The present application discloses a positive electrode active material and its preparation method, a sodium ion battery and an apparatus containing the sodium ion battery. The positive electrode active material satisfies a chemical formula of Na.sub.1-xCu.sub.hFe.sub.kMn.sub.lM.sub.mO.sub.2-y wherein M is one or more selected from Li, Be, B, Mg, Al, K, Ca, Ti, Co, Ni, Zn, Ga, Sr, Y, Nb, Mo, In, Sn, and Ba, 0<x≤0.33, 0<h≤0.24, 0≤k≤0.32, 0<l≤0.68, 0≤m≤0.1, h+k+l+m=1, 0≤y≤0.2, and the positive electrode active material has a water content of 6000 ppm or less.

Coated iron oxide (10) nanocrystal structures, superparamagnetic 10 nanoparticles, methods for synthesizing coated 10 nanocrystal structures, and methods for synthesizing superparamagnetic 10 nanoparticles are described herein. A coated 10 nanocrystal structure may comprise an iron oxide core, a manganese ferrite shell layer surrounding the core, and a bilayer coating surrounding the shell layer. The bilayer coating may include an inner oleic acid layer surrounding the shell layer and an outer layer surrounding the inner oleic acid layer.

Ferrite powder of the present invention is ferrite powder detectable with a metal detector, comprising: soft ferrite particles containing Mn of 3.5 mass % or more and 20.0 mass % or less and Fe of 50.0 mass % or more and 70.0 mass % or less. It is preferable that a volume average particle diameter of the particles constituting the ferrite powder is 0.1 μm or more and 100 μm or less. It is preferable that magnetization by a VSM measurement when magnetic field of 5 K.Math.1000/4πA/m is applied is 85 A.Math.m.sup.2/kg or more and 98 A.Math.m.sup.2/kg or less.

The reversible capacity of P2-type positive electrode active material particle is increased. A positive electrode active material particle of the present disclosure has a P2-type structure, comprises at least one transition metal elements from among Mn, Ni and Co, with Na and O, as constituent elements, and is spherical.

Modified copper chromite spinel pigments exhibit lower coefficients of thermal expansion than unmodified structures. Three methods exist to modify the pigments: (1) the incorporation of secondary modifiers into the pigment core composition, (2) control of the pigment firing profile, including both the temperature and the soak time, and (3) control of the pigment core composition.

The present invention refers to the method for synthesis an absorbent material consisting of a phase of tetravalent manganese feroxyhyte (δ-Fe.sub.(1−1)Mn.sub.xOOH) with a negatively charged grain surface in which a percentage of iron has been isomorphically substituted by manganese atoms at 0.05-25%. Its' production is carried out in two continuous flow stirred-tank reactors arranged in serial configuration, where mild acidic conditions (pH 5-6) prevail in the first reactor and mild alkaline conditions (pH 9-10) together with high redox potential (600-700 mV) in the second reactor. The material can be used to uptake mercury, as well as other heavy metals from both water and hot gas streams. Specifically, the adsorption capacity is determined by the magnitude of the negative surface charge and the isoelectric point that can be both adjusted by the synthesis process parameters.

When manufacturing a magnetic body whose primary component is Ni—Zn ferrite, an iron oxide powder whose Mn content is 0.20 to 0.85 percent by mass is used as a raw material powder, or, in addition to using an iron oxide powder whose Mn content is 0.20 percent by mass or higher as a raw material powder, a mol ratio of Ni to Zn (Ni/Zn) in the ferrite material is determined based on the Mn content in the iron oxide powder and the raw material powders are compounded in such a way that the mol ratio is achieved. The magnetic body does not contain any additives as essential components other than the primary components of the Ni—Zn ferrite material. A coil component using the magnetic body has excellent direct-current superimposition property and magnetic permeability.

An object of the present invention is to provide ferrite particles having a high saturation magnetisation, and being excellent in the dispersibility in a resin, a solvent or a resin composition, a resin composition including the ferrite particles, and a resin film composed of the resin composition. The ferrite particles are a single crystalline body having an average particle size of 1 to 2000 nm, and Mn-based ferrite particles having a spherical shape, and have a saturation magnetisation of 45 to 95 Am.sup.2/kg. The resin composition includes the ferrite particles as a filler. The resin film is composed of the resin composition.

The powder of the magnetoplumbite-type hexagonal ferrite is an aggregate of particles of a compound represented by Formula (1), and, in a particle size distribution based on number measured by a laser diffraction scattering method, in a case where a mode value is defined as a mode diameter, a diameter at a cumulative percentage of 10% is defined as D10 and a diameter at a cumulative percentage of 90% is defined as D90, the mode diameter is equal to or greater than 5 μm and less than 10 μm and an expression of (D90−D10)/mode diameter≤3.0 is satisfied. In Formula (1), A represents at least one metal element selected from the group consisting of Sr, Ba, Ca, and Pb, and x satisfies 1.5≤x≤8.0.

AFe.sub.(12-x)Al.sub.xO.sub.19  Formula(1)

A magnetic nanoparticle, and composites thereof, comprising a ternary host compound comprising a transition metal oxide of size 2-30 nm having two transition metal dopants atom incorporated therein, such that the nanoparticle is converted from superparamagnetic or weak ferromagnetic to strong ferromagnetic material. The strong permanent magnets are formed from non-rare earth materials. The composite material can also include undoped nanoparticles.