The invention relates to a mixed oxide composed of zirconium, cerium, lanthanum and at least one rare earth oxide other than cerium and lanthanum, having a specific porosity and a high specific surface area; to the method for preparing same and to the use thereof in catalysis.

Provided is a method of producing fine particulate barium calcium titanate in which calcium forms a homogeneous solid solution. The present invention relates to a method of producing a perovskite compound represented by the following formula (1):

Ba.sub.(1-x)A.sub.xTiO.sub.3  (1)

wherein A represents Ca or Sr, and x is a number satisfying 0.00<x≤0.30,

the method including: a first step of acid washing barium titanate to provide barium titanate having a ratio of barium element to titanium element of lower than 1.00; a second step of mixing the barium titanate obtained in the first step and a calcium salt or a strontium salt and drying the mixture to provide a dry mixture; and a third step of heating the dry mixture obtained in the second step.

A layered pigment composition comprising a porous mineral substrate and a porous mineral shell is described. Such compositions may be useful in cosmetics, personal care products, printing inks and coatings, and plastics.

An object of the present invention is to provide composite particles capable of suppressing oxidation over time of a Si—C composite material. Composite particles (B) of the present invention contains composite particles (A) containing carbon and silicon; and amorphous layers coating surfaces thereof, where the composite particles (B) have I.sub.Si/I.sub.G of 0.10 or more and 0.65 or less, and have R value (I.sub.D/I.sub.G) of 1.00 or more and 1.30 or less, when a peak due to silicon is present at 450 to 495 cm.sup.−1, an intensity of the peak is defined as I.sub.Si, an intensity of a G band (peak intensity in the vicinity of 1600 cm.sup.−1) is defined as I.sub.G, and an intensity of a D band (peak intensity in the vicinity of 1360 cm.sup.−1) is defined as I.sub.D in a Raman spectrum, and where the composite particles (B) have a full width at half maximum of a peak of a 111 plane of Si of 3.0 deg. or more using a Cu-Kα ray in an XRD pattern.

Disclosed is a method for synthesizing two-dimensional (2D) silicon carbide and other materials. The method includes the use of hexagonal SiC precursor in a wet exfoliation technique. The method may also include synthesizing two-dimensional (2D) silicon carbide by a chemical vapor deposition method, or a combination of a liquid exfoliation technique and a chemical vapor deposition method.

The present invention aims to provide techniques for efficiently synthesizing inorganic microparticles. According to the present invention, inorganic carbonate microparticles can be synthesized by generating ultrafine bubbles containing carbonic acid gas by injecting a gas containing carbonic acid gas and a liquid into a reaction vessel through a nozzle to deposit an inorganic carbonate having an average primary particle size of 300 nm or less in the presence of the ultrafine bubbles.

A lanthanum molybdenum composite oxide is provided. The lanthanum molybdenum composite oxide has a primary crystal phase formed of La.sub.2Mo.sub.2O.sub.9. The lanthanum molybdenum composite oxide also has a secondary crystal phase formed of a lanthanum molybdenum composite oxide species other than La.sub.2Mo.sub.2O.sub.9. The secondary crystal phase may contain at least one species selected from a group consisting of La.sub.2Mo.sub.3O.sub.12, La.sub.6MoO.sub.12, La.sub.7Mo.sub.7O.sub.30, La.sub.2Mo.sub.4O.sub.15, La.sub.2MoO.sub.6, La.sub.4MoO.sub.9, and LaMo.sub.2O.sub.5.

A method for producing an artificial graphite material for a lithium ion secondary battery negative electrode, including at least a step of performing a coking treatment on a raw material oil composition by performing a delayed coking process to generate a raw coke composition, a step of performing a heat treatment on the raw coke composition to obtain a heat-treated raw coke composition, a step of crushing the heat-treated raw coke composition to obtain heat-treated raw coke powder, a step of graphitizing the heat-treated raw coke powder to obtain graphite powder, and a step of crushing the graphite powder, in which a volatile content of the heat-treated raw coke powder is less than 3.71%, and a true density of the heat-treated raw coke powder is greater than 1.22 g/cm.sup.3 and less than 1.73 g/cm.sup.3.

Spherical silica and/or silicate particles having a d50 median particle size from 1 to 5 μm, a d95 particle size less than 8 μm, an oil absorption from 40 to 100 cc/100 g, a pack density from 20 to 60 lb/ft.sup.3, and a sphericity factor (S.sub.80) of at least 0.9, are disclosed, as well as methods for making these spherical particles, and dentifrice compositions containing the spherical particles.

A perovskite-type composite oxide powder is a perovskite-type composite oxide powder represented by a general formula ABO.sub.3-δ (where δ represents an amount of deficiency of oxygen and 0≤δ<1), an element contained in an A site is La, elements contained in a B site are Co and Ni and a crystallite size determined by a Williamson-Hall method is equal to or greater than 20 nm and equal to or less than 100 nm. In this way, when the perovskite-type composite oxide powder is used as an air electrode material for a fuel cell, an air electrode in which the resistance thereof is low and the conductivity thereof is high can be obtained.