C01P2002/50

POSITIVE ELECTRODE ACTIVE MATERIAL, POSITIVE ELECTRODE MATERIAL, BATTERY, AND METHOD FOR MANUFACTURING POSITIVE ELECTRODE ACTIVE MATERIAL
20230093960 · 2023-03-30 ·

The positive electrode active material of the present disclosure includes a complex oxide represented by a formula (1): LiNi.sub.xMe.sub.1-xO.sub.2 as a main component and contains water generated during heating at 300° C. in Karl Fischer titration in an amount of 317.5 ppm by mass or less. Here, x satisfies 0.5 ≤ x ≤ 1, and Me is at least one element selected from the group consisting of Mn, Co, and Al.

PROCESS FOR PREPARING LITHIUM TRANSITION METAL OXIDES
20230030652 · 2023-02-02 ·

A process for producing a lithium transition metal oxide is provided. The process comprises pre-calcination of a transition metal precursor in the absence of a lithium source followed by a high-temperature calcination of the pre-calcined intermediate compound in the presence of a lithium source.

CERAMIC POWDER FOR TIMEPIECE
20220348505 · 2022-11-03 · ·

A ceramic powder for a ceramic component, in particular based on zirconia and/or alumina, in particular for a timepiece or jewelry piece. The powder includes at least one noble metal among platinum, rhodium, osmium, palladium, ruthenium and iridium, at a quantity of less than or equal to 5% by weight.

FERRITE POWDER AND METHOD OF PRODUCING THE SAME

Provided are a ferrite powder capable of maintaining a high withstand voltage even when used in a resin composition having high magnetic properties and electrical resistivity and a high filling ratio, and a method for producing the same. A ferrite powder composed of spherical ferrite particles, wherein the ferrite powder contains iron (Fe): 55.0-70.0 mass % and manganese (Mn): 3.5-18.5 mass %, the ferrite powder containing more than 0.0 mass % to 7.5 mass % α-Fe.sub.2O.sub.3, and the ferrite powder has a volume average particle size (D50) of 15.0 μm or less.

NICKEL ZINC COPPER FERRITE FOR VUHF ANTENNA APPLICATION
20220348479 · 2022-11-03 ·

A composition and a solid material is especially suitable for the manufacture of an antenna adapted to operate in the very high frequency and ultra high frequency or V/UHF band. The composition has the formula Ni.sub.aZn.sub.bCu.sub.cCo.sub.dFe.sub.2-δO.sub.4, in which 2(a+b+c+d)+3(2−δ)=8, 0.05<b<0.5, e.g. 0.1<b<0.5, e.g. 0.1<b<0.4, e.g. 0.15<b<0.35, 0.10<c<0.25, preferably 0.15<c<0.25, alternatively c is 0.20, 0.04<d<0.25, preferably 0.06<d<0.25, and more preferably 0.07<d<0.25, and δ<0.05.

Method for producing zinc oxide platelets with controlled size and morphology

A method for producing polygonic Zn oxide platelets having a median specific surface area of more than 25 square meters per gram, in controlled size and morphology, the method comprising: preparing a medium including Zn or its compounds at a concentration within the range between 1.55 and 7.75 moles of Zn/L, in a medium suitable to substitute Zn ions by releasing free protons thereby forming a complex structure including Zn; agitation of the medium in a vessel at a temperature within the range between 50 and 320° for a duration up to 10 hours to obtain a suspension; filtering the suspension to obtain a filtrate including solid particles; drying and then calcination of the dried filtrate; wherein the agitation is performed with one or more radial flow impellers so that the Reynolds' number in the vessel is higher than 2500 and lower than 10000.

TERNARY POSITIVE MATERIAL OF LARGE MONOCRYSTAL-LIKE PARTICLES, METHOD FOR PREPARING THE SAME, AND LITHIUM-ION BATTERY HAVING THE SAME

A method for preparing ternary positive material in a lithium battery includes mixing nickel salt, cobalt salt, and manganese salt to form a mixed solution. A precipitant and a complexing agent are added into the mixed solution, thereby adjusting a pH value to a range of 10.5 to 12 and obtaining a precursor A. The precursor A and lithium salt are ground by a ball mill to obtain a precursor B, precursor B then being sintered in an air or oxygen atmosphere. The sintering includes heating at a first heating speed of 5 to 15° C./min to a first temperature of 400 to 800° C. and being held at such temperature for 1 to 6 h, and heating at a second heating speed of 1 to 10° C./min to a second temperature of 900 to 980° C. and being held there for 8 to 10 h.

POSITIVE ELECTRODE ACTIVE MATERIAL, POSITIVE ELECTRODE MATERIAL, BATTERY, AND METHOD FOR MANUFACTURING POSITIVE ELECTRODE ACTIVE MATERIAL
20230084392 · 2023-03-16 ·

The positive electrode active material of the present disclosure includes a complex oxide represented by formula (1): LiNi.sub.xMe.sub.1-xO.sub.2 as a main component and has a hydrogen element content of 238.8 ppm by mass or less. Here, x satisfies 0.5≤x≤1, and Me is at least one element selected from the group consisting of Mn, Co, and Al.

CATHODE ACTIVE MATERIAL FOR LITHIUM SECONDARY BATTERY, METHOD OF PREPARING THE SAME, AND LITHIUM SECONDARY BATTERY INCLUDING CATHODE INCLUDING THE SAME

Provided are a cathode active material for a lithium secondary battery, a method of preparing the same, and a lithium secondary battery containing a cathode including the cathode active material, in which the cathode active material includes nickel-based lithium metal oxide containing single-crystal particles, and a particle size of the single-crystal particles is about 1 μm to about 8 μm, and a particle size distribution of the single-crystal particles expressed by (D90-D10)/D50 is 1.4 or less.

Positive Electrode Active Material, Method for Producing the Same, and Positive Electrode and Lithium Secondary Battery Comprising the Same

A positive electrode active material and a method for producing the same are disclosed herein. In some embodiments, a positive electrode active material includes a lithium-nickel-based oxide in the form of at least one of single particles or a pseudo-single particles, wherein each single particle consists of one nodule, wherein each pseudo-primary particles is a composite of 30 or fewer nodules, wherein on the surface of the lithium-nickel-based oxide, a number of nickel ions having an oxidation number of +3 or higher is greater than a number of nickel ions having an oxidation number less than +3.