An iron oxide powder which has an aluminum content of from 10 mol % to 80 mol % (inclusive), and which is composed of porous structures that have a diameter of from 0.3 μm to 2 μm (inclusive).

A positive electrode material for secondary batteries, the material including a Li-rich transition metal oxide having a lithium-to-oxygen atomic ratio: Li/O of 0.8 or more, and a dicarboxylic acid and/or an anhydride of the dicarboxylic acid.

Embodiments disclosed herein relate to using cobalt (Co) to fine tune the magnetic properties, such as permeability and magnetic loss, of nickel-zinc ferrites to improve the material performance in electronic applications. The method comprises replacing nickel (Ni) with sufficient Co.sup.+2 such that the relaxation peak associated with the Co.sup.+2 substitution and the relaxation peak associated with the nickel to zinc (Ni/Zn) ratio are into near coincidence. When the relaxation peaks overlap, the material permeability can be substantially maximized and magnetic loss substantially minimized. The resulting materials are useful and provide superior performance particularly for devices operating at the 13.56 MHz ISM band.

There is provided an oriented body containing platinum group-substituted-6 iron oxide particles typified by Rh-substituted ε-iron oxide or Ru-substituted ε-iron oxide applicable to MAMR, MIMR, or F-MIMR system, and a technique related thereto, containing platinum group element-substituted ε-iron oxide particles in which a part of ε-iron oxide is substituted with at least one element of platinum group elements, as magnetic particles wherein the degree of orientation of the magnetic particles defined by the degree of orientation=SQ (direction of magnetization easy-axes)/SQ (direction of magnetization hard-axes) exceeds 5.0, and a coercive force exceeds 31 kOe.

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.

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.

A polycrystalline ferrite composition comprises a formula of M.sub.5Me.sub.2Ti.sub.3Fe.sub.12O.sub.31, wherein M is Ba.sup.2+, Se.sup.+, or a combination thereof; and Me is Mg.sup.2+, Zn.sup.2+, Cu.sup.2+, Co.sup.2+, or a combination thereof; and has an average grain size of 1 micrometer to 100 micrometers. A composite comprises a polymer matrix; and the polycrystalline ferrite composition. Methods of making the polycrystalline ferrite composition and the composite are also disclosed.

Methods for treating water containing a target anion to remove the target anion can include preparing a treatment composition solution that contains a metal treatment agent, adjusting the treatment composition solution to a first pH that is alkaline and then to a second pH that is acidic, and contacting the treatment composition solution with the water that contains the target anion.

An alkaline aqueous ferric iron salt solution is disclosed. Generally, the alkaline aqueous ferric iron salt solution comprises ferric ions (Fe.sup.3+), potassium ions (K.sup.+), carbonate ions (CO.sub.3.sup.2−), bicarbonate ions (HCO.sub.3.sup.−), hydroxide ions (OH.sup.−), optionally nitrate ions (NO.sub.3.sup.−). Further, a molar ratio of the potassium ions to the ferric ions is generally at least 5.0. The ferric iron is complexed with carbonate, bicarbonate or both to form a water-soluble complex that is anionic in nature and highly soluble in the alkaline aqueous ferric iron salt solution at pH above 8.5, and a pH of the alkaline aqueous ferric iron salt solution is at least 8.5.

An alkaline aqueous ferric iron salt solution is disclosed. Generally, the alkaline aqueous ferric iron salt solution comprises ferric ions (Fe.sup.3+), potassium ions (K.sup.+), carbonate ions (CO.sub.3.sup.2−), bicarbonate ions (HCO.sub.3.sup.−), hydroxide ions (OH.sup.−), optionally nitrate ions (NO.sub.3.sup.−). Further, a molar ratio of the potassium ions to the ferric ions is generally at least 5.0. The ferric iron is complexed with carbonate, bicarbonate or both to form a water-soluble complex that is anionic in nature and highly soluble in the alkaline aqueous ferric iron salt solution at pH above 8.5, and a pH of the alkaline aqueous ferric iron salt solution is at least 8.5.