Highly dense lithium based ceramics can be prepared by a low temperature process including combining a lithium based ceramic with a polar solvent having a lithium based salt dissolved therein and applying pressure and heat to the combination to form a salt-ceramic composite. Advantageously, the lithium salt is one that dissolves in the polar solvent and the heat applied to the combination is no greater than about 250 C. Such composites can also have high ionic conductivity.

It is intended to suppress flaming and smoking due to combustion of combustible substances in a certain-shaped joint material, while maintaining hot sealability of the certain-shaped joint material. A certain-shaped joint material for hot installation is obtained by: adding organic additives to a blend in a combined amount of 26 mass % to 50 mass %, with respect to and in addition to 100 mass % of the blend, wherein the blend comprises 50 mass % to 90 mass % of gibbsite type aluminum hydroxide raw material, 1 mass % to 9 mass % of clay, and 9 mass % to 23 mass % of graphite, with the remainder mainly composed of an additional refractory raw material; and subjecting the resulting mixture to kneading, forming and drying.

The present disclosure provides a high-temperature nano-composite coating and a preparation method thereof, and a small bag flexible packaging coating. The high-temperature nano-composite coating provided by the present disclosure controls the fiber length. Moreover, high-temperature reinforcing filler and high-temperature expansion filler are introduced, to make the coating have ultra-high strength at high temperature without cracks caused by shrinkage at high-temperature. In addition, nanopowder, high-temperature skeleton filler and other additives are introduced to make the coating be uniform and stable and reach a slurry state similar to toothpaste. There is no precipitation and stratification during the placement process. Small packaging can be realized to facilitate construction and operation. Besides, the coating has a good bonding to furnace lining, and will not fall off from the furnace lining, thereby prolonging the service life of the furnace lining.

Set forth herein are garnet material compositions, e.g., lithium-stuffed garnets and lithium-stuffed garnets doped with alumina, which are suitable for use as electrolytes and catholytes in solid state battery applications. Also set forth herein are lithium-stuffed garnet thin films having fine grains therein. Disclosed herein are novel and inventive methods of making and using lithium-stuffed garnets as catholytes, electrolytes and/or anolytes for all solid state lithium rechargeable batteries. Also disclosed herein are novel electrochemical devices which incorporate these garnet catholytes, electrolytes and/or anolytes. Also set forth herein are methods for preparing novel structures, including dense thin (<50 um) free standing membranes of an ionically conducting material for use as a catholyte, electrolyte, and, or, anolyte, in an electrochemical device, a battery component (positive or negative electrode materials), or a complete solid state electrochemical energy storage device. Also, the methods set forth herein disclose novel sintering techniques, e.g., for heating and/or field assisted (FAST) sintering, for solid state energy storage devices and the components thereof.

Set forth herein are garnet material compositions, e.g., lithium-stuffed garnets and lithium-stuffed garnets doped with alumina, which are suitable for use as electrolytes and catholytes in solid state battery applications. Also set forth herein are lithium-stuffed garnet thin films having fine grains therein. Disclosed herein are novel and inventive methods of making and using lithium-stuffed garnets as catholytes, electrolytes and/or anolytes for all solid state lithium rechargeable batteries. Also disclosed herein are novel electrochemical devices which incorporate these garnet catholytes, electrolytes and/or anolytes. Also set forth herein are methods for preparing novel structures, including dense thin (<50 um) free standing membranes of an ionically conducting material for use as a catholyte, electrolyte, and, or, anolyte, in an electrochemical device, a battery component (positive or negative electrode materials), or a complete solid state electrochemical energy storage device. Also, the methods set forth herein disclose novel sintering techniques, e.g., for heating and/or field assisted (FAST) sintering, for solid state energy storage devices and the components thereof.

A ceramic deep-frying device capable of withstanding high temperatures and releasing far-infrared energy is made by grinding and mixing mullite, spodumene, energy ceramic material, ball clay, and kaolin clay into clay blank; molding the blank into ceramic green body; and sintering the green body at 1250-1320 C. for 18-24 hours. The device is completely immersed in the oil in a deep-frying vessel while leaving a gap between the device and heating pipe in the vessel or the inner bottom wall of the vessel, for enabling the oil to circulate through the through holes in the device due to temperature difference in the oil, causing the energy ceramic material to release anions and far-infrared rays that decrease van der Waals forces between oil molecules, and hence split, the oil molecules, thereby extending the service life of the oil, shortening the deep-frying time required, and lowering the oil content of deep-fried food.

Solid electrolytes, anodes and cathodes for SOFC. Doped BaCeO.sub.3 useful for solid electrolytes and anodes in SOFCs exhibiting chemical stability in the presence of CO.sub.2, water vapor or both and exhibiting proton conductivity sufficiently high for practical application. Proton-conducting metal oxides of formula Ba.sub.1xSr.sub.xCe.sub.1y1y2y3Zr.sub.y1Gd.sub.y2Y.sub.y3O.sub.3 where x, y1, y2, and y3 are numbers as follows: x is 0.4 to 0.6; y1 is 0.1-0.5; y2 is 0.05 to 0.15, y3 is 0.05 to 0.15, and cathode materials of formula II GdPrBaCo.sub.2zFe.sub.zO.sub.5+ where z is a number from 0 to 1, and is a number that varies such that the metal oxide compositions are charge neutral. Anodes, cathodes and solid electrolyte containing such materials. SOFC containing anodes, cathodes and solid electrolyte containing such materials.

A multilayer ceramic capacitor includes a multilayer body including a plurality of dielectric layers and a plurality of internal electrodes, wherein the dielectric layers and the internal electrodes are stacked alternately; and external electrodes provided on end surfaces of the multilayer body and electrically connected to the internal electrodes, wherein the dielectric layers each include main crystal grains including calcium and/or strontium, and zirconium; and an additive component including lithium, the internal electrodes include copper, and the dielectric layers have lithium concentrations with a standard deviation of about 1.03 atomic percent or less in the thickness direction.

A ceramic material includes zirconia toughened alumina (ZTA), which is doped with zinc ions and other metal ions, in which the other metal ions are chromium (Cr) ions, titanium (Ti) ions, gadolinium (Gd) ions, manganese (Mn) ions, cobalt (Co) ions, iron (Fe) ions, or a combination thereof. The ceramic material may have a hardness of 1600 Hv10 to 2200 Hv10 and a bending strength of 600 MPa to 645 MPa. The ceramic material can be used as wire bonding capillary.

A multilayer ceramic capacitor includes: a ceramic body including dielectric layers and first and second internal electrodes disposed to face each other with respective dielectric layers interposed therebetween; and first and second external electrodes disposed on an external surface of the ceramic body, wherein the dielectric layer contains a barium titanate-based powder particle having a core-shell structure including a core and a shell around the core, the shell having a structure in which titanium is partially substituted with an element having the same oxidation number as that of the titanium in the barium titanate-based powder particle and having an ionic radius different from that of the titanium in the barium titanate-based powder particle, and the shell covers at least 30% of a surface of the core.