1713 results about "Redox" patented technology

The present application relates to the field of wastewater treatment, and provides a treatment system and method for electroless nickel-plating waste liquid. The treatment system comprises a decomplexing pretreatment system; an oxidation-decomplexing system comprising a redox reactor and a decomplexing reactor which are connected in sequence, wherein an oxidizing agent in the redox reactor is oxygen, and an oxidizing agent in the decomplexing reactor is hydrogen peroxide; a chemical precipitation system comprising a neutralization reaction tank and a sedimentation tank which are connected in sequence, wherein the sedimentation tank is equipped with a filter system; and an evaporation crystallization system comprising an evaporation device, a crystallization device, and a separation device which are arranged in sequence. In the treatment system and method for electroless nickel-plating waste liquid, a two-stage oxidation method is employed to achieve oxidation and decomplexing of the waste liquid; in addition, combining chemical precipitation treatment and evaporation crystallization treatment not only reduces the waste liquid treatment cost but also avoids the introduction of other impurities, and allows for the separation of nickel salts and phosphate salts, so that the operation is easy and convenient, the treatment cost is low, the nickel removal rate is high, and resource utilization of nickel is facilitated.

The present invention relates to novel lignin-derived compounds and compositions comprising the same and their use as redox flow battery electrolytes. The invention further provides a method for preparing said compounds and compositions as well as a redox flow battery comprising said compounds and compositions. Additionally, an assembly for carrying out the inventive method is provided.

The invention discloses a novel photocatalyst for producing hydrogen from organic matter wastewater and a preparation method of the novel photocatalyst, and relates to the technical field of photocatalysis. The photocatalyst disclosed by the invention is combined with oxidation-reduction capability, and can effectively degrade and produce hydrogen under the irradiation of sunlight. Through combination of quaternized porous tungsten oxide and vanadate radicals, silver vanadate load growth is promoted, the sunlight utilization rate is increased, and the electron-hole recombination rate is reduced. Reduced graphene oxide is used for pretreatment, active groups are introduced, the reduced graphene oxide is compounded with tungsten oxide / silver vanadate, the binding force is enhanced through heat treatment, photo-induced electron-hole pair compounding is inhibited through the conductivity, and the visible light catalytic performance is improved. The adsorption effect of porous tungsten trioxide and reduced graphene oxide can accelerate the degradation of organic matters. By optimizing the proportion of silver vanadate, tungsten oxide and reduced graphene oxide, the visible light response and charge separation efficiency are enhanced, the degradation and hydrogen production performance is improved, and light corrosion is reduced.

The invention discloses preparation and application of an organic-inorganic interface layer modified zinc negative electrode. The preparation method comprises the following steps: firstly, dispersing organic polymer polylactic acid and zinc sulfide powder into tetrahydrofuran, then coating the surface of zinc foil with the dispersed solution, and drying a solvent at 70 DEG C, so as to prepare the zinc negative electrode modified by an organic-inorganic interface layer. According to the interface layer, zinc ion deposition is regulated and controlled, and the problem of zinc dendrite growth is solved. In addition, the polylactic acid-zinc sulfide composite coating can effectively improve the redox kinetics of zinc ions and improve the coulombic efficiency of the zinc negative electrode. Due to the good ionic conductivity, the interface modification layer can improve diffusion of zinc ions, and the polarization influence caused by the concentration gradient of the zinc ions is relieved. Therefore, the prepared polylactic acid-zinc sulfide composite interface layer modified zinc negative electrode symmetric battery has more excellent cycling stability, the half battery has more stable coulombic efficiency, and the assembled total battery has more prominent capacity retention rate.

The invention belongs to the technical field of zinc battery electrolyte, and discloses application of pyridine hydrochloride as an electrolyte additive in stabilizing a zinc negative electrode and realizing four-electron transfer of a zinc-iodine secondary battery. The hydrochloride containing the pyridine structure is used as an electrolyte additive, molecules of the pyridine structure are adsorbed on the surface of the zinc negative electrode to form a shielding layer, the deposition / stripping reversibility of the zinc negative electrode is improved, stabilization of the zinc negative electrode can be achieved, and the problems of zinc dendritic crystal, corrosion and hydrogen evolution are solved. Meanwhile, molecules with pyridine structures can activate and stabilize I- / I0 / I < + > four-electron redox reaction, inhibit I < + > hydrolysis side reaction and improve the energy density and cycling stability of the zinc-iodine battery. The problem of poor electrochemical deposition / stripping reversibility of a zinc negative electrode and the problem of poor stability of positive valence I < + > species of an iodine positive electrode of a four-electron transfer reaction are solved. The electrolyte containing the additive is low in cost, simple in method, easy to produce and high in practical value.

The invention discloses a functionalized carbon quantum dot modified all-vanadium redox flow battery electrolyte. The functionalized carbon quantum dot has a large specific surface area and a carboxyl functional group on the surface; the electrolyte of the flow battery is a dilute sulfuric acid solution of vanadium; the main evaluation indexes of the electrochemical performance are the cycle efficiency, the capacity retention ratio and the battery performance of the electrolyte; the invention aims to discuss the catalytic action of the surface functional groups of the functionalized carbon quantum dots on the oxidation-reduction reaction of vanadium ions in the electrolyte of the all-vanadium redox flow battery by using the functionalized carbon quantum dots as an additive of the electrolyte. Meanwhile, the influence of the concentration and doping of the carbon quantum dots on the electrochemical performance of the electrolyte of the all-vanadium redox flow battery is researched, so that the working efficiency and the overall performance of the battery are improved, the characteristics of the electrolyte are improved, and the energy consumption of the battery is reduced.

The invention provides a preparation method of a vanadium electrolyte for an all-vanadium redox flow battery, the vanadium electrolyte and application. The method comprises the following steps: (1) dissolving concentrated sulfuric acid in water to obtain a sulfuric acid solution with a preset concentration, then adding vanadium pentoxide into the sulfuric acid solution, and reacting to obtain a first vanadium solution; (2) the temperature of the first vanadium solution is kept to be the preset temperature, low-valence vanadium oxide is added into the first vanadium solution for reaction, water or hydrochloric acid is supplemented in the reaction process, a second vanadium solution is obtained, and the low-valence vanadium oxide is vanadium oxide with the valence of 3-3.5; and (3) filtering the second vanadium solution to obtain the vanadium electrolyte. The method provided by the invention can save energy consumption, reduce cost and improve dissolution efficiency.

The invention provides a circuit deposition method and device, and relates to the field of electronic circuit manufacturing, and the method comprises the following steps: preparing a deposition solution; deploying a dripping path of the deposition solution on a sample to be processed according to a preset circuit pattern; and dropwise adding the deposition solution on the sample along a dropwise adding path, and irradiating a dropwise adding region by using laser, so that an oxidation-reduction reaction occurs on the sample, thereby forming a line. The method is based on a laser-induced liquid phase deposition technology, a deposition solution containing metal ions is dropwise added to a sample to be processed according to a preset circuit pattern, laser is further used for irradiating a dropwise adding area, and a needed pattern circuit is formed along with movement of a laser irradiation position. The deposition device applying the method is simple in operation step and does not need post-treatment, and a simplified and environment-friendly solution is provided for the circuit manufacturing industry.

The present invention provides a glass sheet having soda-lime-silica glass composition with a high visible light transmittance (LtC) of at least 89% with a dominant wavelength (DW) from about 490 to 505 nanometers and purity (Pe) of no more than 1% for control thickness of 5.66 mm and methods of making the same. The glass composition comprising a low iron raw material, a total iron oxide (Fe2O3) of 0.02 to 0.06 wt. %, ferrous (FeO) from 0.006 to 0.02 wt. %, redox (FeO / Fe2O3) from about 0.30 to 0.55, Cr2O3 from about 0.3 to 10 ppm, TiO2 from about 50 to 500 ppm, SnO2 from about 10 to 500 ppm, and a critical amount from about 0.10 to 0.25 wt. % of SO3. The low content of iron oxide is achieved by the partial substitution of regular raw materials by low iron raw materials, with a complete substitution of regular dolomite by a low iron dolomite with a maximum content of 0.020 wt. % Fe2O3.

This invention belongs to the field of wastewater treatment technology, specifically relating to a method for removing metallic impurities from acidic copper-containing etching wastewater at room temperature and pressure. The method includes the following steps: S1, adding an oxidant to the acidic copper-containing etching wastewater to conduct an oxidation-reduction reaction, obtaining a pretreatment solution; S2, adding phosphoric acid or soluble phosphate to the pretreatment solution, adjusting the pH to 1.3-1.7 using a pH adjuster, stirring, and filtering to obtain a purified copper-containing solution. The method provided by this invention achieves high removal rates for Fe, Ni, Zn, Ca, and Mg, while maintaining a high copper ion content. It can recycle and regenerate high-purity copper salt products for application in food, cosmetics, medical, electroplating, and other fields, while also reducing hazardous waste generation, improving economic efficiency, and significantly reducing costs.

The invention discloses a microbial electrochemical efficient preparation method and application of metal nanoparticles, the metal nanoparticles are prepared and synthesized by regulating the redox metabolism behavior of microorganisms through positive / negative constant potential, and the microorganisms are electroactive microorganisms domesticated and cultured by activated sludge or single bacteria; the metal nanoparticles are in a solid state of a metal simple substance, are formed on the surface of an electroactive biological membrane, and are generated by electroactive microorganisms through extracellular electron transfer dissolved-state metal salt reduction. The palladium or silver and other metal nanoparticles prepared by the method are uniformly distributed on the surface of the electroactive biological membrane, the particle size is 1-10nm, the electroactive biological membrane-metal nanoparticle complex has extremely strong reducibility, and the electroactive biological membrane-metal nanoparticle complex is used for treating a non-biodegradable organic pollutant (4-chlorophenol), so that compared with a non-electroactive biological membrane and a treatment group without metal ions, the electroactive biological membrane-metal nanoparticle complex has the advantages that the biodegradability is greatly improved; the degradation effect is the best.

The invention relates to the technical field of sewage treatment, in particular to a wastewater recycling method which comprises the following steps: cyanide breaking: in an alkaline environment, adding an oxidizing agent to oxidize wastewater; first monitoring: monitoring the oxidation reduction potential and the free cyanide concentration in real time, and adjusting the adding proportion of sodium hypochlorite based on the ORP dynamic range and the cyanide concentration attenuation rate; precipitation: adding hydroxide, and carrying out heavy metal precipitation; second monitoring: acquiring component information in the sewage, and adding sodium hydroxide and sodium sulfide in a gradient compensation manner after triggering judgment; membrane treatment: performing filtration and degradation treatment through a biological membrane; 3, monitoring: dynamically adjusting the aeration intensity and the backwashing period according to the coupling relationship between the pressure difference slope and the sludge concentration; and 4, monitoring: calculating a process capability index, judging whether the process capability index is smaller than a third threshold value, and if so, adjusting the sodium sulfide dosage in the precipitation stage. The method has the effect of reducing resource waste in the wastewater treatment process.

The invention relates to the technical field of preparation of an electrolyte for a vanadium redox flow battery, in particular to a reduction method of an alkaline vanadium-containing solution during short-process preparation of a vanadium electrolyte. The reduction method comprises the following steps: (1) adding a reducing agent sodium sulfite into an alkaline vanadium-containing solution and dissolving; and (2) acid is added into the solution obtained after dissolving in the step (1), the pH is adjusted, a reduction reaction is conducted, and vanadium is reduced to be tetravalent. The method provided by the invention effectively solves the problem of vanadium loss caused by precipitation generated in the sequential operation process of acidification and reduction of the alkaline vanadium-containing solution in the prior art, and meanwhile, the method provided by the invention is easy for engineering implementation.

The invention discloses a KTP type sodium-rich phosphate positive electrode material and a preparation method and application thereof, the chemical formula of the phosphate positive electrode material is NaxV1-yTyPO4F1-zOz, 1 < x < = 2, 0 < y < = 1, and 0 < = z < = 1; the preparation method of the material comprises the following steps: adding a vanadium source, a T source, a phosphorus source and a fluorine source in a stoichiometric ratio into a reaction kettle containing a reaction solvent, adding an ammonium source to keep the pH value to be 6-10, maintaining the temperature to be 120-250 DEG C, and reacting for 2-24 hours; naturally cooling, and washing with clear water to obtain a (NH4) xV < 1-y > TyPO4F < 1-z > Oz precursor; the preparation method comprises the following steps: fully grinding an excessive sodium source and a (NH4) xV < 1-y > TyPO4F < 1-z > Oz precursor, carrying out Na < + > / NH4 < + > molten salt exchange in a tubular furnace at 60-400 DEG C for 1-48 hours, introducing inert gas during reaction, and washing an obtained product with a washing solvent after the reaction is finished to remove the excessive sodium source; and drying in a drying oven at 50-250 DEG C for 1-30 hours to obtain the KTP type sodium-rich phosphate positive electrode material. By utilizing the induction effect of KTP configuration on V-O or T-O bonds, the voltage of V and T transition metal related redox couple is increased, and the energy density is improved.

The invention relates to the technical field of soil remediation, and provides a soil pollution remediation process which comprises the following steps: distributing points in grids of an area to be remediated, measuring the content of heavy metals and the concentration of organic pollutants, applying multi-frequency microwave radiation, synchronously applying ultrasonic treatment, and injecting a complex microbial inoculant containing sphingomonas, aspergillus niger spores and a nitrogen and phosphorus nutrient solution. A direct-current electric field is applied, pH, oxidation-reduction potential Eh and temperature parameters are monitored and measured in real time through an embedded sensor, a repair by-product recovery system is arranged, the purity of recovered metal is not lower than 98%, and mobile repair equipment is used in a matched mode. According to the method, the pollution degree is accurately quantified by constructing the pollution index PI, and dynamic regulation and repair are realized in combination with real-time monitoring parameters of a sensor. The pollutant removal efficiency is improved through the synergistic effect of multiple technologies, metal resource recovery is achieved through a repair by-product recovery system, traditional problems are solved, and efficient and environment-friendly repair is achieved.

The invention relates to the technical field of battery materials, in particular to a sodium-ion battery positive electrode material with a high-entropy superlattice structure and a preparation method of the sodium-ion battery positive electrode material, and the general formula of the sodium-ion battery positive electrode material is Na < 0.67 > MnaNibFecLidCueTifO2, a < lt >; 0.6, 0.1 lt; blt; 0.3, 0.01 lt, 0.01 lt, 0.01 lt; clt; ct; 0, 0.2, 0.03 lt; dlt; 0, 0.2, 0.03 lt; lt, lt; 0.2, 0.01 lt, 0.01 lt, 0.01 lt; flt; 0.2, a + b + c + d + e + f = 1; according to the invention, a plurality of ions with similar sizes are introduced into the sodium ion layered oxide transition metal layer, so that a short-range disordered honeycomb-shaped high-entropy superlattice structure is formed; by means of the hysteresis diffusion effect of the high-entropy material, the oxidation-reduction reaction of oxygen anions activated by lithium is effectively regulated and controlled, and the phenomena of voltage decline and structure degradation caused by the migration process of manganese ions in the transition metal layer are inhibited.

The invention discloses a high-heat-power thermoelectric cell hydrogel for low-grade heat energy collection and a preparation method thereof, and belongs to the technical field of heat energy recovery. The polyacrylamide hydrogel is selected as a substrate of the thermoelectric cell hydrogel, so that a hydrogel internal structure which is easy to regulate and control can be obtained; excellent hydrogel stretchability is obtained by using a cross-linking agent and an initiator with relatively low concentration; potassium ferricyanide and potassium ferrocyanide are used as redox ions to generate a thermoelectric effect, so that stable P-type thermal power is obtained; by using guanidine hydrochloride, the solvation entropy difference between potassium ferricyanide and potassium ferrocyanide is enlarged, and the thermal power of the hydrogel in the thermoelectric cell is greatly improved; sodium pyrrolidone carboxylate is used, so that the concentration of ions in the hydrogel is further improved, the conductivity of the thermoelectric cell hydrogel is improved, meanwhile, a hydrogen bond network between water molecules is destroyed, and the water-retaining property of the thermoelectric cell hydrogel is improved.

The invention discloses a method for preparing cyclohexylamine based on reductive amination of cyclohexanone, and belongs to the technical field of fine chemical engineering. The preparation method comprises the following steps: adding a reactant cyclohexanone into a reaction kettle containing a certain amount of solvent, ammonia water and hydrogen atmosphere, and carrying out reductive amination reaction in the presence of a catalyst to obtain cyclohexylamine. The catalyst is CoyAl-LDHs loaded with metal active components, the CoyAl-LDHs are layered cobalt-aluminum bimetal hydroxides, and cobalt ions and precious metal ions in laminates are subjected to spontaneous oxidation-reduction reaction, so that the precious metal ions can be efficiently reduced into active metal nanoparticles. The layered cobalt-aluminum double-metal hydroxide not only has abundant surface acid-base sites, but also has high dispersity of loaded metal nanoparticles. The catalyst preparation and reductive amination reaction conditions are mild, the yield is high, the reaction system is simple and easy to separate, and the method is suitable for industrial production of cyclohexylamine.

The invention belongs to the technical field of thermoelectricity, and relates to a preparation method and application of a quasi-solid thermoelectric material capable of realizing humidity stability by means of phase separation regulation, the preparation method comprises the following steps: dissolving a negatively charged hydrophilic monomer, an electrically neutral monomer, a cross-linking agent and a photoinitiator in a solvent to obtain a precursor solution, and carrying out an ultraviolet polymerization reaction to form polyelectrolyte gel; mixing the eutectic solvent with an electrolyte aqueous solution containing redox ion pairs and lithium chloride to obtain a quaternary electrolyte system; and immersing the gel into a quaternary electrolyte system, and fully replacing the internal solution through a diffusion effect to obtain the quasi-solid thermoelectric material with stable humidity. The thermoelectric material has the advantages of excellent Seebeck coefficient, good stability, high mechanical strength, large power density and the like, can supply power to wearable electronic products in an actual humidity fluctuation environment, breaks through the main bottleneck of actual application of quasi-solid ionic thermoelectric materials based on ionized water gel, and is wide in application prospect.

The invention provides an efficient chloramphenicol degradation method based on Co-Cu-carbon composite nano-catalyst activated peroxymonosulfate, which comprises the following steps: regulating the Co / Cu molar ratio in a bimetal organic framework precursor, and performing pyrolysis to prepare the Co-Cu-carbon composite catalyst with an optimized pore structure, graphitization degree and metal dispersity; peroxymonosulfate is activated by utilizing the synergistic effect of Co / Co and Cu / Cu redox pairs to generate sulfate free radicals, hydroxyl free radicals, singlet oxygen and superoxide free radicals, and direct oxidative degradation of chloramphenicol is promoted by taking a catalyst as an electron transfer bridge; the method realizes rapid and efficient removal of chloramphenicol, high mineralization rate, excellent cycle stability and strong anti-interference capability, and solves the technical problems of low removal efficiency, high cost and easy secondary pollution in the prior art.

The invention belongs to the technical field of all-vanadium redox flow battery diaphragms, and particularly discloses a sulfonated polyetheretherketone / polyaniline composite membrane as well as a preparation method and application thereof. The preparation method comprises the following steps: mixing polyetheretherketone and concentrated sulfuric acid, and carrying out water bath heating reaction to prepare a sulfonated polyetheretherketone solid; molybdenum disulfide and methylbenzene are mixed and subjected to ultrasonic treatment, 1, 3-propane sultone is added, oil bath heating is conducted, and sulfonated molybdenum disulfide powder is prepared; the preparation method comprises the following steps: mixing and stirring sulfonated molybdenum disulfide powder, polyaniline and a DMF (Dimethyl Formamide) solution, performing ultrasonic treatment, adding a sulfonated polyether-ether-ketone solid, stirring to obtain membrane casting slurry, coating a glass plate with the membrane casting slurry, drying to form a membrane, and soaking the membrane in a sulfuric acid solution and deionized water in sequence to obtain the sulfonated polyether-ether-ketone / polyaniline composite membrane. The invention discloses a sulfonated polyetheretherketone / polyaniline composite membrane as well as a preparation method and application thereof. The sulfonated polyetheretherketone / polyaniline composite membrane has high proton conductivity, can maintain relatively low vanadium ion permeability and can improve the electrochemical performance of an all-vanadium redox flow battery.

The invention discloses a method for promoting acid production and alcohol production through fermentation of clostridium perdali C1 gas by using a biological source carbon-based redox regulation and control medium. The preparation method comprises the following steps: obtaining biochar by adopting a high-temperature pyrolysis method, grinding and sieving to obtain a biogenic carbon-based redox regulation medium, adding the biogenic carbon-based redox regulation medium into a fermentation culture medium, inoculating clostridium perdali into a fermentation device filled with the fermentation culture medium, controlling the volume ratio of H2 to CO2 in the fermentation device to be (1.5: 1)-(2.5: 1), and carrying out anaerobic fermentation for 20-30 days to obtain the biogenic carbon-based redox regulation medium. According to the invention, a biological source carbon-based redox regulation medium is introduced into a clostridium perdali gas fermentation system, and the medium not only can enrich CO2 gas, but also can improve the mass transfer efficiency of a gaseous substrate; the method has the advantages that the method is simple and convenient to operate, extra reducing power is provided for a fermentation system, electron transfer is mediated, the CO2 utilization rate of the strain and the fermentation product generation rate are remarkably increased, secondary resource utilization of solid waste biomass is achieved, C1 gas is effectively converted into high-value chemicals, and a green, economical and sustainable development road is provided for conversion of CO2.

The invention provides a synchronous electrochemical test and hydrogen evolution test experimental device and method, and belongs to the field of metal corrosion research. The experimental device provided by the invention comprises a hydrogen evolution test module, an electrochemical test module and a control system module, and the control system module controls the hydrogen evolution test module and the electrochemical test module to work through circuit connection. By combining the hydrogen evolution test and the electrochemical test, the automatic accurate measurement of the hydrogen evolution amount in the metal corrosion process can be realized, the measurement of the corrosion rate, the corrosion potential and the charge transfer amount in the oxidation-reduction reaction can also be realized, and the problems of poor sustainability and low precision of the traditional hydrogen evolution test method are avoided; the hydrogen evolution test data and the electrochemical test data are automatically obtained while one-time sample preparation is realized.

The invention discloses an all-vanadium redox flow battery positive electrode electrolyte and a redox flow battery. The positive electrolyte comprises an active substance, a supporting electrolyte and an additive; the active substance comprises VO < 2 + > / VO < 2 + >; the additive comprises transition metal salt; positive ions in the transition metal salt are selected from at least one of Ti < 4 + >, Cr < 3 + >, Mn < 2 + >, Co < 2 + >, Ni < 2 + >, Cu < 2 + >, Cd < 2 + > and Ce < 3 + >; anions are selected from at least one of SO4 < 2->, HSO4 <->, PO4 < 3->, HPO4 < 2->, H2PO4 <->, BrO3 <-> and IO3 <->; the concentration of the transition metal salt is greater than or equal to 0.05 moL / L. The transition metal ions change the surrounding chemical environment of VO < 2 + >, so that the pentavalent vanadium ions are prevented from being dehydrated and condensed to generate V2O5 precipitates, the high-temperature stability of the electrolyte is remarkably improved, and stable and efficient operation can be realized at high temperature.

The invention discloses a composite material and application thereof in electrochemical carbon dioxide capture, and belongs to the technical field of electrochemistry and carbon dioxide capture. The composite material provided by the invention comprises a carbon felt and a 1, 4-naphthoquinone compound, the 1, 4-naphthoquinone compound is loaded on the carbon felt; the 1, 4-naphthoquinone compound comprises at least one of 1, 4-naphthoquinone, 2-methyl-1, 4-naphthoquinone or 2, 3-dimethyl-1, 4-naphthoquinone, and the compound is a compound of the 1, 4-naphthoquinone, the 2-methyl-1, 4-naphthoquinone and the 2, 3-dimethyl-1, 4-naphthoquinone. In the composite material disclosed by the invention, a 1, 4-naphthoquinone structure of the 1, 4-naphthoquinone compound can realize specific capture of CO2 through a reversible oxidation-reduction reaction, a carbon felt three-dimensional porous framework provides a smooth channel for CO2 mass transfer and electron transmission, and the 1, 4-naphthoquinone structure and the carbon felt three-dimensional porous framework cooperate with each other to solve the problems of low capture capacity, poor stability and high energy consumption of a traditional carbon material; therefore, the method has a good application prospect in electrochemical carbon dioxide capture.

The invention relates to the field of intelligent medical treatment, in particular to a radioactive monodisperse particle preparation, aerosol generation and animal inhalation deposition in-situ quantification method. Comprising the following steps: acquiring aerosol generation standard particles and radioisotopes; adding the standard particles and radioactive isotopes into a PBS solution, and carrying out an oxidation-reduction reaction to obtain a reaction solution; the reaction solution is washed and filtered through deionized water until no separable gamma activity exists, and the radioactive standard particles used for aerosol generation are obtained.The radioactive aerosol generation particles with the single particle size can be obtained and have good clinical value.

The invention belongs to the technical field of high-entropy metal oxide nano powder materials, and particularly relates to a novel high-entropy metal oxide material for a negative electrode of a lithium ion battery and a preparation method of the novel high-entropy metal oxide material. On the basis of a solution combustion synthesis technology, a redox reaction system is constructed by adopting metal nitrate and organic fuel (such as citric acid, urea and the like), three spinel type high-entropy metal oxide nano powder materials with good electrochemical performance are provided and comprise (FexCoyNizCrmLin) 3O4, (FexCoyNizCrmLinZnq) 3O4 and (FexCoyNizCrmLinMgq) 3O4, the ratio of x: y: z: m: n: q is (0.1-1): (0.1-1): (0.1-1): (0.1-1): (0.1-1): (0.1-1): (0.1-1): (0.1-1): (0.1-1), and the reversible specific capacity can reach 442.2-1190.3 mAhg <-1 > after 400 cycles under the current density of 500 And the rapid synthesis process significantly shortens the time required by traditional sintering, the obtained powder product also has the characteristics of narrow particle size distribution, high grain boundary purity, excellent chemical uniformity and the like, and an effective preparation way is provided for developing a high-performance electrode material.

The invention discloses a preparation method and an application method of a catalyst for producing aromatic aldehyde by oxidizing agricultural waste lignin, and belongs to the field of lignin resource utilization. The preparation method of the catalyst for producing aromatic aldehyde through lignin oxidation comprises the following steps: mixing lanthanum salt, B-site metal salt and citric acid in a solvent to obtain a precursor solution; and soaking a polymethyl methacrylate template in the precursor solution, reacting, and calcining to obtain the catalyst for producing aromatic aldehyde by lignin oxidation. The catalyst for producing aromatic aldehyde through lignin oxidation, provided by the invention, has the advantages of low cost, adjustable electronic structure, high oxygen mobility, excellent oxidation-reduction performance and the like, has good catalytic performance, and is suitable for being used as a lignin alkali-free oxidation catalyst. The prepared porous catalytic material with micropores, mesopores and macropores is beneficial to mass transfer of lignin macromolecules and the catalyst, beta-O-4 bonds of lignin can be efficiently broken, and alkali-free oxidation production of value-added aromatic aldehyde chemicals is facilitated.

The invention provides a sodium ion battery capacitor and a preparation method thereof. The sodium-ion battery capacitor comprises a positive pole piece, a negative pole piece, a diaphragm and an electrolyte, the positive pole piece comprises a composite positive pole material, and the composite positive pole material comprises a capacitive material and a layered oxide; the negative electrode plate comprises a composite negative electrode material, and the composite negative electrode material comprises hard carbon and a surface functional group modified porous carbon nanotube. The capacitive material and the layered oxide are synergistically matched to serve as the composite positive electrode material, a three-dimensional porous network structure is formed, and the synergistic effect of the double-electrode-layer capacity and the oxidation-reduction reaction can be improved; the hard carbon and the surface functional group modified porous carbon nanotube are synergistically matched to serve as the composite negative electrode material, so that the sodium ion diffusion path, the electrolyte infiltration area and the charge-discharge efficiency are favorably optimized, and the sodium ion adsorption capacity is improved. The sodium ion battery capacitor has the characteristics of high energy density, high power density, wide temperature range charging and discharging capability and the like.

The invention belongs to the technical field of wastewater treatment, and particularly relates to a method for removing metal impurities from acidic copper-containing etching wastewater at normal temperature and pressure. The method for removing the metal impurities from the acidic copper-containing etching wastewater at normal temperature and pressure comprises the following steps: S1, adding an oxidizing agent into the acidic copper-containing etching wastewater to carry out oxidation-reduction reaction to obtain a pretreatment solution; and S2, phosphoric acid or soluble phosphate is added into the pretreatment solution, the pH is adjusted to 1.3-1.7 through a pH adjusting agent, stirring and filtering are conducted, and the purified copper-containing solution is obtained. According to the method, the removal rate of Fe, Ni, Zn, Ca and Mg is high, high-content copper ions can be kept, a high-purity copper salt product can be recycled and regenerated to be applied to the fields of food, cosmetics, medical treatment, electroplating and the like, hazardous waste can be reduced, economic benefits are improved, and cost is greatly reduced.