3043 results about "Metal salts" patented technology

An integrated carbon honeycomb structure material and its preparation method are disclosed, belonging to the field of carbon materials technology. Based on a co-sacrificial template low-temperature pyrolysis strategy, the target material can be obtained through three main steps: preparation of a metal salt-colloidal microsphere template precursor, precursor pressing and molding, and subsequent calcination and carbonization. This technology has the characteristics and advantages of simple preparation process, regular and controllable macroscopic structure of the sample (such as shape, area, and thickness), rich and tunable chemical composition, and three-dimensional interconnection of graphene carbon matrix. It has great application potential in many fields such as electrochemical energy storage, catalysis, gas separation, adsorption, and electromagnetic shielding.

A long-term fire retarding biochemical liquid composition including: a dispersing agent realized in the form of a major amount of water, for dispersing alkali metal ions dissolved in the water; a major amount of a first fire retarding agent realized in the form of a primary alkali metal salt of a nonpolymeric saturated carboxylic acid, for example, tripotassium citrate, for providing metal potassium ions dispersed in the water when the at least one alkali metal salt is dissolved in the water to form a mixed retardant solution; a minor amount of a second fire retarding agent realized in the form of a secondary alkali metal salt of a nonpolymeric saturated carboxylic acid, for example, potassium, sodium, calcium and / or magnesium benzoate, for providing benzoate ions dispersed in the water when the secondary alkali metal salt is dissolved in the mixed retardant solution, for functioning as a secondary fire retardant agent.

The invention discloses a metal-doped carbon quantum dot as well as preparation and application of the metal-doped carbon quantum dot in a nano antibacterial agent, citric acid, urea and tea polyphenol are taken as precursors, metal salt is added, carbon dot synthesis and metal ion doping are synchronously completed in one step through a hydrothermal method, and the metal-doped carbon quantum dot is prepared; the surfaces of the metal-doped carbon quantum dots are negatively charged, and the metal-doped carbon quantum dots have peroxidase-like activity and catalase-like activity at the same time; the metal ions adopt any one of Fe < 3 + >, Cu < 2 + > and Ce < 3 + >; the metal-doped carbon quantum dots are in a sphere-like shape. The metal-doped carbon quantum dots prepared by the preparation method disclosed by the invention have peroxidase-like activity and catalase-like activity at the same time through precise doping of metal ions, and the two activities have a synergistic effect in an oral periodontitis microenvironment, so that a good antibacterial effect is achieved.

This invention discloses a method for preparing a CuZnAlGa-based layered double hydroxide (TLH)-derived catalyst for methanol production from carbon dioxide-rich syngas. Using Cu, Zn, Al, and Ga metal salts as precursors, Na₂CO₃ and NaOH as precipitants, and a mixed alcohol-water solution as an auxiliary solvent, co-precipitation is performed under controlled temperature and pH to obtain a LDH-like catalyst precursor. After high-temperature calcination and in-situ reduction in a hydrogen atmosphere, a layered framework structure of Cu nanoparticles immobilized by oxides is obtained. The LDH-like structure provides lattice confinement, preventing Cu particle aggregation, and the interaction between Cu and the oxides enhances the catalyst surface's adsorption capacity for CO and CO₂, thereby improving the activity and stability of methanol production from carbon dioxide-rich syngas.

Adhesive compositions including a multivalent metal salt, an multidentate acidic organic compound, and an aqueous medium are disclosed. The multivalent metal salt and multidentate acidic organic compound can include, as a mixture, a carbonate salt and / or carbonic acid. The aqueous medium can include pH adjusting agent such as sodium hydroxide. The adhesive composition, upon curing, can have a porosity of 10-50%. The adhesive composition, upon curing, can include a plurality of pores. The adhesive composition can be porous, and upon curing can have a plurality of pores having a pore size of between 20 μm to 200 μm. Methods of producing the adhesive composition are disclosed. Methods of using the adhesive composition are further disclosed.

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

The invention belongs to the technical field of lithium batteries, and particularly relates to a lithium-rich manganese-based positive electrode material and a preparation method and application thereof. The preparation method comprises the following steps: mixing a metal salt solution, a precipitator and a complexing agent, and carrying out coprecipitation reaction on an obtained coprecipitation reaction precursor solution to obtain a lithium-rich manganese-based precursor; the metal salt solution comprises a manganese element, a cobalt element and a nickel element; and mixing the lithium-rich manganese-based precursor, a lithium source, an auxiliary agent and a dispersing agent, and calcining to obtain the lithium-rich manganese-based positive electrode material, the auxiliary agent comprises a nitrogen source or a nitrogen source and a carbon source. The first discharge specific capacity, the rate capability and the cycling stability of the lithium-rich manganese-based positive electrode material can be improved, and the problems of capacity fading, discharge voltage drop and dynamic delay in an electrochemical reaction process are solved.

The invention discloses a preparation method for selectively oxidizing thioether into sulfoxide through photo-initiation, and belongs to the field of synthesis of medical compounds. The preparation method comprises the following steps that in the air atmosphere, a thioether compound is dissolved in an acetonitrile-water mixed solvent, inorganic metal salt catalysts such as ferric chloride and copper sulfate are added, the mixture reacts for 8-48 h at the temperature of 0-45 DEG C under illumination with the wavelength of 295-405 nm, selective oxidation is carried out, and the sulfoxide product is obtained, and the molar ratio of thioether to the catalysts is 5: 1. The method overcomes the problems of excessive oxidation risk, complicated operation, environmental pollution and the like caused by dependence of a noble metal catalyst and use of a strong oxidant in the existing thioether oxidation method, has the advantages of high catalytic efficiency, high yield and excellent selectivity, can greatly reduce the production cost, is suitable for later industrial synthesis and amplification, and has wide application prospects. The method has the advantages of no expensive metal catalyst or oxidant, simple preparation process, high efficiency, environmental protection, safety and cost saving.

The invention provides a catalyst, a preparation method and application thereof, and a method for preparing primary amine by catalyzing nitrile compound hydrogenation, and particularly relates to the technical field of catalyst synthesis. The catalyst comprises a nickel / cobalt-based catalyst and a metal salt; wherein the nickel / cobalt-based catalyst is selected from any one of a supported nickel / cobalt-based catalyst, a Raney nickel / cobalt catalyst or a nickel / cobalt nanocrystal; the metal salt comprises any one or a combination of at least two of tungsten salt, molybdenum salt, vanadium salt, aluminum salt and cerium salt. The metal salt and the nickel / cobalt main catalyst have a synergistic effect: the surface electron density is adjusted through electron transfer, the hydrogen dissociation and cyano adsorption activation capacities are enhanced, the hydrogenation activity is improved, and the mild condition reaction is assisted; the surface chemical environment is changed or steric hindrance is borrowed, the primary amine selectivity is improved, and byproducts are inhibited; aluminum salt, cerium salt and the like inhibit nickel / cobalt agglomeration, increase active sites, enhance stability, prolong the service life and reduce the dosage.

The invention belongs to the technical field of lithium ion battery negative electrode materials, and particularly relates to a spinel type metal oxide coated hard carbon composite material based on a lattice matching mechanism, and a gradient doping preparation method of the spinel type metal oxide coated hard carbon composite material can overcome the defects that a hard carbon material is low in initial coulombic efficiency (about 50%), low in lithium ion transmission rate and poor in rate capability. According to the invention, magnesium salt, aluminum salt, copper salt and other metal salts are mixed with hard carbon, a precipitant is added, and a hydrothermal method is combined with a calcination process to obtain the core-shell structure composite material with hard carbon coated with a spinel structure. The technology has the following three obvious advantages: (1) lattice adaptive design of the spar type metal oxide and the hard carbon, (2) molybdenum-copper gradient doping repair of the SEI film, and (3) stable circulation of more than 5000 times at the capacity of 350mAh / g.

The invention relates to the technical field of membrane separation and seawater desalination, in particular to a high-boron-removal-rate reverse osmosis membrane and a preparation method and application thereof. The polyamide reverse osmosis membrane with at least 70% nodular areas on the surface is prepared by introducing the ethylenediamine tetraacetic acid metal salt into the water phase solution as a complexing additive, and the boron removal rate of the membrane can be improved on the basis of ensuring the retention rate and flux of the membrane.

The invention provides a long-acting dripping antifogging master batch as well as a preparation method and application thereof, and the long-acting dripping antifogging master batch comprises the following components in parts by weight: 40-90 parts of matrix resin, 10-40 parts of a dripping agent, 1-20 parts of metal salt and 1-20 parts of a high-molecular-weight slow release agent. According to the long-acting dripping antifogging master batch disclosed by the invention, the dripping agent, the metal salt and the high-molecular-weight slow-release agent are compounded, and the long-acting dripping antifogging master batch is used for preparing a thin film material, so that the dripping lasting period of the thin film material can be effectively prolonged, and meanwhile, the thin film has relatively high light transmittance.

The invention discloses a coated titanium anode and an embedding preparation method thereof, and belongs to the technical field of coated titanium anodes, metal salt powder, an organic additive and inert filler are fully mixed to form embedding agent powder, the mass fraction of metal salt is 45-59%, the mass fraction of the organic additive is 1-5%, and the mass fraction of the inert filler is 40-50%; the sintering treatment is as follows: the pretreated titanium substrate is completely immersed in the embedding agent powder, the sintering temperature is 400-600 DEG C, the sintering time is 1-3 hours, and the heating rate is 5-10 DEG C / min. According to the method, low-temperature sintering is realized by precisely regulating and controlling the components and the proportion of the embedding medium and combining process parameters such as low-temperature sintering, and the damage to a titanium substrate is avoided; and meanwhile, the coating binding force of the titanium anode is improved, the service life of the titanium anode is prolonged, and technical innovation and industrial value are achieved.

The invention belongs to the technical field of energy materials, and provides a multi-functional-layer lithium manganate positive electrode material and a preparation method thereof and a lithium battery, the multi-functional-layer lithium manganate positive electrode material comprises a core body and a coating layer, the core body sequentially comprises a bulk-phase-doped lithium manganate matrix, an induction doping layer and a modification doping layer from inside to outside, the chemical general formula of the core body is Li < 1 + a > Mn < 2-b-c-d > M R < c > X < d > O < 4-e > Z < e >, bulk phase doping elements of the matrix are M and Z, a crystal face induction element is X, and a modification doping element is R; the coating layer is a compound comprising a coating element M '; a supported crystal face inducer is also adopted for further inhibiting the growth of the crystal face (111) and reducing the area of the crystal face (111) so as to form the positive electrode material of a polyhedral spinel crystal structure comprising at least 26 crystal faces, and the crystal face inducer comprises a phosphorus-containing compound, a boron-containing compound or at least + 5 valence metal salt; the Mn dissolution reaction is reduced, and the electrochemical performance of the lithium manganate is improved.

The application discloses a platinum-based high-entropy intermetallic compound and a preparation method and application thereof as a hydrogen fuel cell cathode catalyst, and belongs to the field of fuel cells.The preparation method comprises the following steps: S01, adding platinum salt, at least five other metal salts and a nitrogen-rich organic compound into an organic solvent, uniformly mixing, and obtaining a metal precursor mixed solution; S02, adding a carbon carrier into the metal precursor mixed solution, fully mixing, drying, collecting, and obtaining a precursor; and S03, heat treating the dried precursor under a reducing atmosphere, and performing heat preservation treatment, so as to obtain the platinum-based high-entropy intermetallic compound.The preparation method is simple, low in cost and good in repeatability, the prepared catalyst has the advantages of uniform particle size and high oxygen reduction activity, and has a good development prospect in the field of hydrogen fuel cell catalyst applications.

The invention belongs to the technical field of nano materials, and relates to a carbon thermal reduction driven high-entropy oxide metastable-state material and a preparation method and application thereof.The preparation method comprises the steps that S1, carbon and soluble metal salt are dissolved in a solvent for ultrasonic treatment, and a metal salt solution and a carbon suspension are obtained; s2, adding a metal salt solution into the carbon suspension, adding strong base, and stirring to obtain a coprecipitation polymer; s3, re-dispersing the coprecipitation polymer in the solvent, adding extra ferric salt and urea, mixing and stirring, and freeze-drying the mixed solution to obtain precursor powder; s4, performing staged annealing treatment on the precursor powder under low oxygen partial pressure to obtain a carbon-loaded high-entropy oxide metastable-state material; the prepared high-entropy oxide metastable-state material is of an alloy phase and high-entropy oxide double-phase coupling structure, the polarization loss of electromagnetic waves is enhanced through a heterogeneous interface, and the high-entropy oxide metastable-state material has the advantages of being excellent in impedance matching and wide in electromagnetic wave absorbing bandwidth and can be widely applied to the fields of industrial electronics, medical communication and military stealth.

The invention belongs to the technical field of catalytic materials and hydrocarbon reforming, and particularly relates to a high-entropy catalyst as well as a preparation method and application thereof. The preparation method comprises the following steps: mixing a metal salt solution containing lanthanum, chromium, copper, zinc, manganese, nickel, iron and cobalt ions with a chelating agent and a dispersing agent for reaction, carrying out ultrasonic cavitation treatment to obtain sol, adjusting the pH value, gelatinizing under an oil bath heating condition to obtain a colloidal precursor, drying, and calcining in an air atmosphere to obtain a perovskite type high-entropy oxide precursor; and then treating in a reducing atmosphere to obtain the FeZnCuNiCo perovskite type high-entropy alloy catalyst which contains metal components of La, Cr, Ni, Mn, Fe, Zn, Cu and Co and takes a multi-metal alloy active center of Fe-Zn-Cu-Ni-Co as a main component. The high-entropy catalyst can meet the harsh requirements of high temperature, strong carbon deposition driving force and long-period operation in a propane dry reforming reaction, and is suitable for industrial application scenarios of continuous production of high-temperature synthesis gas.

The present invention discloses coated hydrophobic polyphenol nanoparticles, preparation method therefor and application thereof. The preparation method for coated hydrophobic polyphenol nanoparticles includes: (1) obtaining a hydrophobic polyphenol nanoparticles suspension; (2) injecting a catechin aqueous solution and a metal salt aqueous solution into the hydrophobic polyphenol nanoparticles suspension to obtain a composite nanoparticles suspension; (3) removing excess catechin and metal ions from the composite nanoparticles suspension to obtain a coated hydrophobic polyphenol nanoparticles suspension. The present invention provides an application of the coated hydrophobic polyphenol nanoparticles in the preparation of pectin gel. The coated hydrophobic polyphenol nanoparticles exhibit significantly enhanced biological activity and long-term stability, developing a pectin gel with long-term stability.

The invention relates to a method for preparing a high-quality quasi-two-dimensional perovskite thin film on a gallium nitride substrate, and relates to the technical field of semiconductors. The method for preparing the high-quality quasi-two-dimensional perovskite thin film on the gallium nitride substrate comprises the following steps: cleaning the gallium nitride substrate, and carrying out Plasma treatment; spin-coating a perovskite precursor solution on the processed gallium nitride substrate; the solute of the perovskite precursor solution is butylamine bromide powder, lead bromide powder and cesium bromide powder, and the solvent is a mixed solution of DMF (Dimethyl Formamide) and DMSO (Dimethylsulfoxide); adding a brominated metal salt into the perovskite precursor solution; and performing thermal annealing treatment on the perovskite thin film. According to the invention, a technology of growing a high-quality quasi-two-dimensional perovskite thin film by adopting a spin-coating process is adopted, and the high-quality thin film with uniform phase distribution is obtained by optimizing the proportion of a precursor solution and introducing inorganic salt to regulate and control growth kinetics.

The invention discloses ternary synergistic nano-enzyme hydrogel as well as a preparation method and application thereof, and relates to the technical field of biomedical materials. The preparation method comprises the following steps: dissolving zinc nitrate hexahydrate and ferric nitrate nonahydrate in methanol; dissolving 2-methylimidazole in methanol, adding into a metal salt solution, stirring, and sequentially centrifuging, washing and drying to obtain Fe / ZIF-8 nano-enzyme; the preparation method comprises the following steps: adding methacrylated gelatin and hyaluronic acid into deionized water, stirring, cooling to room temperature, and refrigerating to obtain a GelMA-HA precursor solution; and adding the Fe / ZIF-8 nano-enzyme into the GelMA-HA precursor solution, stirring, injecting into a mold, and carrying out ultraviolet light cross-linking curing to obtain the ternary synergistic nano-enzyme hydrogel. According to the hydrogel disclosed by the invention, active oxygen is efficiently removed and oxygen is produced through Fe / ZIF-8 nano-enzyme, and cartilage repair is promoted in combination with lubrication and slow release functions of gelatin hydrogel, so that a new strategy is provided for treatment of osteoarthritis.

The invention provides a method for preparing a high-voltage medium-nickel ternary positive electrode material by synergistic regeneration of a waste ternary lithium battery, which comprises the following steps: S1, taking a pretreated waste high-nickel and low-nickel ternary positive electrode material, calculating and supplementing a metal source and a lithium source according to the metal proportion of the actual content, and mixing the elements according to the total molar ratio of Li: (Ni + Co + Mn) = 1.0-1.1; s2, a composite fluxing agent containing lithium ion metal salt is added into the calibration mixture obtained in the S1, and two-stage sintering is carried out; and S3, coating the surface of the final product with a metal oxide aqueous solution corresponding to the lithium ion metal salt in the S2 as a coating agent to obtain the ternary positive electrode material. The nickel-rich characteristic of the high-nickel material and the manganese / cobalt-rich characteristic of the low-nickel material are utilized to form element complementation, so that the utilization rate of nickel, manganese and cobalt elements in the waste material is maximized, and the composition proportion limitation during regeneration of a single waste material is broken through.

The invention relates to the technical field of semiconductor material preparation, and provides a TaC composite coating process based on a carbon nanostructure transition layer and a product thereof. The method comprises the following steps: a) pretreating the surface of a base material to form a groove, b) introducing a carbon source gas, carrying out first chemical vapor deposition under the action of a metal salt catalyst to grow carbon nanoparticles, and depositing the base material pretreated in the step a) to obtain a transition layer deposition base material, c) gasifying a tantalum source, mixing the gasified tantalum source with the carbon source gas, a reaction gas and a carrier gas, and carrying out second chemical vapor deposition to obtain the transition layer deposition base material. And second chemical vapor deposition is conducted, the transition layer deposition base material is filled with the fine grain particle layer, then deposition continues to be conducted on the surface of the transition layer deposition base material to form the coarse grain particle layer, and finally the TaC composite coating is obtained. According to the method, the compactness of the coating can be improved, the bonding strength of the coating and the base material is enhanced, the performance of the TaC composite coating is improved, the service life of the TaC composite coating is prolonged, and the reliability of the TaC composite coating is improved.

The invention discloses a metal element doped MnO2 and MnFe oxide composite catalyst as well as a preparation method and application thereof, and belongs to the technical field of flue gas desulfurization and denitrification. The preparation method comprises the following steps: dissolving potassium permanganate, divalent manganese salt and doped metal salt in water for reaction to prepare metal element doped MnO2; and mixing and reacting with a template agent, ferric salt and sodium salt, drying and roasting to obtain the final catalyst. The MnO2 electronic structure is modulated by doping metal elements, and the three-dimensional porous structure of the MnFe oxide is constructed by using the template agent, so that the catalyst has efficient adsorption and strong catalytic oxidation capacity, NO and SO2 can be synergistically removed at the same time, and the catalyst has desulfurization and denitrification activity in a wide temperature range of 30-300 DEG C, and is suitable for industrial production. And liquid ammonia does not need to be used in the purification process, so that the purification agent is high in safety and is particularly suitable for purification treatment under complex flue gas conditions in the non-electric industry.

The invention discloses a preparation method of a metal doped type hydroxyapatite nanoflower. The method specifically comprises the following steps: dispersing a calcium source and soluble metal salt into water, adding acid phosphate, urea and L-histidine, uniformly mixing, carrying out a hydrothermal reaction, mechanically stirring, filtering, washing, and drying a hydrothermal system precipitate to obtain the corresponding metal-doped hydroxyapatite nanoflower. Compared with the prior art, the metal-doped hydroxyapatite nanoflower prepared by the preparation method disclosed by the invention is directly assembled by nanosheets, and a single metal type can be doped in a customized manner. According to the method, water is used as a unique solvent, the use of an organic solvent is avoided, the pH does not need to be adjusted in advance, the technological process is simple, operation is convenient, equipment investment is small, and the method is suitable for industrial production.

The invention relates to a preparation method of a ceramic-based composite material, in particular to a preparation method of a ceramic-based composite material with a pyrolytic carbon-carbon nanotube interface, which is used for solving the problem that in the aspect of improving the thermal conductivity of an interface layer, metals such as Fe, Co, Ni and the like are widely used as catalysts for growing carbon nanotubes at present, so that the thermal conductivity of the interface layer is improved. Carbon nanotubes obtained through a traditional preparation method are prone to agglomeration and uneven in distribution, the risk of the preparation process is high, the carbon nanotubes are not suitable for large-scale production, although metal particles can be reduced through a chemical plating method, the particle sizes of the metal particles are not controlled, the distribution of the metal particles is uneven, and the requirement of a chemical vapor reduction method for distribution of an earlier-stage metal salt solution is high. And the defect is difficult to realize easily. According to the preparation method of the ceramic-based composite material with the pyrolytic carbon-carbon nanotube interface, the ceramic-based composite material with the pyrolytic carbon-carbon nanotube interface is finally obtained through pretreatment, solution A preparation, metal salt solution in-situ reduction and chemical vapor deposition in sequence.

The invention provides a water treatment method for generating singlet oxygen based on electron beam irradiation, belongs to the technical field of water treatment, and aims to provide a universal singlet oxygen generation method for a water treatment process, the method comprises the following steps: adding a metal salt into sewage to be treated, and uniformly stirring to obtain a mixed solution; wherein the metal salt comprises reducing metal ions; continuously aerating air into the mixed solution, so that the mixed solution is rich in oxygen; and carrying out electron beam irradiation on the mixed solution rich in oxygen, so that the reducing metal ions cooperate with the electron beam irradiation to activate the oxygen in the mixed solution to generate singlet oxygen, and removing new pollutants in the sewage to be treated.

The invention belongs to the technical field of catalyst preparation, and particularly relates to a pentachloropropane dehydrochlorination catalyst and a preparation process of tetrachloropropene. The preparation process of the catalyst comprises the following steps: (1) modifying gamma-aluminum oxide powder by adopting an epoxy group-containing silane coupling agent to obtain activated gamma-aluminum oxide powder; (2) dispersing the activated gamma-aluminum oxide powder and polyamino POSS in a solvent, and stirring for reaction to obtain modified gamma-aluminum oxide powder; and (3) preparing trivalent metal salt-loaded modified gamma-alumina powder, and drying to obtain the pentachloropropane dehydrochlorination catalyst. The epoxy group-containing silane coupling agent not only improves the dispersion performance of alumina, but also plays a medium role, so that POSS is attached to the surface of alumina powder, and the stability of the catalyst is improved. Amino groups on POSS are used for complexing trivalent metal ions, and POSS micromolecules can also serve as a transmission track of a substrate, so that the catalytic activity is improved.

The present disclosure is directed to a preservative composition comprising a linear polyetheramine having a molecular weight greater than 118 Daltons (Da) and at least one isothiazolinone, whereby this preservative composition may further comprise a pyrithione salt and / or a metal salt. Also disclosed is an aqueous industrial material comprising the preservative composition as well as a method for enhancing in-contaniner preservative performance of an aqueous industrial material using the preservative composition.

The invention belongs to the technical field of polyether refining, and particularly relates to a methyl-terminated polyether refining treatment method. Comprising the following steps: adding water into a to-be-refined methyl-terminated polyether sample, stirring, dissolving salt in water, layering, adding water into a polyether layer again after separation, stirring, layering, and separating to obtain a primary sample; taking a methyl-terminated polyether sample to be refined again, heating, adding water, adjusting the pH with acid, and stirring to obtain a sample A; adding the preliminary sample into the sample A, and stirring to obtain a sample B; and adding acid into the sample B to adjust the pH value, continuously stirring, crystallizing the metal salt into large particles, settling, separating out solids, deacidifying and decolorizing, dehydrating in vacuum, and filtering to obtain qualified methyl-terminated polyether products, and intercepting part of qualified products as preliminary samples for continuous production. By adding the methyl-terminated polyether primary finished product, the crystallization process of the metal salt can be effectively improved, so that the metal salt tends to generate coarse particles easy to filter, the filtering resistance is reduced, and the filtering period is shortened.

The invention discloses a preparation method and application of a bimetallic sulfide / three-dimensional porous carbon catalyst, and relates to the technical field of electrolyzed water catalysts.The preparation method comprises the following steps that melamine sponge is cleaned, and the clean melamine sponge is obtained; the preparation method comprises the following steps: dissolving metal salt 1 and metal salt 2 in an ethanol aqueous solution, and adding alkali and an aniline monomer to obtain a precursor solution; completely soaking the clean melamine sponge in a precursor solution, carrying out constant-temperature hydrothermal reaction, and sequentially washing and drying to obtain the melamine sponge anchored with bimetal ions; introducing inert gas for protection, and performing high-temperature vulcanization treatment to obtain the three-dimensional porous carbon catalyst embedded with the bimetallic sulfide heterostructure. The catalyst comprises uniformly dispersed bimetallic sulfide nanoparticles and a spongy three-dimensional porous carbon carrier, shows excellent bifunctional catalytic activity and stability when being applied to an electro-catalytic water decomposition reaction, and has a wide application prospect.