Patent classifications
C01P2004/54
ELECTRODE ACTIVE MATERIALS AND PROCESSES TO MAKE THEM
Process for making a particulate lithiated transition metal oxide comprising the steps of: (a) Providing a particulate transition metal precursor comprising Ni, (b) mixing said precursor with at least one compound of lithium and at least one processing additive selected from NaCl, KCl, CuCl.sub.2, B.sub.2O.sub.3, MoO.sub.3, Bi.sub.2O.sub.3, Na.sub.2SO.sub.4, and K.sub.2SO.sub.4 in an amount of from 0.1 to 5% by weight, referring to the entire mixture obtained in step (b), (c) thermally treating the mixture obtained according to step (b) in at least two steps, (c1) at 300 to 500° C. under an atmosphere that may comprise oxygen, (c2) at 650 to 850° C. under an atmosphere of oxygen.
Inhibiting calcium carbonate additive
The use of inhibitory calcium carbonate as additive for a composition containing at least one polymer different from cellulose, wherein the inhibitory calcium carbonate is obtainable by means of a method in which calcium carbonate particles are coated with a composition comprising, based on its total weight, at least 0.1% by weight of at least one weak acid. Further described is a composition containing at least one polymer different from cellulose and inhibitory calcium carbonate.
Nickel-based active material for lithium secondary battery, method of preparing the same, and lithium secondary battery including positive electrode including the nickel-based active material
Provided are a nickel-based active material for a lithium secondary battery, a method of preparing the nickel-based active material, and a lithium secondary battery including a positive electrode including the nickel-based active material. The nickel-based active material includes at least one secondary particle that includes at least two primary particle structures, the primary particle structures each including a porous inner portion and an outer portion having a radially arranged structure, and the secondary particle including at least two radial centers.
BARIUM TITANATE FIBER, RESIN COMPOSITION CONTAINING SAME, POLYMER COMPOSITE PIEZOELECTRIC BODY, PIEZOELECTRIC ELEMENT, METHOD FOR PRODUCING BARIUM TITANATE FIBER, AND METHOD FOR PRODUCING POLYMER COMPOSITE PIEZOELECTRIC BODY
A barium titanate fiber is useful as a filler for a polymer composite piezoelectric body, a polymer composite piezoelectric body has high piezoelectric properties, and a piezoelectric element utilizes the polymer composite piezoelectric body. In the barium titanate fiber, the molar ratio of barium atoms to titanium atoms (Ba/Ti ratio) falls within the range of 1.01 to 1.04. The polymer composite piezoelectric body includes a resin composition containing the barium titanate fiber and a polymer. The piezoelectric element including an electrically conductive layer on one surface or both surfaces of the polymer composite piezoelectric body.
BARIUM TITANATE POWDER AND MANUFACTURING THEREOF
Provided are a barium titanate powder having spherical shape fine particles which have an average particle diameter (D.sub.50) in a range of about 140-270 nm, a tetragonal structure having a markedly improved tetragonality (c/a) in a range of 1.007-1.01 in contrast to the conventional composition, and at the same time, a markedly improved crystallinity in a range of 93-96%, thereby showing improved dielectric properties, and a manufacturing method thereof.
METHOD FOR INCREASING SPECIFIC SURFACE AREA OF TITANIUM PHOSPHATE PLATE-SHAPED PARTICLES, AND POWDER CONTAINING PLATE-SHAPED PARTICLES DERIVED FROM TITANIUM PHOSPHATE
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.
Preparation method of hexagonal molybdenum oxide nanorod
The preparation method according to the present disclosure is to easily prepare hexagonal molybdenum oxide (h-MoO.sub.3) having a nanorod shape even in a low temperature precipitation reaction at atmospheric pressure without applying hydrothermal synthesis under high temperature and high pressure conditions. The hexagonal molybdenum oxide (h-MoO.sub.3) nanorods prepared therefrom can be properly mixed with carbon-based conductive materials such as carbon nanofiber, and thus can be usefully used as an anode material for a pseudocapacitor.
SUPPORT AND FT SYNTHESIS CATALYST, AND PREPARATION METHODS THEREFOR AND APPLICATIONS THEREOF
A microsphere of oxide has an opening on its surface connected to a hollow core inside, forming a cavity. The oxide the microsphere is made of is selected from the group consisting of alumina, silica, zirconia, magnesium oxide, calcium oxide and titania. The microsphere of oxide shows better mass and heat transfer characteristics, and has strength significantly higher than that of existing products with similar structures. A FT synthesis catalyst has the microsphere of oxide as a support and an active metal component disposed on the support. The active metal component is one or more selected from the group consisting of Co, Fe, and Ru.
Positive electrode material for rechargeable lithium ion batteries
The invention provides a positive electrode active material for a lithium ion battery, comprising a lithium transition metal-based oxide powder, the powder comprising single crystal monolithic particles comprising Ni and Co and having a general formula Li.sub.1+a ((Ni.sub.z (Ni.sub.1/2 Mn.sub.1/2).sub.y Co.sub.x).sub.1−kA.sub.k).sub.1-a 02, wherein A is a dopant, −0.02<a≤0.06, 0.10≤x≤0.35, 0≤z≤0.90, x+y+z=1 and k≤0.01, the particles having a cobalt concentration gradient wherein the particle surface has a higher Co content than the particle center.
Positive electrode material for rechargeable lithium ion batteries
A positive electrode active material for a lithium ion battery comprises a lithium transition metal-based oxide powder, the powder comprising single crystal monolithic particles comprising Ni and Co and having a general formula Li.sub.1+a (Ni.sub.z Mn.sub.y Co.sub.x Zr.sub.q A.sub.k).sub.1−a O.sub.2, wherein A is a dopant, −0.025≤a<0.005, 0.60≤z≤0.95, y≤0.20, 0.05≤x≤0.20, k≤0.20, 0≤q≤0.10, and x+y+z+k+q=1. The particles have a cobalt concentration gradient wherein the particle surface has a higher Co content than the particle center.