Abstract: Disclosed herein are composite materials and methods of making and use thereof. The composite materials disclosed herein can comprise: a first metal oxide particle having a thermal stability and a specific reversible oxygen storage capacity, wherein the first metal oxide particle comprises a first metal oxide comprising a transition metal oxide; and a second metal oxide disposed on the first metal oxide particle; wherein the composite material has a thermal stability and a specific reversible oxygen storage capacity; and wherein the thermal stability of the composite material is greater than the thermal stability of the first metal oxide particle. The methods of use of the composite materials described herein can comprise using the composite material as a catalyst, as an oxygen carrier, as a catalyst support, in a fuel cell, in a catalytic converter, or a combination thereof.

Abstract: A method for ammonia decomposition to produce hydrogen, the method comprising the steps of introducing an ammonia stream to a reactor, wherein the ammonia stream comprises ammonia, wherein the reactor comprises a cobalt-based catalyst, the cobalt-based catalyst comprising 15 wt % and 70 wt % of cobalt, 5 wt % and 45 wt % of cerium, and 0.4 wt % and 0.5 wt % barium, wherein a remainder of weight of the cobalt-based catalyst is oxygen; contacting the ammonia in the ammonia stream with the cobalt-based catalyst, wherein the cobalt-based catalyst is operable to catalyze an ammonia decomposition reaction; catalyzing the ammonia decomposition reaction to cause the ammonia decomposition in the presence of the cobalt-based catalyst to produce hydrogen; and withdrawing a product stream from the reactor, the product stream comprising hydrogen.

Abstract: A supported catalyst having rhodium particles with an average diameter of less than 1 nm disposed on a support material containing magnetic iron oxide (e.g. Fe3O4). A method of producing the supported catalyst and a process of reducing nitroarenes to corresponding aromatic amines employing the supported catalyst with a high product yield are also described. The supported catalyst may be recovered with ease using an external magnet and reused.

Abstract: An efficient catalyst for the synthesis of methanol by catalytic hydrogenation of carbon dioxide is provided. A process for the preparation of the catalyst by self-combustion of a gel and a process for the synthesis of methanol by catalytic hydrogenation of carbon dioxide are also presented. The catalyst has the following formula (Cu)x(ZnO)y(ZrO2)z supported on mesoporous silica.

Abstract: A method for producing a catalyst for a fuel cell comprising: a) injecting carbon particles into a fluidized bed reactor; b) evacuating the fluidized bed reactor to form a base pressure; c) introducing a catalytic metal precursor together with a carrier gas into the fluidized bed reactor to contact the catalytic metal precursor with the carbon particles; d d) purging a purge gas into the fluidized bed reactor; e) introducing a reaction gas into the fluidized bed reactor to attach the catalytic metal precursor to the carbon particles; and f) purging a purge gas into the fluidized bed reactor, wherein, the catalytic metal is attached to the carbon particles in a form of nano-sized spot.

Abstract: Disclosed are a Fischer-Tropsch synthesis catalyst, a preparation method therefor and use thereof in a Fischer-Tropsch synthesis reaction. Wherein the catalyst comprises: an active component, being at least one selected from VIIIB transition metals; an optional auxiliary metal; and a nitride carrier having a high specific surface area. The catalyst is characterized in that the active metal is supported on the nitride carrier having the high specific surface, such that the active component in the catalyst is highly dispersed. The catalyst has a high hydrothermal stability, an excellent mechanical wear resistance, a high Fischer-Tropsch synthesis activity and an excellent high-temperature stability.

Abstract: The present invention relates to a porous iron oxide-zirconia composite catalyst, a preparation method thereof, and a method for producing alcohol using the same, and the iron oxide-zirconia composite catalyst having a porous structure may produce alcohol at low cost by carrying out an excellent methane reforming reaction even under room temperature and room pressure conditions through an electrochemical reaction.

Abstract: The present disclosure relates to chromium-on-alumina dehydrogenation catalyst materials, to methods for making such catalysts, and to methods for dehydrogenating hydrocarbons using such catalysts. In one aspect, the disclosure provides a method for preparing a dehydrogenation catalyst material, the method comprising impregnating a chromium-on-alumina material with ascorbic acid, one or more of sodium, lithium and potassium (e.g., sodium), and chromium; and calcining the impregnated material to provide the dehydrogenation catalyst material comprising chromium in the range of 2.5 wt. % to about 35 wt. % and having no more than 100 ppm chromium(VI).

Abstract: Provided in this disclosure are catalyst compositions. The catalyst compositions include an oxidative dehydrogenation catalyst that includes a mixed metal oxide having the empirical formula: Mo1.0V0.12-0.49Te0.05-0.17Nb0.10-0.20AlcOd wherein c is from 0 to 2.0 and d is a number to satisfy the valence of the oxide. The compositions are at least 40 wt. % amorphous as measured by XRD. The disclosure also provides methods of making the compositions.

Abstract: To provide a hexagonal boron nitride powder which contains agglomerates, has a maximum torque calculated by measuring in accordance with JIS-K-6217-4 of 0.20 to 0.50 Nm, a DBP absorption rate of 50 to 100 ml/100 g, a tap bulk density of 0.66 to 0.95 g/cm3 and reduced anisotropy of heat conduction and can provide high heat conductivity and dielectric strength to a resin composition produced by filling a resin therewith and a process for producing the powder by carrying out a reduction nitriding reaction using boron carbide.

Abstract: Methods for making a supported chromium catalyst are disclosed, and can comprise contacting a silica-coated alumina containing at least 30 wt. % silica with a chromium-containing compound in a liquid, drying, and calcining in an oxidizing atmosphere at a peak temperature of at least 650° C. to form the supported chromium catalyst. The supported chromium catalyst can contain from 0.01 to 20 wt. % chromium, and typically can have a pore volume from 0.5 to 2 mL/g and a BET surface area from 275 to 550 m2/g. The supported chromium catalyst subsequently can be used to polymerize olefins to produce, for example, ethylene-based homopolymers and copolymers having high molecular weights and broad molecular weight distributions.

Abstract: The present invention relates to a composite material including a porous titania thin film and a preparation method therefor. A composite material according to the present invention allows for a simple thin film formation process because of the use of cellulose crystals, makes it easy to control the structure of the titanium dioxide thin film provided therefor, has a large specific area, and is superior in terms of scratch resistance and photoactivity, thus finding useful applications in the various fields utilizing titanium dioxide as a photocatalyst.

Abstract: A method for forming and bonding a corrosion resistant perovskite layer on a surface of a steel component, for example, a stainless steel crucible is disclosed. The method comprises preparing an inhibitor mixture comprising about 0.5% to about 5% by weight of a rare-earth oxide and about 0.1% to about 1% by weight of an oxidizer; preparing a molten chloride salt mixture comprising a predetermined concentration of one of a binary eutectic mixture and a ternary eutectic mixture, mixing the inhibitor mixture to the molten chloride salt mixture to produce an inhibitor salt mixture; applying the inhibitor salt mixture to the surface of the steel component to be bonded with the perovskite layer; and heat treating the steel component with said applied inhibitor salt mixture to a predetermined temperature to form and bond the perovskite layer on said surface of said steel component.

Abstract: A method for preparing copper-nickel cobaltate nanowires includes steps of: (1) dissolving a soluble nickel salt, cobalt salt and copper salt in ultrapure water, and preparing same into a mixed salt solution A; (2) adding 1-4 mmol of sodium dodecyl sulfate to solution A, and dissolving same with stirring; (3) dissolving 12-30 mmol of hexamethylenetetramine in 20 mL of ultrapure water to form solution B; (4) slowly dropwise adding solution B to solution A via a separatory funnel to form solution C, and stirring same for 0.5-1 h; and (5) further transferring same into a 100 mL reaction vessel, reacting same at 100-160° C. for 8-20 h, suction filtration and washing, and drying same at 40-60° C. in a vacuum oven, and further reacting same at 350-800° C. for 1-4 h in a muffle furnace.

Abstract: A catalyst for dehydrogenation of hydrocarbons includes a support including zirconium oxide and alumina. A concentration of the zirconium oxide in the catalyst is in a range of from 1 weight percent (wt. %) to 20 wt. %. The catalyst includes from 0.01 wt. % to 2 wt. % of an alkali metal or alkaline earth metal. The catalyst includes from 1 wt. % to 2 wt. % of tin. The catalyst includes from 0.1 wt. % to 2 wt. % of a platinum group metal. The alkali metal or alkaline earth metal, tin, and platinum group metal are disposed on the support.

Abstract: Provided in this disclosure are oxidative dehydrogenation catalysts that include a mixed metal oxide having the empirical formula: Mo1.0V0.12-0.49Te0.05-0.17Nb0.10-0.20Od wherein d is a number to satisfy the valence of the oxide. The oxidative dehydrogenation catalyst is characterized by having XRD diffraction peaks (2? degrees) at 22±0.2, 27±0.2, 28.0±0.2, and 28.3±0.1. The disclosure also provides methods of making the catalysts that include wet ball milling.

Abstract: The present invention relates to a catalyst and a manufacturing method thereof, the catalyst is characterized that a distance between a transition metal of a transition metal oxide nanoparticle and oxygen is controlled by substituting at least a part of surface of the transition metal oxide nanoparticle with an inclusion.

Abstract: An hBN powder containing an aggregate of primary particles of hBN, the hBN powder having a ratio of an average longer diameter (L1) to an average thickness (d1) of the primary particles, [L1/d1], of 10 to 25, a tap density of 0.80 g/cm3 or more, and a BET specific surface area of less than 5.0 m2/g, in which a particle size distribution curve showing a frequency distribution based on volume of the hBN powder is a bimodal distribution curve having a first peak and a second peak in a range of a particle size of 500 ?m or less and having a peak height ratio of a second peak height (HB) to a first peak height (HA), [(HB)/(HA)], of 0.90 or less, a method for producing the same, and a resin composition and a resin sheet each comprising the hBN powder.

Abstract: The present invention relates to a method for preparing a dehydrogenation catalyst for a straight chain-type light hydrocarbon using a stabilized active metal composite, in other words, to a dehydrogenating catalyst for C3 to C4 straight chain hydrocarbons, and more specifically, to a technique for preparing a catalyst in which most of metal components contained in the catalyst are distributed evenly in a support in the form of an alloy rather than in the form of each separate metal, thereby exhibiting a high conversion rate and selectivity when used in dehydrogenation.

Abstract: An hBN powder containing an aggregate of primary particles of hBN, the hBN powder having a ratio of an average longer diameter (L1) to an average thickness (d1) of the primary particles, [L1/d1], of 10 to 25, a tap density of 0.80 g/cm3 or more, and a BET specific surface area of less than 5.0 m2/g, in which a particle size distribution curve showing a frequency distribution based on volume of the hBN powder is a bimodal distribution curve having a first peak and a second peak in a range of a particle size of 500 ?m or less and having a peak height ratio of a second peak height (HB) to a first peak height (HA), [(HB)/(HA)], of 0.90 or less, a method for producing the same, and a resin composition and a resin sheet each comprising the hBN powder.