Abstract: Disclosed is a processing device for a lithium battery positive electrode material, including a base, where the base is fixedly provided with barrel bodies by means of a support, a sleeve is rotatably clamped between the two barrel bodies, a stirring assembly transversely penetrates through interiors of the barrel bodies and the sleeve, the base is further provided with a power mechanism, and the power mechanism separately drives the sleeve and the stirring assembly to rotate. Due to the cooperation of the barrel bodies, the sleeve and the stirring assembly, the stirring assembly can effectively scrape attachments on the inner walls of the barrel bodies, and a first stirring blade in the sleeve and a second stirring blade in the stirring assembly are cooperated to stir, gather and further disperse and disarrange the material, such that the material can be mixed more uniformly.

Abstract: The present disclosure discloses a method for recycling a lithium-ion battery electrolyte. After the waste lithium-ion battery is discharged, it is frozen and disassembled to obtain a battery cell containing an electrolyte. The battery cell is immersed in a lithium hydroxide solution containing a catalyst for reaction. The battery cell after the reaction is taken out and washed. The washing solution is mixed with the lithium hydroxide solution after the reaction to obtain a mixed solution. The mixed solution is filtered to obtain a filtrate and a filter residue. The filter residue is reacted with a hydrofluoric acid solution to obtain anhydrous lithium salt. The anhydrous lithium salt is mixed with an organic solution, and PF5 gas is introduced. The mixture is reacted, and filtered to obtain an organic liquid. The organic solution is frozen and filtered to obtain lithium hexafluorophosphate.

Abstract: A method for recycling and treating an electrolytic solution of a lithium ion battery includes S1: cooling a fully discharged lithium ion battery below a freezing point of the electrolytic solution, and then disassembling and crushing the lithium ion battery to obtain a crushed solid containing the electrolytic solution, S2: under a protection of an inert gas, placing the crushed solid in a supercritical CO2 extraction instrument in which an entrainer is added; S3: conducting extraction; and S4: collection an extraction product with a cryogenic device, and adsorbing water in the extraction product using a 4 ? type lithiated molecular sieve, adsorbing HF in the extraction product using weak-base anion-exchange resin and adsorbing organic acid and alcohol in the extraction product using a 5 ? type lithiated molecular sieve.

Abstract: Disclosed is an apparatus for efficiently pretreating and recycling a waste battery, which includes a bottom plate, a recycling device, a conveying device and a treatment device, and one end of a top portion of the bottom plate is fixedly mounted with a bottom portion of the conveying device. According to the invention, by arranging a fixing assembly and the recycling device, a suction pump can suck a slurry and an electrolyte in a battery downwardly for dropping, and a driving assembly can rapidly convey the slurry and the electrolyte in the battery to the treatment device for treatment at the same time.

Abstract: Disclosed is a method for preparing a graphene-based sodium ion battery negative electrode material, including adding graphene oxide into ethanol absolute, carrying out ultrasonic treatment at a certain temperature to obtain a graphene oxide alcohol dispersion, then preparing a sodium hexanitritocobaltate solution, adding the graphene oxide alcohol dispersion into the sodium hexanitritocobaltate solution, carrying out solid-liquid separation to obtain a solid, isolating the solid from oxygen for calcination, and washing and drying to obtain a graphene-based sodium ion battery negative electrode material.

Abstract: 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.

Abstract: Guaianolide oligomers 1-4 are represented by structural formula (I), a preparation method thereof, and a pharmaceutical composition thereof and the use thereof. The preparation method includes: the preparation of guaianolide diene via epoxy isomerization from arglabin-DMA, and a Diels-Alder reaction between the diene and sesquiterpenoid or oligomeric sesquiterpenoid containing ?, ?-unsaturated ?-lactone fragments and subsequent deprotection of NMe2 to obtain the guaianolide oligomers. The guaianolide oligomers inhibited the growth of human hepatoma cell lines HepG2, Huh7 and SK-Hep-1, and can form a pharmaceutical composition with a pharmaceutically acceptable carrier or excipient to be used for preparing an antihepatoma drug.

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: The present embodiments of the invention disclose methods for implementing ZmARGOS9 gene in drought resistance and high yield of maize. ZmARGOS9 is overexpressed in maize in the present disclosure. The high expression of ZmARGOS9 gene improves the drought resistance and yield of maize. Accordingly, it enables enrichment of drought-resistant and high-yielding genes, contributing to the security of the seed industry.

Abstract: An electronic device is provided that includes one or more image sensors configured to capture a video feed, an image signal processor configured to perform color correction on the captured video feed based on a brightness level computed from the captured video feed and/or based on a color temperature or illuminant type of the lighting in the captured video feed to generate a corresponding color corrected video feed using a first chromatic adaptation model that is adapted to an immersive viewing condition, and one or more displays configured to output the color corrected video feed. The electronic device can further include a recording pipeline configured to record a version of the captured video feed and can share or transmit the recorded content to an external device. The external device can display the recorded content using a second chromatic adaptation model that is adapted to a non-immersive viewing condition.

Abstract: A method for preparing a zinc manganate anode material is disclosed. The method includes the following steps: (1) preparing a solution A containing a manganese ion and a solution B containing zinc alkali; (2) dispersing an adsorption carrier into the solution B; (3) using an alkali solution as a base solution and adding the solution A, the solution B and an oxidant solution to the base solution while stirring; (4) conducting a solid-liquid separation of the materials after reaction to obtain a solid; and (5) washing, drying and calcining the solid to obtain a zinc manganate anode material.

Abstract: Disclosed in the present invention are an NCA positive electrode material precursor having a core-shell structure, a method for preparing same, and use thereof. The precursor is a spherical or spheroid particle and consists of an outer shell and an inner core. The outer shell has a chemical general formula of NiaCobAlc(OH)2+c, wherein a+b+c=1, 0.45?a?0.55, 0.15?b?0.25, and 0.25?c?0.35; the inner core has a chemical general formula of NixCoyAlz(CO3)1?z(OH)3z, wherein x+y+z=1, 0.85?x<0.98, 0<y?0.15, and 0<z?0.15. The inner core has a porous structure. The inner core in the precursor of the present invention has a high nickel content and a porous structure, which can effectively buffer the volume change caused by subsequent charging and discharging of the NCA positive electrode material. The outer shell is a low-nickel material, which alleviates the volume change caused by the high nickel content.

Abstract: Provided are a template growth method for preparing a lithium cobaltate precursor and use. The method comprises: S1: mixing an aqueous ammonium metavanadate solution with a polyvinylpyrrolidone solution for hydrothermal reaction, and calcining the obtained precipitate under an aerobic atmosphere to obtain a vanadium pentoxide structure-directing agent, wherein the polyvinylpyrrolidone solution is prepared by dissolving polyvinylpyrrolidone in an alcohol; S2: adding the vanadium pentoxide structure-directing agent to a cobalt salt solution to obtain a turbid liquid, adding the turbid liquid, a carbonate solution, and a complexing agent in a parallel flow mode for reaction, and performing aging when the reaction material reaches a target particle size; and S3: performing solid-liquid separation on the aged material, and anaerobically calcining the obtained precipitate before aerobic calcination to obtain a lithium cobaltate precursor.

Abstract: Disclosed in the present invention are a wastewater adsorbent, and a preparation method therefor and the use thereof. The method comprises: mixing a carbon black powder and an ammonium salt solution, heating same for a hydrothermal reaction, followed by filtering, and washing the obtained filter residues with acid to obtain an ammonium-salt-modified carbon black; mixing and grinding a nickel-cobalt-manganese mixed salt and a sodium salt to obtain a mixture, mixing the mixture with an organic acid solution, evaporating same to remove water, subjecting same to a heating reaction in an inert atmosphere, and subjecting the reacted material to acid pickling to obtain a nickel-cobalt-manganese-sodium mixed salt; and mixing the nickel-cobalt-manganese-sodium mixed salt, the ammonium-salt-modified carbon black and a binding agent, and compacting, drying and heating same to obtain a multimetal-carbon-based adsorbent.

Abstract: A battery conveyor belt includes a base, a plurality of parallel connecting shafts arranged on the base at intervals, and a plurality of conveying wheels arranged on the connecting shafts and each include a stator sleeved on the connecting shaft and fixed thereto, a rotor, a coil sleeved outside the stator, a pusher, a receiver located on the rotor, a control circuit, and a hub; the rotor is sleeved outside the coil, and there is a gap between the rotor and the coil; the hub is sleeved outside the rotor, and a first bearing is connected between the hub and the rotor; the pusher is connected to the hub and the rotor; the rotor drives the hub to rotate through the pusher; the control circuit is electrically connected to the coil and the receiver; and when a battery is placed on the hub, the pusher is pressed against the receiver.

Abstract: The present disclosure discloses a porous and spherical cobalt oxide particle and a preparation method therefor. The preparation method includes the following steps: (1) mixing a cobalt salt solution, thiourea, and urea to obtain a mixed solution; (2) heating the mixed solution obtained in step (1) to allow a reaction in an aerobic atmosphere; (3) conducting solid-liquid separation (SLS) to obtain a solid product, and subjecting the solid product to calcination in an aerobic atmosphere to obtain a calcined material; and (4) washing and drying the calcined material obtained in step (3) to obtain the porous and spherical cobalt oxide particle. The cobalt oxide particle prepared by the preparation method has a larger specific surface area (SSA), which can significantly improve a specific capacity of a battery.

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: The present application discloses a nickel-cobalt-manganese ternary positive electrode material nanorod and the use thereof. The chemical general formula of the nickel-cobalt-manganese ternary positive electrode material nanorod is LiNi1-x-y-zCoxMnyAlzO2, where 0<x<1, 0<y<1, and 0?z?0.05; the nickel-cobalt-manganese ternary positive electrode material nanorod has a section diameter of 50-200 nm and a length of 0.1-5 ?m. In the present application, a mixed metal salt solution of nickel, cobalt, manganese, aluminum and lithium and 8-hydroxyquinoline are subjected to complex-precipitation to generate a precipitate containing nickel, cobalt, manganese, aluminum and lithium, and then the precipitate is calcined to prepare a ternary positive electrode material nanorod.

Abstract: The present disclosure discloses a silicon-aluminum-iron composite material and a preparation method therefor and use thereof, and belongs to the technical field of wastewater treatment. The silicon-aluminum-iron composite material comprises an inner core and an outer shell wrapping the inner core; the inner core is a silicon-aluminum-based hollow sphere; the outer shell contains iron element; and there are holes on the silicon-aluminum-iron composite material. The silicon-aluminum-iron composite material of the present disclosure improves the specific surface area of the silicon-aluminum-iron composite material through structural adjustment. When it is used to adsorb heavy metal ions, the adsorption sites are correspondingly increased, which finally improves the adsorption capacity for heavy metal ions.

Abstract: The present disclosure discloses a method for recovering active material from waste battery by desorption, comprising steps of: reacting wound cores of cathode and anode current collectors of waste battery with carbon tetrachloride and chlorine to obtain remaining wound cores, a solution of aluminum chloride in carbon tetrachloride and a first desorption powder of cathode; soaking the remaining wound cores and the first desorption powder of cathode in water to obtain soaked wound cores, a lithium salt solution and a second desorption powder of cathode; and reacting the soaked wound cores with nitric acid to obtain a copper nitrate solution and a desorption powder of anode. The waste lithium-ion battery only needs to be discharged and disassembled, and no shredding process is required, which avoids steps of shredding and sorting, reduces equipment investment. In addition, cathode and anode materials can be effectively recovered, and the product has high economic value.