33 results about "Triphenylmethane triisocyanate" patented technology

The present invention discloses an adhesive containing ultra-fine aluminum silicate for packaging and a preparation method thereof. The adhesive comprises the components in parts by weight of 25-30 parts of chloroprene rubber (SN24), 50-60 parts of cyclohexane, 120-160 parts of methylbenzene, 20-30 parts of acetic ether, 10-15 parts of trichloromethane, 20-25 parts of phenolic resin 2402, 5-10 parts of terpene resin, 8-12 parts of polyvinyl alcohol, 2-4 parts of vinyltriethoxysilane, 0.3-0.5 parts of morpholine, 1-2 parts of tri-phenyl methane tri-isocyanate, 4-6 parts of chlorinated paraffinss, 0.2-0.3 parts of Span-60, 8-12 parts of butadiene styrene rubber (SBR1502), 4-8 parts of butyl rubber (BBK232), 1-2 parts of activated zinc oxide, 2-3 parts of active magnesium oxide, 0.5-1 parts of sulphur, 4-6 parts of ultra-fine aluminum silicate, and 2-4 parts of light calcium carbonate, etc. The adhesive provided by the present invention has excellent resistance to high-and-low temperature, good abrasion resistance, high bonding strength, waterproof property, moisture resistance, good storage stability, environmental protection property, good effect and convenient usage.

The invention discloses a high-etherification modified high-performance adhesive and a preparation process thereof, wherein the adhesive comprises, by weight, 100 parts of natural rubber, 45-80 partsof a melamine formaldehyde resin, 25-40 parts of triphenyl methane triisocyanate, 4-12 parts of mineralized nanometer powder, 2-7 parts of magnesium oxide, 1-3 parts of an initiator, 1-3 parts of an anti-aging agent, 1-3 parts of an antioxidant, and 870-960 parts of a solvent. According to the present invention, the adhesive has improved bonding activity, improved aging resistance and improved tear strength so as to improve the wear resistance and the safety of the tire.

The invention discloses a resin self-hardening core sand for casting train iron castings and a preparing method of the resin self-hardening core sand. The resin self-hardening core sand is prepared from, by weight, 160-180 parts of sea sand, 20-30 parts of carborundum, 16-20 parts of refiring magnesia, 10-14 parts of paper clay, 6-8 parts of chalk soil, 10-15 parts of furan resin, 12-14 parts of cashew nut shell oil modified phenolic resin, 4-6 parts of polyimide, 3-5 parts of rare earth tailing, 5-7 parts of pandermite, 8-10 parts of waste foam glass, 3-5 parts of ferro silicon nitride, 1-2 parts of N-(beta-aminoethyl)-gamma-aminopropyl triethoxy silane, 2-4 parts of p-toluenesulfonic acid, 3-5 parts of phosphoric acid, 4-6 parts of castor oil maleic anhydride acid esters, 8-10 parts of triphenylmethane triisocyanate and 2-4 parts of styrene. According to the furan resin self-hardening sand, mixed resin is adopted, the method of adding single resin is changed, mutual effects between different kinds of resin including the furan resin, the cashew nut shell oil modified phenolic resin, the polyimide and the like are adopted for enabling the core sand to have the beneficial effects of being high in strength, small in gas-forming amount, low in thermal expansivity, good in breathability, good in collapsibility and the like, and the produced castings are high in degree of precision and good in surface quality.

The invention discloses an oil resistant silicone rubber material and a preparation method thereof. The material consists of the following raw materials by weight: 75-95 parts of methyl vinyl trifluoropropyl silicone rubber, 40-60 parts of polyethylene naphthalate, 4-8 parts of dihydroxy polydimethylsiloxane, 5-10 parts of nano titanium boride, 3-6 parts of methyl silicone oil, 2-3 parts of aluminum naphthenate, 4-6 parts of lead silicate white, 2-3 parts of triphenylmethane triisocyanate, 10-15 parts of precipitated barium sulfate, 3-6 parts of candelilla wax, 5-10 parts of hydroxyl terminated liquid nitrile rubber, 2-3 parts of dibenzoylquinone dioxime, 1.5-2.5 parts of N,N'-1,3-phenylene bismaleimide, 1-2 parts of polytrimethyldihydroquinoline, 0.5-1.5 parts of TNPP and 3-5 parts of an additive. The silicon rubber material provided by the invention has the advantages of good oil resistant performance, heat resistance, high mechanical strength, tear resistance and aging resistance, can work in the oil medium for a long time, is not easy to age, and has long service life, good processing performance, low cost and broad application prospects.

The invention discloses a polyurethane adhesive which is composed of a component A and a component B. The component A comprises, by mass, 65 parts of triphenyl methane tri-isocyanate and 4 parts of zinc chloride. The component B comprises, by mass, 110 parts of chloroprene rubber, 4 parts of calcium oxide, 3 parts of N-phenyl-2-naphthylamine, 90 parts of methylbenzene and 60 parts of ethyl acetate. The polyurethane adhesive contains isocyanate groups with strong polarity, so the polyurethane adhesive has excellent adhesive properties and excellent mechanical properties such as bending resistance and impact resistance and has the advantages of high peeling strength, acid and alkali resistance, solvent resistance, water resistance, mould prevention and the like. The polyurethane adhesive still has good adhesion strength at a low temperature and especially can keep constant adhesion strength at an ultralow temperature, and the usage temperature range of the polyurethane adhesive is from minus 30 DEG C to 50 DEG C. The invention further provides a manufacturing method and application method of the polyurethane adhesive.

The invention discloses a building sealant composition and application thereof and relates to the technical field of building sealants. The building sealant composition is prepared from the followingraw materials including a vinyl chloride-acrylate copolymer, tert-butyl phenolic tackifying resin, illite powder with the particle size being 20-30 microns, methylisothiazolinone, villus powder with the particle size being 15-30 microns, triphenylmethane triisocyanate, flaxseed gum, tris(butoxyethyl)phosphate, a dispersant FT-78, a crosslinking agent, an accelerator, an antioxidant and a couplingagent. The sealant provided by the invention is simple and convenient to prepare, rapid in surface drying speed, compact and stable in rubber layer crosslinking structure and good in stretching adhesive performance, is flame retardant, resists high-low temperature, water and weather, preserves heat, insulates sound, expels parasites, resists mould, is green and environmentally friendly, saves theenergy and is wide in application places and fields and long in service life.

The invention relates to a microencapsulation ammonium polyphosphate fire retardant and a preparation method thereof. The microencapsulation ammonium polyphosphate fire retardant is prepared from the following raw materials in percentage by weight: 100%-102% of crystal phase APP II (Ammonium Polyphosphate II), 4%-4.5% of melamine, 11%-11.5% of MDI (Diphenylmethane Diisocyanate), 0.4%-0.5% of triphenylmethane triisocyanate, 5%-5.5% of dicyclohexylcarbodiimide, 0.5%-0.8% of trimethylolethane, 120%-125% of acetone and 27%-29% of methylbenzene and is prepared through a double-layer coating process procedure. The microencapsulation ammonium polyphosphate fire retardant disclosed by the invention has the characteristics of easiness for dispersion, good compatibility, high stability, low hygroscopicity and high fire-retardant property.

Belonging to the technical field of coating adhesives, the invention in particular relates to a flame retardant coating adhesive and a preparation method thereof. The flame retardant coating adhesiveis prepared from the following raw materials by weight: 80-120 parts of a waterborne matrix emulsion, 20-35 parts of a polyurethane coating adhesive, 18-22 parts of cyclic phosphate, 10-15 parts of isocyanate, 10-16 parts of tripentaerythritol, 20-26 parts of antimony trioxide, 10-22 parts of ammonium polyphosphate, 8-16 parts of a flame retardant synergist, 5-10 parts of toluene, 5-8 parts of diphenylmethane diisocyanate, 3-8 parts of water-borne blocked isocyanate, 2-5 parts of triphenylmethane triisocyanate and 1-5 parts of trimethylolethane. The flame retardant coating adhesive provided bythe invention has the advantages of good elasticity, corrosion resistance, good flame retardance and the like.

The invention belongs to the technical field of rubber and plastic products, and proposes a low-temperature-resistant rubber and plastic product and a preparation method thereof, comprising the following components in parts by weight: 15 to 20 parts of nitrile rubber, 2 to 3 parts of butadiene rubber, polyvinyl chloride 4-7 parts of resin, 4-7 parts of foaming agent, 3-5 parts of carbon black, 10-13 parts of rubber process oil, 4-7 parts of low-temperature modifier, 0.3-0.5 parts of active agent, 0.1-0.1 parts of stearic acid 0.3 parts, 5-9 parts of aluminum tripolyphosphate, 3-5 parts of barium metaborate, 10-12 parts of filler, 3-5 parts of protective wax, 2-4 parts of accelerator, 0.1-0.3 parts of vulcanizing agent, the low temperature The modifier consists of the following components in parts by weight: 5-8 parts of dioctyl sebacate, 3-5 parts of polydimethylsiloxane, 0.5-1 part of N-methylpyrrolidone, triphenylmethane 2.5-4 parts of isocyanate. Through the above technical solution, the problem that the minimum service temperature of the rubber and plastic products in the prior art can only reach -20°C and the low temperature resistance is poor is solved.

The invention provides a preparation method of a rural experience type light-storing luminescent material. The preparation method comprises the following specific steps: dehydrating a mixed solution of dihydric alcohol and trihydric alcohol at 100-110 DEG C under the vacuum condition of 0.05-0.2 MPa for 3-5 hours; adding an aliphatic ketone solution and an organic tin solution into the dehydratedalcohol solution, mixing, heating to 70-80 DEG C, adding triphenylmethane triisocyanate, and carrying out heat preservation reaction for 1.5-2.5 hours at 70-80 DEG C; and adding the light-storing luminescent material into the catalytic reaction, and continuing the heat preservation reaction to obtain the single-component light-storing polyurethane luminescent material. According to the luminescentmaterial prepared by the method, the light-storing and light-emitting functions of the coating are improved, the problems of the traditional fluorescent coating are solved, and the obtained luminescent material has the advantages of increased light-emitting stable strength, difficulty in migration, lasting and stable maintenance of a light-emitting group, excellent glossiness and weather resistance, difficulty in quenching and typical light-storing and light-emitting enhancement effect.

A nanoparticle reinforced self-lubricated cast nylon composite shaft sleeve is prepared from components including a caprolactam monomer, sodium hydroxide, triphenylmethane triisocyanate, nano graphite fluoride and mica powder in a weight ratio being 100:(0.15-0.45):(0.3-0.6):(0.4-0.5):(2.0-4.0). The manufacturing method of the composite shaft sleeve comprises preparation of reaction melts, preparation of a dispersion liquid as well as molding and demolding, the centrifugal casting method is adopted in the casting process, so that more nano graphite fluoride and mica powder are centralized and distributed on the outer surface of the shaft sleeve, the shaft sleeve has better bearing capacity and more excellent anti-friction and wear-resistance properties, the wear of the shaft sleeve is reduced, and the service life of the shaft sleeve is prolonged.

The invention discloses a method for preparing heat-induced flexible phase change energy storage wood, which is carried out according to the following steps: a. Using N,N dimethylformamide as a solvent, prepare 0.05-0.2mol / L triethanolamine solution 50- 70 parts and 40-60 parts of 0.1-0.4mol / L triphenylmethane triisocyanate solution; b, adding the triethanolamine solution in step a to the triphenylmethane triisocyanate solution, stirring at 60-80°C for 10- 15 hours to obtain a prepolymer; c, adding 10-20 parts of polyethylene glycol-1500 to the prepolymer, stirring at 60-80°C for 20-30 hours to obtain a solid-solid phase change material; d, adding The delignified wood is put into the solid-solid phase change material, vacuum impregnated for 20-40 minutes and then dried to obtain the finished product. The phase change energy storage wood prepared by the invention not only has the ability to store heat and store energy, but also has good flexibility.