4364 results about "High selectivity" patented technology

The invention belongs to the technical field of CO catalytic oxidation, and particularly discloses a method for synthesizing a CuO / CeO2 catalyst through a rapid fluid mixing method and application thereof.The method comprises the steps that a copper salt solution A and a cerium salt solution B are put into a rapid fluid turbulence mixing reactor, the flow speed is controlled, a catalyst precursor is prepared after product treatment, the catalyst precursor is put into a muffle furnace, air is introduced for calcination, and the catalyst is prepared; and high selectivity and high conversion rate in CO oxidation reaction in a hydrogen-rich environment are realized. The method provided by the invention also improves the traditional MOF synthesis method, adopts water as a solvent, and reduces the synthesis conditions. The prepared catalyst has high conversion rate and selectivity, the CO conversion rate at 90 DEG C reaches 100%, and the corresponding selectivity is 100%.

The present disclosure relates to high selectivity doped hardmask films, as well as methods of providing and using such films. In particular examples, the high selectivity doped hardmask film can be employed as a hardmask, an intermediate layer, or a coverage layer.

The invention discloses a self-powered biosensor for double-signal detection of sugarcane pokkah boeng disease, the self-powered biosensor comprises an anode, a cathode and an electrolyte, the anode is a CuCo-MOF / AuNPs / GOD biological anode, the cathode is a CuCo-MOF / AuNPs / DNA chain biosensor, and the electrolyte comprises glucose, MB and a PBS buffer solution. According to the self-powered biosensor, analysis is carried out through two non-interfering modes of electrochemical detection and colorimetric detection, and whether a detection result is a false positive signal or not can be effectively verified. An external power supply is not needed, and real-time outdoor detection can be realized. The material source is wide, the assembly process is simple, and accurate and rapid detection can be realized. The method has the advantages of high sensitivity, good selectivity and real-time detection, and can be used for accurately detecting the sugarcane pokkah boeng rot.

The invention relates to the technical field of catalysts, and discloses a preparation method and application of a copper-based metal-organic framework catalytic material.The preparation method comprises the following steps that S1, cuprous salt, N, N '-bis (5-aminonicotinyl) naphthalimide and a solvent are mixed, and a mixture is obtained; s2, heating the mixture to a reaction temperature, carrying out a constant-temperature reaction, and cooling to obtain a crystal; and S3, washing and drying the crystal to obtain the copper-based metal-organic framework catalytic material. According to the preparation method of the copper-based metal-organic framework catalytic material provided by the invention, N, N '-bis (5-aminonicotinyl) naphthalimide is used as an organic ligand to prepare the copper-based metal framework Cu-PTD with N / O co-coordination, and the copper-based metal framework Cu-PTD has relatively strong electrocatalytic carbon dioxide reduction and electron transfer capabilities; and the catalyst has relatively high selectivity on electrocatalytic carbon dioxide reduction products.

The invention discloses a copper-based nano-enzyme, a preparation method thereof and application of the copper-based nano-enzyme in organophosphorus pesticide detection, and belongs to the technical field of pesticide residue detection. The copper-based nano-enzyme has a netted-like structure, a high specific surface area and many active sites, the valence state of a copper element is zero-valence Cu, Cu < + > and Cu < 2 + >, the copper-based nano-enzyme has high peroxidase-like activity and laccase-like activity, the detection limit is low, and glyphosate can be sensitively detected; and glyphosate, glufosinate-ammonium and isazofos can be well distinguished from six organophosphorus pesticides with medium concentration, and the method has high selectivity. The nano enzyme provided by the invention is prepared from ammonium citrate and copper nitrate in an N, N-dimethylformamide (DMF) solution by using a solvothermal method; the preparation process of the nano enzyme is simple.

The invention belongs to the field of electrochemical biosensors, discloses a preparation method of an electrochemical biosensor capable of being used for multi-mode sweat detection, and particularly provides a single-electrode multifunctional arrangement method in a three-electrode system. A sensor material with high sensitivity and high selectivity is prepared, then the sensor material is printed through screen printing and assembled into a portable device to achieve simultaneous detection of multiple biomarkers in sweat, and the preparation method comprises the steps of selection and modification of an electrode material, sensor assembly and integration of a signal acquisition and analysis system. Through innovative material design and process optimization, the sensor not only can acquire information of various biomarkers in sweat in real time, but also can provide reliable data analysis, and shows excellent long-term stability and anti-interference capability in practical application. The technology provides an effective and reliable solution for real-time health monitoring.

An IPD high-selectivity band-pass filter based on a weak coupling transformer technology comprises an LC parallel resonance circuit, an LC series resonance circuit, an LC parallel resonance circuit and a fourth capacitor C4, and inductors in the LC parallel resonance circuit and inductors in the LC parallel resonance circuit have a weak transformer coupling relation; the coupling coefficient required by the weak coupling transformer provided by the invention is very small and can be realized in a mode of adjacently placing metals on the same layer, so that the structural complexity of the filter is effectively reduced; the band-pass filter is based on an IPD technology, an extra decoupling equivalent inductor is introduced through a weak transformer coupling technology, the extra decoupling equivalent inductor and a parallel capacitor which is connected between the input end and the output end of the filter in a bridging mode form a new resonance path, and a transmission zero point is introduced into an upper stop band and a lower stop band of the filter respectively to improve the selectivity of the filter. According to the invention, the selectivity of the filter can be effectively improved on the premise of not additionally introducing an inductance element and not increasing the order of the filter.

The invention belongs to the technical field of membrane separation, and aims to provide a preparation method and application of a covalent organic framework bipolar membrane. The method comprises the following steps: combining at least one amine, hydrazide or aldehyde monomer containing ionic groups with a monomer without ionic groups, and respectively synthesizing covalent organic framework COF nanosheets with positive charges and negative charges through a one-pot method under the condition of coexistence of an acid catalyst and an organic solvent; sequentially depositing COF nanosheets with positive and negative charges on the surface of the porous carrier by a hot solvent evaporation method; by constructing two COF separation layers with regular pore channels and opposite electrical properties, the covalent organic framework bipolar membrane with charge asymmetry is finally obtained. The product provided by the invention has high selectivity, can realize efficient separation of protons and metal cations, and significantly improves the extraction and recovery purity of hydrochloric acid; through charge repulsion and pore size screening mechanisms, separation of different anions can be further realized, and selective recovery of acid molecules is enhanced.

The invention discloses a method for synthesizing deuterated olefin under catalysis of a palladium membrane by taking D2O as a deuterium source, and belongs to the technical field of synthesis of deuterated olefin building blocks. According to the method, a three-chamber electrolytic tank separated by a palladium membrane and an ion exchange membrane is used as a reactor, the palladium membrane is used as a working electrode, an electrolyte deuterium aqueous solution is used as an electrolyte, deuterium water is electrolyzed through a constant-potential electrolysis method, and formed active deuterium is transmitted to one side of an organic reaction taking absolute ethyl alcohol or cyclohexane as an organic solvent; and catalyzing an alkyne compound by using a palladium membrane modified by sodium thiophenol to perform reduction deuterization so as to synthesize a deuterated olefin compound with high selectivity, and further synthesizing a corresponding deuterated drug. The invention provides a green, efficient, high-universality and low-cost amplification synthesis method for synthesizing a deuterated olefin building block containing a functional group easy to reduce and hydrolyze, and the method has a wide application prospect.

The invention relates to the technical field of analysis and detection, in particular to a molecularly imprinted sensor for in-situ detection of epicatechin in plant leaves and a preparation and application method of the molecularly imprinted sensor. The molecular imprinting sensor for detecting epicatechin is prepared by assembling a zeolite imidazate skeleton-amide functionalized single-walled carbon nanotube composite material, amino-formyl imidazole modified reduced graphene and an MIP film on the surface of an electrode layer by layer. The high-selectivity and high-sensitivity detection on the target molecule epicatechin is realized. The technology can effectively reduce the detection cost, simplify the operation process and improve the performance of the sensor. Particularly, due to the introduction of the MIP, the sensor has the capabilities of in-situ detection and high-precision molecular recognition, can realize rapid and reliable quantitative analysis in a complex sample, and has a wide application prospect.

The invention relates to the technical field of developing, in particular to a high-selectivity developing solution for alkali-soluble photoresist and a developing process. The problem that the developing effect and the dissolving effect are poor in the developing process is solved. The developing solution is prepared from the following synthetic raw materials: a modified active agent, a weakly alkaline mixture, a modified defoaming agent, a composite dispersing agent, an improved chelating agent, an organic solvent and deionized water. According to the invention, the dissolution rate of the unexposed photoresist is improved by preparing the modified active agent and the weakly alkaline mixture, and the high selectivity of the developing solution is embodied; the defoaming performance of the developing solution is improved by preparing the modified defoaming agent and adding the composite dispersing agent; the developing effect of the material can be improved through the synergistic effect of the improved chelating agent and the organic solvent in the developing solution; the developing solution is applied to the developing process, and the pH value and process parameters are adjusted, so that the developing effect and efficiency of the material are improved.

The invention discloses a multi-component gas detection device and method based on a metasurface quasi-continuous domain bound state. The advanced nanometer manufacturing technology and the deep learning algorithm are adopted, and high-precision, high-sensitivity and high-selectivity gas detection is achieved. According to the invention, the metasurface array with specific design is utilized, and the quasi-continuous domain bound state in the middle-infrared band is realized by accurately regulating and controlling the geometric parameters and material characteristics of the microstructure, so that excellent optical response is obtained. In combination with a deep learning algorithm, complex spectral information is converted into accurate gas composition and concentration information, and a reliable solution is provided for the fields of environmental monitoring, industrial production, safety monitoring and the like.

The invention discloses a method for extracting and purifying flavone in litsea coreana through an ultrasonic-assisted eutectic solvent, and belongs to the technical field of green processing of natural products. The invention provides a method for efficiently preparing litsea coreana flavone by integrating computer prediction, green solvent extraction and resin purification technologies. The method comprises the following steps: firstly, calculating and screening a deep eutectic solvent system with the highest affinity with the litsea coreana flavone on the basis of a COSMO-RS theoretical model, then coupling the optimized DES with an ultrasonic-assisted extraction (UAE) technology, and through the synergistic effect of the DES and the UAE technology, remarkably improving the extraction rate of the litsea coreana flavone and furthest keeping the biological activity of a target component; then, a macroporous resin dynamic adsorption-desorption purification process is linked, so that high-selectivity enrichment and impurity removal of the flavonoid compounds in the crude extract are realized, a high-purity product is obtained, and a complete process route from intelligent screening, efficient extraction to precise purification is finally formed.

The invention discloses a polycrystalline silicon etching method, which comprises the following steps of: firstly, carrying out a polycrystalline silicon etching process for the first time, and carrying out a certain amount of transverse etching; an isotropic dry etching process is adopted, so that the polycrystalline silicon has transverse etching. And then a polycrystalline silicon etching process with a high selection ratio is carried out, and an anisotropic etching process is adopted to ensure that the polycrystalline silicon on the surface is etched cleanly. According to the etching process, a step-by-step etching process method is adopted, the isotropic etching process is firstly carried out to control the etching amount of transverse etching, then the anisotropic etching method and the high-selectivity etching method are adopted to carry out etching of different etching amounts on areas with inconsistent feature sizes, and accurate etching of polycrystalline silicon is guaranteed.

The invention discloses an ion exchange membrane based on an intrinsic microporous polymer, and a preparation method and application thereof, and belongs to the technical field of high polymer materials. According to the application, 1, 3, 5-tri (4-aminophenyl) benzene (TAPB) and dimethyl formal are taken as polymeric monomers, a polymer with intrinsic sub-nano micropores and a corresponding homogeneous ion exchange membrane are prepared by utilizing the structural characteristics of rigidity and distortion of the TAPB, an ion transmission channel is formed by a unique micropore structure, and the sub-nano micropores have a size screening effect, so that the ion exchange membrane can be used for preparing the ion exchange membrane. The selective separation of monovalent / multivalent anions can be realized; after quaternization treatment is carried out on the membrane and a positively charged group is introduced, the positively charged group has a strong electrostatic repulsion effect, and selective separation of monovalent / multivalent cations can be realized, so that the polymer ion exchange membrane disclosed by the invention can be simultaneously applied to an acid-base recovery process, and has the characteristics of high selectivity, high permeation flux and stable long-term operation.

The invention relates to the field of catalysts, and discloses a nitrile rubber hydrogenation catalyst and a preparation method and application thereof.The nitrile rubber hydrogenation catalyst comprises a carrier and an active metal component loaded on the carrier, and the carrier comprises a composite metal oxide and silicon dioxide; wherein the composite metal oxide is M < 1-x > Al < x > O (x + 2) / 2, x is 0.1-0.4, and M is selected from at least one of Mg, Ni and Zn; wherein the active metal component is Os; wherein in terms of metal elements, the content of the active metal component is 0.01-5wt% on the basis of the total weight of the catalyst. The catalyst provided by the invention is used for preparing hydrogenated butadiene-acrylonitrile rubber by hydrogenation of butadiene-acrylonitrile rubber, and has high selectivity and hydrogenation degree.

The invention provides a high-molecular adsorption material with high selectivity on platinum group metals as well as a preparation method and application of the high-molecular adsorption material, and belongs to the technical field of material science. Comprising the following steps: (1) preparing a methanol solution containing platinum group metal ions, and adding a functional monomer mixture and modified graphene oxide to form a pre-assembled compound; (2) adding a cross-linking agent and an initiator, removing oxygen, and polymerizing to obtain a polymer; and (3) grinding the polymer, eluting metal ions, washing to be neutral, and drying. The high-molecular adsorption material provided by the invention takes modified graphene oxide as a support body, template molecules and specific functional monomers (4-vinylpyridine and 2-mercaptobenzimidazole) are combined to form a pre-assembled compound, then a cross-linking agent and an initiator are added, recognition sites are fixed through cross-linking polymerization, and finally, the high-molecular adsorption material is obtained after the template molecules are eluted. The adsorbent is high in adsorption rate, capable of specifically adsorbing platinum group metal, good in stability and reproducibility and capable of being repeatedly used.

The invention discloses an electrochemical detection method of dopamine, and belongs to the technical field of analysis. According to the method, SnS2 quantum dots are loaded on Zn-MOF and modified on an electrode, then gold nanoparticles and a sulfydryl-containing dopamine aptamer single chain are sequentially fixed on the electrode, an Apt / AuNPs / SnS2QDs (at) Zn-MOF / GCE composite electrode (in an open state) is formed, an electrochemical signal of the composite electrode is greatly improved, and based on specific recognition between dopamine and an aptamer chain, the electrochemical performance of the composite electrode is improved. A large cavity of Zn-MOF is used for packaging SnS2 quantum dots with excellent electrochemical properties, electrochemical signal amplification is achieved, when a target object dopamine exists, dopamine can quench an ECL signal, an electric signal is obviously reduced (in a closed state), and therefore a linear relation between the change of the electrochemical signal and the concentration of dopamine is constructed, and the electrochemical property of the electrochemical signal is improved. Therefore, high-sensitivity and high-selectivity detection of dopamine is realized.

The invention relates to the technical field of environmental nano-materials, and particularly discloses a chitosan magnetic nano-composite adsorption material as well as a preparation method and application thereof, and the technical key point is that the chitosan magnetic nano-composite adsorption material is successfully prepared by compounding modified chitosan and a Fe3O4 magnetic nano-material. The material has the remarkable advantages of large specific surface area, high selectivity, easiness in separation and the like. Through an ICP-MS (Inductively Coupled Plasma Mass Spectrometry) analysis method, experimental conditions are optimized, and the removal effect of the material on nine harmful elements including Cr, Cu, Zn, As, Se, Ag, Cd, Sb and Pb is evaluated. Experimental results show that the material can efficiently adsorb the heavy metal elements after being subjected to ultrasonic treatment for 120 minutes under the conditions that the temperature is 20 DEG C, the initial concentration is 5mg / L, the material dosage is 10mg and the pH value is about 6, the adsorption rate of the material to the heavy metal in actual industrial wastewater reaches 71.9%-94.2%, and the material shows good application potential.

The invention provides a rigid-flexible metal-organic framework diaphragm with high selectivity as well as a preparation method and application of the rigid-flexible metal-organic framework diaphragm. Through a seed secondary growth strategy, the problems that MOF particles are easy to fall off and are incompatible with a substrate film are successfully avoided. On one hand, grain seeds embedded in the polyvinylidene fluoride (PVDF) substrate film in advance provide stable anchoring points for growth of MOF, and MOF particles are not prone to falling off due to the high adhesive force of the grain seeds. The high Young modulus of the MOF crystal also effectively improves the thermal shrinkage resistance of the diaphragm, the excellent flexibility of PVDF is complementary with the diaphragm in mechanical property, and the battery diaphragm shows excellent mechanical property and thermal stability due to the rigid-flexible combination strategy. The invention provides an efficient diaphragm construction strategy for developing a lithium metal battery with long cycle life and high safety, and shows a wide application prospect in a next-generation high-safety battery.

The invention provides a high-selectivity anti-carbon-deposition CO oxidation catalyst and a preparation method thereof. The CO oxidation catalyst comprises a carrier, an active component loaded on the surface and / or in the carrier, and an auxiliary agent, wherein the active component comprises a noble metal element, and the auxiliary agent comprises a non-noble metal element; by taking the total mass of the carrier as 100%, the content of the auxiliary agent is less than 10%, preferably 3-6%; the total mass of the carrier and the auxiliary agent is 100%, and the content of the active component is less than 1.5%, preferably 0.5-1.5%. The CO oxidation catalyst disclosed by the invention has the characteristics of NOx resistance, carbon deposition resistance, difficulty in oxidizing NO, high CO catalytic combustion activity and the like, and has excellent CO catalytic combustion performance, especially the performance of catalytic combustion of steel sintering flue gas CO.

The invention provides a beneficiation and enrichment method for high-molybdenum oxide ore, which comprises the following steps of: performing fraction magnetic separation on a product after ore grinding, regrinding magnetic separation coarse particle tailings, mixing the reground product with magnetic separation fine fraction tailings to perform low-potential sulphide ore flotation, performing oxidized ore flotation on sulphide ore flotation tailings, and the like. And finally, the molybdenum concentrate with the high recovery rate and grade is obtained, the molybdenum ore separation and enrichment effect is achieved, and the fine disseminated-particle-size refractory molybdenum oxide ore resources in the high-oxidation-type molybdenum ore are effectively and comprehensively recycled. In order to quickly optimize and obtain the optimal condition of oxidized ore flotation, the flotation inhibitor with the good inhibition effect is determined through the pure ore flotation test, the flotation collecting agent with the high selectivity is selected through the molecular simulation calculation method, and the flotation efficiency and selectivity are improved. The method provided by the invention can be widely applied to the fields of development of high-oxidation molybdenum ore mines and recycling of fine-fraction refractory molybdenum oxide ore resources in tailings after sulfuration flotation.

The invention discloses a method for green and efficient removal of thiophene sulfides in fuel oil by using Q [8]. According to the method provided by the invention, a Q [8] solid powder material is adopted to carry out removal treatment on simulated fuel oil containing the thiophene sulfides in a subject-object interaction mode, and the Q [8] solid powder material can be subjected to a regeneration process for reuse through ethanol desorption. The Q [8] solid powder material used in the method is low in cost, the urea is a main raw material for synthesis of the Q [8] solid powder material, and the Q [8] solid powder material is high in selectivity, can be recycled and is more environmentally friendly. The method is simple to operate, convenient to use and low in cost, the combustion simulation oil can be efficiently desulfurized, and environmental pollution is effectively reduced.

The invention provides a plate-type micro-channel reactor and a method for nitrifying trifluoromethoxybenzene by using the plate-type micro-channel reactor, and belongs to the technical field of organic synthesis. The plate type microchannel reactor comprises a first heat exchange plate, a reaction plate and a second heat exchange plate, the reaction plate is positioned between the first heat exchange plate and the second heat exchange plate; a feeding channel, a first shunting section, a first mixing section, a second shunting mixing section, a third shunting mixing section, a fourth shunting mixing section and a discharging channel which are connected in sequence are arranged on the reaction plate; and the feeding channel comprises a first feeding channel and a second feeding channel. According to the method, trifluoromethoxybenzene is taken as a raw material and is subjected to nitration reaction by using plate type micro-channel reactors connected in series, so that high-selectivity continuous nitration of trifluoromethoxybenzene is realized, the nitration reaction can be completed within 5 minutes, and the contents of byproduct meta-position and dinitrate can be controlled to be lower than 0.05% and 0.5% respectively.

The invention discloses a method for preparing furfuryl amine by reductive amination of biomass-based furfural, which comprises the following steps: adding furfural, a catalyst, ammonia water and a solvent into a closed reaction kettle in proportion, replacing air in the reaction kettle with high-purity hydrogen, and reacting in an oil bath pan for a period of time to obtain a target product furfuryl amine, the nano-catalyst provided by the invention is a nitrogen-doped porous hollow carbon sphere loaded nano bimetallic catalyst, takes noble metal and non-noble metal as a metal active center together, and has adjustability of macroscopic size and microstructure at the same time; the method has the advantages of simple reaction system, mild conditions, no pollution to the environment, high efficiency, energy conservation, low cost, few byproducts, high yield, high selectivity and the like, the furfural is efficiently converted into furfuryl amine at low temperature and low pressure within a short time, the used heterogeneous catalyst is stable and easy to recover, a new thought and direction are provided for enterprise production and scientific research, and the method is suitable for industrial production. The method has great significance on development and utilization of biomass-based furfural.

The invention discloses an omariglitazone intermediate as well as a synthesis method and application thereof, and belongs to the technical field of pharmaceutical chemistry synthesis. The invention provides a synthesis method of an omarigliflozin intermediate and application of the intermediate in synthesis of omarigliflozin. The key of the synthesis method provided by the invention lies in the deprotection process of polycyclic indole amide, nitrile groups are not hydrolyzed, indole carboxylic acid is generated with high selectivity, molecular lactamization is avoided in the condensation process with polycyclic imine B, and expensive amidation reagents such as HATU are not needed in the process, so that the synthesis method is simple and easy to implement. And the purpose of preparing omariglitazone with low cost and high yield is achieved. The synthesis method has the advantages of easily available raw materials, mild reaction conditions, small side reaction influence, simplicity and convenience in operation and high yield, improves the yield, is easy to purify, and is suitable for industrial production of omariglitazone.

The invention discloses a La < 3 + >-doped lithium manganese oxide lithium ion sieve as well as a preparation method and application thereof, and belongs to the technical field of salt lake lithium extraction. The preparation method comprises the following steps: by taking Mn2O3 and LiOH as raw materials, carrying out hydrothermal reaction to generate LiMnO2, mixing the LiMnO2 with La2O3, grinding and calcining to form a La < 3 + >-doped spinel structure precursor La-LMO, and carrying out acid pickling to prepare La-HMO. La < 3 + > replaces part of Mn < 3 + >, the average valence state of manganese is improved, meanwhile, the structural stability of the manganese is enhanced through the high bond energy of La-O bonds, the number of exposed manganese atoms is reduced, manganese solution loss caused by Mn < 3 + > disproportionation reaction in the acid treatment process is effectively inhibited, the adsorbed oxygen content and active sites are increased, and the lithium ion adsorption capacity is remarkably improved. The material has high-selectivity adsorption capacity on lithium ions in salt lake brine in a strong alkaline environment, the manganese solution loss rate is obviously lower than that of traditional HMO, the cycle life is remarkably prolonged, and the industrial application potential is remarkably improved. The preparation process of the lithium ion sieve is simple, the raw material cost is low, and the technical bottlenecks that an existing manganese-based lithium ion sieve is poor in structural stability and high in manganese solution loss are solved.

The invention provides a Ga-modified copper-based catalyst, a preparation method thereof and an application of the Ga-modified copper-based catalyst in preparation of methanol by hydrogenation of carbon dioxide, the Ga-modified copper-based catalyst comprises a carrier and an active component loaded on the carrier, the carrier is a Ga-modified TiO2-Al2O3 composite oxide, and the active component is a Cu oxide. The Ga-modified copper-based catalyst has the performance of catalyzing the reaction for preparing methanol through carbon dioxide hydrogenation, and methanol can be generated at high selectivity under the reaction conditions of low temperature and high pressure.

The invention provides a preparation method of a high-flux stable-selection anti-fouling nanofiltration membrane, which comprises the following steps: carrying out amination modification on a nano material by an activation method to prepare a modified nano material; piperazine, an acid absorbent and the modified nano material are added into deionized water to be mixed, and a water phase solution is prepared; the preparation method comprises the following steps: mixing trimesoyl chloride and normal hexane to prepare an organic phase solution; immersing the polyethersulfone-based membrane into the water phase solution, draining, inversely immersing into the organic phase solution, and carrying out interfacial polymerization reaction to generate a polyamide layer to obtain a composite membrane; and then carrying out post-treatment on the composite membrane to obtain the composite membrane. The membrane has high permeability, high selectivity and strong anti-pollution performance.

The invention discloses an electrocatalytic oxidation method for highly selectively converting 5-hydroxymethylfurfural into 2, 5-furandicarboxylic acid by using a cobalt-nickel bimetallic catalyst, and belongs to the technical field of electrochemistry. Firstly, foamed nickel is pretreated; secondly, preparing a cobalt-nickel mixed solution, synthesizing the catalyst by adopting a solvothermal method, and characterizing the catalyst; and thirdly, preparing a three-electrode system by taking the cobalt-nickel catalyst as a working electrode, a spiral platinum wire electrode as a counter electrode, a Hg / HgO electrode as a reference electrode, an alkaline solution as an electrolyte and a Nafion 117 proton membrane as a diaphragm to realize conversion. And finally, testing the stability and cyclicity of the cobalt-nickel catalyst. Under the same potential, the material has the highest current density, the maximum electrochemical active area and the optimal charge transfer rate; the self-degradation of HMF can be effectively inhibited, the electrocatalytic oxidation has lower initial potential than the oxygen evolution reaction, and the electrode cycle stability is good; the method is simple in process, mild in condition and beneficial to industrial production.