C01G45/02

SUBSTITUTED RAMSDELLITE MANGANESE DIOXIDES IN AN ALKALINE ELECTROCHEMICAL CELL

Substituted ramsdellite manganese dioxide (RMnO.sub.2) compounds are provided, where a portion of the Mn is replaced by at least one alternative cation, or a portion of the O is replaced by at least one alternative anion. Electrochemical cells incorporating substituted RMnO.sub.2 into the cathode, as well as methods of preparing the substituted RMnO.sub.2, are also provided.

Water-Gas Shift Catalyst

A sintered pelletized catalyst precursor comprising iron oxides, including haematite, and Cr.sub.2O.sub.3 and optionally one or more of Al.sub.2O.sub.3, ZnO, MnO.sub.2, MgO, and/or CuO, the pelletized catalyst precursor having an iron oxide content of 60 wt % to 95 wt %, when expressed as Fe.sub.2O.sub.3, and a Cr(VI) content of less than 0.1 wt %, is physically stable on ignition or when subjected to a reducing gas sufficient to reduce the haematite to magnetite.

Water-Gas Shift Catalyst

A sintered pelletized catalyst precursor comprising iron oxides, including haematite, and Cr.sub.2O.sub.3 and optionally one or more of Al.sub.2O.sub.3, ZnO, MnO.sub.2, MgO, and/or CuO, the pelletized catalyst precursor having an iron oxide content of 60 wt % to 95 wt %, when expressed as Fe.sub.2O.sub.3, and a Cr(VI) content of less than 0.1 wt %, is physically stable on ignition or when subjected to a reducing gas sufficient to reduce the haematite to magnetite.

Positive electrode active material for nonaqueous secondary batteries, method for producing same, and nonaqueous electrolyte secondary battery using positive electrode active material

Provided are a positive electrode active material for nonagueous secondary batteries, the material having a narrow particle-size distribution and a monodisperse property and being capable of increasing a battery capacity; an industrial production method thereof; and a nonaqueous secondary battery using the positive electrode active material and having excellent electrical characteristics. The positive electrode active material is represented by a general formula: Li.sub.1+uNi.sub.xCo.sub.yMn.sub.zM.sub.tO.sub.2+ (wherein, 0.05u0.95, x+y+z+t=1, 0x0.5, 0y0.5, 0.5z<0.8, 0t0.1, and M is an additive element and at least one element selected from Mg, Ca, Al, Ti, V, Cr, Zr, Nb, Mo, and W), has an average particle diameter of 3 to 12 um, and has [(d.sub.90d.sub.10)/average particle diameter], an index indicating a scale of particle-size distribution, of 0.60 or less.

Positive electrode active material for nonaqueous secondary batteries, method for producing same, and nonaqueous electrolyte secondary battery using positive electrode active material

Provided are a positive electrode active material for nonagueous secondary batteries, the material having a narrow particle-size distribution and a monodisperse property and being capable of increasing a battery capacity; an industrial production method thereof; and a nonaqueous secondary battery using the positive electrode active material and having excellent electrical characteristics. The positive electrode active material is represented by a general formula: Li.sub.1+uNi.sub.xCo.sub.yMn.sub.zM.sub.tO.sub.2+ (wherein, 0.05u0.95, x+y+z+t=1, 0x0.5, 0y0.5, 0.5z<0.8, 0t0.1, and M is an additive element and at least one element selected from Mg, Ca, Al, Ti, V, Cr, Zr, Nb, Mo, and W), has an average particle diameter of 3 to 12 um, and has [(d.sub.90d.sub.10)/average particle diameter], an index indicating a scale of particle-size distribution, of 0.60 or less.

Cathode materials for lithium ion batteries
10833321 · 2020-11-10 · ·

A process of forming a coated cathode active material include preparing a cathode material precursor by co-precipitation; coating the cathode material precursor with an electrochemically inert coating material precursor by precipitation to form a coated cathode material precursor; lithiating the coated cathode material precursor with a lithium source material to form a lithiated coated cathode material precursor; and sintering the lithiated coated cathode material precursor to form a cathode active material coated with an electrochemically inert material.

Method of fabricating metal oxide film

A method of fabricating a metal oxide film includes sequentially laminating a carbon film and a metal oxide film including nano-sized metal oxide nanoparticles on a porous fuel membrane to form a preliminary composite structure and reducing the metal oxide film to form a composite structure by combusting the porous fuel membrane while applying a voltage to the preliminary composite structure.

Method of fabricating metal oxide film

A method of fabricating a metal oxide film includes sequentially laminating a carbon film and a metal oxide film including nano-sized metal oxide nanoparticles on a porous fuel membrane to form a preliminary composite structure and reducing the metal oxide film to form a composite structure by combusting the porous fuel membrane while applying a voltage to the preliminary composite structure.

METHOD FOR PREPARING CATHODE ACTIVE MATERIAL

A method for preparing a cathode active material is provided. The method for preparing a cathode active material can comprise the steps of: preparing a first metal oxide; preparing a second metal oxide having an oxygen ratio lower than that of the first metal oxide by heat treating the first metal oxide in a nitrogen-containing gas atmosphere; and preparing a lithium metal oxide by firing the second metal oxide and a lithium salt.

Filter media for respiratory protection

A respiratory protection filter includes filtration media. The filtration media includes an iron-doped manganese oxide material having an average pore size (BJH method) in a range from 1 to 4 nm and a surface area (BET) of at least 300 m.sup.2/g, or at least 350 m.sup.2/g, or at least 400 m.sup.2/g.