Patent classifications
C01P2004/10
ZIRCONIUM OXIDE NANOPARTICLES
An object of the present invention is to provide zirconium oxide nanoparticles that have excellent dispersibility in a polar solvent and are capable of increasing a core concentration in a dispersion liquid. Zirconium oxide nanoparticles according to the present invention are coated with at least one compound selected from the group consisting of R.sup.1COOH, (R.sup.1O).sub.3-nP(O)(OH).sub.n, (R.sup.1).sub.3-nP(O)(OH).sub.n, (R.sup.1O)S(O)(O)(OH), R.sup.1S(O)(O)(OH), and (R.sup.1).sub.4-mSi(R.sup.4).sub.m, wherein R.sup.1 represents a group comprising a carbon atom and at least one element selected from the group consisting of an oxygen atom, a nitrogen atom, and a sulfur atom, and having the total number of carbon atoms, oxygen atoms, nitrogen atoms, and sulfur atoms of 8 or less; R.sup.4 represents a halogen atom or OR.sup.2, and R.sup.2 represents a hydrogen atom or an alkyl group; and n represents 1 or 2, and m represents an integer of 1 to 3.
Fibrous Structured Amorphous Silica Including Precipitated Calcium Carbonate and Compositions of Matter Made Therewith
A nano-composite structure. A synthetic nano-composite is described having a first component including a fibrous structured amorphous silica structure, and a second component including a precipitated calcium carbonate structure developed by pressure carbonation. The nano-composite may be useful for fillers in paints and coatings. Also, the nano-composite may be useful in coatings used in the manufacture of paper products.
MULTIPLEXED SPECTRAL LIFETIME DETECTION OF PHOSPHORS
New methods and assays for multiplexed detection of analytes using phosphors that are uniform in morphology, size, and composition based on their unique optical lifetime signatures are described herein. The described assays and methods can be used for imaging or detection of multiple unique chemical or biological markers simultaneously in a single assay readout.
MORPHOLOGICALLY AND SIZE UNIFORM MONODISPERSE PARTICLES AND THEIR SHAPE-DIRECTED SELF-ASSEMBLY
Monodisperse particles having: a single pure crystalline phase of a rare earth-containing lattice, a uniform three-dimensional size, and a uniform polyhedral morphology are disclosed. Due to their uniform size and shape, the monodisperse particles self assemble into superlattices. The particles may be luminescent particles such as down-converting phosphor particles and up-converting phosphors. The monodisperse particles of the invention have a rare earth-containing lattice which in one embodiment may be an yttrium-containing lattice or in another may be a lanthanide-containing lattice. The monodisperse particles may have different optical properties based on their composition, their size, and/or their morphology (or shape). Also disclosed is a combination of at least two types of monodisperse particles, where each type is a plurality of monodisperse particles having a single pure crystalline phase of a rare earth-containing lattice, a uniform three-dimensional size, and a uniform polyhedral morphology; and where the types of monodisperse particles differ from one another by composition, by size, or by morphology. In a preferred embodiment, the types of monodisperse particles have the same composition but different morphologies. Methods of making and methods of using the monodisperse particles are disclosed.
Preparation method of doped vanadium dioxide powder
The present invention relates to a hydrothermal method for preparing a doped vanadium dioxide powder, the doped powder having a chemical composition of V.sub.1-XM.sub.XO.sub.2, 0<X0.5, and M is a doping element, which is introduced to control a particle size and a morphology of the doped powder, the doping element M is selected from a group consisting of manganese, iron, cobalt, nickel, copper, zinc, tin, indium, antimony, gallium, germanium, lead and bismuth, the method comprising a step of a precursor treatment of titrating a quadrivalent vanadium aqueous solution with a basic reagent to obtain a precursor suspension, wherein the precursor treatment involves titrating the quadrivalent vanadium aqueous solution until the emergence of the precursor suspension. The preparation methods for the present invention are easy to implement, low in cost, provide high yield, and are suitable for large scale production.
Positive active material for rechargeable lithium battery, method of preparing the same, positive electrode for rechargeable lithium battery including the same and rechargeable lithium battery including the same
A positive active material for a rechargeable lithium battery includes a first compound represented by Chemical Formula 1 and a second compound represented by Chemical Formula 2, the second compound having a smaller particle size than that of the first compound, wherein cation mixing in the surface portion of the positive active material is less than or equal to about 7.5%, cation mixing in the bulk of the positive active material is less than or equal to about 3%, a residual lithium content on the surface of the positive active material is less than or equal to about 3,000 ppm, and the first compound and the second compound each independently include 90 at % to about 98 at % of Ni with respect to the metals excluding Li.
Li.sub.a1Ni.sub.x1Co.sub.y1M.sup.1.sub.1?x1?y1O.sub.2,Chemical Formula 1
Li.sub.a2Ni.sub.x2Co.sub.y2M.sup.2.sub.1?x2?y2O.sub.2.Chemical Formula 2
COMPOSITE HAVING SEMICONDUCTOR STRUCTURES EMBEDDED IN A MATRIX
Semiconductor structures having a nanocrystalline core and corresponding nanocrystalline shell and insulator coating, wherein the semiconductor structure includes an anisotropic nanocrystalline core composed of a first semiconductor material, and an anisotropic nanocrystalline shell composed of a second, different, semiconductor material surrounding the anisotropic nanocrystalline core. The anisotropic nanocrystalline core and the anisotropic nanocrystalline shell form a quantum dot. An insulator layer encapsulates the nanocrystalline shell and anisotropic nanocrystalline core.
Preparation method for rod-shaped molybdenum oxide and preparation method for molybdenum oxide composite
The present specification relates to a preparation method for rod-shaped molybdenum oxide and a preparation method for a molybdenum oxide composite, the preparation method for rod-shaped molybdenum oxide according to the present invention may be carried out under low temperature and pressure conditions, and thus has an advantage in that it is possible to mass produce rod-shaped molybdenum oxide, and the preparation method for a molybdenum oxide composite according to the present invention has an advantage in that the molybdenum oxide composite may be synthesized at a temperature which is equal to or less than the boiling point of ethanol, and the amount of an ethanol solvent used is reduced.
FILLER COMPOSITION
A filler composition comprising fibrous basic magnesium sulfate particles and non-fibrous inorganic micro-particles having an average particle diameter in the range of 0.001 to 0.5 m in a ratio by weight in the range of 100:0.001 to 100:50, is used for providing a molded resin product which shows impact resistance and rigidity balanced at a high level.
METHOD AND SYSTEM FOR RECOVERING RARE EARTH ELEMENTS FROM WITHIN AN OBJECT
Disclosed is a method and system for recovering at least rare earth elements from within an object A consisting of at least one first rare earth portion or a mixture of rare earth elements and a second metal portion. The method includes a solvothermal treatment step that places the object in contact with a fluid for causing at least one rare earth portion and/or mixture of rare earth elements and the metal portion to oxidize in order to separate same, the value of the reaction temperature Tr is selected according to the nature of the object, the reaction following a R-M.fwdarw.R(X)x+M(X)y scheme, where R is the rare earth element or a mixture of rare earth elements, M is the transition metal, and (X) is a group which depends on the fluid used.