The invention belongs to the technical field of material synthesis, and discloses a nitrogen-doped hollow cobaltosic oxide and a preparation method and application thereof. A chemical formula of the nitrogen-doped hollow cobaltosic oxide is Co3O4—COF-T-D@C—N; and the COF-T-D is a covalent organic framework. Due to an open hollow structure, the nitrogen-doped hollow cobaltosic oxide of the invention has a large specific surface area, thus having a large contact area with an electrolyte, which is convenient for lithium ions to transport therein. The open hollow structure also prevents a volume effect from being generated during charging and discharging, and nitrogen is introduced for doping, so that granules can be gradually activated to increase the specific surface area and active sites, a discharge (cycle) stability of the material is improved, and a rate performance of the material is improved.
Disclosed in the present invention is a method for recovering nickel from iron-aluminum slag obtained by battery powder leaching. The method comprises the following steps: adding a sulfuric acid solution into an iron-aluminum slag to dissolve, so as to obtain a sulfate solution; then adding an oxidizing agent; adding ammonia water and carbonate into the oxidized sulfate solution; adjusting the pH to 1.0-3.2 for reaction; separating ferric hydroxide to precipitate to obtain an iron-removed solution; adding carbonate into the iron-removed solution, adjusting the pH to 3.2-5.5 for reaction; separating aluminum hydroxide to precipitate to obtain an aluminum-removed solution; adding ammonia water to the aluminum-removed solution, adjusting the pH to 7.0-8.8 for reaction; washing and removing impurities to obtain a nickel complex; adding an oxidizing agent to the nickel complex to break the complex, so as to obtain a nickel-containing solution. By means of the present method, efficient separation of iron, aluminum and nickel in the iron-aluminum slag is efficiently achieved, the separation effect of iron, aluminum and nickel is improved, the loss of nickel is reduced, and the recovery rate of nickel is improved.
C22B 3/00 - Extraction de composés métalliques par voie humide à partir de minerais ou de concentrés
C01F 7/441 - Déshydratation de l’oxyde ou de l'hydroxyde d'aluminium, c. à d. toutes les conversions d'une forme en une autre impliquant une perte d’eau par calcination
A metal sulfide negative material of a sodium ion battery and a preparation method thereof. The material has porous nanoparticles with a particle size of 5 nm to 500 nm, and the metal sulfide negative material of the sodium ion battery is at least one of zinc sulfide or copper sulfide. The preparation method includes the steps of preparing a mixed solution of stannous chloride and metal salt, adding polyvinylpyrrolidone into the mixed solution to obtain a solution A, introducing reaction gas into the solution A, aging after the reaction to obtain a precipitate, and soaking the precipitate in a persulfide solution to obtain the metal sulfide sodium ion battery negative material.
H01M 10/054 - Accumulateurs à insertion ou intercalation de métaux autres que le lithium, p.ex. au magnésium ou à l'aluminium
H01M 4/02 - PROCÉDÉS OU MOYENS POUR LA CONVERSION DIRECTE DE L'ÉNERGIE CHIMIQUE EN ÉNERGIE ÉLECTRIQUE, p.ex. BATTERIES Électrodes Électrodes composées d'un ou comprenant un matériau actif
4.
DISASSEMBLING AND DISCHARGING DEVICE FOR BATTERY RECYCLING
A disassembling and discharging device for battery recycling includes a crushing assembly, a high pressure tank, at least one pressure relief tank, and a filtering tank. The crushing assembly is provided with a first feed port and a first discharge port communicated with the first feed port; the high pressure tank is provided with a first inner cavity for containing discharging liquid, and the first inner cavity is communicated with the first discharge port; the pressure relief tank is provided with a second inner cavity, and the second inner cavity is communicated with the first inner cavity; and the filtering tank is provided with a third inner cavity, and the third inner cavity is communicated with the second inner cavity.
Disclosed in the present invention is a method for extracting nickel from a high matte nickel leaching residue. The method comprises: firstly, adding a crushed material of a high matte nickel leaching residue to an organic solvent in which sulfur is dissolved, heating same for reaction, and carrying out solid-liquid separation to obtain a first filtrate and a first filter residue; adding the first filter residue to a copper sulfate solution, heating same for reaction, and carrying out solid-liquid separation to obtain a second filtrate and a second filter residue; and evaporating, condensing and concentrating the second filtrate, and filtering same to obtain copper sulfate crystals and a nickel-containing filtrate. Throughout the whole reaction, only a small amount of sulfur and copper sulfate are consumed, and the organic solvent can be recycled.
C22B 3/22 - Traitement ou purification de solutions, p.ex. de solutions obtenues par lixiviation par des procédés physiques, p.ex. par filtration, par des moyens magnétiques
C22B 3/44 - Traitement ou purification de solutions, p.ex. de solutions obtenues par lixiviation par des procédés chimiques
6.
LAYERED SODIUM ION BATTERY POSITIVE ELECTRODE MATERIAL AND PREPARATION METHOD THEREFOR
A layered sodium ion battery positive electrode material and a preparation method therefor. The chemical formula of the layered sodium ion battery positive electrode material is NaxMnO2-a(MO4)a, wherein 0
H01M 4/485 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques d'oxydes ou d'hydroxydes mixtes pour insérer ou intercaler des métaux légers, p.ex. LiTi2O4 ou LiTi2OxFy
H01M 4/36 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs
H01M 4/505 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de manganèse d'oxydes ou d'hydroxydes mixtes contenant du manganèse pour insérer ou intercaler des métaux légers, p.ex. LiMn2O4 ou LiMn2OxFy
H01M 10/0525 - Batteries du type "rocking chair" ou "fauteuil à bascule", p.ex. batteries à insertion ou intercalation de lithium dans les deux électrodes; Batteries à l'ion lithium
7.
PREPARATION METHOD FOR PRUSSIAN BLUE SODIUM-ION BATTERY POSITIVE ELECTRODE MATERIAL
Disclosed is a preparation method for a Prussian blue sodium-ion battery positive electrode material, comprising: adding a first nonionic surfactant and an antioxidant into a sodium ferrocyanide solution to obtain a first solution; adding a second nonionic surfactant into a transition metal salt solution to obtain a second solution; in a protective atmosphere, adding the second solution into the first solution for a precipitation reaction; aging after the reaction has finished; collecting a precipitate, washing same, and carrying out vacuum drying on the washed precipitate; then soaking same in an alcohol solution containing sodium alkoxide; and then filtering same and steam drying to obtain a Prussian blue sodium ion battery positive electrode material. The method may relieve vacuum drying pressure and shorten drying time.
A gas absorption box includes a box body, at least one gas absorption member and an outer housing assembly, the box body has an accommodating cavity; the gas absorption member is elastic and is provided with a first inner cavity, and the first inner cavity is in communication with the outside of the box body; and the outer housing assembly is arranged in the accommodating cavity and is elastically connected to the box body, and the outer housing assembly has a second inner cavity for accommodating a gas absorbent, the second inner cavity being in communication with the first inner cavity, and the gas absorption member being capable of absorbing gas for the second inner cavity. When battery powder or some positive-electrode materials for batteries are transported, hydrogen generated by the battery powder or some positive-electrode materials for batteries gathers towards the upper portion of a ton bag.
B65D 81/32 - Réceptacles, éléments d'emballage ou paquets pour contenus présentant des problèmes particuliers de stockage ou de transport ou adaptés pour servir à d'autres fins que l'emballage après avoir été vidés de leur contenu pour emballer plusieurs matériaux différents qui doivent être maintenus séparés avant d’être mélangés
9.
ROD-SHAPED SODIUM ION POSITIVE ELECTRODE MATERIAL, PREPARATION METHOD THEREFOR AND APPLICATION THEREOF
Disclosed are a rod-shaped sodium ion positive electrode material, a preparation method therefor and an application thereof. The material comprises a rod-shaped base material and nanofibers inserted into the base material. C—Na is loaded on the nanofibers. The chemical general formula of the rod-shaped sodium ion positive electrode material is Na(FeaTb)PO4/CNF-c(C—Na), and 0.001≤c≤0.1, wherein T is at least one of Ni, Co, Zn, Mn, Fe, V, Ti or Mo, 0.9≤a<1, 0
The present disclosure discloses a method for extracting lithium from waste lithium batteries, which comprises: leaching positive electrode powder of the waste lithium battery in hydrochloric acid, and obtaining leaching solution by filtering; removing copper and iron from the leaching solution, and then introducing hydrogen sulfide gas for reaction, and performing solid-liquid separation to obtain first filter residue and first filtrate; adding potassium permanganate to the first filtrate, and performing solid-liquid separation to obtain second filter residue and second filtrate; performing spray pyrolysis on the second filtrate to obtain solid particles and tail gas, washing the solid particles with water to obtain a lotion, washing and collecting the tail gas and then mixing the tail gas with the lotion to obtain lithium salt solution. In the present disclosure, the positive electrode powder is leached with hydrochloric acid to obtain the hydrochloric acid leaching solution, and hydrogen sulfide is used to precipitate nickel and cobalt after removing the copper and iron impurities in the leaching solution in turn, and potassium permanganate is added to precipitate manganese ions to generate manganese dioxide. Spray pyrolysis converts the aluminum and magnesium in the solution into oxides and lithium salt is separated. The entire reaction process does not require organic solvent extraction and reduces the loss of lithium.
The present invention relates to a method for preparing nickel sulfate using low-nickel ferronickel is disclosed. The method comprises the following steps: (1) grinding ferronickel to obtain ferronickel powder, and then sintering the ferronickel powder with an oxidant to prepare ferronickel oxide powder; (2) adding sulfuric acid to the ferronickel oxide powder prepared in step (1), mixing, heating, and washing with water to prepare a sulfate salt water washing solution; (3) adding a base to the sulfate salt water washing solution prepared in step (2) to adjust the pH value, then adding a fluoride salt to form a precipitate, filtering to remove the precipitate, and drying the filtrate to obtain nickel sulfate. The method provided in the present invention can improve the efficiency of preparing nickel sulfate, reduce the loss of nickel, and prepare nickel sulfate with high purity, the content of Ni potentially reaching 19.73%-21.34%.
The disclosure belongs to the technical field of sodium ion battery materials, and discloses a preparation method of a hard carbon anode material and use thereof. The preparation method includes the following steps of: performing first sintering on starch, crushing, and introducing air and nitrogen for secondary sintering to obtain porous hard block granules; and performing third sintering on the porous hard block granules, and then continuously warming up to perform fourth sintering to obtain the hard carbon anode material. The hard carbon anode material prepared by the disclosure has a reversible capacity of no less than 330 mAh/g, excellent cycle stability and initial coulomb efficiency.
Disclosed is a preparation method of porous sodium iron phosphate used as a sodium ion battery cathode material, which includes: mixing ferrous nitrate, silver nitrate and a reducing agent to prepare a mixed solution, adding the mixed solution dropwise to a carbonate solution for reaction to obtain a precipitate, mixing the precipitate with sodium dihydrogen phosphate and sodium iodide and then grinding, sintering the ground material under the condition of air isolation, and soaking the sintered material in an organic solvent to obtain porous sodium iron phosphate used as a sodium ion battery cathode material.
The present disclosure discloses a preparation method of a hard carbon (HC) anode material and use thereof. The preparation method includes the following steps: mixing a substance A, a first alcohol liquid, and an oxidant to obtain a peroxide gel of the substance A, and dissolving a substance B in a second alcohol liquid to obtain an amino-containing solution; mixing the peroxide gel of the substance A with the amino-containing solution to allow a reaction to obtain a post-reaction slurry; and lyophilizing the post-reaction slurry to obtain a dry powder, subjecting the dry powder to calcination in a protective atmosphere to obtain a calcined material, soaking the calcined material in an acid liquid, and water-washing and drying to obtain the HC anode material.
Disclosed are a preparation method of a carbon dioxide capture agent and an application thereof. The method includes: mixing a graphite dispersion, an organic acid solution, a metal salt solution and a silica sol to obtain an organic-inorganic composite gel; standing and aging the organic-inorganic composite gel, drying the same and then carbonizing the same by microwave in a mixed atmosphere of inert gas and sulfur dioxide to obtain an intermediate product; and subjecting the intermediate product to acid washing or alkali washing to obtain a defective carrier, then mixing the defective carrier with an amine substance for ultrasonic treatment and drying to obtain the carbon dioxide capture agent.
B01D 53/22 - SÉPARATION Épuration chimique ou biologique des gaz résiduaires, p.ex. gaz d'échappement des moteurs à combustion, fumées, vapeurs, gaz de combustion ou aérosols par diffusion
B01D 53/02 - SÉPARATION Épuration chimique ou biologique des gaz résiduaires, p.ex. gaz d'échappement des moteurs à combustion, fumées, vapeurs, gaz de combustion ou aérosols par adsorption, p.ex. chromatographie préparatoire en phase gazeuse
B01J 20/22 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtration; Absorbants ou adsorbants pour la chromatographie; Procédés pour leur préparation, régénération ou réactivation contenant une substance organique
The invention belongs to the field of battery material recovery, and discloses a preparation method and application of heterosite phosphate. The method comprises the following steps: mixing lithium iron phosphate with a solvent, adding an acid solution, and adjusting the pH to obtain an acidic lithium iron phosphate liquid; adding a transition metal additive to the acidic lithium iron phosphate liquid, and performing leaching in an intensifying micro-environment, followed by filtrating to obtain heterosite iron phosphate and a lithium-rich solution. The leaching rate of lithium in the leaching solution reaches 90.5-99.9%, and both of the iron and phosphorus content in the leaching solution are less than 0.1 ppm; the recovered heterosite iron phosphate has a purity of 99.9%, and the recovery rate of the heterosite iron phosphate is 99.3%.
A method for preparing a refractory material from waste battery residues. The method comprises the following steps: (1) disassembling waste batteries, then sorting same to obtain positive and negative electrode powders, leaching the positive and negative electrode powders with an acid, filtering same to obtain a graphite slag, and then subjecting the filtrate to copper removal, followed by the addition of an alkali for a precipitation reaction, wherein the resulting precipitate is an iron-aluminum slag; (2) wrapping the graphite slag obtained in step (1) with wet clay to form an inner core material, then mixing wet clay with the iron-aluminum slag, wrapping the inner core material with same, and aging the wrapped inner core material to obtain a blank; (3) pre-sintering, calcining and cooling the blank prepared in step (2) to obtain a fired product; and (4) washing and drying the fired product to obtain the refractory material.
The present invention provides a method for directly preparing nickel sulfate from low nickel matte, a nickel sulfate and an application thereof, the method comprising the following steps: a) pre-treating a low nickel matte to obtain ferronickel powder; b) mixing the ferronickel powder with a sulfuric acid solution, stirring, dissolving, and then evaporating, to obtain a supersaturated sulfate solution; c) cooling the supersaturated sulfate solution to −5° C.-0° C., and performing suction filtration to obtain an insoluble solid; d) washing the insoluble solid with water, and removing impurities from the filtrate to obtain a nickel hydroxide precipitate; impurity removal comprising successively removing iron, and removing calcium and magnesium; e) washing the nickel hydroxide precipitate with water, acid-dissolving and evaporating to obtain nickel sulfate. The present invention increases the amount of nickel recovered, the purity of nickel sulfate being 18.10%-19.24% nickel, and the recovery rate being 94.8%-97.1%.
Disclosed in the present invention is a method for extracting valuable metal from low-matte nickel converter slag. The method comprises: mixing low-matte nickel converter slag and quicklime then calcinating, obtaining a calcinated material; grinding and magnetically separating the calcinated material, obtaining silicate and iron-rich slag; adding a strong alkali solution to the iron-rich slag to perform leaching processing, and performing solid-liquid separation, obtaining a filtrate and a residue; mixing the residue with an acid solution, performing oxygen pressure acid leaching, and performing solid-liquid separation, obtaining a leachate and iron oxide; introducing hydrogen sulfide gas into the leachate, adjusting the pH, and performing solid-liquid separation, obtaining a copper sulfide precipitate and a nickel-cobalt-containing filtrate. In the present invention, first, removing silicon dioxide is removed by means of calcination to prepare silicate, then iron oxide is prepared by means of acid leaching, and finally metal separation is performed on the leachate, causing various components of the converter slag to be effectively utilized. The process flow of the present invention is short and effectively utilizes each component of the low-matte nickel converter slag, waste is turned into valuable material, and the loss of valuable metal elements is reduced.
Disclosed are a method for selectively extracting lithium from a retired battery and an application of the method. According to the method, on the basis of an ion exchange effect between a divalent manganese ion and a lithium ion, a positive electrode material and a divalent manganese salt are mixed according to a certain proportion and prepared into a slurry, and the divalent manganese salt and the positive electrode material are fully mixed by means of a ball milling process, such that a lattice structure of the positive electrode material is effectively damaged, thereby reducing activation energy of exchange of the divalent manganese ion and the lithium ion and greatly reducing reaction energy required by a subsequence lithium extraction process. A mixed material after ball milling is roasted at a lower temperature such that the bivalent manganese in the manganese salt occupies a lithium position in a layered structure, and manganese-lithium replacement is directly performed to obtain a pure lithium-containing leaching solution. The present method greatly improves the leaching rate and selectivity of lithium. The present invention uses a mode of first performing ball-mill mixing and then performing roasting, and thus has low power consumption, high safety, good leaching rate and selectivity of lithium, and wide application prospects.
Disclosed are a nickel-iron wet treatment method and an application thereof. The treatment method comprises: in a high-pressure oxygen environment, mixing a crushed nickel-iron material, sulphuric acid and a corrosion aid, performing an acid leaching reaction, then performing solid-liquid separation on slurry subjected to acid leaching, adding an oxidant into the obtained filtrate, performing heating, removing the corrosion aid, adding a precipitating agent into the filtrate, controlling the pH value of the filtrate, and performing solid-liquid separation to obtain a ferric hydroxide precipitate and a nickel-containing filtrate; and performing extraction and back extraction on the nickel-containing filtrate to prepare battery-grade nickel sulphate. According to the present invention, the nickel-iron is subjected to oxidation acid dissolution in cooperation with the corrosion aid under the high-pressure oxygen and acidic conditions; the nickel-iron is extremely prone to oxidation in the high-pressure oxygen environment; and a strong oxidant is added into the filtrate subsequently, so that ferrous ions in the filtrate are completely converted into ferric ions, and the corrosion aid can be oxidized to generate pollution-free carbon dioxide and water, thereby avoiding the impact of the corrosion aid on the subsequent extraction process.
C22B 3/22 - Traitement ou purification de solutions, p.ex. de solutions obtenues par lixiviation par des procédés physiques, p.ex. par filtration, par des moyens magnétiques
A doped sodium vanadium phosphate and a preparation method and application thereof. Preparation steps of a nitrogen-doped peony-shaped molybdenum oxide in raw materials of the doped sodium vanadium phosphate are as follows: adding a regulator into a molybdenum-containing solution for reaction, concentrating and thermal treatment to obtain a peony-shaped molybdenum oxide; and dissolving the peony-shaped molybdenum oxide in a conditioning agent, and adding an amine source for standing, centrifuging, washing and heat treatment, thus obtaining the nitrogen-doped peony-shaped molybdenum oxide.
H01M 4/58 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs de structures polyanioniques, p.ex. phosphates, silicates ou borates
H01M 10/054 - Accumulateurs à insertion ou intercalation de métaux autres que le lithium, p.ex. au magnésium ou à l'aluminium
H01M 4/02 - PROCÉDÉS OU MOYENS POUR LA CONVERSION DIRECTE DE L'ÉNERGIE CHIMIQUE EN ÉNERGIE ÉLECTRIQUE, p.ex. BATTERIES Électrodes Électrodes composées d'un ou comprenant un matériau actif
23.
PREPARATION METHOD FOR NANO FERRIC PHOSPHATE WITH LOW SULPHUR CONTENT
A method for preparing nano iron phosphate with low sulfur content. The method may include: S1: mixing a phosphorus source and an iron source to obtain a raw material solution, then adding alkali and a surfactant, adjusting a pH, and stirring and reacting to obtain an iron phosphate dihydrate slurry, S2: adding phosphoric acid solution into the iron phosphate dihydrate slurry, adjusting the pH, heating and stirring for aging, and filtering to obtain iron phosphate dihydrate, S3: adding water into the iron phosphate dihydrate for slurrying, and grinding to obtain a ground slurry; and S4: adding the ground slurry into a washing solution to wash, carrying out solid-liquid separation, and calcining a solid phase to obtain the nano iron phosphate with low sulfur content.
The present disclosure discloses a preparation method of a Ni-Rich ternary precursor and use thereof. The preparation method includes the following steps: under specified conditions, feeding an alkali liquor and a metal salt solution simultaneously for a precipitation reaction to obtain particles with D50 of 7.0 μm to 15.0 μm; continuously feeding a seed crystal, and after D10 of the particles is adjusted to 2.0 μm to 7.0 μm, stopping feeding the seed crystal; continuously feeding the alkali liquor and the metal salt solution, and collecting an overflow material; and when a particle size grows to D50 of 7.0 μm to 15.0 μm once again, repeating the above operation of adding a seed crystal, and continuously collecting an overflow material; and washing, drying, and sieving the collected materials to obtain the Ni-Rich ternary precursor.
The present disclosure discloses a preparation method of a ternary precursor, including: S1: mixing a first metal salt solution with a soluble nickel salt, a soluble cobalt salt, and a soluble manganese salt, ammonia water, and a sodium hydroxide solution, adjusting a pH, and heating and stirring a resulting mixture to allow a reaction; and aging and filtering a resulting slurry to obtain a precursor seed crystal; S2: adding the precursor seed crystal to a dilute acid solution, and stirring and filtering a resulting mixture to obtain an acidified seed crystal; and S3: mixing a second metal salt solution with a soluble nickel salt, a soluble cobalt salt, and a soluble manganese salt, a sodium hydroxide solution, and the acidified seed crystal, adjusting a pH, and heating and stirring a resulting mixture to allow a reaction; and aging, filtering, and drying a resulting slurry to obtain the ternary precursor.
The present disclosure belongs to the technical field of battery recycling, and discloses a recycling method and use of lithium iron phosphate (LFP) waste. The method includes the following steps: mixing the LFP waste with water to prepare a slurry; adjusting a pH of the slurry to higher than 7.0 with an alkali, and heating to react; filtering a resulting mixture to obtain a filter residue; dissolving the filter residue in an acid, and filtering to obtain a filtrate; adding an oxalate-containing solution to react, and aging and filtering a resulting mixture to obtain a filter cake and a precipitation mother liquor; and subjecting the filter cake to slurrying, washing, and free water removal to obtain ferrous oxalate.
The present disclosure discloses a high-performance lithium-nickel-manganese-cobalt oxide (LNMCO) cathode material for power batteries and a preparation method thereof, and belongs to the technical field of lithium-ion battery (LIB) materials. The preparation method of an LNMCO cathode material of the present disclosure combines a melting and mixing method, a spray drying method, a sol-gel method, and a high-temperature solid-phase method to achieve thorough mixing of various components of a precursor, such that a prepared product has a uniform particle size, excellent electrochemical performance, and high cycling stability. The method has simple operation steps, low raw material cost, small time consumption, and high production efficiency, and can realize industrialized large-scale production. The present disclosure also provides an LNMCO cathode material prepared by the method, which has high specific charge/discharge capacity, thermal stability, and cycling stability.
H01M 4/505 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de manganèse d'oxydes ou d'hydroxydes mixtes contenant du manganèse pour insérer ou intercaler des métaux légers, p.ex. LiMn2O4 ou LiMn2OxFy
H01M 4/525 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de nickel, de cobalt ou de fer d'oxydes ou d'hydroxydes mixtes contenant du fer, du cobalt ou du nickel pour insérer ou intercaler des métaux légers, p.ex. LiNiO2, LiCoO2 ou LiCoOxFy
28.
METHOD FOR RECOVERING ALUMINUM RESIDUE WITH CONTROLLED PARTICLE SIZE, AND USE THEREOF
The present disclosure belongs to the technical field of battery recycling, and discloses a method for recovering an aluminum residue with a controlled particle size, and use thereof. The method includes the following steps: crushing and sieving a positive electrode sheet of a waste power battery, then, crushing at −198° C. to −196° C. with addition of liquid nitrogen to obtain a granular material; roasting, cooling, and grinding the granular material, adding water, shaking, settling into layers, and separating the layers to obtain a positive electrode active powder layer, a transition layer, and an aluminum residue particle layer; and shaking the aluminum residue particle layer and the transition layer for a second time, settling into layers, and collecting aluminum residue particles and a positive electrode active powder.
The present disclosure discloses a method for recycling iron phosphate waste and use thereof. The method includes: mixing the iron phosphate waste with an acid liquid for dissolution to obtain an iron-phosphorus solution; taking a small portion of the iron-phosphorus solution to prepare an iron phosphate precipitating agent; adding the iron phosphate precipitating agent to a remaining portion of the iron-phosphorus solution to react to obtain an iron phosphate dihydrate precipitate; and keeping a portion of the iron phosphate dihydrate precipitate as a precipitating agent for a reaction in a subsequent batch, and preparing a remaining portion of the iron phosphate dihydrate precipitate into anhydrous iron phosphate. In the present disclosure, an iron phosphate precipitating agent is prepared and used for the subsequent preparation of iron phosphate, and iron phosphate obtained in each preparation can be used for the next preparation of iron phosphate.
The present disclosure belongs to the technical field of metal oxide materials, and discloses a synthesis method of cobalt hydroxide and cobalt hydroxide. The synthesis method includes: (1) stirring and heating ammonium citrate, introducing a protective gas, adding a cobalt salt and a mixed alkali liquor to allow a reaction, and adjusting a pH to obtain a cobalt hydroxide slurry; and (2) subjecting the cobalt hydroxide slurry to alkali-leaching, filtering, and slurrying a resulting filter residue; and washing a resulting slurry with a detergent, and drying the resulting slurry to obtain the cobalt hydroxide. In the present disclosure, ammonium citrate is used as a base solution, and a cobalt solution and a mixed alkali liquor are added to synthesize a cobalt hydroxide slurry in one step under a protective atmosphere.
The present disclosure discloses a method for preparing nickel sulfate from ferronickel, including: S1: in a high-pressure oxygen environment, mixing crushed ferronickel with sulfuric acid, introducing a carbon monoxide gas to allow a reaction, and conducting solid-liquid separation (SLS) to obtain a filtrate and a filter residue; S2: adding an oxidizing agent and a precipitating agent successively to the filtrate, controlling a pH of the filtrate, and conducting SLS to obtain a nickel-containing filtrate and an iron hydroxide precipitate; and S3: subjecting the nickel-containing filtrate to extraction and back-extraction to obtain a nickel sulfate solution. In the present disclosure, the carbon monoxide gas is introduced under high-pressure acidic conditions to first react with nickel and iron to form nickel tetracarbonyl and iron pentacarbonyl, and the nickel tetracarbonyl and iron pentacarbonyl are oxidized by oxygen and then smoothly react with sulfuric acid to form nickel sulfate and iron sulfate.
The present disclosure discloses a method for preparing a ternary cathode material with a molten salt and use thereof. The method includes: mixing a nickel salt, a cobalt salt, a manganese salt, a metal oxide and an acid liquor to obtain a mixed salt solution; concurrently adding the mixed salt solution, a sodium hydroxide solution and ammonia water to a base solution to allow a reaction to obtain a precursor; and mixing the precursor, a lithium source and a molten salt, and subjecting a resulting mixture to sintering, water-washing and annealing to obtain the ternary cathode material. In the present disclosure, a bismuth/antimony-doped ternary precursor is prepared, which is sintered with a molten salt, during which bismuth/antimony oxide is melted in the molten salt, then a resulting mixture is washed with water, and annealed to form a coating layer on a surface of the material.
H01M 4/505 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de manganèse d'oxydes ou d'hydroxydes mixtes contenant du manganèse pour insérer ou intercaler des métaux légers, p.ex. LiMn2O4 ou LiMn2OxFy
H01M 4/525 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de nickel, de cobalt ou de fer d'oxydes ou d'hydroxydes mixtes contenant du fer, du cobalt ou du nickel pour insérer ou intercaler des métaux légers, p.ex. LiNiO2, LiCoO2 ou LiCoOxFy
33.
CATHODE MATERIAL DRYING DEVICE AND CATHODE MATERIAL DRYING PRODUCTION LINE
This application discloses a cathode material drying device and a cathode material drying production line. The cathode material drying device includes: a rotary kiln, where a kiln head and a kiln tail of the rotary kiln each are provided with a sealing structure and the rotary kiln can rotate relative to the sealing structure; and an exhaust system comprising an air inlet pipe, an air outlet pipe, and a first fan, where the air inlet pipe communicates with the kiln tail of the rotary kiln through the sealing structure; the air outlet pipe communicates with the kiln head of the rotary kiln through the sealing structure; and the first fan is arranged on the air inlet pipe and/or the air outlet pipe, so as to make an air flow direction in the rotary kiln opposite to a delivery direction of a cathode material.
F27B 7/24 - Dispositifs d'étanchéité entre les pièces rotatives et fixes
F26B 25/00 - SÉCHAGE DE MATÉRIAUX SOLIDES OU D'OBJETS PAR ÉLIMINATION DU LIQUIDE QUI Y EST CONTENU - Parties constitutives d'application générale non couvertes par un des groupes ou
F27B 7/33 - Aménagement des dispositifs de déchargement
34.
PREPARATION METHOD OF LAYERED CARBON-DOPED SODIUM IRON PHOSPHATE CATHODE MATERIAL
The present disclosure discloses a preparation method of a layered carbon-doped sodium iron phosphate cathode material, including: placing a carbonate powder in an inert atmosphere, introducing a gaseous organic matter, and heating to allow a reaction to obtain a MCO3/C layered carbon material; and mixing the MCO3/C layered carbon material, a sodium source, ferrous phosphate, and a dispersing agent in an inert atmosphere, grinding a resulting mixture, washing and drying to remove the dispersing agent, and heating to allow a reaction in an inert atmosphere to obtain the layered carbon-doped sodium iron phosphate cathode material.
The present disclosure belongs to the technical field of battery materials, and discloses a silicon/carbon composite anode material, and a preparation method and use thereof. The preparation method includes the following steps: S1. dissolving a graphite anode powder in an acid solution, and conducting solid-liquid separation (SLS) to obtain a precipitate; and washing and drying the precipitate, adding a reducing agent, and subjecting a resulting mixture to heat treatment to obtain a purified graphite material; and S2. mixing a modified silicon powder with the graphite material, adding a resulting mixture to a polyimide (PI)-containing N,N-dimethylformamide (DMF) solution, and stirring; and subjecting a resulting mixture to distillation and then to carbonization to obtain the silicon/carbon composite anode material.
H01M 4/36 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs
H01M 4/38 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'éléments simples ou d'alliages
H01M 4/587 - Matériau carboné, p.ex. composés au graphite d'intercalation ou CFx pour insérer ou intercaler des métaux légers
H01M 10/0525 - Batteries du type "rocking chair" ou "fauteuil à bascule", p.ex. batteries à insertion ou intercalation de lithium dans les deux électrodes; Batteries à l'ion lithium
H01M 10/54 - Récupération des parties utiles des accumulateurs usagés
The invention belongs to the technical field of batteries, and discloses a preparation method and application of a lithium cobalt oxide soft-pack battery. The preparation method comprises the following steps: preparation of a lithium cobalt oxide positive electrode; preparation of a graphite negative electrode; preparation of an aluminum plastic film; screening and tab welding the positive and negative electrode, then winding core and packing, injecting an electrolyte to a resulting pack, perform first sealing, formation, second sealing; followed by capacity grading to obtain the lithium cobalt oxide soft pack battery. The preparation method for the lithium cobalt oxide soft-pack battery in a laboratory environment at room temperature provided by the present invention has simple operation and low environmental requirements, can be used in laboratories without dry room conditions, and reduces research and development cost and laboratory maintenance cost.
H01M 4/1391 - Procédés de fabrication d'électrodes à base d'oxydes ou d'hydroxydes mixtes, ou de mélanges d'oxydes ou d'hydroxydes, p.ex. LiCoOx
H01M 10/0525 - Batteries du type "rocking chair" ou "fauteuil à bascule", p.ex. batteries à insertion ou intercalation de lithium dans les deux électrodes; Batteries à l'ion lithium
H01M 10/0587 - Structure ou fabrication d'accumulateurs ayant uniquement des éléments de structure enroulés, c. à d. des électrodes positives enroulées, des électrodes négatives enroulées et des séparateurs enroulés
H01M 50/536 - Connexions d’électrodes dans un boîtier de batterie caractérisées par le procédé de fixation des conducteurs aux électrodes, p.ex. soudage
H01M 4/131 - PROCÉDÉS OU MOYENS POUR LA CONVERSION DIRECTE DE L'ÉNERGIE CHIMIQUE EN ÉNERGIE ÉLECTRIQUE, p.ex. BATTERIES Électrodes Électrodes composées d'un ou comprenant un matériau actif Électrodes pour accumulateurs à électrolyte non aqueux, p.ex. pour accumulateurs au lithium; Leurs procédés de fabrication Électrodes à base d'oxydes ou d'hydroxydes mixtes, ou de mélanges d'oxydes ou d'hydroxydes, p.ex. LiCoOx
The disclosure discloses a precursor with a transformed crystal form and a preparation method thereof. The preparation method includes: (1) heating a carbonate solution, a cobalt salt to allow a reaction, and spray adding a carbonate solution to allow a reaction to obtain a cobalt carbonate slurry; (2) allowing the slurry to stand, spray adding a cobalt salt and a carbonate solution, and spray adding a cobalt salt using a single spray head at a flow rate of 1 m3/h to 3 m3/h and a carbonate solution using no less than three spray heads each at a flow rate of 0.2 m3/h to 5 m3/h to obtain cobalt carbonate with a transformed crystal form; and (3) further spray adding a cobalt salt and a carbonate solution to the cobalt carbonate with a transformed crystal form, heating to allow a constant-temperature reaction, and washing and calcining a product.
Disclosed in the present invention is a method for preparing nickel sulfate from a nickel-iron-copper alloy. The method comprises: in a high-pressure oxygen environment, mixing a nickel-iron-copper alloy crushed material, aqueous ammonia, ammonium sulphate, and a corrosion assisting agent, leaching, then performing solid-liquid separation on the leached slurry, adding a precipitant into a filtrate, and performing ammonia distillation to obtain a nickel-containing leachate; then adding an extractant into the nickel-containing leachate to extract nickel so as to obtain a nickel-containing extraction organic phase; and then adding sulfuric acid into the nickel-containing extraction organic phase to perform back extraction of nickel so as to obtain a nickel sulfate solution. According to the present invention, the nickel-iron-copper alloy is separated by using different properties of nickel and iron, nickel is dissolved in a hexamine complex of nickel, iron cannot be dissolved and then continues to be remained in a solid, after the filtrate is collected, the precipitant is added and ammonia distillation is performed to remove copper, the aqueous ammonia is recycled, and the copper ions react with the precipitant to generate a copper sulfide precipitate, and thus, copper in the filtrate is removed, and the purity of nickel sulfate is further improved.
The present disclosure discloses a preparation method and use of a high-performance modified lithium-nickel-manganese-cobalt oxide (LNMCO) nickel 55 material. In the preparation method of the present disclosure, a silica template-containing nano-precursor coated with a polymer is prepared by electrospinning, and then the nano-precursor is sintered in the air to effectively provide effective embedding and attachment sites for subsequent nickel plating; and after the nickel plating, the silica template is removed such that distributed mesopores are generated in situ on the precursor. The mesopores provide channels for the subsequent penetration of molten lithium into the interior of the precursor material. A final prepared material has a better ion and electron conduction structure compared with traditional granular materials. The present disclosure also discloses a material prepared by the method. The present disclosure also discloses an LIB including the high-performance modified LNMCO nickel 55 material.
H01M 4/525 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de nickel, de cobalt ou de fer d'oxydes ou d'hydroxydes mixtes contenant du fer, du cobalt ou du nickel pour insérer ou intercaler des métaux légers, p.ex. LiNiO2, LiCoO2 ou LiCoOxFy
H01M 4/505 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de manganèse d'oxydes ou d'hydroxydes mixtes contenant du manganèse pour insérer ou intercaler des métaux légers, p.ex. LiMn2O4 ou LiMn2OxFy
H01M 4/62 - Emploi de substances spécifiées inactives comme ingrédients pour les masses actives, p.ex. liants, charges
The present invention discloses a radially-structured nickel-based precursor and a preparation method thereof. An overall shape of the precursor is a secondary sphere formed by agglomeration of primary crystal grains; and the secondary sphere has a loose and porous network core inside and uniform and regular strip primary crystal grains outside, and the strip primary crystal grains grow outward perpendicularly to a surface of the core and are arranged radially and closely. The precursor structure of the present invention is more suitable for high-power battery cathode materials. The internal loose structure is more likely to form a void in the center during a preparation process of a cathode material, which helps to expand a contact area between an active material and an electrolyte.
A method for recovering lithium battery slurry, the method comprising: pretreating lithium battery slurry, and then subjecting the pretreated lithium battery slurry to centrifugal spray drying to separate a solid phase and a solvent. A device for the recovery of lithium battery slurry is a centrifugal spray drying system, and comprises a spray chamber (100), a cyclone separator (200), a condenser (400), a condensate storage tank (500), and a rectification tower (600); the system improves upon original centrifugal spray drying devices, and is designed to combine the processes of centrifugal spray drying and NMP condensation recovery, such that NMP can be directly recovered after separation of positive electrode material and the NMP.
The invention belongs to the technical field of lithium ion battery materials, and discloses a fast ionic conductor coated lithium-transition metal oxide material having a chemical formula of (1−x)Li1+a (Ni(1−m−n)ConMnm) 1−bMbO2·xLicAldTieM′fM″g (PO4)3 and a preparation method thereof. The fast ionic conductor coated lithium-transition metal oxide material of the present invention has lower impedance, excellent cycle performance and safety performance under high voltage, especially when the charging voltage is greater than 4.62V, 4.65V, or higher. The Lithium-transition metal oxide can be obtained by a primary calcination, and the final product of lithium-transition metal oxide material coated with fast ionic conductor can be obtained by a secondary calcination.
H01M 10/0525 - Batteries du type "rocking chair" ou "fauteuil à bascule", p.ex. batteries à insertion ou intercalation de lithium dans les deux électrodes; Batteries à l'ion lithium
43.
SINTERING-RESISTANT MATERIAL, AND PREPARATION METHOD AND USE THEREOF
The present disclosure discloses a sintering-resistant material, and a preparation method and use thereof. The sintering-resistant material includes magnesium oxide, an anti-corrosive agent, an antioxidant, and a binder, where the anti-corrosive agent includes a barite powder and a porous graphite powder; the antioxidant includes aluminum carbide and an aluminum powder; the binder includes a metal chloride and a silica sol; and metals in the raw materials are all extracted from a hydrochloric acid leachate of an electric furnace slag. In the present disclosure, the preparation method of the present disclosure improves the resource utilization of the electric furnace slag. Magnesium and aluminum have the largest proportion among metal elements in the electric furnace slag, and thus magnesium oxide is used as the main material. In addition, other chloride salts leached out from the electric furnace slag by hydrochloric acid can be directly or indirectly used.
C04B 35/04 - Produits céramiques mis en forme, caractérisés par leur composition; Compositions céramiques; Traitement de poudres de composés inorganiques préalablement à la fabrication de produits céramiques à base d'oxydes à base d'oxyde de magnésium, d'oxyde de calcium ou de mélanges d'oxydes dérivés de la dolomite à base d'oxyde de magnésium
C04B 35/622 - Procédés de mise en forme; Traitement de poudres de composés inorganiques préalablement à la fabrication de produits céramiques
C04B 35/63 - Préparation ou traitement des poudres individuellement ou par fournées utilisant des additifs spécialement adaptés à la formation des produits
The present disclosure discloses a preparation method of platy aluminum-doped cobalt carbonate and use thereof. The preparation method includes the following steps: S1: mixing a cobalt salt, an aluminum salt, and a polyhydroxy compound to prepare a mixed solution; S2: mixing the mixed solution with an ammonium bicarbonate solution, adjusting a pH, and heating and stirring to allow a reaction to obtain a seed crystal solution; and S3: adding the mixed solution and an ammonium bicarbonate solution to the seed crystal solution, adjusting a pH, and heating and stirring to allow a reaction, during which a solid content in a slurry is controlled at 20% to 40% until a particle size in the slurry grows to a target value; and separating out, washing, and drying a solid phase to obtain the platy aluminum-doped cobalt carbonate.
The present disclosure discloses a preparation method of tungsten-doped cobalt tetraoxide and use thereof. The preparation method includes the following steps: dissolving a tungsten-containing compound and a molybdenum-containing compound in an alkali liquid to obtain a mixed solution; concurrently feeding the mixed solution, a cobalt salt solution, and a complexing agent into a base solution to allow a reaction to obtain a precipitate; roasting the precipitate in an oxygen-containing atmosphere to obtain a roasted material; and soaking the roasted material in a sodium sulfide solution to obtain the tungsten-doped cobalt tetraoxide. In the present disclosure, tungsten is doped, and tungsten has a large atomic radius, which stabilizes an internal structure of the material, expands the ion channel, and improves the cycling performance of the material; and molybdenum is removed through a soaking process, which provides atomic vacancies to further improve a specific capacity of the material.
H01M 4/525 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de nickel, de cobalt ou de fer d'oxydes ou d'hydroxydes mixtes contenant du fer, du cobalt ou du nickel pour insérer ou intercaler des métaux légers, p.ex. LiNiO2, LiCoO2 ou LiCoOxFy
46.
CATHODE MATERIAL PRECURSOR AND PREPARATION METHOD AND APPLICATION THEREOF
The invention relates to the field of battery materials, and discloses a cathode material precursor and a preparation method and application thereof. The chemical formula of the cathode material precursor is NixCoyMnz(OH)2, wherein 0.2≤x≤1, 0≤y≤0.5, 0≤z≤0.6, and 0.8≤x+y+z≤1. The cathode material precursor is in a shape of a stack of lamellae, and has a particle size broadening factor K, where K≤0.85. In the invention, the preparation process of the precursor is effectively controlled and adjusted by the controlled crystallization method combined with Lamer nucleation and growth theoretical model. The prepared precursor has morphology characteristics of concentrated particle size distribution and high proportion of {010} active crystal plane family, and has capacity retention up to 91.33% at a rate of 20C.
H01M 10/0525 - Batteries du type "rocking chair" ou "fauteuil à bascule", p.ex. batteries à insertion ou intercalation de lithium dans les deux électrodes; Batteries à l'ion lithium
47.
COBALT-FREE NICKEL-MANGANESE CATHODE MATERIAL AND PREPARATION AND APPLICATION THEREOF
The invention relates to the technical field of battery materials and discloses a cobalt-free layered nickel-manganese cathode material and a preparation method and application thereof. The chemical formula of the cobalt-free layered nickel-manganese cathode material is LiaNixMnyMezO2@Mb, and Me is at least one selected from the group consisting of Zr, Al, W, Sr, Ti and Mg; M is at least one selected from the group consisting of Al2O3, CeO2, TiO2, Yb2O3, Nb2O5, La2O3, WO3, titanium sol, aluminum sol, titanium-aluminum sol, aluminum isopropoxide, butyl titanate, aluminum dihydrogen phosphate or lithium tungstate. The present invention achieves a shallow coating through high temperature calcination followed by metal oxide coating, which is beneficial to prevent the material from microcracks expansion caused by the material structure and internal stress change during the charging-discharging cycles.
H01M 10/0525 - Batteries du type "rocking chair" ou "fauteuil à bascule", p.ex. batteries à insertion ou intercalation de lithium dans les deux électrodes; Batteries à l'ion lithium
48.
Device for cutting connection of multi-piece module electrode
The present disclosure discloses a device for cutting connection of multi-piece module electrode which includes a stand, the stand is provided with a workbench and the workbench is connected with a height adjusting device. The device further includes an angle grinding device, the angle grinding device includes a polishing shaft and an angle grinder, the angle grinder is arranged on the polishing shaft, and the angle grinding device is provided with a saw blade. According to the characteristics of the module electrode, the angle grinding device is matched with the workbench to implement simultaneous electrode disconnecting operation of multiple electrodes of the module, so that the device not only has higher efficiency and better cutting effect, but also is suitable for universal saw blades, saves the cost, and is safer.
B24B 41/00 - MACHINES, DISPOSITIFS OU PROCÉDÉS POUR MEULER OU POUR POLIR; DRESSAGE OU REMISE EN ÉTAT DES SURFACES ABRASIVES; ALIMENTATION DES MACHINES EN MATÉRIAUX DE MEULAGE, DE POLISSAGE OU DE RODAGE Éléments constitutifs des machines ou dispositifs à meuler, tels que bâtis, bancs, chariots ou poupées
B24B 41/06 - Supports de pièces, p.ex. lunettes réglables
The invention belongs to the field of an electrolyte solution for a battery, and discloses a lithium-sulfur battery electrolyte and a preparation method and application thereof. The electrolyte solution comprises the following components: an organic solvent, an electrolyte and an additive; the organic solvent is 1,1,2, 2-tetrafluoroethyl 2,2,3,3-tetrafluoropropyl ether and 1,3-dioxolane; the electrolyte is bis(hexafluoroethane) sulfonamide lithium salt and LiCF3SO3; the additive is a lithium-sulfur compound, wherein the lithium-sulfur compound is Li6S2. The invention recovers an electrolyte solution from a lithium-sulfur battery, and then extracts the Li element in the electrolyte solution, which is recycled for preparation of a electrolyte solution of the lithium-sulfur battery; in addition, it can also enrich the organic components in the electrolyte solution of the waste lithium-sulfur battery, facilitating a centralized processing and reduction of leakage pollution.
The invention belongs to the technical field of battery material recycling and discloses a regeneration method of waste ternary cathode materials and application thereof. The regeneration method comprises the following steps: drying, crushing, and sieving a waste ternary cathode material to obtain a cathode powder; adding the cathode powder to a alkali liquid, reacting, stirring, washing, and filtering to obtain a filter residue; drying the filter residue, then mixing with carbonized pitch, and performing reducing calcination to obtain a mixture; after testing the content of nickel, cobalt, manganese, aluminum, and lithium in the mixture, adding a nickel source, a cobalt source, a lithium source, a manganese source, polyethylene glycol, ball milling with water to obtain a suspension; spray granulating the suspension to obtain a ternary precursor; subjecting the precursor to two-stage calcination to obtain a regenerated ternary cathode material.
H01M 10/54 - Récupération des parties utiles des accumulateurs usagés
H01M 4/505 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de manganèse d'oxydes ou d'hydroxydes mixtes contenant du manganèse pour insérer ou intercaler des métaux légers, p.ex. LiMn2O4 ou LiMn2OxFy
H01M 4/525 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de nickel, de cobalt ou de fer d'oxydes ou d'hydroxydes mixtes contenant du fer, du cobalt ou du nickel pour insérer ou intercaler des métaux légers, p.ex. LiNiO2, LiCoO2 ou LiCoOxFy
51.
PREPARATION METHOD FOR LITHIUM IRON PHOSPHATE CATHODE MATERIAL AND APPLICATION THEREOF
The present invention provides a preparation method and application of lithium iron phosphate cathode material, comprising the following steps: (1) Dry mixing an iron source, a phosphorus source, a lithium source, a carbon source and additives and fine grinding to obtain a mixed material; (2) Performing first calcination to the mixed material, and then pulverize to obtain the pulverized material; (3) Perform the second calcination to the pulverized material, while introducing a gasifiable organic carbon source, and then cooling to obtain a lithium iron phosphate cathode material. The invention uses high-efficiency mixing equipment for a one-step mixing and fine grinding of the raw materials, followed by the first calcination and pulverizing, and then performing a second calcination. The gasifiable organic carbon source is used to supplement carbon by forming a carbon coating, so that it has a better carbon coating layer and particle morphology.
H01M 4/58 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs de structures polyanioniques, p.ex. phosphates, silicates ou borates
C01B 25/45 - Phosphates contenant plusieurs métaux ou un métal et l'ammonium
H01M 10/0525 - Batteries du type "rocking chair" ou "fauteuil à bascule", p.ex. batteries à insertion ou intercalation de lithium dans les deux électrodes; Batteries à l'ion lithium
H01M 4/36 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs
H01M 4/60 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs de composés organiques
52.
MIXING PROCESS FOR PREPARING HIGH NICKEL CATHODE MATERIAL AND APPLICATION THEREOF
The invention discloses a mixing process for preparing a high nickel cathode material and its use. The mixing process is to add a precursor and a lithium source to a mixing device for mixing to obtain a mixture. After the mixture is uniformly mixed, the mixture is mixed. While the material equipment continues to operate, spray the liquid into the mixture. After the liquid spray is completed, the material is discharged, and the obtained mixture is put into a sagger for sintering. The liquid is pure water, ethanol, nitrogen methyl pyrrolidone, and additive solution. Or one or more of additive dispersions. The spray mixing process of the present invention can make the mixture more uniform, and because of the presence of a proper amount of mist droplets, the surface of the lithium source is slightly soluble in water and can adsorb the precursor.
H01M 4/525 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de nickel, de cobalt ou de fer d'oxydes ou d'hydroxydes mixtes contenant du fer, du cobalt ou du nickel pour insérer ou intercaler des métaux légers, p.ex. LiNiO2, LiCoO2 ou LiCoOxFy
H01M 10/0525 - Batteries du type "rocking chair" ou "fauteuil à bascule", p.ex. batteries à insertion ou intercalation de lithium dans les deux électrodes; Batteries à l'ion lithium
H01M 4/505 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de manganèse d'oxydes ou d'hydroxydes mixtes contenant du manganèse pour insérer ou intercaler des métaux légers, p.ex. LiMn2O4 ou LiMn2OxFy
H01M 4/485 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques d'oxydes ou d'hydroxydes mixtes pour insérer ou intercaler des métaux légers, p.ex. LiTi2O4 ou LiTi2OxFy
Disclosed are a silicon-doped graphene composite material and a preparation method and application thereof. The silicon-doped graphene composite material comprises silicon and graphene; the silicon is doped in the graphene. The silicon-doped graphene composite material of the present disclosure has excellent charge and discharge capacity and structural stability; the silicon-doped graphene composite material is based on the graphene structure, with silicon atoms replacing the carbon atoms in a two-dimensional network structure of the graphene. The silicon-doped graphene composite material of the present disclosure has a layered structure similar to graphite materials, but is superior to other graphene materials in charge and discharge capacity, which is due to the fact that lithium intercalation sites are constructed by the silicon doped sites.
Disclosed are a method for preparing lithium nickle cobalt manganese oxide by reverse positioning of a power battery and use thereof. The method first mixes and grinds a positive electrode tab and a slagging agent, then dries, cools, adds an aluminum powder, mixes well, conducts a self-propagating reaction to the mixed material, cools, takes a lower layer of rough nickel cobalt manganese alloy, grinds the rough nickel cobalt manganese alloy, adds an alkali liquor, then immerses, filters, takes the filter residue for washing and then dries, to obtain a nickel cobalt manganese alloy powder, adds a lithium salt solution to the porous nickel cobalt manganese alloy powder, mixes and drips an alkali liquor, ages, filters, takes a filter residue for washing and then dries, to obtain a mixed powder of precursor, sinters the mixed powder of precursor and cools, to obtain a lithium nickle cobalt manganese oxide.
Disclosed are a method for recovering lithium from lithium iron phosphate waste and application thereof. The method comprises the following steps: (1) adding water to lithium iron phosphate waste to obtain a lithium iron phosphate slurry (2) adding a soluble iron salt to the lithium iron phosphate slurry to perform a reaction, and filtering a resulting product to obtain an iron phosphate slag and a filtrate containing Li+ and Fe2+; (3) adding an oxidizing agent to the filtrate to perform a reaction and filtering a resulting product to obtain iron hydroxide and a filtrate containing Li+, Fe3+; (4) performing a multi-stage counter-current circulation leaching to the mixture of the filtrate and the lithium iron phosphate waste to obtain a lithium solution. The present disclosure adopts a soluble iron salt capable of accelerating the conversion of lithium iron phosphate.
C22B 7/00 - Mise en œuvre de matériaux autres que des minerais, p.ex. des rognures, pour produire des métaux non ferreux ou leurs composés
H01M 10/54 - Récupération des parties utiles des accumulateurs usagés
C22B 3/22 - Traitement ou purification de solutions, p.ex. de solutions obtenues par lixiviation par des procédés physiques, p.ex. par filtration, par des moyens magnétiques
56.
METHOD FOR REMOVING ELEMENTAL COPPER FROM TERNARY BATTERY WASTE AND APPLICATION THEREOF
Disclosed are a method for removing elemental copper from ternary battery waste and its application. The method comprises the following steps: crushing and screening the ternary battery waste to obtain a powder, and then removing iron by magnetic separation to obtain an iron-removed ternary waste; Adding an alkaline solution to the iron-removed ternary waste to perform an aluminum removal reaction, filtering to obtain a filter slag and aluminum-containing wastewater, washing the filter slag with water and drying to obtain a copper-nickel-cobalt-manganese material. Adding an iron salt solution to the copper-nickel-containing material to perform a leaching process, filtering to obtain a leachate and a nickel-cobalt-manganese waste; adding iron powder to the leachate and stirring to perform a reaction, filtering to obtain a copper residue, washing the copper residue with water and drying to obtain a copper-removed liquid and a sponge copper.
The present disclosure discloses a method for recycling lithium iron phosphate waste and its application. The method comprises the following steps: disassembling, crushing, and sieving the lithium iron phosphate waste to obtain a lithium iron phosphate powder; Diluting a ionic membrane liquid alkali, adding the lithium iron phosphate powder to the alkali, stirring under an oxidizing atmosphere in water bath to perform a reaction; filtering a resulting product to obtain a leachate and a lithium phosphate slag; drying the lithium phosphate slag, adding an ammonia aqueous solution to the slag to perform a reaction, filtering to obtain an ammonia aqueous solution containing lithium phosphate and a filter residue; the ammonia aqueous solution containing lithium phosphate is evaporated to obtain lithium phosphate. By adopting the present method of removing aluminum by alkaline leaching under an oxidizing atmosphere, the aluminum content in the obtained lithium iron phosphate slag is 0.08%.
The present disclosure provides a disassembly mechanism, a disassembly system of a power battery pack with the disassembly mechanism and a disassembly method of the power battery pack. The above disassembly mechanism includes a die base assembly, a pressing assembly and a removal tool assembly. The pressing assembly is movably connected to the die base assembly, and is used to abut against and press a single battery of a power battery pack. The removal tool assembly is slidably connected to the die base assembly and elastically connected to the die base assembly. The removal tool assembly is used to squeeze and separate a casing and the single battery of the power battery pack. The above disassembly mechanism can realize automatic disassembly of the power battery pack with few manual intervention, and solves the problem of low efficiency in the recycling and disassembly process of the power battery pack.
H01M 10/54 - Récupération des parties utiles des accumulateurs usagés
B09B 3/80 - Destruction de déchets solides ou transformation de déchets solides en quelque chose d'utile ou d'inoffensif impliquant une étape d'extraction
The present disclosure discloses a method for recovering and purifying nickel from ferronickel, comprising the following steps: (1) mixing ferronickel with hydrochloric acid, and heating for dissolution; subjecting a resulting slurry to solid-liquid separation to obtain a liquid phase; and adding an oxidant to the liquid phase to obtain a hydrochloric acid-leaching liquor; (2) subjecting the hydrochloric acid-leaching liquor to evaporation, and adding a precipitating agent to allow a reaction; separating out a liquid phase, adding ammonia water to adjust a pH, and adding a water-soluable alcohol solution; and cooling for precipitation to obtain a nickel complex crystal; and (3) dissolving the nickel complex crystal, and adding an oxidant; and subjecting a resulting mixture to a light treatment, and adjusting a pH with an acid to obtain a nickel chloride solution.
A method for recycling a lithium battery cathode material. Residual aluminum on the positive electrode sheet is dissolved by a sodium hydroxide solution, and lithium in the cathode material enters the solution during the dissolution of aluminum, such that an ionic potential is vacated on the cathode material; a residue is washed to avoid sodium ion contamination, then dried, and allowed to react with metallic lithium and lithium sulfide under heating, such that crystal lattices of the material change; a product after first-stage lithium supplementation is directly sintered with a lithium source in an oxygen atmosphere to obtain monocrystalline ternary cathode material agglomerates, where a sintering method and a sintering temperature are controlled; and the agglomerates are crushed, then washed to remove residual lithium on the surface, and dried to obtain a monocrystalline ternary cathode material, which has the performance close to that of the initially synthesized monocrystalline cathode material.
The present disclosure discloses a recycling method for a mixed waste material of lithium nickel manganese cobalt oxide (LNMCO) and lithium iron phosphate (LFP), including: conducting acid-leaching to obtain an acid-leaching liquor with nickel, cobalt, manganese, phosphorus, iron, and lithium; conducting adsorption separation with a resin, washing the resin with sulfuric acid to obtain a mixed solution of nickel sulfate, cobalt sulfate, and manganese sulfate, and subjecting the mixed solution to precipitation to obtain an LNMCO cathode material precursor; and subjecting an obtained solution with phosphorus, iron, and lithium to lithium precipitation to obtain a lithium salt precipitate, and subjecting a post-precipitation solution to concentration and electrospinning to obtain a ferric phosphate/carbon material. The process of the present disclosure can achieve comprehensive recycling of a mixed waste material of LNMCO and LFP and the directed circulation of waste LNMCO and LFP materials.
The present disclosure belongs to the technical field of lithium battery recycling, and discloses a method for separating and recovering valuable metals from waste ternary lithium batteries. The method includes the following steps: adding a persulfate to a waste ternary lithium battery powder, and conducting oxidative acid leaching to obtain a leaching liquor and a leaching residue; adding an alkali to the leaching liquor to allow a precipitation reaction; adding a sulfide salt to allow a reaction; adjusting a pH to allow a precipitation reaction to obtain a nickel hydroxide precipitate and a liquid phase A; adding a carbonate to the liquid phase A to allow a reaction, and conducting solid-liquid separation (SLS) to obtain lithium carbonate; and subjecting the leaching residue to calcination, adding a chlorate, heating a resulting mixture, and conducting SLS to obtain manganese dioxide.
C22B 7/00 - Mise en œuvre de matériaux autres que des minerais, p.ex. des rognures, pour produire des métaux non ferreux ou leurs composés
C22B 3/22 - Traitement ou purification de solutions, p.ex. de solutions obtenues par lixiviation par des procédés physiques, p.ex. par filtration, par des moyens magnétiques
C22B 3/42 - Traitement ou purification de solutions, p.ex. de solutions obtenues par lixiviation par extraction utilisant l'échange d'ions
C22B 3/00 - Extraction de composés métalliques par voie humide à partir de minerais ou de concentrés
The invention belongs to the technical field of lithium ion battery cathode materials, and discloses a preparation method and application of nanosized lithium cobalt oxide cathode materials, comprising the following steps: mixing the carbonate solution with a dispersant, adding a cobalt salt solution to react, then aging, filtering, drying the filter residue to obtain a nano-CoCO3 powder, and then calcinating it to obtain a Co3O4 precursor; mixing the Co3O4 precursor with a lithium salt, and then sintering, cooling, pulverizing and sieving to obtain the nanosized lithium cobalt oxide cathode material. The main advantages of the present invention are that the nano-CoCO3 synthesis process is simple and easy to control, the process is short, no special temperature control is required, the pH value and other conditions are not required to be precisely controlled during the reaction process, and it is suitable for large-scale industrial production.
H01M 4/525 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de nickel, de cobalt ou de fer d'oxydes ou d'hydroxydes mixtes contenant du fer, du cobalt ou du nickel pour insérer ou intercaler des métaux légers, p.ex. LiNiO2, LiCoO2 ou LiCoOxFy
H01M 10/0525 - Batteries du type "rocking chair" ou "fauteuil à bascule", p.ex. batteries à insertion ou intercalation de lithium dans les deux électrodes; Batteries à l'ion lithium
64.
ALUMINUM-BASED LITHIUM ION-SIEVE (LIS), AND PREPARATION METHOD AND USE THEREOF
Disclosed are an aluminum-based lithium ion-sieve (LIS), and a preparation method and use thereof. The aluminum-based LIS is Li2SO4·2Al(OH)3·nH2O coated with Al(OH)3, where n is 1 to 4. The preparation method includes: reacting an aluminum salt and a lithium salt with an alkali to obtain an adsorbent intermediate LiOH·2Al(OH)3·nH2O; using a dilute sulfuric acid to obtain an aluminum-based lithium adsorbent Li2SO4·2Al(OH)3·nH2O; and filtering out and washing the adsorbent, mixing the adsorbent with a metaaluminate, and adjusting a pH to obtain the Li2SO4·2Al(OH)3·nH2O coated with Al(OH)3. The aluminum-based LIS of the present disclosure has the advantages of high adsorption capacity and prominent stability, and can be used to efficiently recover low-concentration lithium in industrial wastewater. Moreover, the LIS is coated with aluminum hydroxide, which can effectively protect the structure from being corroded.
B01J 20/04 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtration; Absorbants ou adsorbants pour la chromatographie; Procédés pour leur préparation, régénération ou réactivation contenant une substance inorganique contenant des composés des métaux alcalins, des métaux alcalino-terreux ou du magnésium
B01J 20/08 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtration; Absorbants ou adsorbants pour la chromatographie; Procédés pour leur préparation, régénération ou réactivation contenant une substance inorganique contenant des oxydes ou des hydroxydes des métaux non prévus dans le groupe contenant de la bauxite
B01J 20/30 - Procédés de préparation, de régénération ou de réactivation
C02F 1/28 - Traitement de l'eau, des eaux résiduaires ou des eaux d'égout par absorption ou adsorption
65.
WET PROCESS FOR RECOVERING VALUABLE METALS FROM LITHIUM BATTERY
The present disclosure discloses a wet process for recovering valuable metals from a lithium battery. In the method, a waste lithium battery powder is subjected to selective leaching under the condition that a hydrogen sulfide gas is introduced through pressurization, such that Mn2+, Li+, and Al3+ metal ions enter a first-stage leaching liquor and nickel, cobalt, copper, and iron exist in a first-stage leaching residue in the form of a sulfide; then a pH of the first-stage leaching liquor is adjusted to remove aluminum and manganese, which achieves extremely thorough metal separation and leads to relatively pure products; a first-stage leaching residue is subjected to leaching in an acid liquor under a negative pressure, such that the sulfides of nickel, cobalt, iron, and copper are dissolved in a second-stage leaching liquor, and a hydrogen sulfide gas produced can be recycled in the first-stage leaching procedure through pressurization.
C22B 3/00 - Extraction de composés métalliques par voie humide à partir de minerais ou de concentrés
C22B 3/22 - Traitement ou purification de solutions, p.ex. de solutions obtenues par lixiviation par des procédés physiques, p.ex. par filtration, par des moyens magnétiques
This disclosure discloses a method for recovering lithium from a waste LFP material, including: S1. adding water to the waste LFP material, controlling a pH thereof at 0.5 to 2.0 and an ORP of the slurry at 0.05 V to 1.2 V, and filtering to obtain a material A; S2. adding sulfuric acid and heating a resulting mixture at 100° C. to 400° C. in the air or an oxygen atmosphere to obtain a material B; S3. adding water to the material B, and stirring and filtering to obtain a material C; S4. controlling a pH of the material C at 9 to 11, and filtering a resulting mixture to obtain a material D; S5. passing the material D through an ion-exchange resin to obtain a material E; and S6. adding the material E to a sodium carbonate solution to react; and collecting a resulting solid to obtain lithium carbonate.
Disclosed are a sagger for sintering lithium composite transition metal oxide and a preparation method thereof. The sagger includes a substrate layer and a shallow layer on a surface of the substrate layer, and a coating layer. The substrate layer is prepared from the following raw materials: silicon carbide, magnesia-alumina spinel, aluminum oxide-magnesium oxide-yttrium oxide composite fiber, zircon powder and a binding agent; the shallow layer is prepared from the following raw materials: silicon carbide, magnesia-alumina spinel, aluminum oxide-titanium oxide composite fiber, yttrium oxide-zirconium oxide composite fiber and a binding agent; and the coating layer is prepared from the following raw materials: silicon carbide, magnesia-alumina spinel, magnesium oxide, zirconium oxide fiber, lithium composite transition metal oxide powder and a binding agent. The sagger of the present disclosure has properties of good corrosion resistance and a small coefficient of thermal expansion.
Disclosed are a preparation method and application of iron phosphate. The preparation method comprises: subjecting iron phosphate waste to calcination, dissolving it in an acid solution, and filtering to obtain filtrate, namely a solution A containing iron phosphorus; stirring a mixed solution of the solution A and a first alkali solution, adjusting pH of the mixed solution to acidity for reaction, and after washing and filtering to obtain second filter residue, namely an amorphous yellow iron phosphate filter cake; subjecting the yellow iron phosphate filter cake to aging and heating, adding phosphoric acid and a second alkali solution for reaction, followed by washing and filtering to obtain third filter residue, namely a basic ammonium iron phosphate filter cake, then drying to obtain basic ammonium iron phosphate crystal powder; and subjecting the basic ammonium iron phosphate crystal powder to calcination for dehydration and cooling to obtain iron phosphate.
Disclosed are a wet sorting process for a waste lithium battery and application thereof, which belong to the field of battery material recycling. The wet sorting process includes the following steps of carrying out wet ball milling on a sorting material of a waste lithium battery to obtain a ball-milled product, screening the ball-milled product to obtain a coarse-grained screened material, a medium-grained screened material and a fine-grained screened material, carrying out wet ball milling, screening, magnetic separation and table concentration on the medium-grained screened material to obtain copper, aluminum and a steel shell, and carrying out flotation, magnetic separation and table concentration on the fine-grained screened material to obtain cathode material powder, graphite, copper and aluminum.
Disclosed are a ternary cathode material and a preparation method and application thereof. The ternary cathode material has a chemical formula of LiNix CoyMn(1-x-y)MO2, wherein 0.5≤x≤1, y≥0, M is at least one selected from the group of niobium, boron and titanium. In the present disclosure, through the reaction between the niobium compound, the boron compound or the titanium compound with the residual lithium on the surface of the calcinated materials, the micro powder deposits in the defect position of the lithium crystal lattice on the surface of the calcinated material, so that the content of the micro powder can be greatly reduced. Meanwhile part of the surface residual lithium is consumed by the reaction to generate lithium niobate, lithium borate or lithium titanate which is uniformly coated on the surface of the material, thereby obtaining the ternary cathode material with excellent cycle and rate performance.
H01M 10/0525 - Batteries du type "rocking chair" ou "fauteuil à bascule", p.ex. batteries à insertion ou intercalation de lithium dans les deux électrodes; Batteries à l'ion lithium
71.
Automatic production line for cascade utilization of power batteries
Disclosed is an automatic production line for cascade utilization of power batteries, which is sequentially provided along the transmission direction of materials with: an appearance detection system, a screening device, a transport system, a residual energy detection device, a tab installation device and an assembling system, and in addition, is provided with a grouping device and a film sticking device, where the grouping device is located among the residual energy detection device, the tab installation device and a grouping station.
H01M 10/48 - Accumulateurs combinés à des dispositions pour mesurer, tester ou indiquer l'état des éléments, p.ex. le niveau ou la densité de l'électrolyte
H01M 10/42 - Procédés ou dispositions pour assurer le fonctionnement ou l'entretien des éléments secondaires ou des demi-éléments secondaires
72.
Method for recycling battery by incomplete extraction
Disclosed is an incomplete extraction method for recycling batteries, which may include: introducing a pretreatment gas into a device loaded with a waste battery powder, and bringing a gas outlet into communication with absorption liquid A and absorption liquid B in order; raising the temperature and introducing the pretreatment gas; reducing the temperature and introducing a reaction gas; raising the temperature, introducing the reaction gas, and then introducing the pretreatment gas; and reducing the temperature, and turning off the pretreatment gas; adding an extractant to absorption liquid A, mixing the mixture, taking organic phase A, adding a stripping agent, and taking aqueous phase A; and adjusting the pH to acidity, then adding an extractant, taking organic phase B, adding a stripping agent to obtain a stock solution enriched in Li, Mn, Ni and Co.
C22B 3/38 - Traitement ou purification de solutions, p.ex. de solutions obtenues par lixiviation par extraction liquide-liquide utilisant des composés organiques contenant du phosphore
Disclosed are a doped nickel-rich ternary material and a preparation method thereof. The preparation method comprises the following steps: (1) Mixing a nickel source, a cobalt source, and a manganese source in a solvent to obtain a solution A, adding oxidant and doping elements to the solution A, and stirring to obtain solution B; (2) Adding a complexing agent and nitric acid to the solution B and stirring to obtain solution C; (3) Drying the solution C to obtain aerogel D; (4) Grinding the aerogel D, and subjecting it to low-temperature pre-calcinating, and heating the aerogel to perform first calcinating to obtain precursor powder E; (5) Mixing the precursor powder E with a lithium source to obtain a mixture, and subjecting the mixture to second calcinating, grinding, and screening to obtain the doped nickel-rich ternary material.
H01M 4/525 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de nickel, de cobalt ou de fer d'oxydes ou d'hydroxydes mixtes contenant du fer, du cobalt ou du nickel pour insérer ou intercaler des métaux légers, p.ex. LiNiO2, LiCoO2 ou LiCoOxFy
H01M 4/505 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de manganèse d'oxydes ou d'hydroxydes mixtes contenant du manganèse pour insérer ou intercaler des métaux légers, p.ex. LiMn2O4 ou LiMn2OxFy
74.
EXTRACTION METHOD FOR REMOVING ALUMINUM FROM TERNARY BATTERY MATERIAL LEACHATE
Disclosed is a method for removing aluminum in a ternary battery material leachate by adopting an extraction method, which comprises the following steps: (1) saponification: mixing an extraction solvent with a saponifying agent to obtain a saponified extraction solvent; (2) extraction: mixing the ternary battery material leachate with the saponified extraction solvent to obtain a loaded organic phase and a raffinate; (3) back extraction: mixing the loaded organic phase with a back-extraction agent, followed by performing a back-extraction to obtain an organic phase and a back-extraction solution; the extraction solvent comprises an extracting agent and a diluent. The extraction method is adopted to separate nickel, cobalt, manganese and aluminum, having the advantages of less heavy metal entrainment, short process flow, and high metal recovery rate. The extraction rate of the aluminum can reach 97.42 percent.
H01M 10/54 - Récupération des parties utiles des accumulateurs usagés
C22B 3/38 - Traitement ou purification de solutions, p.ex. de solutions obtenues par lixiviation par extraction liquide-liquide utilisant des composés organiques contenant du phosphore
The present disclosure belongs to the field of battery materials, and discloses a coated nickel-rich ternary material and a preparation method and application thereof. The coated nickel-rich ternary material has a chemical formula of LiNixCoyMnzO2·a[M3(PO4)2·bH2O], Where 0.6≤x≤0.8, 0.1≤y≤0.2, 0.1≤z≤0.2, x+y+z=1, 0.01≤a≤0.03, 3≤b≤8, M3(PO4)2·bH2O is at least one selected from the group consisting of nickel phosphate, cobalt phosphate and manganese phosphate; the coated nickel-rich ternary material has a flower-like structure. The preparation method of the present disclosure provides phosphate ions through the prepared phosphate solution, performs coating in a liquid phase environment, and synthesizes the precursor simultaneously by microwave hydrothermal synthesis, which is beneficial to the full contact between the phosphates and the precursor, and ensures the surface of the nickel-rich ternary precursor is uniformly coated with the phosphates. The method is simple and has good coating effect.
The present invention relates to the field of waste battery recycling, and discloses a method for treating waste diaphragm paper of a lithium battery, which includes the following steps of: (1) shearing and crushing waste diaphragm paper, and then carrying out pneumatic separation to obtain a light material and a copper-aluminum mixture; (2) putting the light material into a flotation machine for separation to obtain diaphragm paper and battery powder; and (3) pulping the battery powder, and then carrying out leaching of hydrometallurgy, pickling the diaphragm paper, and then filtering and spin-drying to obtain the diaphragm paper. According to the method, the diaphragm paper is treated by a method combining physics and chemistry, so that valuable metals in the waste diaphragm paper of the lithium battery are effectively recycled, and the industrial production requirements of environmental friendliness, low energy consumption and high resource recycling are satisfied.
H01M 50/403 - Procédés de fabrication des séparateurs, des membranes ou des diaphragmes
H01M 6/52 - Récupération des parties utiles des éléments ou batteries usagés
H01M 10/0525 - Batteries du type "rocking chair" ou "fauteuil à bascule", p.ex. batteries à insertion ou intercalation de lithium dans les deux électrodes; Batteries à l'ion lithium
H01M 10/54 - Récupération des parties utiles des accumulateurs usagés
B09B 3/70 - Traitement chimique, p.ex. ajustement du pH ou oxydation
B09B 3/30 - Destruction de déchets solides ou transformation de déchets solides en quelque chose d'utile ou d'inoffensif impliquant un traitement mécanique
A vacuum cracking method and a cracking apparatus for a power battery are disclosed. The vacuum cracking method includes the following steps that: waste power batteries are fed from a feed hopper and then enter a rolling unit for rolling treatment to obtain a crushed material; the crushed material is transported to a cracking unit for preheating, then heated and cracked under an inert atmosphere or vacuum to obtain cracked gas, solid cracked products and non-crackable products; and the solid cracked products and the non-crackable products are transported to a pyrolysis unit for pyrolysis at an aerobic atmosphere to obtain pyrolysis gas and non-pyrolysis products.
B09B 3/40 - Destruction de déchets solides ou transformation de déchets solides en quelque chose d'utile ou d'inoffensif impliquant un traitement thermique, p.ex. évaporation
C10B 53/00 - Distillation destructive spécialement conçue pour des matières premières solides particulières ou sous forme spéciale
H01M 10/54 - Récupération des parties utiles des accumulateurs usagés
The present invention discloses a method for power battery automatic fine-quantity sorting and an apparatus thereof, the method including the following steps of S1. The material is crushed, and leveled, and is then subjected to magnetic sorting processing to sort out iron powder; S2. The material after magnetic sorting is subjected to electrostatic processing to sort out positive electrode material powder; S3. The material after electrostatic processing is subjected to bounce processing to sort out the collector and graphite powder. A magnetic sorting device, an electrostatic sorting device, and a bouncing sorting device are accordingly provided.
B03C 7/08 - Séparateurs ayant des supports pour le matériau traité, en forme de bandes
B03B 9/06 - Disposition générale d'un atelier de séparation, p.ex. schéma opératoire spécialement adapté aux ordures
B03C 1/18 - Séparation magnétique agissant directement sur la substance à séparer ayant des supports pour le matériau traité en forme de bandes avec des aimants se déplaçant pendant l'opération
Disclosed is a device for automatically dismantling a power battery module, including a cutting platform, a clamping mechanism, a first cutting mechanism, a second cutting mechanism, a turnover mechanism, and a stripping mechanism. The clamping mechanism is disposed on the cutting platform. The first cutting mechanism includes a first cutting blade, a cutting blade set, and a first drive assembly. The second cutting mechanism includes a third cutting blade, a fourth cutting blade, and a third drive assembly. The first cutting blade, the cutting blade set, the third cutting blade, and the fourth cutting blade are vertically movable. The cutting blade set includes a plurality of second cutting blades that are movable relative to each other.
H01M 6/00 - PROCÉDÉS OU MOYENS POUR LA CONVERSION DIRECTE DE L'ÉNERGIE CHIMIQUE EN ÉNERGIE ÉLECTRIQUE, p.ex. BATTERIES Éléments primaires; Leur fabrication
H01M 10/54 - Récupération des parties utiles des accumulateurs usagés
The invention discloses a vacuum cracking apparatus for a power battery and a cracking method thereof. The cracking device includes a cylinder and further includes a rolling device, a first sealing device, a cracking device, a second sealing device, a pyrolysis device and a third sealing device which are arranged from top to bottom. The cracking device for the power battery of the present invention is equipped with the first sealing device, the second sealing device and the third sealing device to isolate the cracking device from the pyrolysis device and be capable of realizing material transmission and gas isolation without interference with each other, so that gas stirring between an anaerobic zone and an aerobic zone is avoided; and by combing battery cracking and battery pyrolysis, with cracked gas discharged after cracking as a fuel for cracking and pyrolysis or preheating a pyrolysis device, resources are fully used.
B02C 4/02 - Broyage ou désagrégation par broyeurs cylindriques par plusieurs meules
B09B 3/40 - Destruction de déchets solides ou transformation de déchets solides en quelque chose d'utile ou d'inoffensif impliquant un traitement thermique, p.ex. évaporation
B02C 23/38 - Addition de fluide, dans un but autre que celui de broyer ou de désagréger par l'énergie du fluide dans des appareils comportant plusieurs zones de broyage ou de désagrégation
C10B 47/44 - Autres procédés dans des fours munis de transporteurs mécaniques avec des transporteurs à vis
C10B 53/00 - Distillation destructive spécialement conçue pour des matières premières solides particulières ou sous forme spéciale
F23G 5/027 - Procédés ou appareils, p.ex. incinérateurs, spécialement adaptés à la combustion de déchets ou de combustibles pauvres comportant un traitement préalable par pyrolyse ou par gazéification
F23G 5/033 - Procédés ou appareils, p.ex. incinérateurs, spécialement adaptés à la combustion de déchets ou de combustibles pauvres comportant un traitement préalable consistant en une désagrégation ou un broyage
F23G 5/44 - Procédés ou appareils, p.ex. incinérateurs, spécialement adaptés à la combustion de déchets ou de combustibles pauvres - Parties constitutives; Accessoires
F23G 7/00 - Procédés ou appareils, p.ex. incinérateurs, spécialement adaptés à la combustion de déchets particuliers ou de combustibles pauvres, p.ex. des produits chimiques
H01M 10/54 - Récupération des parties utiles des accumulateurs usagés
Disclosed are a photocatalyst and application thereof in environmentally friendly photocatalytic treatment of a power battery. The photocatalyst is obtained by loading Ag—TaON on a hollow glass microsphere, wherein a mass ratio of the Ag—TaON to the hollow glass microsphere is 1:5 to 10. According to the invention, the Ag—TaON and the hollow glass microsphere are compounded, the hollow glass microsphere has better light permeability, which avoids mutual shielding between catalysts, such that the photocatalyst filled in a reactor is fully excited, which is capable of effectively improving a light utilization rate, thus improving the catalytic conversion efficiency of the photocatalyst.
Disclosed is a method for recycling a hydrogen fuel cell of a new energy vehicle, including the following steps of: (1) discharging and disassembling a hydrogen fuel cell in turn to obtain a hydrogen supply system, an air supply system, a cooling system and a galvanic pile; (2) disassembling the galvanic pile into a catalyst and carbon cloth, and ashing to obtain ash; (3) adding an auxiliary agent into the ash, mixing, introducing inert gas, heating, introducing oxidizing gas, and absorbing tail gas by using an ammonium salt solution; and (4) adding a reducing agent into the ammonium salt solution absorbing the tail gas in step (3) to react, filtering, taking and cleaning a filter residue to obtain Pt.
H01M 8/00 - PROCÉDÉS OU MOYENS POUR LA CONVERSION DIRECTE DE L'ÉNERGIE CHIMIQUE EN ÉNERGIE ÉLECTRIQUE, p.ex. BATTERIES Éléments à combustible; Leur fabrication
H01M 8/008 - PROCÉDÉS OU MOYENS POUR LA CONVERSION DIRECTE DE L'ÉNERGIE CHIMIQUE EN ÉNERGIE ÉLECTRIQUE, p.ex. BATTERIES Éléments à combustible; Leur fabrication Élimination ou recyclage des éléments à combustible
Disclosed is a method for purification and lattice reconstruction of graphite in a power battery, which includes the following steps: subjecting a waste power battery to discharging, coarse breaking, pyrolysis, fine breaking and sorting sequentially to obtain electrode material powder; mixing the electrode material powder with a metal extractant, standing still, then washing with a purifying agent A, filtering to obtain a filter residue A, mixing the filter residue A with the metal extractant, standing still, then washing with a purifying agent B, and filtering to obtain a crude graphite; subjecting the crude graphite to the de-organic treatment, cooling, ball milling, and ventilation replacement to obtain a primary purified graphite; and introducing a rare gas into a primary purified graphite to repair the graphite lattice.
brevets
