103 results about "Yttrium silicate" patented technology

An article comprising a silicon-containing substrate, a silicide-containing bond coat layer overlying the substrate, and typically an environmental barrier coating overlaying the bond coat layer. An article is also provided wherein the environmental barrier coating comprises: (1) an optional inner silica scale layer overlaying the bond coat layer; (2) intermediate layer overlaying the inner silica scale layer, or the bond coat layer in the absence of the inner silica scale layer, and comprising mullite, or a combination of mullite with a barium strontium aluminosilicate, a yttrium silicate, or a calcium aluminosilicate; and (3) an outer steam-resistant barrier layer overlaying the intermediate layer and consisting essentially of an alkaline earth silicate/aluminosilicate. Processes are also provided for forming the silicide-containing bond coat layer over the substrate, followed by forming the environmental barrier coating over the bond coat layer.

A shell mold for casting molten material to form an article is described. The mold includes a shell for containing the molten material, formed from at least one of yttrium silicates, zirconium silicates, hafnium silicates, and rare earth silicates. The mold also includes a facecoat disposed on an inner surface of the shell that contacts the molten material. The facecoat can be made from the materials described above. A method of casting a niobium-silicide article is also described, using the shell mold described herein. A method of making the ceramic shell mold is described as well, along with a slurry composition used in the manufacture of the shell mold.

Embodiments relate to a coated substrate and a method of making and using the same. A plasma-spray coated layer may be formed on a substrate, wherein the plasma-sprayed coated layer comprises a rare-earth oxide (e.g., yttrium oxide), a rare-earth fluoride (e.g. yttrium fluoride), or a rare-earth silicate (e.g. yttrium silicate). An exposed surface of the plasma-spray coated layer may be irradiated to form a treated portion of the layer, wherein the treated portion of the layer has a mean spacing of local peaks (S value) between about 100 and 200 microns. A second layer may be formed on the treated portion of the plasma-spray coated layer, wherein the second layer comprises a dielectric material.

The present invention provides a surface coating system of fiber reinforced ceramic matrix composite material, wherein the surface coating system is arranged on the substrate surface of the fiber reinforced ceramic matrix composite material and comprises a Sic coating layer, a mullite coating layer and a yttrium silicate coating layer laid in order from bottom to top. The preparation method comprises the following steps of preparing sludge raw materials of the Sic coating layer, the mullite coating layer and the yttrium silicate coating layer respectively, and preparing the Sic coating layer, the mullite coating layer and the yttrium silicate coating layer. The present invention is used for the surface coating system of the fiber reinforced ceramic matrix composite material, has the advantages of high density, high temperature resistance and anti-oxidation.

The invention relates to a yttrium silicate modified silicon carbide fiber reinforced silicon carbide composite material and a preparation method thereof. The preparation method comprises the following steps: (1) sequentially preparing a yttrium silicate interface layer and a silicon carbide interface layer on the surface of a silicon carbide fiber prefabricated body so as to obtain a yttrium silicate modified silicon carbide fiber prefabricated body; (2) soaking the yttrium silicate modified silicon carbide fiber prefabricated body prepared in the step (1) into a carbon precursor solution, and sequentially carrying out a curing step and a cracking step on the soaked yttrium silicate modified silicon carbide fiber prefabricated body; (3) at least repeating the step (2) once so as to obtaina porous silicon carbide fiber prefabricated body; (4) carrying out a liquid silicon infiltration reaction on the porous silicon carbide fiber prefabricated body prepared in the step (3), thereby obtaining a yttrium silicate modified SiC/SiC composite material. The yttrium silicate modified SiC/SiC composite material provided by the invention has excellent oxidation resistance, temperature resistance, vapor corrosion resistance, and the like, and is excellent in comprehensive property.

The invention relates to a method for preparing an yttrium silicate coat by cathode rotation hydrothermal electrophoretic deposition. A cathode rotation hydrothermal electrophoretic deposition method is used for preparing an yttrium silicate antioxidant coat on the surface of carbon/carbon-carborundum composite. Yttrium silicate powder is used as raw material to be respectively made into the yttrium silicate coats with compact structure, microcrack and different thickness in certain powder material proportion, under certain temperature and voltage and at different cathode rotation speeds. The method has the advantages of simple technical control and uniform coat, avoids repeated operation to certain extent and can be used for product with complex surface, and the method can obtain the yttrium silicate coat with controllable structure and good performance under low temperature.

The invention relates to a preparation method of a controllable yttrium silicate nano-rod. The preparation method comprises the following steps: respectively adding NaOH and analytically pure (NO3)3.6H2O and Na2SiO3.9H2O into distilled water, adjusting the pH to 4-13 and obtaining a solution A; adding the solution A into a hydro-thermal reaction kettle, sealing the hydro-thermal reaction kettle, placing the hydro-thermal reaction kettle into a temperature and pressure double-control microwave hydro-thermal reaction instrument, naturally cooling to room temperature after reaction, and obtaining a solution B; opening the hydro-thermal reaction kettle, collecting the product through filtering, washing the product by respectively adopting de-ionized water and absolute ethyl alcohol or isopropanol, drying the product in an electrothermal blowing dry box and obtaining a final product, i.e. yttrium silicate nano-powder. The invention adopts microwave hydro-thermal method to synthesize yttrium silicate nano-crystal, and then controls the yttrium silicate nano-structure through processes of anneal, and the like. The invention has the advantages of simple process preparation, convenient operation, easily obtained materials, low preparation cost, short reaction period, low temperature and good repetitiveness. The yttrium silicate nano-powder prepared by the method has narrow distribution of grain diameter, controllable crystal grain shape and higher purity.

The invention relates to a preparation method of yttrium silicate ceramic powder, in particular relates to a preparation method of yttrium silicate ceramic powder for environment barrier coating, and belongs to the technical field of oxide ceramic material preparation. The method comprises the following steps: using a yttrium solution with Y<3+> ion concentration of 0.6-1.5 mol/L as solution A; weighing silicate ester according to a molar ratio of Y to Si being 2: 1; adding alcohol and water in the weighed silicate ester according to a volume ratio of the silicate ester to alcohol to water being 1: 1-2: 2-6 to obtain solution B; uniformly mixing the solutions A and B solution to obtain the mixed solution containing aluminum and silicon; adding the mixed solution containing aluminum and silicon into ammonium hydroxide with pH value of 9-10 at a speed of dropwise adding 0.2-0.5 L of the mixed solution containing aluminum and silicon in 1L of precipitator every minute, and stirring to obtain the co-precipitate; after the reaction is finished, standing, filtering, washing and drying the residue, calcining for at least 4 hours at 800-1000 DEG.C to obtain the Y2SiO5 ceramic composite powder. The method provided by the invention is short in reaction period and good in repeatability; and the obtained product is high in purity and is of a single crystal form.

The invention is a gadolinium silicate scintillator growing method, mainly using the crystals with structures similar to gadolinium silicate's, like lutecium silicate, yttrium silicate and lutecium yttrium silicate, their chemical general formula: (Lu1-xYx)2SiO5(0<=x<=1), as seed crystals, and by selecting a proper seeding temperature, generally at 2200-1980 deg.C, able to grow uncracked gadolinium silicate crystal. It solves the cracking problem of seed crystals when processing, primely solves the problem of cracking or breaking at the seed crystals when crystal growing, and extremely enhancing the yield.

The invention relates to a cerous ion-doped rare earth silicate polycrystal material and a preparation method thereof, which is characterized in that the rare earth silicate is lutecium silicate, yttrium silicate or lutecium and yttrium silicate; the mol percentage of the doped cerous compound is 0.2 percent to 2 percent; the general formula of the doped rare earth silicate is Ln<2(1-x)>Ce2xSiO3, wherein, x is equal to0.002 to 0.02, and Lu is one or two types of Y and Lu. The doped cerous compound is Ce2(CO3)3, Ce(NO3)3, Ce2(C2O4)3, Ce(CH3COO)3 or Ce(OH)3. The polycrystal material is directly synthesized or prepared by doping the cerous compound and liquid-phase mixing. The invention most reduces the introduction of Ce<+4> raw material, eliminates the quenching impact of the Ce<+4> on the luminescence of Ce<+3>, reduces the sintering temperature of the polycrystal material, and improves the scintillation properties of the material, such as light output, energy resolution and the like.

The invention discloses Sc/Ce-codoped lutetium silicate and lutetium yttrium silicate crystals and a melt-process growth method thereof. The molecular formulae are Sc[2x]Ce[2y]Lu2[(1-x-y)]SiO[5] and Sc[2x]Ce[2y]Y[2z]Lu[2(1-x-y-z)]SiO[5]. The melt-process growth method comprises the following steps: as for the Sc[2x]Ce[2y]Lu2[(1-x-y)]SiO[5], proportionally preparing Sc2O3, CeO2, Lu2O3 and SiO2, sufficiently mixing, carrying out press forming, and carrying out high-temperature sintering to obtain a crystal growth initial raw material; or as for the Sc[2x]Ce[2y]Y[2z]Lu[2(1-x-y-z)]SiO[5], proportionally preparing Sc2O3, CeO2, Y2O3, Lu2O3 and SiO2, sufficiently mixing, carrying out press forming, and carrying out high-temperature sintering to obtain a crystal growth initial raw material; and heating to melt the growth initial raw material, and growing by a dip coating process or crucible descent process to obtain the scintillator monocrystals.

The invention relates to a rare earth silicate coating and a method for preparing a coating on the surface of a C/SiC composite material. In the method, a yttrium silicate coating and a ytterbium silicate coating with a relatively wide application prospect are synthesized by virtue of a chemical vapor reaction mechanism, combination of the coatings and a substrate is relatively tight, and the coatings are relatively dense. The method is simple in principle; the preparation temperature is relatively low; the coatings are not affected by the external shape of the substrate, so that large-scale industrial production can be achieved.

The invention relates to a method for preparing a carbon/carbon composite yttrium silicate whisker reinforced C-AlPO4-SiCn complex external coating. An induction heating auxiliary impulse arc discharge deposition method is adopted for preparing the carbon/carbon composite yttrium silicate whisker reinforced C-AlPO4-SiCn complex external coating which has a uniform surface free from microcracks, is uniform in thickness, has no penetrable holes or cracks, and is higher in binding force and good in oxidation resistance. As suspended charge particles have high energy and are high in diffusion migration rate under the condition of induction heating, the reaction is accomplished in a water heat kettle at one time, and pulsed arc discharge sintering is accompanied; the coating is dense and uniform, has a higher interface binding force, and is not required to be subjected to post heat treatment; the preparation cost is low; and the method is simple to operate and short in preparation cycle. In addition, the electromagnetic induction heating can allow local high temperature and high pressure to be generated in a reaction system rapidly, so that the reaction activation energy of yttrium silicate whiskers, and C-AlPO4 and SiCn suspended particles is reduced effectively, the yttrium silicate whiskers, and C-AlPO4 and SiCn suspended particles can react more completely and sufficiently during the pulsed arc discharge deposition process; and the coating with a dense structure is obtained.

The invention relates to a SiC/SiC composite material wide temperature range thermal protective coating. The coating is composed of a transition layer, a hole-sealing layer and an anti-washout layer.The transition layer is made of SiC and SiBCN ceramic prepared through a polymer precursor infiltration and pyrolysis (PIP) technology. The hole-sealing layer is made of SiBCN ceramic prepared througha slurry method and CVD-SiC prepared through a chemical vapor deposition technology. The anti-washout layer is made of a yttrium silicate coating prepared through a molten-salt growth method. The invention further relates to a preparation method of the SiC/SiC composite material wide temperature range thermal protective coating. The coating has excellent thermal shock resistance and antioxidant property in the wide temperature range of 800-1300 DEG C, and has wide application prospects in hot end parts such as aero-engine exhaust nozzles, heat shields and turbine outer rings and thermal protective structures of aircrafts with high Mach number such as leading edges and rudders.

The invention discloses a brake pad friction material composition and a preparation method thereof, and a brake pad. The brake pad friction material composition comprises a binding agent, a reinforcing material and a friction performance modifier. The binding agent comprises modified phenolic resin and silicone resin. The reinforcing material comprises aluminum silicate fiber, steel fiber, carbonfiber, aramid fiber, polybenzimidazole fiber, polyphenylene sulfide fiber and polytetrafluoroethylene fiber. The friction performance modifier comprises mullite whisker, silicon nitride, yttrium silicate, silicon carbide, boron nitride, silicon dioxide aerosol, titanium nitride and titanium carbide. The friction coefficient of the brake pad manufactured by the adoption of the brake pad friction material composition is high and stable in the braking process, the wear rate is small, and the brake pad has excellent heat stability, is low in noise and shakes little.

The invention provides a preparation method of an yttrium silicates coating having the oxidation resistance, the method adopts a novel hydrothermal electrophoretic deposition technique to prepare the yttrium silicates coating with oxidation resistance, and the method has the advantages of high efficiency, low manufacturing cost, good coating compactness and excellent oxidation resistance of the coating.

The invention relates to a method for preparing a carbon/carbon composite yttrium silicate whisker reinforced mullite-C-AlPO4 complex external coating. A pulsed arc discharge deposition method is adopted to prepare the yttrium silicate whisker reinforced mullite-C-AlPO4 complex antioxidant external coating; the reaction is accomplished in a water heat kettle at one time; pulsed arc discharge sintering is accompanied; the obtained coating is dense and uniform, has a higher interface binding force and is not required to be subjected to post heat treatment; the advantages of yttrium silicate whiskers, mullite and C-AlPO4 are integrated well; and the prepared yttrium silicate whisker reinforced mullite-C-AlPO4 complex antioxidant external coating has a uniform surface without microcracks, is uniform in thickness, has no penetrable holes or cracks, and is higher in binding force and good in oxidation resistance.

The invention relates to the field of hot-spray coating materials, particularly an yttrium silicate hot-spray composite powder and a preparation method thereof. The hot-spray composite powder is prepared from the following raw materials in percentage by weight: 23-27% of SiO2 and 73-77% of Y2O3. The particle size of SiO2 is smaller than 25 mu m, and the particle size of the Y2O3 is smaller than 15 mu m. The preparation method comprises the following steps: evenly mixing SiO2 and Y2O3 powder in a mixer for 20-24 hours, prepressing the mixed powder under the pressure of 600-800kPa, sintering at 1500-1700 DEG C in air for 4-6 hours, and finally, carrying out mechanical crushing and screening. The components of the hot-spray composite powder are Y2SiO5 and Y2Si2O7, the particle size is 45-125 mu m, the flowability is smaller than or equal to 55s/50g, and the loose density is 1.5-3.0g/cm<3>. The coating prepared by the powder can effectively enhance the high-temperature oxidation resistance of the C/C-SiC composite material surface, has important application value, and can solve the problem of high-temperature oxidation of the material.

The invention belongs to the field of fluorescent powder, and discloses an yttrium silicate upconversion luminous fluorescent powder, and a preparation method and application thereof. The fluorescent powder has a structure of Y2-xSiO5:xHo<3+>; Ho<3+> is a doping ion; and x is in the range from 0.02 to 0.1. The yttrium silicate upconversion luminous fluorescent powder prepared by the invention can realize blue short-wavelength light emitting through excitation by long-wave radiation from infrared to green ray. Therefore, the fluorescent powder can make up for the lack of blue material in current display and luminous material.