Patents
Literature
Patsnap Copilot is an intelligent assistant for R&D personnel, combined with Patent DNA, to facilitate innovative research.
Patsnap Copilot

144results about How to "Large reaction interface" patented technology

Phosphate material having mesoporous structure for lithium secondary batteries and preparation method thereof

The invention relates to a phosphate material having a mesoporous structure for lithium secondary batteries and a preparation method thereof. The material having a mesoporous structure is secondary particles which have a mesoporous spherical or spheroid shape and are formed by the agglomeration of primary particles; the chemical composition of the material having the mesoporous structure is represented by the formula of LixAaMmBbPOzNn; the average particle diameter of the primary particles is 10nm to 1mum, the average particle diameter of the secondary particles is 100nm to 50mum, the average pore diameter of mesopores is 2 to 500nm; and the material having the mesoporous structure also comprises a layer of 2 to 100nm thick carbon coated outside the secondary particles and on the inner walls of the mesopores, wherein the content of the carbon accounts for 1 to 20 weight percent of the total weight of a substrate. The material is prepared by the steps of: firstly preparing pure-phase phosphate LiMPO4 or doped LiMPO4 sol; secondly, forming dry gel through heat treatment; and finally, forming the agglomerate secondary particles through sintering at high temperature. The phosphate material having the mesoporous structure can be directly used in secondary lithium batteries as an anode active material and can also be used by being mixed with the prior anode material as an additive. The material having the mesoporous structure can improve the rate performance and energy density of the prior anode material and batteries. The secondary lithium batteries containing the phosphate material having the mesoporous structure has high power density and high safety.
Owner:INST OF PHYSICS - CHINESE ACAD OF SCI

Wind-crushing water-cooling granulating method and device for high-temperature liquid-state steel slag, granulating steel slag and use thereof

ActiveCN101259991ALarge reaction interfaceImproved React interfaceSolid waste managementSlagLiquid state
The invention provides a wind-crushing water-cooling granulating method of high-temperature liquid steel slag, a granulating device and granulated steel slag and use thereof. The invention belongs to the industrial waste comprehensive utilization filed and particularly relates to the treatment and the utilization of high-temperature liquid steel slag. The wind-crushing water-cooling granulating method of high-temperature liquid steel slag comprises the following steps: liquid steel slag flowing out from a tundish is granulated in the air through the high-speed compressed airflow ejected by a granulator; the granulated steel slag is dropped into a water pool so as to be cooled down; moreover, the pressure of the compressed air is controlled between 0.59 MPa and 0.70 MPa, and the degree of superheat of the liquid steel slag is controlled above 110 DEG C. The granulating device comprises a tundish, a granulator and a water pool, and is characterized in that: a tundish rapid heating-up device is arranged near the granulator; and a compressed air pipe is connected with a compressed air pressure automatic display monitoring device. The final blow rate of steel slag is increased from the 80 percent of the prior art to 95 percent and the steel slag has fine particle diameter; moreover, because unstable phase is eliminated, the steel slag can be directly used in the preparation of cement concrete of various strength grade labels from C30 to C80.
Owner:MAANSHAN IRON & STEEL CO LTD

Stannic selenide/graphene oxide negative pole composite material for sodium ion battery and preparation method thereof

The invention discloses a stannic selenide / graphene oxide negative pole composite material for a sodium ion battery and a preparation method thereof. The negative pole composite material is formed by uniformly growing nanometer stannic selenide on the surface of graphene oxide. The preparation method comprises the following steps of: ultrasonically dispersing graphene oxide powder into a mixed solution of water and ethylene glycol to obtain a dispersion solution; adding tin salt and selenite to the dispersion solution, then carrying out hydrothermal reaction, and placing a hydrothermal reaction product into an inert gas protective tube furnace for heat treatment so as to obtain a negative pole composite material which has nanometer sheet-like morphology and is formed by uniformly growing nanometer stannic selenide on the surface of graphene oxide. The composite material disclosed by the invention can be used for preparing the sodium ion battery which has the characteristics of high discharging specific capacity, excellent magnification property, long cycle life and the like. The preparation method disclosed by the invention has the advantages of simplicity, reliability, good process repeatability, high operability, low cost and suitability for industrialized production.
Owner:CENT SOUTH UNIV

Generating and energy storage integrated device based on direct carbon fuel cells (DCFCs) with liquid metal positive electrode

The invention belongs to the field of fuel cells, and particularly relates to a generating and energy storage integrated device based on direct carbon fuel cells (DCFCs) with a liquid metal positive electrode. The generating and energy storage integrated device comprises a metal molten pool, the liquid metal positive electrode, the tubular solid oxide direct carbon fuel cells (SO-DCFCs) and a fluidization air distributing feeding system, wherein the tubular SO-DCFCs can be blind pipes and through pipes and can be inserted into the metal molten pool vertically or horizontally; the feeding system carries a fuel and a positive electrode material into the metal molten pool by virtue of carrier gas, and substances in the molten pool are stirred. The generating and energy storage integrated device provided by the invention has the advantages that chemical energy in the fuel and surplus electric energy in an power grid are changed into chemical energy in the liquid metal positive electrode to be stored, and the integration of a generating device and an energy storage device is realized; the integrated device is simple and compact, the reactivity of the carbon fuel and the metal positive electrode is high, the property of the cell is good, the friction of the cell caused by liquid state positive electrode fluidization is small, the service life of the cell is long, the seal is easy, the collection is convenient, and a large-scale electric pile is convenient to form.
Owner:TSINGHUA UNIV

pH (potential of hydrogen) responsive metal organic framework nanometer crystal, preparation method and application

The invention discloses a pH (potential of hydrogen) responsive metal organic framework nanometer crystal, a preparation method and application. The pH responsive metal organic framework nanometer crystal comprises a metal organic framework and a pH responsive segment, wherein the pH responsive segment is graftedadhered to an organic ligand of the metal organic framework, and can be a pH responsive polymer, a chain segment containing a carboxylic group, or a chain segment containing a pyridine group. The pH responsive metal organic framework nanometer crystal has the advantages that the pH responsive segment is grafted onto the organic ligand of the metal organic framework, so that the contact angle of the metal organic framework is changed, namely that the hydrophilicity and hydrophobicity properties of the metal organic framework are changed, thereby increasing the interface activity of the pH responsive metal organic framework; the pH responsive segment has response property to the change of the pH value of the surrounding environment, the pH responsive metal organic framework has different hydrophilicity and hydrophobicity properties under different pH values, and then the pH responsive metal organic framework can be separated and recycled by adjusting the pH value.
Owner:SHANDONG NORMAL UNIV

Process for applying hydrogen to deoxygenation of liquid steel

The invention relates to a process for applying hydrogen to deoxygenation of liquid steel. The invention adopts the technical scheme that: when the oxygen blowing decarbonization in a converter comes to an end, or when steel ladle is refined or when the oxygen blowing decarbonization for RH ultra-low-carbon steel production comes to an end, the mixed gas of H2 or Ar-H2 is blown into liquid steel for deoxygenation, the flowrate of the mixed gas ranges from 40 to 3000m3/h, the pressure ranges from 0.5 to 2.0 MPa, and the time of blowing the mixed gas into the liquid steel ranges from 5 to 30min. When converter or steel ladle or RH hydrogen blowing deoxygenation comes to an end, hydrogen which is dissolved in the steel is removed by argon blowing and vacuum treatment, wherein the step of blowing the gas into the liquid steel for deoxygenation is that the gas is blown into the liquid steel for deoxygenation by a gas permeable brick from the bottom of a top-bottom combined blown converter or from the bottom of the steel ladle or from an RH ascending tube; and in the mixed gas of Ar-H2, the volume content of Ar ranges from 10 to 80 percent, and the volume content of H2 ranges from 20 to 90 percent. The invention has the advantages that the process is simple, and the pollution of the liquid steel caused by deoxygenation can be reduced. The process used for removing oxygen in the steel can effectively increase the cleaness of the liquid steel and the quality of steel products.
Owner:WUHAN UNIV OF SCI & TECH

Method for removing ceramic core of hollow blade of turbine of aircraft engine

ActiveCN104368801ASuccessfully developedSmooth productivityAviationChemical reaction
A method for removing a ceramic core of a hollow blade of a turbine of an aircraft engine comprises the four steps of primary core removing, secondary core removing, third core removing and ultrasonic cleaning. The concentration of KOH alkali liquor used in primary core removing is 40%, the concentration of KOH alkali liquor used in secondary core removing is 30%, and the concentration of KOH alkali liquor used in third core removing is 40%. Every time core removing is conducted, the temperature of the alkali liquor ranges from 160 DEG C to 200 DEG C, the pressure of the alkali liquor fluctuates between 0.4 MPa and 0.5 MPa, water is added every six hours, and soaking time is 48 hours. According to the method, the concentration of the alkali liquor is reduced, the water is added every six hours, and it is guaranteed that salt generated due to reactions is sufficiently dissolved; the alkali liquor is replaced every 48 hours, the concentration of the alkali liquor changes in a stepped mode, and it can be guaranteed that the chemical reactions are conducted effectively; the pressure of the alkali liquor fluctuates in a pulse mode, core cracking can be facilitated, the reaction interface between the alkali liquor and the core is enlarged, and the reacting dose is increased. Through the method, the ceramic core removing period can be shortened to six days from over twenty days, and the first pass yield of core removing can be higher than 90%.
Owner:SHENYANG LIMING AERO-ENGINE GROUP CORPORATION

High-catalytic activity composite negative electrode material of intermediate-temperature solid oxide fuel cell and preparation method of composite negative electrode material

The invention relates to a high-catalytic activity composite negative electrode material of an intermediate-temperature solid oxide fuel cell and a preparation method of the composite negative electrode material, and belongs to the technical field of an energy material. The composite negative electrode comprises a perovskite structured oxide PrBa<1-x>Co<2>O<6-Delta>, Pr<1-y>BaCo<2>O<6-Delta> or Pr<1-n>Ba<1-m>Co<2>O<6-Delta> in the absence of A-position cation and an oxygen ion conductor material Sm<0.2>Ce<0.8>O<1.9> or Gd<0.1>Ce<0.9>O<1.95>, wherein the mass percent of the oxygen ion conductor material accounts for 20-50%. The preparation method of the composite negative electrode material comprises the following steps of firstly, respectively preparing synthesis solutions of two constituents; secondly, mixing and uniformly stirring the two solutions to obtain a mixed synthesis solution of the two constituents, and heating the mixed synthesis solution to obtain mixed precursor gel; and finally, carrying out high-temperature sintering reaction to obtain composite negative electrode powder. The composite negative electrode material is prepared by a synchronous sintering reaction method, the preparation method has the advantages of simplicity in process, short preparation period, low cost and high efficiency, and is easy to operate, and the oxygen reduction catalytic activity of the negative electrode of the intermediate-temperature solid oxide fuel cell is effectively improved.
Owner:DALIAN UNIV OF TECH

Magnesium-calcium-based hydride powder for wide-temperature zone hydrolysis hydrogen generation and preparation method for magnesium-calcium-based hydride powder

The invention discloses magnesium-calcium-based hydride powder for hydrolysis hydrogen generation. The magnesium-calcium-based hydride powder comprises the following components in percentage by mass: 14.2 to 50.2 percent of Ca4Mg3H14, 34.8 to 85.7 percent of MgH2 and 0.1 to 15 percent of Mg. In order to increase the hydrolysis hydrogen generation rate, other hydrides and/or salts can also be compounded, and the mass content of the other hydrides is 0 to 5 percent based on the total mass of the components Ca4Mg3H14, MgH2 and Mg; the mass content of the salts is 0 to 11 percent based on the total mass of the components Ca4Mg3H14, MgH2 and Mg; the content of the other hydrides and the content of the salts is not 0 simultaneously. According to the preparation method for the magnesium-calcium-based hydride powder, a magnesium-calcium alloy is activated for hydrogen absorption after being crushed and ball-milled. According to the magnesium-calcium-based hydride powder for the hydrolysis hydrogen generation, the hydrogen yield can be increased on the premise of ensuring the reaction safety and controllability, and particularly the hydrogen yield at room temperature and low temperature is increased.
Owner:SICHUAN UNIV

Low-surface-alkalinity lithium nickel cobalt aluminate positive electrode material and preparation method thereof

InactiveCN108417796ALow structural firmnessSmall latticeCell electrodesSecondary cellsPhosphatePyrophosphate
The invention discloses a low-surface-alkalinity lithium nickel cobalt aluminate positive electrode material and a preparation method thereof. The lithium nickel cobalt aluminate positive electrode material is obtained by performing calcining on metal hydrogen phosphate and a lithium nickel cobalt aluminate positive electrode active material in oxygen flow. By adoption of metal hydrogen phosphatewhich is decomposed into pyrophosphate in calcining, reactant activity is improved, and a reaction with the residual alkali in the lithium nickel cobalt aluminate positive electrode active material ispromoted to generate a Li<3>PO<4> coating layer; compared with phosphate, hydrogen phosphate is lower in structural firmness, lower in lattice energy and easier in reaction, so that the calcining temperature can be obviously lowered; dry method coating of the lithium nickel cobalt aluminate positive electrode active material is converted from high temperature solid phase reaction (700 DEG C) in the prior art into a medium temperature solid phase reaction (400-600 DEG C), so that reaction difficulty is greatly lowered; and in addition, simple process, low cost and high production efficiency are achieved, so that realization of large-scale industrial production can be facilitated.
Owner:CHENGDU ORGANIC CHEM CO LTD CHINESE ACAD OF SCI +1

Battery anode material and preparation method thereof and lithium battery

The invention provides a battery anode material and a preparation method thereof and a lithium battery. The preparation method of the battery anode material comprises the following steps: epitaxiallygrowing a high-quality gallium nitride thin film on a conductive crystal substrate to obtain an epitaxial structure; and modifying the epitaxial structure through electrochemical corrosion, forming holes in the surface of the high-quality gallium nitride thin film and making the holes run through the epitaxial structure and forming a crystal gallium nitride material serving as the battery anode material. The crystal gallium nitride material is first used as the battery anode material and is directly used as an electrode in the lithium battery; the preparation method overcomes the technical challenge that the preparation technique of the crystal gallium nitride material is not compatible with the traditional electrode technique; and through adoption of the high-conductivity homogeneous substrate, epitaxial growth of the gallium nitride materials with different properties and structures and modification of the material through the electrochemical corrosion process, the high-quality gallium nitride electrode material is obtained, wherein the material has good cycle stability and high capacity, and has a good application prospect.
Owner:INST OF SEMICONDUCTORS - CHINESE ACAD OF SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products