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174results about How to "High batch stability" patented technology

Preparation method for inverted LED white-light chip of chip scale package

The invention discloses a preparation method for an inverted LED white-light chip of chip scale package, and the method comprises the following steps: temporarily fixing an UV solidifying adhesive tape (2-1) on the upper surface of a die bonding positioning light cover (1); setting flip chips (3) on the upper surface of the UV solidified adhesive tape (2-1) according to the position of the die bonding positioning light cover (1); employing a fluorescent glue film (4) to cover the flip chips (3); carrying out vacuumizing and heating, and enabling the fluorescent glue film (4) to be solidified and packaged on the flip chips (3); carrying out cutting along gaps among the all packaged flip chips (3); removing the die bonding positioning light cover (1); carrying out UV irradiation and enabling the UV solidified adhesive tape (2-1) to be solidified, and obtaining the inverted LED white-light chip (5) of chip scale package. The method simplifies the technological flow, avoids glue mixing and dispensing in the original technology, improves the production efficiency and yield, and greatly reduces the production cost. The method completely avoids the sinking of phosphor, enables the batch stability of the inverted LED white-light chips (5) to be high, and enabling the color temperature of the inverted LED white-light chips (5) to be consistent.
Owner:TECORE SYNCHEM

Method for treatment on high-voltage Ni-Co-Mn ternary positive electrode material by surface drying method

InactiveCN105374996AReduce the amount of residual lithium on the surfaceImprove adaptabilityCell electrodesSecondary cellsAir atmosphereManganese
A method for treatment on a high-voltage Ni-Co-Mn ternary positive electrode material by a surface drying method comprises the following steps of firstly, sieving and dispersing a lithium salt, weighing and adding the lithium salt and a Ni-Co-Mn hydroxide into a blending mixer for mixing according to a mole ratio of (1.0-1.2):1, mixing the lithium salt and the Ni-Co-Mn hydroxide to obtain mixed raw powder; secondly, loading and compacting the mixed raw powder in a pot, carrying out sintering in a high-temperature air atmosphere, cooling until the tapping temperature is less than or equal to 80 DEG C, taking a powder body out, and carrying out weak breaking, dispersing and sieving on the powder body in a drying room to obtain a high-dispersion Ni-Co-Mn ternary material substrate; thirdly, weighing and adding the high-dispersion Ni-Co-Mn ternary material substrate and a cladding agent A into a grinding blending mixer for mixing according to a mole ratio of 1:(0.1-0.001), and allowing the high-dispersion Ni-Co-Mn ternary material substrate and the cladding agent to be in mixed contact, thereby obtaining a mixed material; loading the mixed material in the pot, cooling after sintering the mixed material in the high-temperature air atmosphere to a solid phase until the tapping temperature is less than or equal to 80 DEG C, taking the powder body out, and carrying out sieving to obtain the high-voltage Ni-Co-Mn ternary material. According to the method, the high-voltage Ni-Co-Mn ternary positive electrode material which has the characteristics of high capacity, high cycle, high temperature and favorable safety can be prepared.
Owner:CAIHONG GRP ELECTRONICS CO LTD

Novel process for preparing battery-grade iron phosphate material by using iron hydroxide

The invention discloses a novel process for preparing a low-cost battery-grade iron phosphate material by using iron hydroxide. The process comprises the following steps: mixing a zero-valent iron source and corrosive acid in a molar ratio, and adding a certain amount of primary water and ammonia water; stirring to react for 0 to 24 hours, and slowly adding hydrogen peroxide until the iron source disappears and the solution turns to orange; adding surfactant which is 1 to 5 percent that of the mass of the iron source into the solution; adding a reagent containing phosphate radicals into the solution according to a certain molar ratio of iron element to phosphor element under a stirring condition to obtain iron phosphate precipitate; filtering and washing the product 3 to 5 times with the primary water which is 3 to 7 times the weight of the iron phosphate; drying in vacuum for 4 to 12 hours at 50 and 80 DEG C to obtain FePO4.2H2O. The process for preparing battery grade iron phosphate is simple and easy to carry out and low in cost; and the prepared product has good product crystal structure, few impurities and uniform granularity and is suitable for industrial scale production; moreover, the lithium iron phosphate prepared by the process has high specific capacity, low self-discharge, high tap density, stable product performance and good processing performance.
Owner:ZHEJIANG NARADA POWER SOURCE CO LTD +2

Secondary sintering synthesis method for lithium iron phosphate

The invention discloses a secondary sintering synthesis method for lithium iron phosphate, which comprises the following process steps of: 1, preparing materials in a molar ratio of lithium to iron to phosphorus element of (0.98-1.02): 1: 1, and mixing the materials uniformly; 2, heating the obtained mixture to between 350 and 550 DEG C, preserving the heat for 5 to 15 hours, then cooling the mixture along with a furnace to room temperature, and crushing the obtained material to obtain lithium iron phosphate powder; 3, mixing the obtained lithium iron phosphate powder, a carbon source and a solvent uniformly, drying the mixture and then heating the mixture to between 650 and 850 DEG C, preserving the heat for 10 to 20 hours, then cooling the mixture along with the furnace to room temperature, and crushing, screening and grading the mixture to obtain a screened product which is a lithium iron phosphate product produced by the method. The method is simple; the operation is convenient; the prepared lithium iron phosphate has high electric conductivity, good storage performance, good low-temperature performance and good batch consistency; and the method greatly improves the electric conductivity, low-temperature performance, storage performance and batch stability of the lithium iron phosphate. The method is suitable for industrialized production and can replace the conventional one-time high temperature sintering process.
Owner:谢朝华 +3

Working electrolyte for ultrahigh-voltage aluminium electrolytic capacitor and manufacturing method thereof

Disclosed in the invention is a working electrolyte for an ultrahigh-voltage aluminium electrolytic capacitor. The working electrolyte comprises the following raw materials, by mass percent: 49 to 76% of a main solvent, 5 to 20% of a secondary solvent, 6 to 25% of a solute, and 3 to 10% of a property-modifying additive. According to the manufacturing method, the main solvent and the secondary solvent are mixed; the solute is added at the temperature of 100 to 115 DEG C, and stirring is carried out and the temperature rises 130 to 135 DEG C; heat-preservation stirring is carried out and reaction is also carried out for 10 to 40 minutes; and cooling is carried out until the temperature is reduced to 70 to 90 DEG C and then the property-modifying additive is added, thereby completing preparation. According to the invention, with application of special materials, the special preparation process is used; and on the basis of optimized formulas, the combined effect of the materials is realized. The prepared working electrolyte having advantages of reasonable cost, long service life, high high-temperature stability, and high batch stability can meet the urgent need of factories in the country, especially the need of the high-end manufacturers.
Owner:上海洪微电子科技有限公司

Preparation method of GH4169 alloy bars

The invention relates to a preparation method of GH4169 alloy bars, and belongs to the technical field of high-temperature alloy hot machining. The problems that the grain sizes of GH4169 alloy bars in the prior art are not uniform, and batch-to-batch production is not stable are solved. The preparation method includes the following steps that 1, a free forging press is used for upsetting cast ingots in a closed upsetting or free forging upsetting manner, wherein the upsetting deformation temperature is 1,110+ / -20 DEG C; 2, forging blanks obtained after upsetting are subjected to surface machining, black skin and defects are removed, and cylindrical forging blanks are obtained; and 3, the machined blanks are heated, the heating temperature is 980 DEG C-1,060 DEG C, the forging blanks continue to be subjected to heat preservation for 60 min-480 min after being fully heated, then the forging blanks are discharged out of a furnace to be subjected to hot extrusion, the time between furnacedischarging and extrusion starting is controlled within 5 min, the surfaces of the forging blanks are coated with a lubricant before the forging blanks are extruded, and a glass cushion is arranged between an extrusion die and the forging blanks. High-stability manufacturing that the structures of the sections, the heads and the tails of the GH4169 alloy bars with the diameters larger than or equal to 250 mm are uniform and fine, and the grain sizes are smaller than the level 4 or even the level 6 is achieved.
Owner:TIANJIN HEAVY EQUIP ENG RES +1

Environment-friendly stable polyamide acid solution and preparation method thereof

The invention relates to a polyamide acid solution and a preparation method thereof, in particular to an environment-friendly stable polyamide acid solution and a preparation method thereof. The environment-friendly stable polyamide acid solution and the preparation method thereof aim at solving the problems of difficultly of large-scale preparation of a polyamide acid aqueous solution, wide molecular weight distribution and poor batch stability in the prior art. The environment-friendly stable polyamide acid solution is prepared from tertiary amine, aromatic primary amine, aromatic dianhydride, aromatic diamine and water, wherein repetitive units of polyamide acid in the polyamide acid aqueous solution are shown in the specification. The preparation method includes the steps that tertiary amine, aromatic primary amine, aromatic dianhydride, aromatic diamine and water are taken, and weighed tertiary amine is divided into tertiary amine A and tertiary amine B; water and aromatic primary amine are added into a three-necked bottle under certain conditions for a reaction; weighed tertiary amine A and weighed aromatic diamine are added into the three-necked bottle for a reaction, reaction liquid is heated, then weighed aromatic dianhydride is added into the three-necked bottle and stirred for a reaction, then the reaction liquid is cooled, weighed tertiary amine B is added and stirred for a reaction, and the reaction liquid is cooled and subjected to standing.
Owner:INST OF PETROCHEM HEILONGJIANG ACADEMY OF SCI

Preparation method of Mg-contained hydrogen storage alloy

The invention belongs to the technical field of functional metal alloy materials and relates to a smelting method applicable to La-Mg-Ni series and Mg2Ni type hydrogen storage alloys, which comprises the following concrete steps of: weighing the components of the La-Mg-Ni series hydrogen storage alloy as ABy according to a stoichiometric proportion, wherein the A is LaxMg1-x, the B is Niy-zCz, and the C is Mn, Fe, Mo, Co, Al, Ti, Si, V, Cr, Cu, Zn, Zr, Nb, W, Hf, Ta, B, P or / and Sn, La, Mg and Ni, adding into a crucible of a medium-frequency induction smelting furnace, and placing on a feeding device in the furnace after carrying out surface processing on Mg blocks; carrying out vacuum pumping until the vacuum degree is 10-2 Pa, introducing He and Ar protective gases mixed according to a certain proportion until the air pressure in the furnace reaches 0.01-0.1MPa, regulating the power range to be 15-35kW, and controlling the temperature at 600-1300 DEG C until metals are molten; and stopping electrifying for 1-10 minutes, adding the Mg into the crucible through the feeding device in the furnace, regulating the power range to be 15-35kW, controlling the temperature at 600-1300 DEG C and casting after smelting for 1-10 minutes. The process has simple operation, good controllability, stable components of the prepared hydrogen storage alloy and lower cost and can realize low-cost and large-scale production.
Owner:UNIV OF SCI & TECH BEIJING

Polytetrafluoroethylene composite, polytetrafluoroethylene composite holder for bearing and preparation method of polytetrafluoroethylene composite holder for bearing

The invention discloses a polytetrafluoroethylene composite, a polytetrafluoroethylene composite holder for a bearing and a preparation method of the polytetrafluoroethylene composite holder for the bearing. The polytetrafluoroethylene composite is prepared from, by mass, 3%-8% of coupling agent modified nano aluminum oxide, 2%-5% of molybdenum disulfide and 90%-95% of polytetrafluoroethylene. The polytetrafluoroethylene composite is prepared by compounding polytetrafluoroethylene, coupling agent modified nano aluminum oxide and molybdenum disulfide. Nano aluminum oxide is large in heat conductivity and small in grain size, the crushing resistance, heat conductivity and wear resistance of the composite can be remarkably improved, the material surface activity can be improved after nano aluminum oxide is modified with a coupling agent, and surface binding force is increased. The friction and wear resistance of the composite can be enhanced through molybdenum disulfide; the composite has excellent self-lubricating performance and high tensile strength, crushing resistance, heat conductivity and friction and wear resistance are obviously improved, and the requirement of the ultralow-temperature high-speed bearing on the holder is met.
Owner:LUOYANG BEARING RES INST CO LTD

Silicide/oxide composite negative electrode material with lithium silicate interface layer and preparation method

The invention provides a silicide / oxide composite negative electrode material with a lithium silicate interface layer and a preparation method, and belongs to the field of lithium ion batteries. The silicide / oxide composite negative electrode material with the lithium silicate interface layer comprises a silicon active center, an oxide substrate and the lithium silicate interface layer, wherein the lithium silicate interface layer is positioned between the silicon active center and the oxide substrate. By adopting a method that chemical deposition is combined with high-temperature solid-phase reaction, excessive lithium ions are adsorbed by virtue of good adsorption properties of deposition reaction products, so that the lithium silicate interface layer is formed in situ between the silicon active center and the oxide substrate through high-temperature solid-phase reaction of the lithium ions and trace silicon oxide on a silicon surface, not only is a continuous channel for lithium ion transmission provided, but also the lithium silicate interface layer can be used as an effective protection interface to reduce the reaction property of the active center and the oxide substrate, and therefore, good electrochemical circulation properties can be achieved. The processes related to the silicide / oxide composite negative electrode material are very simple, and the composite material prepared by using the method is excellent in interfacial compatibility.
Owner:DALIAN MARITIME UNIVERSITY

Method for controlling homogeneity of structure properties of high-strength and high-plasticity TB6 titanium alloy wires

ActiveCN108893691AOptimizing the preparation process parametersHigh room temperature tensile strengthStructure propertyRoom temperature
The invention belongs to the technical field of preparation of titanium alloy wires, and particularly relates to a method for controlling homogeneity of structure properties of high-strength and high-plasticity TB6 titanium alloy wires. The method comprises the following steps: carrying out multi-pass large deformation hot rolling on a TB6 titanium alloy bar with the specification of phi 40mm- phi45mm* 800mm-1200mm at first to obtain a bar with the specification of phi 9 mm-phi 10 mm; then carrying out single-phase region solid-solution treatment and then carrying out cold rolling, and controlling total deformation of cold rolling to be 15-36% to obtain a wire with the specification of phi 6 mm-phi 7 mm; and finally, carrying out ageing treatment on the wire at the temperature of 520-560 DEG C. The method is simple in process parameter setting, convenient to operate and high in process controllability, and the tensile strength sigma b of the wire in an aged state at the room temperature is greater than or equal to 1050 MPa, the yield strength sigma 0.2 is greater than or equal to 1000 MPa, the elongation delta 5 is greater than or equal to 15%, the percentage reduction of area psiis greater than or equal to 50%, the batch stability is high, and the repeatability is good.
Owner:AVIC BEIJING INST OF AERONAUTICAL MATERIALS
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