Patent classifications
C01G39/00
TANTALUM OXIDE PARTICLE AND METHOD FOR PRODUCING TANTALUM OXIDE PARTICLE
It relates to tantalum oxide particles containing molybdenum. The tantalum oxide particles preferably have a polyhedral shape, and the crystallite size of the tantalum oxide particles at 2=22.8 is preferably 160 nm or more. It also relates to a method for producing the tantalum oxide particles, the method including firing a tantalum compound in the presence of a molybdenum compound.
Active material, nonaqueous electrolyte battery, battery pack, and vehicle
According to one embodiment, an active material is provided. This active material includes active material particles containing orthorhombic Na-containing niobium titanium composite oxide, and satisfies the following formula (1):
1A5/A0(1) where A5 is a mole content ratio of a Li mole content L5 to a total of a Ti mole content T5 and a Nb mole content N5, and A0 is a mole content ratio of a Li mole content L0 to a total of a Ti mole content T0 and a Nb mole content N0.
HYDROTHERMAL SYNTHESIS OF THE MOLYBDENUM DIOXIDE NANOPARTICLES DIRECTLY ONTO A METAL SUBSTRATE
Provided are a method of synthesizing molybdenum dioxide (MoO.sub.2) directly onto a metal substrate to form a coating on the surface of the substrate, products having a coated metal surface produced by the disclosed method, and their uses to decontaminate water and/or air. The coated metal surface disclosed herein also may be used as a structural component of a Li-ion battery, a supercapacitor, or a sensor for detecting a molecule.
Cathodes and electrolytes for rechargeable magnesium batteries and methods of manufacture
The invention relates to Chevrel-phase materials and methods of preparing these materials utilizing a precursor approach. The Chevrel-phase materials are useful in assembling electrodes, e.g., cathodes, for use in electrochemical cells, such as rechargeable batteries. The Chevrel-phase materials have a general formula of Mo.sub.6Z.sub.8 and the precursors have a general formula of M.sub.xMo.sub.6Z.sub.8. The cathode containing the Chevrel-phase material in accordance with the invention can be combined with a magnesium-containing anode and an electrolyte.
Opportunities for recovery augmentation process as applied to molybdenum production
A copper/molybdenum separation processor is provided featuring a slurry/media mixture stage configured to receive a conditioned pulp containing hydrophobic molybdenite and hydrophilic copper, iron and other minerals that is conditioned with sodium hydrosulfide together with an engineered polymeric hydrophobic media, and provide a slurry/media mixture; and a slurry/media separation stage configured to receive the slurry/media mixture, and provide a slurry product having a copper concentrate and a polymerized hydrophobic media product having a molybdenum concentrate that are separately directed for further processing. The slurry/media mixture stage include a molybdenum loading stage configured to contact the conditioned pulp with the engineered polymeric hydrophobic media in an agitated reaction chamber, and load the hydrophobic molybdenite on the engineered polymeric hydrophobic media.
Mo-doped Co.SUB.2.Z-type ferrite composite material for use ultra-high frequency antennas
A Co.sub.2Z hexaferrite composition is provided containing molybdenum and one or both of barium and strontium, having the formula (Ba.sub.2Sr.sub.(3-Z)Co.sub.(2+X))Mo.sub.xFe.sub.(y-2x)O.sub.41 where x=0.01 to 0.20; y=20 to 24; and z=0 to 3. The composition can exhibit high permeabilities and equal or substantially equal values of permeability and permittivity while retaining low magnetic and dielectric loss tangents and loss factors. The composition is suitable for high frequency applications such as ultrahigh frequency and microwave antennas and other devices.
Mask free methods of depositing compositions to form heterostructures
The present disclosure provides methods of preparing heterostructures of two or more transition metal dichalcogenides on a surface in a pattern in which the method does not require a mask or blocking agent to create a pattern on the surface. Also provided herein are ink compositions which are used in the methods described herein and include precursor materials that generate these transition metal dichalcogenides.
Carbide, nitride and silicide enhancers for laser absorption
A universal or all-purpose laser marking composition for forming satisfactorily dark laser marks on a wide variety of substrates is provided. The marking composition comprises an enhancer of nitrides, carbides, silicides, and combinations thereof. The enhancer may be selected one or more of ferromanganese, ferrosilicon, Fe.sub.xSi.sub.(1-x) where X can range from about 0.005 to 0.995, Fe.sub.5Si.sub.2, MgFeSi, SiC, CaSi, (Co)Mo, MoSi.sub.2, TiSi.sub.2, ZrSi.sub.2, WSi.sub.2, MnSi.sub.2, YSi, Cu.sub.5Si, Ni.sub.2Si, Fe.sub.3C, Fe.sub.7C.sub.3 and Fe.sub.2C, MoC, Mo.sub.2C, Mo.sub.3C.sub.2, YC.sub.2, WC, Al.sub.4C.sub.3, Mg.sub.2C, Mg.sub.2C.sub.3, CaC.sub.2, LaC.sub.2, Ta.sub.4C.sub.3, Fe.sub.2N, Fe.sub.3N, Fe.sub.4N, Fe.sub.7N.sub.3, Fe.sub.16N.sub.2, MoN, Mo.sub.2N, W.sub.2N, WN, WN.sub.2, and combinations thereof and combinations thereof. Upon disposing the marking composition on a substrate and exposing the marking composition to laser radiation, the marking composition absorbs the laser radiation, increases in temperature, chemically bonds with the substrate, and when formed on each of a metal, glass, ceramic, stone, and plastic substrates, the mark has a negative L dark contrast value of at least 1 compared to a mark formed by the marking composition without the enhancer.
Carbide, nitride and silicide enhancers for laser absorption
A universal or all-purpose laser marking composition for forming satisfactorily dark laser marks on a wide variety of substrates is provided. The marking composition comprises an enhancer of nitrides, carbides, silicides, and combinations thereof. The enhancer may be selected one or more of ferromanganese, ferrosilicon, Fe.sub.xSi.sub.(1-x) where X can range from about 0.005 to 0.995, Fe.sub.5Si.sub.2, MgFeSi, SiC, CaSi, (Co)Mo, MoSi.sub.2, TiSi.sub.2, ZrSi.sub.2, WSi.sub.2, MnSi.sub.2, YSi, Cu.sub.5Si, Ni.sub.2Si, Fe.sub.3C, Fe.sub.7C.sub.3 and Fe.sub.2C, MoC, Mo.sub.2C, Mo.sub.3C.sub.2, YC.sub.2, WC, Al.sub.4C.sub.3, Mg.sub.2C, Mg.sub.2C.sub.3, CaC.sub.2, LaC.sub.2, Ta.sub.4C.sub.3, Fe.sub.2N, Fe.sub.3N, Fe.sub.4N, Fe.sub.7N.sub.3, Fe.sub.16N.sub.2, MoN, Mo.sub.2N, W.sub.2N, WN, WN.sub.2, and combinations thereof and combinations thereof. Upon disposing the marking composition on a substrate and exposing the marking composition to laser radiation, the marking composition absorbs the laser radiation, increases in temperature, chemically bonds with the substrate, and when formed on each of a metal, glass, ceramic, stone, and plastic substrates, the mark has a negative L dark contrast value of at least 1 compared to a mark formed by the marking composition without the enhancer.
Template-Assisted Synthesis of 2D Nanosheets Using Nanoparticle Templates
A template-assisted method for the synthesis of 2D nanosheets comprises growing a 2D material on the surface of a nanoparticle substrate that acts as a template for nanosheet growth. The 2D nanosheets may then be released from the template surface, e.g. via chemical intercalation and exfoliation, purified, and the templates may be reused.