A negative electrode material for a lithium-ion secondary battery includes composite particles, each of the composite particles having a structure in which plural flat graphite particles are stacked, wherein the composite particles have a particle size distribution D90/D10 of from 2.0 to 5.0, or wherein the plural flat graphite particles have a particle size distribution D90/D10 of from 2.0 to 4.4.

A production method for growing a carbon nanotube assembly on a substrate having a catalyst on a surface thereof. In this production method, in each of a formation unit that carries out a formation step of reducing a catalyst on the substrate and a growth unit that carries out a growth step of growing a carbon nanotube assembly, the substrate is continuously being conveyed using conveyance units that convey the substrate by screw rotations. In carrying out the formation step and the growth step, these steps are carried out while the gas environments in these steps are prevented from mixing with each other.

The present disclosure is directed to providing a carbon film having an excellent shield performance against electromagnetic waves. The carbon film of the present disclosure is a carbon film made of a carbon nanotube assembly, wherein a pore distribution curve of the carbon film indicating the relationship between the pore size and the Log differential pore capacity obtained from an adsorption isotherm at 77 K of liquid nitrogen based on the Barrett-Joyner-Halenda method has a peak in which the Log differential pore capacity is maximized within a pore size range of 10 nm or more and 100 nm or less, and the value of the Log differential pore capacity at the peak is 1.2 cm.sup.3/g or more.

A lithium metal composite oxide having a layered structure, containing at least Li, Ni, and an element X, in which the element X is one or more elements selected from the group consisting of Co, Mn, Fe, Cu, Ti, Mg, Al, B, W, Mo, Nb, Zn, Sn, Zr, Ga, La, and V, and characteristic values obtained from adsorption isotherm measurement of nitrogen gas obtained by a gas adsorption method satisfy requirements (1) and (2).

A method of preparing a bimodal positive electrode active material precursor and a positive electrode active material prepared from the same are disclosed herein. In some embodiments, the method includes inputting a first reaction source material including a first aqueous transition metal solution into a reactor, precipitating at pH 12 or more to induce nucleation of a first positive electrode active material precursor particle, and at less than pH 12 to induce growth of the same, inputting a second reaction source material including a second aqueous transition metal solution into the reactor containing the first positive electrode active material precursor particle, precipitating at pH 12 or more to induce the nucleation of a second positive electrode active material precursor particle, and at less than pH 12 to induce simultaneous growth of the first and second positive electrode active material precursor particles, thereby preparing a bimodal positive electrode active material precursor.

A dispersion, methods of making the same, applications of the dispersion to graphitic material and the resulting coated particles are disclosed. The dispersion includes ≤55% wt. coal tar pitch (softening point 100° C.-95° C.), ≤60% wt. dispersant, and the balance a non-aromatic solvent such as water or alcohol. Pitch particles in the dispersion are preferably ≤10 μm with a distribution of D50<15 μm. The pitch particles are micronized, such as by dry and/or wet milling with the dispersant and aqueous solvent to achieve the desired pitch particle size and distribution. This aqueous dispersion may be mixed with natural or synthetic graphitic material having a diameter of 5-20 μm in a ratio of 5%-30% pitch to graphite, dried and carbonized to form coated particles having a graphitic core at least partially coated by pitch particles.

A process may produce mixed oxides including lithium, zirconium, and optionally at least one other than Li and Zr metal, by flame spray pyrolysis. Mixed oxides are obtainable by such a process. Such mixed oxides may be used in lithium ion batteries.

A synthesis method for producing a refractory oxide-ceramic material of CaZrO.sub.3, in particular in the form of a refractory granular material that is preferably mechanically comminuted, in particular crushed and/or ground, as well as to a batch and a coarse ceramic, shaped or unshaped, refractory product containing at least one pre-synthesized refractory calcium zirconate-containing granular material.

A carbon nanotube assembly satisfies at least one of the following conditions (1) to (3): (1) an FT-IR spectrum of a CNT dispersion obtained by dispersing the CNT assembly has a peak based on plasmon resonance of the CNTs in a wave number range of greater than 300 cm.sup.−1 and 2000 cm.sup.−1 or less; (2) the highest peak in a differential pore capacity distribution of the CNT assembly is located within a pore size range of more than 100 nm and less than 400 nm; and (3) a two-dimensional spatial frequency spectrum of an electronic micrographic image of the CNT assembly has at least one peak within a range of 1 μm.sup.−1 or more and 100 μm.sup.−1 or less.

Provided is a silica that exhibits a high matting property when utilized as a matting agent for a paint, and can also suppress the occurrence of cloudiness. The silica has an aggregated structure in which primary particles are aggregated, has a particle diameter ratio R represented by the following equation (1) of from 4.3 to 5.2, has an absorbance of 0.6 or less for light having a wavelength of 700 nm as an aqueous dispersion having a concentration of 1.48 mass %, and has a particle density measured with a He pycnometer of 2.18 g/cm.sup.3 or more: Equation (1) R=.sup.LD50/.sup.CD50 (in the equation (1), .sup.LD50 represents a volume-based 50% cumulative particle diameter (μm) of the silica measured based on a laser diffraction/scattering method, and .sup.CD50 represents a volume-based 50% cumulative particle diameter (μm) of the silica measured based on a Coulter counter method).