43 results about "Tributyltin chloride" patented technology

The invention discloses an anti-fatigue cable material and a preparation method thereof. The material is prepared by the following raw materials by weight:80 to 90 of SG-5-type PVC, 15 to 25 of impact-resistance polystyrene, 10 to 15 of PEEK, 5 to 10 of epoxidized soybean oil, 10 to 15 of antimony trioxide, 8 to 12 of active aluminum hydroxide, 15 to 20 of nano bauxite , 4 to 8 of glass fiber, 5 to 10 of composite filler, 10 to 15 of TOTM, 5 to 10 of acetyl tributyl citrate, 4 to 8 of dioctyl phthalate, 2 to 3 of calcium zinc composite stabilizer, 1 to 2 of tributyltin chloride, 0.5 to 1 of isopropyl three (two octyl pyrophosphateacyloxy) titanate, 0.4 to 0.6 of erucamide, and 0.5 to 1 of oxidized polyethylene wax. The cable material is good in flexibility and has excellent mechanical performance of fatigue resistance, tearing resistance, oil resistance, heat resistance, flame retardancy and the like, and the cable material is safe, reliable, and durable in use.

The invention relates to an oligothiophene derivative and a preparation method thereof. The preparation method of the oligothiophene derivative mainly comprises the following steps of: dissolving 3TB into dichloromethane, adding NBS (N-bromosuccinimide), stirring and reacting so as to obtain 3TB-3Br; adding EDOT (3,4-ethylenedioxythiophene) and tetrahydrofuran into a three-neck flask, controlling the reaction temperature to be minus 78 DEG C, dropwise adding n-butyllithium, gradually raising to be room temperature after the dropwise adding, and continuously reacting; subsequently decreasing the reaction temperature to be minus 78 DEG C, dropwise adding tributyl stannic chloride, gradually raising to be the room temperature after the dripping, and reacting to obtain an EDOT tin reagent; under the protection of nitrogen, adding methylbenzene into the three-neck flask, further adding the 3TB-3Br and the EDOT tin reagent, carrying out backflow reaction so as to obtain a 3TB-3Br crude product, thus obtaining pure 3TB-3EDOT through separation. As cation (or anion) free radicals generated in electrochemical doping are stable, the oligothiophene derivative can be used as a novel organic electrochromic material.

An industrial water treatment bactericide consists of three ingredients of alkyl quaternary phosphonium salt, quaternary ammonium salt and tributyltin chloride, wherein the alkyl quaternary phosphonium salt is one of or a composition of tributyltetradecylphosphonium chloride and tetrakisphosphonium sulfate; the quaternary ammonium salt is one of or a composition of dodecyl dimethyl benzyl ammonium chloride and 12-alkyl dimethyl ammonium chloride.

The invention discloses a moldproof polyethylene sheath material for cables and a preparation method thereof. The moldproof polyethylene sheath material for cables is prepared from the following raw materials in parts by weight: 80-90 parts of linear low density polyethylene, 15-20 parts of chlorosulfonated polyethylene, 10-15 parts of poly(4-methyl-1-pentene), 20-30 parts of carbon black N660, 4-8 parts of turpentine, 5-10 parts of dioctyl terephthalate, 1-2 parts of anilinomethyl triethoxy silane, 3-5 parts of methyl p-hydroxybenzoate, 8-12 parts of decabromodiphenyl oxide, 5-10 parts of zinc borate, 10-15 parts of aluminum hydroxide, 4-8 parts of brucite powder, 5-10 parts of tri(2-chloropropyl)phosphate, 2-4 parts of light magnesium oxide, 1-2 parts of tributyltin chloride, 2-3 parts of barium stearate, 3-6 parts of calcium hydroxide, 3-4 parts of oxidized polyethylene wax, 5-8 parts of quartz powder, 3-5 parts of nano silver and 4-6 parts of composite filler. On the premise that the excellent moldproof function of the sheath material is ensured, the sheath material can effectively inhibit Aspergillus niger, Aspergillus terreus and other molds from growth and reproduction, so that the cable is free from mold invasion, and the service life of the sheath is prolonged.

The invention discloses a mould-prevention polyethylene water supply tubular product and a preparation method thereof. The mould-prevention polyethylene water supply tubular product is prepared from the following raw materials in parts by weight: 50-70 parts of medium density polyethylene, 25-45 parts of metallocene linear low density polyethylene, 20-30 parts of nylon 12, 15-20 parts of dimethyl fumarate, 4-8 parts of perfluorinated polyether lubricating grease, 3-6 parts of liquid paraffin, 1-2 parts of protocatechuic acid ethyl ester, 2-3 parts of propylparaben, 1.5-2.5 parts of trichlamide, 2.5-4.5 parts of antimony sulfate, 5-10 parts of jade powder, 15-20 parts of calcining loess, 2-3 parts of dodecanoic acid monoester with triglycerol, 1-2 parts of zinc undecylenate, 5-10 parts of epoxidized soybean oil, 1-2 parts of calcium stearate, 1-2 parts of barium stearate, 20-25 parts of filling master batch, 10-15 parts of dicyclohexyl phthalate, 2-3 parts of N,N'-Bis(1-methylpropyl)-1,4-phenylenediamine and 1.5-2.5 parts of chlorotributyltin. The mould-prevention polyethylene water supply tubular product has excellent antibacterial property, can effectively restrain and prevent attachment and breeding of mould, prevents mould from corroding the tubular product, has excellent mechanical property, ageing resistance, heat resistance and processability, and is long in service life and wide in application prospect.

The invention discloses a high temperature resistant and corrosion resistant coating for the surface of a distribution box and a preparation method of the high temperature resistant and corrosion resistant coating. The high temperature resistant and corrosion resistant coating for surface of the distribution box is prepared from the following raw materials in parts by weight: 50 to 80 parts of epoxy resin modified organic silicon resin, 10 to 20 parts of dimethylbenzene, 5 to 15 parts of propylene glycol, 5 to 8 parts of zinc naphthenate, 3 to 8 parts of tributyltin chloride, 3 to 5 parts of barium petroleum sulfonate, 3 to 10 parts of kerosene, 6 to 10 parts of lauryl diethanolamine, 2 to 8 parts of p-methylaniline, 5 to 8 parts of zinc powder, 3 to 6 parts of silicon nitride, 5 to 8 parts of chromium carbide, 5 to 10 parts of aluminium-plated glass micro-beads, 6 to 15 parts of silicon dioxide, 5 to 8 parts of aluminium oxide, 3 to 5 parts of calcium sulphate whisker powder, 5 to 10 parts of polytetrafluoroethylene, 5 to 10 parts of aloe juice, 10 to 20 parts of filler, 5 to 15 parts of pigment, 3 to 5 parts of a cardanol modified amine curing agent, 1 to 3 parts of a levelling agent, and 1 to 3 parts of an antifoaming agent. According to the high temperature resistant and corrosion resistant coating for the surface of the distribution box and the preparation method of the coating, reasonable raw materials and proportions are selected, so that the coating is dense and neat, does not crack, does not swell, does not fall off, and has high resistance to high temperature and corrosion; normal work of a distribution box is ensured; and the service life of the distribution box is prolonged.

The invention discloses a triphenylamine benzothiadiazole polymer containing a biphenyl structure as well as a preparation method and an application thereof. The triphenylamine benzothiadiazole polymer aims to solve the problems of low solubility and poor heat resistance of small organic molecule compounds in organic solvents in the existing photoelectric field. The preparation method comprises the following steps: firstly, taking 4-(9H-carbazole-9-yl) aniline, N', N'-bis(4-(tert-butyl) phenyl) benzene-1, 4-diamine and 4-amino triphenylamine monomers as raw materials, and carrying out a substitution reaction on the raw materials and p-bromoiodobenzidine to generate triphenylamine monomers containing biphenyl structures; the benzothiadiazole derivative is prepared by the following steps: substituting two bromides on 4, 7-dibromo-2, 1, 3-benzothiadiazole with tributyltin chloride to form a reaction active site, and reacting the reaction active site with a triphenylamine monomer containing a biphenyl structure to generate the polymer. The triphenylamine benzothiadiazole polymer is easily soluble in polar solvents and good in thermal stability, and is applied to the field of multifunctional materials.

The invention relates to an OFF-ON type TBT-detecting fluorescent probe shown by a structural general formula (I). The R1 represents H or CH2CH3, and the R2 is selected from H, Cl, Br or NO2. The fluorescent probe has very good fluorescence response to tributyl tin chloride (TBT), has the advantages of high selectivity, high sensitivity and the like, has the TBT detection capability in a complex environment, can be applied to fluorescent confocal imaging of cells and is wide in application prospect.

The invention discloses a method for recovering and utilizing tributyl tin chloride. The method comprises following steps: (1) heating and distilling tributyl tin chloride with a weight content less than 80% in a hydrogen chloride atmosphere with a high vacuum degree of 20 Pa, wherein the final temperature is 140 to 160 DEG C; (2) after vacuum distillation, mixing obtained tributyl tin chloride product with tin tetrachloride, carrying out reactions at a controlled temperature to obtain a mixture composed of monobutyl tin trichloride and dibutyl tin dichloride; and (3) distilling and separatingthe mixture obtained in the step (2) to obtain monobutyl tin trichloride and dibutyl tin dichloride. The method has the advantages that the difference between the melting points of monobutyl tin trichloride and dibutyl tin dichloride is large, thus the separation is easy, the generated wastes are little, the production is easy, monobutyl tin trichloride and dibutyl tin dichloride can be individually sold, and the waste tributyl tin chloride catalysts are fully recovered and utilized.

The invention provides a method for simultaneously detecting inorganic tin and organotin compounds through low pressure ion chromatography-inductively coupled plasma-mass spectrometry. Analysis devices comprising a low pressure pump, a six-way injection valve, a sample introduction ring, a cation separating column and an inductively coupled plasma mass spectrometer are adopted. The method comprises the following steps: 1, plotting a baseline; 2, platting the spectra of the inorganic tin and the organotin compounds in a sample; 3, plotting the spectra of the inorganic tin and the organotin compounds in a standard sample, and drawing the working curves of the inorganic tin and the organotin compounds; and 4, calculating the concentrations of the inorganic tin and the organotin compounds in the sample. The method can be used to simultaneously detect the concentrations of total inorganic tin, monomethyltin trichloride, dibutyltin dichloride, diphenyltin dichloride, trimethyltin chloride and tributyltin chloride in the sample.

The invention relates to the field of candesartan preparation, and particularly discloses a synthesis method of triphenyl candesartan. The synthesis method of triphenyl candesartan comprises the following steps: S1, preparation of tributyl tin azide: carrying out azide reaction on tributyl tin chloride and sodium azide to obtain tributyl tin azide; S2, preparation of a candesartan intermediate C7:carrying out a tetrazole reaction on 2-ethoxy-1-[[(2'-nitrile biphenyl-4-substituted)methyl]benzimidazole]-7-carboxylic acid ethyl ester and tributyltin azide to obtain a candesartan intermediate C7;S3, preparation of a candesartan intermediate C8: carrying out hydrolysis reaction on the candesartan intermediate C7 in an alkaline agent, then reacting with hydrochloric acid, and acidifying to obtain a candesartan intermediate C8; and S4, preparation of a triphenyl candesartan intermediate: reacting the candesartan intermediate C8 with a triphenyl compound to obtain the triphenyl candesartan intermediate. The preparation method disclosed by the invention has the advantages of shortening the process flow and improving the yield.

The invention discloses a triphenylamine isoindigo polymer containing a biphenyl structure as well as a preparation method and application thereof. The invention aims to solve the problem of narrow application range of isoindigo caused by low solubility of isoindigo in organic solvents in the prior art. The preparation method comprises the following steps: preparing a triphenylamine monomer with abiphenyl structure, introducing a long alkyl chain into 6-bromoisoindole, and substituting two bromides of 6-bromoisoindole with tributyl tin chloride to form reaction active sites to react with thetriphenylamine monomer with the biphenyl structure so as to generate the polymer. The finished product is easy to dissolve in a polar solvent, and 1-1.5 g of the polymer can be dissolved in every 10 ml of a polar solution. The polymer is applied to the field of multifunctional materials.

A process for preparing irbesartan comprises pentanoylation of cycloleucine in the presence of sodium hydroxide to form n-pentanoyl cycloleucine, condensing this product with 2-(4-aminomethyl phenyl) benzonitrile using dicyclohexyl carbodiimide and 1-hydroxy benzotriazole as a catalyst to form the 4-(&quest-N-pentanoyl amino) cyclopentamido methyl-2′-cyano biphenyl compound, and then cyclizing using trifluoroacetic acid in the presence of an aromatic solvent to form cyano irbesartan. Cyano irbesartan is converted to irbesartan by reaction with tributyltin chloride and sodium azide in the presence of an aromatic solvent.

An alkyd impregnating varnish and a preparation method thereof are disclosed. The varnish is characterized by being composed of following raw materials in parts by weight: 40 to 45 parts of medium-oil-length alkyd resin, 24 to 26 parts of terpolycyantoamino-formaldehyde resin, 12 to 14 parts of m-phenylenediamine, 6 to 8 parts of diaminodiphenyl-methane, 3 to 4 parts of calcium naphthenate, 4 to 6 parts of dimethicone, 1 to 2 parts of triphenethylphenoxypoly(ethyleneoxy)ethanol, 2 to 3 parts of ricinoleic acid, 4 to 5 parts of vinyl tri(beta-metoxyethoxy) silane, 3 to 4 parts of styrene, 8 to 10 parts of vinyl carboxylic ester, 2 to 3 parts of tributyltin chloride and 4 to 5 parts of film forming agent. The alkyd resin impregnating varnish has the advantages of compact coating membrane, fast drying, high-temperature resistance, high dampness resistance, good electric insulation property and high mechanic performance. The heat conductivity of the varnish is improved, so the varnish can work at the temperature of 200 DEG C for a long period and at the temperature of 220 DEG C for a short period. The design requirements are fulfilled.

The invention discloses an anti-yellowing epoxy resin coating, which is prepared from the following raw materials in parts by weight: 50 to 60 parts of epoxy resin, 50 to 60 parts of rosin water, 20 to 25 parts of butyl acetate, 15 to 18 parts of propylene glycol methyl ether acetate, 10 to 15 parts of polyving akohol, 10 to 12 parts of diatomaceous earth, 5 to 10 pats of sodium dehydroacetate, 5 to 8 parts of xylene, 5 to 10 parts of tributyltin chloride, 3 to 5 parts of diphenyl ketone and 2 to 5 parts of nipagin ester. The preparation method comprises the steps as follows: adding the epoxy resin and the rosin water into a reaction vessel; stirring, fully dissolving and then adding the diatomaceous earth and nipagin ester; heating, stirring, reacting; adding butyl acetate, propylene glycol methyl ether acetate, polyving akohol, sodium dehydroacetate, xylene, tributyltin chloride and diphenyl ketone, and then reheating, stirring, reacting and cooling to obtain the anti-yellowing epoxy resin coating. The anti-yellowing epoxy resin coating is excellent in anti-yellowing performance, and remains pure white as before after being used for a number of years.

The invention provides a method for synthesizing diphenyl through Stille reaction recycling with an organotin compound, and relates to a method for preparing diphenyl through a Stille reaction. A purpose of the present invention is to solve the problem of low organotin utilization rate of the existing Stille method for preparing the diphenyl compound. The method comprises: 1, adopting tri-butyltin chloride and bromobenzene as raw materials, and carrying out a reaction under the effect of a Grignard reagent to synthesize tributylphenyltin; 2, carrying out a reaction of a mixed solution of halogenated benzene, tributylphenyltin, cuprous iodide, lithium chloride, palladium(triphenylphosphine)dichloride and cesium fluoride DMF to prepare diphenyl, and collecting the filter residue; 3, dissolving the filter residue with acetone, dissolving the insoluble matter with absolute alcohol, and concentrating to obtain fluorotributyltin; and 4, converting the tin fluoride into the organic tin chloride with saturated ammonium chloride tetrahydrofuran. According to the present invention, the synthesis process conditions are optimized, the highest yield of the diphenyl compound achieves 97%, and the effective separation utilization of the organic tin chloride is achieved.

The invention discloses a small molecular material with yellow mechanoluminescence of 10-membered fused ring benzothiadiazole as well as a preparation method and application of the small molecular material. The preparation method comprises the steps of 1) carrying out reduction reaction on a benzo [1, 2-b: 4, 5-b '] dithiophene-4, 8-diketone compound and sodium borohydride; 2) reacting the product in the step 1) with halogenated alkane; (3) reacting the product obtained in the step (2) with n-butyllithium and tributyltin chloride; (4) carrying out Stille coupling reaction; (5) carrying out a Cadogan reaction; and 6) reacting the product in the step 5) with halogenated alkane. The material prepared by the invention can be applied to a yellow mechanoluminescent material and a white mechanoluminescent material. The preparation method disclosed by the invention is relatively simple in process and relatively low in cost, and the prepared product has high fluorescence quantum yield in a solid state, has excellent yellow mechanoluminescence property, can generate mechanoluminescence white light emission with the CIE coordinate of (0.325, 0.346) after being doped with a blue mechanoluminescence material, and has good white light mechanoluminescence property.

The invention provides a sealant composite and a sealant. The sealant composite comprises basic glue and a mould inhibitor, wherein the mould inhibitor is selected from one or a plurality of 8-oxine copper, ethyl tin chloride, tributyltin chloride, phenyl mercury oleate, pentachlorophenol, N-phenylmaleimide and trichlorophenyl maleimide. With the adoption of the sealant, the problems that marine organism are eroded and attached, mould massively propagates under humid marine environment can be effectively solved and prevented.

The invention relates to a composite high polymer material. Specifically, the composite high polymer material provided by the invention comprises the following components in parts by weight: 50-80 parts of butyl rubber, 5-10 parts of styrene-butadiene rubber, 5-10 parts of butadiene-acrylonitrile rubber, 5-8 parts of tributyltin chloride, 3-5 parts of melamine, 4-6 parts of magnesium phosphate, 2-5 parts of liquid paraffin, 0.1-0.5 part of dimethyl silicone oil and 1-5 parts of zinc stearate. The composite high polymer material provided by the invention is energy-saving and environment-friendly, high in mechanical strength, high in temperature resistance and good in thermal insulating effect, is not added with any harmful ingredients in a production process, achieves non-toxic, harmless, clean and environment-friendly effects, has a simple and feasible preparation method and is suitable for industrial production.

The invention relates to a high decorative coating for an outer wall and a preparation method of the high decorative coating. The high decorative coating comprises the following components in parts by mass: 20-30 parts of water, 0.4-0.8 part of an ethylene-vinyl acetate copolymer, 10-22 parts of calcite powder, 5-12 parts of anatase type TiO2 nanopowder, 3-9 parts of zinc oxide whiskers, 1-5 parts of sericite, 2-7 parts of kaolin, 0.3-0.7 part of dimethylsiloxane, 0.2-0.48 part of molecular sieve, 3-7 parts of succinimide, 0.1-0.3 part of 2-amino-2-methyl-1-propanol, 0.1-0.3 part of 2-ethyl hexyl acrylate, 0.15-0.45 part of tributyl tin chloride, 0.008-0.015 part of cumene hydroperoxide, 1-4 parts of propylene glycol, 0.7-3.2 parts of a self-crosslinking elastic acrylic emulsion and 30-44 parts of a silicone emulsion. The coating provided by the invention has an excellent decorative effect.

The invention discloses a building interior wall insulation coating and a preparation method thereof, and relates to the technical field of coatings. The insulation coating comprises the following rawmaterials in parts by weight: 70-80 parts of epoxy resin emulsion, 40-50 parts of acrylate emulsion, 16-22 parts of brucite fibers, 25-30 parts of white carbon black, 5-8 parts of glyceryl monostearate, 3-10 parts of sodium tripolyphosphate, 1-5 parts of salt, 10-16 parts of silica, 6-14 parts of octamethylcyclotetrasiloxane, 8-12 parts of hydroxypropyl methylcellulose, 10-14 parts of paraffin, 3-6 parts of sodium stearate, 4-8 parts of stearic acid, 6-10 parts of propylene glycol methyl ether acetate, and 3-7 parts of tributyltin chloride. The preparation method of the insulation coating comprises the steps of ball milling, mixing and stirring. The insulation coating has very good thermal insulation, high mechanical strength, strong bonding property with materials, and long service life.

The invention discloses wire enamel which is characterized by being prepared by raw materials in parts by weight (kilogram) as follows: 3-5 parts of isocyanate, 7-9 parts of di-tetradecyl carbon alcohol ester, 12-15 parts of epoxy phenolic resin, 8-12 parts of polyester acrylate, 1-2 parts of a cross-linking agent TAC, 2-3 parts of chlorotributylstannane tributyltin chloride, 14-18 parts of nylon 12, 6-9 parts of 582-2 amino resin, 0.5-1.0 part of simethicone, 3-4 parts of nano brick slag powder, 1-2 parts of potassium tetraborate, 7-9 parts of an auxiliary, 120-130 parts of cresol and 100-120 parts of xylene. A product is high in paint hardness and cannot turn yellow, a paint film is waterproof, chemically resistant, good in ageing resistant, firm in adhesion, not prone to spalling, convenient to use and small in adhesion pollution, the adherence is improved, and the problems that withstand voltage of a copper-clad aluminum electromagnetic wire does not reach the standard as well as wear resistance, salt mist resistance, severe environment resistance and the like do not reach the standard all the time are solved.

The invention relates to a preparation method of tributyltin chloride. The preparation method includes: preparing tin tetrachloride and tetrabutyltin or a mixture containing tetrabutyltin according toa mole ratio of 1:1; adding the tetrabutyltin or the mixture containing tetrabutyltin into a reaction kettle, starting stirring, and adding chilled water, performing cooling to 0DEG C or below, vacuumizing the reaction kettle to ultimate vacuum, and closing a vacuum valve; continuously adding tin tetrachloride dropwise when the temperature in the reaction kettle is controlled ranging from -10DEGC to 0DEG C, keeping reaction for half an hour at the end of feeding, then transferring materials in the reaction kettle to a washing kettle, adding pure water, performing stirring, and conducting full standing; separating a monobutyltin trichloride aqueous solution at a lower layer in the washing kettle into a storage tank, leaving an upper layer organic phase in the washing kettle, controlling the temperature of the washing kettle at 90-110DEG C, and carrying out vacuum drying; and cooling the dried material to obtain a tributyltin chloride product. The process provided by the invention is simple and is easy to control, and the prepared product has high purity.

The invention discloses a synthesis method of a medical intermediate iodomethyl tributyltin. The synthesis method specifically comprises the following steps: dropwise adding n-butyllithium to the raw materials including diiodomethane and tributyltin chloride at minus 78 DEG C to carry out in-situ reaction to generate the target product iodomethyl tributyltin. The method has the obvious advantages that the reaction raw materials are easy to obtain; the reaction operation is simple; large-scale production is easy to achieve; the yield is high; the purity is good; the production cost is low.

The invention relates to a high decorative coating for an outer wall and a preparation method of the high decorative coating. The high decorative coating comprises the following components in parts by mass: 20-30 parts of water, 0.4-0.8 part of an ethylene-vinyl acetate copolymer, 10-22 parts of calcite powder, 5-12 parts of anatase type TiO2 nanopowder, 3-9 parts of zinc oxide whiskers, 1-5 parts of sericite, 2-7 parts of kaolin, 0.3-0.7 part of dimethylsiloxane, 0.2-0.48 part of molecular sieve, 3-7 parts of succinimide, 0.1-0.3 part of 2-amino-2-methyl-1-propanol, 0.1-0.3 part of 2-ethyl hexyl acrylate, 0.15-0.45 part of tributyl tin chloride, 0.008-0.015 part of cumene hydroperoxide, 1-4 parts of propylene glycol, 0.7-3.2 parts of a self-crosslinking elastic acrylic emulsion and 30-44 parts of a silicone emulsion. The coating provided by the invention has an excellent decorative effect.

The invention discloses a method of preparing monobutyl tin trichloride and dibutyl tin dichloride from low purity tributyl tin chloride. The method comprises following steps: (1) mixing tributyl tinchloride with a purity lower than 95% with tin tetrachloride, controlling the temperature to carry out reactions to obtain a mixture composed of monobutyl tin trichloride and dibutyl tin dichloride; and (2) distilling and separating the mixture obtained in the step (1) to obtain monobutyl tin trichloride and dibutyl tin dichloride. Low purity and waste tributyl tin chloride is fully utilized to generate monobutyl tin trichloride and dibutyl tin dichloride that can be used, the cost for processing sewage of organic tin catalysts is reduced, and the utilization rate is improved.

The invention relates to the field of high polymer materials, in particular to a wear-resistant antibacterial degradable high polymer composite material. The composite material is prepared from the following raw materials in parts by weight: an ABS material, carbon fibers, ethylene pure fibers, polylactic acid, chitosan, plant fibers, tributyltin chloride, trichlorobenzeneurea, polyaniline, an ultra-high molecular weight wear-resistant agent, a coupling agent, a curing agent and a compatilizer. The high-molecular composite material has the advantages that the ABS material and the ultra-high molecular weight wear-resistant agent are added into the high-molecular composite material, so that the strength and hardness of the high-molecular composite material are obviously improved, the wear resistance is greatly improved, and meanwhile, the elasticity, toughness and antibacterial persistence of the material are improved by combining other raw material components; the application range of the polymer composite material is greatly widened, and the polymer material is mainly prepared from environment-friendly fiber material components, so that the degradability is greatly improved, and the environmental pollution rate is low.