Patent classifications
C01G39/00
METHOD FOR INCREASING THE PARTICLE SIZE OF AMMOIUM OCTAMOLYBDATE (AOM)
Methods of increasing the particle size of ammonium octamolybdate (AOM) pigment powder are provided. A method can include heating the AOM pigment powder to a temperature above 20° C. for a given amount of time. An ink composition can be produced by formulating AOM pigment powder with increased particle size and incorporating the AOM pigment powder into an ink composition.
METHOD FOR INCREASING THE PARTICLE SIZE OF AMMOIUM OCTAMOLYBDATE (AOM)
Methods of increasing the particle size of ammonium octamolybdate (AOM) pigment powder are provided. A method can include heating the AOM pigment powder to a temperature above 20° C. for a given amount of time. An ink composition can be produced by formulating AOM pigment powder with increased particle size and incorporating the AOM pigment powder into an ink composition.
Non-lithium metal ion battery electrode material architecture
A method for configuring a non-lithium-intercalation electrode includes intercalating an insertion species between multiple layers of a stacked or layered electrode material. The method forms an electrode architecture with increased interlayer spacing for non-lithium metal ion migration. A laminate electrode material is constructed such that pillaring agents are intercalated between multiple layers of the stacked electrode material and installed in a battery.
PREPARATION METHOD FOR ROD-SHAPED MOLYBDENUM OXIDE AND PREPARATION METHOD FOR MOLYBDENUM OXIDE COMPOSITE
The present specification relates to a preparation method for rod-shaped molybdenum oxide and a preparation method for a molybdenum oxide composite, the preparation method for rod-shaped molybdenum oxide according to the present invention may be carried out under low temperature and pressure conditions, and thus has an advantage in that it is possible to mass produce rod-shaped molybdenum oxide, and the preparation method for a molybdenum oxide composite according to the present invention has an advantage in that the molybdenum oxide composite may be synthesized at a temperature which is equal to or less than the boiling point of ethanol, and the amount of an ethanol solvent used is reduced.
Method of making hydrocarbon soluble metal compositions
The present invention relates to a method of making of hydrocarbon soluble metal composition comprising of one or more metals of group VIB of the periodic table, wherein the metal having 4+ oxidation state predominantly forms highly active metal sulfide catalyst for hydro-conversion of heavy oil feedstocks in liquid phase. More particularly, present invention relates to a hydrocarbon soluble metal composition comprising of reaction products of a metal source, a lipophilic phenolic acid, a surfactant and an organophosphorus compound. The present invention also provides a one-pot process for preparation of the hydrocarbon soluble metal composition comprising reacting a metal source, a lipophilic phenolic acid, a surfactant, an organophosphorus compound and water to obtain a reaction product and drying the reaction product to obtain the hydrocarbon soluble metal composition.
Method of making hydrocarbon soluble metal compositions
The present invention relates to a method of making of hydrocarbon soluble metal composition comprising of one or more metals of group VIB of the periodic table, wherein the metal having 4+ oxidation state predominantly forms highly active metal sulfide catalyst for hydro-conversion of heavy oil feedstocks in liquid phase. More particularly, present invention relates to a hydrocarbon soluble metal composition comprising of reaction products of a metal source, a lipophilic phenolic acid, a surfactant and an organophosphorus compound. The present invention also provides a one-pot process for preparation of the hydrocarbon soluble metal composition comprising reacting a metal source, a lipophilic phenolic acid, a surfactant, an organophosphorus compound and water to obtain a reaction product and drying the reaction product to obtain the hydrocarbon soluble metal composition.
MoS.SUB.x.O.SUB.y./carbon nanocomposite material, preparation method therefor and use thereof
Provided are a MoS.sub.xO.sub.y/carbon nanocomposite material, a preparation method therefor and a use thereof. In the MoS.sub.xO.sub.y/carbon nanocomposite material, 2.5≤x≤3.1, 0.2≤y≤0.7, and the mass percent of MoS.sub.xO.sub.y is 5%-50% based on the total mass of the nanocomposite material. When the MoS.sub.xO.sub.y/carbon nanocomposite material is used as a catalyst for an electrocatalytic hydrogen evolution reaction, the current density is 150 mA/cm.sup.2 or more at an overpotential of 300 mV. The difference between this performance and the performance of a commercial 20% Pt/C catalyst is relatively small, or even equivalent; and this performance is far better than the catalytic performance of an existing MOS.sub.2 composite material. The MoS.sub.xO.sub.y/carbon nanocomposite material also has a good catalytic stability, and after 8,000 catalytic cycles, the current density thereof is only decreased by 3%, thus exhibiting a very good catalytic performance and cycle stability.
DEVICE AND METHOD FOR PRODUCING NANO-SIZED ZINC MOLYBDATE AND APPLICATION OF SAME
A production device, method and application of nano-sized zinc molybdate. The device includes a double-cone mixer; an elevator is obliquely provided at a bottom of a discharge port of the double-cone mixer; a rear end of the elevator is located above a feeder; the feeder is connected to one end of an electric heating converter, an other end of the electric heating converter is connected to a finished product bin; a top of the finished product bin is provided with an atomizing nozzle for adding nanomaterial dispersant; the atomizing nozzle is connected to a syringe pump by pipeline. High-purity nano-sized molybdenum trioxide and nano-sized zinc oxide are adopted to synthesize nano-sized zinc molybdate in an electric heating converter. The nano-sized zinc molybdate prepared by the device and method can be used for treatment of African swine fever virus, coronavirus, and AIDS phase I, Ebola, dengue fever, polio viruses.
MATERIALS, COMPONENTS, AND METHODS FOR USE WITH EXTREME ULTRAVIOLET RADIATION IN LITHOGRAPHY AND OTHER APPLICATIONS
Nanostructured photonic materials, and associated components for use in devices and systems operating at ultraviolet (UV), extreme ultraviolet (EUV), and/or soft Xray wavelengths are described. Such a material may be fabricated with nanoscale features tailored for a selected wavelength range, such as at particular UV, EUV, or soft Xray wavelengths or wavelength ranges. Such a material may be used to make components such as mirrors, lenses or other optics, panels, lightsources, masks, photoresists, or other components for use in applications such as lithography, wafer patterning, astronomical and space applications, biomedical applications, biotech or other applications.
MATERIALS, COMPONENTS, AND METHODS FOR USE WITH EXTREME ULTRAVIOLET RADIATION IN LITHOGRAPHY AND OTHER APPLICATIONS
Nanostructured photonic materials, and associated components for use in devices and systems operating at ultraviolet (UV), extreme ultraviolet (EUV), and/or soft Xray wavelengths are described. Such a material may be fabricated with nanoscale features tailored for a selected wavelength range, such as at particular UV, EUV, or soft Xray wavelengths or wavelength ranges. Such a material may be used to make components such as mirrors, lenses or other optics, panels, lightsources, masks, photoresists, or other components for use in applications such as lithography, wafer patterning, astronomical and space applications, biomedical applications, biotech or other applications.