1081 results about "Tetrahydrofuran" patented technology

The invention belongs to the technical field of conductive adhesives, and particularly relates to a salt-fog-resistant waterborne conductive adhesive and a preparation method thereof.The salt-fog-resistant waterborne conductive adhesive is mainly prepared from, by weight, 5-10 parts of salt-fog-resistant waterborne polyurethane; 5 to 10 parts of water-based tackifying resin; 30 to 50 parts of conductive silver powder; 10 to 20 parts of ethanol; 2-10 parts of an anti-hydrolysis agent; and 10-30 parts of deionized water. According to the salt-fog-resistant aqueous conductive adhesive, polyurethane resin with polytetrahydrofuran alcohol and polycaprolactone polyol as main structures is used as matrix resin, a system is endowed with excellent water resistance and salt-fog resistance, the salt-fog-resistant aqueous conductive adhesive shows outstanding hydrolysis-resistant stability after being cured, and the salt-fog-resistant aqueous conductive adhesive and the conductive silver powder have a synergistic effect, so that the anti-settling performance is effectively improved.

The invention relates to a hyaluronic acid-polyurethane composite material based on a double dynamic network and a preparation method and application thereof, and the preparation method comprises the following steps: carrying out hydrophobic modification reaction on hyaluronic acid and aminophenylboronic acid to obtain aminophenylboronic acid modified hyaluronic acid; the preparation method comprises the following steps: mixing polytetrahydrofuran ether glycol, polyethylene glycol and isophorone diisocyanate, carrying out a primary reaction, adding trimethylolpropane tri (3-mercaptopropionic acid) ester, carrying out a secondary reaction, adding tannic acid, and carrying out a third reaction to obtain tannic acid-terminated dynamic thionocarbamate polyurethane; and mixing the amino phenylboronic acid modified hyaluronic acid with the tannic acid terminated dynamic thionocarbamate polyurethane for reaction to obtain the hyaluronic acid-polyurethane composite material with the double dynamic networks. Compared with the prior art, by introducing a'thionocarbamate-borate 'double-dynamic network, high toughness, high strength, good self-repairability and repeatable processability in an extreme environment are realized, and the material is particularly suitable for manufacturing and repairing of key components in an LNG ship body and a heat insulation system thereof.

The invention discloses a crown ether functionalized covalent organic framework material as well as a preparation method and application thereof, and the method comprises the following steps: adding a covalent organic framework material, 4-bromobenzo-15-crown-5, potassium carbonate and potassium iodide into an acetone solution for reaction, washing the obtained crude product, performing Soxhlet extraction with tetrahydrofuran for a certain time, and drying to obtain the crown ether functionalized covalent organic framework material. The crown ether functionalized covalent organic framework material is obtained. Compared with a synthesis method of crown ether functionalized COFs in the prior art, the method has the advantages that the crown ether (4-bromobenzo-15-crown-5) can be grafted to the COFs in one step, the Na < + > adsorption capacity and the adsorbent recycling performance are greatly improved, the synthesis method is simple, and synthesis of the crown ether functionalized COFs is greener, more convenient and more economical.

The invention belongs to the technical field of batteries, discloses a battery electrolyte solvent capable of adapting to a wide temperature range and preparation of a battery, and provides application of a mixed organic solvent as an energy storage battery electrolyte solvent, the mixed organic solvent is composed of tetrahydrofuran, 1, 3-dioxolame and 1, 1, 2, 2-tetrafluoroethyl-2, 2, 2-trifluoroethyl ether, and the 1, 1, 2, 2-tetrafluoroethyl-2, 2, 2-trifluoroethyl ether is composed of tetrahydrofuran, 1, 3-dioxolame and 1, 1, 2, 2-tetrafluoroethyl-2, 2, 2-trifluoroethyl ether. The volume percent content of the 1, 2, 2-trifluoroethyl ether is 10%-50%. The solvent composition of the energy storage battery electrolyte is improved, 1, 1, 2, 2-tetrafluoroethyl-2, 2, 2-trifluoroethyl ether is introduced into an ether organic solvent (namely tetrahydrofuran and 1, 3-dioxolame) to serve as a diluent, meanwhile, the volume percentage of the diluent is controlled, and the obtained electrolyte solvent formula can adapt to the wide temperature range of the full temperature interval of-130 DEG C to 60 DEG C, so that the energy storage battery electrolyte is suitable for being used as an energy storage battery electrolyte. And the problem of battery failure of the current energy storage battery under the extremely low-temperature and high-temperature conditions can be effectively solved.

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 preparation method and application of a reproducible self-healing polyurethane elastomer with synergism of dynamic silicon oxygen bonds and multiple hydrogen bonds. The method comprises the following steps: (1) carrying out a pre-polymerization chain extension reaction on polytetrahydrofuran, isophorone diisocyanate and a catalyst; (2) adding a 3, 13-dihydroxy propyl octaphenyl double-layer silsesquioxane monomer to carry out a chain extension reaction, and then adding carbohydrazide to carry out a reaction; and (3) adding glycerol and camphorsulfonic acid, uniformly stirring, pouring into a mold, curing and drying, thereby obtaining the reproducible self-healing polyurethane elastomer with synergistic dynamic silicon-oxygen bonds and multiple hydrogen bonds. According to the invention, a common fabric is soaked in a dispersion liquid formed by uniformly mixing diluted polyurethane and hydrophobically modified MXene to obtain the multifunctional composite material with the functions of self-cleaning, self-repairing, photo-thermal conversion and human body sensing.

The invention discloses an aluminum oxide coated diaphragm and a preparation method thereof in the field of lithium ion battery diaphragms. The diaphragm comprises aluminum oxide particles, a fluorine-containing porous organosilicon compound, a phosphorus heterocyclic covalent organic framework, a binder, a dispersant and deionized water. The fluorine-containing porous organosilicon compound is prepared by mixing methyltrimethoxysilane, perfluorohexyltrimethoxysilane and water, adding ammonia water to adjust the pH value, then reacting to form a sol-gel system, adding amino silane to continue reacting, and then carrying out rotary evaporation, calcination and grinding. The phosphorus heterocycle covalent organic framework is prepared by dissolving cyanuric chloride, triphenylphosphine oxide and anhydrous tetrahydrofuran, adding imidazole bromide to react to form an intermediate, then adding ethylene glycol to continuously react, and performing vacuum drying and grinding to obtain the phosphorus heterocycle covalent organic framework. According to the diaphragm, the interface adhesion and electrolyte wettability are enhanced synergistically through the bifunctional compound, and the thermal stability and the cycle performance are improved.

Disclosed in the present application are a compound as represented by formula (I), a pharmaceutically acceptable salt, a stereoisomer, a tautomer, or an N-oxide, and the use thereof in the preparation of a drug for treating, preventing or alleviating voltage-gated sodium ion channel-related diseases.

The invention provides bio-based MS base resin, bio-based MS glue and a preparation method of the bio-based MS base resin and the bio-based MS glue, and belongs to the technical field of high polymer materials. The MS base resin is isocyanate group silane terminated bio-based polyether polyol or polyether polyol subjected to chain extension. The polyether polyol is selected from one or more of bio-based polyethylene glycol, bio-based polypropylene glycol, bio-based poly (trimethylene ether glycol) and bio-based polytetrahydrofuran ether glycol. And mixing the bio-based MS base resin, the plasticizer, the filler, the catalyst III, the coupling agent and the auxiliary agent, and stirring under a vacuum condition to obtain the bio-based MS adhesive. The bio-based MS adhesive prepared by the invention is high in bio-based material content, uncomplicated in preparation process and low in energy consumption, and meanwhile, an adhesive body is good in mechanical property, high in stability and good in high temperature resistance and humidity and heat resistance.

The invention discloses an application of a novel miscellaneous [3] aromatic hydrocarbon crystal material in adsorptive separation of a pyrrolidine and tetrahydrofuran mixture and / or capture of iodine vapor, and relates to the technical field of adsorption.Firstly, the novel miscellaneous [3] aromatic hydrocarbon crystal material capable of adsorptive separation of pyrrolidine and tetrahydrofuran so as to realize iodine capture is synthesized; the application method comprises the following steps: selectively adsorbing pyrrolidine in a mixture of pyrrolidine and tetrahydrofuran by adopting the novel miscellaneous [3] aromatic hydrocarbon crystal material to obtain a pyrrolidine-miscellaneous [3] aromatic hydrocarbon crystal material, realizing separation of tetrahydrofuran and pyrrolidine, and capturing iodine vapor by adopting the pyrrolidine-miscellaneous [3] aromatic hydrocarbon crystal material. Compared with other macrocyclic aromatic hydrocarbons, the method provided by the invention not only can realize separation of tetrahydrofuran and pyrrolidine, but also has the advantages of high iodine adsorption capacity, good thermal stability and the like; meanwhile, the synthesis method has the advantages of simplicity in operation, high yield, simplicity in post-treatment, easiness in separation and purification of products and the like.

The technology of the present disclosure generally relates to the field of power storage devices, and more specifically to a solid electrolyte, an electrode, a solid-state battery, and a method for producing the same. An aspect of the present disclosure relates to a process for producing a solid electrolyte, comprising the steps of: - contacting, in the presence of a catalyst: - a polymer precursor compound comprising polyethylene glycol (PEG) and / or polytetrahydrofuran (PTHF), wherein the polymer precursor compound comprises on average per polymer precursor molecule, -at least 2.0 alkoxysilyl functional groups, with a functionality of at least 2.0, preferably at least 2.5, preferably at least 3.0; and / or -at least 1.0 alkoxysilyl functional groups, with a functionality of at least 3.0; - optionally, an organo-tri-alkoxy silane, an organo-tetra-alkoxy silane, and / or a mixture thereof comprising a metal ion (M+) chelating moiety being a cyanurate, a crown ether, an aza-crown ether, a thia-crown ether, a cryptand, a carbamate, a cyano group, a thiocyanate group, or a metallacrown,, - a metal (M+) salt, preferably does the metal salt comprises Li+, Na+, Mg+, Ca+, Al+, and / or a combination thereof, preferably lithium (Li+); - a solvent, preferably an organic solvent; and, - optionally, an ionically conductive compound; thereby obtaining a solid electrolyte; - optionally, drying the obtained solid electrolyte.

The invention discloses cyclodextrin alkyl ether sulfonic acid as well as a preparation method and application thereof, and relates to the technical field of oil and gas field auxiliaries. The preparation method of the cyclodextrin alkyl ether sulfonic acid comprises the following steps: adding hydroxyl alkyl sulfonic acid into dichloromethane, adding alkali and a sulfonyl chloride reagent, and reacting for 3-5 hours to obtain sulfonate; the preparation method comprises the following steps: adding sulfonate into iodide, adding acetone, reacting for 5-8 hours, and removing excessive iodide after the reaction is finished, so as to obtain iodo-hydrocarbyl sulfonic acid; the preparation method comprises the following steps: dissolving cyclodextrin in tetrahydrofuran, cooling to 0 DEG C, adding alkali under the protection of nitrogen, reacting for 0.5-2 hours, then adding iodo-alkyl sulfonic acid, reacting for 30-60 hours at room temperature, cooling to 0 DEG C, and carrying out reduced pressure distillation to obtain cyclodextrin alkyl ether sulfonic acid; the cyclodextrin alkyl ether sulfonic acid prepared by the invention is used as a cosolvent of the powder resistance-reducing agent, can effectively prevent aggregation among molecules of the powder resistance-reducing agent, improves the dispersity, reduces agglomeration and precipitation phenomena, and meanwhile, can avoid pipeline blockage in a conveying process.

The invention discloses a crystal compound, a preparation method thereof and application of the crystal compound in X-ray detection, imaging and anti-counterfeiting encryption, and belongs to the technical field of crystals. The molecular formula of the crystal compound is [Cu (totp) (CH3CN) 3] [Cu2I3 (totp) (PN)]. (CH3CN), wherein totp is tris (o-tolyl) phosphine; and PN is diphenyl-2-pyridine phosphine. The crystal compound disclosed by the invention is simple in preparation method, and has the characteristics of large mass attenuation coefficient of X-ray energy, high light yield and low detection limit when being used as a material of an X-ray detector. The compound also has the characteristic of structural transformation in solvents such as methanol, ethanol, acetone, dichloromethane, tetrahydrofuran and the like, and meanwhile, the conversion of luminescence color under the excitation of 365nm ultraviolet light and X rays is accompanied. The material can be applied to the aspects of scintillator materials, room-temperature X-ray radiation indirect detection materials, radiation detection dosimeters, X-ray scintillator medical imaging, anti-counterfeiting encryption and the like.

The invention relates to a preparation technology of a multifunctional plastic clothes hanger through cooperation of degradable color master batches and nitrogen filling injection molding, and belongs to the technical field of plastic products. Adding the polylactic acid, the styrene-acrylonitrile copolymer, the modified stone powder, the degradable color master batch and the compound additive into a horizontal helical ribbon mixer, stirring and drying to obtain a mixture; the dried mixture is added into an injection molding machine to be melted and plasticized, a screw pushes melt to be injected into a mold, high-pressure nitrogen is injected into the melt, and the melt is pushed to completely fill a cavity; the plastic clothes hanger is obtained through pressure maintaining, cooling and demolding; the compound additive is prepared from allyl alcohol polyoxyethylene ether, 2-octenyl succinic anhydride, 14-mercaptotetradecanoic acid, anhydrous tetrahydrofuran, 2-hydroxy-4 '-(2-hydroxyethoxy)-2-methyl propiophenone and triethylamine. The preparation method comprises the following steps: preparing the compound additive; the degradable material is adopted, the biodegradation rate is high, the mechanical property is stable, the coloring effect is good, fading is not prone to occurring, and the service life is long.

The invention provides an ultrathin temperature-sensitive hydrogel flexible electrode and a preparation method thereof, and belongs to the technical field of hydrogel electrodes. The preparation method comprises the following steps: mixing monomer acryloyl glycinamide and acrylic acid, and dissolving in deionized water to obtain a mixed solution A; adding a chemical cross-linking agent and a poly (3, 4-ethylenedioxythiophene)-poly (styrene sulfonate) solution into the mixed solution A to obtain a mixed solution B; adding sodium sulfate and tannic acid into the mixed solution B to obtain a prepolymerization solution; adding an initiator into the pre-polymerized solution to obtain a polymerized solution; the preparation method comprises the following steps: adding thermoplastic polyurethane particles into a mixed solution of N, N-dimethylformamide and tetrahydrofuran to form a precursor solution, and carrying out electrostatic spinning on the precursor solution to obtain a film matrix; and coating the polymerization solution on the surface of a thin film substrate, and packaging a conductive copper foil to obtain the ultrathin temperature-sensitive hydrogel flexible electrode. The mechanical property and the adhesion property of the flexible electrode are improved, and the adhesion strength can be dynamically adjusted by regulating and controlling the temperature.

The invention discloses a bio-based modified high polymer material and a preparation method thereof, and relates to the technical field of high polymer materials. When the bio-based modified high polymer material is prepared, firstly, lignin reacts with terephthalaldehyde to prepare formylated lignin; carrying out multi-component reaction on the aldehyde lignin to obtain modified lignin; the preparation method comprises the following steps: reacting 4-mercaptophenylboronic acid with 1-mercaptoglycerol to prepare a dimercaptoborate cross-linking agent; the preparation method comprises the following steps: reacting isophorone diisocyanate with polytetrahydrofuran ether glycol, and then reacting with a flame-retardant chain extender, 1, 2-propylene glycol and hydroxyethyl methylacrylate to prepare modified polyurethane; and mixing the modified polyurethane, the modified lignin and a dimercaptoborate cross-linking agent, casting and curing to obtain the bio-based modified high polymer material. The bio-based modified high polymer material prepared by the invention has the advantages of flame retardance, antibacterial property, aging resistance, self-repairing property, repeatable processing and high mechanical strength.

The invention discloses a method for preparing high-purity lithium sulfide based on a solution double decomposition method, and belongs to the technical field of battery materials, and the method comprises the following steps: adding lithium chloride and sodium sulfide into ethanol, mixing, and reacting in the mixing process to generate lithium sulfide; performing solid-liquid separation on the reaction system to obtain a solid product; washing the solid product with tetrahydrofuran and drying; and continuously introducing inert gas into the heat treatment chamber to purge a solid product in the heat treatment chamber, carrying out heat treatment on the solid product under the conditions of 200-300 DEG C and 10-1000 Pa, and removing complex impurities in the solid product to obtain the high-purity lithium sulfide. Compared with the prior art, the method has the advantages that the Li2S.EtOH impurity in the lithium sulfide is removed, the lithium carbonate impurity generated by the reaction of the impurity at high temperature is reduced, and the risk of electrolyte and battery performance is further reduced.

The invention discloses a preparation method of an antibacterial warm-keeping fabric, and relates to the technical field of textiles. When the antibacterial warm-keeping fabric is prepared, firstly, (E)-butyl-2-ene-1, 4-diamine, glyoxal, formaldehyde and butyric acid are used as raw materials to synthesize a polyimidazolium salt antibacterial agent, then the polyimidazolium salt antibacterial agent is copolymerized with polytetrahydrofuran ether glycol and diphenylmethane diisocyanate to prepare an antibacterial polyurethane spinning solution, and the antibacterial fabric is obtained through wet spinning and weaving. The preparation method comprises the following steps: reacting L-cysteine with 3-amino propyl triethoxy silane to prepare cysteamine acyl propyl triethoxy silane, reacting with formaldehyde and phosphorous acid to obtain flame-retardant modified silane, and further preparing a silicon dioxide solution from the flame-retardant modified silane and sol-gel such as methyltrimethoxysilane; finally, the antibacterial fabric is treated with a benzophenone solution and then soaked with a silicon dioxide solution, and the antibacterial thermal fabric is prepared through ultraviolet irradiation, standing gelation, aging and hexane washing. The prepared fabric has excellent antibacterial property, heat retention property and flame retardant property.

The invention discloses synthetic resin and an adhesive for a medical oxygen anaesthetic mask as well as a preparation method and application of the synthetic resin and the adhesive, and the synthetic resin is prepared by the following steps: carrying out ring-opening reaction on KH-560 and KH-550 to generate a siloxane intermediate with hydroxyl, and modifying polyurethane by using the siloxane intermediate; the adhesive comprises the following components in parts by weight: 100 parts of synthetic resin, 45-95 parts of a reactive diluent and 4-14 parts of a photoinitiator, and the reactive diluent mainly comprises isobornyl acrylate, N, N-dimethylacrylamide, tetrahydrofuran acrylate and hydroxyethyl acrylate; compared with the prior art, the adhesive prepared from the synthesized modified resin has the advantages that the adhesive can be quickly cured under the irradiation of an LED lamp, the energy consumption is low, and automatic production is facilitated; the oxygen mask has the characteristics of good surface dryness, good flexibility, no blistering at constant temperature and humidity, firmness of a PC (Poly Carbonate) surface cup and a PVC (Polyvinyl Chloride) air bag for bonding the oxygen mask, and the like.

The utility model belongs to the technical field of chemical solvent preparation, and particularly relates to a tetrahydrofuran purification device. The utility model provides a tetrahydrofuran purification device. The tetrahydrofuran purification device comprises a feed port, a catalytic hydrogenation reaction part, a gas phase discharge port, a liquid phase discharge port, a heavy component removal tower and an absorption tower. In the application, through the catalytic hydrogenation part, the impurity dihydrofuran in the tetrahydrofuran is hydrogenated to generate the tetrahydrofuran, the impurities n-butyraldehyde and isobutyraldehyde are hydrogenated to generate alcohols which are easily separated from the tetrahydrofuran, through determination, the content of the impurity dihydrofuran in the purified tetrahydrofuran is reduced to 3 ppm or below, the alcohols are separated in the heavy component removal tower, and the content of the tetrahydrofuran in the tetrahydrofuran is reduced to 3 ppm or below. The purity and the quality of tetrahydrofuran are effectively improved, and the purification device structure and the purification process are simple.

The invention relates to the technical field of tetrahydrofuran polymerization catalysts, in particular to a circular reaction device of a high-purity tetrahydrofuran polymerization catalyst and a polymerization technology.The circular reaction device comprises a base, the left side of the top of the base is fixedly connected with a reaction kettle, and the rear side of the reaction kettle is fixedly connected with a feeding mechanism; the right side of the top of the base is fixedly connected with an inert gas injection mechanism, and the left end of the inert gas injection mechanism extends to the inner wall of the reaction kettle. Accurate feeding, real-time monitoring and efficient polymerization of a high-purity tetrahydrofuran polymerization catalyst are achieved, the discharging speed and amount are accurately controlled through an electric push rod in the feeding mechanism, the purity and the component proportion of a catalyst raw material are monitored in real time in combination with a chromatographic detection head, the stability of polymerization reaction and the product quality are ensured, and the production efficiency is improved. Due to the design of a circular reaction polymerization process, the whole reaction process is carried out in an oxygen-free environment.

The application relates to the technical field of packaging cartons, and discloses a high-strength lightweight packaging carton and a preparation method thereof. The preparation steps are as follows: S1: uniformly mixing trihydroxy heptaoctyl poss, 3-bromopropylene, sodium carbonate and tetrahydrofuran, reacting at 50-60 DEG C for 3-5 h to obtain modified poss; S2: taking hexamethoxymethyl melamine, ethanol and the modified poss to prepare a modified etherified amino resin; S3: uniformly mixing the modified etherified amino resin, mercapto-modified silicon dioxide and a photoinitiator to obtain an additive; uniformly stirring acrylic emulsion, epoxy / acrylic core-shell emulsion, hyperbranched polyurethane acrylate and the additive to obtain reinforcing coating; and coating the reinforcing coating on the surface of the lightweight packaging carton, drying and curing to obtain the high-strength lightweight packaging carton.

The invention belongs to the technical field of foaming polyurethane, and provides a microsphere foaming polyurethane material, a base plate and a preparation method and application of the base plate, raw materials are prepared from a polyol component and an isocyanate component according to the proportion that the isocyanate index is 1.05-1.15; wherein the polyol component is prepared from the following components in parts by mass: 60 to 65 parts of polytetrahydrofuran polyol, 10 to 15 parts of poly trimethylene ether glycol, 6 to 8 parts of polypropylene oxide polyol A, 6 to 10 parts of polypropylene oxide polyol B, 4 to 6 parts of 1, 4-butanediol, 0.5 to 1.5 parts of trimethylolpropane, 0.3 to 0.5 part of a catalyst, 0.8 to 1.5 parts of a foam stabilizer, 0.5 to 0.7 part of a dispersing agent EFKA-4040 and 0.1 to 0.3 part of polyether modified polysiloxane BYK-333; 0.4 to 0.6 part of expansion microspheres and 0.1 to 0.3 part of water. According to the technical scheme, the problem that a polyurethane material in the prior art cannot have low compression set and excellent fatigue resistance at the same time is solved.

The application belongs to the field of catalyst synthesis, and relates to a polymer polynuclear boron organic catalyst, a preparation method and application thereof, the preparation method of the catalyst comprises the following steps: adding tetrahydrofuran into a catalyst precursor, then adding a borohydride reagent drop by drop, heating the reaction mixture at 25-80 DEG C for 22-26 h, vacuum concentrating the reaction mixture to obtain a crude product, purifying the crude product by washing with pentane for 2-5 times, and vacuum drying the product at normal temperature for 10-14 h to obtain the catalyst; the catalyst precursor and a preparation method thereof are also provided; the polymer polynuclear boron organic catalyst provided by the application has the advantages of high activity, simple preparation method and low cost, and the catalyst can control the polymer substrate type and the polymer type by adjusting the reaction conditions, the catalytic system and the substrate, and can efficiently prepare polymers such as polyether, polyester and polycarbonate due to the synergistic effect of the polynuclear boron center, so that the types of the organic catalyst and the polymer are greatly expanded.

The application discloses a preparation method and application of a zirconium dioxide loaded iridium oxide nanocluster oxygen evolution electrocatalyst. A mixed solution of zirconium salt, amide solvent and organic acid is prepared, and the mixed solution is kept at 120 DEG C for 24 hours; after cooling, the white product is separated, washed and dried. Then, the product and iridium salt are dispersed in a mixed solution of tetrahydrofuran and water, and sodium nitrate and potassium nitrate aqueous solution are added under stirring; after stirring, rotary evaporation is carried out at 60 DEG C, and the greenish powder obtained after drying is vacuum dried at 60 DEG C for 12 hours; the greenish powder is kept in a muffle furnace at 450 DEG C for 30 minutes, and then cooled in air; the greenish powder is washed with deionized water and anhydrous ethanol for multiple times, and finally vacuum dried at 60 DEG C for 12 hours. The zirconium dioxide loaded iridium oxide material based on oxygen overflow stable tetragonal zirconia can be specially applied to an electrocatalyst for an oxygen evolution reaction in an acidic electrolyte, has excellent oxygen evolution reaction activity, follows a lattice oxygen mechanism in the reaction process, and can realize an oxygen overflow effect from tetragonal zirconia to iridium oxide nanoclusters to stabilize the catalyst.

The application relates to the technical field of metal organic thin layer material preparation, in particular to a kilogram-level preparation method of metal organic thin layer material. The preparation method comprises the following steps: S1, adding zirconium tetrachloride and H2BPYDC into a polytetrafluoroethylene reaction kettle, dissolving the zirconium tetrachloride and the H2BPYDC, and then adding a composite; S2, sequentially adding a DMF solution of palladium fluoroacetate, a catalyst and concentrated hydrochloric acid into the reaction kettle; S3, transferring the reaction kettle into an oven, centrifuging to obtain a cyan suspension after 18-20 hours, dispersing the cyan suspension in a DMF solution in batches at 60 DEG C, placing for 5-6 hours, removing unreacted substrates, and obtaining a solid; S4, cleaning the solid obtained in S3 by using DMF and tetrahydrofuran respectively, and vacuum drying for 12 hours to obtain the metal organic thin layer material. The kilogram-level preparation method of metal organic thin layer material is provided, so as to solve the problems of low preparation yield, slow rate and difficulty in kilogram-level preparation of metal organic thin layer material in the related art.

A method for preparing a polyolefin adhesive sheet with low dielectric constant and low dielectric loss, the method comprising the following steps: soaking a porous polytetrafluoroethylene film in a sodium-naphthalene-tetrahydrofuran solution, rinsing and air-drying to obtain an activated porous polytetrafluoroethylene film; adding a silane coupling agent to ethanol to form a silane coupling agent ethanol solution, immersing the porous polytetrafluoroethylene film in the silane coupling agent ethanol solution, and drying to obtain a porous polytetrafluoroethylene film with double bonds bonded to the surface; immersing inorganic fillers in the silane coupling agent ethanol solution, and drying to obtain inorganic fillers with double bonds bonded to the surface; stirring polyolefin, inorganic fillers, a flame retardant, an antioxidant, and an initiator to form a polyolefin composite glue solution; immersing the porous polytetrafluoroethylene film with double bonds bonded to the surface in the polyolefin composite glue solution, and drying to obtain a polyolefin adhesive sheet, which has the advantages of low dielectric constant, low dielectric loss, low water absorption, and the like.

The application provides a preparation method of a polyurethane foaming material. The preparation method comprises the following steps: firstly, pre-polymerization of polytetrahydrofuran ether glycol and hexamethylene diisocyanate; then, mixing, extruding, and granulating of polyhexalactone dihydric alcohol and a catalyst to obtain polyurethane granules. The granules are dried and injection molded into a small embryo to be foamed. The small embryo is immersed in supercritical carbon dioxide, nitrogen is introduced for auxiliary foaming, and gradient pressure relief control is implemented in the foaming process. After foaming, curing treatment is performed to obtain the polyurethane foaming material. The preparation method is beneficial to improving the cell uniformity of the polyurethane foaming material and improving the performance stability of the material after rebound, compression, and aging.

SOLVENT COMPOSITIONS The present invention relates to a solvent composition for solvent-based paints or other coatings characterized in that it comprises a combination of dimethyl glutarate and at least one other compound selected from isobutyl acetate, ethyl lactate, dimethyl 2-methylglutarate, 2-methyltetrahydrofuran, ethyl acetate, cyclopentyl methyl ether, dithoxymethane, dimethyl carbonate, dimethyl succinate, benzyl alcohol, dimethyl adipate, and glyceryl triacetate. Fig. 1

The present application relates to the technical field of pipeline drainage, and particularly relates to a composite hydrophobic material for inhibiting crystallization of a tunnel drainage pipeline and a preparation method thereof; the composite hydrophobic material comprises a hydrophobic inner layer and a scale inhibition outer layer attached to the outer surface of the hydrophobic inner layer; the hydrophobic inner layer comprises tetrahydrofuran, a solvent volatilizing agent, a surfactant, nano-silicon dioxide, a cross-linking agent and a curing agent; the scale inhibition outer layer comprises a scale inhibitor solution and a gum material, wherein the scale inhibitor solution comprises EDTA, hydrolyzed maleic anhydride and sulfamic acid; the preparation method comprises the following steps: S1, coating the hydrophobic inner layer material; S2, air-drying to obtain the hydrophobic inner layer; S3, coating the scale inhibition outer layer material on the surface of the hydrophobic inner layer to obtain the composite material; the composite material prepared by the present application still has excellent hydrophobic performance after being left for 24 hours and can be maintained for a long time; the scale inhibition outer layer protects the hydrophobic inner layer and simultaneously plays a scale inhibition role, thereby improving the functionality of the material.