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3236 results about "Coprecipitation" patented technology

In chemistry, coprecipitation (CPT) or co-precipitation is the carrying down by a precipitate of substances normally soluble under the conditions employed. Analogously, in medicine, coprecipitation is specifically the precipitation of an unbound "antigen along with an antigen-antibody complex".

Method of forming nanoparticles and microparticles of controllable size using supercritical fluids with enhanced mass transfer

The current invention, Supercritical Antisolvent Precipitation with Enhanced Mass Transfer (SAS-EM) provides a significantly improved method for the production of nano and micro-particles with a narrow size distribution. The processes of the invention utilize the properties of supercritical fluids and also the principles of virbrational atomization to provide an efficient technique for the effective nanonization or micronization of particles. Like the SAS technique, SAS-EM, also uses a supercritical fluid as the antisolvent, but in the present invention the dispersion jet is deflected by a vibrating surface that atomizes the jet into fine droplets. The vibrating surface also generates a vibrational flow field within the supercritical phase that enhances mass transfer through increased mixing. Sizes of the particles obtained by this technique are easily controlled by changing the vibration intensity of the deflecting surface, which in turn is controlled by adjusting the power input to the vibration source. A major advantage of the SAS-EM technique is that it can be successfully used to obtain nanoparticles of materials that usually yield fibers or large crystals in SAS method. Microencapsulation via coprecipitation of two or more materials can also be achieved using the SAS-EM technique.
Owner:UNIV AUBURN

Method of forming nanoparticles and microparticles of controllable size using supercritical fluids and ultrasound

The current invention, Supercritical Antisolvent Precipitation with Enhanced Mass Transfer (SAS-EM) provides a significantly improved method for the production of nano and micro-particles with a narrow size distribution. The processes of the invention utilize the properties of supercritical fluids and also the principles of virbrational atomization to provide an efficient technique for the effective nanonization or micronization of particles. Like the SAS technique, SAS-EM, also uses a supercritical fluid as the antisolvent, but in the present invention the dispersion jet is deflected by a vibrating surface that atomizes the jet into fine droplets. The vibrating surface also generates a vibrational flow field within the supercritical phase that enhances mass transfer through increased mixing. Sizes of the particles obtained by this technique are easily controlled by changing the vibration intensity of the deflecting surface, which in turn is controlled by adjusting the power input to the vibration source. A major advantage of the SAS-EM technique is that it can be successfully used to obtain nanoparticles of materials that usually yield fibers or large crystals in SAS method. Microencapsulation via coprecipitation of two or more materials can also be achieved using the SAS-EM technique.
Owner:UNIV AUBURN

Full-component resource reclamation method for waste positive electrode materials of lithium ion batteries

The invention provides a full-component resource reclamation method for waste positive electrode materials of lithium ion batteries. The method comprises the following steps: 1) separating active substances and aluminum foils in waste positive electrode materials of lithium ion batteries by using an aqueous solution of fluorine-containing organic acid and carrying out liquid-solid-solid separation so as to obtain leachate, the lithium-containing active substances and the aluminum foils; 2) respectively carrying out high temperature roasting and impurity removal with alkali liquor on the lithium-containing active substances; 3) respectively carrying out recovery of the fluorine-containing organic acid through addition of acid and distillation, deposition of impurity ions through addition of alkali and ammonium carbonate coprecipitation on the leachate so as to prepare nickel-cobalt-manganese carbonate ternary precursor; and 4) carrying out component regulation on a mixture of the treated active substances and the nickel-cobalt-manganese carbonate ternary precursor, adding lithium carbonate in a certain proportion and carrying out high temperature solid phase sintering so as to prepare a lithium nickel cobalt manganese oxide ternary positive electrode material. The method provided in the invention has the following advantages: the application scope of the method is wide; separation efficiency of the lithium-containing active substances and the aluminum foils is high; short-flow direct re-preparation of positive electrode materials in waste lithium ion batteries is realized; and the method is applicable to large-scale resource reclamation of waste lithium ion batteries.
Owner:INST OF PROCESS ENG CHINESE ACAD OF SCI

Spinel nickel manganese acid lithium and layered lithium-rich manganese-based composite cathode material with core-shell structure and preparation method thereof

The invention relates to a spinel nickel manganese acid lithium and layered lithium-rich manganese-based composite cathode material with a core-shell structure and a preparation method thereof, which belongs to the technical field of material synthesis. The prepared lithium ion composite cathode material takes a layered lithium-rich manganese-based Li[Lia(NixCoyMnz)]O2 as a core material, takes spinel nickel manganese acid lithium LiNi0.5Mn1.5O4 as a shell material; a coprecipitation method is employed to obtain a core-shell precursor, the core-shell precursor and the lithium source are uniformly mixed and calcined to obtain the spinel nickel manganese acid lithium and layered lithium-rich manganese-based composite cathode material with the core-shell structure. According to the invention, the layered lithium-rich manganese-based is taken as the core material, and the spinel nickel manganese acid lithium is taken as the shell material; under the prerequisite that material gram capacity is kept, material structural stability is increased, material cycle, multiplying power and safety performances are improved, function composite and complementation of the core material and the shell layer material can be realized, and the problem that high capacity and high security can not be achieved simultaneously is solved. The composite cathode material has the advantages of simple process and obviously increased performance.
Owner:南京时拓能源科技有限公司

Lithium ion battery gradient core shell cathode material and synthetic method thereof

The invention provides a lithium ion battery gradient core shell cathode material and synthetic method thereof, and relates to a lithium ion battery cathode material and synthetic method thereof. The lithium ion battery gradient core shell cathode material provided by the present invention may have two kinds of core shell structures as follows: a two-layer structure: a ternary material is used as a core material, and a binary material or a unitary material is casing material, and the ternary material external layer is covered by the binary material or the unitary material; three-layer structure: the ternary material is used as a core material, and the binary material and the unitary material are casing materials, and the ternary material external layer is covered with the binary material, and the binary material is covered with the unitary material. The synthetic method includes: employing a coprecipitation method for obtaining a precursor, and then adding lithium source, calcining and coating to obtain the ternary gradient core shell material. Under the prerequisite that the structure stability of the material is kept, the cost is reduced, and the gram capacity of the material is improved, and the material circulating performance and rate capability of the material are improved, and the safety performance and low temperature performance of the ternary cathode material are increased, and the preparation technology is optimized and improved.
Owner:HARBIN INST OF TECH

Active material for lithium secondary battery, lithium secondary battery, and method for producing the same

ActiveUS20100233542A1Decrease in battery performanceSufficient discharge capacityBatteries circuit arrangementsElectrode manufacturing processesX-rayCrystal structure
The present invention provides an active material for a lithium secondary battery with a high discharge capacity, particularly for a lithium secondary battery that can increase the discharge capacity in a potential region of 4.3 V or lower, a method for producing the same, a lithium secondary battery having a high discharge capacity, and a method for producing the same. The active material for a lithium secondary battery includes a solid solution of a lithium transition metal composite oxide having an α-NaFeO2 type crystal structure, in which the composition ratio of Li, Co, Ni, and Mn contained in the solid solution satisfies Li1+(1/3)xCo1−x−yNi(1/2)yMn(2/3)x+(1/2)y (x+y≦1, 0≦y and 1−x−y=z); in an Li[Li1/3Mn2/3]O2(x)-LiNi1/2Mn1/2O2(y)-LiCoO2(z) type ternary phase diagram, (x, y, z) is represented by values in a range present on or within a line of a heptagon (ABCDEFG) defined by the vertexes; point A(0.45, 0.55, 0), point B(0.63, 0.37, 0), point C(0.7, 0.25, 0.05), point D(0.67, 0.18, 0.15), point E(0.75, 0, 0.25), point F(0.55, 0, 0.45), and point G(0.45, 0.2, 0.35); and the intensity ratio between the diffraction peaks on (003) plane and (104) plane measured by X-ray diffractometry before charge-discharge is I(003)/I(104)≧1.56 and at the end of discharge is I(003)/I(104)>1. The invention provides a method for producing the active material for a lithium secondary battery using a coprecipitation method, a lithium secondary battery including a positive electrode containing the active material and a method for producing the lithium secondary battery.
Owner:GS YUASA INT LTD

High-density small-particle-size nickel-cobalt-manganese hydroxide and preparing method thereof

The invention relates to a high-density small-particle-size nickel-cobalt-manganese hydroxide and a preparing method thereof. The nickel-cobalt-manganese hydroxide and the preparing method thereof are characterized in that: the general chemical formula of the nickel-cobalt-manganese hydroxide is NixCoyMnz(OH)2, wherein the sum of the x, the y and the z is 1, the x is not more than 0.8 and not less than 0.3, the y is not more than 0.4 and not less than 0.1, and the z is not more than 0.4 and not less than 0.1. The nickel-cobalt-manganese hydroxide is provided, so that problems of small-particle-size nickel-cobalt-manganese hydroxides prepared by methods at present, namely nonuniform element distribution, poor particle appearance, loose surfaces, difficult particle size control, nonuniformity, low tap density, and the like are overcome. A complexing control crystallization coprecipitation method is adopted. By a special technical process of producing nucleuses, growing, and subjecting particles to continuous frictional collision under a continuously increased solid liquid ratio, an aqueous solution of a nickel-cobalt-manganese soluble salt and an aqueous sodium hydroxide solution are subjected to coprecipitation under complexing of ammonia to obtain the small-particle-size nickel-cobalt-manganese hydroxide having characteristics of uniform element distribution, good degree of sphericity, uniform particle size distribution and high tap density.
Owner:宁夏中色金辉新能源有限公司

Method for preparing corrosion inhibition anion intercalated layered double hydroxides/oxide composite material and application

The invention provides a corrosion-inhibiting anionic intercalated hydrotalcite/nano oxide composite material, a preparation method thereof and application of the corrosion-inhibiting anionic intercalated hydrotalcite/nano oxide composite material. The preparation method is as follows: corrosion-inhibiting anions are directly inserted between hydrotalcite layers by the one-step coprecipitation method and the roasting restoring method; the nano oxide is generated by means of in situ synchronization during the process of generation of hydrotalcite crystals by controlling the mixture ratio of divalent metal ions to trivalent metal ions, the pH value of a reaction solution and the reaction temperature; and the corrosion-inhibiting anionic intercalated hydrotalcite/nano oxide composite material with the anti-corrosive function is prepared. The invention is mainly characterized in that the in situ preparation method for the hydrotalcite/oxide composite material provided with a nano lamellar structure improves the release amount of a corrosion inhibitor and reduces the water absorption of a coating by leading into the corrosion inhibitor with the anti-corrosive function and the nano oxide which is generated in situ during the reaction process. The composite material can be used to be pigment of an anti-corrosive metallic coating system, and particularly has potential application value in improving the anti-corrosive performance of a magnesium alloy anti-corrosive coating.
Owner:HARBIN ENG UNIV

Acid-resistant magnetic chitosan microspheres as well as preparation method and application thereof

The invention relates to an acid-resistant magnetic chitosan microsphere adsorbent as well as a preparation method and the application thereof, and in particular relates to acid-resistant magnetic chitosan microspheres which have the excellent absorption performance and recycling performance for acid waste water containing hexavalent chromium, a preparation method of the acid-resistant magnetic chitosan microspheres and the application of the acid-resistant magnetic chitosan microspheres. The preparation method of the acid-resistant magnetic chitosan microspheres comprises the following steps: (1) preparing Fe3O4 nano-particles modified by citric acid by using a coprecipitation method; (2) preparing single-coated magnetic SiO2 nano-particles by using a sodium silicate hydrolysis method or a sol-gel method; and (3) preparing the chitosan microspheres coated with magnetic SiO2 by taking chitosan powder as a raw material by adopting an emulsion crosslinking method. Furthermore, in order to further improve the adsorbing capacity of the microspheres, in the method, dendritic polyethylene imine is taken as a functional group for modifying the adsorbent, so that the modified chitosan microspheres can be obtained. The magnetic chitosan microspheres prepared by adopting the method not only have the excellent acid resistance, but also have the good absorption performance on Cr (VI) ions.
Owner:INST OF PROCESS ENG CHINESE ACAD OF SCI

Method for preparing nickel-cobalt lithium aluminate as anode material of lithium ion battery

The invention discloses a method for preparing nickel-cobalt lithium aluminate as an anode material of a lithium ion battery. The method comprises the following steps: (1) mixing a nickel-cobalt metal salt water solution, a sodium metaaluminate solution, a complexing agent and a precipitant, regulating the pH value of a reaction system to be 9 to 12, and then maintaining a stirring state to carrying out a reaction at the temperature of 30 to 80 DEG C for 20 to 200 hours, thereby obtaining nickel-cobalt aluminum hydroxide precipitates; (2) washing the nickel-cobalt aluminum hydroxide precipitates by using pure water of 50 to 100 DEG C, drying, screening the part of precipitates capable of passing through a sieve being 300 meshes, adding a lithium source to the precipitates, mixing evenly, and sintering at the temperature of 600 to 1000 DEG C, wherein oxygen is filled during the sintering process; and finally sintering for 5 to 50 hours, thereby obtaining the nickel-cobalt lithium aluminate. According to the method, the sodium metaaluminate is adopted as the lithium source, so that the nickel-cobalt aluminum elements can evenly form a coprecipitation, so that the aluminum is evenly distributed in the nickel-cobalt lithium aluminate material. As a result, the electrical performance of the material is improved, and especially the cycling performance of the material is improved.
Owner:HUNAN BRUNP RECYCLING TECH +1

Method for preparing hydrogenation catalyst composite

The invention discloses a method for preparing a hydrogenation catalyst composite, comprising the following steps of: (1) preparing a NixWyOz composite oxide precursor by using a coprecipitation method; (2) pulping, mixing and filtering the NixWyOz composite oxide precursor and MoO3; and (3) forming and activating the NixWyOz composite oxide precursor and the MoO3 to form a final catalyst, wherein the process of manufacturing the NixWyOz composite oxide precursor comprises the steps of: preparing acid solution A containing an active metal Ni component according to a component content proportion of the catalyst; preparing solution B containing an active metal W component according to the component content proportion of the catalyst; merging the solution A and the solution B, and adding the mixture of the solution A and the solution B into a reaction tank to gelatinize; and generating a deposited mixture to obtain the precursor containing the composite oxide NixWyOz. The catalyst prepared by the method has the advantages of uniform dispersion of metals, high use performance, and particularly higher activity for deep impurity removal process of hydrocarbon. The method is simple and convenient, and has low metal loss. The method is mainly used for preparing a bulk phase catalyst with higher metal content.
Owner:CHINA PETROLEUM & CHEM CORP +1
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