949 results about "Cobalt salt" patented technology

The invention discloses preparation and application of a diatomic catalyst modified carbon felt electrode. The preparation method of the modified carbon felt electrode comprises the following steps: dissolving bismuth salt, cobalt salt and urea in water to obtain a complexing solution; immersing the carbon felt substrate subjected to acid activation into a complexing solution for soaking treatment, then taking out the carbon felt substrate, and drying to obtain a precursor-loaded carbon felt; and sequentially carrying out primary heating, cold shock and secondary heating treatment on the precursor-loaded carbon felt, and cooling to obtain the Bi-Co diatom modified carbon felt electrode. The carbon felt electrode can be applied to an all-vanadium redox flow battery. The innovation point of the invention lies in that through the synergistic effect of double atoms and the mutual cooperation of the nitrogen-doped carbon substrate, the intrinsic activity bottleneck of the traditional catalyst is broken through, the comprehensive advantages of high catalytic activity, excellent stability and low cost are achieved, and a new technical solution is provided for the high performance and large-scale application of the flow battery.

The invention relates to a preparation method of Pt monatomic nano-enzyme and application of Pt monatomic nano-enzyme in cardiac troponin I. The preparation method comprises the following steps: 1) ultrasonically dispersing cobalt salt, selenium powder, chloroplatinic acid, urea and sodium chloride in an alcohol solvent, heating and stirring until the solvent is completely volatilized to obtain a solid mixture, and grinding the solid mixture into powder; and 2) placing the powder in a heating device, carrying out Joule heat treatment in an air atmosphere, washing a reactant, and carrying out vacuum drying to obtain the Pt monatomic nano-enzyme. Se doping is introduced in the one-step chemical reaction process to construct oxygen vacancies, rapid heating and structural shaping are achieved in combination with Joule heat treatment, the Se-doped Co3O4-loaded Pt monatomic catalyst is obtained, the oxygen vacancies and Se doping sites are synergistically used as anchoring sites, Pt monatomic atoms are effectively fixed, and the loading capacity and dispersity of the Pt monatomic atoms are improved. The obtained material shows excellent POD-like enzyme activity, can be used for constructing a high-sensitivity colorimetric immunoassay system, and realizes rapid and accurate detection of cTnI.

The invention belongs to the technical field of catalysts, and relates to a surface-reconstructed heterojunction catalyst and a preparation method and application thereof. The preparation method comprises the following steps: dissolving cobalt salt, ferric salt and praseodymium salt in deionized water, heating and spraying on a carrier to prepare praseodymium-doped ferrocobalt layered double hydroxide; mixing the praseodymium-doped ferrocobalt layered double hydroxide with a phosphorus source, and calcining in an inert atmosphere to prepare praseodymium-doped CoP / Fe2P; and carrying out electrooxidation treatment on the praseodymium doped CoP / Fe2P, so as to prepare the Pr6O11 cluster modified CoFeOOH heterojunction catalyst. Through cooperation of three technologies of spray thermal deposition, phosphating and electrooxidation, stable construction and electrochemical activation of a heterogeneous interface are realized, the corrosion resistance and chlorine evolution resistance competitive capacity of the catalyst in a chlorine-containing alkaline system are remarkably improved, the current density of 100 mA. Cm <-2 > can be achieved only through 223 mV overpotential, and meanwhile, stable operation is performed for 500 h.

The invention relates to the technical field of electro-catalysis and hydrogen energy, in particular to a modified LDH-based catalyst and a preparation method and application thereof. The preparation method comprises the following steps: mixing trimesic acid, water, an organic solvent, a nickel salt, a cobalt salt and an iron salt, carrying out electro-deposition, washing and drying to obtain a NiFeCo-LDH (TA) catalyst; the preparation method comprises the following steps: soaking a NiFeCo-LDH (TA) catalyst in a silver salt solution, washing and drying to obtain the modified LDH-based catalyst. The modified LDH-based catalyst provided by the invention can effectively resist chloride ion corrosion and inhibit dissolution of active metals in layered double hydroxides (LDH) under high current density in seawater, can reach industrial grade current density under relatively low overpotential, and can stably run for more than 1000 hours.

The invention relates to a sunken porous magnetic alloy ball wave-absorbing material and a preparation method and application thereof.The wave-absorbing material is prepared through the following steps that S1, citric acid, soluble ferric salt, soluble cobalt salt and soluble nickel salt are dissolved in a mixed solvent of ethylene glycol and water, and the mixture is fully stirred to form a uniform mixed solution; and S2, the mixed solution obtained in the step S1 is subjected to spray drying, obtained precursor powder is placed in the air atmosphere to be calcined to remove the carbon source, then the precursor powder is placed in the H2 / Ar atmosphere to be subjected to heating reduction, and the porous FeCoNi alloy balls with the surface pits are obtained and are the target product. The surface of the prepared alloy microsphere has an obvious concave structure, magnetic anisotropy and magnetic performance are enhanced, a small number of pores are generated in the reduction process, impedance matching of the material is optimized, and effective high-frequency electromagnetic absorption is achieved; and due to the synergistic effect of the recesses and the pores, the obtained alloy microspheres have obvious lightweight characteristic, and have good application prospects in the field of electromagnetic absorption.

The invention discloses a high-entropy metal oxide catalyst as well as a preparation method and application thereof in CO catalytic oxidation, and belongs to the technical field of flue gas treatment. The preparation method comprises the following steps: dissolving copper salt, manganese salt, cerium salt, cobalt salt, vanadium salt and a dispersing agent into water to form a uniform solution, and slowly adding excessive alkali precipitant into the uniform solution to form a solid-liquid mixture; the solid-liquid mixture is transferred into a high-pressure kettle to be subjected to a hydrothermal reaction and then quenched, an obtained hydrothermal reaction product is calcined, and the high-entropy metal oxide catalyst is obtained and is high in catalytic oxidation activity on carbon monoxide at the low temperature, excellent in water resistance and sulfur resistance and particularly suitable for treatment of complex flue gas.

The present invention discloses a layered metal hydroxide composite catalytic material, its preparation method and application. The composite catalytic material comprises a carrier carbon nanotube and a metal hydroxide loaded on the carbon nanotube, and the metal is iron, cobalt and nickel. Preparation method: (1) Dissolve nickel salt, cobalt salt, iron salt and urea in an alcohol solution, stir evenly, then add carbon nanotubes, and continue to stir evenly to obtain a mixed solution; (2) Carry out a solvothermal synthesis reaction on the mixed solution obtained in step (1), filter, wash and dry after the reaction is completed to obtain the layered metal hydroxide composite catalytic material. The carbon nanotubes are introduced into the layered metal hydroxide in this composite catalytic material, reducing the precipitation of metal ions, avoiding the aggregation of hydroxides, improving the stability and catalytic activity of the catalytic material, and being used for activating persulfate to degrade organic pollutants, realizing the efficient activation of persulfate so as to improve the degradation rate of pollutants.

The invention discloses a preparation method of CoWO (cobalt tungsten oxide) modified NbOp-n heterojunction NbO5 / CoWO photocatalyst powder. The preparation method comprises the following steps: dissolving cobalt salt and tungsten salt in deionized water, stirring and mixing, carrying out hydrothermal reaction in an autoclave, washing and drying to obtain CoWO powder; the preparation method comprises the following steps: dissolving niobium oxalate and ammonium carbonate in deionized water, adding CoWO powder, carrying out a hydrothermal reaction in an autoclave, and carrying out washing and drying treatment to prepare NbO / CoWO photocatalyst powder. According to the method, the hydrothermal reaction temperature is regulated and controlled, and the mass ratio of raw materials is optimized, so that the catalyst forms a p-n heterojunction structure of NbOmicron flower loaded CoWOnano particles. The prepared catalyst has high norfloxacin wastewater degradation efficiency under visible light irradiation, has the advantages of simple preparation process, low reagent cost, high catalytic activity and good structural stability, and can be effectively applied to purification treatment of antibiotic polluted water.

The invention discloses a catalytic electrode which comprises a substrate, and an anti-corrosion layer and a sulfur-phobic layer which are sequentially attached to the substrate, the substrate is a blank foamed nickel substrate, the anti-corrosion layer is formed by dipping the foamed nickel substrate with a ferric salt solution, and the sulfur-phobic layer is formed by processing a precursor with a cobalt salt solution through electro-deposition. Accordingly, a corresponding preparation method is also established, a blank foamed nickel substrate is adopted, firstly, the foamed nickel substrate is subjected to dipping treatment with an iron salt solution to obtain a precursor with an anti-corrosion layer, and then the precursor is subjected to electro-deposition treatment with a cobalt salt solution to form the sulfur-phobic layer on the anti-corrosion layer. Wherein the anti-corrosion layer can isolate a high-sulfur environment and prevent the substrate from being corroded; the sulfur phobic layer may prevent sulfur products from depositing and passivating the electrode. The catalytic electrode provided by the invention solves the problems of sulfur reaction corrosion and passivation, shows excellent catalytic activity and stability, and can be used for catalyzing sulfur oxidation reaction for a long time. In conclusion, the method has the advantages of mild conditions, simple process, economy and practicability, and has obvious large-scale industrial production potential.

The invention belongs to the technical field of new energy and electrochemistry, and particularly relates to a corrosion-resistant structured transition metal alloy electrode suitable for hydrogen production from alkaline water and a preparation method of the corrosion-resistant structured transition metal alloy electrode. The method comprises the following steps: sequentially carrying out sand blasting treatment and electrochemical activation treatment on a nickel net substrate so as to improve the surface roughness and the number of active sites; and then performing constant-current deposition in an electro-deposition solution containing nickel salt and ferric salt and / or cobalt salt, and constructing a nickel-based alloy catalyst layer in a micron array shape to obtain the alloy electrode. Through observation of a scanning electron microscope, the surface of the obtained electrode has a sphere-like microstructure, the arrangement is compact, and the catalytic efficiency and durability can be improved. The prepared structured alloy electrode has the advantages of being high in interface bonding force, high in electro-catalytic performance, high in alkali corrosion resistance and the like, and is suitable for efficient and long-term operation of hydrogen production through alkaline electrolysis of water.

The invention discloses cobalt molybdenum nitride / cobalt modified nitrogen-doped hollow carbon microspheres as well as preparation and application thereof, and relates to the technical field of electrochemical energy storage devices. Carboxylated polystyrene microspheres, soluble zinc salt and cobalt salt, phosphomolybdic acid and 2-methylimidazole are dispersed in methanol, a PMA (at) ZnCo-ZIFs / PS precursor of a spherical structure is obtained, then the PMA (at) ZnCo-ZIFs / PS precursor is placed in an inert atmosphere for carbonization treatment, and the cobalt molybdenum nitride / cobalt modified nitrogen-doped hollow carbon microsphere material is obtained. According to the structure and the preparation method, the nitride / metal cobalt component and the nitrogen-doped sodium affinity sites are introduced at the same time, uniform transportation and nucleation of sodium ions are effectively induced, sodium metal is guided to deposit in a specific three-dimensional structure, growth of sodium dendrites is effectively inhibited, volume expansion of metal sodium in the reaction process is relieved, the preparation method is simple and convenient, and the preparation method is suitable for industrial production. The cost is low, the electrochemical performance of the sodium metal battery assembled by using the composite material can be remarkably improved, and the composite material has a good large-scale application prospect.

The invention discloses an efficient NiMo-Co MOF alkaline electrolysis water electrode and a preparation method thereof.The efficient NiMo-Co MOF alkaline electrolysis water electrode comprises a nickel net, a NiMo deposition layer deposited on the nickel net and a Co MOF deposition layer deposited on the NiMo deposition layer, and during preparation, the nickel net is pretreated firstly; dissolving a nickel salt, a molybdenum salt, a conductive salt and a complexing agent in water to obtain a NiMo electro-deposition solution; the method comprises the following steps: dissolving cobalt salt and a ligand in a mixed solution of DMF and water to obtain a Co MOF electro-deposition solution; the pretreated nickel net is placed in a NiMo electro-deposition solution for constant-current deposition, and a NiMo electrode with a NiMo deposition layer loaded on the nickel net is obtained; the NiMo electrode is placed in the Co MOF electro-deposition solution for constant-voltage deposition, and the NiMo-Co MOF composite electrode with the Co MOF deposition layer loaded on the NiMo electrode is obtained. The method is simple and easy to control, low in preparation cost and good in electrode stability and hydrogen production effect.

The present invention discloses a cobalt-based armor nanozyme and its preparation method and application. The method comprises uniformly mixing a cobalt salt solution, a 2,2'-bipyridine solution, and a g-C3N4 dispersion, performing sufficient reaction followed by pretreatment to obtain a precursor, and grinding and calcining the precursor to obtain the cobalt-based armor nanozyme. The cobalt-based armor nanozyme prepared by the present invention has high catalytic activity and the stability of carbonaceous materials. While ensuring efficient catalysis, it greatly reduces secondary pollution caused by cobalt metal leaching. The cobalt-based armor nanozyme can be used to remove organic pollutants from solid pollutants such as soil and water, and can also be used for targeted enrichment of numerous organic pollutants in contaminated wastewater, thereby improving removal efficiency.

The invention relates to the technical field of multifunctional composite materials, in particular to wave-absorbing, photo-thermal and deicing integrated carbon aerogel and a preparation method thereof. The wave-absorbing, photo-thermal and deicing integrated carbon aerogel is characterized by comprising the following raw materials: 5-15 parts of a dominant bio-based material; 3-10 parts of an auxiliary bio-based material; 0.5 to 3 parts of cobalt salt; 1-5 parts of a photo-thermal material, namely an MXene material; a dispersion medium: 40-80 ml of a 1% v / v acetic acid solution; the concentration of the photo-thermal material dispersion liquid is 0.5 mg / mL to 2 mg / mL, and the concentration of the photo-thermal Compared with the prior art, the wave-absorbing, photo-thermal and deicing integrated carbon aerogel and the preparation method thereof have the advantages that through the collaborative design of a bio-based framework and MXene, the problems of function splitting, non-uniform photo-thermal material loading and insufficient wave-absorbing strength of an existing material are solved, collaborative fusion of photo-thermal deicing and wave-absorbing functions is realized, and the wave-absorbing performance of the wave-absorbing, photo-thermal and deicing integrated carbon aerogel is improved. The method is suitable for extreme environment protection scenes such as aerospace and wind power equipment.

The invention belongs to the technical field of air power supplies, and relates to modification treatment of an oxide, in particular to a cerium oxide doped transition metal oxide and a preparation method thereof, an air cathode and an air power supply. The preparation method comprises the following steps: dissolving cerium salt, cobalt salt and manganese salt in water, uniformly mixing to obtain a mixed solution, adjusting the pH value of the mixed solution to 9-11, and carrying out a sedimentation reaction to obtain a sediment; and drying the precipitate, and calcining in an air atmosphere at 300 + / -10 DEG C for 2-4 hours to obtain the cerium oxide doped transition metal oxide. The cerium oxide doped transition metal oxide is cerium doped cobalt manganese oxide with a spinel structure, and the doping amount of cerium is 20 + / -1wt%. The cerium oxide doped transition metal oxide provided by the invention is applied to an air cathode as a catalyst, and has good stability and high catalytic activity. The performance of an air power supply containing the oxide is remarkably improved. The method for preparing the oxide provided by the invention is simple and easy to operate, and is suitable for large-scale production.

The invention discloses a multilayer graphene-loaded cobalt-nitrogen-carbon monatomic catalyst for an advanced oxidation process, and a preparation method and application thereof, and belongs to the technical field of catalysis. The catalyst is prepared by the following method: dispersing reduced graphene oxide in a solvent, performing ultrasonic treatment, then adding cobalt salt, and performing ultrasonic treatment; then carrying out hydrothermal reaction on the mixed solution, and after the reaction is finished, washing and drying a product to obtain the multi-layer graphene loaded cobalt nitrogen carbon monatomic catalyst. The prepared catalyst overcomes the defects of a traditional symmetric coordination catalyst in the aspects of activity, selectivity, stability and the like, the application range of a monatomic catalyst is further widened, and the catalyst has very excellent activation performance on persulfate; the catalyst can be applied to advanced treatment of sewage containing organic pollutants together with persulfate, and the biodegradability of the sewage is improved, so that the catalyst shows a relatively good application prospect in the technical field of catalysis.

The invention provides a sulfo-spinel composite catalyst, a preparation method thereof and an electrolyzed water catalyst. The preparation method comprises the following steps: adding a carrier into a mixed solution of cobalt salt, a morphology regulator and a precipitator, carrying out hydrothermal reaction, washing and drying to obtain a cobalt precursor; the cobalt precursor is subjected to calcination treatment, and a Co3O4 catalyst is obtained; mixing the Co3O4 catalyst with a sulfur source solution, carrying out vulcanization reaction, washing and drying; and mixing a product of the sulfuration reaction with a reducing agent, carrying out reduction treatment, washing and drying to obtain the sulfo-spinel composite catalyst. The invention also provides the sulfo-spinel composite catalyst obtained by the preparation method, and an electrolyzed water catalyst containing the sulfo-spinel composite catalyst. The catalyst has relatively high OER catalytic activity and HER catalytic activity.

The present disclosure relates to the technical field of powder metallurgy, especially to a coarse grain cemented carbide and a preparation method thereof. Pseudo particles in coarse grain tungsten carbide are removed by pretreating process. Broken of the coarse grain tungsten carbide in traditional wet milling is avoid by solid-liquid stirring, spay granulating and surface covering, which also guarantee the uniform distribution of PEG and cobalt salt. Transformation from cobalt salt to cobalt is safely and effectively guaranteed by performing two sintering stages with different atmosphere and temperature to obtain a WC—Co mixture material. By performing spark plasma sintering process, the precipitation of nano fine grain tungsten carbide guarantees regrowth of defect occurred in pretreating process. The coarse grain cemented carbide with the average grain size of WC above 10 μm, the uniform cobalt phase distribution and be bending strength not less than 2200 MPa is prepared.

The invention provides a nitrogen modified iron-cobalt bimetallic catalyst as well as a preparation method and application thereof, and belongs to the technical field of catalysts. The catalyst takes iron and cobalt as active components, and is prepared by adopting a coprecipitation-hydrothermal-step atmosphere heat treatment process: firstly, carrying out coprecipitation reaction on iron salt and cobalt salt, controlling the pH value to be 11 + / -0.5, carrying out aging and hydrothermal treatment, filtering, washing, drying and grinding to obtain a precursor; and calcining the precursor in a hydrogen-containing mixed atmosphere at 400-500 DEG C, and then calcining the precursor in an ammonia-containing mixed atmosphere at 450-600 DEG C to obtain the nitrogen surface modified iron-cobalt bimetallic catalyst. The catalyst is of a carrier-free iron-cobalt bimetallic structure, nitrogen atoms are embedded into alloy lattices or adsorbed on the surface in the form of pyridine nitrogen, pyrrole nitrogen or graphite nitrogen, and a Fe / Co-N high-activity interface is formed.

The invention belongs to the field of chemical catalysis, and particularly relates to a Fischer-Tropsch synthesis catalyst and a preparation method and application thereof. The preparation method comprises the following steps: adding a carrier into a cobalt salt solution, uniformly stirring, separating, and drying to obtain a cobalt-based catalyst precursor; and carrying out vacuum roasting on the cobalt-based catalyst precursor to obtain the Fischer-Tropsch synthesis catalyst. Compared with a catalyst obtained by traditional dipping-roasting, the supported cobalt-based catalyst prepared by the preparation method provided by the invention has the advantages of high dispersion, small-size nanoparticles and enhanced interaction between metal and a carrier, and shows better catalytic performance. After reduction, the Fischer-Tropsch synthesis catalyst provided by the invention not only has high catalytic activity, but also has good Fischer-Tropsch synthesis reaction selectivity, high C < 5 + > selectivity, low CH4 selectivity and excellent stability, and is an excellent Fischer-Tropsch synthesis reaction catalyst.

The invention provides spherical cobaltosic oxide as well as a preparation method and application thereof, the preparation method comprises the following steps: (1) injecting a cobalt salt-containing solution and a carbonate solution into a base solution in a parallel flow manner for a coprecipitation reaction to obtain a mixed-phase precursor; and (2) calcining the mixed phase precursor to obtain the spherical cobaltosic oxide, wherein the solute of the base solution in the step (1) is alkali metal hydroxide. According to the method disclosed by the invention, the precursor of the hydroxyl cobalt oxide and cobalt carbonate mixed phase can be prepared without separating kettles, the content of foreign ions in the precursor is low, and small-particle and high-purity cobaltosic oxide can be prepared by directly sintering.

The invention belongs to the technical field of electro-catalysis water decomposition, and relates to a self-supporting W-NiCoP / NF composite material and a preparation method and application thereof. Cobalt salt, terephthalic acid, acetic acid and foamed nickel are subjected to a first solvothermal reaction, and defect type Co-MOF / NF is obtained; immersing the defect type Co-MOF / NF into a tungstate solution, and then carrying out a second solvothermal reaction to obtain a defect type W-Co-MOF / NF precursor; and carrying out phosphating heat treatment on the defect type W-Co-MOF / NF precursor and a phosphorus source in an inert atmosphere to obtain the W-Co-MOF / NF composite material. According to the preparation method disclosed by the invention, the tungsten-doped nickel-cobalt bimetallic phosphide with rich defect structures is successfully constructed on the foamed nickel substrate through a step-by-step solvothermal and gas-phase phosphating strategy, so that organic combination of a bimetallic synergistic effect and defect engineering is realized; the prepared self-supporting composite material has more active sites, a better electronic structure regulation effect and better stability.

The invention provides a chlorine corrosion resistant cathode for electrolyzing seawater as well as a preparation method and application of the chlorine corrosion resistant cathode. The preparation method comprises the following steps: S1, dissolving a cobalt salt, a nickel salt, a morphology regulating agent and a structure-directing agent in a solvent according to a molar ratio of (1-2.5): (1-2.5): (8-12): (6-10), and stirring to form a first solution; s2, a titanium mesh and the first solution are subjected to a hydrothermal reaction at the temperature of 100-150 DEG C, and CoNi layered double hydroxide with the shape of a nanoneedle array grows on the titanium mesh in situ; s3, selenium powder and a reducing agent are dissolved in a solvent according to the molar ratio of 1: (0.8-1.5) and stirred to form a second solution; and S4, carrying out hydrothermal reaction on the titanium mesh on which the CoNi layered double hydroxides grow in situ and a second solution at 150-190 DEG C so as to grow cobalt-nickel bimetallic selenide of which the morphology is a nanoneedle array in situ on the titanium mesh, thereby obtaining the chlorine corrosion resistant cathode.

The invention discloses a catalytic system for preparing amine compounds through nitro reduction and application of the catalytic system. The catalytic system comprises an alkaline aqueous solution, a reducing agent and a catalyst, the alkaline aqueous solution is an alkali metal hydroxide aqueous solution; the reducing agent is alkali metal hydroboron and / or alkaline earth metal hydroboron; the catalyst is copper salt lewis acid and / or other lewis acid; the other Lewis acid is selected from one or a combination of more of cobalt salt, ferric salt, zinc salt, manganese salt and palladium salt. When the catalytic system is used for reducing the aromatic nitro-compound, the using amount of a reducing agent is small, meanwhile, the using amount of an organic solvent is reduced, the reaction yield is high, the reaction is milder, and amplified production of the process is facilitated.

The invention discloses a lithium-rich manganese-based solid-state battery positive electrode active material and a preparation method and application thereof, and the preparation method comprises the following steps: S1, taking a manganese salt, a cobalt salt and a nickel salt, and preparing a mixed salt solution; s2, adding an oxalic acid solution into the mixed salt solution, and stirring to form an oxalate precipitate; s3, carrying out vacuum drying and collecting precipitates to obtain an oxalic acid precursor; s4, mixing and uniformly grinding the oxalic acid precursor, LiOH and Li2WO4 to obtain mixed powder; and S5, pre-sintering the mixed powder, then calcining, and naturally cooling to room temperature to obtain the composite material. The invention also discloses the lithium-rich manganese-based solid-state battery positive electrode active material prepared by the preparation method, and a battery positive electrode and a solid-state battery comprising the active material. Li2WO4 is introduced into the lithium-rich manganese-based solid-state battery positive electrode material to construct a Li < + > / e <-> transmission channel, so that the initial specific capacity of the battery is increased; and a protective layer is formed on the surface of the positive electrode material to enhance the redox reversibility and improve the cycle stability of the battery.

The invention discloses an iron-cobalt spinel oxide, which is prepared by the following steps: with ferric salt and cobalt salt as raw materials, dissolving the ferric salt, the cobalt salt and sodium acetate in an ethanol aqueous solution to obtain a precursor solution, carrying out hydrothermal treatment on the precursor solution, and washing and drying a reaction product to obtain the iron-cobalt spinel oxide. The iron-cobalt spinel type oxide is stable in crystal structure, the leaching rate of metal ions is remarkably reduced due to existence of metal-oxygen bonds, the recycling rate is increased, and meanwhile the risk of secondary pollution of water is reduced. In the process of degrading nitrogen-containing organic wastewater by an advanced oxidation technology for generating sulfate free radicals based on peroxymonosulfate, the iron-cobalt spinel type oxide has good catalytic performance, and can basically complete degradation of multi-nitrogen organic pollutants in water; and the method has relatively strong capability of resisting interference of inorganic ions and organic matters, and has relatively great application potential in actual wastewater treatment. The invention also discloses a method for degrading the multi-nitrogen explosive wastewater by using the ferrocobalt spinel type oxide.

The invention provides a preparation method of a CoFe alloy fiber microwave absorbent, which comprises the following steps: immersing cotton fibers in an aqueous solution containing ferric salt and cobalt salt for dipping, taking out, and drying to obtain cotton fibers loaded with iron ions and cobalt ions; under the nitrogen atmosphere, the temperature is increased to 600-800 DEG C from the room temperature at the speed of 4 DEG C / min, after constant-temperature roasting, natural cooling is conducted to the room temperature, and the CoFe alloy fiber microwave absorbent is obtained. The invention further provides application of the CoFe alloy fiber microwave absorbent, and the CoFe alloy fiber microwave absorbent is used for preparing stealth materials or / and electromagnetic protection materials. The raw materials are wide in source and low in cost, only an impregnation method and a roasting method are adopted, no organic solvent is used, and the method is green and environmentally friendly; the technological process is simple, easy to operate, low in synthesis cost and suitable for industrial production; the prepared CoFe alloy fiber microwave absorbent is high in magnetism, facilitates double-layer optimization design of microwave absorption performance, and has the advantages of being good in microwave absorption performance and light in weight.

The invention provides a cobalt-doped nickel-based coordination polymer catalyst and a preparation method and application thereof.The preparation method comprises the following steps that S1, Schiff base and 4, 4 '-dipyridyl are placed in a mixed solvent to be mixed, acid is added into the mixed solvent to obtain a precursor solution, the precursor solution and foamed nickel are mixed, a coordination reaction is conducted through a hydrothermal method, and a nickel-based coordination polymer is obtained; and S2, dissolving cobalt salt in an organic solvent, adding into the nickel-based coordination polymer, mixing, and carrying out a hydrothermal method to obtain the cobalt-doped nickel-based coordination polymer catalyst. The preparation method is simple in process, low in cost and good in repeatability.

The invention relates to a high-entropy metal oxide catalyst and a preparation method and application thereof.The preparation method comprises the following steps that S1, ferric salt, cobalt salt, manganese salt, nickel salt, copper salt and organic alkaline matter are mixed to obtain a mixed solution, hydrothermal reaction is conducted, and a precursor is obtained; and S2, calcining the precursor at the temperature of 500-600 DEG C to obtain the high-entropy metal oxide catalyst. The high-entropy metal oxide catalyst uniformly doped with iron, cobalt, manganese, nickel and copper is prepared by adopting a hydrothermal reaction and calcination method, and the high-entropy metal oxide catalyst not only can efficiently catalyze ozone to remove antibiotics, but also can still keep an excellent antibiotic removal rate constant in a water body containing hetero ions and humic acid; and the anti-interference capability is excellent.

The invention discloses a ZIF-67 sodium alginate composite gel bead and a preparation method and application thereof, and belongs to the technical field of environmental functional materials.The preparation method comprises the steps that sodium alginate serves as a gel raw material and is evenly mixed in water, and a sodium alginate precursor liquid is formed; the preparation method comprises the following steps: taking acrylamide and a vinyl monomer as raw materials, adding a cross-linking agent, and dissolving in water to obtain a gel matrix solution; adding the sodium alginate precursor liquid into the gel matrix liquid to obtain primary gel beads, radiating the primary gel beads by adopting a 60Co gamma ray source, inducing free radicals to generate and initiating a graft copolymerization reaction of monomers on a network of the primary gel beads to obtain the cross-linked gel beads. And sequentially immersing the cross-linked gel beads into a soluble cobalt salt solution and a 2-methylimidazole solution to obtain the ZIF-67 sodium alginate composite gel beads.