2339 results about "Aniline" patented technology

The invention relates to a pharmaceutically acceptable salt of a fused ring compound, and a crystal form and application thereof. Specifically, the present disclosure provides a pharmaceutically acceptable salt of 3-chloro-5-((5S, 5aS, 6S, 9R)-1-fluoro-12-((1-((4-(fluoromethylsubunit) piperidine-1-yl) methyl) cyclopropyl) methoxy)-5-methyl-5a, 6, 7, 8, 9, 10-hexahydro-5H-4-oxa-3, 10a, 11, 13, 14-pentaaza-6, 9-methylbridged naphtho [1, 8-ab] heptan-2-yl)-4-(trifluoromethyl) aniline, a crystal form, and a preparation method thereof, and a preparation method thereof. Corresponding salts have good stability and can be better used for clinical treatment. # imgabs0 #

The invention relates to a pharmaceutically acceptable salt of a fused ring compound, and a crystal form and application thereof. Specifically, the present disclosure provides a pharmaceutically acceptable salt of 3-chloro-5-((5S, 5aS, 6S, 9R)-1-fluoro-12-((1-((4-(fluoromethylsubunit) piperidine-1-yl) methyl) cyclopropyl) methoxy)-5-methyl-5a, 6, 7, 8, 9, 10-hexahydro-5H-4-oxa-3, 10a, 11, 13, 14-pentaaza-6, 9-methylbridged naphtho [1, 8-ab] heptan-2-yl)-4-(trifluoromethyl) aniline, a crystal form, and a preparation method thereof, and a preparation method thereof. Corresponding salts have good stability and can be better used for clinical treatment. # imgabs0 #

The invention relates to a pharmaceutically acceptable salt of a fused ring compound, and a crystal form and application thereof. Specifically, the present disclosure provides a pharmaceutically acceptable salt of 3-chloro-5-((5S, 5aS, 6S, 9R)-1-fluoro-12-((1-((4-(fluoromethylsubunit) piperidine-1-yl) methyl) cyclopropyl) methoxy)-5-methyl-5a, 6, 7, 8, 9, 10-hexahydro-5H-4-oxa-3, 10a, 11, 13, 14-pentaaza-6, 9-methylbridged naphtho [1, 8-ab] heptan-2-yl)-4-(trifluoromethyl) aniline, a crystal form, and a preparation method thereof, and a preparation method thereof. Corresponding salts have good stability and can be better used for clinical treatment. # imgabs0 #

The invention discloses a preparation method of a fluorine-containing carbazole phosphonic acid compound, which solves the technical problems of harsh reaction conditions, high raw material price and low yield in the existing preparation process, 4-trifluoromethoxyaniline and 4-trifluoromethoxyiodobenzene are used as initial raw materials, and Ullmann reaction is performed under a solvent-free condition to obtain 4, 4 '-difluorocarbazole phosphonic acid. The preparation method comprises the following steps: taking 3, 4 '-bis (trifluoromethoxy) diphenylamine as a raw material, carrying out palladium acetate catalytic oxidation cyclization to obtain 3, 6-bis (trifluoromethoxy) carbazole, reacting the 3, 6-bis (trifluoromethoxy) carbazole with 2-bromoethyl dimethyl phosphonate to obtain N-(2-ethyl dimethyl phosphonate) 3, 6-bis (trifluoromethoxy) carbazole, and finally hydrolyzing to obtain the N-(2-ethyl phosphonate) 3, 6-bis (trifluoromethoxy) carbazole. The reaction process is simpler to operate, the yield is guaranteed, and the method is suitable for large-scale production. In the preparation method disclosed by the invention, a solvent is not required to be used in multiple steps, the reaction is performed under a solvent-free condition, and the preparation method is high in safety and environment-friendly.

The invention belongs to the technical field of aerogel materials, and particularly relates to antistatic aerogel for 3D printing as well as a preparation method and application of the antistatic aerogel. The preparation method comprises the following steps: (1) dispersing inorganic nanoparticles modified by a silane coupling agent containing epoxy groups and an aniline monomer in an acidic solvent to obtain a monomer mixed solution; (2) stirring and dissolving polyamide in the monomer mixed solution; (3) initiating a reaction to obtain a polyaniline modified polyamide solution; and (4) freeze-drying to obtain the antistatic aerogel for 3D printing. By controlling synthesis conditions, a core-shell structure of acid-doped polyaniline coated inorganic nanoparticles is formed, and a good conductive path is formed in polyamide with a small addition amount of polyaniline. The antistatic aerogel for 3D printing can be applied to technologies such as photocuring molding and fused deposition of polyurethane resin in a 3D printing technology, and the antistatic property and the mechanical property of a 3D printed product are improved.

The invention belongs to the technical field of aerogel materials, and particularly relates to high-performance antistatic aerogel for 3D printing as well as a preparation method and application thereof. According to the invention, inorganic hollow nanoparticles are selected as a nucleating modifier for in-situ polymerization of aniline monomers in a polyamide solution, so that polyaniline-coated inorganic hollow nanoparticles are uniformly dispersed in polyamide, and the aerogel composite material with polyamide as a continuous phase and polyaniline-coated inorganic hollow nanoparticles as a conductive and reinforced phase is formed. The use of the hollow inorganic nanoparticles avoids the problem that the solid inorganic nanoparticles lose the characteristics of the inorganic nanoparticles due to high specific gravity and high surface energy, and easy agglomeration or adsorption with other substances in the preparation process of the solid inorganic nanoparticles. The inorganic hollow nanoparticles are adopted as a nucleating modifier, so that the problems of agglomeration of solid nanoparticles and dispersion in a polyamide matrix are well solved.

The invention provides a polyaniline / modified graphene oxide composite material and a preparation method thereof. The preparation method comprises the following steps: dispersing purified graphene oxide, performing ultrasonic treatment, heating, adding a modifier for modification, centrifuging, taking precipitate, freezing, drying and grinding to obtain modified graphene oxide powder; mixing the powder with an aniline solution in doped acid to form a modified graphene oxide / aniline acid solution; dissolving ammonium persulfate in the doped acid to prepare an ammonium persulfate acid solution; and slowly dropwise adding the solution into the solution, carrying out in-situ polymerization, and carrying out suction filtration, washing and drying to obtain the composite material. According to the method, through chemical modification and in-situ polymerization processes, the problems that a single filler is poor in dispersity, a conductive network is discontinuous, and anti-corrosion and anti-static performance is difficult to synergistically improve are solved, and the process is simple and convenient and suitable for industrialization.

The invention discloses a waterproof anticorrosive coating and a preparation method and application thereof, and relates to the technical field of coatings, and the waterproof anticorrosive coating is prepared from the following raw materials in parts by weight: 30-40 parts of carboxyl-terminated hyperbranched polyester resin, 20-30 parts of carboxyl-terminated functional polyamide, 10-15 parts of hyperbranched polyurethane containing epoxy groups, 15-20 parts of filler, 1-3 parts of (3, 6-diamino acridine-9-yl) boric acid, 1-3 parts of 1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5- the component A is prepared from the following components in parts by weight: 3-5 parts of 2, 3, 5-triglycidyl-S-triazinetrione, 1-2 parts of a coupling agent, 0.8-1.2 parts of a flatting agent and 0.6-1.3 parts of a defoaming agent; the carboxyl-terminated functional polyamide comprises a structural unit introduced by the following monomers: N-(4H-1, 2, 4-triazole-4-yl) diphenylamine-4, 4 '-dicarboxylic acid, and 3, 3'-diamino-4, 4 '-difluorodiphenyl sulfone. The coating is good in waterproof and anti-corrosion performance, high in adhesive force with a base material, sufficient in solvent resistance and aging resistance and long in service life.

The invention discloses a waterborne epoxy resin coating, a preparation method and application in bridge protection, and belongs to the technical field of coatings. The water-borne epoxy resin coating comprises the following raw material components in parts by weight: 15-25 parts of epoxy composite resin emulsion, 100 parts of emulsified asphalt, 3-5 parts of a curing agent and 6-10 parts of water, wherein the epoxy composite resin emulsion is obtained by carrying out a composite reaction on 30-60 parts by mass of epoxy resin, 2-3 parts by mass of an emulsifier, 6-9 parts by mass of an acrylate composition and 1.4-1.6 parts by mass of a co-stabilizer; the acrylate composition is prepared by prepolymerizing 15 to 16 parts by mass of butyl methacrylate, 10 to 12 parts by mass of 2-isopropenyl aniline, 5 to 7 parts by mass of allyl glycidyl ether and 1 to 1.2 parts by mass of allyl polyhedral oligomeric silsesquioxane and then combining the prepolymerized materials with 1 to 3 parts by mass of acrylic acid.

The invention belongs to the technical field of organic photoelectric materials, and particularly relates to preparation and application of a benzoselenadiazole covalent organic framework material. According to the invention, benzoselenadiazolyl tetraaldehyde is used as a construction unit, o-toluidine, 4, 4 '-biphenyl diamine or 3, 3'-dihydroxybenzidine is used as a connecting body, and three kinds of novel rigid COFs, namely HBU-COF-CH3, HBU-COF-H and HBU-COF-OH, are synthesized in sequence. The COFs has high cycling stability, has outstanding advantages in the aspect of sustainable heterogeneity of molecular catalysts, and can be used as a heterogeneous photocatalyst to realize efficient hydrogen peroxide production under visible light, and the photocatalytic hydrogen peroxide production performance of the COFs is superior to that of most reported COFs materials. Wherein the yields of HBU-COF-CH3, HBU-COF-H and HBU-COF-OH are as high as 12910 [mu] mol g <-1 > h <-1 >, 8838 [mu] mol g <-1 > h <-1 > and 7679 [mu] mol g <-1 > h <-1 > in sequence.

The preparation method comprises the following steps: S1, mixing a hydrochloric acid solution with organic sodium sulfonate, then adding aniline and water, stirring and dissolving, then adding an oxidizing agent to carry out doping reaction, and carrying out suction filtration, washing, drying and grinding on a reaction product to obtain sodium-modified polyaniline; s2, uniformly mixing a negative electrode active material, a conductive agent and polytetrafluoroethylene, and then adding sodium polyaniline and an organic sodium supplement agent in a nitrogen or inert atmosphere for fibration treatment to obtain fibration powder; and S3, performing hot pressing on the fiberized powder onto the current collector to obtain the lithium ion battery. The prepared pre-sodium-modified negative electrode dry-method electrode has relatively good peeling strength and pole piece flexibility, and the condition that a traditional wet-method thick electrode is easy to crack is relieved; meanwhile, the dry-method electrode subjected to sodium modification treatment can induce uniform deposition of sodium ions, so that the dynamic performance of the whole sodium battery is improved, the problem of cyclic sodium precipitation is avoided, and the service life of the battery is further prolonged.

The invention discloses a positive electrode material of an upward flow type electrochemical dephosphorization system, and the preparation method comprises the following steps: preparing a polyaniline-coated ZIF-8 derived carbon loaded magnesium-aluminum double-metal hydroxide electrode material, and the preparation process comprises ZIF-8 carbonization in a nitrogen atmosphere, aniline oxidation polymerization, and loading of magnesium-aluminum double-metal hydroxide by a coprecipitation method; the electro-adsorption positive electrode material belongs to a polyaniline magnesium aluminum double-metal hydroxide mesoporous synergistic platform in ZIF-8 derived carbon, and has a nano frame with strong pore accessibility and high electrochemical activity; the synergistic process comprises attraction of polyaniline to phosphate ions and trapping of the magnesium-aluminum double-metal hydroxide. The electrode prepared by the method has a unique mesoporous framework, a large number of phosphorus removal sites are obtained on the surface of the electrode, a rapid ion storage behavior mainly based on a capacitance control process is realized on a solid-liquid interface, phosphate in water can be effectively separated in an electro-adsorption system, and the method is a pollution control process with a clear mechanism.

The invention discloses an aniline pyridine amino-aluminum catalyst and a preparation method and application thereof, belonging to the technical field of polyester catalysts. The invention can directly utilize an aniline pyridine amino ligand to react with an aluminum source, and directly drain the solvent after the reaction to obtain a corresponding catalyst. The invention also utilizes the synthesized catalyst to catalyze monomers such as cyclic esters and lactones to prepare biodegradable aliphatic polyesters, and the monomer conversion rate is greater than 96%. Compared with the currently commercialized stannous isooctanoate catalyst, the aniline pyridine amino-aluminum catalyst provided by the invention has higher catalytic activity and lower biological toxicity, and has certain application prospects.

The invention discloses a pyridyl anti-aging agent as well as a synthesis method and application thereof, the anti-aging agent is obtained by taking 5-nitro-N-phenylpyridine-2-amine synthesized by 2-chloro-5-nitropyridine and aniline and iodide synthesized by alcohol and iodine as raw materials, and reacting in the presence of a hydrogen source and a catalyst. The anti-aging agent provided by the invention can effectively slow down the emigration speed of the anti-aging agent in rubber and greatly improve the phenomenon that the appearance of a tire becomes red, has one more N heteroatom than other anti-aging agents in the structure, has good oxidation resistance and flex cracking resistance, and is high in anti-ozone activity, environment-friendly and small in pollution.

The invention relates to a preparation method of a polyurethane-based flexible phase-change material and a battery heat management device. Polyethylene glycol is used as a phase-change material, and adipic dihydrazide (ADH) and 4, 4 '-diphenyltetracarboxylic dianhydride (ADH) are integrated at a condensation end of a heat pipe; at least one of 4, 4 '-diaminobenzanilide (DABA) is used as a cross-linking agent, and at least one of HMDI or IPDI is used as a chain extender to prepare the polyurethane-based flexible phase change material with enthalpy value, flexible rigidity and appropriate phase change temperature. The material not only has excellent mechanical strength and thermal stability, but also has healing property, recoverability and shape memory function. The polyurethane-based flexible phase change material serves as an energy storage film and forms a sealing structure with the condensation end through mechanical pressing. When the temperature rises, the energy storage film B1 absorbs heat and expands, the contact area with the outside is increased, the heat dissipation power is improved, and the heat dissipation efficiency and the heat load management capacity are remarkably improved by maximizing the heat transfer area and utilizing the high latent heat characteristic.

The invention discloses an acrylate conductive composite pressure-sensitive adhesive and a preparation method thereof. The acrylate conductive composite pressure-sensitive adhesive comprises a raw material A and a raw material B, wherein the raw material A comprises 5-15 parts of acrylate polymer; 0.10 to 1.00 parts of epoxy resin; 1.0 to 10.0 parts of aniline; 0.1 to 1.0 part of an initiator; 1-5 parts of conductive particles; and 0.010 to 0.100 part of an amine curing agent. The acrylate conductive composite pressure-sensitive adhesive disclosed by the invention has excellent conductivity and capacitance sensing performance, and shows excellent capacitance stability and relatively high sensitivity in a pressure cycle test; on the basis of containing the conductive filler, the pressure-sensitive adhesive still has better hardness, adhesion strength and tensile strength, and the conductive filler is well dispersed and combined in a pressure-sensitive adhesive system.

The invention discloses an organic fiber AGM separator and application thereof, and belongs to the field of storage batteries. The organic fiber AGM separator comprises high-alkali glass wool, medium-alkali glass fiber, bi-component polyester fiber and slurry containing a nitrogen-doped reduced graphene oxide / lead oxide composite material, the nitrogen-doped reduced graphene oxide / lead oxide composite material is prepared by the following steps: uniformly ultrasonically dispersing graphene oxide, deionized water and absolute ethyl alcohol, slowly dropwise adding aniline, and ultrasonically stirring to obtain a mixed solution; and adding lead acetate powder into the mixed solution, carrying out ultrasonic stirring, hydrothermal reaction, washing and freeze drying, and carrying out pyrolysis in a rare gas atmosphere to obtain the nitrogen-doped reduced graphene oxide / lead oxide composite material. After being prepared into slurry, the AGM separator substrate is coated with the slurry, and then acid leaching and curing are carried out; the material has excellent dendritic stabbing resistance, and the service life of the storage battery is prolonged.

The invention provides a method for monitoring the degradation process of 3-chloroaniline, and relates to the technical field of water environment pollution remediation. According to the method, by combining multi-dimensional monomer isotope fractionation characteristics and experimental test results, theoretical calculation and experimental test are combined, possible degradation ways, degradation mechanisms and environmental attribution of 3-chloroaniline are deduced, and the results are complete and accurate. Compared with a mode of capturing and degrading intermediate products and free radicals only through a test means so as to reversely deduce a degradation pathway, the monitoring method provided by the invention can well make up the defects of experimental tests, deeply understand a degradation mechanism, more scientifically and reliably analyze the degradation pathway, the mechanism and the environmental destination of the pollutant 3-chloroaniline, and has a good application prospect. Key steps are favorably controlled, and the development of a high-efficiency and low-cost remediation technology for the polluted water environment is promoted.

The invention is applicable to the technical field of intelligent response materials, and provides a three-dimensional azobenzene functionalized covalent organic framework intelligent response material and a preparation method thereof. The three-dimensional azobenzene functionalized covalent organic framework intelligent response material is prepared by uniformly grinding 3, 3 ', 5'-tetra [(3 ', 5'-diformylphenyl)]-hexamethyl biphenyl and azobenzene-4, 4 '-diaminotriphenylamine, adding an organic solvent, adding a catalyst acetic acid aqueous solution, quickly freezing, emptying air, sealing with flame, heating after recovering to room temperature, and obtaining the three-dimensional azobenzene functionalized covalent organic framework intelligent response material. According to the invention, the azobenzene functionalized covalent organic framework material with a bcu topological structure is synthesized; the material has excellent photostimulation response CO2 adsorption performance; reversible control of CO2 adsorption capacity can be realized through ultraviolet light and heating conditions, at least five times of circulation can be maintained, and good circulation stability is achieved.

The invention discloses a corrosion-resistant polypropylene edge band material and a preparation method thereof, and belongs to the technical field of preparation of edge band materials. The corrosion-resistant polypropylene edge sealing strip material is prepared from, by weight, 50-75 parts of polypropylene, 2-5 parts of an antioxidant, 3-6 parts of a corrosion-resistant agent, 2-4 parts of a composite flame retardant, 8-15 parts of calcium carbonate and 2-4 parts of dye, the corrosion-resistant agent is prepared from 2, 6-dichlorobenzonitrile, 1, 2, 4-triazole, a sulfuric acid solution, sodium nitrite and parachloroaniline, and the corrosion-resistant agent is prepared from 2, 6-dichlorobenzonitrile, 1, 2, 4-triazole, a sulfuric acid solution, sodium nitrite and parachloroaniline. The composite flame retardant is prepared from 3-glycidyl ether oxypropyl trimethoxy silane, diphenyl silanediol, barium hydroxide and boric acid. The edge band material prepared by the method has excellent corrosion resistance, flame retardance, heat resistance and mechanical properties.

The invention discloses a super-hydrophobic road ice-inhibiting coating based on a photothermal effect and nano modified particles and a preparation method of the super-hydrophobic road ice-inhibiting coating. The preparation method comprises the following steps: introducing silane modified nano silicon dioxide (SiO2) and titanium dioxide (TiO2) particles into a polyaniline solution, and preparing the composite super-hydrophobic powder through a chemical oxidation polymerization method. The preparation method comprises the following steps: firstly, modifying the surfaces of SiO2 and TiO2 nanoparticles by adopting a silane coupling agent, and endowing the SiO2 and TiO2 nanoparticles with low surface energy and hydrophobic property; and then adding the modified nano-particles into an aniline monomer solution, reacting with doped acid and an oxidizing agent, so that polyaniline molecules are subjected to in-situ polymerization on the surfaces of the particles, and the composite super-hydrophobic powder with a micro-nano structure is formed. The obtained composite material has excellent photothermal conversion performance and super-hydrophobic performance at the same time, and the efficient photothermal material heat absorption ice melting effect and the synergistic ice restraining effect of the photothermal material and the super-hydrophobic material can be achieved. Compared with a traditional ice-inhibiting coating, the coating disclosed by the invention shows stronger ice-resisting capability in a low-temperature and high-humidity environment, has good durability, mechanical stability and environmental protection property, and is suitable for the field of ice prevention and ice inhibition in cold regions such as roads, bridges, airport runways and the like.

The invention discloses a method for joint production of cyclohexylamine and dicyclohexylamine, which comprises the following steps: 1) feeding aniline tail gas of a nitrobenzene catalytic hydrogenation production device into a gas-liquid separator for gas-liquid separation to obtain aniline tail hydrogen and aniline condensate; 2) mixing aniline tail hydrogen and new hydrogen as a raw material A, and mixing defective aniline and fresh aniline in proportion as a raw material B; (3) feeding the vaporized raw material B and the vaporized raw material A into a fixed bed reactor according to a certain hydrogen-oil ratio, and carrying out hydrogenation reaction; a hydrogenation reaction product is subjected to heat exchange condensation and then enters a gas-liquid separator for gas-liquid separation, a gas phase serves as recycle hydrogen to be mixed with the raw material A, and a liquid phase is fed into a distillation device; and 4) carrying out primary distillation and rectification purification in sequence to obtain cyclohexylamine and dicyclohexylamine. According to the method, aniline tail gas resources and defective aniline are fully utilized, the three-waste treatment cost is reduced, product benefits can be improved, pollution to the environment can be reduced, and economic benefits and social benefits are remarkable.

The invention relates to the technical field of ton bag lining materials, and particularly discloses a shielding antistatic ton bag lining bag and a preparation method thereof. The invention relates to a shielding antistatic ton bag lining bag, which is prepared by processing a multi-layer composite film with a structure of PET / antistatic layer / PA / PE, and the antistatic layer is prepared from the following raw materials by weight: 40-75 parts of a resin material; 20 to 40 parts of filler; 5-10 parts of a color master batch; 1-3 parts of an antistatic agent; 2-5 parts of a dispersant; 0.2 to 0.4 part of an antioxidant; 4 to 6 parts of polyimide nanofiber; 1-3 parts of a modified carbon nanotube; the modified carbon nanotube is prepared by the following method: S1, pretreating a carbon nanotube raw material with a concentrated nitric acid solution to obtain a pretreated carbon nanotube; and S2, dispersing the pretreated carbon nanotubes in xylene, then adding deionized water and p-toluenesulfonic acid, then adding an aniline monomer, then adding ammonium persulfate, and carrying out a reaction to obtain the composite material after the reaction is finished. The shielding anti-static ton bag lining bag can keep stable anti-static performance under the influence of a severe temperature change environment.

The invention discloses a stress whitening resistant polyamide composite material, which comprises the following components by weight: 74-86 parts of polyamide; 0.1-1 part of rice bran wax metal salt; 5-30 parts of a toughening agent; and 0.3 to 0.8 part of carbon black and 0.1 to 0.5 part of aniline black. The rice bran wax salt is used as a nucleating agent to reduce the grain size of the crystal, the aniline black can improve the tinting power to a crystalline region to reduce light reflection at a stress whitening position, the carbon black can also adjust the tinting power to the crystal and an amorphous region, and under the cooperation of the three, the grain size of the crystal is reduced to be smaller than the wavelength of visible light to realize absorption of visible light. Light reflection caused by tiny gaps generated by separation of the flexibilizer and a polyamide resin matrix after the polyamide composite material is bent under stress is improved, and the defect of stress whitening of the polyamide composite material is remarkably reduced.

The invention discloses a preparation method and application of a zinc-bromine flow battery positive electrode material, and belongs to the field of zinc-bromine flow batteries. The preparation method comprises the following steps: dissolving aniline and a dithio compound in an acidic ice bath, dropwise adding a peroxy strong oxidant to generate a polyaniline-disulfide bond copolymer, dialyzing, and freeze-drying to obtain powder; then heating soluble silver salt, a reducing agent, a hydrophilic dispersing agent and an organic sulfydryl silane coupling agent to prepare functionalized nano-silver particles; the powder and nano-silver particles are dispersed in N-methyl pyrrolidone for ultrasonic treatment, and dynamic self-repairing coating slurry is prepared; and performing acid pretreatment on the carbon fiber paper, and performing electrochemical deposition on the slurry to prepare the zinc-bromine battery positive electrode material. According to the zinc-bromine battery positive electrode material, the coulombic efficiency and the voltage efficiency of a zinc-bromine flow battery are remarkably improved and the cycle life of the zinc-bromine flow battery is remarkably prolonged through methods of dynamic covalent bonds, nano-silver catalysis, a hierarchical pore structure, carbon fiber pretreatment and the like, and the zinc-bromine flow battery positive electrode material has chemical stability, efficient bromine adsorption capacity and excellent catalytic activity.

The invention belongs to the technical field of water-based ink, and particularly relates to low-dielectric-loss black water-based ink and a preparation method thereof.The preparation method comprises the following steps that aniline black is ground to the nanoscale particle size; the preparation method comprises the following steps: mixing nano aniline black, an emulsifier, a coupling agent, an initiator and deionized water to prepare a pre-dispersion liquid; the preparation method comprises the following steps: mixing and emulsifying an acrylate monomer, an emulsifier, a PH buffer agent and deionized water to prepare a seed emulsion; dropwise adding the pre-dispersion liquid into a seed emulsion, and carrying out a graft polymerization reaction to generate a nigrosine-acrylate hybrid emulsion; and mixing the hybrid emulsion with an auxiliary agent to prepare the black water-based ink. The dielectric loss of the black ink layer is reduced, and the process requirements that the black ink layer is not prone to overheating and scorching when the black ink layer is subjected to microwave drying to remove moisture are met. The compatibility of aniline black powder and water-based resin is improved, and the problems of dispersion and precipitation of high-concentration aniline black powder are solved. And the secondary agglomeration condition of the nigrosine powder is obviously reduced.

The invention belongs to the technical field of polyether polyol, and particularly relates to flame-retardant polyether polyol with a low heat conductivity coefficient as well as a preparation method and application of the flame-retardant polyether polyol. The flame-retardant polyether polyol with the low heat conductivity coefficient is obtained by polymerizing bis (2-hydroxyethyl) aminomethyl diethyl phosphonate, halogen-containing aniline and small molecular alcohol / alcohol amine as a ternary mixed initiator with alkylene oxide under the action of a catalyst, the ternary mixed initiator comprises the following components in percentage by mass: 12.15 to 22.78 percent of bis (2-hydroxyethyl) amino methyl diethyl phosphonate, 43.21 to 63.89 percent of halogen-containing aniline, and 23.96 to 34.01 percent of small molecular alcohol / alcohol amine. The polyether polyol realizes comprehensive properties of lasting flame retardance, high strength and low heat conductivity. The invention also provides a preparation method of the polyether polyol and application of the polyether polyol in rigid polyurethane foam.

The invention discloses a production process of a modified p-phenylenediamine rubber anti-aging agent, which comprises the following steps: S1, catalyzing a ring-closure reaction through lipase, and accurately controlling pH by combining a phosphate buffer solution, so that the bonding efficiency of 6PPD and tea polyphenol is remarkably improved, and the release amount of aniline is effectively reduced; s2, carrying out spray drying to obtain EP-TP powder to control the particle morphology; s3, increasing the load rate of the anti-aging agent and effectively inhibiting the migration rate of the anti-aging agent through the pore diameter physical confinement of mesoporous silica and an amination gas phase modification technology, and ensuring uniform dispersion of anti-aging agent particles through the synergistic effect of staged load reaction and a polyethylene glycol dispersant; and S4, the particle morphology is cooperatively controlled through vacuum microwave drying, the dispersion requirement of the rubber mixing technology is met, and the interface bonding strength is improved by combining the staged loading reaction with a polyethylene glycol dispersing agent.

The invention discloses an organic wastewater adsorbent as well as a preparation method and application thereof, and belongs to the technical field of sewage treatment. Comprising the following steps: carrying out nitration reaction on styrene porous microsphere resin, and then carrying out reduction reaction to obtain amino-modified porous microsphere resin; the preparation method comprises the following steps: carrying out polymerization reaction on high-nitrogen-content amino organic small molecules and aldehyde group small molecules under the action of a basic catalyst in an adsorption polymerization manner to generate a nitrogen-doped organic porous polymer, and coating the surface of amino-modified porous microsphere resin with the nitrogen-doped organic porous polymer to obtain the organic wastewater adsorbent. The porous microsphere resin adsorbent with large adsorption capacity and high organic matter removal rate is synthesized by using the carrier advantage of styrene microsphere resin and introducing a porous heteroatom polymer on the microsphere resin. When the adsorbent is used, the adsorbent is directly added into an organic wastewater solution, and the removal rate of bisphenol A, aniline and tetracycline can reach 90% or above.

The invention belongs to the technical field of lithium battery positive electrode materials, and provides high-compaction-density lithium iron phosphate and a preparation method thereof.The preparation method comprises the following steps that 1, pretreated polyvinyl alcohol is added into deionized water, the temperature is increased to 80-85 DEG C, stirring is conducted, the pH value is adjusted to 10.5-11.0, epichlorohydrin is added for a reaction, aniline is added for a continuous reaction, cooling is conducted, and a product is obtained; adjusting the pH value to 1-2, adding ammonium persulfate for reaction, and dialyzing to remove impurities to obtain modified polyvinyl alcohol; step 2, adding a lithium source, an iron source and a phosphorus source into deionized water for mixing, and performing ball milling and drying to obtain a lithium iron phosphate precursor; step 3, putting the lithium iron phosphate precursor into a tubular furnace, adding an inorganic carbon source, heating for reaction, cooling and crushing to obtain primary sintered lithium iron phosphate; and step 4, mixing the primarily sintered lithium iron phosphate and the modified polyvinyl alcohol, placing the mixture in a tubular furnace, carrying out heating reaction, cooling and crushing to obtain the lithium iron phosphate.