548results about How to "Morphological rules" patented technology

The invention relates to soft magnetic composite powder and a magnetic powder core preparation method thereof, and belongs to the technical field of powder metallurgy and magnetic materials. According to different magnetic performance characteristics of metal soft magnetic powder, amorphous and nano-crystalline powder and ferrite powder, magnetic performances are linearly calculated and optimally designed, so that the requirements of different magnetic properties are met. Besides, powder sizes are calculated and coordinately designed, the powder is shaped, screened, annealed, coated in an insulated manner and mixed, and the powder with different components is respectively passivated and insulated, weighed according to weight ratio and uniformly mixed to form the composite powder. The prepared soft magnetic composite powder is regular in morphology and good in dispersity and has good apparent density and flowability. In addition, the magnetic performance of a magnetic powder core prepared from the soft magnetic composite powder can be calculated and designed as required, the magnetic powder core has high cost performance and good comprehensive magnetic performance, and the blank of the performance and application of an existing magnetic powder core is effectively filled in.

The invention relates to a nickel disulfide carbon nano composite material and a preparation method and an application thereof, wherein the composite material is formed by coating a nickel disulfide nanosheet with a carbon layer. The preparation method comprises the following steps of preparing a nickel hydroxide nanosheet precursor by a hydrothermal method, performing magnetic stirring and dispersing in deionized water to obtain a uniform dispersion liquid of the nickel hydroxide nanosheet precursor, adding a buffering agent tris(hydroxymethyl) aminomethane hydrochloride, and adjusting the pHvalue to be 8.5 by adopting an alkali solution with the pH value of 13, adding dopamine hydrochloride, and magnetically stirring at room temperature for in-situ polymerization, and carrying out washing and centrifugally drying to obtain a nickel hydroxide nanosheet precursor/polydopamine composite material, and carrying out heat treatment and vulcanization with sublimed sulfur powder in a tubularfurnace in nitrogen atmosphere at a certain temperature to obtain the composite material. The preparation process is simple, easy to operate, green and non-toxic and friendly in material preparationprocess; and the prepared nickel disulfide carbon nano composite material is stable in structure, uniform in morphology and high in dispersion. The obtained nickel disulfide carbon nano composite material can be an ideal electrode material of a high-performance lithium ion battery, a supercapacitor and other new energy devices.

The invention discloses a method for preparing a porous spherical Li(1-x)MxFe(1-y)Ny(PO4)([3+(alpha-1)x+(beta-2) y]/3)/C material, comprising the specific steps of: dissolving a lithium-containing compound, an iron-containing compound, a phosphor-containing compound and a element-doped compound additive in a dispersing agent to form a sizing agent; dispersing a mixture of a pore-forming agent, a cladding agent and a stabilizer in a dispersing agent through ultrasound, then adding into the sizing agent and mixing to form a new sizing agent; carrying out a physical method or a chemical method on the new sizing agent to obtain a sizing agent with the primary particles in nano grade; carrying out spraying drying and granulating on the obtained sizing agent with the primary particles in nano scale to obtain a dry mixed material with secondary particles with spherical appearances; then carrying out a sintering process on the dry mixed material to obtain the product of the invention. The method has the advantages that besides that the primary particles reach the nano scale, the particle diameters are more uniform in distribution and more regular in appearance, an iron phosphate product synthesized from the material has the particle diameters with uniform distribution, and the material has favorable processability, good electric conductivity, excellent power multiplication performance and higher actual capacity.

The invention relates to a method for preparing a small-size nickel-cobalt lithium manganate precursor. The method is characterized by comprising the following steps of: (1) preparing a solution from soluble salts of nickel, cobalt and manganese as materials, adopting a sodium hydroxide water solution as a precipitator, and adopting ammonia water or ammonium salt as a complexing agent; (2) merging and adding the obtained three solutions into a reaction kettle which contains bottom water and includes stirring and temperature control devices; leading in nitrogen to protect in a reaction process, and continuously carrying out reaction; and (3) stirring and aging for 4-6 hours after a temporary kettle is full, putting the aged material into washing and press filtering equipment to wash; removing moisture in a filter pressing manner; and then mixing and sieving by a 200mesh screen after baking and crushing. By adopting the method disclosed by the invention, industrialized production of the small-size nickel-cobalt lithium manganate precursor can be conveniently achieved; and the method is stable to control the particle size, and convenient to achieve requirements of the materials and equipment.

A nickel lithium ion battery positive electrode material having a concentration gradient, and a preparation method therefor. The material is a core-shell material having a concentration gradient, the core material is a material having a high content of nickel, and the shell material is a ternary material having a low content of nickel. The method comprises: synthesizing a material precursor having a high content of nickel by means of co-precipitation, co-precipitating a ternary material solution having a low content of nickel outside the material precursor having a high content of nickel, aging, washing, and drying to form a composite precursor in which the low nickel material coats the high nickel material, adding a lithium source, grinding, mixing, calcining, and cooling to prepare a high nickel lithium ion battery positive electrode material. The obtained material has regular morphology, uniform coating, narrow particle size distribution range, gradient distribution of the concentration of the nickel element, high content of the nickel element in the core, and low content of the nickel element in the shell; the nickel element in the core guarantees the specific capacity of the material, and the shell coating material maintains the stability of the structure of the material, so as to improve the safety of the material in the charge and discharge process, and improve the cycle and rate performance of the material.

The invention relates to a lithium titanate-carbon co-cladded lithium manganese iron phosphate positive electrode material. According to the invention, the characteristic of zero stress of a lithium titanate material is utilized for inhibition of deformation of a positive electrode during charging and discharging so as to improve cycle performance and resistance to over-charge and over-discharge of the positive electrode material, and conductivity and electrochemical properties of the positive electrode material are improved through co-cladding of the lithium titanate material and carbon; meanwhile, tap density of lithium titanate is as high as 1.68 g/cm<3>, which enables influence of carbon cladding on the tap density of the positive electrode material to be reduced. A preparation method for the positive electrode material provided by the invention is simple, is easy to operate and can easily realize industrial application.

A process for preparing the WC-based spherical powder for thermospray coating includes such steps as proportionally mixing WC, Co or mixture of Co and Cr, hexane and paraffin wax, wet grinding, spray drying, granulating, sieving, sintering under protection of H2, and classifying.

The invention provides a preparation method of lithium-nickel-cobalt-aluminum oxide for anode materials of lithium ion batteries. The method comprises: step 1, using a nickel-cobalt-aluminum precursor prepared through a coprecipitation method and doped with mixed ions as raw materials, putting the raw materials into a sealed hearth of a pressure furnace, continuously introducing oxygen until a fixed pressure value is formed, then heating to a pre-burning temperature and keeping warm for a period of time, and cooling to obtain an oxidized precursor; and step 2, adding measured lithium salt or lithium hydroxide into the oxidized precursor, ball milling and uniformly mixing; heating the uniformly mixed raw materials to a certain temperature and keeping warm for a period of time, and meanwhile continuously introducing oxygen to complete a sintering process, thereby obtaining the finish product. According to the invention, through a hyperbaric oxygen atmosphere, the oxygen are enabled to fully infiltrate into particles of the raw materials which has a certain accumulation thickness, thereby preventing situations that only surface materials are oxidized under a normal pressure, and ensuring a full conversion of Ni<2+> to Ni<3+> by a full pre-oxidation.

The invention discloses a method for preparing gold nanoparticles by annealing of a gold film. The method comprises the following steps: depositing a gold nano film (2) on a base material (1) by a magnetron sputtering method or vacuum evaporation method, wherein the vacuum degree of a magnetron sputtering chamber or a vacuum evaporation chamber is 10<-3>-10<-4>Pa, and the thickness of the deposited gold nano film (2) is 5-20nano; integrally arranging the deposited gold nano film (2) and the base material (1) in an annealing furnace to be heated for 30-120min, wherein the heating temperature is 350-600 DEG C; and cooling to the room temperature, and forming gold nanoparticles (3) on the base material (1). According to the invention, through controlling the thickness of the gold film, the annealing temperature, the annealing time and other parameters, the gold nanoparticles in different sizes and shapes can be obtained. The method disclosed by the invention has the advantages that the preparation is simple, the sizes and the shapes of the nanoparticles can be controlled, the preparation efficiency is high, and the like.

The invention provides a preparation method for synthesizing metal organic framework UiO-66 adsorbents by the aid of mixed ligands. The preparation method includes mixing zirconium sources and regulators with one another and then dissolving the zirconium sources and the regulators in solvents to obtain solution A; uniformly dissolving 2-aminoterephthalic acid, terephthalic acid and solvents to obtain mixed ligand solution B; dropwise adding the solution A into the solution B at the constant speed to obtain solution C; injecting the solution C into reaction kettles with polytetrafluoroethylenelinings and carrying out crystallization at the temperatures of 100-160 DEG C for 18-24 h; carrying out reaction, and then carrying out treatment to obtain target products. As proved by XRD (X-ray diffraction) analysis, the obtained products are UiO-66 adsorbent materials. The preparation method for synthesizing the adsorbent materials has the advantages that the preparation method is simple; theUiO-66 adsorbents synthesized by the aid of the mixed ligands are excellent in chemical and thermal stability; the hydrogen adsorption capacity of the metal organic framework UiO-66 adsorbents can beimproved to a great extent, and effective treatment methods and research directions can be provided to hydrogen adsorption separation and storage.

The invention discloses a preparation method of RGD-modified ultra-small magnetic iron oxide nanoparticles. The preparation method comprises the following steps: preparing ultra-small magnetic iron oxide nanoparticles by taking ferric acetylacetonate as a reaction raw material and a precursor, taking oleylamine as a surfactant and a reducing agent and taking dibenzyl ether as a solvent; replacing oleylamine molecules wrapped on the surfaces of the nanoparticles by utilizing dopamine-modified HOOC-PEG-COOH to realize PEG-modification of the surfaces of the nanoparticles; and finally, chemically coupling RGD cyclic peptide by virtue of free carboxyl at the tail end of the PEG to obtain the RGD-modified ultra-small magnetic iron oxide nanoparticles. The method of synthesizing the ultra-small magnetic iron oxide nanoparticles has the characteristics of a simple process, a high raw material conversion ratio, strong repeatability and the like. The synthesized magnetic iron oxide nanoparticles have the characteristics of a regular morphology, an ultra-small dimension, good stability, good monodispersity, high biocompatibility, and tumor specific targeting, and the like, and can be used as a T1-weighted imaging high-performance magnetic resonance imaging contrast agent with a tumor active targeting function.

A preparation method of polyvinyl alcohol/hydroxyapatite (PVA/HA) composite microspheres belongs to preparation methods of composite water-in-oil emulsion system microspheres. PVA and HA precursors are used as raw materials to prepare a clear and transparent mixed solution; the clear and transparent mixed solution is dispersed into an oil phase containing a surfactant to form a homogeneous water-in-oil microemulsion; and the PVA/HA composite microspheres can be finally obtained by successive crosslinking reaction under acid-catalyzed conditions, HA deposition under alkaline conditions, product centrifugation, washing, drying and other processes. The method has the advantages of simple process, good repeatability, low energy consumption and low cost, and effectively solves the problems that inorganic nanoparticles are easy to agglomerate in the microspheres to cause uneven structures and poor comprehensive performances and the like. The composite microspheres prepared by the method have the advantages of regular morphology, high dispersibility, uniform microstructure, good biocompatibility, biological activity and adsorption performance, and can be used as drug carrier materials, bone repair materials, environmental water treatment materials, cosmetics or food additives and the like.

The invention relates to a method for preparing an anode material of a lithium ion battery of spinel lithium titanate. The invention provides a method for preparing a Li4Ti5O12 material through a low-temperature ionic diffusion reaction, aiming at the drawbacks of a high-temperature solid-phase Li4Ti5O12 synthesis process of high temperature, long time and high energy consumption and the drawbacks of a sol-gel synthesis process of complex process and higher cost. The method adopts a technical proposal that: titanium dioxide or metatitanic acid is uniformly dispersed in 1 to 20mol/L aqueous solution of LiOH, wherein the Lithium to Titanium ratio is (10-100):1; under a condition of uniform stirring, the mixed solution is heated to 60 to 150 DEG C to react for 6 to 72 hours; the obtained products are washed till the pH is equal to 7 to 8, filtered and dried to form a precursor of Lithium-titanium oxide precursor; and the prepared precursor is roasted at 500 to 800 DEG C for 3 to 12 hours to form the final product of Li4Ti5O12.

The invention relates to the technical field of preparation of heterojunction composite photocatalysts, in particular to a method for preparing BiOI/WO ₃ A method for heterojunction composite photocatalysts. Disperse tungsten oxide in deionized water, add potassium iodide and bismuth nitrate, stir and mix evenly, filter and wash, and then obtain BiOI/WO ₃ Heterojunction composite photocatalysts. The prepared nanocomposite photocatalysts have excellent visible light catalytic activity, especially bismuth nitrate and WO ₃ The sample with a molar ratio of 1.0 has the best activity in degrading rhodamine B, and the degradation rate reaches 92% after visible light reaction for 100min, which is higher than that of pure BiOI and WO ₃ high degradation activity.

The invention relates to a sea urchin shaped copper oxide catalyst, as well as a preparation method and application thereof, and belongs to the field of catalysts. The preparation method for the sea urchin shaped copper oxide catalyst comprises the following steps of: dissolving a copper salt and a dispersant into an organic solvent, performing solvent heat reaction in an alkali environment, and thus obtaining the sea urchin shaped copper oxide catalyst. The method for preparing the sea urchin shaped copper oxide is concise, easy and convenient to operate, efficient, low in price and environment-friendly, and realizes large-scale preparation. The sea urchin shaped copper oxide catalyst prepared by the method is controllable in shape and granular size, and can be used for synthesizing organic silicon monomers.

The invention provides a method for preparing SrCuSi4O10 and BaCuSi4O10 blue pigments through a hydrothermal technique, and belongs to the technical field of hydrothermal chemistry. The method uses copper oxide powder or copper salt, barium salt or strontium salt, and silicate as raw materials, and NH4OH as a mineralizing agent and comprises the following hydrothermal reaction processes: mixing a reactant with distilled water according to a stoichiometric ratio of an objective product, adjusting the pH value of a solution to be greater than 10 and less than 14, putting in a high-pressure reactor so as to enable the filling degree to reach 40%-90%, sealing and reacting for 5-72 hours at the temperature of 230-300 DEG C; and cooling and filtering so as to obtain products. The invention provides a new reaction route and a green preparation method for SrCuSi4O10 and BaCuSi4O10 difficult to prepare. The products are multi-level structure microparticles, have high purity, regular morphology and good dispersity and are uniform in particle size. The preparation method is simple, efficient and high in yield; waste liquid generated in a hydrothermal reaction process can be recycled.

For overcoming the problems of irregular shape, uneven element distribution and partial agglomeration of metal elements of a positive electrode active material prepared by a method in the prior art, the invention provides a preparation method for the positive electrode active material, comprising the steps of S1, mixing a reaction seed crystal with a complexing agent solution, wherein the reaction seed crystal is hydroxide of one or more of nickel, cobalt, manganese or aluminum; and the D50 of the reaction seed crystal is less than or equal to 2-6 [mu]m; S2, under a condition of stirring and ultrasonic processing, adding a metal salt solution and a precipitator solution, regulating PH to 9-13; and then washing and drying to obtain a precursor, wherein the metal salt solution is a solution containing nickel salt, cobalt salt, manganese salt and aluminum salt; and S3, mixing the precursor with a lithium source, performing heat preservation at a temperature of 500-950 DEG C for 2-24h, and cooling. Meanwhile, the invention also discloses the positive electrode active material prepared by the method. The positive electrode active material provided by the invention is regular in shape, high in degree of sphericity, uniform in element distribution and free of partial agglomeration of metal elements; and in addition, the positive electrode active material is high in cycling performance, thermal stability and security.

The invention discloses a synthesizing method for organic silicon micro-balls with performances of super hydrophobicity and high temperature resistant, which relates to the synthesizing method of organic silicon. The synthesizing method for the organic silicon micro-balls comprises the following steps: firstly hydrolyzing n-silicate ester of which the structural formula is Si(ORn)4 (n is the number of carbon atom), and then forming a spherical pre-polymer after polycondensation; adding alkylchlorosilane of which the structural formula is Cl2Si(Rn)2 (n is the number of carbon atoms) or alkoxy silane of which the structural formula is (Rn)2Si(ORn)2 (n is the number of carbon atoms), so as to obtain the organic silicon micro-balls of which surfaces are fully provided with alkyls after copolycondensation. The obtained micro-balls have good dispersibility, and have characteristics of super hydrophobicity and high temperature resistant and the range of particle diameter is within 0.5-10 microns. The organic silicon micro-balls are simple in production technology, free form pollution during the production process and convenient for post-treatment technology, and can be widely applied to rubber, plastic and adhesive, so as to improve the temperature resistant performance of basis materials. The organic silicon micro-balls also can be applied to coating and self-prepared hydrophobic self-cleaned coating.

The invention discloses a method for preparing an NH4V3O8 anode material for a lithium ion battery. The method comprises the steps that ammonium metavanadate is dissolved in deionized water, an NH4VO3 solution is prepared, pre-oxidization short carbon fibers of 1 mm to 3 mm are added, the NH4VO3 solution is transferred into a reaction still after the pH value is adjusted, forced mixing is carried out, after the reaction still is sealed, the reaction still is placed in a water and heat induction heater, and suspension liquid is obtained after a heating reaction; centrifugal separation is carried out on the suspension liquid to obtain a powder product, the powder product is soaked in the deionized water and the absolute ethyl alcohol, repeated washing is carried out, and then drying and grinding are carried out. The NH4V3O8 microcrystal prepared through the method is uniform in chemical component, high in purity and uniform in form, and the electrochemical performance of the material can be effectively improved. The preparation method is simple, low in reaction temperature, short in reaction period, high in productivity, free of any subsequent treatment, environmentally friendly and capable of being suitable for large-scale production.