A preparation method of an alumina-carbon nano tube composite powder material includes the steps of using an organometallic precursor as a raw material, using metal nanoparticles formed on the surface of the alumina powder as a catalyst, and simultaneously feeding a carbonaceous gas such as methane and acetylene, so as to grow a carbon nano tube in situ, and obtain an alumina-metal nanoparticle-carbon nano tube composite powder material through a chemical vapor deposition method under a temperature condition of 400 to 800 C. Through changing various parameters such as the weight of the organic raw material, the flow or constituent of reactant gases and reaction temperature, the decomposition of the organic raw material and the generation of the metal nanoparticles and the carbon nano tube are adjusted, and the size and the microstructure of the powder are controlled.

In a monolithic refractory, in terms of a proportion in 100 mass % of a refractory raw material having a grain size of 8 mm or smaller, an amount of Ca.sub.XSr.sub.1XAl.sub.2O.sub.4 (where, 0X0.5) is 0.5 mass % or more and 10 mass % or less, and a polyvalent metal salt of oxycarboxylic acid is 0.05 mass % or more and 1.0 mass % or less.

A multiferroic material for magnetic and electric switching including Iron selenide (Fe.sub.3Se.sub.4) nanoparticles and its derivatives or doped with at least one element selected from transitional metals, rare earths elements or combination of the two and chalcogens. Ferroelectric polarization and coupling of magnetic and ferroelectric behavior in the doped Fe3Se4 is observed at a temperature ranging from 15 to 30 C.

A body including a first phase having silicon carbide, a second phase comprising a metal oxide, the second phase being a discrete intergranular phase located at the grain boundaries of the first phase, and the body has an average strength of at least 700 MPa.

A method for masking the appearance of a support structure underlying a highly translucent ceramic dental restoration is provided. The porous form of a zirconia ceramic dental restoration is treated with a liquid masking composition comprising 0.4 wt % to 50 wt % of one or more masking agents. The masking composition is applied to the internal surface of a restoration and a region of the facial surface of the restoration that is opposite the internal surface. After application of the masking compositions, treated zirconia restoration is sintered to greater than 98% theoretical density.

A coating apparatus is provided that includes: a mixer configured to generate mixed ceramic powder in which a material which contains an organic compound imparting lubricity to raw ceramic powder whose average particle size is smaller than or equal to 10 m and acts as an additive is mixed into the raw ceramic powder; a jetting device configured to jet the mixed ceramic powder toward a surface of a base material; and a heating device configured to heat the mixed ceramic powder jetted from the jetting device, and to evaporate the organic compound of the additive contained in the mixed ceramic powder.

Provided is a liquid material for forming a three-dimensional object. The liquid material is adapted to harden a powder material for forming a three-dimensional object containing an organic material. The liquid material contains a solvent and a cross-linking agent. A dynamic contact angle of the liquid material over a film made of the organic material is from 20 to 80.

Nanopowders containing nanoparticles having a core particle with a thin film coating. The core particles and thin film coatings are, independently, formed from at least one of a rare earth metal-containing oxide, a rare earth metal-containing fluoride, a rare earth metal-containing oxyfluoride or combinations thereof. The thin film coating may be formed using a non-line of sight technique such as atomic layer deposition (ALD). Also disclosed herein are nanoceramic materials formed from the nanopowders and methods of making and using the nanopowders.

A solid electrolyte which reduces grain boundary resistance and exhibits a high total ion conductivity is provided.

The solid electrolyte includes a first area which has a cubic garnet type crystalline and a second area which is amorphous, around the first area, in which each of the first area and the second area contains a composite oxide represented by formula (1) or (2) as a forming material, and an abundance ratio of metal atoms each having an ionic radius of 78 pm or more gradually increases from the first area to the second area.

Li.sub.7+xLa.sub.3xZr.sub.2A.sub.xO.sub.12(1)

[In formula (1), A is at least one selected from the group consisting of Mg, Ca, Sr, and Ba. In addition, x is 0.1 or more and 0.6 or less.]

Li.sub.7La.sub.3xZr.sub.2B.sub.xO.sub.12(2)

[In formula (2), B is at least one selected from the group consisting of Sc and Y. In addition, x is 0.1 or more and 0.6 or less.]

The present invention relates to a composite of a cobalt-based perovskite material with a negative thermal expansion material, and a preparation method of the same, and a solid oxide fuel cell (SOFC) comprising the same, and belongs to the technical field of fuel cells. In the present invention, a negative thermal expansion material is introduced into a cobalt-based perovskite oxide to successfully prepare an SOFC cathode material with excellent electrochemical performance and low thermal expansivity. The composite electrode achieves prominent mechanical tolerance in SOFC, which can moderate a volume change during the whole calcination process and enable a smooth transition to a high-temperature stage. The composite electrode has a thermal expansion coefficient (TEC) only of 12.9?10.sup.?6 K.sup.?1, which is perfectly matched with that of an SDC electrolyte. In addition, the composite shows excellent oxygen reduction reaction (ORR) activity, high TEC, and extremely-excellent anti-CO.sub.2 poisoning performance.