90results about How to "Fast migration" patented technology

The invention provides positive slurry of a lithium ion battery as well as a preparation method and application of the positive slurry of the lithium ion battery. The preparation method of the positive slurry of the lithium ion battery comprises the following steps: (1) uniformly agitating and mixing a solvent and an oily binding agent to obtain a mixture A; (2) adding graphene into the mixture A at 25-40 DEG C and agitating uniformly to obtain a mixture B; and (3) adding nickel cobalt lithium aluminate powder into the mixture B; agitating to obtain the positive slurry; and during the agitating period, adding oxalic acid to adjust the pH value of the slurry to 8-9.5. The battery prepared from the positive slurry of the lithium ion battery has the excellent charging/discharging circulating service life and has the high power and safety performance. The battery prepared by the invention is applicable to the fields of hybrid electric vehicles, telecommunication networks, outer spaces, defending equipment and the like.

The present invention is efficient oxidizing catalyst for organic waste water treating and its preparation process and application. The carrier prepared with composite powder of Ti, Si, Al and RE oxide and in the average granularity smaller than 100 nm is loaded with at least two kinds of transition metal to prepare the catalyst. The catalyst contains TiO2-SiO2-Al2O3 65-85 wt%, RE oxide 5-15 wt%, and transition oxide 5-30 wt%. The preparation process of the catalyst includes preparing carrier powder with the carrier components and through precipitation, homogenization, ageing, filtering, washing, pulping, dispersing, fluidizing at supercritical condition to eliminate water and activating; forming the carrier, soaking, fluidizing and drying, and activating to obtain the catalyst. The catalyst is used in acid organic waste water treatment and has COD degrading rate higher than 95 %, ammonia nitrogen oxidizing conversion rate higher than 99 % and chroma eliminating rate higher than 95 %.

The invention discloses an electrolyte for improving the low temperature performance of a lithium ion battery and a lithium ion battery comprising the same. The electrolyte comprises conductive lithium salt, a non-aqueous organic solvent, and additives, wherein the additives include a conventional negative electrode film forming additive, an additive with the structure of Formula I, and an anhydride-type compound additive with the structure of Formula II. According to the battery electrolyte provided by the invention, under synergistic effects among the additive with the structure of Formula I, the anhydride-type compound additive with the structure of Formula II, a nitrogen-containing lithium salt type additive and the conventional negative electrode film forming additive, the electrolytethus has excellent film forming performance on the electrode surface, the cycle performance and the rate performance of the lithium ion battery in a low temperature condition can be effectively improved, and the high temperature cycle performance and the storage performance of the battery are little affected.

The invention relates to a method for preparing nanoscale spherical Si-phase Al-Si alloy through selective laser melting. The method comprises the steps that a CAD three-dimensional model for forming parts is designed, and is converted into a data format STL file capable of being slit, a supporting body of a certain height is built at the bottom of the three-dimensional model, the three-dimensional model and the supporting body are slit into a plurality of layers, technological parameter setting is carried out, and data and parameters are guided into SLM equipment; a sealing device is filled with inert gas for atmosphere protection after being vacuumized, a base plate is fixed to a work table capable of ascending and descending, a layer of Al-Si alloy powder is evenly laid on the base plate through a powder feeding system, corresponding cutting layers are selectively scanned according to guided-in parameter lasers, the base plate is lowered by the thickness of one layer, and a layer of new Al-Si alloy powder is evenly laid on the base plate until scanning of all the layers is finished. In the method, no mold is needed, the utilization rate of materials is high, the mechanical property of the Al-Si alloy can be improved, and the production cost of parts in a complex shape can be lowered.

The invention discloses a positive plate and a lithium ion battery containing the positive plate. The positive plate comprises a current collector and a coating located in a coating area of the current collector; the coating comprises a first coating area and a second coating area; the first coating area is located on the surface of the current collector coating area, and the contact surface of the first coating area and the current collector coating area completely covers the current collector coating area; the second coating area is located above the first coating area and comprises an areaE and an area E', the area E and the area E' are located on the long edge sides of the first coating area respectively, and the area E and the area E' are independent of each other or at least have one intersection point; and both the first coating area and the second coating area contain active substances. The problem of lithium precipitation in the edge area of the negative electrode is fully solved, a cruising ability of the lithium ion battery is improved, the problems of cyclic expansion and battery cell deformation are solved, and a safety risk is reduced.

The invention discloses a three-dimensional porous nanocarbon composite lithium manganate spherical positive electrode material and a preparation method thereof. The preparation method comprises the following steps of adsorbing Mn<2+> ions onto a carbonyl (-COH-) group in a microgel three-dimensional macromolecular network by adopting poly(acrylamide, acrylic acid) microgel spheres as a template; increasing the pH value of the poly(acrylamide, acrylic acid) microgel spheres so as to in-situ hydrolyze the Mn<2+> ions to generate Mn(OH)2 crystal nucleus, depositing the Mn(OH)2 crystal nucleus into a space formed by the three-dimensional macromolecular network to form nano composite polymer microspheres; placing the obtained nano composite polymer microspheres into a tubular furnace to be calcined at a high temperature in an inert gas atmosphere to prepare the three-dimensional porous nanocarbon composite lithium manganate spherical positive electrode material. The positive electrode material has the advantages of excellent high-temperature cycling performance, large multiplying power charging-discharging performance and the like, and can be widely applied to the production of a lithium battery.

Provided is a thin-film transistor comprising a low-temperature polysilicon transistor having a low off-current, excellent potential-holding characteristics, low power usage, and a high operating speed. Also provided are a liquid-crystal display device using said thin-film transistor and a method for manufacturing the thin-film transistor. The provided thin-film transistor uses an inversely staggered structure with a gate electrode, a gate insulation film, a channel region, and source/drain electrodes formed on top of a glass substrate. The channel region comprises a polysilicon film and an a-Si:H film that covers the top and sides of the polysilicon

The invention discloses a cross cobalto-cobaltic oxide nanosheet array, a gas sensor containing the array and application thereof. The nanosheets in the special cross cobalto-cobaltic oxide nanosheet array cross with each other. The nanosheets have a mesoporous structure, and the highest sensitivity of 16.5 for selective detection of acetone at about 111 DEG C. The cross cobalto-cobaltic oxide nanosheet array overcomes the problem that traditional cobalto-cobaltic oxide nanosheet cannot directly generate array on an insulation substrate with only supporting effect, and has the advantages of low production cost, high efficiency, and simple and controllable operation. The cross cobalto-cobaltic oxide nanosheet array has open structure, large specific surface area and electron mobility, and can provide more space for the benefit of rapid adsorption and detachment of gas molecules, and significantly improve the gas sensitive properties of the material. The cross cobalto-cobaltic oxide nanosheet array has good stability; test is carried out every 3 days in 60 days; and after 20 times of test, the performance change rate is only +/- 8%. The invention is quite applicable to sensor, acetone detection and medical detection.

The related preparation method for anti-CO composite positive electrode catalysis layer of proton-exchange member fuel cell comprises: with Pt/C or PtM/C(M is one or more of Ru, Mo, Sn, Ni, Au/Fe2O3,Au/Al2O3, Au/Co2O3, Fe, Co and W) as electric catalyst, a hydrophilic catalyst layer named inner catalyst layer with former catalyst and polymer solid as main components connected to the proton exchange member, a hydrophobic catalyst layer named outer catalyst layer with the catalyst and some hydrophober as main components connected to a diffused layer, and one or more middle catalyst layer with hydrophilic and hydrophobic feather gradient change. This invention has well performances.

The invention relates to a solid powder multi-element composite infiltration agent and a composite infiltration process, and belongs to the technical field of metal surface treatment. The composite infiltration agent is composed of a chromium source, a vanadium source, a boron source, nickel powder, an activating agent, a filling agent, an oxygen scavenger and a rare-earth infiltration enhancer. The composite infiltration agent has the effects of rapid infiltration speed, no pollution, improving the structural density of an infiltration layer, and avoiding the embrittlement of the infiltrationlayer. The composite infiltration process comprises the following steps of carrying out acid pickling activation pretreatment on a base body material, then burying the base body material into the composite infiltration agent, heating and preserving heat in a carbon-containing or nitrogen-containing atmosphere, and then carrying out quenching treatment after furnace cooling. According to the process, the method is simple, no pollution occurs, the infiltration speed is rapid, the infiltration agent is free of hardening, and the surface of an infiltrated workpiece is clean. The prepared composite infiltration layer is fine in the crystalline grains and compact in the structure, has a good gradient structure, has the toughness, the wear resistance, the corrosion resistance, the high-temperature oxidation resistance and the like, and can be applied to parts such as a tool, a mold, a bearing, and a gear.

The invention relates to the field of preparation of new materials, in particular to a preparation method of a carbon nanotube amidation grafted polysilsesquioxane flame retardant. The preparation method comprises the following steps: surface modification is carried out on a carbon nano tube by adopting tetramethyl guanidino propyl trimethoxy silane; octaaminophenyl silsesquioxane, aminoferroceneand biphenyl phosphoramidate are grafted and introduced into the modified carbon nanotube material by adopting an amidation reaction, and high-heat-resistance and high-smoke-suppression cage-shaped polysilsesquioxane is obtained by virtue of a synergistic effect. The flame retardant has very excellent flame retardance, is used for polycarbonate products, and has the characteristics of small addition amount, strong carbon forming ability and high migration speed.

The invention provides a method for producing a pair of tritium-proof gloves and belongs to the field of a radiation proof material. The method comprises the step of: preparing a three-layer compound rubber thin film by using a method of compounding layer by layer, wherein the outer layer is a rubber barrier layer which is good in hydrogen stopping property; the middle layer is a tritium absorption layer in which an organic hydrogen absorption agent prepared by DEB and a catalyst is dispersed; and the third layer is a rubber layer which is good in compatibility with the skin and is made of the same material as the outer layer. The gloves produced by using the method has the advantages that tritium permeating into each tritium-proof glove through surface layer rubber is fixed in the rubber layer of the middle layer of each glove, thereby achieving the tritium-proof effect; and the preparation process is simple, the tritium-proof effect is obvious and the tritium recycle and the environmental protection can be realized.

The invention relates to a fluorine-containing acrylate-based random copolymer, which has a number average molecular weight of 20000-500000 and molecular weight distribution of 1.6-3, and is obtainedby carrying out free radical copolymerization on 40-80 wt% of a monomer component A and 20-60 wt% of a monomer component B, wherein the monomer component A is fluorine-containing (meth)acrylate, and the monomer component B is C8-C30 alkyl (meth)acrylate. The invention further relates to a preparation method of the fluorine-containing acrylate-based random copolymer, wherein the preparation methodcomprises: heating a solvent to a temperature of 80-140 DEG C, mixing the monomer component A, the monomer component B and an initiator to obtain a mixed solution, adding the mixed solution into the heated solvent in a dropwise manner within 1.5-3 h, and carrying out a copolymerization reaction to obtain the fluorine-containing acrylate-based random copolymer. The invention further relates to usesof the fluorine-containing acrylate-based random copolymer as an anti-foaming agent in coating materials, inks or plastic materials. According to the present invention, the fluorine-containing acrylate-based random copolymer has advantages of strong foam inhibition and defoaming performance and good system compatibility, the preparation is simple, and the continuous production can be achieved.

The invention discloses a data migration method used for hierarchical storage. The method comprises the steps of A: comparing whether a proportion of used spaces in an online storage device is greaterthan or equal to a first preset threshold by a preset cycle, and if yes, executing the step B, otherwise, re-executing the step A; B: when the proportion of the used spaces in the online storage device is greater than or equal to the first preset threshold, obtaining attribute information of all data tables in the online storage device, and executing the step C; C: based on the attribute information, calculating migration values of all the data tables, and executing the step D; D: migrating data corresponding to the data table with a maximum migration value in the online storage device to anoffline storage device, and executing the step E; and E: comparing whether the proportion of the used spaces in the online storage device is smaller than or equal to the second preset threshold, and if yes, executing the step A, otherwise, executing the step D. The purposes of high migration speed, large released space, small influence range and high access efficiency are achieved.

The invention provides a virtual machine processing method and device and equipment. The virtual machine processing method can comprise the steps that a resource request message sent by terminal equipment is received; the resource request message comprises a type of virtual machines; a virtual machine is determined from a buffer pool according to the type of the virtual machines to be used for virtual machine migration; and at least one type of virtual machines operates in the buffer pool. Through the virtual machine processing method and device and the equipment, delivery speed of the virtualmachine can be increased, delivery time is shortened, it is guaranteed that a user uses the requested virtual machine normally in time, and user experience is improved.

The embodiments of the present invention disclose an electrochromic grating, a manufacturing method thereof, a display panel and a display device. The method of manufacturing the electrochromic grating comprises: forming a first transparent electrode layer on a first substrate; forming a resin layer on the first transparent electrode layer and forming a plurality of grooves in the resin layer; forming a second transparent electrode layer on a second substrate; perfusing at least one of solution type or gel type electrochromic material into the plurality of grooves; and then, encapsulating the first substrate and the second substrate. In this way, by using the at least one of solution type or gel type electrochromic material filled in the grooves, the conversion speed of the electrochromic grating between the transparent state and the colored state can be increased, the conversion response speed of the display panel between 2D picture and 3D picture can be further increased, so as to realize a higher contrast, thereby improving the display effect.

The invention relates to a water-based cutting fluid for diamond wire cutting and a preparation method and a use method thereof. The cutting fluid is mainly prepared from the following components in parts by weight: 8-33 parts by weight of silicone modified polyether; 3-7 parts by weight of a silane hydrolysis inhibiting stabilizer; and the balance of water, wherein the total weight part is 100. By implementing the embodiment of the invention, the cutting fluid has the following beneficial effects that the cutting fluid has a low-foam self-defoaming function, and a defoaming agent component does not need to be additionally added; the silicon modified polyether can be subjected to hydrolysis endothermic reaction on a cutting contact interface, and heat which cannot be taken away in time in the cutting process is balanced; meanwhile, the hydrolyzed silicon hydroxyl has a strong adsorption effect and can play roles in protecting the diamond wire, enhancing the lubricating property, reducing the cutting resistance and reducing the wire breakage probability; the dispersion of silicon powder is enhanced and the silicon powder is enabled not to be agglomerateand, active sites on the surface of the silicon powder are adsorbed and combined in time so that the problem of spontaneous combustion caused by high reaction activity of the filter-pressing silicon powder is avoided.

The invention relates to a multistage micropore composite electrode material and a manufacturing method thereof. A structure is a three-dimensional pore structure. The material is characterized in that a small pore material possessing a three-dimensional mesh structure and a large pore material possessing the three-dimensional mesh structure are mutually wrapped; the small pore material is filled in pores of the large pore material and incompletely-filled gaps exist in the pores of the large pore material. The manufacturing method of the electrode material comprises the following steps that the large pore material possessing the three-dimensional mesh structure is dipped in a hydrogel solution so that the hydrogel solution is filled in large pores possessing the three-dimensional mesh structure; and then, the hydrogel is solidified so as to form a three-dimensional small gap material; during a solidified process, the size of the hydrogel is contracted to a certain degree so that unfilled gaps exist in the large pores. The material and the method have the advantages that the composite electrode material possesses a high specific surface area (high energy storage density) and rapid ion migration and diffusion speeds (short charge and discharge time); a manufacturing technology is simple and material cost is low.

The invention relates to the technical field of preparation of nano-materials and photoelectrochemistry and in particular discloses a porous flower-petal-shaped anatase TiO2 nano-crystal thin film anda preparation method thereof. The porous flower-petal-shaped anatase TiO2 nano-crystal thin film is prepared by adopting hydrothermal synthesis and high-temperature crystallization methods; the prepared thin film is composed of porous TiO2 nano-crystals and has the advantages of large specific surface area and low compounding probability of photoelectron cavities; the TiO2 nano-crystal thin filmis an anatase phase and has a strong photoelectron cavity oxidization capability; the TiO2 nano-crystal thin film is obtained by direct hydrothermal growth of a Ti substrate and is combined with the substrate very well; the TiO2 nano-crystal thin film has relatively low charge migration resistance and the thin film does not easily fall off.