327 results about "N-Butyl methacrylate" patented technology

A polymer for a medical device, particularly for a drug eluting stent, is described. The polymer can be derived from n-butyl methacrylate and can have a degree of an elongation at failure from about 20% to about 500%

The invention discloses an isolating membrane of lithium ion secondary battery, comprising a porous substrate and a polymer coating distributed only on a surface of the porous substrate which faces an anode of the lithium ion secondary battery, wherein the polymer in the polymer coating is selected from poly(methyl methacrylate-acrylonitrile), poly(methyl methacrylate-vinyl acetate), poly(methyl methacrylate-acrylonitrile-vinyl acetate), poly(n-butyl methacrylate-styrene), or blends of the polymers. The polymer unit in the polymer coating of the isolating membrane of the lithium ion secondary battery contains carbonyl, wherein very strong effect exists between the carbonyl and oxygen in carbonic acid ester type organic solvent so as to have fine solution suction ability and good interface stability of lithium electrode or anode; the membrane has strong adhesive property and film formation, and can provide fine mechanical tensile strength; and the membrane has fine cycle performance and safety performance. The invention further discloses a polymer lithium ion secondary battery using the membrane.

The invention discloses a plastic-wooden composite tray which is prepared from the raw materials in parts by weight: 50-60 parts of high density polyethylene, 20-30 parts of copolymerization polypropylene, 30-40 parts of modified wood meal, 40-50 parts of plastic renewable material, 20-30 parts of active calcium, 1-2 parts of zinc stearate, 1-2 parts of calcium stearate, 2-3 parts of n-butyl methacrylate, 0.3-0.5 part of polyethylene wax, 0.4-0.6 part of triethoxyvinylsilane, 0.3-0.4 part of antioxidant 1010, 0.4-0.6 part of anti-aging agent MB, 8-10 parts of foaming modifier, 4-8 parts of ACM, 4-8 parts of MBS, 25-30 parts of oxidized polyethlene wax, 0.2-0.3 part of foaming agent, 4-8 parts of TPE (Thermoplastic Polyurethane Elastomer), 8-12 parts of chlorinated polyvinyl chloride, 5-8 parts of glass fiber and 3-4 parts of semi-reinforced carbon black. The plastic-wooden composite tray produced by using the preparation method has the advantages of excellent mechanical property, capability of being sawed, planed and nailed, good durability, high repeated usage rate, capability of being recycled, resistance to insect biting, acid and alkaline resistance, aging resistance, and low water absorption and low deformation rate.

The invention discloses a high-temperature oil resistant nitrile rubber gasket, comprising the following ingredients in parts by weight: 35-145 parts of nitrile rubber N411, 30-35 parts of active chloride type acrylic rubber, 10-15 parts of SG-1 type polyvinyl chloride, 2-5 parts of triethyl citrate, 3-5 parts of epoxy butyl oleate, and 2-5 parts of n-butyl methacrylate. The nitrile rubber gasket disclosed by the invention has excellent oil resistance and solvent resistance, also has excellent compressibility and rebound resilience and weak permanent deformation, does not soften and not decompose at high temperature, does not harden and not crack at low temperature, has excellent corrosion property, can work for a long time in mediums of acid, alkali, oil and the like, has small change in volume and rigidity and can adhered on metal surfaces, and has the following advantages of low friction coefficient, excellent wearing resistance, flexibility of being combined with a seal surface, excellent weather aging and ozone aging resistance, endurance, and the like.

The invention discloses a CBN (cubic boron nitride) resin grinding wheel and a preparation method of the CBN resin grinding wheel. The CBN resin grinding wheel is prepared from the following components in parts by weight, 50-60 parts of CBN grinding material, 5-10 parts of white corundum grinding material, 5-10 parts of silicon carbide powder, 5-15 parts of phenolic resin powder, 2-6 parts of phenolic resin liquid, 1-2 parts of n-butyl methacrylate, 5-10 parts of nano dolomite dust, 5-10 parts of nano quartz sand powder, 2-5 parts of micro polyamide wax mist and 2-5 parts of steel scrap powder. According to the CBN resin grinding wheel and the preparation method of the CBN resin grinding wheel, as a ceramic material is added into padding, the adhesive property is good, the grinding materials hardly fall off, the heat resistance and hardness of the resin grinding wheel are improved, and cracks formed by rigid grinding are reduced, thereby the use efficiency and service life of the resin grinding wheel are improved further; and in addition, as steel power is added, fast heat dissipation effect is achieved, a great deal of heat generated in a cutting process of the grinding wheel can be dissipated quickly, and the effect of lowering cutting temperature is achieved.

The invention discloses attapulgite-modified polyvinyl chloride (PVC) synthetic leather. The attapulgite-modified PVC synthetic leather comprises a surface layer, a foamed layer, a bonding layer and a brushing fabric, and is characterized in that the surface layer is prepared by mixing the following raw materials in parts by weight to form slurry: 70 to 80 parts of SG-2 type PVC resin, 30 to 40 parts of SG-5 type PVC resin, 10 to 15 parts of triethyl citrate, 30 to 35 parts of epoxy butyl oleate, 20 to 25 parts of n-butyl methacrylate, 5 to 6 parts of PVC color paste, 1 to 2 parts of dibasic lead phosphate, 1 to 2 parts of tribasic lead sulfate and 5 to 10 parts of modified diatomite. Through the improvements of the formula and the process, the flexibility of the synthetic leather is improved, and the synthetic leather has a natural comfortable hand feeling similar to that of natural leather and is difficult to damage or tear after being used for 3 to 5 years.

The invention discloses a scratch-resistant optical diffusion film, which comprises a substrate layer, an optical diffusion layer and an anti-adhesion layer, wherein the optical diffusion layer comprises a resin film former, diffusion particles, a cross-linking agent and a solvent; the diffusion particles comprise organic particles and inorganic particles; the organic particles consist of large particles, medium particles and small particles; the large particles are PBMA (poly(n-butyl methacrylate)) particles or PIBMA (poly(isobutyl methacrylate) particles; the particle diameter ratio of the large particles to the medium particles is 5:1 to 3:1, and the mass ratio of the large particles to the medium particles is 1:6 to 1:3; the particle diameter ratio of the large particles to the small particles is 15:1 to 10:1, and the mass ratio of the large particles to the small particles is 1:1 to 1:3; the particle diameter ratio of organic particles to inorganic particles is 130:1 to 10:1, and the mass ratio of the organic particles to the inorganic particles is 50:1 to 5:1. The substrate layer, the surface optical diffusion layer and the anti-adhesion layer of the optical diffusion film are prepared by particle diffusion, dilution and drying and curing treatment. A preparation method is simple. A flexible contact surface is formed on the surface, so that high scratch resistance is achieved.

The invention relates to a monodisperse nano-polymer carrier with biological compatibility and a method for preparation and carrying drug thereof. Firstly, a reversible addition fragmentation chain transfer (RAFT) polymerization method is used for preparing amphiphilic block copolymers with smaller polydispersity index, wherein the hydrophilic segment is methylacryoyloxyethyl phosphorylcholine (MPC) and the hydrophobic segment is n-butyl methacrylate (BMA). Then through the method of solvent evaporation, the amphiphilic block copolymers are used for preparing nano-polymer micelle, drugs are encapsulated in the micelle through physical action, thus obtaining the monodisperse nano-polymer carrier system with good biological compatibility.

The invention discloses a quantum dot with high transparency and high fluorescence efficiency/epoxy resin nano composite material, preparation and applications thereof, and belongs to the technical field of nano composite material. Poly(n-butyl methacrylate-glycidyl methacrylate) P(BMA-GMA) amphiphilic two-section copolymer compatibilizer is introduced, the PBMA section of the P(BMA-GMA) copolymer is utilized to soak the oleic acid ligand on the quantum dot surface, the PGMA section of the P(BMA-GMA) is utilized to soak the epoxy substrate, and thus a good interface compatibilizing effect is achieved. The amphiphilic compatibilizing effect of the two-section copolymer is utilized to increase the interface compatibility of quantum dots in epoxy resin substrate, thus the quantum dots are evenly dispersed in the substrate, and the prepared quantum dot/epoxy resin nano composite material has excellent transparency and fluorescence performance, and has a wide application prospect in the field of white light packaging.

The invention discloses a sealing gasket for a hydraulic cylinder and a preparation method thereof. The sealing gasket is prepared from the raw materials including nitrile rubber, epichlorohydrin rubber, polyformaldehyde (POM), polyisobutene, 2,4-dichlorobenzoyl peroxide, 2,2'-disulfide dibenzo thiazine, dioctyl sebacate, n-butyl methacrylate, microcrystalline wax, modified wollastonite, nano sepiolite, calcium sulfate whiskers and the like. On the basis of blending of the nitrile rubber and the epichlorohydrin rubber, POM and polyisobutene are also added, so that the performances such as the oil resistance, the temperature tolerance, the abrasive resistance, the compressive strength and the like of the rubber can be improved; and the modified wollastonite is also added, so that the dispersibility of the wollastonite in the rubber can be obviously improved; and the performances such as the mechanical strength, the oil resistance, the abrasive resistance, the high thermal resistance and the like of a seal material are improved.

the invention discloses a fluorine modified acrylic resin and preparing method for helicopter covering paint, which comprises the following steps: blending composite monomer methacrylic acid borneol ester, n-butyl methacrylate, hydroxyethyl methacrylate, butyl acrylate, methacrylic acid and fluorine monomer in the composite solvent with xylene, propylene glycol methyl ether acetic ester, methyl isobutyl ketone and 100# solvent oil; dripping carbonic glycide ester to polymerize acted by trigger pentaphen peroxide to obtain the product.

The invention discloses polyvinyl chloride synthetic leather, which comprises a face layer, a foaming layer, a bonding layer and a brushing fabric. The polyvinyl chloride synthetic leather is characterized in that the face layer is made of slurry prepared from the following raw materials in parts by weight: 40-50 parts of SG-1 type PVC (polyvinyl chloride), 70-80 parts of SG-6 type PVC resin, 20-25 parts of phthalate, 15-20 parts of sebacic propylene glycol polyester, 20-25 parts of n-butyl methacrylate, 5-6 parts of PVC color paste, 1-2 parts of imarcaptoacetate dioctyltin, 1-2 parts of zinc stearate, 5-10 parts of light calcium carbonate and 35-50 parts of modified attapulgite. According to the invention, through formula and process improvement, the toughness of the synthetic leather is increased, and the polyvinyl chloride synthetic leather has natural and comfortable handfeel similar to that of natural leather; and the polyvinyl chloride synthetic leather is not easy to damage or tear within 3-5 years.

The invention discloses a veneer glue and a preparation method thereof. The veneer glue is composed of the following raw materials: vinyl acetate, vinyl versatate, n-butyl methacrylate, acrylic acid, methacrylic acid, an environment-friendly plasticizer, polyvinyl alcohol, a special cross-linking monomer, an environmentally reactive anionic emulsifying agent, an environmentally reactive nonionic emulsifying agent and deionized water. The veneer glue finished product does not contain formaldehyde, heavy metal, halide and the like, and meets the state promulgated Interior Decoration Material Adhesive Harmful Substance Limit GB18583-2008 standard. The veneer glue is nontoxic, odor-free, safe and reliable. When the glue is used in fireproof board and veneer binding, the veneer is prevented from yellowing, and has a good anti-aging effect. With the glue, the veneer is flexible, and can resist bending and glue failure. The veneer can resist glue failure after 7 days of soaking in 45 DEG C water.

The invention discloses an absorbing fiber and a manufacturing method thereof. The absorbing fiber comprises 100wt% of polymer monomer by mass percent, wherein n-butyl methacrylate monomer accounts for 70-90wt%, and methyl methacrylate monomer accounts for 10-30wt%; beta-hydroxyethyl methacrylate accounts for 10-20wt% of the polymer monomer (the following are the same); and benzoperoxide accounts for 0.1-0.5wt% of the total mass of the polymer monomer. The manufacturing method adopting the mass percent composition of the absorbing fiber comprises the following steps: 1, refining the methyl methacrylate and the n-butyl methacrylate in a reduced pressure distillation mode; 2, synthesizing methyl methacrylate/n-butyl methacrylate/beta-hydroxyethyl methacrylate multipolymer by using a water-phase suspension polymerizing method; 3 thoroughly drying the multipolymer, and adding 30-50wt% of N,N-dimethyl acetamide solvent according to the mass ratio of 3:7-1:1 to sufficiently swell the multipolymer for 24-48 hours; and 4 under the spinning temperature of 100-150 DEG C, preparing the absorbing fiber by using a gel spinning method and a double-screw spinning machine.

The invention relates to a method for manufacturing organic-matter adsorbing fibers. The technical process includes that 1) first monomer n-butyl methacrylate covering 50-90 percent of the total mass of the two monomers (the same below) and 50-10 percent of second monomer acrylonitrile and 0.1-1 percent of dispersing agent, 0.1-1 percent of initiator and two types of deionized water (monomer total volume: 3:1) are used to produce resin; 2) proper amount of solvent and the achieved resin are used to prepare spinning stock-solution; 3) the achieved spinning stock-solution is used for spinning by solution spinning technology, and nascent fiber is achieved; 4) after stretching treatment of the nascent fiber, the organic-matter adsorbing fiber is achieved. The invention has the advantages of that the manufacturing technique is simple, the prepared fiber is in three-dimensional mesh texture, and the fiber has sound organic-matter adsorbing capacity and mechanical property.

The invention discloses water-borne acrylic compound adhesive. The water-borne acrylic compound adhesive is prepared from the following raw materials in parts by weight: 5-10 parts of emulsifying agent, 0.2-0.6 part of initiating agent, 4-6 parts of hydroxyl-terminated polydimethylsiloxane organosilicone modifying agent, 20-30 parts of soft monomer, 0.5-0.7 part of buffering agent, 20-30 parts of hard monomer, 8-12 parts of functional monomer, 4-6 parts of pH conditioning agent and 70-90 parts of deionized water. The hard monomer is one or more than two kinds of methyl acrylate, methyl methacrylate, vinyl acetate, ethyl methacrylate and n-butyl methacrylate. The prepared water-borne acrylic compound adhesive is good in stability, high in viscosity, free of organic solvent, free of poison, favorable for environmental friendliness and health of operating workers and easy to convey and store. By means of adding various kinds of water-borne additives with excellent performance, foam of the water-borne acrylic compound adhesive during use is reduced, moistening and leveling property of emulsion on the surface of a plastic film is improved, the convenientce of operation is realized, the affinity between glue and a PET film is improved, and the peel strength is improved.

The invention discloses a solvent-resistant and corrosion-resistant rubber and a preparation method thereof. The solvent-resistant and corrosion-resistant rubber consists of the following parts by mass: 30-50 parts of natural rubber, 20-30 parts of nitrile rubber, and 20-30 parts of fluorosilicone rubber 30 parts, 3-7 parts of active zinc oxide, 3-9 parts of PE wax, 4-10 parts of n-butyl methacrylate, 3-8 parts of epoxy resin, 0.3-1.2 parts of anti-aging agent, 1-part of resorcinol 3 parts, polytetrafluoroethylene 6‑10 parts, coumarone resin 2‑5 parts, stearic acid 3‑6 parts, white carbon black 8‑15 parts, sulfur 10‑15 parts, accelerator AM‑2 3‑ 5 parts, 0.1-0.3 parts of anti-scorch agent CTP, the present invention is prepared by two-stage mixing method. The solvent-resistant and corrosion-resistant rubber of the invention has good resistance to organic solvents, strong acid and alkali resistance, corrosion resistance, excellent wear resistance and high temperature resistance, simple preparation, low cost and certain promotion value.

The invention relates to a water-base ambient crosslinking acrylate wood paint resin and a preparation method thereof. The resin comprises the following components: n-butyl acrylate, n-butyl methacrylate, methyl methacrylate, styrene, acrylic acid, diacetone acrylamide, adipic dihydrazide, potassium persulfate, emulsifier NP-40, emulsifier sodium dodecyl benzene sulfonate, ammonia and deionized water. The resin takes water as the diluent, is harmless to human bodies and the environment, has no pollution and does not contain harmful substances, such as triphenyl, formaldehyde and the like, the resin grain fineness is less than 100 nanometers, the paint film has high brightness and good hand feeling, and the resin can be used as the primer and finish paint for all kinds of water-base wood varnish and colored paints.

The invention discloses an application of a block polymer as a dielectric elastomer. The structural general formula of the block polymer is B-C-D, wherein B and D are independently selected from a styrene homopolymer or a methyl methacrylate homopolymer; C is selected from a butyl acrylate homopolymer, a n-butyl acrylate homopolymer, a n-butyl methacrylate homopolymer, a isobutyl methacrylate homopolymer, a tert-butyl acrylate homopolymer, a 2-ethylhexyl acrylate homopolymer, an iso-octyl acrylate homopolymer, an ethyl acrylate homopolymer or a homopolymer of at least two kinds of butyl acrylate, n-butyl acrylate, n-butyl methacrylate, isobutyl methacrylate, tert-butyl acrylate, 2-ethylhexyl acrylate, iso-octyl acrylate and ethyl acrylate. The block polymer can have larger deformation under high-frequency driving without swelling by a solvent and can be used as the dielectric elastomer.

The invention belongs to the technical field of a negative electrode material for a lithium-ion battery, and discloses a nitrogen-doped carbon-coated iron oxide negative electrode material for the lithium-ion battery and a preparation method of the nitrogen-doped carbon-coated iron oxide negative electrode material. The method comprises the following steps of adding ferrite to a mixed solution of water and ethanol, stirring, dissolving, adding oxalate and stirring to obtain a turbid liquid; heating the turbid liquid to 120-220 DEG C for reaction for 8-15 hours to obtain a ferrous oxalate precursor; heating the ferrous oxalate precursor to 500-600 DEG C and burning the ferrous oxalate precursor for 4-8 hours to obtain an iron oxide; dissolving an emulsifier into water, adding n-butyl methacrylate, acrylonitrile and styrene, heating the solution to 55-65 DEG C, adding an initiator, stirring for 4-10 hours to obtain an emulsion and carrying out demulsification to obtain a polymer; and dispersing the polymer into an organic solvent, adding the iron oxide, stirring for 12-36 hours, separating to obtain a solid, heating the solid to 500-600 DEG C and burning the solid for 2-4 hours to obtain the nitrogen-doped carbon-coated iron oxide negative electrode material with excellent cycle performance and rate capability.

A plasticized, copolymerized and modified organic glass is prepared by copolymerizing methyl methacrylate, comonomer and plasticizer with a main body, and carrying out casting molding. The comonomer used belongs to butyl acrylate type, and includes n-butyl acrylate or n-butyl methacrylate; and the plasticizer belongs to phthalic acid esters, and includes Di-n-octyl phthalate (DOP), Diisooctyl ortho-phthalate (DIOP) and dibutyl phthalate (DBP). The preparation method is used for preparing an organic glass cast sheet with super flexibility and high light transmittance.