Patent classifications
C04B35/632
Method for making ceramic thin exterior part
A method for making a thin ceramic part involves making a casting slurry including a ceramic powder, a solvent, a binder, a plasticizer, and a dispersant. The casting slurry is tape casted to achieve a single layer green tape. At least two single layer green tapes are laminated to form a green tape lamination. The green tape lamination is dry pressed, dried, shaped, degreased, and fired to achieve the exterior component required.
Dental ceramic article, process of production and use thereof
The present disclosure relates to a dental ceramic article comprising ceramic components, the ceramic components having ZrO2 and Al2O3 and at least one component comprising Mn, Er or mixtures thereof, Al2O3 being present in an amount below about 0.15 wt.-% with respect to the weight of the ceramic article. The present disclosure relates also to kit of parts comprising a ceramic article and a coloring solution and processes for producing a dental ceramic article.
Dental ceramic article, process of production and use thereof
The present disclosure relates to a dental ceramic article comprising ceramic components, the ceramic components having ZrO2 and Al2O3 and at least one component comprising Mn, Er or mixtures thereof, Al2O3 being present in an amount below about 0.15 wt.-% with respect to the weight of the ceramic article. The present disclosure relates also to kit of parts comprising a ceramic article and a coloring solution and processes for producing a dental ceramic article.
SILICON NITRIDE CERAMIC MATERIAL FOR MOBILE PHONE REAR COVER AND PREPARATION METHOD THEREFOR
A silicon nitride ceramic material for a mobile phone rear cover and a preparation method therefor. The method comprises: using a mixture of a silicon source, a colorant, and a sintering aid as raw materials, mixing the raw material components, and performing shaping and sintering to obtain the silicon nitride ceramic material. The toughness of the silicon nitride ceramic material can reach more than 12 MPa.Math.m.sup.1/2; the thermal conductivity thereof can reach 40 to 70 W/m.Math.K; and a dielectric loss thereof is 10.sup.−4.
High Strength Shaped Aluminas and a Method of Producing Such High Strength Shaped Aluminas
A method of producing high strength shaped alumina by feeding alumina power into an agglomerator having a shaft with mixers able to displace the alumina power along the shaft, spraying a liquid binder onto the alumina power as it is displaced along the shaft to form a shaped alumina, and calcining the shaped alumina. The shaped alumina produced having a loose bulk density of greater than or equal to 1.20 g/ml, a surface area less than 10 m.sup.2/g, impurities of less than 5 ppm of individual metals and less than 9 ppm of impurities in total, and/or crush strength of greater than 12,000 psi.
High Strength Shaped Aluminas and a Method of Producing Such High Strength Shaped Aluminas
A method of producing high strength shaped alumina by feeding alumina power into an agglomerator having a shaft with mixers able to displace the alumina power along the shaft, spraying a liquid binder onto the alumina power as it is displaced along the shaft to form a shaped alumina, and calcining the shaped alumina. The shaped alumina produced having a loose bulk density of greater than or equal to 1.20 g/ml, a surface area less than 10 m.sup.2/g, impurities of less than 5 ppm of individual metals and less than 9 ppm of impurities in total, and/or crush strength of greater than 12,000 psi.
Phase-change material and method for producing same
A method for producing a form-stable phase-change material includes freezing a slurry of solid and solvent to provide a frozen slurry, exposing the frozen slurry to conditions causing sublimation of the frozen solvent to remove solvent and provide a body having vacancies therein, sintering the body to provide a scaffold, and adding a molten phase-change material to the scaffold to provide the form-stable phase-change material. The same scaffold when ground acts as a phase-change nucleating aid.
Dental Mill Blank, Process for Production and Use Thereof
The invention relates to a coloured zirconia ceramic dental mill blank having fluorescing properties, processes of production such a mill blank and uses thereof, in particular for producing zirconia ceramic dental restorations.
The dental mill blank having a shape allowing the dental mill blank to be attached or fixed to a machining device, the dental mill blank comprising a porous zirconia material, the porous zirconia material comprising the oxides Zr oxide calculated as ZrO.sub.2: from about 80 to about 97 wt.-%, Al oxide calculated as Al.sub.2O.sub.3: from about 0 to about 0.15 wt.-%, Y oxide calculated as Y.sub.2O.sub.3: from about 1 to about 10 wt.-%, Bi oxide calculated as Bi.sub.2O.sub.3: from about 0.01 to about 0.20 wt.-%, Tb oxide calculated as Tb.sub.2O.sub.3: from about 0.01 to about 0.8 wt.-%, and optionally one or two of the following oxides: Er oxide calculated as Er.sub.2O.sub.3: from about 0.01 to about 3.0 wt.-%, Mn oxide calculated as MnO.sub.2: from about 0.0001 to about 0.08 wt.-%, wt.-% with respect to the weight of the porous zirconia material.
Dental Mill Blank, Process for Production and Use Thereof
The invention relates to a coloured zirconia ceramic dental mill blank having fluorescing properties, processes of production such a mill blank and uses thereof, in particular for producing zirconia ceramic dental restorations.
The dental mill blank having a shape allowing the dental mill blank to be attached or fixed to a machining device, the dental mill blank comprising a porous zirconia material, the porous zirconia material comprising the oxides Zr oxide calculated as ZrO.sub.2: from about 80 to about 97 wt.-%, Al oxide calculated as Al.sub.2O.sub.3: from about 0 to about 0.15 wt.-%, Y oxide calculated as Y.sub.2O.sub.3: from about 1 to about 10 wt.-%, Bi oxide calculated as Bi.sub.2O.sub.3: from about 0.01 to about 0.20 wt.-%, Tb oxide calculated as Tb.sub.2O.sub.3: from about 0.01 to about 0.8 wt.-%, and optionally one or two of the following oxides: Er oxide calculated as Er.sub.2O.sub.3: from about 0.01 to about 3.0 wt.-%, Mn oxide calculated as MnO.sub.2: from about 0.0001 to about 0.08 wt.-%, wt.-% with respect to the weight of the porous zirconia material.
VAPORIZATION CORE, ELECTRONIC VAPORIZATION DEVICE, AND METHOD FOR MANUFACTURING THE SAME
A vaporization core, a method of manufacturing the same, and an electronic vaporization device comprising the same are disclosed. The vaporization core includes a tubular porous substrate for forming a vaporization cavity and configured to guide liquid outside the tubular porous substrate into the vaporization cavity and a heating element disposed on an inner wall of the tubular porous substrate and configured to heat and vaporize the liquid guided into the vaporization cavity.