1078results about How to "High impact strength" patented technology

Disclosed are a crystalline polypropylene resin composition comprising a crystalline polyproplylene resin and a beta-nucleating agent, and a method of increasing the proportion of beta-form crystals in a crystalline polypropylene resin molding comprising molding the composition, the beta-nucleating agent being a diamide compound.

The invention relates to a wood plastic composite material comprising the following materials in parts by weight: 100 parts of wood meals, 20-80 parts of waste plastics, 5-50 parts of waste rubbers, 10-60 parts of high-melt index thermoplastic resins, 1-12 parts of surface active agents, 2-8 parts of lubricating agents, 0.1-4 parts of cross-linking agents, 0.1-4 parts of antioxygens and 0.05-1.5 parts of processing agents, wherein the grain diameter of the wood meals ranges from 10 meshes to 325 meshes; the flow velocity of the high-melt index thermoplastic resins is higher than 20 g/10 minutes; the cross-linking agents are peroxides, thus the invention improves the dispersibility and the flowability of the wood meals contained in the composite and the compatibility of plastics by adding the high-melt index thermoplastic resins, can not only better utilize the resources, but also enhances the mechanical strength (such as tensile strength, bending strength, impact strength, and the like) of the composite material by adding the waste rubbers, has the advantages of good processing property, low water absorption rate, good stability of products, and the like and is suitable for injection moulding and beneficial to market promotion.

Described are polyester compositions comprising at least one polyester which comprises terephthalic acid residues, 2,2,4,4-tetramethyl-1,3-cyclobutanediol, and cyclohexanedimethanol, wherein the inherent viscosity and the Tg of the polyester provides for certain polyester properties. The polyesters may be manufactured into articles such as fibers, films, bottles or sheets.

The invention relates to a high-performance halogen-free flame retardant ABS modified resin and a preparation method thereof. The resin comprises the following components with the content (in parts by weight): 100 ABS resin, 4-30 polyamide, 5-25 phosphate fire retardant, 0.1-0.5 anti-drippage agent, 5-10 toughening agent, 1-5 nano filler, 1-5 compatilizer, 0.2-1 antioxidant, 0.1-0.5 light stabilizer and 1-5 processing agent. Compared with the prior art, the invention has reasonable technique, and overcomes the defects of poor flame retardant property and low impact strength of the existing halogen-free flame retardant ABS; and the invention adopts a novel high-efficiency halogen-free flame retardant compounding synergism technology, a novel polyamide coal-forming agent, the high-efficiency synergism between organic and inorganic fire retardants, and the master batch method processing technique, thus endowing the resin with high fire resistance on the basis of improving the original good performances (especially the impact performance) of the ABS resin, and having wide application prospect.

The invention relates to a radiation curable resin composition comprising a cationically polymerizable component, a cationic photoinitiator, a hydroxy component, an impact modifier and wherein the resin composition after full cure has a modulus of >2 GPa; a yield stress<70 MPa; and a K_1c value>1.3 MPa. (m)^1/2 or an Izod value>0.45 J/cm. The resin composition can preferably be used in the preparation of three dimensional objects.

A thermoplastic olefin (TPO) composition comprises (1) a major amount by weight of (a) a substantially linear homopolymer or copolymer of a C₂-C₁₀ α-olefin in major proportion to (b) a long chain branched a linear homopolymer or copolymer of a C₂-C₁₀ α-olefin, (2) a minor amount by weight of a cross linkable elastomer, and (3) at least one thermally decomposing free radical generating agent present in an amount sufficient to promote an increase in melt strength of the composition over that of the melt strength of the linear homopolymer or copolymer of a C₂-C₁₀ α-olefin alone and insufficient to substantially degrade the α-olefinic polymers. The TPO composition is prepared by melt blending the components at a temperature sufficient to melt said homopolymers or copolymers of a C₂-C₁₀ α-olefin and thermally decompose said agent. Articles are thermoformed from the thermoplastic olefin.

The invention provides a preparation method of a polylactic acid/nano cellulose composite material. The composite material comprises the following components in percentage by weight: 55 to 99.8% of polylactic acid, 0.1 to 15% of nano cellulose, and 0.1 to 30% of polyethylene glycol. The method comprises the following steps of: preparing a 5 to 15% an aqueous solution of microcrystalline cellulose, dripping concentrated sulfuric acid until the concentration of sulfuric acid reaches 40 to 60%, stirring and reacting for 1 to 2hours, carrying out centrifugation, ultrasound treatment and adjusting pH value to be neutral to obtain a nano cellulose suspension; dissolving polyethylene glycol, mixing with the nano cellulose suspension, stirring for 1 to 3hours at the temperature of 90 DEG C and carrying out vacuum drying to obtain a polyethylene glycol/nano cellulose comixture; and carrying out melt blending on the polyethylene glycol/nano cellulose comixture and polylactic acid for 5 to 8minutes at the temperature of 120 to 170 DEG C to obtain the composite material. The method is convenient and simple to operate, short in the time of the preparation process and solves the problem of uniform dispersion of nano-cellulose in the polylactic acid.

Described are polyesters containing (a) a dicarboxylic acid component having from 70 to 100 mole % of terephthalic acid residues, and up to 30 mole% of aromatic dicarboxylic acid residues or aliphatic dicarboxylic acid residues; and (b) a glycol component having from 40 to 65 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, and from 35 to 60 mole % of cyclohexanedimethanol residues; wherein the total mole % of the dicarboxylic acid component is 100 mole %, and the total mole % of the glycol component is 100 mole %. The polyesters may be manufactured into articles such as fibers, films, containers, bottles or sheets.

The invention discloses a solvent-free polyurethane adhesive for a composite film, which consists of an A component and a B component, wherein the A component is end-OH polyester polyol, and the B component is end NCO-polyurethane prepolymer; and the A component and the B component are mixed in the molar ratio of functional groups of NCO to OH being 1.2-1.9:1.0. The polyurethane adhesive for the composite film does not need to adopt solvent and has high safety. The adhesive shows low hydroscopic property as well as low hydrolysis and high shock strength due to introducing dimeric dibasic acid, and shows good adhesive property for some substrates which are particularly difficult to adhere and attach. The invention improves the adhesive strength of the composite film through the design of compositions and a molecular structure of the adhesive, the T peeling strength reaches more than 3.8N/15mm after the plastic films are compounded for 3 to 5 days, and the T peeling strength between the plastic and an aluminum-plating film reaches more than 4.2N/15mm.

The invention provides a composite material special for blow molding of a reinforced nylon air inlet pipe. The composite material comprises the following components in percentage by mass: 20-83 percent of main material, 3-10 percent of modifier, 3-35 percent of elastomer, 10-30 percent of enhancing filler and 1-5 percent of auxiliary agent. The composite material special for blow molding of the reinforced nylon air inlet pipe can be used in blow molded products of air inlet pipelines, oil paths or cooling system pipelines at the peripheries of automobile engines. The composite material contains the reinforcing filler; the strength and the high temperature resistance performance of the composite material are improved; and the composite material is rich and cheap in raw materials and is suitable for promotion and application.

The invention relates to high-temperature resistant and strong corrosive resistant water-based baking varnish for metal and a preparation method for the water-based baking varnish. The water-based baking varnish consists of the following raw materials: 40 to 60 percent of resin, 8 to 18 percent of amino resin, 1 to 5 percent of adhesion promoter, 8 to 15 percent of pigment, 1 to 3 percent of salt mist resistant aid, 0.2 to 0.5 percent of pH regulator, 0.1 to 0.5 percent of flatting agent, 0.2 to 0.8 percent of wetting dispersant, 0.1 to 0.2 percent of defoaming agent, 5 to 8 percent of cosolvent, and the balance of water. The volatile organic compound (VOC) content of the obtained water-based baking varnish is low; and the water is used for replacing an organic solvent and used as a thinning agent, so that the water-based baking varnish is nontoxic, odorless and environment-friendly, improves the working environment of construction personnel and protects the body health of the construction personnel. A prepared varnish film has good physical and mechanical properties, high temperature resistance and corrosion resistance, the adhesive force of the varnish film is level 0, the varnish film resists a high temperature of 200 DEG C for 4 hours and yellows lightly, and the salt mist resistance reaches 300h.

The invention discloses a high-strength biodegradable polycaprolactone 3D printing material which comprises the following components in parts by weight: 70-90 parts of polycaprolactone, 1-5 parts of a crosslinking agent, 2-10 parts of an inorganic filler, 0.5-1.5 parts of an inorganic filler dispersing wetting auxiliary agent, 0.5-1 part of a stabilizer, 0.1-0.5 part of a degassing agent, and 1-2 parts of a leveling agent. With targeted selection of the inorganic components for modification treatment on polycaprolactone, the polycaprolactone modified material exerts excellent impact-resistance strength and creeping resistance. The material allows the degradable 3D printing material to exert better mechanical properties while broadening the 3D printing material type.

The invention discloses an enhanced toughened halogen-free flame-retardant polypropylene mixture and a preparation method thereof. The method comprises the steps of: diluting 0.5-3 parts by weight of surfactants with 20-30 parts by weight of absolute ethyl alcohol, then adding into 100 parts by weight of alkaline magnesium sulfate whiskers, mixing for 15-30 min in a mixer, and then drying in a dryer to obtain the modified alkaline magnesium sulfate whiskers, wherein the alkaline magnesium sulfate whiskers is required to be 10-60 mum in average length and less than 10 mu m in diameter; adding polypropylene resin firstly on an open type warming mill with double-roll temperature of 170-180 DEG C, sequentially adding an antioxidant, a toughened modifier, the modified alkaline magnesium sulfate whiskers, a synergistic flame retardant, a molten-drop prevention modifier and a compatibilization modifier after the polypropylene resin is molten and covers the rolls, and evenly mixing to obtain the enhanced toughened halogen-free flame-retardant polypropylene mixture. The polypropylene mixture prepared in the invention has the advantages of high strength, good toughness, low smoke, no toxicity, no molten drop, remarkable flame retardant property and the like.

The present invention provides a thermoplastic resin composition containing 100 parts by mass of a mixture of a thermoplastic resin (A) and carbon nanotubes (B), the mixture being composed of the component (A) in an amount of 20 to 99.95 mass % and the component (B) in an amount of 0.05 to 20 mass %; a flame retardant (C) in an amount of 0.05 to 30 parts by mass; and a polyfluoroolefin resin in an amount of 0 to 2 parts by mass. The flame retardant is preferably a phosphorus compound, and the thermoplastic resin preferably contains, as a component, an aromatic polycarbonate-polyorganosiloxane copolymer.

The invention discloses a method for preparing a 3D printing material by use of recycled waste high-density polyethylene plastics. The raw material adopted by method is the waste high-density polyethylene plastics which are prepared from the following components in parts by weight: 100 parts of high-density polyethylene, 10-40 parts of jute fibers, 10-30 parts of calcium lignosulfonate, 10-30 parts of calciumsilicate, 0.8-1.4 parts of a coupling agent, 10 parts of a compatilizer and 20-30 parts of a plasticizer. The method comprises the following steps: 1, breaking and cleaning the waste plastics; 2, preprocessing the jute fibers; 3, adding additives, and grinding at low temperature; 4, extruding and pelletizing. According to the method, the waste high-density polyethylene plastics are recycled, and the additives are added to modify the recycled plastics and enhance the toughness, tensile strength and impact strength of the plastics, so that the plastics can be accepted as a material meeting 3D printing requirements, and the cost of the 3D printing material is greatly reduced.

The invention relates to a high-strength binding band and a production method thereof, solving the problems that the existing high-strength steel bands are complex in production method and process, high in control difficulty, high in equipment investment and high in product cost and are not environment-friendly. In the process, the weight percentage of chemical elements of steel is as follows: 0.03-0.25 percent of C, 0.50-2.00 percent of Si, 0.50-2.50 percent of Mn, 0.10-0.20 percent of P, 0-0.015 percent of S, 0.01-0.20 percent of Als, and the balance of Fe and other unavoidable impurities; and the high-strength binding band is obtained by molten iron steelmaking, hot rolling, cold rolling and blue annealing, wherein in the blue annealing process, the annealing temperature is controlled to be 450-600 DEG C, the temperature of a lead bath furnace is controlled to be 400-550 DEG C, and the band speed is controlled to be 5-7m/min. In the invention, the process control is simple, the cost is low, environmental pollution is less, the performances are better, the process is simple and convenient as well as feasible, the production efficiency is high, and the tensile strength reaches 980MP.

The invention discloses a buffering anti-collision guardrail on an expressway. The guardrail comprises a guardrail plate, a connection vertical column, a connection buffering tray, a reinforcing vertical column, a reinforcing buffering tray and a built-in steel plate, wherein the guardrail plate consists of an outer layer pipe plate, an inner layer pipe plate body, a steel plate clamping groove pipe body and a supporting buffer column; three layers of buffering structures are formed in the guardrail, the first layer is a three-layer pressure-reducing and buffering honeycomb, the second layer is a wave-shaped built-in steel plate manufactured in the pressure-reducing and buffering honeycomb, and the third layer is a connection buffering tray or a reinforcing buffering tray arranged between the guardrail and the vertical columns. The strength, toughness and bounciness of the guardrail are enhanced; the guard rail is connected with the vertical column elastically, so that the buffering anti-collision guardrail has high buffering capacity, bounciness, elasticity and impact resistance, phenomena that automobile accidents occur, and loss is caused by the automobile accidents can be effectively avoided; and the guardrail has the advantages of long service life and low using cost.

Articulating devices for replacing damaged or degenerated weight bearing joints are provided. The devices may have two or more surfaces that articulate against one another that are coated or fully formed of PEEK or similar materials to provide improved wear capabilities while maintaining sufficient strength to operate in a weight bearing capacity.

The invention discloses a halogen-free flame-retardant and cold-resistant PC/ABS (Poly Carbonate/Acrylonitrile Butadiene Styrene) material and a preparation method thereof. The halogen-free flame-retardant and cold-resistant PC/ABS material mainly comprises components of PC and ABS and further comprises a silicon fire retardant, a phosphorus fire retardant, an anti-dripping agent, a compatilizer, a flexibilizer, a lubricant, an antioxidant, and an anti-ultraviolet agent. A preparation process is a twin-screw melting extrusion pelletizing process. According to the preparation method disclosed by the invention, the silicon fire retardant and the phosphorus fire retardant are composited so that the fire resistance 1.2 mm of the obtained PC-ABS alloy material can meet the UL94V-0 class requirement in the United States. The compatilizer MBS (Methyl methacrylate-Butadiene-Styrene) not only enables the PC and the ABS to be better dissolved but also can be used for increasing the compatibility between the silicon fire retardant and a substrate. Therefore, not only can the impact property of the alloy be improved but also the flame retardant efficiency can be effectively improved. The alloy material has the good low-temperature impact property due to the flexibilizer. The silicon fire retardant has a fire retardant synergy effect and further has a smoke suppression effect, so that the fire resistance 1.2 mm of the obtained PC-ABS alloy material can meet the UL94V-0 class requirement in the United States.

The invention relates to a material used for buildings and a production method of the material. The hybrid nanocomposite material used for buildings provided in the invention includes the following components by weight: 100 parts of cement, 10-30 parts of water-based resin, 0.01-45 parts of a water-based resin curing agent, 25-50 parts of water, 0.5-2 parts of a super plasticizer, 0.1-5 parts of a nano-fiber, 0.1-5 parts of a nano-fiber dispersing agent, 0.01-3 parts of a thickening stabilizer, and 0.02-0.2 part of a foam inhibitor. With the method provided in the invention, the nano-fiber can realize good dispersion and network distribution in a water-based resin system and a subsequent resin/cement hybrid matrix, and can form a compact reticular cemented structure together with hardening resin and cement, thus improving the dynamic shock resistance and dynamic vibration damping performance of the hybrid composite material.

The present invention relates to communication equipment, and is especially cellphone window protecting screen making process. The process includes the following steps: CNC machining superthin glass to the required size and shape, toughening glass part chemically, coating transparent color insulating film to the lower surface of the glass part through low temperature electronic beam evaporation, adhering anticracking film to the lower side of the insulating film, and coating hard film to the upper surface of the glass part through magnetically controlled sputtering. The cellphone window protecting screen has high impact strength, high scratch resistance and high safety, and the process has low production cost, high production efficiency and high product quality.

A polycarbonate-base mixture suitable for the engineering plastics in wet or hot water environment is prepared through mixing polyethene with maleic acid anhydride modified polyolefine or ionic polymer, kneading, granulating, mixing with polycarbonate and acrylonitrile-butadiene-styrene copolymer, and extruding out. Its advantages are high mechanical performance, size stability and refractory nature, and high antiageing nature in boiling water.

The invention discloses water borne epoxy intermediate paint. The intermediate paint comprises a component A and a component B, and the weight ratio of the component A to the component B is between 0.5 and 10, wherein the component A comprises the following ingredients in percentage by weight: 23-55 percent of water borne epoxy resin curing agent, 0.1-1 percent of wetting dispersant, 1-5 percent of antirust pigment, 5-10 percent of tinting pigment, 1-5 percent of filler, 1-2 percent of film forming auxiliary, 0.1-1 percent of defoaming agent, 0.1-0.5 percent of flatting agent, 0.01-0.5 percent of antiseptic, 0.5-2 percent of rust inhibitor, 0.01-0.1 percent of rheology modifier and 36.09-49.9 percent of softened water; and the component B comprises the following ingredients in percentage by weight: 10-30 percent of self-emulsified water borne epoxy resin and 70-90 percent of softened water. By compounding a self-emulsified epoxy resin emulsion and a self-emulsified water borne epoxy resin curing agent, the mechanical performance and the salt mist resistance of the paint can be improved, and the environmentally friendly requirement can be fulfilled.

A method of creating a modified heterophasic polyolefin composition is provided, whereby a polyolefin composition having at least two phases is melt mixed with a free radical generator, such as a peroxide, and a compatibilizing agent characterized by at least one nitroxide radical and at least one unsaturated bond capable of undergoing a radical addition reaction. Modified heterophasic polyolefin compositions with increased melt flow rates, impact strength, and clarity, which incorporate the compatibilizing agent, are also included within the scope of the invention.

The invention discloses a blended foam material based on PLC and modified PLA and a preparation method thereof, and belongs to the foam material field. The foam material comprises, by weight, 60-90 parts of PLA, 1-25 parts of PCL, 2-10 parts of reinforcing agents, 1-3 parts of nanometer nucleating agents, 4 parts of foaming agents, 0.1-1 part of a blowing promoter, 1-3 parts of environment-friendly flame retardants and 0.5-1 part of a surfactant. According to the foam material and the preparation method thereof, composite foamed plastics with good mechanical properties and superior surface quality can be prepared.

The invention relates to a filling masterbatch used for polypropylene wire-drawing and its preparation method. The said masterbatch includes (weight parts): CaCO3 25~50, and superfine talc (SFT) 5~30, homopolymerized PP 17.5~25, dual EPDM 5~10, ethylene-vinyl acetate copolymer wax 1.5~6, stearic acid 1~4, and zinc stearate 1~2, wherein the average particle size of CaCO3 is 5~10 micron and the average size of SFT is 6-10 micron. The said method comprises: mixing CaCO3 and SFT in a stirring mixer at 100degreeC-130degreeC, adding ethylene-vinyl acetate copolymer wax and mixing 3~5 minutes, respectively adding stearic acid, zinc stearate, dual EPDM, and homopolymerized PP, stirring for 3 min to obtain the pre-mixture, placing the pre-mixture into a cocurrent twin-screw granulation machine, granulating and pelleting, cooling and sifting, separating, and packaging to obtain the final product. The prepared filling masterbatch has good mechanical properties, dispersion, and high economy.

We disclose novel metallic nanoparticles coated with a thin protective carbon shell, and three-dimensional nano-metallic sponges; methods of preparation of the nanoparticles; and uses for these novel materials, including wood preservation, strengthening of polymer and fiber/polymer building materials, and catalysis.

The present invention relates to copolycarbonates and a composition comprising the same. The copolycarbonate according to the present invention has a structure in which specific siloxane compounds are introduced in the main chain of polycarbonate and thus exhibits the effects of improving impact strength at room temperature, impact strength at low-temperature and melt index.

The invention relates to a manufacturing method for a wood-plastic composite floor, in particular to the manufacturing method for the wood-plastic composite floor. The manufacturing method comprises the following steps: wood flour is carbonized in the temperature of 200 to 240 DEG C for 5 to 15 min to obtain modified wood flour; 50 to 70 parts by weight of modified wood flour and 30 to 50 parts by weight of plastic powder are mixed and plasticized in advance to obtain wood-plastic blended powder; the obtained wood-plastic blended powder is put into an extruder and extruded to take on a plate shape by a die head to obtain the wood-plastic composite board; and the wood-plastic composite board is cooled, shaped, and professionally processed in later period to obtain the wood-plastic composite board. The wood flour is processed in the wood flour processing step so that polar groups on the surface of wood fiber are destroyed; the water absorption rate of the processed modified wood flour is reduced by more than 50%; and then powder blending step is carried out so as to reduce the water absorption rebound resilience of the wood-plastic composite material, thus achieving the purpose of reducing plastic proportion and increasing the quality of products.

The invention belongs to technical field of modification of high molecular materials and the technical field of processing, and discloses a glass fiber-reinforced polypropylene foaming material and a preparation method and an application thereof. The material comprises the following components in parts by weight: 35-80 parts of polypropylene, 1-10 parts of a toughening agent, 1-10 parts of a compatilizer, 0.2-0.4 part of an antioxidant and 15-45 parts of glass fibers. The preparation method of the material comprises the following steps of: putting the raw materials into a high-speed mixing machine according to the parts by weight for mixing for 3-5 minutes, adding into an extruder, adding 15-45 parts of glass fibers into a dual-screw extruder from a fiber inlet for extruding, and pelletizing to obtain a needed glass fiber-reinforced polypropylene material; and injecting a supercritical fluid into the glass fiber-reinforced polypropylene material molten at the homogenizing section of a screw rod of an injection molding machine to form a homogeneous solution, and injecting the homogeneous solution into an injection mold through injection molding to obtain a glass fiber-reinforced polypropylene foaming material. The material disclosed by the invention is a most suitable material for an engineering plastic marsh gas pond.