2991 results about "Acyl chloride" patented technology

The invention relates to the technical field of organic synthesis, and discloses a preparation method of bromo-pyrrole nitrile. The method comprises the following steps: (1) mixing p-chlorophenylglycine, acetonitrile, trifluoroacetic acid and a catalyst, then dropwise adding acyl chloride and carrying out acylation reaction, and after the reaction is completed, purging with an inert gas; (2) under the inert gas, mixing the mixture obtained in the step (1) with inorganic salt, then dropwise adding 2-chloroacrylonitrile, carrying out cyclization reaction, and separating a liquid phase from the obtained mixture; and (3) under the inert gas, mixing the liquid phase obtained in the step (2), hydrobromic acid and hydrogen peroxide, carrying out a bromination reaction, then extracting with acetonitrile to obtain an acetonitrile layer, then removing the acetonitrile, and then carrying out cooling crystallization to obtain the bromo-pyrrolenitrile. According to the technical scheme, the reaction yield is high, different solvents do not need to be frequently replaced, and the solvents can be recycled.

The invention belongs to the technical field of flame-retardant materials, and particularly relates to a phenylboronic acid-based P / N / B-containing halogen-free flame retardant, a preparation method thereof and application of the phenylboronic acid-based P / N / B-containing halogen-free flame retardant in epoxy resin. The preparation method comprises the following steps: by taking diphenyl hypophosphorous chloride as a basis, preparing a flame-retardant intermediate through nucleophilic substitution reaction between diphenyl hypophosphorous chloride and an aldehyde group-containing phenolic compound, then reacting a phenylboronic acid structure with 3-amino-1, 2-propylene glycol to obtain an amino group-containing phenylboronic acid compound, and finally reacting the phenylboronic acid compound with 3-amino-1, 2-propylene glycol to obtain the amino group-containing phenylboronic acid compound. And finally, carrying out a Schiff base reaction on the flame-retardant intermediate and an amino-containing phenylboronic acid compound to obtain the halogen-free flame retardant containing phosphorus, nitrogen and boron elements. The flame retardant provided by the invention can significantly improve the flame retardant property and mechanical property of epoxy resin. A flame-retardant epoxy resin prepared based on the flame retardant; the influence on Tg of an epoxy resin cured product is small, the smoke suppression and char formation performance and the mechanical performance of the cured product can be remarkably improved, and meanwhile, the flame retardant has excellent flame retardant efficiency; the limit oxygen index of the flame-retardant epoxy resin can reach 31%; the vertical combustion grade is V-0 or above, and the carbon residue amount can reach 18% or above.

The invention provides a PVDF (Polyvinylidene Fluoride) nanofiltration membrane constructed on the basis of microwave-enhanced bridging interfacial polymerization as well as a preparation method and application of the PVDF nanofiltration membrane. The method comprises the following steps: reacting PVDF powder with an organic alkali to prepare a modified film-forming solution, blade-coating the modified film-forming solution on a non-woven fabric supporting layer, placing the non-woven fabric supporting layer in an ethanol-water or methanol-water coagulating bath, and preparing a PVDF supporting film by virtue of assistance of an ice template; weighing the functionalized nano material and an amino silane coupling agent, performing ultrasonic dispersion, and adding a catalyst for reaction to obtain dispersion liquid; immersing a PVDF support membrane into the dispersion liquid to obtain a modified membrane; immersing the modified membrane into an aqueous solution containing an amine monomer and an organic solution containing an acyl chloride monomer, and carrying out microwave radiation. The interface reaction rate and selectivity are enhanced through the microwave excitation effect, and meanwhile, the hydrophilicity and reaction activity of the PVDF base membrane are cooperatively regulated and controlled, so that the separation efficiency and the anti-pollution capacity of the membrane are remarkably improved. The obtained PVDF nanofiltration membrane has high flux, high selectivity and excellent structural stability, and is suitable for efficient purification and resource recovery application in a complex water system.

The invention discloses a desalting membrane as well as a preparation method and application thereof, and relates to the technical field of membrane separation. The desalting membrane comprises a porous ultrafiltration base membrane and a functional layer formed on the surface of the porous ultrafiltration base membrane; the functional layer is formed by copolymerizing and cross-linking a polyamine monomer, a zwitterionic multi-element hydroxyl monomer and an acyl chloride monomer through an interfacial polymerization reaction. The preparation method comprises the following steps: providing the porous ultrafiltration base membrane; coating the surface of the porous ultrafiltration base membrane with an alkaline water-phase solution containing a polyamine monomer and a zwitterionic multi-hydroxyl monomer to form a water-phase solution layer; coating an oil-phase solution containing an acyl chloride monomer on the surface of the water-phase solution layer to form a functional layer; and performing heat treatment. The invention also provides application of the desalination membrane in any one of seawater desalination, brackish water desalination, wastewater treatment and material separation and concentration. According to the invention, zwitter-ion-based multi-hydroxyl monomers are introduced into water-phase monomers to participate in interfacial polymerization, and a super-hydrophilic nano-channel is constructed in a separation layer, so that the water flux and the desalination rate of the membrane are remarkably improved.

The present invention discloses a perfluoromethylcyclohexanone microcapsule fire extinguishing medium and its preparation process, which relates to the field of fire fighting technology. A perfluoromethylcyclohexanone microcapsule fire extinguishing medium is composed of a core material and a shell material. The core material includes perfluoromethylcyclohexanone, silicon dioxide, and azobisisobutyronitrile. The shell material includes modified guar gum, acrylic resin, aluminum hydroxide, potassium nitrate, and an emulsifier. The modified guar gum is prepared by the following method: tetrahydrofuran, guar gum, and triethylamine are sequentially added into a reactor, stirred and mixed evenly, and then a tetrahydrofuran solution of diphenylphosphinyl chloride is added dropwise. After the addition is completed, the temperature is raised to 75-85°C and the reaction is carried out for 10-14 hours, followed by post-treatment to obtain diphenylphosphinyl chloride-modified guar gum. The present invention modifies guar gum with diphenylphosphinyl chloride and then uses the modified guar gum for the shell material of perfluoromethylcyclohexanone microcapsules, improving the fire extinguishing performance, heat resistance, and long-term stability of perfluoromethylcyclohexanone microcapsules.

The invention discloses a low-cost and environment-friendly process for producing 1, 4-bis (4-fluorobenzoyl) benzene, and belongs to the technical field of Friedel-Craft reaction, fluorobenzene and paraphthaloyl chloride react to generate 1, 4-bis (4-fluorobenzoyl) benzene, after reaction quenching, filtering is performed to obtain a crude product 1, 4-bis (4-fluorobenzoyl) benzene and filtrate, and the 1, 4-bis (4-fluorobenzoyl) benzene is purified in a sublimation crystallization mode; standing and layering the filtrate in an inclined plate layering device, respectively treating an oil layer and a water layer, dehydrating a fluorobenzene layer in a dehydrating tower, and returning fluorobenzene; the water phase is firstly subjected to organic matter removal treatment, the obtained organic matter enters a fluorobenzene recovery device to be sleeved back, and the obtained water phase is a byproduct of crystallized aluminum chloride in an evaporative crystallization device. According to the process, the 1, 4-bis (4-fluorobenzoyl) benzene is produced in a sublimation crystallization mode instead of a solution crystallization mode, no waste solvent is generated, the waste solvent does not need to be recycled, the cost is low, organic matter removal and evaporative crystallization treatment is carried out on wastewater, organic matter recycling is carried out, crystalline aluminum chloride is produced as a byproduct, and wastewater and waste salt are not discharged.

The invention relates to the technical field of material science and engineering, and discloses a nanocellulose-based oil-water separation and adsorption composite material, which is prepared from the following raw materials in parts by mass: 35 to 45 parts of nanocellulose; 8 to 11 parts of bagasse cellulose; 10 to 15 parts of sodium lignin sulfonate; 4 to 8 parts of chitosan; 5-10 parts of oxidized starch; 5 to 8 parts of cellulose nanowhiskers; 2-5 parts of silicon dioxide nanoparticles; 0.5 to 1 part of calcium carbonate nanoparticles; 1-2 parts of a citric acid cross-linking agent; 1-2 parts of graphene oxide; 0.3 to 0.6 part of ethylene diamine tetraacetic acid; 2-5 parts of glycerol; 0.4 to 1 part of stearoyl chloride; 2-4 parts of nano iron oxide; the preparation method comprises the following steps: pretreating the raw materials, mixing the pretreated raw materials into slurry, carrying out crosslinking and ultrasonic dispersion, standing to obtain a basic mixture, injecting the basic mixture into a mold, carrying out freeze drying to form a photocatalytic layer, carrying out centrifugal dewatering, carrying out chelation reaction, spraying a composite solution, and carrying out vacuum drying to obtain the photocatalytic material. The obtained composite material has the advantages of efficient adsorption capacity, good mechanical properties, environmental friendliness, degradability and low preparation cost.

The invention relates to the field of cables, and discloses a modified polyvinyl chloride composite material for cables and a preparation method thereof.The composite material comprises low-density polyethylene, polyvinyl chloride, ethylene-vinyl acetate copolymer, nitrile rubber, modified graphene oxide, modified nano calcium carbonate and auxiliaries; the modified graphene oxide is prepared by reacting acylating chlorination of graphene oxide with an anti-aging derivative, the anti-aging derivative is prepared by reducing a benzoxazole-containing intermediate generated by a reaction of 2-amino-4-bromophenol and 4-cyanobenzaldehyde to obtain an aminated benzoxazole-containing intermediate, then the aminated benzoxazole-containing intermediate reacts with p-phenylenediamine, and then the product reacts with 3-(3, 4-dichlorophenyl)-1, 2, 3-triazole-3-one to obtain the anti-aging graphene oxide. 2, 5-di-tert-butyl-4-hydroxyphenyl) propionyl chloride is subjected to a reaction to prepare the product. And the modified nano calcium carbonate is prepared by reacting phosphonitrilic chloride trimer with an amino silane coupling agent and 2-amino benzoxazole-5-borate and then grafting on the surface of the nano calcium carbonate. The composite material prepared by the invention has excellent flame retardance, heat resistance and long-acting oxidation resistance.

The invention belongs to the technical field of acyclic compounds, and particularly relates to a preparation method of tert-butyl peroxyisobutyrate. Stirring and cooling a solvent, a tert-butyl hydroperoxide aqueous solution and deionized water to obtain a mixed solution A; adding liquid caustic soda and a solid base catalyst into the mixed solution A under a stirring condition, and continuously stirring for reaction to obtain a mixed solution B; under the stirring condition, isobutyryl chloride and a water-soluble distributing agent are added into the mixed solution B, stirring reaction continues to be conducted, and a mixed solution C is obtained; standing and layering the mixed solution C, separating to obtain a tert-butyl peroxyisobutyrate crude product, and refining the tert-butyl peroxyisobutyrate crude product to obtain the tert-butyl peroxyisobutyrate. According to the method, the raw material utilization rate is increased, the reaction speed is increased, the reaction time is shortened, and the product yield is high.

A flame-retardant laminated solid wood composite floor and a manufacturing method therefor. The manufacturing method comprising: first reacting dopamine hydrochloride with acryloyl chloride to generate a dopamine acrylamide monomer; by means of a double bond in the dopamine acrylamide monomer, carrying out a click reaction with a phosphate monomer containing a sulfydryl group, so as to introduce a catechol group into a side chain of the phosphate monomer and obtain a flame-retardant monomer containing the double bond; and then mixing pentaerythritol tetra(3-mercaptopropionate), pentaerythritol triacrylate, perfluorodecanethiol and the flame-retardant monomer containing the double bond to obtain a photocurable coating material. The coating material is photocured after being coated on the surface of a wood veneer, thus effectively improving the flame-retardant performance of the wood veneer; moreover, the adhesion between the coating layer and the wood veneer is excellent. The wood veneers are laminated in multiple layers, are glued and assembled into a layered structure, and then hot-pressed to form the solid wood composite floor, thus improving the comprehensive performance.

The invention relates to the technical field of polyester fibers, and discloses a preparation method of antibacterial modified polyester hollow fibers, which comprises the following steps: by taking nitrilotriacetic acid, thionyl chloride, epoxy chloropropane, eugenol and the like as raw materials, carrying out acylating chlorination reaction, quaternization reaction and esterification reaction to obtain eugenol epoxy quaternary ammonium salt. The preparation method comprises the following steps: carrying out ring-opening reaction on carboxyl groups in graphene oxide and epoxy groups in eugenol epoxy quaternary ammonium salt to obtain modified graphene, uniformly mixing the modified graphene with polyethylene glycol terephthalate, and carrying out a series of steps to finally obtain the antibacterial modified polyester hollow fiber. Eugenol and quaternary ammonium salt are utilized to improve the antibacterial property of the polyester hollow fiber, and graphene is utilized to improve the mechanical property of the polyester hollow fiber. The polyester hollow fiber prepared by the invention has excellent mechanical properties and antibacterial properties.

The invention provides a polyimide multilayer composite membrane material as well as a preparation method and application thereof, and belongs to the technical field of gas separation. According to the method, through collaborative design of a functional support layer, a gradient MOF layer and an ultrathin selection layer structure, the problems of support layer pore seepage, MOF agglomeration, weak interface bonding and the like in an existing composite membrane material are solved. The preparation method comprises the following steps: firstly, carrying out electrostatic spinning on a polyamide acid glue solution, and synchronously introducing dopamine by adopting a chemical imidization method to prepare a functionalized polyimide fiber membrane containing hydroxyl and amino on the surface, so that the mechanical property of a supporting layer and the MOF anchoring capability are remarkably improved; growing MOF layers with different particle sizes on the surface of the fiber membrane by regulating and controlling the concentration gradient of ligand / metal salt and the reaction time, and passivating through a silane coupling agent after each step of growth so as to avoid heterogeneous nucleation and construct a gradient structure; after the MOF gradient layer is subjected to Ar plasma pretreatment to introduce hydroxyl, the ultrathin polyamide selection layer is formed by utilizing interfacial polymerization of fluorine-containing acyl chloride and a macrocyclic amine monomer, and the ultrathin polyamide selection layer is suitable for gas separation work.

The invention relates to the field of plastic bags, and discloses a biodegradable plastic bag and a preparation method thereof, the biodegradable plastic bag comprises polylactic acid, poly (butylene adipate-co-terephthalate), a functional additive, modified starch, a lubricant and an antioxidant; the functional additive is prepared by grafting hydroxylated modified castor oil and isocyanated montmorillonite loaded titanium dioxide; the hydroxylation modified castor oil is prepared by modifying castor oil with chloroethyl isocyanate, then reacting with N-allylimidazole, and then reacting with 6-mercaptohexyl-1-alcohol; the isocyanated montmorillonite loaded titanium dioxide is prepared by reacting montmorillonite loaded titanium dioxide obtained by a sol-gel method with isophorone diisocyanate; the modified starch is prepared by reacting octadecanoyl chloride and acryloyl chloride with starch, then carrying out graft copolymerization with ethyl acrylate and further introducing glycidyl methacrylate, so that the plastic bag is endowed with excellent mechanical properties, biodegradability and antibacterial property.

The invention discloses a surface-enhanced tryptophan modified nanofiltration membrane as well as a preparation method and application thereof. Belongs to the field of water treatment membrane preparation. The invention aims to solve the technical problems of non-uniform pore size distribution and surface hydrophobicity of the conventional nanofiltration membrane. The method comprises the following steps: adding tryptophan into a piperazine water-phase solution, and carrying out interfacial polymerization with oil-phase trimesoyl chloride to prepare the tryptophan modified nanofiltration membrane. According to the preparation method, the diffusion rate of the piperazine monomer can be adjusted in the interfacial polymerization process by utilizing a similar surfactant structure of tryptophan, meanwhile, the tryptophan has hydrophilicity and can improve the hydrophilicity of the surface of an active layer, and the prepared modified nanofiltration membrane is reduced in molecular weight cut-off, improved in surface hydrophilicity and good in water resistance. The retention rate of organic micro-pollutants is improved, and meanwhile, good anti-pollution performance is achieved.

The invention discloses an electrolytic adhesive, an electrolytic cotton adhesive tape and a preparation method of the electrolytic adhesive. The electrolytic cotton adhesive tape comprises the following components in parts by weight: 5-10 parts of 1, 1 '-ferrocene diformyl chloride, 10-15 parts of acrylic acid beta-cyclodextrin ester, 3-8 parts of polyethylene glycol diglycidyl ether, 10-20 parts of ionic liquid, 1.5-3 parts of a cross-linking agent, 10-15 parts of tackifying resin and 0.5-1.5 parts of an initiator, and a polymer matrix comprises an acrylic acid-hydroxypropyl acrylate copolymer and acrylic acid-2-ethylhexyl ester. Comprising an adhesive layer and an adhesive tape base layer, the adhesive layer is prepared from the electrolytic adhesive, and the adhesive tape base layer is prepared from acrylic foam; the obtained electrolytic cotton adhesive tape has high initial adhesion and viscosity strength after power-on and power-off re-adhesion.

The invention relates to the field of packaging materials, and discloses low-temperature heat-sealing water-based coated paper and a preparation method and application thereof.The water-based coated paper comprises a base paper layer and a water-based coating, and the water-based coating comprises water-based ethylene-acrylic acid copolymer emulsion, modified nano-silica, a coalescing agent and water; a cardanol derivative is introduced into the water-based ethylene-acrylic acid copolymer emulsion as a functional component; the cardanol derivative is prepared by reacting epoxidized cardanol with 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide and then grafting with acryloyl chloride. The preparation method comprises the following steps: reacting epoxidized cardanol with 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide; the modified nano silicon dioxide is prepared by mixing aminated nano silicon dioxide and chitosan and adding a cross-linking agent prepared by grafting phytic acid and ethylene glycol diglycidyl ether. The water-based coating paper prepared by the invention overcomes the defects that the existing BOPP film is not environment-friendly, and the conventional coating paper is high in heat sealing temperature and easy to stick; meanwhile, good mechanical properties, water resistance and flame retardance are achieved.

The invention relates to the technical field of polymer photoelectric materials, in particular to a preparation method of a supramolecular gel electrolyte. The method comprises the following steps: esterifying tetraphenylethylene alcohol and methacryloyl chloride to form tetraphenylethylene methacrylate, and performing staged linear heating polymerization on the tetraphenylethylene methacrylate, 3-(methacrylamido) propyl dimethyl 3-thiopropyl ammonium oxide inner salt, acrylic acid, tetraphenylethylene methacrylate and 4-vinylpyridine under the action of ammonium persulfate to obtain a tetraphenylethylene copolymer. And finally, soaking in a lithium chloride aqueous solution to obtain the supramolecular hydrogel electrolyte. The hydrogel obtained by the invention has high mechanical strength and high ionic conductivity, and is suitable for energy storage devices such as flexible supercapacitors and the like.

The invention discloses a preparation method of a dotenorad key intermediate, and belongs to the technical field of compound synthesis. In the preparation method of the dotenorad key intermediate, provided by the invention, 2-aminothiophenol and formaldehyde are used as raw materials to carry out cyclization reaction to prepare a compound as shown in a formula 1, and then the compound as shown in the formula 1 and 3, 3, 3, 3, 3, 3, 3, 3, 3, 3, 3, 3, 3, 3, 3, 3, 3, 3, 3, 3, 3, 3, 3, 3, 3, 3, 3 According to the method, 3-(3, 5-dichloro-4-methoxybenzoyl chloride)-2, 3-dihydro-1, 3-benzothiazole is used as a raw material, an amidation reaction is carried out on 3, 5-dichloro-4-methoxybenzoyl chloride in an aqueous solution of an organic solvent, and the key intermediate 3-(3, 5-dichloro-4-methoxybenzoyl)-2, 3-dihydro-1, 3-benzothiazole of dotenorad can be effectively prepared; the obtained dotenorad key intermediate is relatively high in yield and purity; moreover, benzothiazoline which is widely used in the prior art does not need to be used in the preparation method, an activating agent or a solubilizer does not need to be used, the operation method is simple, reaction conditions are mild, and the method is suitable for actual industrial production.

The invention discloses a method for preparing a polyvinyl polyamide composite reverse osmosis membrane by coupling reversed-phase interfacial polymerization with lignosulfonate, which adopts a reversed-phase interfacial polymerization method and comprises the following steps: firstly adding an oil phase containing polyacyl chloride, and then adding a water phase containing amine monomers and lignosulfonate. Molecules of the lignosulfonate contain more sulfonate radicals, so that the lignosulfonate is endowed with hydrophilicity, meanwhile, a large number of active functional groups such as phenolic hydroxyl groups, alcoholic hydroxyl groups and carboxymethyl exist, and oxygen atoms, sulfur atoms and the like in the functional groups contain unbonded electron pairs and can participate in interfacial polymerization reaction to form a cross-linked structure; the trade-off effect of the flux and the rejection rate of the reverse osmosis membrane is broken, and the polyvinyl polyamide reverse osmosis membrane with high flux and high rejection rate is obtained. The raw material of the polyethylene base material is low in price, and the product can be applied to the fields of water treatment, seawater desalination, brackish water desalination and the like on a large scale.

The invention relates to an electromagnetic shielding resistant PPS alloy material containing modified carbon nanotubes, and belongs to the technical field of polymer composite materials. The PPS alloy material comprises 70-85 parts of polyphenylene sulfide, 5-15 parts of polyether-ether-ketone or a liquid crystal polymer, 3-8 parts of carbon nanotubes subjected to acyl chloride-amido double-step modification and 5-12 parts of carbon fibers subjected to oxidation treatment, and the carbon fibers subjected to oxidation treatment are covalently connected with the carbon nanotubes subjected to double-step modification. 0.5 to 1.5 parts of a coupling agent, 0.3 to 0.8 part of an antioxidant and 0.2 to 0.6 part of a lubricant. According to the invention, the carbon nanotubes are subjected to surface grafting group modification, and the carbon fibers are subjected to surface oxidation treatment, so that the technical problems that the carbon nanotubes are easy to agglomerate, the interface between the carbon fibers and the matrix is weak, and the shielding efficiency and the mechanical property are difficult to consider are solved, and the carbon nanotubes and the PPS matrix form a composite reinforced structure; the comprehensive improvement of the material in the aspects of electromagnetic shielding, mechanical property, thermal stability and the like is realized.

The invention discloses a polyetherketoneketone high-temperature-resistant wear-resistant non-stick coating and a preparation method thereof. The coating is prepared from the following components in parts by mass: 13 to 30 parts of a resin matrix group (containing 12 to 25 parts of titanium modified polyether ketone ketone resin, 1 to 5 parts of fluorine-free viscous resin and 0.65 to 6 parts of aluminum oxide), 0.5 to 3 parts of a nano reinforced group (containing 0.5 to 3 parts of KH-550 modified nano titanium dioxide, 0.025 to 0.6 part of cerium dioxide and 0.5 to 3 parts of boron nitride) and 62 to 71 parts of an auxiliary agent group. The preparation method comprises the following steps: 1) taking diphenyl ether, paraphthaloyl chloride and isophthaloyl chloride as monomers, and synthesizing titanium modified polyether ketone ketone resins with different viscosities through segmented polymerization (1.5-2.0 hours or 3.0-4.0 hours); 2) respectively preparing a smooth bottom layer water dispersion slurry and a wrinkled surface layer water dispersion slurry; and (3) forming a compact bottom layer and a micro-wrinkle surface layer on the base material by adopting a layered spraying and stepped sintering process (280-320 DEG C, 10-20 minutes). The whole system of the coating is fluorine-free and has temperature resistance gt; the coating has the characteristics of high temperature resistance (350DEG C), wear resistance (Taber wear rate of 3-5mg / 1000r), non-sticking (contact angle gt, 100 DEG C) and heavy corrosion resistance, and is suitable for cooking utensils and chemical equipment.

The invention relates to the technical field of membrane separation, in particular to a preparation method of a pH-step-by-step thermocuring regulation sodium-magnesium separation nanofiltration membrane. The method comprises the following steps: (1) pre-treating a base membrane; (2) preparation and treatment of an aqueous phase solution: S1, preparing the aqueous phase solution according to mass fraction: sequentially adding 1.2%-1.6% of piperazine, 0.10%-0.14% of triaminopyrimidine and 0.14%-0.18% of polyethylene glycol into deionized water, and stirring until the piperazine, the triaminopyrimidine and the polyethylene glycol are completely dissolved to form the aqueous phase solution; s2, adjusting the pH value of the water-phase solution to 10-11 by using hydrochloric acid; s3, pouring the water-phase solution of which the pH is adjusted on the surface of the pretreated base membrane, standing, and blow-drying to form a uniform water-phase layer; (3) interfacial polymerization reaction: S1, preparing an oil phase solution: adding 0.10-0.14% of trimesoyl chloride into n-hexane, and performing ultrasonic treatment until the trimesoyl chloride is completely dissolved; s2, pouring the oil-phase solution on the surface of the base membrane subjected to water-phase treatment, and after reaction, pouring out redundant solution to form a polyamide separation layer, so as to obtain a membrane sheet; (4) performing a step-by-step thermocuring process; and (5) cleaning and storing.

The invention discloses a preparation method of lithium trifluoromethanesulfinate, and belongs to the field of lithium ion battery materials. The preparation method of the lithium trifluoromethanesulfinate comprises the following steps: 1, mixing trifluoromethanesulfonyl chloride, lithium sulfite, lithium bicarbonate and a first solvent, and heating to react; 2, dissolving the concentrated crude product in a second solvent, and filtering and separating a lithium sulfate solid; and 3, concentrating the filtrate, adding a third solvent, uniformly stirring, filtering and separating the lithium chloride solid, and concentrating to obtain the lithium trifluoromethanesulfinate. According to the method for preparing the lithium trifluoromethanesulfinate, the yield can reach 94%, the operation is simple, byproducts are easy to separate, and the method is suitable for industrial production. In addition, the obtained by-product lithium sulfate can be used for preparing lithium sulfide, the by-product lithium chloride can be used for preparing solid electrolyte, and resource utilization is achieved.

The invention relates to the technical field of aramid fibers, in particular to a heterocyclic aramid fiber and a preparation method thereof.The preparation method comprises the steps that S1, p-phenylenediamine, benzimidazole diamine and terephthaloyl chloride are subjected to a polymerization reaction in an amide solvent, and a polymer stock solution is obtained; s2, the polymer stock solution is subjected to spinning through a spinning nozzle, coagulating bath forming, drafting bath, alkali washing, water bath, drying, hot drafting, oiling and winding into a barrel, and the heterocyclic aramid fiber is obtained. In the step S1, the polymerization reaction temperature is-10 DEG C to 0 DEG C. According to the heterocyclic aramid fiber prepared by the preparation method, the problems of broken filaments, doubled filaments, sticky filaments, broken filaments and the like are obviously improved, the mechanical property is improved, the irregularity is reduced, and the product quality is excellent. The tensile strength of the heterocyclic aramid fiber is 30 to 37 cN / dtex, the elongation at break of the heterocyclic aramid fiber is 3.0 to 4.0 percent, and the elastic modulus of the heterocyclic aramid fiber is 950 to 1150 cN / dtex.

A preparation method of an emulsion type aramid fiber sizing agent belongs to the technical field of fiber surface treatment, and the specific scheme is as follows: preparing aromatic polyamide from corresponding diamine and acyl chloride, then reacting with epoxy resin to prepare modified epoxy resin, and preparing the emulsion type aramid fiber sizing agent under the action of a compound emulsifier. The preparation method disclosed by the invention is simple and relatively low in cost, better interface bonding can be formed between the aramid fiber and the epoxy resin after sizing by the sizing agent, and particularly, the interlayer shear strength of the aramid fiber / epoxy resin composite material is relatively well improved; the preparation method has important significance in improving the use performance and stability of the aramid fiber composite material and expanding the application of the aramid fiber.

The invention discloses an inorganic atomic layer reinforced high-temperature-resistant nanofiltration membrane and a preparation method and application thereof, and belongs to the technical field of water treatment.The preparation method comprises the steps that firstly, a polymer porous basement membrane is modified through an atomic layer deposition technology, an inorganic atomic layer is introduced to the porous basement membrane, and the modified porous basement membrane is prepared; and performing interfacial polymerization reaction on a water-phase solution containing an amine monomer and a surfactant and an oil-phase solution containing a multi-acyl chloride monomer on the modified porous substrate membrane, and curing and cross-linking to prepare the inorganic atomic layer reinforced high-temperature-resistant nanofiltration membrane. According to the method, the thickness of the inorganic atomic layer can be accurately controlled, the mechanical strength and thermal stability of the porous basement membrane are improved, and the product high-temperature-resistant nanofiltration membrane has excellent high-temperature nanofiltration performance, water flux and long-term stability and is suitable for water treatment, ion screening and the like in a high-temperature environment.

The invention provides a preparation method of a high-flux stable-selection anti-fouling nanofiltration membrane, which comprises the following steps: carrying out amination modification on a nano material by an activation method to prepare a modified nano material; piperazine, an acid absorbent and the modified nano material are added into deionized water to be mixed, and a water phase solution is prepared; the preparation method comprises the following steps: mixing trimesoyl chloride and normal hexane to prepare an organic phase solution; immersing the polyethersulfone-based membrane into the water phase solution, draining, inversely immersing into the organic phase solution, and carrying out interfacial polymerization reaction to generate a polyamide layer to obtain a composite membrane; and then carrying out post-treatment on the composite membrane to obtain the composite membrane. The membrane has high permeability, high selectivity and strong anti-pollution performance.

The present invention relates to the technical field of nanofiltration membranes, and particularly relates to a high-temperature resistant nanofiltration membrane and a preparation method thereof. The nanofiltration membrane is prepared by this method. The method includes preparing a nano-layer; coating a CHO-SiO2 nano-particle solution with a required mass concentration on the surface of a porous support layer to form a base membrane containing the nano-layer; preparing a high-temperature resistant nanofiltration membrane; immersing the base membrane in an aqueous solution, taking out the base membrane after the first immersion treatment and air-drying the water droplets on its surface; secondly, immersing the base membrane in an oil-phase solution, taking out the base membrane after the second immersion treatment and performing a drying treatment to obtain a high-temperature resistant nanofiltration membrane; the aqueous solution includes polyamine, an acid absorbent, inorganic salts and a first organic solvent; the polyamine is a bis-benzene N-heterocyclic derivative; the oil-phase solution includes polyacyl chloride. The present invention can solve the problem that the directly introduced nano-particles are liable to fall off after film formation in the prior art.

The invention belongs to the technical field of oil well paraffin removal and prevention, and relates to a paraffin removal and prevention agent for a shale oil shaft and a preparation method thereof. The paraffin remover and inhibitor for the shale oil wellbore comprises the following raw materials in percentage by mass: 40-55% of an oily solvent, 1-3% of a cosolvent, 1-2% of imidazole bis (trifluoromethanesulfonyl) imide salt, 10-20% of a wax crystal modifier, 3-5% of an emulsifier, 1-2% of an alkaline regulator and 25-35% of water, wherein the sum of the mass percentages of the raw materials is 100%. The wax crystal modifier is prepared by copolymerizing (methyl) acrylic acid C12-C16 ester, (methyl) acrylic acid C1-C3 ester and (methyl) acryloyl chloride and then reacting with C20-C30 alkyl alcohol. The wax crystal modifier provided by the invention has long-medium-short branched chains, and interacts with the imidazole bis (trifluoromethanesulfonimide) salt capable of improving the paraffin removal effect and low-temperature fluidity, so that the efficient paraffin removal and inhibition effect is realized, and the better paraffin removal and inhibition effect can still be kept at low temperature.

The invention discloses a preparation method of a solvent-resistant nanofiltration membrane with a polydopamine / amino silicon dioxide middle layer, belongs to the technical field of membrane separation, and solves the technical problems of low flux and poor stability of the solvent-resistant nanofiltration membrane. The preparation method of the solvent-resistant nanofiltration membrane with the polydopamine / amino silicon dioxide middle layer comprises the following steps: preparing a polyetherimide-based membrane by a phase inversion method-crosslinking method; preparing amino silicon dioxide nanoparticles by adopting a sol-gel method; preparing a deposition solution containing dopamine, an oxidizing agent and amino silicon dioxide by using a Tris buffer solution; depositing the polydopamine / amino silicon dioxide intermediate layer on the upper surface of the polyetherimide base film; carrying out interfacial polymerization reaction of piperazine and trimesoyl chloride on the surface of the membrane deposited with the middle layer, and carrying out heat treatment to obtain a composite membrane; and immersing the composite membrane into an organic solvent for activation to obtain the solvent-resistant nanofiltration membrane with a polydopamine / amino silicon dioxide intermediate layer. The solvent-resistant nanofiltration membrane constructed by taking polyetherimide as a base membrane, polydopamine / amino silicon dioxide as a middle layer and polyamide as a separation layer has excellent flux and stability, and has a wide application prospect in the aspects of drug separation, organic solvent recovery and the like.