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871 results about "Nickel content" patented technology

Alkaline electroplating Zn-Ni alloy additive, electroplating solution and preparation method

InactiveCN101942684AOptimum metal distributionStable nickel contentZincElectroplating
The invention relates to an alkaline electroplating Zn-Ni alloy additive, an electroplating solution and a preparation method. The additive comprises the following components in parts by weight: 3.5 to 4.5 parts of nickel complex agent, 6 to 8 parts of nickel source, 7 to 8.5 parts of zinc complex agent, 1.5 to 2.5 parts of brightening agent and 0.2 to 0.3 part of throwing agent. The preparation method comprises the following steps: adding zinc oxide into dissolved sodium hydroxide, stirring and dissolving; adding the zinc complex agent, the nickel complex agent, nickel replenisher, the brightening agent and the throwing agent in turn; and stirring to ensure that the mixture is mixed uniformly so as to prepare the electroplating solution containing the additive. The alkaline electroplating Zn-Ni alloy additive can acquire excellent metal distribution and constant alloy composition within a wide current density range, has stable nickel content of the plating in a range of between 12 and 15 percent, excellent corrosion resistance which is over five times more than a conventional zinc coating, excellent dispersive power and higher current efficiency, and can be used for barrel plating or rack plating with small coating stress, high ductility and excellent brightness.
Owner:济南德锡科技有限公司

Catalyst for continuous production of succinic anhydride from hydrogenation of maleic anhydride and preparation method thereof

The invention provides a catalyst for continuously producing butanedioic anhydride by maleic anhydride hydrogenation. The catalyst is a nickel loaded catalyst prepared by an equivalent-volume impregnation method, wherein in the catalyst, the content of nickel is 13 to 20 weight percent, the content of accelerating agent is 1 to 7 weight percent, and a carrier is a composite oxide of SiO2 and Al2O3 or SiO2-Al2O3. A preparation method for the catalyst comprises the following steps: impregnating impregnation solution blended by ammonia water and active metal salt solution on a carrier subjected to baking pretreatment at a temperature between 400 and 800 DEG C by the equivalent-volume impregnation method to form the catalyst through drying, baking and reducing treatment. The catalyst is applied to continuously preparing the butanedioic anhydride by maleic anhydride hydrogenation on a fixed bed reactor, the conversion rate of maleic anhydride is more than or equal to 99.98 percent, and the selectivity of the butanedioic anhydride is more than or equal to 98.85 percent. The catalyst achieves the technical-scale continuous production of the butanedioic anhydride, and has the advantages of high activity, good selectivity, high yield (more than or equal to 98.83 percent) and long service life.
Owner:SHANXI UNIV

Nickel lithium ion battery positive electrode material having concentration gradient, and preparation method therefor

A nickel lithium ion battery positive electrode material having a concentration gradient, and a preparation method therefor. The material is a core-shell material having a concentration gradient, the core material is a material having a high content of nickel, and the shell material is a ternary material having a low content of nickel. The method comprises: synthesizing a material precursor having a high content of nickel by means of co-precipitation, co-precipitating a ternary material solution having a low content of nickel outside the material precursor having a high content of nickel, aging, washing, and drying to form a composite precursor in which the low nickel material coats the high nickel material, adding a lithium source, grinding, mixing, calcining, and cooling to prepare a high nickel lithium ion battery positive electrode material. The obtained material has regular morphology, uniform coating, narrow particle size distribution range, gradient distribution of the concentration of the nickel element, high content of the nickel element in the core, and low content of the nickel element in the shell; the nickel element in the core guarantees the specific capacity of the material, and the shell coating material maintains the stability of the structure of the material, so as to improve the safety of the material in the charge and discharge process, and improve the cycle and rate performance of the material.
Owner:INST OF PROCESS ENG CHINESE ACAD OF SCI

1000MPa grade nickel-saving type metastable austenite stainless steel

The invention provides 1000MPa class nickel-saving type metastable austenite stainless steel. The chemical components of the nickel-saving type metastable austenite stainless steel of the invention calculated by weight percentage include 0.06 to 0.15 percent of C, less than 1 percent of Si, 8 to 10 percent of Mn, 15 to 17 percent of Cr, 0.5 to 1.2 percent of Ni, 0.15 to 0.30 percent of N, less than 0.03 percent of P, less than 0.02 percent of S and the rest are Fe and unavoidable impurities. The room temperature yield stress of a cold processing state of the invention can reach 1250MPa, the anti-tension intensity can reach 1460MPa and the average room temperature extension rate can be maintained to be 16.8 percent. Under different states, the room temperature yield stress of the material is 370 to 1250MPa and the room temperature anti-tension intensity is 860 to 1460MPa. The room temperature anti-tension intensity of a cold-rolling solid solution state can reach over 1000MPa and the extension rate is larger than 40 percent. The invention has high intensity and excellent plasticity. The excellent room temperature mechanical performance of the 1000MPa class nickel-saving type metastable austenite stainless steel of the invention can be remarkably distinguished from the normal metastable austenite stainless steel and is suitable for weak-corrosion environments such as the fields of traffic, construction and hardware, etc., and can partially replace the austenitic stainless steels with high nickel contents like AISI304, AISI301 and AISI201, etc., so as to save the expensive metal nickel.
Owner:BAOSHAN IRON & STEEL CO LTD

Method for preparing high-performance iron nickel magnetically soft alloy by using powder metallurgy process

The invention discloses a method for preparing high-performance iron nickel magnetically soft alloy by using a powder metallurgy process, which belongs to the technical field of powder metallurgy. The method comprises the following steps of: 1, uniformly mixing various powder such as iron powder, nickel powder, molybdenum powder, silicon powder, copper powder, cobalt powder, chrome powder, niobium powder, tungsten powder, aluminum powder and titanium powder according to a certain ratio, wherein the nickel content ranges from 30 to 78 percent; or the alloy powder prepared according to a certain alloy component ratio is directly used as a raw material; 2, forming the powder which is obtained by step 1 into a blank with a certain shape by using a powder metallurgy forming method; 3, sintering the formed blank, which is obtained by the step 2, under the pressure of between 0 and 1,000 MPa and at the temperature of between 600 and 1,500 DEG C for 10 to 4,000 minutes; and 4, processing the sintered body obtained by the step 3 under the pressure of between 0 and 4,000 MPa and at the temperature of between 600 and 1,600 DEG C for 0 and 4,000 minutes. The method has the characteristic that: by improving the sintering and thermal treatment systems, the material density is improved, the micro texture and structure of the material are improved, the impurity content is reduced, and the magnetically soft alloy product with the maximal magnetic conductivity of no less than 40 mH/m and with the coercive force of no more than 20 A/m can be prepared.
Owner:UNIV OF SCI & TECH BEIJING

Core-shell polynary lithium ion battery anode material distributed in all-concentration gradient way and preparation method thereof

The invention relates to a core-shell polynary lithium ion battery anode material distributed in an all-concentration gradient way and a preparation method thereof, and belongs to the field of lithium ion battery anode materials. The structural formula of the anode material is LiaNixCoyMn1-x-yO2@LibNimConMn1-m-nO2, wherein a is more than or equal to 0.9 and less than or equal to 1.2, x is more than or equal to 0.6 and less than or equal to 0.9, y is more than or equal to 0.05 and less than or equal to 0.4, b is more than or equal to 0.9 and less than or equal to 1.2, m is more than or equal to 0.2 and less than or equal to 0.7, and n is more than or equal to 0.1 and less than or equal to 0.6. The anode material is spherical or sphere-like, and is of a core-shell structure; a core part is an all-concentration gradient part being 2-10 microns in diameter; a shell part is a protective layer part being 0.5-2 microns in thickness; the concentration of the protective layer part is an all-concentration gradient end-point concentration; and from the center of a core to the surface of a shell, the nickel content decreases gradually while the cobalt content and manganese content increase gradually. The material has the advantages of low cost, high cycle performance, high safety performance, high discharge capacity and the like. Moreover, the core-shell polynary lithium ion battery anode material is simple in process flow, and easy for realizing industrial production.
Owner:CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI

Lithium ion battery cathode material and preparation method thereof

Belonging to the technical field of lithium ion batteries, the invention discloses a lithium ion battery cathode material and a preparation method thereof. The chemical molecular formula of the cathode material is Lix(NiaCobMnc)1-yMyO2, wherein x is greater than or equal to 0.96 and smaller than or equal to 1.04, y is greater than or equal to 0.01 and smaller than or equal to 0.06, a is greater than or equal to 0.8 and smaller than or equal to 0.9, and a+b+c=1, M has a general formula of BzM'1-z, M' is composed of one or several of the following elements: Al, Mg, Ti and Zr, and z is greater than or equal to 0.1 and smaller than or equal to 0.5. The cathode material is coated by a layer of compound containing L, B, Ni, Co and Mn, the content of B in the outermost surface of the coating layer is at least two times that of the B in the innermost layer of the coating layer. According to the invention, the high capacity cathode material is acquired from a high nickel content ternary system, additionally multielement doping is employed to stabilize the crystal structure of the material, and then by means of washing, boron element surface modification and two-step sintering process, the material surface structure can be improved, and the surface residual alkali content can be reduced to improve the interface stability. The whole technological process of the invention is simple, and is easy for large scale production.
Owner:HEFEI GUOXUAN HIGH TECH POWER ENERGY

Core-shell structure high nickel gradient nickel cobalt manganese aluminum quaternary positive electrode material and preparation method thereof

The invention provides a core-shell structure high nickel gradient nickel cobalt manganese aluminum quaternary positive electrode material and a preparation method thereof. The quaternary positive electrode material is spherical particles with an average particle size of 8-10 microns, the diameter of the inner core is 4-6 microns, the thickness of the shell layer is 2-3 microns and the surface ofthe shell layer is sheet-shaped. The nickel content gradually decreases from the center of the core to the surface of the shell structure, the manganese content gradually increases from the center ofthe core to the surface of the shell structure, the cobalt content is uniformly distributed and the aluminum content is uniformly or gradient distributed. The preparation method comprises the follow steps: a low nickel solution I is continuously added into a high nickel solution so that the nickel content in the high nickel solution is continuously reduced, and then the low nickel solution I is continuously pumped into an ammonia aqueous solution to form a continuous reaction system with reduced nickel content, and further hydroxide and carbonate are successively used as precipitants and ammonia water is used as a complexing agent to successively coprecipitate to generate a precursor with a core-shell structure; and then the precursor is sintered with lithium so as to prepare the core-shell structure high nickel gradient nickel cobalt manganese aluminum quaternary positive electrode material. The battery assembled by the positive electrode prepared by the core-shell structure high nickel gradient nickel cobalt manganese aluminum quaternary positive electrode material has high capacity, excellent cycle and rate performance and highly reversible charge-discharge reaction.
Owner:CENT SOUTH UNIV

Method for separating nickel and iron from nickel-iron alloy and application

The invention belongs to the field of hydrometallurgy, and discloses a method for separating nickel and iron from a nickel-iron alloy and application. The method comprises the following steps: dissolving the nickel-iron alloy in an acid solution, filtering, and taking filtrate to obtain an acidic nickel-iron solution; adjusting the pH value of the acidic nickel-iron solution, heating, stirring, adding iron powder, and continuously heating and stirring to obtain sponge nickel and nickel precipitation mother liquor; enabling the nickel precipitation mother liquor to be subjected to oxidation iron precipitation to obtain ferric hydroxide slag and iron precipitation mother liquor; and dissolving sponge nickel into sulfuric acid, filtering, collecting filtrate, heating, and adjusting the pH value to obtain a nickel sulfate solution; According to the method, after the nickel-iron alloy is dissolved by using the acid liquor, nickel in the solution is replaced by iron powder to obtain sponge nickel, the nickel precipitation mother liquor is oxidized to generate ferric hydroxide, the nickel content is lower than 0.4%, the iron precipitation mother liquor can be returned to a leaching section, and the sponge nickel is subjected to acid dissolution, impurity removal and evaporative crystallization to obtain a battery-grade nickel sulfate product.
Owner:HUNAN BRUNP RECYCLING TECH +2

High-nickel gradient nickel cobalt manganese aluminum quaternary positive electrode material and preparation method thereof

The invention provides a high-nickel gradient nickel cobalt manganese aluminum quaternary positive electrode material and a preparation method thereof. The positive electrode material is spherical particles with an average particle size of 5-8 microns, the nickel content of the positive electrode material gradually decreases from the center to the surface of the spherical particles, the manganesecontent gradually increases from the center to the surface of the spherical particles, the cobalt content is uniformly distributed in the spherical particles and the aluminum content is uniformly or gradiently distributed in the spherical particles. The preparation method comprises the steps: the solution I with low nickel content is continuously added into the solution II with high nickel content, then the solution II with gradually decreasing nickel content is continuously pumped into the ammonia aqueous solution to form a continuous reaction system with decreasing nickel content, and then the precursor with gradient change of nickel, cobalt, manganese and aluminum content is precipitated in an inert gas environment by taking hydroxide as the precipitant and ammonia water as the complexing agent; and then the nickel cobalt manganese aluminum hydroxide precursor is sintered with lithium so as to prepare the high-nickel gradient nickel cobalt manganese aluminum quaternary positive electrode material. The quaternary positive electrode material obtained by the preparation method has high capacity, excellent cycle and rate performance and highly reversible charge-discharge reaction.
Owner:CENT SOUTH UNIV
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