The present disclosure discloses a W-containing high-nickel ternary cathode material, including both spherical secondary particles and single-crystal particles. There is basically no W inside the single-crystal particles, and the spherical secondary particles are doped with W. A preparation method of the W-containing high-nickel ternary cathode material includes: mixing a nickel salt, a cobalt salt, and a manganese salt according to a specified molar ratio, and adding an ammonia solution and a sodium hydroxide solution for co-precipitation to prepare a precursor A; mixing a nickel salt, a cobalt salt, a manganese salt, and a tungsten salt, and adding an ammonia solution and a sodium hydroxide solution for co-precipitation to prepare a W-containing precursor B; and mixing the precursor A, the precursor B, a lithium source, and a doping element M-containing compound, and subjecting a resulting mixture to high-temperature sintering in an oxygen atmosphere to obtain the high-nickel ternary cathode material including both spherical secondary particles and single-crystal particles. While increasing the capacity, the spherical secondary particles in the product of the present disclosure can ensure that a crystal structure will not undergo obvious phase transition when lithium ions are deintercalated during a cycling process, which helps to improve the cycling performance.

The present invention aims to provide an activated carbon for adsorbing a molecular polar substance with excellent adsorption property to a molecular polar substance and regeneratability. The present invention provides an activated carbon for adsorbing a molecular polar substance obtained by an alkali activation method, wherein the activated carbon has an acidic functional group in an amount of 2.1 meq/g or more, a basic functional group in an amount of more than 0 to 0.6 meq/g, and a specific surface area of 1000 to 4000 m.sup.2/g.

The present invention relates to a method for producing a metal nitride by igniting a raw material powder containing a metal powder filled in a reaction vessel under a nitrogen atmosphere and propagating nitriding combustion heat generated by a nitriding reaction of the metal to the whole raw material powder, the method including forming a heat insulating layer made of a material having nitrogen permeability and inert to the nitriding reaction on an upper surface of a layer made of the raw material powder. According to the present invention, it is possible to provide a method for reducing the amount of unreacted metal powder when producing a metal nitride by a combustion synthesis method.

Producing a molded body made of opaque quartz glass includes providing SiO.sub.2 grains obtained by comminuting quartz glass having a purity of at least 99.9 wt % SiO.sub.2, forming a slurry containing a suspension liquid and the SiO.sub.2 grains and which has a total solids content, wet grinding the SiO.sub.2 grains in the slurry so as to form ground SiO.sub.2 grain particles, forming a porous green body from the slurry, and sintering the porous green body. To provide a low cost quartz glass, the wet grinding of the SiO.sub.2 grains takes place at least temporarily in the presence of SiO.sub.2 nanoparticles, the proportion of which in the total solids content of the slurry is in the range of 0.1 wt % to 10 wt %, and the slurry has a solids content in the range of 76 to 80 wt % after addition of the SiO.sub.2 nanoparticles and after the wet grinding.

This application discloses a negative-electrode active material and a preparation method thereof, a secondary battery, and a battery module, a battery pack, and an apparatus that include such secondary battery. The negative-electrode active material includes a core and a coating layer covering at least part of a surface of the core, where the core includes artificial graphite, the coating layer includes amorphous carbon, a volume-based particle size distribution of the negative-electrode active material satisfies D.sub.v99≤24 μm, a volume-based median particle size D.sub.v50 of the negative-electrode active material satisfies 8 μm≤D.sub.v≤15 μm, D.sub.v99 is a particle size corresponding to a cumulative volume distribution percentage of the negative-electrode active material reaching 99%, and WO is a particle size corresponding to a cumulative volume distribution percentage of the negative-electrode active material reaching 50%.

The invention relates to a method for producing hydrophilic silicia moulded bodies, in which i) a mixture containing hydrophilic silicic acid is added at a maximum temperature of 55° C. to hydrophobic means and ii) the mixture obtained in step i) is compacted after a maximum storage time of 30 days to form moulded bodies, iii) during steps ii and iii and until the moulded bodies are used, the temperature is at a maximum of 55° C.

Inorganic particulate compositions containing inorganic particles associated with a copolymer of a hydrophilic monomer and a hydrophobic monomer associated with the inorganic particles are provided. The particulate composition satisfies at least one of the following properties: a BET surface area of the inorganic particles is greater than 8 m.sup.2/g, a Hegman value of the inorganic particles is 75 microns or less, and a rate of water loss from the composition upon drying from a moisture level greater than 2% wt % is at least 30% greater than a composition having a corresponding content of a polyacrylate polymer associated with the particles. A method to prepare the composition and formulations for inks, paints, coatings and filled polymeric articles containing the inorganic particulate composition are also provided.

Provided are a cathode active material having a suitable particle size and high uniformity, and a nickel composite hydroxide as a precursor of the cathode active material. When obtaining nickel composite hydroxide by a crystallization reaction, nucleation is performed by controlling a nucleation aqueous solution that includes a metal compound, which includes nickel, and an ammonium ion donor so that the pH value at a standard solution temperature of 25° C. becomes 12.0 to 14.0, after which, particles are grown by controlling a particle growth aqueous solution that includes the formed nuclei so that the pH value at a standard solution temperature of 25° C. becomes 10.5 to 12.0, and so that the pH value is lower than the pH value during nucleation. The crystallization reaction is performed in a non-oxidizing atmosphere at least in a range after the processing time exceeds at least 40% of the total time of the particle growth process from the start of the particle growth process where the oxygen concentration is 1 volume % or less, and with controlling an agitation power requirement per unit volume into a range of 0.5 kW/m.sup.3 to 4 kW/m.sup.3 at least during the nucleation process.

Molybdenum oxychloride consolidated masses, comprising molybdenum oxychloride and less than 10 wt % binder. The consolidated masses have a bulk density greater than 0.85 g/cc.

A method for increasing the specific surface area of titanium phosphate plate-shaped particles of this invention includes: obtaining a liquid in a state where a powder containing titanium phosphate plate-shaped particles is dispersed in an aqueous alkaline solution.