This application discloses a positive electrode active material, including bulk particles and a coating layer applied on an exterior surface of each of the bulk particles, where the bulk particle includes a lithium composite oxide that contains element nickel and a doping element M.sup.1, and the coating layer includes an oxide of element M.sup.2. When the positive electrode active material is in a 11% delithiated state, average valences of element M.sup.1 and M.sup.2 are α.sup.1 and β.sup.1, respectively; when the positive electrode active material is in a 78% delithiated state, average valences of element M.sup.1 and M.sup.2 are α.sup.2 and β.sup.2, respectively; and α.sup.2>α.sup.1, β.sup.1=β.sup.2. Element M.sup.1 includes one or more of Si, Ti, Cr, Mo, V, Se, Nb, Ru, Rh, Pd, Sb, Te, Ce, and W, and element M.sup.2 is selected from one or more of Mg, Al, Ca, Zr, Zn, Y, and B.

A reflective granular composition including a reflective pigment material including a majority of kaolin clay and a hardening additive including a sodium salt or another salt. A method for making a reflective granular composition includes the steps of mixing together a reflective pigment material including a majority of kaolin clay and a hardening additive including a sodium salt or another salt to form a particulate mixture, forming a slurry from the particulate mixture by adding to the particulate mixture water and a binder material, granulating the slurry, drying the granulated slurry, and kilning the dried, granulated slurry to form the reflective granular composition. Methods of analyzing the strength of a reflective granular composition are also disclosed.

Embodiments of the present disclosure generally relate to carbon foams, processes for forming carbon foams, doped carbon composites, processes for forming doped carbon composites, and uses thereof, e.g., as electrodes. Processes described herein relate to fabrication of carbon foam and materials derived from the pyrolyzation of biomass at supercritical and subcritical conditions for CO.sub.2, N.sub.2, H.sub.2O, or combinations thereof. The process includes exposing biomass to CO.sub.2, N.sub.2, H.sub.2O, or combinations thereof under various parameters for temperature, pressure, heating rate and fluid flow rate. Silicon-carbon composites and sulfur-carbon composites for use as, e.g., electrodes, are also described.

Provided are a nickel-based active material precursor for a lithium secondary battery including: a first porous core; a second core located on the first porous core and having a higher density than that of the first porous core, a shell located on the second core; and having a radial arrangement structure, wherein an amount of nickel included in the first porous core is greater than or equal to an amount of nickel included in the second core, and the amount of nickel included in the second core is greater than an amount of nickel included in the shell, a method of producing the nickel-based active precursor, a nickel-based active material for a lithium secondary battery, obtained from the nickel-based active precursor, and a lithium secondary battery including a cathode containing the nickel-based active material.

The present invention relates to a bundle-type carbon nanotube which has a bulk density of 25 to 45 kg/m.sup.3, a ratio of the bulk density to a production yield of 1 to 3, and a ratio of a tap density to the bulk density of 1.3 to 2.0, and a method for preparing the same.

A spherical silica powder with a low dielectric tangent, wherein after formulating the spherical silica powder in a resin and molding it into a sheet, in a dielectric tangent of the spherical silica powder calculated by using he following Formula (I) based on a dielectric tangent (tan δc) of the sheet which is measured under the conditions a frequency is 35-40 GHz with a resonator method, B/A is 0.70 or lower, wherein “A” represents a dielectric tangent (tan δf.sub.A) of the spherical silica powder before a dielectric tangent reduction treatment and “B” represents a dielectric tangent (tan δf.sub.B) of the spherical silica powder after a dielectric tangent reduction treatment; and a specific surface area of said spherical silica powder after a dielectric tangent reduction treatment is 1-30 m.sup.2/g.

The present invention relates to a carbonaceous material that is suitable for the negative pole active substance of a nonaqueous electrolyte secondary battery, a negative pole for a nonaqueous electrolyte secondary battery comprising the carbonaceous material, a nonaqueous electrolyte secondary battery having the negative pole, and a method for producing the carbonaceous material. This carbonaceous material is for a negative pole active substance of a nonaqueous electrolyte secondary battery. The carbonaceous material is derived from plants, the half-width of the peak at approximately 1360 cm-1 of the Raman spectrum observed by laser Raman spectroscopy is 190 to 240 cm-1, and the specific surface area as found by multipoint BET analysis of nitrogen adsorption is 10 to 100 m2/g.

One aspect relates to a process for the preparation of a quartz glass body. The process includes providing a silicon dioxide granulate I prepared from a pyrogenically produced silicon dioxide powder, treating the silicon dioxide granulate I with a reactant at a temperature in a range from 1000 to 1300° C., and making a glass melt out of the silicon dioxide granulate. A quartz glass body is made out of at least a part of the glass melt. Furthermore, one aspect relates to a quartz glass body obtainable by this process. Furthermore, one aspect relates to a light guide, an illuminant, and a formed body, each of which is obtainable by further processing of the quartz glass body. One aspect additionally relates to a process for the preparation of a silicon dioxide granulate II.

A ceramic powder material which contains an LLZ-based garnet-type compound represented by Li.sub.7−3xAl.sub.xLa.sub.3Zr.sub.2O.sub.12 (where x satisfies 0≤x≤0.3) and in which a main phase of a crystal phase undergoes phase transition from a tetragonal phase to a cubic phase in the process of raising a temperature from 25° C. to 1050° C. and the main phase is the cubic phase even after the temperature is lowered to 25° C.

A sputtering target for a gallium nitride thin film, which has a low oxygen content, a high density and a low resistivity. A gallium nitride powder having powder physical properties of a low oxygen content and a high bulk density is used and hot pressing is conducted at high temperature in high vacuum to prepare a gallium nitride sintered body having a low oxygen content, a high density and a low resistivity.