Patent classifications
C01G37/02
Preparation method of particle size-controlled, chromium oxide particles or composite particles of iron oxide-chromium alloy and chromium oxide
Provided are particle size-controlled, chromium oxide particles or composite particles of iron oxide-chromium alloy and chromium oxide; a preparation method thereof; and use thereof, in which the chromium oxide particles or the composite particles of iron oxide-chromium alloy and chromium oxide having a desired particle size are prepared in a simpler and more efficient manner by using porous carbon material particles having a large pore volume as a sacrificial template. When the chromium oxide particles or the composite particles of iron oxide-chromium alloy and chromium oxide thus obtained are applied to gas-phase and liquid-phase catalytic reactions, they are advantageous in terms of diffusion of reactants due to particle uniformity, high-temperature stability may be obtained, and excellent reaction results may be obtained under severe reaction environment.
Preparation method of particle size-controlled, chromium oxide particles or composite particles of iron oxide-chromium alloy and chromium oxide
Provided are particle size-controlled, chromium oxide particles or composite particles of iron oxide-chromium alloy and chromium oxide; a preparation method thereof; and use thereof, in which the chromium oxide particles or the composite particles of iron oxide-chromium alloy and chromium oxide having a desired particle size are prepared in a simpler and more efficient manner by using porous carbon material particles having a large pore volume as a sacrificial template. When the chromium oxide particles or the composite particles of iron oxide-chromium alloy and chromium oxide thus obtained are applied to gas-phase and liquid-phase catalytic reactions, they are advantageous in terms of diffusion of reactants due to particle uniformity, high-temperature stability may be obtained, and excellent reaction results may be obtained under severe reaction environment.
Mesoporous materials and processes for preparation thereof
A process for preparing a mesoporous material, e.g., transition metal oxide, sulfide, selenide or telluride, Lanthanide metal oxide, sulfide, selenide or telluride, a post-transition metal oxide, sulfide, selenide or telluride, and metalloid oxide, sulfide, selenide or telluride. The process comprises providing a micellar solution comprising a metal precursor, an interface modifier, a hydrotropic or lyotropic ion precursor, and a surfactant; and heating the micellar solution at a temperature and for a period of time sufficient to form the mesoporous material. A mesoporous material prepared by the above process. A method of controlling nano-sized wall crystallinity and mesoporosity in mesoporous materials. The method comprises providing a micellar solution comprising a metal precursor, an interface modifier, a hydrotropic or lyotropic ion precursor, and a surfactant; and heating the micellar solution at a temperature and for a period of time sufficient to control nano-sized wall crystallinity and mesoporosity in the mesoporous materials. Mesoporous materials and a method of tuning structural properties of mesoporous materials.
Mesoporous materials and processes for preparation thereof
A process for preparing a mesoporous material, e.g., transition metal oxide, sulfide, selenide or telluride, Lanthanide metal oxide, sulfide, selenide or telluride, a post-transition metal oxide, sulfide, selenide or telluride, and metalloid oxide, sulfide, selenide or telluride. The process comprises providing a micellar solution comprising a metal precursor, an interface modifier, a hydrotropic or lyotropic ion precursor, and a surfactant; and heating the micellar solution at a temperature and for a period of time sufficient to form the mesoporous material. A mesoporous material prepared by the above process. A method of controlling nano-sized wall crystallinity and mesoporosity in mesoporous materials. The method comprises providing a micellar solution comprising a metal precursor, an interface modifier, a hydrotropic or lyotropic ion precursor, and a surfactant; and heating the micellar solution at a temperature and for a period of time sufficient to control nano-sized wall crystallinity and mesoporosity in the mesoporous materials. Mesoporous materials and a method of tuning structural properties of mesoporous materials.
USE OF IONIC LIQUIDS IN COMPOSITIONS FOR GENERATING OXYGEN
The present invention is directed to the use of an ionic liquid as a dispersant or solvent and as a heat sink in a composition for generating oxygen, the composition further comprising at least one oxygen source formulation, and at least one metal oxide compound formulation, wherein the oxygen source formulation comprises a peroxide compound, the ionic liquid is in the liquid state at least in a temperature range from 10 C. to +50 C., and the metal oxide compound formulation comprises a metal oxide compound which is an oxide of one single metal or of two or more different metals, said metal(s) being selected from the metals of groups 2 to 14 of the periodic table of the elements.
USE OF IONIC LIQUIDS IN COMPOSITIONS FOR GENERATING OXYGEN
The present invention is directed to the use of an ionic liquid as a dispersant or solvent and as a heat sink in a composition for generating oxygen, the composition further comprising at least one oxygen source formulation, and at least one metal oxide compound formulation, wherein the oxygen source formulation comprises a peroxide compound, the ionic liquid is in the liquid state at least in a temperature range from 10 C. to +50 C., and the metal oxide compound formulation comprises a metal oxide compound which is an oxide of one single metal or of two or more different metals, said metal(s) being selected from the metals of groups 2 to 14 of the periodic table of the elements.
METHOD FOR GENERATING OXYGEN FROM COMPOSITIONS COMPRISING IONIC LIQUIDS
The present invention is directed to a method for generating oxygen comprising providing at least one oxygen source, providing at least one ionic liquid, providing at least one metal oxide compound, wherein the oxygen source is a peroxide compound, the ionic liquid is in the liquid state at least in the temperature range from 10 C. to +50 C., and the metal oxide compound is an oxide of one single metal or of two or more different metals, said metal(s) being selected from the metals of groups 2 to 14 of the periodic table of the elements, and contacting the oxygen source, the ionic liquid, and the metal oxide compound.
METHOD FOR GENERATING OXYGEN FROM COMPOSITIONS COMPRISING IONIC LIQUIDS
The present invention is directed to a method for generating oxygen comprising providing at least one oxygen source, providing at least one ionic liquid, providing at least one metal oxide compound, wherein the oxygen source is a peroxide compound, the ionic liquid is in the liquid state at least in the temperature range from 10 C. to +50 C., and the metal oxide compound is an oxide of one single metal or of two or more different metals, said metal(s) being selected from the metals of groups 2 to 14 of the periodic table of the elements, and contacting the oxygen source, the ionic liquid, and the metal oxide compound.
PROCESS FOR PREPARING AN IRON-CHROMIUM CATALYST WITH A PLATINUM PROMOTER, AND CATALYST CONSISTING OF IRON CHROMIUM WITH A PLATINUM PROMOTER
The present invention relates to catalysts of iron and chromium with a platinum promoter for use in water-gas shift reactions, both at low temperatures (LTS) and at high temperatures (HTS). Their characteristics of higher activity due to the addition of Pt compared to the conventional catalysts make them superior to the commercial catalysts in the same operating conditions. Because precursors of the active phase (Fe.sub.3O.sub.4) are obtained in greater quantity per unit area, it was possible to prepare catalysts that are more promising with a smaller surface area.
SPECTRALLY SELECTIVE SOLAR ABSORBING COATING AND A METHOD FOR MAKING IT
Disclosed is a spectrally selective solar absorbing coating and a method for making same. The spectrally selective solar absorbing coating includes a multilayer stack including, from the substrate to the air interface: substrate (1), infrared reflective layer (2), barrier layer (3), composite absorbing layer (4) consisting of metal absorbing sublayer (4.1), metal nitride absorbing sublayer (4.2), and metal oxynitride absorbing sublayer (4.3), and antireflective layer (5). Therefore, the solar absorbing coating has good high and low temperature cycle stability and superior spectrum selectivity, with a steep transition zone between solar absorption and infrared reflection zones. It has a relatively high absorptance >95%, and a low thermal emissivity 4%, PC (performance criterion)=0.3. The solar absorbing multilayer stack can be obtained by reactively magnetron sputtering the metal target in argon or other inert gas with some amounts of gas containing oxygen or nitrogen or their combination.