obtain the lithium battery diaphragm. According to the invention, the OPBI matrix and the propenyl SCOF react to form a covalent cross-linked network, so that the mechanical properties of the diaphragm in the aspects of thermal shrinkage rate, tensile strength, puncture strength and the like and the electrical properties in the aspects of wettability and ionic conductivity are improved.

The invention relates to the technical field of release films, and particularly provides a preparation method of a low-temperature-curable and high-wettability release film for MLCC (multilayer ceramic capacitor) tape casting. The release film comprises a base material layer and a release agent layer, the release agent layer is prepared from the following raw materials in percentage by weight: 30%-40% of methylbenzene, 10%-15% of ethyl acetate, 20%-35% of butanone, 10%-20% of organic silicon modified acrylic resin, 2%-3% of a curing agent and 1%-2% of a flatting agent, and the organic silicon modified acrylic resin is prepared from fluoropropenyl trimethoxy silane modified acrylic resin. The surface flatness and wettability of the release film obtained by adopting the scheme are equivalent to those of an imported MLCC release film, and the cost of the release film is far lower than that of the imported MLCC release film.

The invention relates to a polypropylene material and a preparation method thereof, and discloses a high molecular weight propenyl elastomer toughened polypropylene blend composite material and a preparation method thereof. The preparation method comprises the following steps: toughening polypropylene by using a high-molecular-weight propenyl elastomer; the high-molecular-weight propenyl elastomer is prepared from propylene monomers and comonomers (one or more of 1-butene, styrene, 1-hexene, 1-octylene, 1-decene and the like) through a quinoline amino binuclear metal hafnium catalyst and co-catalysts (tri-pentafluorophenyl boron, triphenylcarbonium tetra (pentafluorophenyl) borate, aluminoxane, aluminum alkyl and the like). And one or more of alkyl aluminum chloride and the like). According to the present invention, the polypropylene-based blend composite material has characteristics of PP toughness improving, excellent strength and excellent rigidity maintaining, and excellent low temperature toughness, specifically, after the toughening modification, the normal temperature (25 DEG C) toughness and the low temperature (-25 DEG C) toughness of the polypropylene-based blend composite material are significantly improved, and the tensile strength change is not significant. Therefore, the invention has original innovation, and provides a new direction for the development of the field of polyolefin materials.

The invention discloses a composite pipe and a preparation method thereof, and relates to the technical field of water supply pipes. The composite pipe sequentially comprises an outer layer, a middle layer and an inner layer from outside to inside, raw materials of the outer layer comprise polypropylene random copolymer and composite rubber, and the mass ratio of the polypropylene random copolymer to the composite rubber is (3-9): 1; the composite rubber comprises ethylene propylene rubber, isoprene rubber and nano silicon dioxide, the mass ratio of the ethylene propylene rubber to the isoprene rubber in the composite rubber is (2.3-4): 1, and the mass ratio of the nano silicon dioxide to the composite rubber is (2-3): 10; the raw material of the middle layer is a propenyl block copolymer; the raw materials of the inner layer comprise heat-resistant polyethylene and glass fibers. The composite pipe provided by the invention has excellent mechanical strength and impact resistance.

The invention belongs to the technical field of battery materials, and particularly relates to a lithium ion battery electrolyte containing a cyano sulfonamide compound and a lithium ion secondary battery, the lithium ion battery electrolyte containing the cyano sulfonamide compound comprises an organic solvent, a lithium salt and an additive, the additive comprises at least one substance of fluoroethylene carbonate, ethylene sulfate, ethylene sulfite, 1, 3-propane sultone, 1, 3-propenyl sultone, vinylene carbonate and vinylethylene carbonate, and a cyano sulfonamide compound, and the additive comprises at least one substance of fluoroethylene carbonate, ethylene sulfate, ethylene sulfite, 1, 3-propane sultone, 1, 3-propenyl sultone, vinylene carbonate and vinylethylene carbonate; the invention relates to a lithium ion secondary battery which comprises a battery cell, a battery shell and electrolyte, the electrolyte additive, the organic solvent and the lithium salt of specific types are matched, so that the cycle performance of the lithium ion battery under high voltage can be effectively improved, and the lithium ion battery prepared from the lithium ion battery electrolyte has excellent cycle performance under high voltage.

The invention belongs to the technical field of preparation of thickening agents, and particularly relates to a preparation method of a polymer thickening agent for fracturing. The preparation method comprises the following steps: preparing a pretreated methacrylic acid (triethoxysilyl) methyl ester solution; preparing a pretreated 2-[[2-(methacryloyloxy) ethyl] dimethylammonium] acetate solution; preparing a water phase; and preparing the polymer thickening agent for fracturing. According to the preparation method of the polymer thickening agent for fracturing, acrylamide is used as a main monomer, maleic acid mono [2 (1-oxy-2-propenyl) oxyethyl] ester, methacrylic acid (triethoxysilyl) methyl ester and 2-[[2-(methacryloyloxy) ethyl] dimethylammonium] acetate are used as functional monomers, and the acrylamide, the maleic acid mono [2 (1-oxy-2-propenyl) oxyethyl] ester, the methacrylic acid (triethoxysilyl) methyl ester, the methacrylic acid (triethoxysilyl) methyl ester and the 2-[[2-(methacryloyloxy) ethyl] dimethylammonium] acetate are used as functional monomers. A redox initiator and an azo initiator are combined to serve as an initiator system, multi-monomer copolymerization is achieved through gradient temperature polymerization, and the temperature-resistant and salt-resistant polymer thickening agent for fracturing is prepared.

The invention discloses antistatic medical gauze and a preparation method thereof. The antistatic medical gauze is formed by blending carbon nanotube graphene conductive fibers, medical chitosan fibers and functional synthetic fibers, the functional synthetic fiber is prepared from the following raw materials in parts by weight: 100 parts of a functional synthetic copolymer and 3-5 parts of (3, 6-diamino-9-acridinyl) boric acid, the functional synthetic copolymer comprises structural units introduced by the following monomers: 1-allyl-3-methylimidazole chloride, N-vinyl oxazolidinone, 3-[N, N-dimethyl-[2-(2-methylpropyl-2-enoyloxy) ethyl] ammonium] propane-1-sulfonic acid inner salt, N-(4-cyano-3-trifluoromethylphenyl) methacrylamide, 1, 2, 3, 4-tetramethyl-1, 3, 4-tetramethyl-1, 3, 4, 5-tetramethyl-1, 3, 5-tetramethyl-1, 3, 5-tetramethyl-1, 3, 5-tetramethyl-1, 3, 5-tetramethyl-1, 3, 5-tetramethyl-1, 3, 5-tetramethyl-1, 3, 5-tetramethyl-1, the catalyst is 1, 3-bis (oxiranyl methyl)-5-(2-propenyl)-1, 3, 5-triazine-2, 4, 6 (1H, 3H, 5H)-triketone. The gauze is good in antibacterial property, excellent in air permeability and antistatic property and long in service life.

Described herein is N-[4-[4-(4-morpholinyl)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]phenyl]-4-[[3(R)-[(1-oxo-2-propen-1-yl)amino]-1-piperidinyl]methyl]-2-pyridinecarboxamide (Compound A) (Formula I),including crystalline forms, solvates, and pharmaceutically acceptable salts thereof. Also disclosed are pharmaceutical compositions or pharmaceutical formulations that include the compound, as well as methods of using the compound, alone or in combination with other therapeutic agents, for the treatment of autoimmune diseases or conditions, heteroimmune diseases or conditions, cancer, including lymphoma, diabetes, and inflammatory diseases or conditions.

The invention discloses a high-performance composite geotextile and a preparation method thereof, and relates to the technical field of geotextile, the high-performance composite geotextile sequentially comprises a functional protective layer, a fiber reinforced layer and a base layer from top to bottom; the functional protection layer is prepared from the following raw materials in parts by weight: 5-8 parts of 2-[3-(2H-benzotriazole-2-yl)-4-hydroxyphenyl] ethyl 2-methacrylate, 6-10 parts of 1-allyl-3-vinyl imidazole chlorine salt, 1-3 parts of 2, 4, 6-trivinyl boroxane, 1-3 parts of 3-(1, 2, 4-triazole-2-yl)-4-hydroxyphenyl)-1, 2, 3-triazole-2-yl)-1, 2, 3-triazole-2-yl)-1, 2, 3-triazole-2-yl)-1, 2, 3-triazole-2-yl)-1, 2, 3-triazole-2 The invention relates to a high-temperature-resistant coating which is prepared from the following raw materials in parts by weight: 1-3 parts of 1, 1-difluoro-2-propylene-1-yl)-2 (1H)-quinoxalinone, 2-4 parts of vinyl trimethoxy silane and 0.1-0.3 part of an initiator. The composite geotextile is sufficient in mechanical property and good in antibacterial property and aging resistance.

The invention provides a novel mineral separation activating agent for sulphide ores and a preparation method of the novel mineral separation activating agent. The cleaning agent comprises 1-2 parts of basic cupric carbonate, 2-4 parts of ammonium chloride, 2-4 parts of nanometer jade powder, 2-3 parts of alginic acid, 1-2 parts of allyl glycidyl ether, 2-3 parts of peregal O, 2-3 parts of sodium di-sec-octyl maleate sulfonate, 2-3 parts of vinyl acetate, 4-7 parts of hydrogen peroxide, 4-6 parts of disodium hydrogen phosphate and 40-50 parts of water. The preparation method comprises the following steps: firstly mixing basic cupric carbonate and ammonium chloride to obtain a first mixture, then mixing the rest components, heating and stirring to obtain a second mixture, and finally uniformly mixing the first mixture and the second mixture. The activating agent overcomes the defects of a traditional activating agent, has efficient activating performance, can improve the beneficiation efficiency of low-grade, complex and refractory sulfide ore, is environmentally friendly, good in stability and high in adaptability, and provides technical support for efficient development of sulfide ore resources.

The invention provides an organic silicon modified perfluoropolyether UV anti-fingerprint agent and a preparation method thereof. The method comprises the following steps: adding organic silicon modified perfluoropolyether into a fluorocarbon solvent, and adding an alcohol compound containing a propenyl terminal group and a catalyst for reaction to obtain a hydroxyl-containing organic silicon modified perfluoropolyether solution; the preparation method comprises the following steps: adding an acid-binding agent into a hydroxyl-containing organosilicon modified perfluoropolyether solution, and slowly dropwise adding acryloyloxy chloride for reaction to obtain a crude product; and adding an organic alcohol compound into the crude product for treatment, carrying out liquid separation and standing, taking out subnatant, and carrying out rotary evaporation to obtain the organic silicon modified perfluoropolyether UV anti-fingerprint agent. According to the method disclosed by the invention, the problem of compatibility of the perfluoropolyether-based anti-fingerprint agent and the UV coating is solved under the condition of reducing the fluorocarbon solvent through chemical synthesis. In the curing process, the perfluoropolyether-based anti-fingerprint agent part is quickly migrated to the surface of the UV coating, and in-situ curing and crosslinking are achieved.

The invention discloses an organosilicon pesticide wetting agent and a preparation process thereof, and relates to the technical field of wetting agents, the organosilicon pesticide wetting agent comprises the following raw material components: 50-150 parts of hydrogen-containing silicone oil, 50-150 parts of allyl polyether, 0.1-3 parts of a catalyst, and 30-80 parts of a nonionic surfactant, the invention relates to a polystyrolsulfon acid composition which comprises the following components in parts by weight: 50-150 parts of polystyrolsulfon acid, 1-10 parts of a thickening agent, 100-250 parts of glycerol, 25-55 parts of a first additive substance, 20-50 parts of a second additive substance and 5-15 parts of trace elements. The allyl polyether and the hydrogen-containing silicone oil are subjected to an addition reaction to generate polyether modified organic silicon with small molecular weight, the wettability of the wetting agent is improved, the modified organic silicon wetting agent is combined with the nonionic surfactant, the wettability is further improved, and the wetting effect is improved. And by grafting the branched chain on the hydrophobic group of the organosilicon compound wetting agent, the wetting effect of the wetting agent can be effectively improved, and the effective components of the pesticide can wet the surfaces of crops.

The invention belongs to an insulating material, relates to a polypropylene-based insulating material, and in particular relates to a high-temperature-resistant intrinsic self-recovery polypropylene insulating material as well as a preparation method and application thereof. The material is formed by blending a polypropylene grafting material and an ethylene-tetrafluoroethylene copolymer grafting material according to a mass ratio of 6.0: 4.0-9.5: 0.5, wherein the PP graft material comprises a PP graft polymer and an antioxidant, and the PP graft polymer is a graft polymer formed by grafting 4-propenyloxy-2-hydroxybenzophenone to polypropylene; the ETFE graft material comprises an ETFE graft polymer and an antioxidant, and the ETFE graft polymer is a graft polymer of glycerol grafted ethylene-tetrafluoroethylene copolymer. On the basis of keeping the original excellent performance of polypropylene, the polypropylene has higher heat resistance and self-recovery capability through a grafting modification technical means.

The invention provides a propenyl copolymer as well as a preparation method and application thereof. The weight-average molecular weight of the propenyl copolymer is 2.0 * 10 < 4 >-40.0 * 10 < 4 > g / mol, and the density of the propenyl copolymer is 0.860-0.890 g / cm < 3 >. The gamma value of the propenyl copolymer is greater than or equal to 80%. Through design of specific molecular weight, density and gamma value, regulation and control of material structure and composition are realized. The propenyl copolymer is used for a polyolefin film material, and can effectively reduce the initial sealing temperature and broaden the heat sealing temperature range, so that the polyolefin film containing the propenyl copolymer has significantly improved heat sealing performance.

The invention discloses a propenyl olefin block copolymer with a flame-retardant function, a preparation method of the propenyl olefin block copolymer and a composition containing recycled plastic. The allyl olefin block copolymer with the flame-retardant function comprises a first block and a second block, the first block contains a polypropylene block, and the second block contains propylene, ethylene and a copolymer block of a monomer containing a phosphonic acid group and a carbon-carbon double bond. The composition containing the recycled plastic comprises polyethylene recycled plastic, polypropylene recycled plastic and the allyl olefin block copolymer with the flame retardant function. The allyl olefin block copolymer with the flame-retardant function can be used as a compatilizer in ethylene-propylene recycled plastics, so that the ethylene-propylene recycled plastics have excellent mechanical properties and flame-retardant properties at the same time.

The invention discloses a preparation method of a warm-keeping and health-care composite fabric, and relates to the technical field of functional fabrics. The preparation method comprises the following steps: firstly, combining fumed silica with graphene oxide hydrogel to prepare mixed aerogel; the mixed aerogel is combined with allyl trichlorosilane, and is grafted to a macromolecular chain of polypropylene through maleic anhydride, so that the compatibility is improved, and the agglomeration problem is solved; secondly, calcining tourmaline, then directly carrying out quenching hydration modification, combining Si-OH groups on the surface with active groups in a polyester molecular chain, and spinning into hollow fibers; the mixed aerogel can absorb far infrared rays dissipated and emitted by the modified tourmaline, and the aerogel absorbing the far infrared rays can generate a resonance effect and a warm effect and permeate into the deep layer of the skin; the modified tourmaline has the capability of generating negative ions, and the gull rock powder is added for combined action, so that the antibacterial effect is achieved by destroying the structure of bacteria, and the health-care effect is achieved. The composite fabric prepared by the invention has warm-keeping and health-care effects.

The invention relates to a preparation method of bio-based ink of cardanol modified acrylic resin, and belongs to the technical field of ink preparation. The preparation method comprises the following steps: stirring and mixing cardanol, a 6, 6 '-dihydroxy-3, 3'-biphenyl dicarboxylic acid / Cu complex, triethylamine and a dichloromethane solvent at room temperature, slowly dropwise adding a mixture of acryloyl chloride and dichloromethane, and performing reduced pressure distillation to remove dichloromethane after reaction to obtain a propenyl cardanol ester / propenyl biphenyl dicarboxylic acid ester / Cu complex mixture; the preparation method comprises the following steps: carrying out a reaction on the obtained product, methyl methacrylate, pentaerythritol tetramercaptoacetate, acrylic acid, a triazine trithiol trisodium salt hydrate, toluene and a photoinitiator under ultraviolet irradiation; dropwise adding ammonia water to adjust pH, and performing reduced pressure distillation after reaction to obtain cardanol modified acrylic resin; and dispersing the cardanol modified acrylic resin with deionized water, ethanol, a pigment, a defoaming agent, a thickening agent and a coupling agent at a high speed, and adjusting the pH value with ammonia water to obtain the cardanol modified acrylic resin bio-based ink.

The present invention provides an organosilicon-modified-perfluoropolyether-based UV anti-fingerprint agent and a preparation method therefor. The method comprises the following steps: adding an organosilicon-modified perfluoropolyether to a fluorocarbon solvent, adding an alcohol compound containing a propenyl-terminated group and a catalyst thereto, and reacting same, so as to obtain a hydroxyl-containing organosilicon-modified perfluoropolyether solution; adding an acid-binding agent to the hydroxyl-containing organosilicon-modified perfluoropolyether solution, and slowly adding, in a dropwise manner, an acryloyloxy chloride, and reacting same, so as to obtain a crude product; and adding an organic alcohol compound to the crude product for a treatment, subjecting same to liquid separation, leaving same to stand, taking out a subnatant, and subjecting same to rotary evaporation, so as to obtain an organosilicon-modified-perfluoropolyether-based UV anti-fingerprint agent. By means of chemical synthesis, the method of the present invention solves the problem of compatibility between a perfluoropolyether-based anti-fingerprint agent and a UV coating, whilst reducing the amount of fluorocarbon solvent. During the process of curing, the present invention further achieves the rapid migration of part of the perfluoropolyether-based anti-fingerprint agent to the surface of the UV coating for curing and cross-linking in situ.

The invention discloses an anti-ultraviolet solar cell backboard film and a preparation method thereof, and relates to the technical field of solar cell backboards, the anti-ultraviolet solar cell backboard film comprises a first anti-ultraviolet functional layer, a polyester base layer and a second anti-ultraviolet functional layer from top to bottom in sequence; the first uvioresistant functional layer and the second uvioresistant functional layer are independently prepared from the following raw materials: a functional polymer, 2-acrylamido-2-methylpropanesulfonic acid, 1, 3-bis (oxiranyl methyl)-5-(2-propenyl)-1, 3, 5-triazine-2, 4, 6 (1H, 3H, 3H, 3H, 3H, 3H, 3H, 3H, 3H, 3H, 3H, 3H, 3H, 3H, 3H, 3H, 3H, 3H, 3H, 3H, 3H, 3H, 3H The invention relates to a high-temperature-resistant nano-emulsion which is prepared from N-(4-cyano-3-trifluoromethylphenyl) methacrylamide, N-(4-cyano-3-trifluoromethylphenyl) methacrylamide, a nano-assistant, a coupling agent, an initiator, polyphosphoric acid and phosphorus pentoxide. The backboard film is good in ultraviolet aging resistance, good in interlayer peel strength and excellent in barrier property.

According to the invention, rigid anthracene is introduced as a framework of bridged binuclear metal, a pyridylamino binuclear metal titanium-zirconium-hafnium catalyst is constructed, and the molecular weight of the obtained polymer can be effectively improved through the synergistic effect between the binuclear metal and the steric hindrance and electronic effect on the catalyst structure; the polyolefin elastomer (POE), the isotatic polypropylene (iPP) and the propenyl elastomer (PBE) are efficiently synthesized. The pyridylamino binuclear metal titanium-zirconium-hafnium catalyst has the advantages that synthesis is simple, raw materials are easy to obtain, and the product yield is high. In copolymerization of ethylene and alpha-olefin, the catalyst shows excellent activity (5.75 * 10 < 7 > g (POE). Mol <-1 > (M). H <-1 >) and alpha-olefin selectivity (the insertion rate reaches 16.2 mol%), and the polyolefin elastomer POE with excellent performance is prepared. In propylene polymerization, the regularity of the polypropylene chain segment can be effectively regulated and controlled by adjusting the steric hindrance and the electronic effect of the catalyst, and the regularity gt is prepared with high activity (3.84 * 10 < 7 > g (PP). Mol <-1 > (M). H <-1 >); and the polypropylene material with high stereoregularity is prepared from 80 mmmm% of polypropylene with high stereoregularity. In copolymerization of ethylene and propylene, an elastomer material which takes propylene as a main material, can regulate and control the ethylene content to be 5-50 wt% and has unique characteristics of a propylene-ethylene semi-crystalline copolymer is prepared. In addition, the pyridylamino binuclear metal titanium-zirconium-hafnium catalyst also shows excellent high-temperature resistance (higher than 160 DEG C), is suitable for high-temperature solution polymerization, and can be used for preparing high-performance polyolefin elastomers. Therefore, the invention has original innovation, and provides a new direction for the development of the field of polyolefin materials.

The invention relates to a preparation method of a high-speed rail brake pad, and belongs to the technical field of brake pads. Iron powder, silicon dioxide powder, carbon powder, nickel powder, copper powder and a grinding aid are subjected to wet grinding, drying, sieving, cold pressing forming and sintering, and a matrix is obtained; and after a base body is polished, derusted and ultrasonically cleaned, the iron-chromium-aluminum mixed powder is heated to be in a molten state, plasma spraying is conducted on the surface of the base body, and then the high-speed rail brake pad is obtained. The grinding aid disclosed by the invention is prepared from dioctadecylamine, allyl triphenyltin, methacrylated sodium alginate, triethanolamine and DMF (Dimethyl Formamide). The high-speed rail brake pad prepared by the invention has the advantages of stable friction coefficient, low abrasion loss, good wear resistance and the like.