2043 results about "Crystallinity" patented technology

The invention discloses a high-bio-based PHA-acrylate emulsion paint as well as a preparation method and application thereof, and belongs to the technical field of water-based paints. The film former of the latex paint comprises 60% to 90% of polyhydroxyalkanoate (PHA) with a moderate crystallinity of 40% to 60%, and 10% to 40% of a specific bio-based acrylate copolymer with a Tg of not higher than 5 DEG C. According to the invention, a core-shell microstructure in which a rigid PHA phase is wrapped by a flexible acrylate phase is constructed through a key process including ultrasonic treatment. According to the structure, low-temperature film forming can be achieved without a VOC coalescing agent, the bio-based content of an obtained paint film is higher than 70%, the VOC content is lower than 0.5 g / L, the scrub resistance is larger than 7000 times, and the technical problem that high bio-based content and high performance of a PHA coating are difficult to achieve at the same time is solved.

The invention discloses a p-type or n-type COF film, the film thickness is 50 nm to 5 m, the aperture is 0.7 nm to 4 nm, and the film has a regular pore channel structure and light response performance. According to the invention, proper monomers are selected, and liquid-solid interface polymerization reaction is carried out, so that COF membranes grow along the tube wall, and p-type and n-type COF membranes are respectively prepared. The growth direction of the film is inconsistent with the transmission direction of the monomer and the catalyst, and the process can effectively promote the dissolution growth and self-repair of the COF film, so that the crystallinity and stacking orientation of the film are improved, and the structural characteristics of the COF film are optimized. The obtained COF film has a remarkable advantage of light-driven ion pump performance. The obtained COF membrane is used for preparing a desalting device.

The invention discloses a double-PHA barrier system for a paper-based container and a paperboard as well as a preparation method and application of the double-PHA barrier system, and belongs to the technical field of paper-based material surface engineering and green packaging. The system sequentially comprises a paper base material, a water-based PHA dispersion hole sealing layer and a PHA extrusion compact layer from inside to outside. According to the invention, the micron-sized PHA dispersoid without cell debris is utilized, so that an efficient hole sealing effect which is difficult to achieve by a high coating amount in a traditional process can be achieved by only needing an extremely low coating amount, and the pinhole defect of an extrusion layer is eliminated from the source. And in cooperation with the modified PHA extrusion layer with the specific crystallinity, the problem of micro-cracking of a single coating during edge rolling forming is cooperatively solved. According to the system, excellent barrier performance is achieved through a thinner bio-based structure, and meanwhile the system has a wide heat sealing window and excellent repulp recycling performance. Compared with the prior art, on the premise that high performance is guaranteed, the consumption amount of packaging materials and the environmental burden are remarkably reduced.

The invention discloses a glass ceramic and a preparation method thereof, and an electronic equipment cover plate and an electronic equipment cover plate assembly prepared from the glass ceramic, the overall crystallinity of the glass ceramic is 60%-95%, the crystalline phase is lithium disilicate and petalite, and the weight ratio of the lithium disilicate crystalline phase to the petalite crystalline phase is greater than or equal to 1.5. The microcrystalline glass provided by the invention has specific glass composition and crystalline phase structure, and by utilizing the synergistic effect of the glass composition and the high lithium disilicate crystalline phase structure, not only is the microcrystalline glass product endowed with high elastic modulus, but also the microcrystalline glass product can obtain an expected stress structure after chemical strengthening treatment; particularly, the high center tensile stress (CT-CV) and the large average tensile stress (CT-AV) are achieved.

The invention belongs to the technical field of chemical process intelligent control, and discloses an iron phosphate synthesis parameter self-adaptive control system based on an intelligent algorithm. The system is composed of a target quality sensing module, a reaction data acquisition and preprocessing module, a sensitive section identification module, a process boundary modeling module, a multi-strategy control model library module, a strategy evaluation and structure evolution module and a control execution and feedback module. According to the method, a multi-module cooperation mechanism including target scoring modeling, dynamic sensitive segment identification and reaction boundary modeling is constructed, so that whole-process online identification and segmented precise control of the crystal form, the particle size and the crystallinity of a product in the iron phosphate synthesis process are realized; compared with a traditional control system depending on experience setting and univariate feedback, the system has the advantages of being higher in state sensing depth, more accurate in crystal form conversion process recognition, finer in reaction stage regulation and control and the like, and the problems of crystal form deviation, particle size drift and inter-batch quality fluctuation are effectively solved.

An AI-based euryale ferox processing process quality control system of the present invention belongs to the technical field of food processing and quality control, and comprises a quality perception quantification module used for carrying out real-time nondestructive detection on a material unit entering a processing flow, and determining the quality of the material unit through a pre-established chemometrics model. The system comprises a material unit acquisition module for acquiring original spectrum data, a quality dynamic evolution prediction module for analyzing and quantifying the acquired original spectrum data into an initial starch crystallinity index, and a quality dynamic evolution prediction module for predicting a quality evolution track of the material unit in future processing time through a dynamic evolution prediction model based on the initial starch crystallinity index, a current quality state and real-time process parameters. According to the method, different processing paths can be predictively planned for materials with different characteristics, so that disturbance caused by heterogeneity of the raw materials is effectively overcome.

The invention discloses an air pressure control method for microwave plasma chemical vapor deposition diamond, and particularly relates to the technical field of microwave plasma chemical vapor deposition, and the method comprises the steps of S1, spectrum real-time monitoring, S2, machine learning prediction, S3, multi-stage air pressure regulation and control, S4, multi-parameter cooperative control, and S5, air pressure closed-loop control. According to the method, high-precision prediction of the optimal air pressure value is achieved through combination of spectrum real-time monitoring and a machine learning model, the diamond deposition quality is effectively improved by means of a multi-stage air pressure regulation and control and multi-parameter cooperative control strategy, the surface flatness and crystallinity are remarkably improved, meanwhile, precise air pressure closed-loop control and efficient gas flow are coordinated, and the precision of the diamond deposition is improved. In addition, all the modules of the system are in close fit, the stability of the deposition environment is guaranteed, the process fluctuation is reduced, the stability and reliability of the whole deposition process are enhanced, and powerful guarantee is provided for high-quality and high-efficiency production of diamonds.

The invention discloses a bio-based PHA oil-resistant and moisture-permeable coating for hamburger paper, coated paper and a preparation method, and belongs to the technical field of bio-based high polymer materials and paper-based food packaging. The coating is a PHA aqueous dispersion, and mainly comprises a semi-crystalline matrix PHA and a low-crystallinity or amorphous toughening PHA. The core of the coating is that after the coating is dried to form a film, a functional gradient structure can be spontaneously formed in the thickness direction of the coating: an interface layer close to a paper base is rich in toughening PHA so as to enhance toughness and adhesive force; and the surface layer of the coating is rich in matrix PHA so as to maximize the oil resistance. By means of the functional gradient structural design, the packaging material integrates oil resistance, moisture permeability and flexibility of the packaging material, has the degradable environment-friendly characteristic and is suitable for packaging high-grease food.

The invention discloses a covalent organic framework membrane and a preparation method thereof, and belongs to the technical field of organic porous materials and membrane materials. The preparation method of the covalent organic framework membrane comprises the following steps: S1, respectively dissolving an amine compound containing a plurality of amino groups and a compound containing a plurality of aldehyde groups in a mixed solution of trifluoroacetic acid and water to respectively obtain a first monomer solution and a second monomer solution; in the mixed solution, the volume ratio of trifluoroacetic acid to water is (95-96): (4-5); s2, mixing the first monomer solution and the second monomer solution, and performing ultrasonic treatment to obtain a reaction solution; and heating the reaction liquid at 95-100 DEG C to react for 3-5 minutes to form the covalent organic framework film. In addition, the invention also provides the covalent organic framework film which is prepared by the preparation method. The COF film which is complete in structure, excellent in crystallinity and flexible can be prepared in a short time through a simple method.

The invention relates to the technical field of functional materials, in particular to a polyvinyl butyral flexible material as well as a preparation method and application thereof. The molecular chain regularity is destroyed through an isobutyraldehyde branched chain, the crystallinity is reduced, and the flexibility is improved; cesium-tin co-doped tungsten oxide has high infrared rejection rate and good dispersity, and the influence on the flexibility of the material is reduced; magnesium salicylate and magnesium formate are compounded, so that the reaction activity with resin is reduced, and the bonding stability in the bending process is ensured; the flexibility and migration resistance of the material are synergistically improved through the flexible plasticizer, and the interlayer sheet is prevented from being sticky; the flexible reinforcing agent polycaprolactone micro powder is used for forming an elastic node, bending stress is absorbed, and the recovery performance is improved. The polyvinyl butyral flexible material provided by the invention has flexible bending performance, an efficient infrared barrier function and stable bonding performance, is suitable for scenes such as curved building curtain walls, special-shaped automobile sunroofs or arc-shaped rail traffic windows, and has a wide application prospect.

The invention relates to the technical field of material polishing, and discloses a PEEK material composite polishing method and system based on multi-process collaboration.The method comprises the steps that surface detection is conducted on a PEEK material, and crystallinity gradient distribution information is obtained; according to the crystallinity gradient distribution information, process parameter calculation is conducted on the crystalline area and the amorphous area, and a polishing process parameter combination is obtained; inputting the polishing process parameter combination into multi-process collaborative composite polishing equipment, and carrying out gradient interface strengthening polishing on the PEEK material to obtain an interface strengthening polishing semi-finished product; and dynamically adjusting the process parameters of the semi-finished interface strengthening and polishing product to obtain the finished interface strengthening and polishing product, so that accurate division of a crystallization area and an amorphous area of the PEEK material and differential process parameter calculation are realized, and the composite polishing precision of the PEEK material is improved.

The invention belongs to the field of synthesis of inorganic non-metallic materials, and particularly relates to an equimolar-ratio seven-element high-entropy oxide and a preparation process thereof. The preparation process comprises the following steps: putting seven oxide powder Al2O3, Y2O3, TiO2, ZrO2, NiO, CuO and CeO2 into a ball milling tank according to a molar ratio of 1: 1: 2: 2: 2: 2: 2: 2, adding absolute ethyl alcohol and zirconium oxide grinding balls, performing ball milling in a ball mill, and fully drying and sieving after ball milling to obtain mixed powder; carrying out tabletting treatment on the mixed powder to obtain a to-be-sintered green body; and putting the to-be-sintered green body into an alumina crucible, and putting the alumina crucible into a microwave oven for microwave sintering. According to the method, the equimolar-ratio seven-element high-entropy oxide (AlYTiZrNiCuCe) Ox with good solid solution is obtained, the crystallinity and element uniformity of the seven-element high-entropy oxide are improved, all the raw materials react completely, meanwhile, the process efficiency is high, and energy consumption is low.

The invention relates to the technical field of capacitor films. The invention discloses a preparation process of a high-performance polypropylene capacitor film. The preparation process comprises the following steps: A1, preparing a polypropylene capacitor film; a2, carrying out surface cleaning and activation pretreatment on the polypropylene capacitance film; a3, evaporating a gradient modified layer on the surface of the pretreated polypropylene capacitance film; a4, carrying out laser plasma synergistic treatment and crystallinity regulation and control on the modified polypropylene capacitor film; and A5, coating the outer layer of the modified polypropylene capacitance film with a functional layer, and carrying out annealing post-treatment to prepare the high-performance polypropylene capacitance film. The mechanical strength and the electrical stability are improved through nano filler dispersion, two-way stretching and crystallinity regulation and control; through the collaborative design of surface cleaning and activation and a gradient functional layer, excellent interface bonding force and environmental adaptability are given; and by means of technologies such as multi-source evaporation and laser plasma co-processing, precise regulation and control and diversified expansion of the performance are achieved, the method is suitable for various scenes, and the process repeatability is good.

The invention relates to the technical field of environmental chemistry, in particular to a double-vacancy Fe0. 96S (at) MoS2 nano composite material as well as a wet-type mechanochemical synthesis method and application thereof. The preparation method comprises the following steps: firstly carrying out co-ball milling by utilizing a wet mechanical chemical synthesis method to obtain a low-crystallinity Fe0. 96S (at) MoS2 precursor, and then carrying out further calcination treatment to accelerate the thermal reaction of the precursor, improve the crystallinity and remove redundant sulfur powder impurities, thereby obtaining the high-crystallinity Fe0. 96S (at) MoS2 nano composite material. Iron powder is introduced in the process of preparing MoS2 nanosheets from molybdenum powder and sulfur powder, the reaction activity of the molybdenum powder and the sulfur powder is improved and the formation energy of MoS2 is reduced by utilizing the characteristic of ball-milling heat release of the iron powder and the sulfur powder, the reaction barrier that MoS2 is difficult to prepare between Mo and S through a mechanical ball-milling process originally is broken, and the generation of the MoS2 nanosheets is promoted.

The recycled bis(4-hydroxybutyl) terephthalate according to one embodiment has a low amount of residual ethylene glycol derivatives and can therefore be used as a polymerization raw material for high crystallinity engineering polyester products or biodegradable polyesters, offering superior qualities, for example, color.

The invention discloses a method for synthesizing a Mn0. 43Cd0. 57S / Cu2MoS4 photocatalyst by adopting a solvothermal method, and belongs to the technical field of catalysts. The preparation method comprises the following steps: preparing copper molybdenum sulfide by using cuprous oxide as a template, synthesizing copper molybdenum sulfide with high purity and good crystallinity by combining a solvothermal method, preparing manganese cadmium sulfide by using manganese acetate, cadmium acetate, sodium hydroxide and thioacetamide as raw materials, adding copper molybdenum sulfide before a hydrothermal reaction, successfully modifying the manganese cadmium sulfide by constructing a heterojunction, and preparing the copper molybdenum sulfide modified manganese cadmium sulfide. The Mn0. 43Cd0. 57S / Cu2MoS4 photocatalyst is synthesized, and the photocatalytic hydrogen production rate of the cadmium manganese sulfide is improved. Moreover, the hydrogen production rate of the Mn0. 43Cd0. 57S / Cu2MoS4 photocatalyst prepared by the invention can reach 8233 mu mol / (g.h), which is 2.08 times of the hydrogen production rate of pure cadmium manganese sulfide, and 1.24 times of the hydrogen production rate of cadmium manganese sulfide loaded with 1% platinum.

The invention provides a cable insulation aging state evaluation method and device and a detection system. The method comprises the following steps: acquiring near-infrared spectrum data which is a light intensity value of a cable for absorbing near-infrared light; according to the near infrared spectrum data, the crystallinity of the cable is determined, and the crystallinity is the proportion of the volume of a crystallization area of a polymer material of the cable to the material volume of the whole cable; according to the crystallinity and a first preset mapping relation, the aging index of the cable is determined, and the first preset mapping relation is the mapping relation between the crystallinity and the aging index; and when the aging index is greater than a first preset index threshold, controlling the alarm device to give an alarm. The method solves the problem that the aging state of the cable cannot be accurately evaluated in the prior art.

The invention provides high-performance silver powder suitable for TOPCon battery fine grid silver paste, a preparation method of the high-performance silver powder and the silver paste, and belongs to the technical field of photovoltaic materials. The preparation method comprises the steps that a silver salt solution and a composite reducing agent are mixed, a first-stage hydrothermal reaction is carried out at the first temperature, a second-stage hydrothermal reaction is carried out at the second temperature, and silver powder is obtained after centrifugation, washing and drying; wherein the composite reducing agent is selected from a mixture of two of potassium tartrate, sodium sulfite and ferrous sulfate. According to the method, gradual growth and crystallinity improvement of silver crystal nucleuses are achieved through two-stage heating, particle aggregation or uneven morphology caused by rapid reduction is avoided, in addition, the adopted composite reducing agent combination is remarkably superior to a single reducing agent (such as ascorbic acid), and the morphology and particle size distribution of the silver powder can be more accurately regulated and controlled.

The invention discloses a memristor based on a covalent organic framework and a preparation method and application thereof.The memristor comprises a substrate, a semiconductor electrode, a covalent organic framework film and a metal electrode which are sequentially arranged in a stacked mode, and the covalent organic framework film is composed of 1, 3, 4, 5, 6, 7, 8, 8, 9, 10, 11, 12, 13, 14, 16, 17, 17, 17, 17, 17, 17, 17, 17, the catalyst is prepared by condensing 1, 3, 5-tri (4-aminophenyl) benzene and terephthalaldehyde or terephthalaldehyde with an alkyl or alkoxy side chain. The covalent organic framework film has a highly ordered structure and an adjustable porous structure, the preparation process is simple, the film thickness is uniform, the flatness and the crystallinity are high, and the dielectric property is adjusted, so that the switching voltage and the cycling stability of the memristor are adjusted, and the memristor has stable and repeatable switching performance; the COFs-based memristor has high on / off ratio, low device variability and high flexibility, can be used for preparing the COFs-based memristor, can provide technical support for neuromorphic devices with high efficiency, adjustability, structure adjustability and rich functions, and can be applied to the field of intelligent sensing and autonomous system control such as an auxiliary driving system.

The invention provides a high-crystallinity modified iron oxide as well as a preparation method and application thereof, and relates to the technical field of organic solid waste treatment. The preparation method comprises the following steps: preparing a precursor MIL-88B by utilizing a hydrothermal method; the precursor MIL-88B is subjected to calcination treatment, and an iron oxide with the MIL-88B as the precursor is obtained; the temperature condition of the calcination treatment is 550-850 DEG C. The high-crystallinity modified iron oxide prepared by the preparation method improves methane production efficiency and stability, avoids competition of iron reducing bacteria, is stable in long-term operation and low in cost, and has both environmental and economic benefits.

The invention belongs to the field of functional material preparation, and relates to an MOFs crystal film and a preparation method and application thereof. According to the MOFs crystal film, a porous polymer supporting film is used as a carrier, a high-crystallinity, compact and continuous rigid MOFs crystal layer grows on the surface of the porous polymer supporting film in situ, and a solid / quasi-solid electrolyte system is formed by matching polymer electrolyte or electrolyte. The MOFs ordered pore channel ion screening effect and metal ion sites are used for limiting anions, so that the ion transference number is increased; a physical-chemical synergistic dendritic crystal inhibiting mechanism is realized by utilizing high mechanical strength and a high crystal structure; the low-tortuosity compact ordered MOFs crystal film is used for improving the conductivity, the MOFs electrolyte with wide temperature range stability and high voltage resistance is obtained, and a support is provided for realizing a secondary battery with high energy density and high safety.

The invention discloses a method for improving the crystallinity of a flexible covalent organic framework film through solvent heat treatment, and relates to the technical field of flexible functional film materials, and the method comprises the following steps: (1) synthesizing a COF film; (2) soaking the COF membrane in a triethylamine methanol solution to remove residual acidic components; and (3) putting the treated membrane into an acetic acid acetonitrile solution, and heating at 100 DEG C for 0.5-6 hours to improve the crystallinity of the membrane. According to the method, rearrangement of framework chain segments in a film body and enhancement of crystallinity are achieved through the mild two-step solution treatment step, the XRD diffraction intensity, the film body compactness and the structural orderliness of the COF film are remarkably improved, and meanwhile the flexibility and the mechanical property of an original film are kept.

This invention discloses a bio-based PHA oil-blocking and moisture-permeable coating for hamburger paper, the coated paper, and its preparation method, belonging to the fields of bio-based polymer materials and paper-based food packaging technology. The coating is an aqueous dispersion of PHA, mainly comprising semi-crystalline matrix PHA and low-crystallinity or amorphous toughening PHA. Its core feature is that after the coating dries and forms a film, it spontaneously forms a functional gradient structure along the coating thickness direction: the interfacial layer near the paper substrate is rich in toughening PHA to enhance toughness and adhesion; while the surface layer is rich in matrix PHA to maximize oil-blocking performance. Through this functional gradient structure design, this invention balances the oil-blocking, moisture-permeable, and flexible properties of the packaging material, and possesses biodegradable environmental characteristics, making it suitable for high-oil food packaging.

The present plated member includes, on an outer surface, a plated film mainly composed of chromium deposited from a trivalent chromium bath containing at least chromium, carbon, and oxygen, in which the plated film contains 60 to 80 at % of chromium and 16.5 to 30 at % of carbon and has an indentation hardness of 7 GPa or more on the outer surface, and a degree of crystallinity calculated from a peak integrated intensity ratio of a measured value of X-ray diffraction measurement and the following expression (1) is 4% or less.

The invention provides a heat insulation and energy storage polylactic acid-based composite material, the polylactic acid-based composite material is a three-layer composite material, and comprises a surface layer, an energy storage layer and a heat conduction buffer layer, the surface layer comprises high-crystallinity polylactic acid, mesoporous SiO2, micron hollow glass beads, nano TiO2, nano ZnO and an antioxidant 1010, the energy storage layer comprises low-crystallinity polylactic acid and phase change microcapsules, and the heat conduction buffer layer comprises a heat conduction buffer layer. The composite material comprises polylactic acid, hydroxylated carbon nanotubes, polycaprolactone, tributyl citrate and an antioxidant 1010, and the composite material comprises medium-crystallinity polylactic acid, hydroxylated carbon nanotubes and polycaprolactone. The polylactic acid-based composite material prepared by the preparation method disclosed by the invention realizes the balance of heat insulation, energy storage and mechanical properties.

The invention discloses preparation and application of a millimeter-scale high-uniformity bastnaesite single crystal electron probe standard sample, and the preparation method comprises the following steps: taking CeF3 and carbonate as raw materials, carrying out solid phase mixing, carrying out a hydrothermal reaction at 400-500 DEG C under water self-generated saturated vapor pressure, and carrying out programmed cooling, washing and drying to obtain a CeCO3F single crystal which has a millimeter-scale size and does not contain Nd and other rare earth impurities. The spectrum peak overlapping interference in EPMA analysis is eliminated from the source, the internal elements are highly uniformly distributed, and the relative standard deviation (RSD) of the distribution of the key element Ce is less than 1.0%. The method is simple in process, low in cost and mild in condition, the limitation that millimeter-level single crystals are difficult to prepare through a traditional method is broken through, and the obtained single crystal standard sample has the advantages of being high in crystallinity, good in stability, high in matching degree with a natural geological sample matrix and the like, is suitable for electron probe analysis, especially high-precision quantitative analysis of rare earth element Ce and has good application prospects. And the accuracy and reliability of an analysis result can be effectively improved.

The present invention discloses a kind of mesoporous ZSM 5 molecular sieve and preparation method thereof, the preparation method comprises the following steps:Silicon source, aluminum source, alkali source, crystallization inducer, auxiliary agent, water are mixed to obtain crystallized gel, the crystallized gel is crystallized under hydrothermal conditions, washed, filtered, dried, roasted, and mesoporous ZSM 5 molecular sieve is obtained;Wherein, the silicon source is magadiite, the crystallization inducer is organic ammonium salt and seed crystal, and the auxiliary agent is selected from at least one of alcohol or amine. The molecular sieve obtained by the method of the present invention has the characteristics of high crystallinity, large specific surface area, and large micro-mesopore volume. The preparation method of the present invention adopts cheap silicon source, and in the case of adding a small amount of mesoporous template agent, mesoporous ZSM 5 molecular sieve can be synthesized, which is applied to light hydrocarbon catalytic cracking reaction with good low-carbon olefin selectivity.

The invention discloses a preparation method of a lithium battery positive electrode precursor with narrow half-peak width, which comprises the following steps: firstly preparing reaction solutions of a mixed salt solution, a precipitator, a complexing agent and a half-peak width regulator, and then preparing a reaction base solution in a reaction kettle; adding other reaction solutions into the reaction base solution in the reaction kettle, and carrying out precursor nucleation and growth to obtain precursor slurry; and finally, carrying out subsequent treatment on the synthesized precursor slurry to obtain the narrow half-peak width precursor material. The concentration of the free nickel is controlled within a certain range, so that the nucleation rate and the growth rate of crystals are controlled, the adsorption of the residual free nickel on the surfaces of precipitated particles is controlled, the influence of the residual free nickel on the ordered arrangement of crystal faces is inhibited, and surface dislocation or grain boundary defects are reduced, so that the crystallinity of the precursor is improved, and the narrow half-peak width is realized.

The invention relates to the technical field of batteries, in particular to a high-dispersity and low-crystallinity composite solid electrolyte and an all-solid-state lithium metal battery. The composite solid electrolyte comprises a polymer matrix, a lithium salt, an inorganic filler and a quaternary ammonium salt surfactant, the mass ratio of the polymer matrix to the lithium salt to the inorganic filler to the quaternary ammonium salt surfactant is 100: (60-80): (10-20): (1-15). Through the quaternary ammonium salt additive, the inorganic filler is uniformly dispersed in a polymer matrix, and the crystallinity of polyethylene oxide (PEO) is effectively reduced, so that the ion transmission performance of the electrolyte and the cycling stability of a battery are remarkably improved, and the problem that organic-inorganic interfaces between PEO and LLZTO in the composite solid electrolyte are incompatible is systematically solved; and a key technical path is provided for developing a new generation of energy storage devices with high safety, long cycle life and excellent electrochemical performance.

The present application relates to the technical field of ZSM-5 molecular sieve preparation, and provides a high-crystallinity aluminum-rich ZSM-5 molecular sieve, a preparation method and application thereof.The preparation method of the high-crystallinity aluminum-rich ZSM-5 molecular sieve provided by the present application realizes the skeleton composition control of the ZSM-5 molecular sieve by adding a second aluminum source and then performing secondary crystallization, solves the technical bottleneck that it is difficult to directly synthesize the high-crystallinity aluminum-rich ZSM-5, breaks through the lower limit of the Si / Al ratio phase region of the artificial in-situ synthesis of the molecular sieve, effectively controls the crystal parameter and improves the production efficiency, realizes the precise construction of the high-crystallinity aluminum-rich ZSM-5 molecular sieve, and thus enhances the micropore crystallinity of the molecular sieve, optimizes the acid distribution, greatly enriches the metastable surface active acid center distribution of the molecular sieve, and has good aromatic hydrocarbon conversion performance.