Abstract: 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.

Abstract: 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.

Abstract: A method of preparing lithium iron phosphate by recycling and utilizing waste batteries. The method may include pre-processing a waste lithium iron phosphate battery to obtain lithium iron phosphate powder, adding alkaline liquid to the lithium iron phosphate powder, and filtering to obtain a filter residue; an iron source, a lithium source or a phosphorus source to the filter residue, and performing ball milling to obtain a ball-milled product; preparing a carbon source solution, and adding a surfactant to the carbon source solution to obtain a mixed solution; mixing the ball-milled product and the mixed solution, performing spray pyrolysis to obtain a high-temperature powder, spraying atomized water to the high-temperature powder to remove impurities, and then calcining to obtain a finished product of lithium iron phosphate.

Abstract: Disclosed is a method for producing battery-grade nickel sulfate by using laterite nickel ore comprising the following steps: sorting the laterite nickel ore to obtain lump ore and sediment ore; crushing the lump ore, and then performing heap leaching, to obtain a crude nickel sulfate solution A; separating the sediment ore to obtain high chromium ore, low iron, high magnesium ore, and high iron, low magnesium ore, and drying, roasting, reducing, and sulfurating the low iron, high magnesium ore to obtain low nickel matte; blowing and performing water extraction on the low nickel matte, and then performing oxygen pressure leaching, to obtain a crude nickel sulfate solution B; performing pressure leaching on the high iron, low magnesium ore to obtain a crude nickel sulfate solution C; and performing extraction on the crude nickel sulfate solutions A, B, and C, and then evaporating and crystallizing, to obtain battery-grade nickel sulfate.

Abstract: 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.

Abstract: 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.

Abstract: A reaction kettle cleaning apparatus, includes a kettle body and a stirrer, the stirrer being located in the kettle body and including a stirring rod and a stirring portion, where a movable frame is disposed on the stirring rod and is movable along the stirring rod; and a cleaning device is disposed on the movable frame is configured to clean the kettle body; and the reaction kettle cleaning apparatus further includes a movable control apparatus configured to control the movable frame to move.

Abstract: 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.

Abstract: 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.

Abstract: 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.

Abstract: 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.

Abstract: 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.

Abstract: A fire-extinguishing agent capable of extinguishing the combustion of aluminum slag, and a preparation method therefor and the use thereof. The fire-extinguishing agent comprises the following raw materials: a sulfate, a chlorine salt, a mineral, a silica gel, a surfactant and a stearate. The main materials of sulfate and chlorine salt are solid waste containing sulfate and chlorine salt obtained by separating high-salt wastewater generated during a resynthesis process of a positive electrode material of a waste lithium battery. The solid waste containing sulfate and chlorine salt is used as a material for a fire-extinguishing agent, which can effectively recycle waste resources.

Abstract: 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.

Abstract: 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<x?1, 0.01?a?0.2, and M is one or two of W and Mo. The preparation method comprises: preparing a manganese salt solution and a basic potassium permanganate solution mixed with an M element material, wherein the M element material is one or two of molybdate or tungstate; adding the basic potassium permanganate solution to the manganese salt solution, and potassium permanganate solution to the manganese salt solution, and after a reaction is finished, carrying out solid-liquid separation to obtain a solid material; and washing and drying the solid material, mixing the solid material with a sodium source, and then sintering same to obtain a layered sodium ion battery positive electrode material.

Abstract: 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.

Abstract: 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.

Abstract: 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.

Abstract: 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%.

Abstract: 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.