422results about How to "Improve sinterability" patented technology

Stable supply of a cathode material for a lithium secondary battery that exels in sinterbility and composition stability and can exhibit satisfactory battery performance is accomplished by reducing to 100 ppm or less both the contents of Na and S being impurity elements in multiple oxides as materials for a cathode material for a lithium secondary battery and carbonic salts as precursor materials for the production of a cathode material for a lithium secondary battery.

A method of performing direct current pressurized sintering to powder in a mold having a cylindrical molding space, wherein sintering is continuously effected while relatively moving a current portion and a sintering subject; and a sintering device characterized in that the vertical position of the current electrodes is unchanged and the mold and the sintering subject are successively moved with respect to the current electrodes, so as to effect continuous sintering. A sintering method and a sintering device that are superior in sintering ability are provided wherein even if the sintered body is in the form of a long-size rod or has an uneven cross-section, the sintered body is uniform in quality.

The invention relates to a method for preparing black zirconia ceramics at the low temperature and belongs to the technical field of the preparation of high-temperature structural material. The method respectively uses a homogeneous precipitation method for synthesizing a nanometer coloring agent, and a coprecipitation method for synthesizing nanometer zirconia powder, and adopts Fe-Co-Ni-Mn as a coloring agent. The zirconia powder is not added with any sintering additive, only added with small amount of coloring agent and sintered at the temperature of 1150-1350 DEG C, thus obtaining the black zirconia ceramics with excellent performance and bright color. As the homogeneous precipitation method is adopted for synthesizing coloring agent powder, the monodisperse nanometer particles with uniform powder granules, narrow size distribution and high purity are obtained so that the coloring agent easily colors the particles. As the coprecipitation method is used for synthesizing zirconia powder, nanometer particles with small granularity, big superficial area and high activity are obtained, and can reduce the temperature of the solid-phase reaction, greatly reduce the sintering temperature and solve the problem that the black coloring agent oxide decomposes and volatiles at the high temperature. Simultaneously the method adopts the Fe-Co-Ni-Mn as the coloring agent, thus avoiding the poisonous function of Cr on the human body.

A selective laser sintering quick manufacturing of the mold comprises CAD three dimension model design, storing STL files after treatment by the section software, sending the STL data to SLS quick forming machine. Spreading a composite powder of polyamide and copper on the power bed of selective laser sintering machine, with copper powder grain side 200--400, their weight ratio ranging 2:1-7:1, scanning and sintering in the selected zone of the laser harness, laser speckle 10-250 mum, scanning distance 0.04-0.1mm, scanning speed 1000- 3000mm/s, single layer thickness 70-150 mum, repeating till the formation of the complete mold inlaid, coating the surface with epoxide resin or acrylic acid series solidification system, polishing the surface thereafter. It is simple in process, short in processing period, low in cost, suitable for small volume plastic parts pilot run, testing and production.

The invention relates to the technical field of high molecular materials and particularly relates to preparation and application methods of a selective laser sintering polypropylene powdery material. The method comprises the following steps: obtaining polypropylene powder by a freeze grinding method; grading and collecting by an airflow screening machine, selecting polypropylene powder with the granularity in a range of 200-800 meshes and returning coarse materials which do not meet the fineness requirement to a stock bin and continuously smashing; and adding 100 parts of polypropylene powder, 0.1-1 part of graphite powder, 0.01-0.5 part of antioxidant and 0.5-6 parts of metallic soap salt and uniformly mixing in a high speed mixer, wherein the granularity of the graphite powder is 1000-5000 meshes and the antioxidant is a compound antioxidant consisting of phenols and phosphonate or thioester in a weight ratio of 1:1. The polypropylene powder prepared by the invention has excellent sintering performance and the SLS (Selective Laser Sintering) formed piece prepared by the polypropylene powder has high mechanical property and dimensional precision.

The invention discloses a high-strength light foam ceramic plate and a manufacturing method thereof, and belongs to the field of building material manufacturing. The ceramic plate comprises the following materials in percentage by weight: 10-30 percent of sludge/bottom mud, 20-30 percent of building waste, 15-25 percent of waste ceramic, 10-25 percent of waste glass, 5-15 percent of bentonite, 5-15 percent of kaolin, 0.5-5 percent of aluminum powder, 5-10 percent of sodium bicarbonate, 0.5-1.5 percent of animal albumen foaming agent and 9-16 percent (percentage of total amount of the solid matters) of water. The manufacturing method comprises the following steps of: mixing and crushing the main raw material; adding the animal albumen foaming agent and water; granulating; filling a granular material into a refractory combined mould; leveling; filling in a kiln; firing; and performing cold processing to produce a ceramic plate finished product. The high-strength light foam ceramic plate has the advantages of high product strength, small volume weight, fire proofing, excellent freeze proofing, long-term water proofing, readily available main raw material which basically comes from environmental solid waste, has a wide source and is low in cost and adoption of the animal albumen foaming agent of small using amount and wide source; the manufacturing process has the advantages of simplicity, high efficiency, energy conservation, environmental friendliness, no secondary pollution; and the high-strength light foam ceramic plate can be used as thermal insulation decorative materials, fire barriers and the like of exterior walls of buildings.

A process for preparing the superfine alloy powder by codeposition-coreduction method includes such steps as liquid-phase codeposition to prepare the precursor powder of each component in alloy, calcining to obtain nano-class composite metallic oxide powder, and reducing by H2 or decomposed ammonia in tubular reducing furnace while alloying to obtain superfine alloy powder.

An alumina ceramic composition comprising 10 weight % or less (calculated as MgO) of Mg, and 0.2-10 weight % or more (calculated as TiO2) of Ti, the balance being substantially an Al2O3 phase and inevitable impurities. An Al2TiO5 phase is precipitated in grain boundaries. The Al2TiO5 phase surrounds inevitable impurities in the grain boundaries. The alumina ceramic composition exhibits a Q factor of 850 or more when measured at a frequency of 10 GHz.

The invention relates to a preparation method of zirconium carbide ceramics powder; the method for rapidly preparing zirconium carbide ceramics powder is characterized in that: the method comprises the following steps: 1) raw material selection: the raw materials are selected according to 12:4-12:5 of mass ratio of zirconium propoxide solution and sugar and 8:32:1:1-8:64:2:4 of volume ratio of zirconium propoxide solution, normal propyl alcohol, chelant-acetic acid and water; the solvent acetic acid is selected according to (7-8)g:50ml of proportion of the sugar and the solvent acetic acid; 2) the preparation of dried gel power; 3) preparation of precursor powder; 4) heat treatment of the precursor powder; carbothermal reduction reaction is carried out under the conditions of high heating rate and short temperature preservation time, the synthesizing process of the zirconium carbide powder is shortened into dozens of minutes even several minutes, so as to obtain high-purity and refined zirconium carbide ceramics powder with good sintering character; single zirconium carbide phase can be analyzed by X-ray diffraction, the oxygen content in the product is 0.5-3 percent, and the free carbon content is from 0.2 to 2 percent; the crystal particles are uniform and tiny, and the mean grain size is less than 500nm.

The invention discloses an Al2O3/Ti(C,N) nano-composite metal ceramic die material. The Al2O3/Ti(C,N) nano-composite metal ceramic die material is characterized by being formed by performing hot-pressed sintering by taking nano-Al2O3 as a matrix, taking nano-Ti(C,N) as a hard dispersed phase, taking micron metals Mo, Ni and Cr as binding phases, and adding one or two of oxides Y2O3 and TiO2, and two or more of carbides TaC, NbC and VC as sintering aids. Compared with a die taking die steel or hard alloy as a material, the metal ceramic die material disclosed by the invention is more excellent in wear resistance, antioxidation and thermal shock resistance, and good in strength and toughness, as well as also has an application prospect in the aspects of tools and wear-resistant and corrosion-resistant components besides production for dies.

The invention discloses a high-temperature stable medium material for multilayer ceramic capacitors and a preparation method thereof. The medium material consists of a main component and a doping component; the chemical constitution of the main component is (1-x) BaTiO3-xBiScO3, wherein x is equal to between 0.5 and 0.15; the doping component is CaF2+4LiF, wherein the purity of the CaF2+4LiF is more than 99 percent and the molar doping quantity of the CaF2+4LiF is 1 to 5 percent of the total mol number of the main component. The preparation method comprises the following steps: firstly, using BaCO3 and TiO2 as raw materials and mixing the materials according to the stoichiometric proportion of the BaTiO3 to synthesize BaTiO3 powder with a tetragonal phase structure; secondly, mixing BaTiO3, Bi2O3 and Sc2O3 according to the stoichiometric proportion of (1-x) BaTiO3-xBiScO3, wherein x is equal to between 0.05 and 0.15; and finally, adding CaF2 and LiF powder which have a purity of more than 99 percent, mixing and ball milling the mixture in absolute ethanol for 48 hours, drying the milled mixture, adding a solution of polyvinylalcohol into the dried mixture for granulation, passing the product obtained after granulation through an 80 mesh sieve, subjecting the product to press forming and sintering and obtaining the medium material. The material has high dielectric constant, low dielectric loss and excellent temperature stability, can be sintered at intermediate temperature and is suitable to be sintered together with cheap base metals. The medium material can be used to produce multilayer ceramic capacitors having X8R and X9R properties.

The invention relates to a method for preparing boron carbon zirconium materials by liquid phase method, which belongs to the field of structural ceramics. By using carbothermal reduction as the basic principle and adopting zirconium oxychloride, boric acid and phenolic resin as the main materials, the method comprises the steps as follows: the phenolic resin is mixed with zirconia sol which is formed by titration of ammonia; then gel is formed by the titration of the ammonia; finally ball milling is carried out; after drying, screening and heat treatment, the ultrafine boron carbon zirconium materials can be obtained. The boron carbon zirconium materials which are prepared by the invention, with product granularity smaller than 200nm and excellent molding and sintering performance, can be applied to fields such as electron materials and refractory materials.

A refractory self-lubricating coated layer is prepared through proportionally mixing Ni, Cr, Cr2O3, BaF2, CaF2 and Ag high-energy ball grinding, preparing slurry, coating on the target surface, baking, cold isostatic pressing for compacting it, and sintering at 800-1200 deg.C for 1-3 hr. Its strength is more than 40 MPa.

The invention relates to a high intensity low conductivity magnesium aluminate spinel brick. The high intensity low conductivity magnesium aluminate spinel brick comprises the following ingredients: 20-25% magnesium aluminate composite material with granularity of 5-3 mm, 20-25% magnesium aluminate composite material with granularity of 3-1 mm, 12-16% fused magnesite with granularity of 1-0 mm, 12-16% fused magnesite with granularity of 180 F, 10-12% magnesium aluminate composite material with granularity of 180 F, 4-8% fused magnesium aluminate spinel with granularity of 180 F, 2-5% Alpha-Al2O3 fine powder, and calcium lignosulphonate which accounts for 3.5-5 weight percentage of the raw material. The high intensity low conductivity magnesium aluminate spinel brick is suitable for cement rotary kiln, has good sintering performance, thermal shock resistance, erosion resistance and permeating resistance, and has good economic and social benefits.

The purpose of the present invention is to provide a photosensitive conduction paste which is excellent in both of formability of high-fineness patterns and firing properties at <= 600 DEG C. The photosensitive conduction paste contains (A) silver powders having a low degree of crystallinity, (B) an organic binder, (C) a photopolymerizable monomer, and (D) a photopolymerization initiator, in which the silver powder (A) having the low degree of crystallinity exhibits a value of >= 0.15 DEG at a half peak width of the Ag (111) face peak in X-ray analysis patterns.

The invention discloses a preparation method for indium tin oxide (ITO) powder, which uses tin alloys as raw materials. The preparation method for the ITO powder comprises dissolving the tin alloys into nitric acid to generate metastannic acid polymer (H2SnO3) n, enabling In (OH) 3 to precipitate simultaneously with the (H2SnO3) n as the center, and sintering to obtain the ITO powder. Compared with the prior art, the preparation method for the ITO powder uses the tin alloys as the raw materials, the tin alloys react with the nitric acid to simultaneously generate indium oxide and tin oxide, evenness of the particle size of the prepared ITO powder is guaranteed, and sintering performance is good. Test results show that the crystallization sub diameter of the prepared ITO powder is D90/D50 and not larger than 3.5. In addition, the invention further provides a method using the ITO powder to prepare an ITO sintering body. The sintering body is even in constituent, even in crystallization particle size and high in density.