Patent classifications
C01G37/00
Iron sulfide dissolver
An aqueous iron sulfide dissolver including zinc, chromium, a methoxybenzoic acid, formic acid, acetic acid, and hydrochloric acid. The iron sulfide dissolver is made by combining these components, and dissolves compounds including iron sulfide upon contact. Evolved hydrogen sulfide reacts with the methoxybenzoic acid to yield solubilized methanethiol as an intermediate product, which is further oxidized to yield dissolved dimethyl disulfide.
Iron sulfide dissolver
An aqueous iron sulfide dissolver including zinc, chromium, a methoxybenzoic acid, formic acid, acetic acid, and hydrochloric acid. The iron sulfide dissolver is made by combining these components, and dissolves compounds including iron sulfide upon contact. Evolved hydrogen sulfide reacts with the methoxybenzoic acid to yield solubilized methanethiol as an intermediate product, which is further oxidized to yield dissolved dimethyl disulfide.
POSITIVE ELECTRODE ACTIVE MATERIAL FOR SECONDARY BATTERY, AND SECONDARY BATTERY INCLUDING THE SAME
A method for positive electrode active material for a secondary battery includes preparing a precursor by reacting a nickel raw material, a cobalt raw material and an M1 raw material; forming a first surface-treated layer including an oxide of Formula 2 below, on a surface of a core including a lithium composite metal oxide of Formula 1 below, by mixing the precursor with a lithium raw material and an M3 raw material, firing the resultant mixture; and forming a second surface-treated layer including a lithium compound of Formula 3 below, on the core with the first surface-treated layer formed thereon,
Li.sub.aNi.sub.1xyCo.sub.xM1.sub.yM3.sub.zM2.sub.wO.sub.2 [Formula 1]
Li.sub.mM4O.sub.(m+n)/2 [Formula 2]
Li.sub.pM5.sub.qA.sub.r [Formula 3]
wherein, in Formulae 1 to 3, A, M1 to M5, a, x, y, z, w, m, n, p, and q are the same as those defined in the specification.
ABSORBER COATING FOR SOLAR HEAT POWER GENERATION AND MANUFACTURING METHOD THEREOF
An absorber coating is provided for solar heat power generation that has excellent thermal oxidation resistance and a high spectral absorptance and manufacturing method thereof. The absorber coating for solar heat power generation has a network structure of composite particles comprising: particles of metal oxide containing mainly two or more metals selected from Mn, Cr, Cu, Zr, Mo, Fe, Co and Bi, and titanium oxide partly or entirely coating on the surface of the particle of the metal oxide. The arithmetic mean estimation of the surface of the coating is 1.0 m or more, and a ratio of a network area of the composite particle to a plane area of the coating is 7 or more.
Shaded zirconia ceramic material and machinable sintered ceramic bodies made therefrom
Shaded, zirconia ceramic materials are disclosed that are suitable for use in dental applications. Ceramic bodies are made from a zirconia-containing ceramic material and a coloring composition comprising a terbium (Tb)-containing component and a chromium (Cr)-containing component as a coloring agent. The pre-shaded ceramic body is machinable into a dental restoration either as a bisque body or sintered body. A pre-shaded machinable sintered ceramic body may obviate the need for further processing steps, such as shading or sintering, and may be suitable for use in chair-side machining applications, such as in a dentist's office, significantly reducing the time to create a custom finished product.
Shaded zirconia ceramic material and machinable sintered ceramic bodies made therefrom
Shaded, zirconia ceramic materials are disclosed that are suitable for use in dental applications. Ceramic bodies are made from a zirconia-containing ceramic material and a coloring composition comprising a terbium (Tb)-containing component and a chromium (Cr)-containing component as a coloring agent. The pre-shaded ceramic body is machinable into a dental restoration either as a bisque body or sintered body. A pre-shaded machinable sintered ceramic body may obviate the need for further processing steps, such as shading or sintering, and may be suitable for use in chair-side machining applications, such as in a dentist's office, significantly reducing the time to create a custom finished product.
Positive electrode active material for secondary battery, and secondary battery including the same
The present invention provides a positive electrode active material for secondary battery and a secondary battery including the same. The positive electrode active material includes a core including a lithium composite metal oxide of Formula 1 below, a first surface-treated layer positioned on the surface of the core and including a lithium oxide of Formula 2 below, and a second surface treated layer positioned on the core or the first surface-treated layer and including a lithium compound of Formula 3. Thus, the present invention can improve capacity characteristics and output characteristics of a battery and also reduce the generation of gas,
Li.sub.aNi.sub.1-x-yCo.sub.xM1.sub.yM3.sub.zM2.sub.wO.sub.2 [Formula 1]
Li.sub.mM4O.sub.(m+n)/2 [Formula 2]
Li.sub.pM5.sub.qA.sub.r [Formula 3] (in formulae 1 to 3, A, M1 to M5, a, x, y, z, w, m, n, p, and q are the same as those defined in the specification).
IRON SULFIDE DISSOLVER
An aqueous iron sulfide dissolver including zinc, chromium, a methoxybenzoic acid, formic acid, acetic acid, and hydrochloric acid. The iron sulfide dissolver is made by combining these components, and dissolves compounds including iron sulfide upon contact. Evolved hydrogen sulfide reacts with the methoxybenzoic acid to yield solubilized methanethiol as an intermediate product, which is further oxidized to yield dissolved dimethyl disulfide.
IRON SULFIDE DISSOLVER
An aqueous iron sulfide dissolver including zinc, chromium, a methoxybenzoic acid, formic acid, acetic acid, and hydrochloric acid. The iron sulfide dissolver is made by combining these components, and dissolves compounds including iron sulfide upon contact. Evolved hydrogen sulfide reacts with the methoxybenzoic acid to yield solubilized methanethiol as an intermediate product, which is further oxidized to yield dissolved dimethyl disulfide.
Mn-activated oxidohalides as conversion luminescent materials for LED-based solid state light sources
The present invention relates to Mn-activated luminescent materials, to a process for preparation thereof and to the use thereof as luminophores or conversion luminophores in light sources. The present invention further relates to a radiation-converting mixture comprising the luminescent material of the invention and a light source comprising the luminescent material of the invention or the radiation-converting mixture. The present invention further provides light sources, especially LEDs, and lighting units comprising a primary light source and the luminescent material of the invention or the radiation-converting mixture. The Mn-activated luminescent materials of the invention are especially suitable for creation of warm white light in LEDs.