A solution of acid deficient uranyl nitrate has a formula of UO.sub.2(OH).sub.y(NO.sub.3).sub.2-y, where y ranges from 0.1 to 0.5. The solution is prepared by placing U.sub.xO.sub.z in aqueous nitric acid to produce a uranium solution, wherein x is 1 to 3 and z is 2 to 8; placing the uranium solution under a pressure greater than atmospheric pressure in a sealed reaction chamber; and heating the uranium solution to a desired temperature of between 150 C. and 250 C. by applying microwave energy to the uranium solution. The uranium solution is maintained at the desired temperature under a pressure of from 5 atmospheres to 40 atmospheres for a hold time of 15 minutes to 6 hours to produce the desired acid deficient uranyl nitrate.

A film-forming material of the present invention contains an oxyfluoride of yttrium represented by YO.sub.XF.sub.Y (X and Y are numbers satisfying 0<X and X<Y) and YF.sub.3, wherein a ratio I.sub.2/I.sub.1 of a peak height I.sub.2 of the (020) plane of YF.sub.3 to a peak height I.sub.1 of the main peak of YO.sub.XF.sub.Y as analyzed by XRD is from 0.005 to 100. It is preferable that a ratio I.sub.4/I.sub.1 of a peak height I.sub.4 of the main peak of Y.sub.2O.sub.3 to the peak height I.sub.1 of the main peak of YO.sub.XF.sub.Y as analyzed by XRD is 0.01 or less.

In an embodiment, a metal or metal-ion battery cell, includes anode and cathode electrodes, a separator electrically separating the anode and the cathode, and a solid electrolyte ionically coupling the anode and the cathode, wherein the solid electrolyte comprises a material having one or more rearrangeable chalcogen-metal-hydrogen groups that are configured to transport at least one metal-ion or metal-ion mixture through the solid electrolyte, wherein the solid electrolyte exhibits a melting point below about 350 C. In an example, the solid electrolyte may be produced by mixing different dry metal-ion compositions together, arranging the mixture inside of a mold, and heating the mixture while arranged inside of the mold at least to a melting point (e.g., below about 350 C.) of the mixture so as to produce a material comprising one or more rearrangeable chalcogen-metal-hydrogen groups.

In an embodiment, a metal or metal-ion battery cell, includes anode and cathode electrodes, a separator electrically separating the anode and the cathode, and a solid electrolyte ionically coupling the anode and the cathode, wherein the solid electrolyte comprises a material having one or more rearrangeable chalcogen-metal-hydrogen groups that are configured to transport at least one metal-ion or metal-ion mixture through the solid electrolyte, wherein the solid electrolyte exhibits a melting point below about 350 C. In an example, the solid electrolyte may be produced by mixing different dry metal-ion compositions together, arranging the mixture inside of a mold, and heating the mixture while arranged inside of the mold at least to a melting point (e.g., below about 350 C.) of the mixture so as to produce a material comprising one or more rearrangeable chalcogen-metal-hydrogen groups.

The present invention relates to a bio-electrode for current measurement including silicon carbide (SiC) doped at least partially with nitrogen (N). The bio-electrode for current measurement according to an embodiment of the present invention is a bio-electrode for a current measurement which is contact with an object to be analyzed, which generates a current signal by an electrochemical reaction, and includes silicon carbide (SiC) doped at least partially with nitrogen (N). The electrode may be used in a high-sensitive bio-quantification kit, a high-sensitive bio-quantification device, and an immunoassay device.

The present invention relates to a bio-electrode for current measurement including silicon carbide (SiC) doped at least partially with nitrogen (N). The bio-electrode for current measurement according to an embodiment of the present invention is a bio-electrode for a current measurement which is contact with an object to be analyzed, which generates a current signal by an electrochemical reaction, and includes silicon carbide (SiC) doped at least partially with nitrogen (N). The electrode may be used in a high-sensitive bio-quantification kit, a high-sensitive bio-quantification device, and an immunoassay device.

A method comprises reacting an aluminum feedstock with an acid in the presence of water to provide an aluminum salt solution comprising an aluminum salt in water, wherein the aluminum salt comprises a reaction product of the acid and aluminum, and spray roasting the aluminum salt solution at a temperature of at least about 450 C. to provide an aluminum oxide powder, wherein the spray roasting is performed in a furnace lined with a refractory comprising alumina that is at least about 99.2% purity alumina, and wherein the aluminum oxide powder is 99.2% pure aluminum oxide or greater.

A solid electrolyte material is represented by the following compositional formula (1): Li.sub.33+aY.sub.1+aM.sub.aCl.sub.6xyBr.sub.xI.sub.y where, M is at least one selected from the group consisting of Mg, Ca, Sr, Ba, and Zn; and 1<<2, 0<a<3, 0<(33+a), 0<(1+a), 0x6, 0y6, and (x+y)6 are satisfied.

Provided is a ceramic composition capable of achieving a light scattering function while maintaining optical properties at a high level. The ceramic composition comprises a fluorescence phase comprising a fluorescent material and a light-scattering phase comprising a lanthanum oxide. The lanthanum oxide may be, for example, at least one selected from LaAlO.sub.3 and La.sub.2O.sub.3. The ratio of the fluorescent material (or the fluorescence phase) to the lanthanum oxide (or the light-scattering phase), the former/the latter, may be 99.9/0.1 to 50/50 in terms of volume ratio.

An electrochemical metal alloy identification device employing electrolytes to measure and identify different potentials of alloys is presented. This includes physical structure, disposables, electrical systems, control circuitry, and algorithms to identify alloys.