3493 results about "High selectivity" patented technology

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.

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 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 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 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 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 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.

The invention provides a high-selectivity broadband millimeter wave three-dimensional printing filtering antenna based on a half-mode slot gap waveguide, and belongs to the technical field of antennae, the half-mode slot gap waveguide antenna comprises a metal column cover plate, an input waveguide port, a first slot, a second slot, a first resonance iris and a second resonance iris, a third resonance iris and a stepped radiation waveguide port; the first slot is arranged on the device body and connected with the right side of the first resonant iris, and the left side of the first resonant iris is connected with the input waveguide interface; the second slot is formed in the device body, the second slot is connected with the left side of the third resonance iris, the right side of the third resonance iris is connected with the stepped radiation waveguide, and the first slot and the second slot are connected through the second resonance iris. The cover plate is arranged on the device body and forms a second resonant cavity and a fourth resonant cavity with the first open groove and the second open groove, and the first resonant iris, the second resonant iris and the third resonant iris form a first resonant cavity, a third resonant cavity and a fifth resonant cavity.

The invention relates to a coumarin-based fluorescent probe as well as a preparation method and application thereof in the aspect of HClO detection, and belongs to the technical field of HClO detection. The invention discloses a coumarin-based fluorescent probe W (O-(3-((2-morpholinyl ethyl) carbamoyl)-2-oxo-2hydrogen-benzopyran-7-yl) dimethyl thiocarbamate) prepared on the basis of an intramolecular charge transfer (ICT) mechanism, and a preparation method of the coumarin-based fluorescent probe W. The novel lysosome targeting fluorescent probe contains coumarin as a fluorophore, a morpholine group as a targeting group and a dimethyl thiocarbamate group as a recognition group, is a novel lysosome targeting fluorescent probe, and has excellent performances of high selectivity, low detection limit, low cytotoxicity, high resolution and the like in the aspect of HClO detection; the method can be used for detecting the content of endogenous and exogenous hypochlorous acid in living cells.

The invention relates to the technical field of analysis and detection, in particular to a fluorescent switch sensor based on quantum dot-nano porphyrin and application. The specific technical scheme is as follows: the fluorescent switch sensor is constructed by utilizing cadmium telluride quantum dots modified by mercaptosuccinic acid and a 5, 10, 15, 20-tetra (4-nitrophenyl) porphyrin nano material modified by a cationic surfactant hexadecyl trimethyl ammonium bromide. And the method has a good enrichment effect on zearalenone. The sensor has high sensitivity, high selectivity and anti-interference performance, can accurately analyze trace zearalenone in actual grain samples (corn, rice, soybean and the like), and has the advantages of simplicity in operation, low detection limit, high sensitivity, low cost and the like.

The invention relates to the technical field of fine chemical engineering and flame retardant preparation, and discloses a preparation method of bromo-triazine capable of improving thermal stability, and the preparation method comprises the following steps: mixing phenol, water and dichloromethane, controlling the temperature, and carrying out oxidative bromination reaction to prepare an organic phase containing tribromophenol; then, under the action of an organic amine catalyst, carrying out condensation reaction on the organic phase, liquid caustic soda and cyanuric chloride; after the reaction, washing with water to remove impurities; and in the presence of process water, firstly controlling the temperature at 38-42 DEG C for azeotropic desolvation, then raising the temperature to 85-95 DEG C for high-temperature crystallization and crystal growing, and finally cooling, filtering and drying to obtain the bromo-triazine product. By utilizing the high selectivity of the organic amine catalyst and a two-stage azeotropic crystallization process, the side reaction is effectively reduced, the solvent wrapped in the crystal is eliminated, the prepared product is high in main content and extremely low in volatile component, the temperature can reach 370 DEG C or above when the thermal weight loss is 2%, and the thermal stability is remarkably improved.

The invention relates to the technical field of analysis and detection, in particular to a surface enhanced Raman spectroscopy (SERS)-based nano material detection method, which is characterized in that a heterojunction composite structure consisting of noble metal nano stars and semiconductor oxide nano particles is used as an SERS active substrate; and a specific recognition molecule carrying a Raman reporter molecule is used as a detection probe. During detection, the recognition molecules are firstly combined with the to-be-detected nano material, and then the compound is adsorbed on the surface of the substrate. The tip structure of the noble metal nanostar and a heterojunction interface jointly generate a synergistic effect of electromagnetic enhancement and chemical enhancement, and a reporter molecule signal is doubly amplified, so that high-sensitivity and high-selectivity detection on a to-be-detected nano material is realized. The method solves the problems of weak signal and poor selectivity of the traditional method, and is suitable for rapid and quantitative analysis of trace nano materials in the environment.

The invention provides a self-cleaning liquid crystal display screen system based on nanostructure enhancement, and relates to the technical field of liquid crystal display screens, the self-cleaning liquid crystal display screen system comprises a liquid crystal display panel, a reconfigurable surface phonon polariton regulation and control layer, a pollutant identification module, an excitation source module, a central control processing unit and an energy recovery module, by dynamically tuning the surface phonon polariton resonance characteristics of the reconfigurable surface phonon polariton regulation and control layer micro-nano structure unit, selective resonance coupling with a target pollutant detected by the pollutant identification module is carried out, and selective activation is carried out by an excitation source. High-selectivity energy transfer generated by resonance causes molecular decomposition or generates field gradient force to achieve physical effects such as particle stripping migration, pollutants are efficiently and intelligently removed, and meanwhile the integrated energy recovery module collects panel waste heat and converts the panel waste heat into driving energy to assist system operation so as to improve energy efficiency. The problems of poor selectivity, low efficiency, high energy consumption and screen damage in the traditional technology are solved.

The invention provides a method for accurately regulating and controlling pores of an MXene material by utilizing a phosphonic acid ligand, which mainly comprises the following key steps of: directionally removing a main group element (A) layer of an MAX precursor by wet etching to obtain lamellar MXene, and then introducing a protonated quaternary amine compound intercalator to strip the MXene. And finally, carrying out functional modification and conversion by adopting a phosphonic acid ligand, and stably introducing phosphonic acid groups between layers and on the surface of MXene through solvothermal reaction to realize accurate regulation and control of interlayer spacing. The prepared material can realize efficient adsorption of uranyl in an acidic environment, shows high selectivity, high adsorption capacity and good acid stability and regeneration capacity to uranyl, provides a stable and efficient selective adsorption solution for treating high-acidity uranium-containing nuclear wastewater, and has a remarkable industrial application prospect.

The invention relates to a screening method and an activity evaluation method of a natural antioxidant, and the screening method is characterized in that a cerium dioxide-based nano composite material with a specific structure is used as oxidase, a nano oxidase + natural antioxidant reaction system is constructed, and the activity of the natural antioxidant is evaluated through a high performance liquid chromatography-ultraviolet detector-tandem mass spectrometry analysis technology. Screening of the natural antioxidant is realized; according to the activity evaluation method, a cerium dioxide-based nano composite material with a specific structure is used as oxidase, a nano oxidase + natural antioxidant + TMB reaction system is constructed, and the activity evaluation of the natural antioxidant is realized through an oxidized TMB photo-thermal detection technology. According to the method disclosed by the invention, the used reaction system is high in applicability, high in accuracy and good in selectivity.

The invention belongs to the technical field of preparation and application of nano materials, and relates to a preparation method and application of amino-functionalized cerium oxide nano enzyme, and the preparation method comprises the following steps: adding 3-aminophenylboronic acid into a cerous nitrate hexahydrate aqueous solution to obtain a mixed solution; dropwise adding a sodium hydroxide aqueous solution into the mixed solution, carrying out hydrothermal reaction, cooling after the reaction is finished, centrifuging, washing and drying to obtain milk white powder, namely the amino-functionalized cerium oxide nano-enzyme. The boron element is introduced in the preparation of the cerium oxide nano-enzyme, and the amino-functionalized cerium oxide nano-enzyme is prepared by adopting a simple one-step hydrothermal synthesis method, so that the nano-enzyme has good phosphatase-like activity, has high selectivity and sensitivity to LPS, and is short in detection time, high in sensitivity, low in detection limit, simple in preparation process and high in preparation efficiency; the product is good in quality, high in stability, environment-friendly and extremely wide in market prospect.

The invention discloses an electrocatalyst for biomass conversion and plastic degradation as well as a preparation method and application of the electrocatalyst. According to the catalyst, a carbon-based material serves as a catalyst carrier, multi-component metal and multi-component metal oxide are loaded to prepare the catalyst of a binary metal interface structure, and the catalyst is recorded as NM / TMOx / C, NM is one or more of precious metal Au, Ag, Ir, In, Pd, Pt, Ru and Rh, TM is one or more of transition metal Co, Cu, Mn, Ni, Fe and Ti, the loading amount of NM is 0.5 wt%-35 wt%, and the loading amount of TM is 1 wt%-30 wt%; the invention also provides a preparation method and an application method of the catalyst. The catalyst NM / TMO / C is high in reaction rate of electrocatalytic oxidation of biomass and plastic degradation under low potential, high in selectivity of corresponding multi-electron products, good in CO toxicity resistance, good in stability and high in repeatability.

The invention relates to a preparation method of ordered mesoporous MOFs with a hollow structure and uranium extraction application of the ordered mesoporous MOFs, the molar ratio of terephthalic acid to aminoterephthalic acid is controlled at 92: 8 by accurately regulating and controlling the variety and content of organic ligands in a reaction system, and the uranium extraction application of the ordered mesoporous MOFs with the hollow structure can be realized while amino functionalization is realized. The ordered mesoporous MOFs with the hollow structure are rapidly synthesized in one step, and the method is simple and high in operability. Experiments prove that the ordered mesoporous MOFs with the hollow structure have excellent anti-interference capability, show high-selectivity adsorption on uranium, and provide a new idea and choice for extraction of uranium from seawater.

The invention discloses an organelle-targeted fluorescent probe for specific detection of tumor cells as well as preparation and application of the organelle-targeted fluorescent probe, and the specific structural formula of the fluorescent probe is as follows: BCY-DP shows obvious specific targeting ability of tumor cell mitochondria and has been applied to ONOO-selective imaging in living cell mitochondria; results show that the BCY-DP has high selectivity on ONOO <-> in tumor cells, can successfully distinguish the ovarian cancer cells from normal ovarian cells, and can be used for diagnosis of cancer cells.

The invention relates to the field of sensors, and discloses a solid electrolyte for ammonia gas detection, an electrochemical luminescence sensor, a preparation method and a detection method, and the solid electrolyte for ammonia gas detection comprises the following raw materials: a second electrolyte, a luminescent substance, an optional first electrolyte and an optional binder. The solid electrolyte for ammonia gas detection provided by the invention can realize ppb-level NH3 selective detection with high sensitivity, wide linear response range and low detection limit at room temperature for an electrochemical luminescence sensor for detecting ammonia gas. The electrochemical luminescence sensor for detecting the ammonia gas can be used for sensing the ammonia gas through a cyclic voltammetry method and a constant potential-luminescence technology, and ppb-level high-sensitivity and high-selectivity ammonia gas detection is realized.

According to the present invention, glycosyl transferase UGTBL1 derived from Bacillus licheniformis ZSP01 is adopted as a research object, AlphaFold 2 is adopted to carry out modeling, molecular docking, molecular dynamics simulation and other technologies, amino acids in an active pocket region of glycosyl transferase are analyzed, site-directed mutagenesis is performed on the amino acids to obtain a series of glycosyl transferase mutants, and salidroside can be highly selectively catalyzed and synthesized.

Provided is a method for etching a silicon nitride film with high accuracy and high selectivity with respect to a silicon oxide film, while preventing deterioration of the shape of a silicon oxide film portion during etching. A dry etching method according to the present invention is used for etching a film structure that is formed in advance on a wafer disposed in a processing chamber, and that is configured such that an end portion of a film layer obtained by laminating a silicon nitride film so as to be vertically sandwiched by silicon oxide films constitutes a side wall of a groove or a hole, in a state in which a gas for processing is supplied into the processing chamber and no plasma is used, wherein: the method comprises (a) a step for reacting a hydrogen fluoride gas at a prescribed temperature to form a reaction layer on the silicon nitride film, (b) a step for channeling a gas of a polar solvent to process the reaction layer formed in step (a), and (c) a step for performing heating at a temperature higher than that in step (a) in a state in which no hydrogen fluoride gas is channeled and volatilizing the reaction layer formed in step (a) and processed in step (b) to remove the reaction layer; and steps (a) to (c) are repeated a plurality of times.

The invention provides a cation exchange membrane chromatography medium and a preparation method and application thereof, the cation exchange membrane chromatography medium comprises a homo-porous membrane, polydopamine is loaded on two side surfaces and in a pore structure of the homo-porous membrane, and a cation exchange functional ligand is grafted on the polydopamine; a homogeneous pore membrane is selected as a matrix membrane, polydopamine is loaded on the surface and in an internal pore structure of the homogeneous pore membrane, and then a cation exchange functional ligand is further grafted, so that the surface of a chromatography medium of the obtained cation exchange membrane has relatively strong negative charges, and biomolecules with positive charges can be effectively adsorbed, thereby being separated from biomolecules with negative charges; meanwhile, the membrane is relatively low in transmembrane pressure and relatively high in separation degree, also has the characteristics of high permeability and high selectivity, and is suitable for being applied to separation and purification of biological drug macromolecules.

The invention discloses an internal-acid and external-alkali type organic-inorganic hybrid molecular sieve catalyst as well as a preparation method and application thereof, and belongs to the technical field of heterogeneous catalytic materials and chemical processes. According to the catalyst, a hydrogen type Beta molecular sieve is used as an acidic inner core, polyvinylpyrrolidone (PVP) is used as an organic shell, and a unique inner-acid outer-alkali structure is formed. The preparation method comprises the following steps: hydrothermally synthesizing a hydrogen type Beta molecular sieve with a specific silica-alumina ratio, and then coating PVP through surface adsorption. The catalyst is used for catalyzing the condensation of methylal and trioxymethylene under mild conditions (40-70 DEG C and normal pressure) to prepare polyoxymethylene dimethyl ethers (DMMn). The PVP shell covers acidic sites on the outer surface of the molecular sieve to form an external neutral / weak base and internal strong acid microenvironment, so that the secondary side reaction of the product is effectively inhibited, the trioxymethylene conversion rate of more than 98% and the DMMn selectivity of more than 96% can be obtained in the reaction at 50 DEG C and normal pressure, the product distribution can be regulated and controlled, and the traditional Anderson-Schulz-Flory distribution limitation is broken through. The catalyst disclosed by the invention has the advantages of high activity, high selectivity, mild conditions and easiness in separation, and has a good industrial application prospect.

The invention discloses a binder-free granular carbon molecular sieve and application thereof in C4 olefin mixture separation, and belongs to the technical field of C4 olefin adsorption and separation. The granular carbon molecular sieve for C4 olefin mixture component separation is obtained by crushing a precursor, screening particles with a proper particle size as a carbon source, and then performing carbonization and pyrolysis in a tubular furnace. The granular carbon molecular sieve disclosed by the invention is high in adsorption capacity, high in selectivity, good in stability, high in particle strength and easy to recycle and regenerate, and can be directly used for industrial devices. Compared with the traditional solvent absorption, extractive distillation and low-temperature distillation technologies, the separation method provided by the invention has the advantages of low energy consumption, small equipment investment, environmental friendliness and the like, and has a wide application prospect in the field of C4 olefin component separation.

The invention belongs to the technical field of synthesis of polyol carbonate materials, and discloses a preparation method of polyol carbonate. The preparation method disclosed by the invention comprises the following steps: mixing solid polyol with a eutectic component to form a low-melting-point eutectic substance, and then adding a reactant to carry out cyclization reaction, so as to prepare the cyclic or multi-cyclic polyol carbonate. According to the method, the polyol and the eutectic component are mixed to form a low-melting-point eutectic substance, and the hydrogen-bond interaction of the polyol is weakened through the intermolecular interaction of the eutectic component and the polyol, so that the cyclic or multi-cyclic polyol carbonate can be prepared at high selectivity and high yield under mild conditions.

The invention belongs to the field of methanol conversion and utilization, and particularly relates to a three-layer multi-core structure catalyst for high-selectivity synthesis of monomethylamine and a preparation method of the three-layer multi-core structure catalyst. The core layer of the catalyst is gamma-aluminum oxide, the middle layer of the catalyst is a mordenite (MOR) molecular sieve, and the outer layer of the catalyst is porous SiO2. The preparation of the multi-core MOR layer adopts a steam-assisted crystallization method, the preparation method is simple, no organic waste liquid is generated, the preparation method is environment-friendly, the multi-core MOR layer can be used in a reaction for preparing methylamine through continuous gas phase catalytic amination of methanol after being modified by ammonium ion exchange and chemical liquid phase deposition (CLD), the methanol conversion rate reaches 98.6% under the reaction conditions that the temperature is 340 DEG C, the methanol liquid hourly space velocity is 1.5 h <-1 >, the ammonia-alcohol ratio is 3 and the pressure is normal, and the method is suitable for industrial production. The mass ratio of monomethylamine is greater than 60%, and the method has a good application prospect.

The invention discloses a double-morphology boron-containing Zn / Cu metal organic framework composite material as well as preparation and application thereof, and belongs to the technical field of fine chemical engineering. The double-morphology boron-containing Zn / Cu metal organic framework composite material is prepared through a one-pot hydrothermal reaction, and the double morphology comprises a three-dimensional nanoflower structure and a three-dimensional rod / columnar structure. Specifically, by adjusting the molar ratio of Zn to Cu in the coordination process with corresponding ligands, when the molar ratio of Zn to Cu reaches 1: 1, the original single nanoflower structure can generate a new three-dimensional rod / columnar structure, so that two composite forms are formed. The double-morphology boron-containing Zn / Cu metal organic framework composite material shows high activity and high selectivity when being used for two key reactions of electrochemical hydrogenation reduction and electrochemical oxidation of furfural.