1423 results about "Nickel salt" patented technology

A method of preserving wood includes injecting into the wood an effective amount of a aqueous wood-injectable biocidal slurry, said a wood-injectable biocidal slurry containing dispersants and sub-micron biocidal particles selected from at least one of the following classes: 1) a plurality of particles containing at least 25% by weight of a solid phase of sparingly soluble salts selected from copper salts, nickel salts, tin salts, and/or zinc salts; 2) a plurality of particles containing at least 25% by weight of a solid phase of sparingly soluble metal hydroxides selected from copper hydroxide, nickel hydroxide, tin hydroxide, and/or zinc hydroxide; 3) a plurality of particles containing at least 25% by weight of a solid phase comprising a substantially-insoluble organic biocide selected from triazoles, chlorothalonil, iodo-propynyl butyl carbamate, copper-8-quinolate, fipronil, imidacloprid, bifenthrin, carbaryl, strobulurins, and indoxacarb; 4) a plurality of particles containing on the outer surface thereof a substantially-insoluble organic biocide; 5) a plurality of particles containing a solid phase of a biocidal, partially or fully glassified composition comprising at least one of Zn, B, Cu, and P. The particles may advantageously contain metallic copper, a leachability barrier, pigments, dyes, or other adjuvants disposed on the outer surface thereof.

The invention discloses a method for preparing nickel cobalt aluminum serving as a cathodic material of a lithium ion battery, which comprises the following steps of: mixing nickel salt solution and cobalt salt solution uniformly, adding complexing agent solution, precipitant solution and the mixed solution into a reaction kettle with base solution in a parallel flow mode to perform precipitation reaction, performing solid-liquid separation after the reaction is performed fully, and washing; adding the washed solid material into the reaction kettle, dripping aluminum salt solution and the precipitant solution slowly to perform secondary precipitation reaction, so that an aluminum element is precipitated on the surface of the solid material gradually, stirring continuously in the integral process, performing solid-liquid separation after the reaction is finished, and washing and drying the solid material to a precursor of the cathodic material of the lithium ion battery; and mixing the precursor and a lithium source, performing two-section sintering under the condition of introducing oxygen, and crushing the calcined material which is subjected to the two-section sintering and performing subsequent processing to obtain the nickel cobalt aluminum serving as the cathodic material of the lithium ion battery. The method has the advantages of low requirement on equipment, high automation degree, environment friendliness, few wastes, high quality of products and the like and is easy to operate.

The invention relates to a preparation method of nickel-coated alumina oxide powder, in particular to the preparation method of nickel-coated aluminum oxide powder for thermal spraying in aviation, aerospace and military fields. The invention is characterized in that: a suspension is made from a mixing liquid of nano-aluminum oxide and dispersant, stirred and added with nickel salt solution at the same time, and the obtained mixture liquid is dropped with ammonium water after being fully stirred, added with distilled water, when dark blue mixing solution C of nickel ammonia complex ([Ni (NH3)) 2+and alumina oxide is obtained; the mixing solution C is aged by water, filtered, washed and dried, and a green middle coated product is obtained; the green middle coated product is further reduced and roasted, finally, black nickel-coated aluminum oxide powder is prepared. The nickel-coated aluminum oxide powder prepared through the invention has uniform granularity, with average size less than or equal to 1.0Mum, and can enhance the application performance of nano-alumina and expand the application of nano-aluminum oxide; the product is mainly used for aviation, aerospace and military materials and other high-tech fields. The method of the invention is simple, reproducible and easy to be industrialized.

The invention relates to a rare-earth doping modified lithium ion battery ternary positive electrode material and a preparation method of the rare-earth doping modified lithium ion battery ternary positive electrode material. The chemical general formula of the material is as follows: LiNiaCo<1-a-b>MnbRxO2/M, wherein a is more than 0 and less than 1, b is more than 0 and less than 1, (1-a-b) is more than 0 and less than 1, x is more than 0.005 and less than 0.1, R is one or more of rare-earth lanthanum, cerium, praseodymium and samarium, and M is a composite cladding layer of oxide of aluminum, titanium or magnesium and carbon. The soluble metal nickel salt, cobalt salt, manganese salt and rare-earth compound are mixed to prepare a mixed salt solution, the mixed salt solution is reacted with a mixed alkaline solution prepared by mixing NaOH and ammonium hydroxide, after the reaction solution is filtered, washed and dried, the obtained product is uniformly mixed with lithium salt powder to be ball milled, then the mixture is calcined at the high temperature and coated with the composite cladding layer of the aluminum, titanium or magnesium oxide and carbon, and finally the calcined mixture is calcined at a constant temperature to obtain the rare-earth doping modified lithium ion battery ternary positive electrode material. After doping the rare earth, the metal oxide and carbon composite cladding layer, which are cheap and easy to obtain, are adopted, so that the cycling performance and the rate performance can be improved, and the charging-discharging efficiency of the material also can be improved.

The invention involves an aluminum or aluminum alloy super-hydrophobic surface preparation method. The method is: polishing the surface of aluminum or aluminum alloy using metallographic sandpaper or polishing paste, pure water washing, acetone ultrasonic cleaning, pure water washing and other clean treatment, handing it with chemical etching solution containing nitric acid and metal salts (copper or nickel salt) 30s-20min under 90 ~ 100 degree C, then coating low surface energy material on its surface to get super-hydrophobic property. The aluminum or aluminum alloy surface treated by the invention has excellent hydrophobicity, the contact angle of water and surface can be as high as 150-165 degree, droplets are easy to roll on the surface. The method of the invention need not complex equipment, cost is low, technology is simple and repeatability is good.

Disclosed herein are antimicrobial compositions comprising an effective concentration of a metal salt combined with a plant extract. In some embodiments the composition comprises a copper salt and/or an iron salt and/or a nickel salt and/or a cobalt salt; and an extract of a plant selected from a group consisting of Punka granatum, Viburnum plicatum, Camellia sinensis, and Acer spp. The invention extends to uses of such compositions as medicaments, and to methods of treating microbial infections. The invention extends to methods for preventing microbial infections by coating objects and surfaces with the compositions.

The invention relates to a modified lithium ion battery ternary positive electrode material and a preparation method of the modified lithium ion battery ternary positive electrode material. The chemical generation formula of the material is as follows: LiNiaCo<1-a-b>MnbBxO2/TiO2, wherein a is more than 0 and less than 1, b is more than 0 and less than 1, (1-a-b) is more than 0 and less than 1, x is more than 0.005 and less than 0.1, and the TiO2 is a cladding layer. The soluble nickel salt, cobalt salt and manganese salt are prepared into a mixed salt solution, the mixed salt solution is reacted with a mixed alkaline solution prepared by mixing the NaOH and ammonium hydroxide, after being filtered, washed and dried, the reaction product is mixed with a boronic compound and roasted for 4h to 12h at the temperature of 300 to 800 DEG C under an air atmosphere, then the roasted product is ball milled with the lithium salt to be uniformly mixed together, the mixture is coated with titanium dioxide after being calcined at the high temperature to obtain the modified lithium ion battery ternary positive electrode material. The prepared boron doping modified ternary positive electrode material is high in specific capacity and good in cycling performance.

The invention relates to a nickel cobaltate-graphene composite material and a preparation method thereof. The composite material comprises graphene and nickel cobaltate, wherein nickel cobaltate nanowires are uniformly grown on a graphene sheet, the wire length of the nickel cobaltate nanowires is 50-300nm, and the wire width is 5-30nm. The preparation method comprises the following steps of: taking a graphene oxide water solution and a cobalt salt and nickel salt water solution which are dispersed in an ultrasonic manner, mixing, further adding a precipitator, uniformly stirring and mixing, transferring into a high-temperature reaction kettle, performing hydro-thermal reaction for a certain period of time, filtering, washing and drying an obtained product, and further performing thermal treatment so as to obtain the nickel cobaltate nanowire-graphene composite material. The nickel cobaltate nanowire-graphene composite material prepared by the method disclosed by the invention has the advantages of high single-electrode capacitance and good cycle performance, and is suitable for being used as an electrode material of a super-capacitor.

The invention relates to a method for preparing a catalyst for preparing synthesis gas by reforming methane and carbon dioxide, which comprises the following steps: soaking a carrier into a mixed solution of cerium(III) nitrate and lanthanum nitrate, and drying and roasting the soaked carrier for 2 to 10 hours to obtain a modified carrier (A); soaking the (A) into a soluble nickel salt solution orsoaking the (A) into a chloroplatinic acid solution, and drying and roasting the soaked carrier to obtain (B) or (C); soaking the (B) into the chloroplatinic acid solution or soaking the (C) into thesoluble nickel salt solution, and drying and roasting the soaked carrier to obtain a catalyst precursor, or soaking the modified carrier into a mixed solution of the soluble nickel salt solution andthe chloroplatinic acid, and drying and roasting the soaked carrier to obtain a catalyst precursor; and reducing the precursor in hydrogen and nitrogen mixed gas to obtain the catalyst. The catalyst has the advantages of low cost, good catalytic activity under the reaction condition of large space velocity, high selectivity for H2 and CO, and good sintering resistance and carbon deposition resistance.

The invention discloses a method for preparing a nickel cobalt lithium aluminate cathode material. The method comprises the following steps of: uniformly mixing a nickel salt solution, a cobalt salt solution and an aluminum salt solution in a certain mole ratio of metal ions; adding a complexing agent solution, a precipitator solution and a metal salt solution together into a high-speed stirring reaction kettle with a base solution, and performing precipitation reaction; after complete reaction, performing oxidizing reaction on discharged slurry and an oxidizing agent with certain concentration in an alkaline environment; after the oxidizing reaction is finished, performing solid liquid separation on the slurry, washing in pure water, and drying to obtain a nickel cobalt aluminum hydroxyl oxide precursor of a lithium ion battery cathode material; fully mixing the precursor with a lithium source, and performing multi-step sintering in an oxygen atmosphere; and performing crushing and subsequent treatment on a material obtained by sintering, and thus obtaining the nickel cobalt lithium aluminate cathode material. The method is low in equipment requirement, simple in flow, low in energy consumption and low in waste. The produced material is high in tap density and high in capacity.

The invention discloses a novel cleaning plating technology by using an ionic liquid which is a non-aqueous media as an electroplate liquid. Through using the technology, problems of bad environment and unstable qualities of electroplates existing in the condition of electroplating zinc, nickel, molybdenum and their alloys in an aqueous system can be solved. Qualities of coatings generated by using the technology are better than the qualities of coatings generated in the traditional system. The technology comprises the following steps: dissolving zinc salts, nickel salts and molybdate salt into the ionic liquid which is regarded as an electrolyte to prepare the electroplate liquid; electroplating at a current density of 1-30mA/cm2, wherein metallic zinc, nickel, molybdenum and their alloys are taken as soluble anode or graphite, complex carbon, glassy carbon, metal tungsten and titanium base plating platinum are taken as insoluble anode, and components which are needed to be electroplated are taken as cathode. Needed depth of coating can be obtained through controlling the current density and electroplating time.

The invention discloses an eggshell type nickel-based catalyst and a preparation method and application thereof, belonging to the technical field of nickel-based catalysts and aiming at developing the eggshell type nickel-based catalyst for meeting the demand. The research shows that the eggshell type nickel-based catalyst can be prepared by dissolving nickel salt into ammonia water solution, loading the mixed solution on a catalyst carrier by adopting a spraying or immersing mode, drying, roasting and reducing. The active component of nickel is mostly centralized in an area from the surface of the carrier to the part of 0.7mm below the surface and can remarkably improve the conversion rate and the selectivity of the catalyst. The invention can be applied to the technical fields of hydrogen addition and trace amount of carbon monoxide removal from hydrogen and the like.

The invention relates to a method for preparing aluminum-coated anode materials of lithium-ion batteries, which is characterized in that: firstly, soluble nickel salts, cobalt salts, and manganese salts are formulated into salt solutions, and then mixed with ammonia-water-mixed sodium hydroxide or potassium hydroxide solutions React to form precursor particles, wash and dry; add water to the dried precursor particles to prepare a flowable slurry, stir, and add trivalent aluminum salt solution and sodium hydroxide or potassium hydroxide solution dropwise to the slurry at the same time , to obtain the precursor of nickel hydroxide cobalt manganese coated with aluminum; then mix the precursor with lithium source, and then sinter to obtain the positive electrode material of lithium ion battery coated with aluminum. The present invention has the following obvious advantages: raw materials are easy to obtain; coated The process conditions are easy to control, and it is easy to obtain a relatively uniform coating body; the prepared positive electrode material can make the lithium ion battery have superior high temperature stability and better cycle characteristics.

The invention relates to a preparation method for a double-metal-sulfide catalyst. Soluble molybdate and nickel salt or cobalt salt serves as a raw material, thiourea or thioacetamide serves as a sulfur source, and a Ni(Co)-S/MoS2 catalyst is prepared through a two-step hydrothermal method. The method particularly comprises the following steps: MoS2 is prepared in a high pressure reactor through the hydrothermal method first, then the nickel salt or cobalt salt and the sulfur source are added into the reactor of the obtained MoS2 to be evenly mixed, the reactor is sealed and heated, a reaction is conducted for a certain period of time, and Ni-S or Co-S is deposited on the MoS2, so that the Ni(Co)-S/MoS2 catalyst is prepared. The preparation method is characterized in that the specific area of the Ni(Co)-S/MoS2 catalyst prepared through the two-step hydrothermal method is large, high temperature vulcanization is not required in the preparation process, the preparation condition is mild, the catalyst is used for hydrodeoxygenation, a target product has high yield and good repeatability, and hydrodeoxygenation activity of the catalyst is high.

The invention discloses a preparation method of a high density nickel cobalt lithium manganate positive electrode material, LiNixCoyMnzO2. The preparation method comprises the following steps: firstly, mixing a nickel salt solution, a cobalt salt solution and a manganese salt solution according to a certain mol ratio, adding the mixed solution, a complexing agent solution and a precipitant solution together to a stirring reaction kettle with a base solution, fully reacting, carrying out solid-liquid separation, and washing and drying to obtain a globular nickel cobalt manganese oxyhydroxide precursor; calcining the precursor at the temperature of 350-900 DEG C for 2-20 hours to obtain a globular nickel cobalt manganese oxide precursor, and smashing the globular nickel cobalt manganese oxide precursor at high speed to obtain a mono-crystalline nickel cobalt manganese oxide precursor; mixing a lithium source and the mono-crystalline precursor according to a certain mol ratio, calcining at the temperature of 700-980 DEG C for 2-20 hours, and smashing and classing to obtain the mono-crystalline nickel cobalt lithium manganate positive electrode material. The preparation method provided by the invention has the advantages that the compacted density of the prepared nickel cobalt lithium manganate material is large, the specific capacity is high, the rate property and consistency are good, the preparation method is simple, and the preparation process is easy to control and operate.

The invention relates to a method for preparing a lithium-enriched lithium manganese oxide solid solution cathode material. The method comprises the following steps of: adding a mixed aqueous solution of nickel salt, cobalt salt and manganese salt into an oxalic acid or oxalate aqueous solution by an oxalate coprecipitation high-temperature solid state method, and stirring and reacting to generate nickel, cobalt and manganese oxalate coprecipitation; performing solid and liquid separation, washing and drying to obtain a nickel, cobalt and manganese oxalate precursor; and mixing and grinding the precursor and lithium salt, drying, baking at high temperature in an air atmosphere, and thus obtaining the lithium-enriched lithium manganese oxide solid solution cathode material. During preparation of the precursor, the proportion of the nickel salt, the cobalt salt and the manganese salt is adjusted, so that the constituents of the lithium-enriched lithium manganese oxide solid solution cathode material can be adjusted flexibly. The preparation method is suitable for large-scale, economic, stable and reliable production of the lithium-enriched lithium manganese oxide solid solution cathode material, has obvious advantages, and is high in practical value.

The present invention discloses a high -vibration -shaped triggea orthopedic material preparation method. Put nickel salt, cobalt salt, manganese salt and alkaline aquatic solution, complexing agent in the reactor.Synthetic spherical or spherical ternary orthopedic material front -drive body, chemical formula is NIXCOYMNZ (OH) 2,0.5 ≤ x ≤1,0≤y ≤ 0.5, 0 ≤Z ≤ 0.5, x+y+z = 1, add alkaline pH pHSurface treatment, washing dry and drying the three -yuan positive electrode material front drive body.The present invention improves the processing performance of ternary positive electrode materials, vibrating density, overcoming material capacity and stability defects. By controlling the appearance and particle size of the front -drive body, the materialization performance of the three yuan positive pole material is achieved, and the stability of the material is improved.

The invention relates to a preparation method of 5V level anode material of a lithium ion battery, namely, ball LiNi0.5Mn1.5O4, and pertains to the energy material and novel material preparation technology field. The method includes the steps that: a liquid mixture of manganese salt and nickel salt which is prepared according to a molar ration of 3:1, reacts with dissoluble carbonate or bicarbonate water solution and ammonia or ethylene diamine water solution to obtain ball MnCO3-NiCO3, processes of centrifugal separation, washing and drying are carried out, ball Mn2O3-Ni2O3 powder is obtained by heat treatment at 400 DEG C to 600 DEG C, the ball Mn2O3-Ni2O3 powder is mixed with lithium salt compound, ball LiNi0.5Mn1.5O4 is obtained by heat treatment at 700 DEG C to 900 DEG C. The LiNi0.5Mn1.5O4 anode material obtained by the method has high purity and relatively high specific capacity; the product grain is a ball shape, with high tap density which can reach 2.2 to 2.5 g question mark cm <-3>; the ball grain can provide a beneficial condition to the further carrying out of surface coating and to the improvement of the cycle stability of the material, and has great practical value in the field of high energy density and high power lithium ion battery.

The invention discloses a high-activity amorphous silica-alumina, a hydrocracking catalyst supported by amorphous silica-alumina, and preparation methods thereof. The preparation method of the amorphous silica-alumina supporter comprises the following steps: preparing a silicon source-aluminum source mixed water solution, mixing the mixed water solution with a precipitant solution, carrying out cocurrent flow coprecipitation to obtain a precipitated slurry, transferring the slurry into a closed vessel, aging, molding, and roasting. The invention also provides a preparation method of a hydrocracking catalyst by using the amorphous silica-alumina as the supporter. The preparation method of the hydrocracking catalyst is as follows: in the preparation method of the amorphous silica-alumina supporter, a nickel salt or nickel salt and metal aid M salt is/are added into the silicon source-aluminum source mixed water solution in the step (1), and the rest steps are the same as those in the preparation method of the amorphous silica-alumina supporter. The coprecipitation process is adopted in the preparation process, and the silicon source and aluminum source finally exist in the catalyst in the form of the amorphous silica-alumina, but the catalyst has much higher activity than the common amorphous silica-alumina catalyst.

The invention relates to a preparation method of a magnetic-alloy-loaded porous carbon sphere composite wave-absorbing material. The method comprises the following steps: 1) preparing a precursor solution containing two or more magnetic metal ion salts; 2) stirring the porous carbon spheres in the precursor solution for impregnation; 3) filtering out the porous carbon spheres, washing and drying; 4) calcining the dried porous carbon spheres in an inert atmosphere; and 5) cooling to room temperature in an inert atmosphere to obtain the magnetic-alloy-loaded porous carbon sphere composite wave-absorbing material. The iron salt/cobalt salt, iron salt/nickel salt and cobalt salt/nickel salt mixed precursor solution are introduced to the inside of the ducts of the carbon spheres by using the high specific area and strong adsorptivity of the porous carbon spheres through the capillary actions and are combined with the hydrophilic oxygen-containing functional group; and finally, the drying and sintering treatment in the inert atmosphere are performed to obtain the iron-cobalt/iron-nickel/cobalt-nickel-alloy-loaded porous carbon sphere composite material. The whole preparation process is simple in technique and convenient to operate, and has low requirements for the production equipment.

An inkjet recording method which suppresses feathering and color bleeding and is excellent in fixability to a recording medium. The inkjet recording method includes the steps of applying an ink-receiving solution prepared by dissolving in an aqueous solvent at least one metal salt having a water solubility of 0.1 mol/l or more, selected from calcium salts, magnesium salts, nickel salts and zinc salts having a valence of 2 or more, to at least the surface to be printed by using an inkjet ink or the entire surface of a recording medium; and printing on the metal salt adhered part by using the inkjet ink comprising at least a pigment, a resin emulsion and an aqueous solvent containing a surfactant. Further, a phosphorus-containing group having at least one P—O or P═O bond is bound to the surface of the pigment.

The invention provides an oxidation catalyst to purify CO in room temperature, which is prepared in coprecipitation method or deposition-precipitation method. The catalyst consists of non precious metal active components and carrier, wherein the loading of the active components is 5 to 80 percent of the conversion value of metal element. The active components come from cobalt salt liquid, iron salt liquid, nickel salt liquid, manganese salt liquid, copper salt liquid, zinc salt liquid, tin salt liquid and cerium salt liquid. The carrier comes from alumina, silica, molecular sieve, honeycomb ceramics, wire fence, cobalt oxide, iron oxide, manganese oxide, copper oxide, zinc oxide, tin oxide and cerium oxide. The precipitant is Na₂CO₃, K₂CO₃, sodium hydroxide, urea or ammonia. The catalyst preparation solution needs to be fully stirred for 1 to 8 hours and the retrogradation duration is 1 to 16 hours. The dried solution needs to be treated in in-situ remediation in air, oxygen, and hydrogen or nitrogen atmosphere in temperature from 100 to 500 degrees centigrade. The catalyst disuses precious metal as active component, so the cost is low and the preparation process is simple.

The present invention provides high density cobalt-manganese coprecipitated nickel hydroxide, particularly having a tapping density of 1.5 g/cc or greater, and a process for its production characterized by continuous supply of an aqueous solution of a nickel salt which contains a cobalt salt and a manganese salt, of a complexing agent and of an alkali metal hydroxide, into a reactor either in an inert gas atmosphere or in the presence of a reducing agent, continuous crystal growth and continuous removal.

The invention discloses a preparation method of a spherical high-voltage lithium nickel manganate anode material represented by the formula of [Li (Ni0.5-XMn1.5MX) FyO4-Y] 1-Z.[NO]Z. The preparation method comprises the following steps of: evenly mixing a nickel salt solution and a manganese salt solution, and then adding a mixed metal salt solution, a complexing agent solution and a precipitator solution into a reaction kettle with a base solution and a protective gas for coprecipitation reaction; carrying out solid-liquid separation on an overflowing material after the complete reaction; aging the separated solid material; carrying out solid-liquid separation on the aged solid material, thereby obtaining a spherical nickel-manganese binary precursor; evenly mixing a lithium source, the nickel-manganese binary precursor and an M source compound, sintering twice under an oxygen enrichment atmosphere condition, and annealing, thereby obtaining spherical high-voltage lithium nickel manganate. The spherical material prepared by the invention has the advantages of high voltage, high compaction, high volume, excellent rate capability and high-temperature circulating performance, low material cost and the like.

The invention discloses an ammonia-free chemical nickel plating bath which adopts an ammonia-free pH modifying agent to regulate the pH value of the bath. Each liter of the bath contains the components that nickel salt is 24 to 30g, reducing agent is 24 to 33g, buffering agent is 10 to 18g, complexing agent is 20 to 30g, stabilizing agent is 0.5 to 1.5mL, brightener is 1.5 to 3.0mL, and others are water. In the ammonia-free chemical nickel plating bath, the ammonia-free pH modifying agent is selected from one or the mixture of sodium hydroxide, and potassium hydroxide or potassium carbonate. All materials in the ammonia-free chemical nickel plating bath do not contain heavy metal, ammonia water is not utilized to regulate the pH value, the problems of environment pollution, invalidation caused by overlong storing time of the bath, etc. are not caused, and the obtained chemical plating bath is friendly to the environment, in addition, the luminance brightness of the made plating layer can be full-bright. The bath has wide application prospect.

The invention provides a trivalent-chromium blue-white passivator for a zinc-plated permanent magnetic material and a passivation method thereof. The trivalent-chromium blue-white passivator contains a main film-forming agent, an auxiliary film-forming agent, a stabilizer, an oxidant and a surfactant, wherein the main film-forming agent is a soluble salt of trivalent chromium, the stabilizer is selected from at least one of fluoride, citric acid and oxalic acid, the auxiliary film-forming agent is selected from at least one of soluble cobalt salt, soluble nickel salt or soluble salts of rare-earth elements, the oxidant is nitrate ions or hydrogen peroxide, and the surfactant is NPE (Nonylphenol Polyoxyethylene Ether) or sodium dodecyl benzene sulfonate. The trivalent-chromium blue-white passivator provided by the invention has a low cost, does not pollute the environment, and also does not cause damage to the health of operators.

The invention relates to a modified nickel-cobalt lithium aluminate positive electrode material and a preparation method of the material. The chemical general formula of the material is LiNi(1-a-b)CoaAlbO2/TiO2, wherein a is greater than 0.1 and less than 0.3; b is greater than 0.01 and less than 0.2; 1-a-b is greater than 0 and less than 1; the TiO2 layer is a coating layer; the preparation method of the material comprises the following steps: preparing soluble metal nickel salt, cobalt salt and aluminium salt into a mixed salt solution, preparing the mixed salt solution, NaOH and ammonia water into a mixed alkali solution for reacting, filtering, washing, drying and then roasting the mixed alkali solution for 5-10 hours at the temperature of 400-600 DEG C in the oxygen atmosphere, then carrying out ball milling and uniformly mixing with lithium salt, roasting the mixed alkali solution for 6-16 hours at the high temperature of 800-1000 DEG C in the oxygen atmosphere, coating the mixed alkali solution by titanium dioxide to prepare the modified nickel-cobalt lithium aluminate positive electrode material. The prepared modified ternary positive electrode material of the lithium ion battery is good in electrochemical performance; the dry coating process is free of waste liquid and high-temperature sintering, so that the energy consumption and the cost are reduced.

The invention discloses a nickel oxide nano rod array material, a method for preparing the same and application thereof, and belongs to the technical field of inorganic advanced nano materials. The nickel oxide nano rods are vertically and orderly grown on the nickel foam substrate, and the nickel oxide nano rods are 100 to 800 nanometers long and 5 to 30 nanometers wide. The preparation method comprises the following steps of: putting the nickel foam substrate in concentrated hydrochloric acid, deionized water and ethanol for ultrasonic cleaning respectively; dissolving soluble nickel salt and urea in deionized water to obtain clear solution; obliquely putting the nickel foam substrate in a reaction kettle, and moving the clear solution to the reaction kettle for hydrothermal reaction, and after reaction, using the cooling water to cool the reaction kettle to the room temperature; taking the nickel foam substrate out of the reaction kettle, and cleaning the nickel foam substrate withwater and ethanol; and drying the product in an oven, and calcining the dried product. The one-piece product has a very big capacitance value which can be well kept even under high current density and is high in cycle performance, so that the product is a super capacitor material with a great application prospect.

The invention belongs to the technical field of nanometer material preparation, and in particular relates to a graphene with high specific capacitance and a preparation method thereof. The method specifically comprises the following steps: firstly soaking an MCM-22 molecular sieve into a mixture liquor of carbon source, nickel salt and concentrated sulphuric acid, so that carbon source molecules and Ni2<+> ions fully enter spaces between the layers of the MCM-22 molecular sieve; then pre-carbonizing the MCM-22 molecular sieve at low temperature; in the presence of high-temperature inert gases, calcinating the MCM-22 molecular sieve for a certain time to obtain a compound of the graphene and the MCM-22 molecular sieve; and finally, the MCM-22 molecular sieve and nickel in the compound are dissolved, are centrifugally separated out and are dried to obtain the graphene. The graphene which is prepared through the method has the advantages of large specific area, high electric conductivity and controllable two-dimensional size and layers. The graphene can be used as a capacitance material of supercapacitors and has excellent capacitance performance. The method is simple to operate, is low in cost, has reproducibility and can be used for large-scale production.

The invention discloses a preparation method of lithium-ion battery positive electrode material spherical nickel-cobalt-lithium aluminate. The preparation method comprises the following steps of: firstly dissolving aluminum salt in deionized water, and preparing AlOOH aluminum sol by adding HNO3 or ammonium hydroxide and nitric acid; preparing nickel salt and cobalt salt into uniform aqueous solution according to a certain ratio; enabling the mixed salt solution to be collectively reacted with the aluminum sol and a mixed alkali solution, adjusting the pH value to be 9 to 12, controlling the reaction temperature, carrying out the solid-liquid separation after 20 to 30h of the reaction, and washing, filtering and drying the reaction product to obtain spherical nickel-cobalt-aluminum hydroxide precursor powder; then mixing the spherical nickel-cobalt-aluminum hydroxide precursor powder with lithium, sintering the mixture, and pulverizing and grading sintered material to obtain the lithium-ion battery positive electrode material spherical nickel-cobalt-lithium aluminate. The prepared spherical nickel-cobalt-lithium aluminate particles are controllable in shape and granularity, high in compacting density, high in specific discharge capacity, good in cycling stability and low in cost.