2312 results about "Toluene" patented technology

Disclosed in the present invention are a reinforced polyurethane rigid foam material and a preparation method therefor, belonging to the technical field of high polymer materials. The material comprises: 5-10 parts of glass fiber yarn, 40-60 parts of an aromatic polyether polyol, 30-50 parts of an aromatic polyester polyol, 30-50 parts of toluene diisocyanate, 40-60 parts of polymethylene polyphenyl polyisocyanate, 5-10 parts of a flame retardant, 5-15 parts of a foaming agent, 1-5 parts of a catalyst and 1-5 parts of a surfactant. The present invention can achieve continuous production of the reinforced polyurethane rigid foam material and can improve the tensile property of the material by 20% or above and increase the utilization rate of glass fibers by 5% or above. The reinforced polyurethane rigid foam material can be widely applied to the field of liquefied gas storage and transportation.

A method for continuously producing m-xylylenediamine belongs to the technical field of organic synthesis and comprises the following steps: (1) mixing isophthalonitrile, toluene and liquid ammonia according to a mass ratio of 1: (3-5): (13-17) in a nitrogen atmosphere to form a reaction mixture; (2) heating the interior of a reaction bed containing a catalyst to 90-95 DEG C, continuously introducing hydrogen into the reaction bed, introducing the reaction mixture after the pressure intensity of the reaction bed is stable, and carrying out a catalytic hydrogenation reaction to generate a reaction product; and (3) carrying out gas-liquid separation on the reaction product, removing liquid ammonia from the liquid-phase product through an ammonia distillation process, and separating toluene and m-xylylenediamine through a rectification process to obtain m-xylylenediamine. According to the method, isophthalonitrile and hydrogen are used as raw materials, liquid ammonia and methylbenzene are used as reaction solvents, the raw materials and the reaction solvents are heated to 90-95 DEG C under the catalytic action of a catalyst for an exothermic reaction, m-xylylenediamine is generated through the reaction, and the reaction yield is larger than 99%.

The invention relates to the field of fine chemical engineering, and discloses a green process for preparing chloramine T by a continuous flow reactor. The method comprises the following steps: respectively pumping p-toluenesulfonamide, a sodium hydroxide solution and a sodium hypochlorite solution into a micro-channel mixer for instantaneous mixing, and carrying out chlorination reaction in a multi-stage temperature control tubular reaction unit; the concentration of free chlorine is detected on line at an outlet, and the flow rate of a chlorine source is dynamically adjusted through a PID algorithm, so that closed-loop control is realized; the reaction liquid is directly crystallized and separated to obtain the product without alkali wash. The system comprises a base solution and chlorine source conveying subsystem, a micro-channel mixer, a multi-stage reaction unit, an online monitoring module, a central controller and a crystallization unit. The side reaction is inhibited from the source, so that the free chlorine is less than or equal to 0.5 mg / L, the alkali washing step is omitted, the COD (Chemical Oxygen Demand) of the wastewater is reduced by more than 80%, the product purity is more than or equal to 99.5%, and the productivity is improved by 3 times.

The invention relates to the technical field of functional ceramic materials, and discloses complex-phase gradient isomeric zinc spinel-based composite activated zinc oxide, a preparation method thereof and a ceramic glaze, and the preparation method comprises the following steps: mixing zinc oxide, aluminum oxide, silicon oxide, magnesium oxide and rare earth oxide in proportion to obtain a mixture, adding the mixture and an alkoxy compound into a solvent, and dispersing to form nano precursor slurry; carrying out reduction-oxidation calcination treatment on the obtained nano precursor slurry to obtain a calcined product; and carrying out hydration treatment on the obtained calcined product to obtain the complex-phase gradient isomeric zinc spinel-based composite activated zinc oxide. By implementing the preparation method, the obtained complex-phase gradient isomeric zinc spinel-based composite activated zinc oxide contains a zinc oxide phase and a spinel phase, is low in high-temperature lattice distortion rate and has super wear resistance, and a rare earth element R is introduced, so that the catalytic activity of the zinc oxide is improved, the degradation rate of the zinc oxide to formaldehyde and toluene is increased, and the antibacterial property of the zinc oxide is also improved.

The present invention relates to the field of polyurethane materials and particularly to a temperature-induced color-changing vehicle film and a preparation method therefor. The method of the present invention comprises: firstly, using polyurethane to wrap vanadium dioxide powder to obtain color-changing microcapsules; then using 1,1,1,3,5,5,5-heptamethyltrisiloxane and 3-allyloxy-1,2-propanediol as raw materials to synthesize an organosilicon-modified diol, and enabling trimellitic anhydride to react with toluene diisocyanate to synthesize a dicarboximide compound; enabling the organosilicon-modified diol and the dicarboximide compound to undergo an esterification reaction and a polymerization reaction to obtain an organosilicon-modified imide polyester diol; then mixing the organosilicon-modified imide polyester diol with polytetrahydrofuran ether glycol 2000, and then enabling the mixture to react with toluene diisocyanate to obtain a polyurethane elastomer; and mixing the polyurethane elastomer, the color-changing microcapsules, a silane coupling agent, a plasticizer, an antioxidant, and an ultraviolet light absorber, followed by melt extrusion and blow molding into a film, so as to obtain the temperature-induced color-changing vehicle film.

The invention discloses a normal-temperature curing ablation-resistant coating and a preparation method thereof, the normal-temperature curing ablation-resistant coating comprises a component A, a component B and a component C, the component A comprises the following raw materials by weight: 20-30 parts of epoxy resin, 30-40 parts of liquid nitrile rubber, 27-50 parts of an ablation-resistant filler, 10-20 parts of a heat-insulating functional filler, and 200-300 parts of toluene; the component B is a curing agent; and the component C is a curing accelerator. By selecting the high-performance polymer-based resin material and adding the ablation-resistant filler and the heat-insulating functional filler, the ablation-resistant and heat-insulating coating protection construction of the equipment under the normal-temperature curing condition is realized; the problems of ablation-resistant coating construction and thermal protection when a fragile cover, a launcher and the like in a launching system cannot use a high-temperature curing system ablation-resistant coating are solved. The coating can realize military technology and civil use, and can be widely applied to fire prevention and heat insulation construction of buildings.

The present invention relates to the field of the preparation of polyurethane elastic fibers, and relates to a preparation method for a bio-based polyurethane elastic fiber, comprising: preparing polyether polyol from sucrose, glycerol, dimethylamine and propylene oxide; adding a solvent, i.e., N,N-dimethylacetamide, and polyether polyol and polyisocyanate into a reaction tank, and adding p-Toluenesulfonyl semicarbazide and aluminum methylenebis(2,4-di-tert-butylphenoxy) phosphate to prepare a spinning solution; and subjecting the spinning solution to spinning and oil application by means of dry spinning technology to obtain the bio-based polyurethane elastic fiber. The present invention ensures that the properties of polyurethane elastic fibers do not deteriorate or are partially enhanced, while the cost and performance advantages are achieved.

The invention discloses silicon-based flame-retardant high-heat-resistance hydrocarbon resin as well as a preparation method and application thereof in preparation of a copper-clad plate, and belongs to the technical field of electronic resin synthesis. The preparation method of the silicon-based flame-retardant high-heat-resistance hydrocarbon resin comprises the following steps: S1, adding a first monomer, organic silicon and a catalyst into a reaction container, then adding dehydrated toluene and fully stirring, and after the reaction is finished, carrying out silica gel adsorption, filtration and reduced pressure distillation to obtain a silicon-containing unsaturated monomer; s2, sequentially adding a first monomer, a silicon-containing unsaturated monomer, a second monomer and a third monomer into a reaction container, then adding a solvent A and a cationic initiator, fully stirring, and washing and distilling after the reaction is finished to obtain the silicon-based flame-retardant high-heat-resistance hydrocarbon resin. The prepared silicon-based flame-retardant high-heat-resistance hydrocarbon resin has excellent dielectric property, heat resistance, mechanical strength and flame retardance, and can endow a copper-clad plate with excellent dielectric property, heat resistance, mechanical strength, flame retardance and the like when being applied to preparation of the copper-clad plate.

The invention discloses a preparation method of salt-resistant sodium carboxymethyl cellulose, and relates to the technical field of petroleum fracturing materials. The preparation method comprises the following steps: reacting stearic acid with ethylenediamine to obtain a monosubstituted intermediate, reacting the monosubstituted intermediate with cocoyl chloride to obtain an intermediate 1, reacting the intermediate 1 with epoxypropane to obtain an intermediate 2, and reacting the intermediate 2 with paratoluensulfonyl chloride to obtain a hydrophobic intermediate; reacting a sodium carboxymethyl cellulose solution with the hydrophobic intermediate to obtain modified sodium carboxymethyl cellulose, and sulfonating the modified sodium carboxymethyl cellulose with sulfamic acid to obtain crude salt-tolerant sodium carboxymethyl cellulose; and reacting the crude product salt-resistant sodium carboxymethyl cellulose with borax to obtain the salt-resistant sodium carboxymethyl cellulose. The salt-resistant sodium carboxymethyl cellulose prepared by adopting a step-by-step synthesis strategy has excellent salt resistance, temperature resistance, shearing resistance and dissolution rate, and is suitable for thickening and sand carrying of high-temperature and high-salt oil and gas field fracturing fluid.

The invention discloses environmentally degradable plastic as well as a preparation method and application thereof, and belongs to the technical field of degradable plastic. The degradable modified plastic is prepared from the following raw materials: polylactic acid, poly (butylene terephthalate)-adipate, modified thermoplastic starch, modified cellulose, poly (butylene succinate), epoxidized soybean oil, polyvinyl alcohol, glycerol monolaurate and ethylenediaminetetraacetic acid. Wherein the modified thermoplastic starch is obtained by thermoplastic modification of starch through a plasticizer and modification of castor oil and toluene diisocynate; the modified cellulose is obtained by modifying cellulose acetate with chitosan. By regulating and controlling the types and proportions of the raw materials for preparing the plastic, the plastic with excellent degradation performance and mechanical performance can be obtained, the shopping bag is prepared from the plastic, the loading capacity can be remarkably improved, the plastic is easily degraded by microorganisms in the environment after being discarded, and environmental pollution is avoided.

The invention relates to the technical field of anti-yellowing, in particular to anti-yellowing lining cloth with a hot melt coating and a preparation method of the anti-yellowing lining cloth. Composite carbon dots, an anti-yellowing agent and a composite chitosan solution are adopted to prepare finishing liquid for finishing the lining cloth; the preparation method comprises the following steps: selecting furfural and urea as a carbon source and a nitrogen source, performing one-step hydrothermal synthesis to obtain a nitrogen-doped furfural-based carbon dot, and grafting an amino-terminated polyimidazolium salt antibacterial compound to obtain a composite carbon dot; wherein the amino-terminated polyimidazolium salt antibacterial compound is an amino-terminated halogen-free polyimidazolium salt antibacterial compound which is prepared by taking ethylenediamine, butyric acid, glyoxal and formaldehyde as raw materials based on amine-aldehyde polycondensation and has good biocompatibility; the preparation method comprises the following steps: by taking polybutylene adipate, toluene diisocynate and isophorone diisocyanate as main monomers, polypropylene oxide triol as a crosslinking monomer, 2, 2-dimethylolpropionic acid and 4, 4 '-diaminodiphenyl disulfide as chain extenders and composite carbon dots as an end-capping reagent, adding water and emulsifying to obtain the waterborne polyurethane hot melt adhesive.

A photoelectric composite cable for an underwater buoy, and a preparation process therefor. A polyurethane, a self-repairing polyurethane prepolymer, and a composite nano zinc oxide are selected as an outer sheath base material. A modified polysiloxane having a B-O six-membered ring dynamic cross-linked network and a long-chain alkane group and an amino is introduced into the self-repairing polyurethane prepolymer; 5,5'-methylenedisalicylaldehyde and isophorone diisocyanate are together subjected to stepwise polymerization with the modified polysiloxane, and the 5,5'-methylenedisalicylaldehyde is cross-linked with diphenylmethane diisocyanate to obtain a self-repairing polyurethane prepolymer; and nano zinc oxide is subjected to a modification treatment, wherein dodecyltrimethoxysilane and 3-glycidoxypropyltrimethoxysilane are used for dual modification, such that super-hydrophobic nano zinc oxide having good thermal stability and high dispersity is prepared in a toluene system.

The invention relates to the technical field of automobile air purification, and particularly discloses a filtering material, a preparation method of the filtering material and a novel automobile air conditioner multi-effect catalytic formaldehyde removal filter. The filtering material comprises a PET (Polyethylene Terephthalate) supporting layer, a gas filtering layer and a PP (Polypropylene) electrostatic filtering layer which are arranged in sequence, the gas filtering layer is prepared from the following raw materials in parts by weight: 30 to 90 parts of activated carbon and 10 to 70 parts of manganese catalyst. The gas filtering layer composed of the activated carbon and the manganese catalyst is matched with the filtering material composed of the PET supporting layer and the PP electrostatic filtering layer, four gases of n-butane, methylbenzene, sulfur dioxide and nitrogen dioxide can be adsorbed, the manganese catalyst degrades formaldehyde at normal temperature, meanwhile, the reaction on the formaldehyde is a catalytic reaction, and the environment-friendly effect is achieved. Therefore, the filter material disclosed by the invention also has longer service life, so that a filter made of the filter material has a better formaldehyde removal effect and longer service life.

The invention relates to the technical field of sealing detection, in particular to a toluene cooler sealing detection assembly which is installed on the outer wall of the connecting position of a pipeline and a cooler and comprises a positioning belt, a fixing belt, a supporting belt, a covering belt, a sealing performance detection assembly and a strain gauge. The inner wall of the fixing belt is connected with the outer wall of the positioning belt, the supporting belt is wound on the outer wall of the cooler, the left side and the right side of the inner wall of the covering belt are connected with the outer wall of the supporting belt and the outer wall of the fixing belt respectively, and the positioning belt, the fixing belt, the supporting belt and the covering belt are matched with the pipeline and the cooler to form a cavity. The sealing performance detection assembly is connected between the positioning belt and the fixing belt, the strain gauge is connected to the sealing performance detection assembly, and the left side of the sealing performance detection assembly is located in the cavity. And the monitoring precision is effectively improved.

The invention discloses a precise construction strategy of a dibenzothiophene sulfuryl covalent organic framework material and systematically explains efficient application of the dibenzothiophene sulfuryl covalent organic framework material in photocatalytic synthesis of thiadiazole and derivatives thereof. The achievement relates to a plurality of leading subjects such as catalytic chemistry, organic synthesis, material science, environmental engineering and green chemistry. According to the method, 2, 4, 6-triformyl phloroglucinol and 3, 7-diaminodibenzo [b, d] thiophene-5, 5-dioxide are taken as construction units, and the crystalline S-COF rich in sulfuryl active sites can be quantitatively obtained through topology-oriented Schiff base condensation under the conditions of protonic acid catalysis, no water and no oxygen. Under the radiation condition of visible blue light, S-COF is used as a heterogeneous photocatalyst to drive green synthesis of 3, 5-di-p-tolyl-1, 2, 4-thiadiazole and series of derivatives thereof; the invention provides a new catalyst design normal form for light-induced organic conversion, and lays a solid foundation for sustainable development-oriented efficient synthesis chemistry.

The invention discloses a triazine desulfurizer and a preparation method thereof, and belongs to the technical field of gas purification. The triazine desulfurizer is mainly prepared from the following raw materials in percentage by weight: 20 to 50 weight percent of triazine derivative, 10 to 15 weight percent of sterically hindered amine, 3 to 7 weight percent of stabilizer, 1 to 3 weight percent of synergist, 0.5 to 1.5 weight percent of penetrant, 0.5 to 1.5 weight percent of inhibitor, 1 to 2 weight percent of additive and the balance of water, the preparation method of the triazine derivative comprises the following steps: adding 2-(diphenylphosphino) ethylamine into a toluene solvent, adding a paraformaldehyde aqueous solution in batches under a stirring condition, and reacting for 2-8 hours to obtain the triazine derivative. According to the triazine desulfurizer and the preparation method thereof provided by the invention, the triazine derivative and the sterically hindered amine are taken as a host, and the stabilizer, the synergist, the penetrant, the inhibitor and the assistant are compounded, so that the scaling trend of the triazine desulfurizer in an oil and gas well can be slowed down, the dissolution rate of hydrogen sulfide and the mass transfer rate in a solution are increased, and the desulfurization reaction is promoted; the desulfurization effect and the desulfurization rate are improved, and meanwhile, a very good scale inhibition effect is also achieved.

The invention discloses a high-performance anti-corrosion coating based on a layered nano material and a preparation method of the high-performance anti-corrosion coating. The anticorrosive paint is prepared from raw materials including a component A and a component B. The component A comprises epoxy resin, modified MXene nanosheets, modified graphene oxide, nano clay, zinc powder, a corrosion inhibitor, a defoaming agent, a flatting agent and ethylene glycol butyl ether, the modified MXene nanosheets are obtained by conducting surface treatment on the MXene nanosheets through a silane coupling agent, and the modified graphene oxide is obtained by conducting surface treatment on the modified MXene nanosheets through a silane coupling agent. The modified graphene oxide is obtained by modifying graphene with toluene diisocynate and dibutyltin dilaurate; and the component B is a polyamide resin curing agent. According to the anticorrosive paint disclosed by the invention, through interlayer intercalation and surface functional modification of MXene and graphene oxide, a compact physical barrier is formed, the interface bonding force is enhanced, and the permeability resistance is remarkably improved; the corrosion inhibitor is encapsulated in the layered structure, and when the coating is damaged, the corrosion inhibitor can be actively released to repair local microcracks.

The invention discloses a plant-based deodorant and a preparation method thereof, and relates to the technical field of high polymer materials. When the plant-based deodorant is prepared, beta-cyclodextrin reacts with paratoluensulfonyl chloride and then reacts with ethylenediamine, and amino modified cyclodextrin is prepared; the plant-based extract is subjected to inclusion with amino modified cyclodextrin, and a cyclodextrin inclusion compound is prepared; the preparation method comprises the following steps: reacting hydroxyethyl cellulose with methacrylic anhydride to prepare double-bond modified cellulose; carrying out hydrothermal reaction on titanium sulfate, the carboxylated multi-walled carbon nanotube, ammonium fluoride and cerous nitrate to prepare a co-doped titanium dioxide / carbon nanotube; coating the co-doped titanium dioxide / carbon nano-tubes with oleic acid to prepare modified nano-particles; and reacting the double-bond modified cellulose with the cyclodextrin inclusion compound, and then copolymerizing with the modified nanoparticles and the comonomer to obtain the plant-based deodorant. The prepared plant-based deodorant has the advantages of good deodorization effect, slow release and photocatalytic degradation.

The invention discloses a hexamethyldisiloxane preparation method capable of purifying a raw material, and relates to the technical field of chemical preparation, the hexamethyldisiloxane preparation method capable of purifying the raw material comprises the following steps: S1, raw material preparation: cooling deionized water through a cooling system, and maintaining the temperature to be less than or equal to 10 DEG C, then injecting part of the cooled deionized water into a tubular reactor, pumping trimethylchlorosilane and methylbenzene into a premixing tank according to a proportion, and uniformly stirring and mixing; s2, catalytic promotion: injecting diluted hydrochloric acid into the tubular reactor, uniformly mixing the diluted hydrochloric acid with deionized water, and maintaining the pH value to 2-3; according to the hexamethyldisiloxane preparation method capable of purifying the raw materials, redundant steps such as catalyst recovery and repeated washing can be omitted through the hydrolysis reaction, the method is suitable for continuous production, meanwhile, the process of the hydrolysis reaction is optimized by changing the use steps and the input method of the deionized water, and the stability in the preparation process is further maintained.

The invention provides a method for synthesizing diethyl adipate through dynamic covalent chemical regulation. Comprising the following steps: S1, sequentially adding 80-120g of adipic acid, 160-240mL of absolute ethyl alcohol, 5-8g of a difunctional dynamic regulation and control carrier, 2-4g of a ternary composite catalyst, 1-2g of a synergistic additive and 100-150mL of a mixed solvent consisting of cyclohexane and methylbenzene into a 500mL four-neck flask provided with a thermometer, a water segregator and a pH sensor, and adjusting the initial pH value to 8.0-8.5; stirring and reacting for 6 to 8 hours at the rotating speed of 450 to 500r / min under the condition of 70 to 75 DEG C; and S2, after the reaction is finished, cooling to 25 DEG C, separating and recovering the bifunctional dynamic regulation and control carrier and the ternary composite catalyst, introducing CO2 into the filtrate to regulate the pH value to 5.0-5.5, releasing the captured moisture, and carrying out reduced pressure distillation under the conditions of 80-90 DEG C and-0.08 MPa to obtain diethyl adipate. By means of the rare earth ion-carbon quantum dot-ionic liquid ternary composite catalyst, efficient catalysis under the strong acid-free condition is achieved, and the catalyst recovery rate and the product purity are greatly improved.

The invention discloses a high-entropy metal oxide with efficient toluene photo-thermal catalytic efficiency and a synthesis method thereof. The high-entropy metal oxide is composed of oxides of Co, Mn, Ni, Zn and Fe, the metal molar ratio of Co to Mn to Ni to Zn to Fe is equal to (3.0-4.0): (3.0-4.0): (0.5-1.0): (0.5-1.0): (0.5-1.0), the high-entropy metal oxide is synthesized through an ethanol-water solvent coprecipitation combined hydrothermal crystallization and programmed calcination process, and the high-entropy metal oxide has excellent light absorption and heat transfer capacity, high toluene catalytic degradation activity and excellent catalytic stability, so that the high-entropy metal oxide can be used for photo-thermal catalytic oxidation of toluene.

The invention discloses a high-elastic material for an anti-slip sole and a preparation method of the high-elastic material in the field of high polymer materials. The high-elastic material is prepared from the following raw materials: modified polyurethane, modified silicone rubber, calcium carbonate, dicumyl peroxide, 2-mercaptobenzothiazole, N-isopropyl-N '-phenyl p-phenylenediamine and naphthenic oil. Wherein the modified polyurethane is prepared by the following steps: carrying out vacuum dehydration on polybutylene adipate, reacting with toluene diisocynate to prepare an isocyanate-terminated prepolymer, adding dimethylolpropionic acid, triethylamine and deionized water to obtain a water-based dispersion, and carrying out graft copolymerization on the water-based dispersion, methyl methacrylate and the like; the preparation method comprises the following steps: preheating modified polyurethane, mixing with modified silicone rubber at a high speed, adding calcium carbonate and naphthenic oil, carrying out double-roller open milling and thin-passing, adding a vulcanizing agent and the like, carrying out overturning milling, and carrying out flat plate vulcanization molding. The material is used for anti-skid soles, and has the advantages of high elasticity, lasting skid resistance and excellent weather resistance.

The invention relates to a formaldehyde-free environment-friendly polyurethane adhesive and a preparation method thereof, relates to the technical field of high polymer materials, and aims to solve the problems of formaldehyde residue, poor water resistance, high process energy consumption, high cost and the like of the existing formaldehyde-free adhesive. According to the invention, dimethylolpropionic acid and wood metal ions form coordinate bonds to strengthen interface bonding, trimethylolpropane constructs a three-dimensional hydrophobic network, and toluene diisocynate isomers are subjected to fractional reaction to optimize crosslinking uniformity. The content of free formaldehyde in the adhesive is not detected, the adhesive strength retention rate is greatly improved after the adhesive is boiled in boiling water for 72 hours, the hot pressing time is shortened to 8 minutes, and the raw material cost is reduced by 40% or above compared with similar products.

The invention provides an oxygen vacancy adjustable catalyst for synergistically removing nitrogen oxides and volatile organic compounds as well as a preparation method and application of the oxygen vacancy adjustable catalyst. The catalyst takes natural ore as a raw material, main active components are MnO2 and Fe2O3, and an inert component is mainly SiO2. The catalyst with different oxygen vacancy concentrations is obtained by regulating and controlling the ratio of the active components and the calcining atmosphere, and the catalyst has good catalytic performance of synergistically removing nitrogen oxides and volatile organic compounds. Under the conditions that the volume space velocity (24000 h <-1 >) is high, the concentration of NO and NH3 is 500 ppm, the concentration of toluene is 50 ppm and 5 vol.% O2 / N2, the conversion rate of NO is kept at 80% or above within the range of 90-260 DEG C, and the conversion rate of toluene reaches 50% at the temperature of 114 DEG C and reaches 90% at the temperature of 224 DEG C. The simple preparation method is utilized, ores are selected as active components, the catalyst with the adjustable oxygen vacancy is prepared, and the catalyst is suitable for collaborative purification of NOx and VOCs in flue gas in the industries of coal-fired power plants, cement, metallurgy and the like.

The invention discloses an amino alcohol nickel complex as well as a preparation method and application thereof, and belongs to the technical field of organic metal synthesis. The molecular formula of the amino alcohol nickel complex is Ni [OCR1R2 (CH2) mNR3R4] 2, comprising the following raw materials: a nickel-containing complex, 60wt.% of NaH and HOCR1R2 (CH2) mNR3R4, the preparation method specifically comprises the following steps: (1) under the protection of nitrogen, mixing a nickel-containing complex, 60wt.% NaH, HOCR1R2 (CH2) mNR3R4 and toluene, carrying out heating reaction, and carrying out heating reaction again; and (2) filtering, concentrating, cooling, filtering again, and washing to obtain the product. The nickel-containing complex, sodium hydride and amino alcohol are synthesized into the amino alcohol nickel complex through a one-pot method, the raw materials are simple, easy to obtain and convenient to store, expensive active intermediates do not need to be synthesized or purchased, and the cost and risk of amplified production are reduced. Meanwhile, the purification method of the product is improved, the high-purity amino alcohol nickel complex is obtained through a low-temperature crystallization method, operation is safe and convenient, the industrial purification efficiency is improved, and the purity of the obtained product is as high as 6N-7N through ICP-MS testing.

The invention belongs to the technical field of cables, and particularly relates to a weather-proof new energy automobile charging cable which is composed of a cable core, a shielding layer wrapping the cable core and a sheath layer wrapping the shielding layer. Each cable core is composed of a conductor and an insulating layer. The invention discloses a preparation method of a traditional Chinese medicine. A sheath layer of the weather-resistant new energy automobile charging cable is prepared from 70 to 90 parts of thermoplastic elastomer (TPE), 20 to 30 parts of lignin, 25 to 30 parts of propylene oxide, 20 to 25 parts of furfuryl alcohol, 2 to 5 parts of 4-chloromethyl styrene, 1.5 to 3 parts of tetrabutyl ammonium hydroxide, 5 to 6 parts of methylbenzene, 10 to 25 parts of methyl tert-butyl ether, 45 to 7 parts of anhydrous MgSO4, 0.5 to 2.5 parts of initiator, 2 to 3 parts of cross-linking agent, 5 to 8 parts of metal salt additive and 1 to 3 parts of lubricant. 0.3 to 0.6 part of antioxidant and 3 to 4 parts of color master batch.

The invention provides a preparation method of (S)-oxetane-2-methylamine. The preparation method of (S)-oxetane-2-methylamine comprises the following steps: (1) carrying out ring closing reaction on a compound A under an alkaline condition to obtain a compound B; (2) reacting the compound B with dibenzylamine to obtain a compound C; (3) reacting the compound C with a reducing agent to obtain a compound D; (4) reacting the compound D with paratoluensulfonyl chloride to obtain a compound E; (5) reacting the compound E with alkali to obtain a compound F; and (6) carrying out a reaction on the compound F and palladium on carbon to obtain the (S)-oxetane-2-methylamine. According to the preparation method provided by the invention, ring expansion reaction using trimethylsulfoxide iodide in the prior art is avoided, the problem that residual sulfur elements cause poisoning of a palladium-carbon catalyst is solved, meanwhile, sodium azide is also avoided, and the preparation method is safe and reliable in process, high in chiral purity and yield and suitable for industrial large-scale production.

The application relates to the technical field of film materials, in particular to a mixed matrix membrane and a preparation method and application thereof. Toluene is added into a viscous polyamine acid solution, the temperature is increased to 200-250 DEG C, and stirring reaction is carried out for 5-8 hours, then the precipitate is obtained through centrifugation, the precipitate is washed with methanol for 3-5 times, and the product COOH-PI is obtained through drying; zinc nitrate hexahydrate and 2-methyl imidazole are dissolved in methanol, stirring reaction is carried out at room temperature for 3-8 hours, then the product is taken out and centrifuged, the product is washed with anhydrous methanol for 3-5 times, and ZIF-8 is obtained through drying; NH2-ZIF-8 is synthesized by using the same method; COOH-PI is added into DMF and stirred to obtain a PI solution, ZIF-8 and NH2-ZIF-8 are respectively added into DMF, and MOF suspension is obtained through ultrasonic treatment for 2-5 hours, then the MOF suspension is added into the PI solution, stirring is carried out at room temperature for 24-36 hours, the casting solution obtained is poured into a flat and clean glass plate, heating is carried out at 60-65 DEG C for 24-48 hours, then the formed membrane is dried to obtain the mixed matrix membrane. The preparation condition of the mixed matrix membrane is mild, the stability of the membrane is obviously improved, and the mixed matrix membrane has high selective permeability to helium.

The invention discloses a carbamoyl-substituted diarylethene derivative as well as a preparation method and application thereof, and the preparation method comprises the following steps: reacting R-substituted 3-bromo-2-hydroxybenzaldehyde with an arylmethyl triphenylphosphonium bromide compound or an aryl acetic acid compound to obtain an intermediate A; then the intermediate A and cuprous cyanide are subjected to a heating reaction in N, N-dimethylformamide and nitrogen atmosphere, and an intermediate B is obtained; and finally, heating the intermediate B, acetaldoxime and indium trichloride in toluene for reaction to obtain the carbamoyl-substituted diarylethene derivative. The carbamoyl-substituted diarylethene derivative disclosed by the invention has a remarkable effect in an in-vitro anti-tumor activity test, particularly has excellent anti-proliferation ability to human BRCA mutant tumor cells, and can be used for preparing medicines for treating PARP-1 activity abnormity related diseases. The synthesis route is simple, the cost is low, and large-scale implementation is facilitated.

The invention relates to the technical field of gas adsorbents, in particular to an MOF-based gas adsorbent with a core-shell-shell structure as well as a preparation method and application of the MOF-based gas adsorbent. According to the MOF-based gas adsorbent disclosed by the invention, UiO-66 regulated and controlled by defect engineering is taken as a core layer, and the defect density in a UiO-66 crystal structure is accurately controlled by introducing a specific regulator glacial acetic acid, so that a sufficient physical adsorption space is provided for toluene molecules, and abundant acidic adsorption sites are formed; the PDA middle layer has dual functions of interface bonding and performance collaboration, so that the adsorption affinity of the material to toluene is further enhanced, and the adsorption performance is synergistically improved; the super-hydrophobic ZIF-8 is used as the outermost shell layer, on one hand, the super-hydrophobic ZIF-8 can be used as a molecular barrier to efficiently block external water molecules from entering the core layer UiO-66, the inactivation of core Zr active sites due to hydration is avoided, and the stability problem in a high-humidity environment is solved; and secondly, the diffusion behavior of toluene molecules can be regulated and controlled through a molecular sieving effect, so that high-selectivity and high-stability adsorption on toluene under a high-humidity condition is realized.