488 results about "Ammonium fluoride" patented technology

The invention discloses a silicon-carbon negative electrode material, porous carbon and a preparation method, the porous carbon is prepared by mixing ammonium fluoride and a pre-carbonized material to prepare a premix; and putting the premix in an inert atmosphere, and carrying out pre-activation, drying, carbonization, activation and crushing treatment to obtain the composite material. And uniformly depositing the nano silicon particles into the porous carbon skeleton through a mature CVD (Chemical Vapor Deposition) process to obtain the silicon-carbon composite material. Fluorine and nitrogen co-doping modification can increase the defect degree of a carbon skeleton, efficiently relieve mechanical stress accompanied by lithium storage volume expansion of the silicon negative electrode in a micro scale, provide abundant lithium ion transport and mass transfer channels and enhance the conductivity of porous carbon, and ammonium fluoride is used as a supplementary activator besides water vapor, so that the porosity of the porous carbon is further improved, and the conductivity of the porous carbon is improved. An effective space is provided for uniform deposition of silicon, the fluorine-containing carbon layer can induce formation of a high-stability SEI film rich in LiF on the surface of the nano silicon material, and the interface stability and coulombic efficiency of the silicon negative electrode are further improved.

The invention discloses a composite coated graphite negative electrode material, a preparation method thereof and a lithium ion solid-state battery, and belongs to the technical field of lithium ion solid-state batteries, the composite coated graphite negative electrode material comprises a graphite matrix and a composite coating layer, and the composite coating layer comprises an inner layer amorphous lithium chloride and an outer layer nanocrystalline LiF / Li3N composite phase. Mixing graphite, lithium chloride containing crystal water and ammonium fluoride to obtain a mixed material; placing the mixed material in a microwave reaction cavity, heating the mixed material to 600-700 DEG C at the microwave power of 800-1200 W in an H2 / Ar mixed atmosphere, and keeping the temperature for 20-60 minutes; and cooling the sintered mixed material, grinding, and sieving with a 100-300 mesh sieve to obtain the composite coated graphite negative electrode material with a coating layer thickness of 10-50 nm. The invention provides an innovative amorphous LiCl / nanocrystalline LiF-Li3N gradient coating layer design, the performance of the lithium ion battery is remarkably improved by optimizing an ion migration path, enhancing the interface stability and reducing the process cost, and a new engineering way is provided for realizing high magnification and long cycle performance of the sulfide all-solid-state battery.

The invention relates to an elementary substance / alloy-metal oxyhydroxide anchored noble metal single atom / cluster heterojunction catalyst. A preparation method comprises the following steps: 1) dissolving a metal salt A, urea and ammonium fluoride in deionized water to obtain a mixed solution B; 2) performing hydrothermal reaction on the mixed solution B and a carrier to obtain a primary sample 1; 3) performing high-temperature calcination on the primary sample 1 in a mixed atmosphere of hydrogen and argon to obtain a primary sample 2; and 4) putting the preliminary sample 2 into a noble metal compound C solution for vacuum impregnation, taking out the sample after impregnation, and drying to obtain the catalyst. According to the scheme, the metal salt A is used as a metal source of a simple substance / alloy, the metal salt A is subjected to hydro-thermal synthesis to form a metal hydroxide and then subjected to high-temperature calcination reduction, the metal salt A is calcined to form the simple substance / alloy, then the simple substance / alloy is soaked in the precious metal compound solution C to form a metal oxyhydroxide, and meanwhile precious metal single atoms / clusters are anchored; the prepared catalyst is high in activity, and the preparation method is simple.

The invention discloses a catalyst for an n-butene isomerization reaction and a preparation method thereof, and belongs to the technical field of catalysts. The preparation method comprises the following steps: mixing a silicon source, an aluminum source, tetrapropylammonium hydroxide and water, adding boric acid, and crystallizing to obtain a seed crystal; the method comprises the following steps: mixing a silicon source, an aluminum source, pyridine and water, adding a seed crystal and ammonium fluoride, and crystallizing to obtain a core-shell type molecular sieve; adding the core-shell type molecular sieve into the bimetallic complex solution for dipping to obtain a metal-loaded type molecular sieve; adding the metal-loaded molecular sieve into a triethyl phosphine ethanol solution for treatment to obtain a phosphorus-modified molecular sieve; uniformly mixing the phosphorus-modified molecular sieve, pseudo-boehmite, sesbania powder and water, kneading, performing extrusion molding, drying and calcining to obtain the catalyst. The catalyst prepared by the invention is used for n-butene isomerization reaction, and has excellent catalytic activity and isobutene selectivity.

The invention belongs to the technical field of fly ash solid waste resource utilization, and particularly relates to a method for preparing flaky alumina by using fly ash, which is characterized by comprising the steps of fly ash pretreatment, intermediate preparation and alumina preparation, ammonium fluoride used in the alumina preparation step is a recycling product of fluorine-containing tail gas in the step, and ammonium fluoride used in the alumina preparation step is a recycling product of fluorine-containing tail gas in the step. The preparation method comprises the following specific operation steps: 1) pretreating fly ash, namely treating fly ash with a NaOH solution and an HCl solution to obtain a mixture of quartz and mullite; (2) preparing an intermediate, namely reacting a mixture of quartz and mullite with CeO2 to obtain a K3Al (SO4) 3 intermediate; and 3) preparing aluminum oxide, purifying the K3Al (SO4) 3 intermediate, grinding and mixing the purified K3Al (SO4) 3 intermediate and ammonium fluoride crystals according to the F / Al molar ratio, and roasting at high temperature to obtain a flaky aluminum oxide product. The method has the beneficial effects that the problem of low purity of flaky aluminum oxide in the existing method for preparing the aluminum oxide from the fly ash is solved, and the purity of the flaky aluminum oxide is 99.2-99.8%.

Provided are a wide-temperature-range solid-state electrolyte, a preparation method thereof and use thereof in solid-state lithium metal batteries. The preparation method includes: dissolving a lithium salt and a magnesium salt in a solvent to obtain a mixed salt solution; and mixing the mixed salt solution with an ammonia fluoride solution, subjecting a resulting mixture to reaction, and subjecting a resulting reaction product to centrifugation, washing, and drying in sequence to obtain magnesium-doped lithium fluoride nanoparticles; and mixing the magnesium-doped lithium fluoride nanoparticles, a liquid plasticizer, a polymer monomer and a thermal initiator to obtain a liquid precursor, and subjecting the liquid precursor to curing to obtain the wide-temperature-range solid-state electrolyte, where the polymer monomer is a mixture of ethoxylated trimethylolpropane triacrylate and hexafluorobutyl methacrylate.

The invention belongs to the technical field of chemical detection, and particularly relates to a method for detecting the content of boron in soil and sediment, which comprises the following detection methods: S1, weighing a sample and putting the sample into a digestion tank; s2, adding a digestion solution into the digestion tank; s3, after uniform stirring, putting the digestion tank into a microwave digestion instrument for microwave digestion; s4, after digestion is completed, closing the microwave digestion instrument, and after the digestion tank is cooled to the room temperature, filtering to remove precipitates; s5, transferring the digestion solution into a volumetric flask, and fixing the volume for subsequent analysis; and S6, analyzing the digestion solution by using ICP-OES / MS (Inductively Coupled Plasma-Optical Emission According to the method for detecting the boron content in the soil and the sediment, ammonium fluoride is used for replacing hydrofluoric acid in boron detection of the soil and the sediment, use of toxic reagents is reduced, mannitol is added, a stable complex is formed by mannitol and boron, and the recovery rate of boron is increased.

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

The invention discloses a preparation method of high-purity bis (fluorosulfonyl) imide alkali metal salt. The method comprises the following steps: (1) synthesizing bis (chlorosulfonic acid) imide by taking sulfamic acid, chlorosulfonic acid, thionyl chloride and chlorosulfonic acid isocyanate as raw materials; (2) fluorinating the bis (chlorosulfonic acid) imide by ammonium fluoride to obtain bis (fluorosulfonyl) imide ammonium salt; (3) treating the imidodisulfuryl fluoride ammonium salt solution with a strong acid ion exchange column and concentrating under reduced pressure to obtain imidodisulfuryl fluoride; (4) reacting the alkali metal salt with bis (fluorosulfonyl) imide to obtain bis (fluorosulfonyl) imide alkali metal salt; and (5) carrying out a series of purification processes on the bis (fluorosulfonyl) imide alkali metal salt to obtain the high-purity bis (fluorosulfonyl) imide alkali metal salt. The preparation method has the advantages of mild reaction conditions, low danger coefficient in the technological process, easiness in control, no use and generation of corrosive acid, greenness and environmental protection, and high yield and high purity of the bis (fluorosulfonyl) imide alkali metal salt, and is suitable for large-scale industrial application.

The invention belongs to the technical field of new energy batteries, and particularly relates to a method for preparing sodium tetrafluoroborate. The method uses relatively cheap and readily available ammonium fluoride, sodium bicarbonate, and boron trichloride gas as raw materials, wherein ammonium fluoride and sodium bicarbonate are added to an organic solvent and stirred uniformly to obtain a dispersion, boron trichloride gas is introduced, the dispersion is fully reacted, nitrogen is purged from the reaction liquid, and the filtrate is filtered to obtain a filtrate, which is concentrated, crystallized, filtered, washed, and dried to obtain sodium tetrafluoroborate. The method has the advantages of simple process, rapid and thorough reaction, no water by-product, and reduced preparation cost of sodium tetrafluoroborate while achieving a yield and purity equivalent to or even superior to that of existing sodium tetrafluoroborate.

The invention provides high-transparency rare earth doped fluoride glass and a preparation method thereof, and belongs to the technical field of glass. The calcium fluoride ensures high transparency and chemical stability, the magnesium fluoride improves the ultraviolet transmittance and the mechanical strength, and the barium fluoride optimizes the melting fluidity and the rare earth doping uniformity; aluminum fluoride is added to inhibit crystallization and enhance uniformity, the rare earth element realizes optical function regulation and control, and ammonium fluoride provides a fluorine source and reduces impurities; in a preparation link, quick lime is dedusted and then reacts with pure water in proportion, impurities in a calcium nitrate solution are removed by hydrogen peroxide, uniform growth of calcium carbonate crystal nucleuses is controlled by ammonia water and carbon dioxide, and calcium fluoride is synthesized by hydrofluoric acid in proportion and dried at low temperature after plate-frame pressure filtration and purification; after the raw materials are refined through ball milling, the melting temperature is controlled in stages, impurities, reaction integrity and a microstructure are accurately controlled in the whole process, and finally the high-transparency functional glass is prepared.

The invention belongs to the technical field of photoelectric ceramic material manufacturing, and relates to high-density calcium fluoride photoelectric ceramic and an ultralow-temperature preparation method thereof. The method comprises the following steps: S1, wet mixing: weighing calcium hydroxide (Ca (OH) 2) powder and ammonium fluoride (NH4F) powder according to a molar ratio of 1: (1.5-2), and mixing by taking an organic solvent as a medium to form slurry; s2, rapid drying: rapidly drying the slurry obtained in the step (1) to obtain mixed precursor powder; and S3, reaction cold sintering: putting the mixed precursor powder into a mold, and carrying out reaction cold sintering. The sintering temperature used in the method is not higher than 350 DEG C, and the sintering temperature can be changed according to actual needs so as to improve the mechanical property of the ceramic, and the mechanical property is improved by 2-4 times compared with that of a conventional hot pressed sintering sample.

The invention relates to the technical field of niobium-tantalum-iron ore purification, in particular to a method for preparing high-purity tantalum pentoxide and niobium pentoxide from niobium-tantalum-iron ore. The method comprises the following steps: firstly, adding ammonium fluoride and ammonium sulfate to help mineral decomposition and reduce the roasting temperature, then treating the niobium-tantalum iron ore by using a sulfuric acid-hydrofluoric acid mixed solution to fully dissolve niobium-tantalum oxides, then extracting and separating niobium and tantalum by using a specific solvent system, and finally adding ammonia water to precipitate and calcine to obtain the niobium-tantalum iron ore. The high-purity niobium pentoxide and tantalum pentoxide are prepared, the product yield is high, the impurity content is low, and the niobium pentoxide and tantalum pentoxide are suitable for being used as raw materials of capacitor-grade tantalum powder and niobium powder.

The invention provides porous alumina ceramic and a preparation method thereof, and relates to the technical field of ceramic materials. The invention relates to a preparation method of porous alumina ceramic. The preparation method comprises the following steps: dispersing alpha-cellulose powder in deionized water to form a cellulose suspension; stirring to fully swell the cellulose and form uniform gel, and freeze-drying to obtain a template; dissolving aluminum nitrate hexahydrate, magnesium nitrate hexahydrate and yttrium nitrate hexahydrate in absolute ethyl alcohol to obtain a precursor solution; putting gamma-Al2O3 micro powder and ammonium fluoride into a ball milling tank, adding the precursor solution and a dispersing agent, adding zirconium oxide balls and absolute ethyl alcohol into the ball milling tank, and performing ball milling to obtain ceramic slurry; dipping a template into the ceramic slurry, and performing dipping treatment under a vacuum condition to form a composite green body; and sintering to obtain the porous alumina ceramic. According to the porous aluminum oxide ceramic, the process stability is improved, and the problem that the strength is sharply reduced when the porosity is too high is solved.

The invention provides a method for preparing high-purity flaky alumina based on a hydrolysis method, and belongs to the field of high-purity flaky alumina powder. The method comprises the steps that metal aluminum scraps are pretreated; the method comprises the following steps: putting metal aluminum scraps, an alkaline organic matter catalyst and a morphology control agent into water, and carrying out a hydrolysis reaction at a set temperature for a set time to obtain a reaction mixed solution; carrying out solid-liquid separation, washing and drying on the reaction mixed solution to obtain flaky aluminum hydroxide; and roasting the flaky aluminum hydroxide to remove crystal water so as to obtain high-purity flaky aluminum oxide, wherein the alkaline organic matter catalyst comprises at least one of the following components: tetraethylammonium hydroxide, tetramethylammonium hydroxide, tetrapropylammonium hydroxide and tetrabutylammonium hydroxide; the morphology control agent comprises at least one of ammonium bifluoride and ammonium fluoride. The preparation method disclosed by the invention is simple in process flow, free of an impurity removal process, mild in reaction condition, short in reaction time and free of environmental pollution, and the product is regular in shape and high in purity.

The application discloses a kind of microspheroidal high-entropy spinel type ferrite wave-absorbing materials and preparation method thereof, belong to electromagnetic wave absorbing material technical field, the preparation method includes with the designed molar ratio six metal nitrate is weighed and dissolved in deionized water, then add ammonium fluoride, urea, after stirring, the obtained solution is hydrothermal reaction at a certain temperature for a certain time to obtain precursor, the precursor is calcined to obtain microspheroidal high-entropy spinel type ferrite.The obtained wave-absorbing material is single-phase spinel structure, micron-sized spherical morphology, its chemical formula is MFe2O4;Wherein M=Co, Ni, Cu, Zn, Cr.The microspheroidal high-entropy spinel type ferrite wave-absorbing material and preparation method thereof are used, and the performance of pure ferrite wave-absorbing material can be effectively improved, with the characteristics of simple preparation, strong absorption performance, absorption frequency bandwidth.

The invention provides a preparation process of an ultra-clean high-purity ammonium fluoride solution, and belongs to the technical field of preparation of electronic-grade chemicals. The microcapsule adsorbent is creatively introduced, various purification technologies are combined, the content of metal ions, particles and organic impurities in the ammonium fluoride solution is remarkably reduced, and the strict requirement of the semiconductor industry for high-purity chemicals is met. Wherein the hollow structure of the microcapsule adsorbent and the amide modified cyclodextrin have a synergistic effect, so that the microcapsule adsorbent is endowed with high specific surface area and strong adsorption capacity and has a strong adsorption effect on heavy metal ions and impurity particles, and the polyacrylate shell material enhances the stability of the microcapsule adsorbent in a strong acid / alkali environment. The traditional process has the problem of poor filtering effect and needs to use complex equipment (such as a centrifugal machine and an ultrafiltration device) for multi-step separation, while the method can achieve an efficient separation effect through conventional filtering operation, has the characteristics of high purification efficiency, convenience in separation, stable product quality and the like, and is suitable for industrial production.

The invention relates to a controllable electrochemical etching strategy based on solubility product difference, in particular to a preparation method of a barium sulfate modified NiCo-LDH aqueous alkaline zinc battery positive electrode material, which comprises the following steps: firstly, dissolving 1, 4-phthalic acid and sodium hydroxide in a molar ratio of 1: 2 in water to obtain a solution A; dissolving barium nitrate pentahydrate, cobalt nitrate hexahydrate, nickel nitrate hexahydrate and ammonium fluoride in water according to a molar ratio of (0-1.5): 1: 4: 10 to obtain a solution B; the preparation method comprises the following steps: fully mixing the solutions, transferring the mixed solution into an autoclave containing foamed nickel (NF), and carrying out solvothermal reaction to obtain a tri-metal Co / Ni / Ba-MOF precursor (CNBx-BDC); cNBx-BDC is used as a working electrode, a platinum wire is used as a counter electrode, Hg / HgO is used as a reference electrode, 5-6M potassium hydroxide and 0.05-0.06 M sodium sulfate are used as electrolyte, a three-electrode system and a cyclic voltammetry method are adopted, electrochemical etching is carried out at the scanning rate of 20-30mV s <-1 > under the voltage range of 0-0.5 V, and the barium sulfate nanodot functionalized Co / Ni / Ba-LDH electrode (BS (at) CN-LDH) is obtained after six times of circulation. The unique porous structure can provide more electrochemical active sites and enhance electrolyte infiltration capacity, and the constructed heterostructure forms a strong built-in electric field, accelerates charge transfer, reduces ion diffusion energy barriers and improves energy utilization efficiency.

The aluminum fluoride coated nano silicon material is prepared from nano silicon powder, aluminum nitrate nonahydrate, ammonium fluoride, absolute ethyl alcohol and deionized water, and an aluminum fluoride coating layer and a nano silicon negative electrode material are compounded to form an aluminum fluoride coated nano silicon material structure. The aluminum fluoride coating layer on the surface can be converted into a fast ion conductor in the battery circulation process, so that the lithium ion diffusion rate is increased, and migration of lithium ions between the nanometer silicon negative electrode and the electrolyte is promoted. Under the coating protection effect of the coating layer, the volume expansion of the nano-silicon material is improved, the voltage attenuation speed is slowed down, the cycling stability is greatly improved, the cycling performance of the nano-silicon negative electrode material is improved, and silicon particle breakage, material pulverization and falling off from a pole piece are avoided. The coating amount of the aluminum fluoride coating layer is compared, and the optimal coating amount is given. The method has the advantages of low cost and high controllability.

The invention discloses carbon-coated lithium manganese iron phosphate as well as a preparation method and application thereof, and belongs to the technical field of battery positive electrode materials. A preparation method of carbon-coated lithium manganese iron phosphate comprises the following steps: S1, mixing and dispersing a manganese source, an iron source, a lithium source, a phosphorus source and a carbon source, grinding, spray-drying and sintering to prepare carbon-coated lithium manganese iron phosphate; and S2, ammonium fluoride and the carbon-coated lithium manganese iron phosphate obtained in the step S1 are sequentially subjected to low-temperature fluorination sintering treatment and high-temperature defluorination sintering treatment. According to the preparation method, the carbon coating layer is modified through fluorine doping subjected to low-temperature fluorination sintering treatment in the step S2, so that the electronic structure distribution and the conductivity of the material are regulated and controlled, and the doped fluorine atoms leave the system in a fluorine gas form through fluorine-doped defluorination sintering treatment at a high temperature; and then proper sintering is performed to accelerate polymerization and heal excessive defect sites, so that the specific surface area of the material is reduced, and controllable adjustment of the specific surface area of the material is realized.

The invention relates to the technical field of etching solutions, and particularly discloses an etching solution for inhibiting etching of metallic titanium and application of the etching solution. The etching solution contains hydrofluoric acid, ammonium fluoride, an additive 1 and an additive 2; wherein the additive 1 is a fluorine capture type inhibitor, and the additive 2 is a surface adsorption type organic protective agent. The etching solution can effectively inhibit the corrosion of a titanium layer while keeping the high etching rate of silicon oxide, obviously improves the etching selection ratio of silicon oxide to titanium, has lower surface tension and higher uniformity, and is suitable for a wet etching scene with a complex structure. The additive 1 captures free fluorine ions through complexation or precipitation, the activity of the fluorine ions is reduced, and therefore the chemical attack on the titanium surface is reduced; and the additive 2 can form a transient adsorption protective film on the titanium surface to further delay the dissolution of titanium. The synergistic effect of the two additives can effectively inhibit titanium corrosion and maintain high etching efficiency.

The invention discloses preparation of an Ag-modified Ni2P composite material and application of the Ag-modified Ni2P composite material to ammonia production through electro-catalysis of nitrate reduction, and belongs to the technical field of ammonia production through electro-catalysis of nitrate reduction. The preparation method of the Ag modified Ni2P composite material comprises the following steps: mixing a silver source, a nickel source, urea and ammonium fluoride, and reacting to obtain an Ag-Ni (OH) x precursor; and mixing the Ag-Ni (OH) x precursor with a phosphorus source, and carrying out phosphating treatment to obtain the Ag modified Ni2P composite material. According to the invention, Ni2P is used as a main catalytic substrate, and abundant Ni active sites are provided and are responsible for activating N-O bonds and carrying out multi-step electron transfer; ag is a doping element, so that the electron utilization rate of the catalyst can be increased, the electron structure of a Ni site can be optimized, and intermediate adsorption can be improved; and the two components cooperate to jointly promote efficient nitrate electro-catalysis ammonia preparation reaction, and convenience is provided for starting the whole reduction reaction chain, so that the yield of the target product NH4 < + > is improved.

The invention relates to the field of catalyst preparation and application thereof, in particular to a preparation method and application of zirconium dioxide catalysts with different crystal phases, a zirconium precursor and P123 are dissolved in deionized water, then ammonia water is added, and then the mixture is subjected to oil bath, product filtering and washing; and drying and then roasting to obtain tetragonal phase ZrO2. The preparation method comprises the following steps: dissolving a zirconium precursor and yttrium nitrate in deionized water, adding citric acid, adding ammonia water, carrying out oil bath, drying, and roasting to obtain cubic phase ZrO2; the preparation method comprises the following steps: dissolving a zirconium precursor in deionized water, adding ammonium fluoride, stirring, carrying out a hydrothermal reaction, cooling, carrying out centrifugal washing, drying, and roasting in a muffle to obtain the monoclinic phase ZrO2. Compared with a traditional metal supported catalyst, the problems of metal sintering, agglomeration, loss and the like are avoided. Therefore, the prepared ZrO2 catalyst with different crystal phases is an effective catalyst.

The invention discloses a ruthenium-loaded nickel-cobalt oxide heterostructure electrocatalyst and a preparation method thereof.The preparation method of the ruthenium-loaded nickel-cobalt oxide heterostructure electrocatalyst comprises the steps that nickel nitrate hexahydrate, cobalt nitrate hexahydrate, ammonium fluoride and urea are dissolved in deionized water and stirred for 30 min, the mixture and carbon cloth are subjected to a hydrothermal reaction, cleaning, drying and calcination are conducted, and the ruthenium-loaded nickel-cobalt oxide heterostructure electrocatalyst is obtained; forming a second intermediate product; ruCl3.xH2O and KCl are added into H2O, magnetic stirring is conducted for 30 min, and a second process solution is obtained; and performing electrochemical deposition of ruthenium on the second intermediate product through cyclic voltammetry to obtain a third intermediate product, and drying the third intermediate product to obtain the ruthenium-loaded nickel-cobalt oxide heterostructure electrocatalyst. According to the preparation method of the ruthenium-loaded nickel-cobalt oxide heterostructure electrocatalyst provided by the embodiment of the invention, the proportion of ruthenium in the product is more easily regulated and controlled, so that the optimal nitrate electrocatalysis reduction performance is obtained.

The invention provides a nitrogen-fluorine double-element doped porous carbon material, a silicon-carbon negative electrode material and a preparation method thereof, and the preparation method of the porous carbon material comprises the following steps: mixing porous carbon with ammonium fluoride and / or ammonium bifluoride, and carrying out vapor deposition coating or liquid phase coating; and calcining the coated porous carbon material in a closed environment in an inert atmosphere to obtain the nitrogen-fluorine double-element doped porous carbon material. According to the invention, by utilizing the characteristics of nano-scale micropores and super-large specific surface of porous carbon and the properties of low melting point and low boiling point of ammonium fluoride and ammonium bifluoride, a uniformly coated ammonium fluoride and ammonium bifluoride coating layer is obtained by adopting a vapor deposition or liquid phase coating method, and then the porous carbon material is obtained by utilizing high-temperature calcination treatment. According to the present invention, the characteristics of high specific surface and nano-scale micropores can be simultaneously retained, and after the silicon-carbon negative electrode material is prepared, the expansion of the silicon-carbon negative electrode material is substantially reduced, the cycle performance of the material is ensured, and the rate capability of the obtained silicon-carbon negative electrode material is improved.

The invention discloses a preparation method and application of a high-entropy layered double hydroxide oxygen evolution catalyst, and relates to the field of oxygen evolution reaction catalysis, and the preparation method comprises the following steps: S1, washing foamed nickel in absolute ethyl alcohol and deionized water, and then carrying out ultrasonic treatment in a hydrochloric acid solution to obtain pretreated foamed nickel; s2, adding ferric salt, cobalt salt, nickel salt, manganese salt, zinc salt and a proper amount of urea into deionized water, then adding ammonium fluoride, and uniformly stirring to obtain a mixed solution; and S3, transferring the mixed solution and the pretreated foamed nickel into a reaction kettle, carrying out a hydrothermal reaction, and washing and drying the obtained product to obtain the high-entropy layered double hydroxide oxygen evolution catalyst. According to the method, the key regulation and control effect of NH4F on the structure, chemical and electro-catalytic properties of HELDHs in the synthesis process of the HELDHs is analyzed, and the performance enhancement is attributed to NH4F-induced morphology and crystal engineering and catalytic active cation vacancies generated in situ through selective leaching of Zn < 2 + > and adsorption of sulfate under the alkaline condition.

The invention discloses a preparation method and application of double-doped biochar, and belongs to the technical field of biochar preparation, and the preparation method comprises the following steps: cleaning, drying and crushing apple branches to obtain branch powder with uniform particles; uniformly blending the branch powder, urea and potassium formate with deionized water, drying, and carrying out calcination reaction at 600-800 DEG C; cooling to room temperature, sequentially washing with diluted hydrochloric acid and deionized water until the pH is constant, and drying to obtain N-doped biochar; and uniformly blending the N-doped biochar and ammonium fluoride by using deionized water, drying, and carrying out calcination reaction at 400-600 DEG C to obtain the double-doped biochar. Compared with single N doping, the preparation method of the N and F double-doped biochar provided by the invention can more efficiently regulate and control pore development of the biochar, the step-by-step preparation method can accurately regulate and control the introduction effect of doped elements, the specific surface area of the prepared N and F double-doped biochar is greatly increased, and the preparation method is suitable for large-scale industrial production. And a sufficient structure bearing foundation is provided for the high-efficiency adsorption performance of the material.

This invention relates to a method for preparing carbon materials based on in-situ surface fluoride modification, comprising the following steps: ① dissolving carbon material powder, aluminum nitrate, and polyvinyl alcohol in anhydrous ethanol to obtain an aluminum nitrate solution; ② dissolving ammonium fluoride in a mixed solvent to obtain an ammonium fluoride solution; slowly adding the ammonium fluoride solution dropwise to the aluminum nitrate solution to carry out an in-situ AlF3 growth reaction to obtain a composite material precursor; ③ drying the composite material precursor and then calcining it using a programmed temperature rise method to solidify the coating layer, thereby obtaining the AlF3@C composite material. This invention also discloses the application of this carbon material. The preparation method of this invention is simple and low-cost, and can efficiently prepare AlF3@C composite materials. The obtained AlF3@C composite material, as a negative electrode material for potassium-ion or lithium-ion secondary batteries, can significantly improve a series of properties such as the initial coulombic efficiency, rate performance, cycle stability, and potassium ion diffusion kinetics of the battery.

The application provides a preparation method of a zeolite adsorbent, comprising the following steps: a) treating a zeolite in an oxalic acid solution, and drying to obtain a zeolite precursor; b) treating the zeolite precursor obtained in the step a) in an ammonium fluoride solution, and drying to obtain a zeolite adsorbent. The application also provides a zeolite adsorbent and an ammonia adsorption method. The preparation method provided by the application is mild and controllable in structure adjustment, and the zeolite is post-treated to make the zeolite framework selectively rearrange or slightly adjust in local areas, so that mesoporous channels with appropriate sizes and good connectivity are generated. The preparation method provided by the application can introduce mesopores while maintaining the integrity of the microporous framework structure as much as possible, avoids damage to the micropores or collapse of the framework, and has the characteristics of simple process route, wide range of control parameters, good repeatability and suitability for large-scale preparation.

The invention belongs to the technical field of auxiliary preparation, and provides a curing material applied to a flameless combustion process of copper-containing sludge and a preparation method. The preparation method comprises the following steps: firstly, mixing iron nitrate nonahydrate, ferrous sulfate heptahydrate, a manganous nitrate solution and citric acid to prepare a ferrite precursor; further, a rare earth phosphate nano dispersion is synthesized through a hydrothermal method, lanthanum nitrate hexahydrate and cerium nitrate hexahydrate are used as rare earth sources, and ammonium dihydrogen phosphate and ammonium fluoride are introduced to provide phosphate radicals and fluorine ions; meanwhile, multi-element co-doped amorphous powder is prepared through a sol-gel method, tetraethoxysilane serves as a silicon source, zirconium oxychloride octahydrate, tetra-n-butyl titanate and niobium pentachloride are supplemented, a thermally stable amorphous oxide matrix is formed under high-temperature heat treatment, and the high-temperature mechanical property is provided; and finally, mixing kaolin or bentonite mineral powder with the synthesized ferrite precursor, the rare earth phosphate nano dispersion, the multi-element amorphous powder and other auxiliaries to form slurry, and drying to form the curing material.