72 results about "Acetylacetone" patented technology

The invention provides an acetylacetone-based composite thermal stabilizer which is a mixture obtained by mixing zinc acetylacetonate, calcium acetylacetonate or magnesium acetylacetonate and hydrotalcite pro rata. The composite thermal stabilizer is suitable for chloride-containing high polymer, such as polyvinyl chloride, chlorinated polyethylene, chlorinated polyvinyl chloride, copolymer of vinyl chloride-ethylene or copolymer of vinyl chloride-vinyl acetate, has better thermal stability, prolongs the thermal aging time of the chloride-containing high polymer, and overcomes the shortcomings of poor long-term performance of single stabilizer of zinc acetylacetonate, poor transparency of stabilizer of calcium acetylacetonate, and poor initial colorability of stabilizer of hydrotalcite. The composite thermal stabilizer has low cost, good initial colorability, excellent long-term performance and good transparency, and is an efficient composite thermal stabilizer.

The application discloses a polyester synthesis method and application thereof. The polyester synthesis method comprises the following steps: preparing a sol containing cellulose nanocrystals, and an alcohol solution containing an aluminum alkoxide; adding the alcohol solution into the sol to react; separating a solid phase to obtain a composite catalyst; and synthesizing polyester under the co-catalysis of the composite catalyst and diisopropyl bis(acetylacetonyl) titanate. The polyester synthesized by the method has low carboxyl content, high light transmittance, high mechanical property and hydrolysis resistance, and can be used for preparing a polyester film. The application also provides application of the polyester prepared by the method.

This invention pertains to photothermal evaporation and its water purification, specifically relating to a biochar metal membrane. It is composed of a copper foam mesh, titanium acetylacetonate, lychee charcoal, and alcohol. The composition, by mass, includes one sheet of copper foam mesh, 75g of alcohol, 2g of lychee charcoal, and 0.2g of titanium acetylacetonate. The invention also discloses a method for preparing the biochar metal membrane, specifically involving: stirring titanium acetylacetonate and lychee charcoal in alcohol; immersing the copper foam mesh in the solution repeatedly for several dozen times to obtain a hydrophilic biochar metal membrane. The XRD and contact angle images of the obtained hydrophilic biochar metal membrane are shown in Figure 1a. The prepared biochar metal membrane has a porous structure, further enhancing its photothermal performance. This invention also discloses the photothermal evaporation performance of the biochar metal membrane and its application in seawater desalination. The biochar metal membrane of this invention is non-salt-accumulating, hydrophilic, and possesses highly efficient photothermal performance, enabling its application in multiple fields.

The application discloses a rhodium-catalyzed desymmetrization hydroformylation method for constructing polychiral center carbon ring nucleosides. The method for constructing polychiral center carbon ring nucleosides comprises the following steps: under the condition of an inert atmosphere, an acetylacetone dicarbonyl rhodium metal precursor and a chiral ligand are added into an organic solvent to prepare a catalyst solution, the catalyst solution is mixed with a substrate, and a reaction is carried out under the condition of a hydrogen atmosphere and a carbon monoxide atmosphere; after the reaction is completed, filtration and purification are carried out, and polychiral center cycloalkyl aldehyde is obtained; and the aldehyde group is converted to obtain the polychiral center carbon ring nucleosides. The method for constructing polychiral center carbon ring nucleosides has the advantages of high selectivity, wide substrate compatibility, high reaction efficiency, easy conversion of products, and the like. The whole reaction process can obtain polychiral center cycloalkyl aldehyde in one step with extremely high enantioselectivity and diastereoselectivity, the aldehyde group is converted, polychiral center carbon rings can be obtained with high yield, high dr value and high ee value, and the method is simple and easy to operate.

The present application belongs to the field of heterogeneous catalysis and material synthesis, and relates to a hollow ceramic fibrous iron-based catalyst for preparing biofuel from synthesis gas, a preparation method and application thereof. The catalyst is prepared by a coaxial electrospinning process, with polyborosilazane as a shell layer, polymethyl methacrylate, polyvinylpyrrolidone and acetylacetone iron as a core layer, and through spinning, solidification, gradient temperature pyrolysis and reduction steps, a hollow ceramic fibrous iron-based catalyst is prepared. The shell layer of the catalyst is converted into a high-strength and high-temperature stable SiBCN ceramic carrier, the core layer is pyrolyzed to form a hollow cavity and in-situ load high-dispersion iron active species, and the catalyst has good mechanical strength, high hydrothermal stability and excellent catalytic activity. The application of the catalyst in a continuous flow fixed bed reactor for preparing biofuel from synthesis gas is suitable for the synthesis of sustainable aviation fuel and other biofuels.

The application discloses a high-capacity capacitor electrode material and a preparation method thereof, and relates to the technical field of capacitor electrode materials. In the preparation of the high-capacity capacitor electrode material, polyacrylonitrile, lignin, pitch, zinc acetate and acetylacetone iron are uniformly mixed to prepare a spinning solution, and a composite fiber filament is obtained through electrostatic spinning; the composite fiber filament is high-temperature carbonized to obtain a composite carbon nanofiber; polythiophene is polymerized and deposited on the composite carbon nanofiber to obtain a polythiophene modified composite carbon nanofiber; the polythiophene modified composite carbon nanofiber and poly(ethylene glycol) methacrylate are reacted to obtain a functionalized composite carbon nanofiber; the functionalized composite carbon nanofiber, acetylene black and a bonding agent are mixed and ground to obtain a mixed slurry, and the high-capacity capacitor electrode material is prepared by coating and drying the mixed slurry. The high-capacity capacitor electrode material obtained by the application has excellent electrochemical performance.

This invention relates to the field of photoelectrocatalytic organic synthesis technology, specifically to a composite photoelectrode for photoelectrocatalytic preparation of ketone compounds from polyols, its preparation method, and its application. The method includes: dropping a dimethyl sulfoxide solution of vanadium acetylacetonate onto an FTO conductive glass plated with bismuth iodide, wherein the ratio of the amount of vanadium acetylacetonate to the deposition area of ​​bismuth iodide is 10-15 mmol:1 cm². 2 The bismuth oxy iodide deposition on the FTO conductive glass was carried out until the dimethyl sulfoxide solution of vanadium acetylacetonate completely covered the bismuth oxy iodide deposition, followed by calcination to obtain a BiVO4 photoanode. An ethanol solution of [2-(9H-carbazole-9-yl)ethyl]phosphonic acid was spin-coated onto the BiVO4 photoanode and dried to obtain a 2PACz / BiVO4 photoanode. A second constant-potential electrodeposition was performed, followed by washing to obtain the composite photoelectrode. The calcination conditions included a calcination temperature of 600-800℃, a calcination time of 2-4 h, and a heating rate of 8-12℃ / min. This composite photoelectrode can photocatalyze the conversion of polyols into ketone compounds.

A highly transparent conductive film comprises an electrode substrate and a top layer. The electrode substrate is a silver nanowire film, and the top layer is a pyrolytic zirconium acetylacetonate protective layer. The pyrolytic zirconium acetylacetonate protective layer is a precursor solution prepared using zirconium acetylacetonate as a solute and ethanol and dimethylformamide as a composite solvent. This precursor solution is deposited onto the surface of the silver nanowire film via atomization pyrolysis, followed by vacuum annealing to obtain a pyrolytic zirconium acetylacetonate protective layer composed of complex components. This invention achieves a transparent conductive film by dissolving zirconium acetylacetonate in a composite solvent of DMF and ethanol, and then depositing it onto the surface of an Ag nanowire film via spray pyrolysis. This transparent conductive film achieves a transmittance of 97.7% at 310 nm ultraviolet light, comparable to that of an unprotected Ag nanowire film, effectively improving the charge collection capacity and transport stability of the electrode.

This invention discloses a process for preparing rare-earth modified automotive pearl paint and its application, relating to the field of automotive pearl paint technology. The process includes: mixing cerium dioxide and neodymium acetylacetone to obtain a composite rare earth; adding the composite rare earth to an aqueous solution of a silane coupling agent to obtain a composite rare earth solution; adding a certain mass proportion of silicone-containing defoamer, anti-settling agent, and leveling agent to obtain a rare earth modifier; adding the rare earth modifier to the automotive pearl paint, stirring, ultrasonically dispersing, and allowing it to stand in the dark for thorough integration. This invention modifies automotive pearl paint using composite rare earth, significantly improving the structural stability and anti-aging ability of the coating under long-term ultraviolet irradiation, while also enhancing the weather resistance and color retention of the automotive pearl paint.

This invention relates to the field of ceramic technology, specifically to a corrosion-resistant daily-use ceramic and its preparation method. The ceramic body is obtained by firing basic green body particles that have undergone outer coating and sequential treatment with a dual zirconium source. The core of the method lies in: at the end of the spray granulation stage, a carboxyl-grafted polysiloxane precursor and aluminum nitrate nonahydrate are used to coat the outer layer of the basic green body particles; subsequently, zirconium acetylacetonate and zirconium oxynitrate are introduced sequentially for treatment. This technical solution can precisely enrich the modified components in the outer layer and interface region of the green body particles, thereby significantly improving the ceramic's acid and alkali corrosion resistance, post-corrosion mechanical strength retention, and mechanical washing resistance without significantly altering the traditional potassium feldspar-quartz-kaolin main formulation.

This invention discloses a PdCu intermetallic compound catalyst, its preparation method, and its application, belonging to the field of electrochemical ammonia synthesis and catalyst preparation technology. The preparation method includes: dispersing palladium acetylacetonate, copper acetylacetonate, glucose monohydrate, a surfactant, and a carbon support in an oleylamine solvent to obtain a mixture; subjecting the mixture to ultrasonic treatment to form a uniform dispersion; subjecting the dispersion to an oil bath reaction; collecting the reaction product, washing, and drying to obtain a PdCu intermetallic compound catalyst supported on a carbon support. The catalyst of this invention achieves approximately 224.25 mgh in the electrocatalytic reduction of nitrate to ammonia under alkaline conditions at -1.3V (vs. RHE). ‑1 mg ‑1 The ammonia yield is high, with a Faraday efficiency of 93.48%. Furthermore, this catalyst can be used as a cathode in zinc-nitrate batteries, achieving both power output and ammonia synthesis, demonstrating promising application prospects.

The application discloses a kind of biological hybrid nanoscale enzyme robot pills, with multi-mode regulation intestinal redox homeostasis and dysbiosis in inflammatory bowel disease, steps are as follows: step one, using zinc nitrate, acetylacetone iron and methanol and other drugs synthesis metal organic framework precursor, then calcination obtains iron single atom nanoscale enzyme;Step two, cultivate enrichment long bifidobacterium and human induced pluripotent stem cells, and extract the exosome or outer vesicle membrane of both respectively;Step three, nanoscale enzyme and probiotic vesicle membrane and stem cell exosome are co-extruded, and biological membrane-nanoscale enzyme composite robot is prepared;Step four, the prepared biological membrane-nanoscale enzyme composite particle is encapsulated in magnetic response pill, and engineering biological hybrid nanoscale enzyme robot pill is formed.Engineering biological hybrid nanoscale enzyme robot pill can be targeted to stay in intestinal inflammatory site under the control of rotating magnetic field after entering the intestinal tract of organism, then promote nanoscale enzyme release and enhance enzyme activity under the action of pulse magnetic field, so as to improve the treatment effect.Engineering biological hybrid nanoscale enzyme robot pill has biocompatibility and treatment safety, and has wide application prospect in the field of treating digestive tract inflammation.

The application belongs to the technical field of carbon dioxide hydrogenation, and particularly relates to a preparation method and application of an Ir monatomic catalyst for carbon dioxide hydrogenation to produce formic acid. A metal precursor, acetylacetone iridium Ir(acac)3, is in-situ coordinated and encapsulated in a complex cavity assembled with gallic acid coordination, and is carbonized at different temperatures (800 DEG C, 900 DEG C and 1000 DEG C) respectively, thereby successfully preparing monatomic catalysts with different coordination environments (Ir-N4, Ir-N3 and Ir-N2). The method is simple in operation, the obtained material structure is controllable, the carbon skeleton has good thermal stability and has a high specific surface area, the Ir is atomically dispersed and does not agglomerate, and in addition, the metal loading is low. The precise synthesis strategy of the catalyst is simple and feasible, easy to industrial production, can meet the needs of future carbon dioxide resource utilization and industrial production of bulk chemicals formic acid, and has good application prospect.

This invention discloses an environmentally friendly calcium / zinc stabilizer and its preparation method. The stabilizer comprises the following raw materials in the indicated mass percentages: calcium salt 25-40%, zinc salt 10-15%, zinc acetylacetonate 5-10%, uracil 5-10%, antioxidant 5-10%, pentaerythritol sodium tetrastearate 5-10%, nano-sized montmorillonite 5-10%, polyethylene glycol 3-5%, and lubricant 22-35%. The stabilizer is prepared through the steps of raw material weighing, premixing, activation, homogenization, cooling, pulverization, and sieving. This invention utilizes a specific three-stage temperature-controlled blending process to achieve an in-situ stable three-dimensional structure formed by nano-montmorillonite, calcium and zinc ions, and polyethylene glycol polymer chains. This three-dimensional structure not only achieves uniform dispersion and synergistic effect of the components, endowing the stabilizer with excellent long-term thermal stability, but also simplifies the production process, avoids the use of expensive or complex modified raw materials, and significantly reduces production costs while ensuring performance, thus combining high efficiency, environmental friendliness, and economy.

The present application uses the mixture of residual liquid and cracking product (LPS) after the cracking of polydimethylsilane (PDMS) as raw material, and the polymerization reaction with tributyl borate or triethyl borate obtains viscous liquid (LPCS), which introduces the heterogeneous element boron; the viscous liquid (LPCS) further reacts with zirconium acetylacetonate to introduce the heterogeneous element zirconium, and the polycarbosilane ceramic precursor (PBZCS) doped with boron and zirconium elements is obtained; the precursor silk obtained after the melt spinning can be inosculated by the relatively simple air oxidation crosslinking method, and the boron and zirconium elements act as sintering agents to densify the fiber in high-temperature sintering, and the high-temperature-resistant ceramic fiber is obtained.

The application discloses a kind of catalysts for hydrogen storage material and its preparation method and application, belong to hydrogen storage material and its preparation technical field.The present application is to solve the problems such as high dehydrogenation temperature of existing magnesium-based solid hydrogen storage material and slow low-temperature kinetics.The present application is prepared by using nickel chloride hexahydrate, acetylacetone manganese, polyether P123, polyether P127, dopamine hydrochloride, 1,3,5-trimethylbenzene and ammonia as raw materials to obtain carbon as carrier wrapped with elemental Ni nanoparticle catalyst with a large number of edge dislocations, and is applied to Mg-based hydrogen storage material by ball milling method.The introduced dislocation has a dual role: not only directly accelerates the dissociation of H2 molecule, but also indirectly improves the activity of catalytic phase (Mg2NiH4 / Mg2Ni).The preparation process of the composite hydrogen storage material provided by the present application is simple and mature, and the raw materials are cheap and easy to obtain, only a small amount of MNC needs to be added to greatly improve the hydrogen storage performance of Mg, and it is convenient for large-scale industrial production.

This invention relates to a nuclear-targeted multimodal imaging diagnostic probe with BNCT therapeutic efficacy, its preparation, and its application, belonging to the fields of biomedicine and nuclear medicine technology. This boron drug contains... 10 Using acetylacetone difluoroborate as the parent nucleus, this invention endows the tumor with nuclear targeting ability by introducing N- or S-containing heterocyclic structures, while utilizing its conjugated structure to provide fluorescence / photoacoustic dual-modal imaging functionality. Based on this, the invention achieves three core functions: first, through fluorescence / photoacoustic dual-modal imaging, it enables the visual localization and real-time monitoring of tumor sites; second, by leveraging the binding of nuclear targeting groups to nuclear DNA / RNA, it... 10 B is precisely delivered into the nucleus, significantly improving the killing efficiency of BNCT; thirdly, thermal neutron irradiation is performed under imaging guidance, triggering... 10 The B(n,α)⁷Li nuclear fission reaction ultimately enables high-precision integrated diagnosis and treatment. This invention also discloses a method for preparing this probe, which has promising clinical application prospects.

This invention provides a mononuclear manganese complex containing acetylacetone and β-ketoimine ligands, and a method for its preparation. This invention synthesizes a novel mononuclear divalent manganese complex Mn. II (acac)2(Hki)2. This compound is readily soluble in a variety of organic solvents, exhibits good stability, and is not easily deliquescent, making it an ideal source of divalent manganese. This invention employs a solution method to synthesize the aforementioned mononuclear divalent manganese complex, utilizing inexpensive and readily available raw materials; the reaction conditions are mild and can be carried out at room temperature; only water is used as the solvent, making it environmentally friendly; the reaction product is singular, easily purified, and yields the target compound in high quantities. This invention also synthesizes a novel mononuclear trivalent manganese complex, Mn. III (acac)2(ki), which differs from manganese acetylacetonate (III) in that one acetylacetonate anion is replaced by a ⁻-ketoimine anion. Mn III (acac)2(ki) is soluble in a variety of organic solvents and is an ideal trivalent manganese source reagent for anhydrous organic reactions.

The present application belongs to the technical field of environmental functional materials, and particularly relates to an environmentally-friendly purifying agent for fireworks and firecrackers as well as a preparation method and application thereof. The purifying agent is composed of two self-made core compounds and various commercially available materials. The first core compound is phosphotungstic acid-titania mesoporous spheres, which are prepared by a reverse microemulsion method combined with hydrothermal crystallization, and the inner core of phosphotungstic acid is coated with titania formed by hydrolysis of tetrabutyl titanate. The second core compound is a transition metal-nitrogen co-doped graphene-coated spinel composite. The magnesium-aluminum spinel precursor is prepared by a coprecipitation method, and after pre-carbonization by melamine, cobalt acetylacetonate and manganese acetylacetonate are introduced into a chemical vapor deposition system to in-situ grow a doped graphene film on the surface of the spinel. The present application utilizes the synergistic effect of adsorption, catalysis and disinfection of the two modified compounds to efficiently remove the smoke, PM2.5 and harmful gases generated by the burning of fireworks and firecrackers, and is suitable for various types of fireworks and firecrackers.

The application discloses a titanium-doped bismuth vanadate film photo-anode and a preparation method thereof. A precursor solution formed by mixing bismuth nitrate, an aqueous potassium iodide solution and an ethanol solution of benzoquinone is used as an electrolyte, fluorine-doped tin dioxide conductive glass (FTO) is used as a working electrode, a platinum sheet is used as a counter electrode, Ag / AgCl is used as a reference electrode, a bias voltage of -0.1 V vs. Ag / AgCl is applied to the working electrode, and a bismuth oxyiodide precursor film is deposited on the FTO. Then, a mixed solution of titanium tetrachloride and acetylacetone vanadyl dimethyl sulfoxide is added dropwise to the bismuth oxyiodide precursor film, and the titanium-doped bismuth vanadate film photo-anode is obtained through calcination and neutralization treatment. The titanium-doped bismuth vanadate film photo-anode has higher photoelectrocatalytic efficiency and charge transport efficiency, and can be widely applied to the fields of photoelectrocatalytic hydrogen production and photoelectrocatalytic degradation of pollutants.

The application provides a preparation method and application of a nanoscale porous hydroxyapatite material, and belongs to the field of inorganic material synthesis. The hydroxyapatite material with high crystallinity, nanoscale, microspherical morphology and multi-level pore structure of microporous and mesoporous is obtained through one reaction of a calcium source suspension liquid containing calcium acetylacetonate and a phosphorus solution containing a trisalt of phosphoric acid through a microchannel reactor, and then secondary crystallization through high-temperature calcination. The material particle size is 30-90nm, the pore size range is 0.5-50nm, heavy metal ion adsorption can be realized, the adsorption rate reaches more than 93.0% when the heavy metal ion concentration is 100-500mg / L, is 1.21 times of the adsorption rate of a hydroxyapatite material prepared by a simple chemical precipitation method, and has a wide application prospect in the field of heavy metal ion adsorption.

The application discloses a MgH2-V2O3 / VN@NC hydrogen storage composite material, which is prepared by mixing and mechanically ball-milling MgH2 and calcined V2O3 / VN@NC. The V2O3 / VN@NC raw material is obtained by fully grinding urea and vanadium acetylacetonate and then high-temperature calcination, wherein the doping amount of the V2O3 / VN@NC accounts for 5-10 wt% of the total mass of the composite material. The preparation method comprises the following steps: 1) preparation of the V2O3 / VN@NC material; and 2) preparation of the MgH2-V2O3 / VN@NC hydrogen storage composite material. The MgH2-V2O3 / VN@NC hydrogen storage composite material and the preparation method thereof have the following advantages: 1) excellent hydrogen absorption and desorption kinetic performance; 2) high hydrogen storage capacity; and 3) fewer synthesis steps and easy cost control.

The application relates to the technical field of high polymer coating, and discloses a super-hydrophobic mildew-proof and algae-resistant high polymer preparation and a preparation process thereof. The super-hydrophobic mildew-proof and algae-resistant high polymer preparation is made of raw materials containing the following components by weight: 100 parts of hydroxyl-terminated polydimethylsiloxane, 5-15 parts of hydrophilic fumed silica, 3-7 parts of methyltrimethoxysilane, 1-3 parts of vinyltriisopropoxysilane, 1.0-2.0 parts of diisopropoxybisacetylacetone titanium, 13.2-21.39 parts of an acetic acid type quaternary ammonium salt polar solution, and 3.2-9.5 parts of a composite anchoring powder. The preparation process comprises the following steps: material heating, pressure reduction and dehydration, nitrogen filling and temperature reduction, stirring and end-capping of silane and a catalyst, and finally, solution and powder are added to perform air extraction and defoaming to obtain the super-hydrophobic mildew-proof and algae-resistant high polymer preparation. The super-hydrophobic mildew-proof and algae-resistant high polymer preparation of the application excludes halogen interference to guarantee coating solidification and film formation, and utilizes acid-sensitive response to release an agent outward, so that long-acting protection is realized.

The application provides a preparation method of a foamed copper-based organic catalytic material for treating chloride ion wastewater, comprising the following steps in sequence: step [1], forming a cobalt aminoacetate [Co(gly)3] organic compound layer on the surface of a foamed copper base; step [2], converting the cobalt aminoacetate [Co(gly)3] on the surface of the foamed copper base into cobalt samarium aminoacetate [CoSm(gly)6] through a samarium Sm replacement reaction; and step [3], converting the cobalt samarium aminoacetate [CoSm(gly)6] on the surface of the foamed copper base into samarium acetylacetone ethylenediamine / cobalt aminoacetate [Sm(acac)2(en)][Co(gly)3], and finally obtaining the foamed copper-based organic catalytic material. The catalytic material prepared according to the application has the advantages of high chloride ion removal rate, excellent corrosion resistance and long-term stability.

The present disclosure relates to a solid electrolyte layer, an all-solid-state battery including the solid electrolyte layer, and a method for manufacturing the solid electrolyte layer. The solid electrolyte layer includes a sulfide-based solid electrolyte, a binder, and an additive. The additive includes a metal acetylacetonate.

The application relates to a synthesis method of a Bose factor, which comprises the following process steps: step (1): mixing xylose, acetylacetone and an alkaline substance in a solvent and heating to react to obtain a first intermediate product crude product; step (2): mixing potassium phosphate buffer, the first intermediate product crude product obtained in step (1), a KRED2935 crude enzyme solution, glucose dehydrogenase, glucose and beta-nicotinamide adenine dinucleotide phosphate monosodium salt, and converting at 25-35 DEG C for 1-2 h; after the conversion is completed, adding ethyl acetate to terminate the reaction, extracting, combining the organic phases, adding anhydrous sodium sulfate to dry, and then removing the solvent under reduced pressure through rotary evaporation to obtain the Bose factor. The application can obtain the Bose factor with high stereoselectivity, the conversion rate is high, the obtained product is easy to separate, and the problems of low stereoselectivity and difficult process amplification production in the prior art are overcome.

The application discloses a kind of corrosion-resistant fireproof plate and preparation method thereof, it is related to functional composite material technical field.The application first phosphorizes graphene oxide and obtains phosphorized graphene oxide;With 1,4-ditolyl dibromide and 1-(3-aminopropyl) imidazole as raw material, double-cation ionic liquid is synthesized, and then phosphorized graphene oxide is reacted with double-cation ionic liquid under the action of condensing agent to obtain ionic liquid functionalized graphene oxide, which is further reacted with molybdenum acetylacetone to obtain ionic liquid functionalized flame-retardant and smoke-suppressing graphene oxide;Bis (4-fluorophenyl) sulfone, bis (3-amino-4-hydroxyphenyl) sulfone and hexafluorobisphenol A are polycondensed to obtain fluorine-containing and amino-containing polyether sulfone;Finally, epoxy resin, fluorine-containing and amino-containing polyether sulfone, ionic liquid functionalized flame-retardant and smoke-suppressing graphene oxide and curing agent are mixed, defoamed and cured to obtain the corrosion-resistant fireproof plate.The corrosion-resistant fireproof plate prepared by the application has high flame retardancy, low smoke toxicity and excellent corrosion resistance.