Embodiments of the present disclosure are directed to hydrogen-selective oxygen carrier materials and methods of using hydrogen-selective oxygen carrier materials. The hydrogen-selective oxygen carrier material may comprise a core material, which includes a redox-active transition metal oxide; a shell material, which includes one or more alkali transition metal oxides; and a support material. The shell material may be in direct contact with at least a majority of an outer surface of the core material. At least a portion of the core material may be in direct contact with the support material. The hydrogen-selective oxygen carrier material may be selective to combust hydrogen in an environment that includes hydrogen and hydrocarbons.

Embodiments of the present disclosure are directed to hydrogen-selective oxygen carrier materials and methods of using hydrogen-selective oxygen carrier materials. The hydrogen-selective oxygen carrier material may comprise a core material, which includes a redox-active transition metal oxide; a shell material, which includes one or more alkali transition metal oxides; and a support material. The shell material may be in direct contact with at least a majority of an outer surface of the core material. At least a portion of the core material may be in direct contact with the support material. The hydrogen-selective oxygen carrier material may be selective to combust hydrogen in an environment that includes hydrogen and hydrocarbons.

An object of the present invention is mainly to provide a catalyst with which an ,-unsaturated aldehyde and/or an ,-unsaturated carboxylic acid can be produced with a high selectivity. Provided is a catalyst used for producing, by an oxidation reaction of a hydrocarbon, a corresponding ,-unsaturated aldehyde and/or ,-unsaturated carboxylic acid, and the catalyst contains molybdenum, bismuth, and cobalt, and satisfies the following Formula (I-1): (x2x1)/11.5 (I-1) In Formula (I-1), x1, x2, and 1 are values obtained by binarizing a reflected electron image of the catalyst, which is obtained using a scanning electron microscope (SEM) at an accelerating voltage of 15 kV, into black and white and subsequently performing an energy dispersive X-ray spectroscopy (EDS) analysis; x1 represents a bismuth concentration [% by mass] in black parts; x2 represents a bismuth concentration [% by mass] in white parts; and 1 represents a standard deviation of the bismuth concentration in the black parts.

A method and a system for converting ethane to ethylene are provided. An exemplary method includes providing a feed stream including the ethane and oxygen to an oxidative dehydrogenation reactor and converting at least a portion of the ethane to ethylene in the oxidative dehydrogenation reactor to provide a reactor effluent stream including ethane, ethylene, and oxygen, acetylene, or both. The method includes cooling the reactor effluent stream to form a cooled effluent stream and providing the cooled effluent stream to an oxygen removal reactor including an ODH catalyst bed. A deoxygenation stream including water and an alcohol is provided to the oxygen removal reactor to form a deoxygenated effluent.

A method and a system for converting ethane to ethylene are provided. An exemplary method includes providing a feed stream including the ethane and oxygen to an oxidative dehydrogenation reactor and converting at least a portion of the ethane to ethylene in the oxidative dehydrogenation reactor to provide a reactor effluent stream including ethane, ethylene, and oxygen, acetylene, or both. The method includes cooling the reactor effluent stream to form a cooled effluent stream and providing the cooled effluent stream to an oxygen removal reactor including an ODH catalyst bed. A deoxygenation stream including water and an alcohol is provided to the oxygen removal reactor to form a deoxygenated effluent.

The present invention relates to a catalyst containing a vanadium-phosphorus oxide and an alkali metal, wherein the proportion by weight of alkali metal in the vanadium-phosphorus oxide is in the range from 10 to 400 ppm, based on the total weight of the vanadium-phosphorus oxide, a process for producing it and also the use of the catalyst for the gas-phase oxidation of hydrocarbons, in particular for preparing maleic anhydride.

The present invention relates to a catalyst containing a vanadium-phosphorus oxide and an alkali metal, wherein the proportion by weight of alkali metal in the vanadium-phosphorus oxide is in the range from 10 to 400 ppm, based on the total weight of the vanadium-phosphorus oxide, a process for producing it and also the use of the catalyst for the gas-phase oxidation of hydrocarbons, in particular for preparing maleic anhydride.

The present invention provides a method for producing an oxide catalyst comprising Mo, V, Sb, and Nb for use in a gas-phase catalytic oxidation reaction or a gas-phase catalytic ammoxidation reaction of propane or isobutane, the method comprising: a preparation step of preparing a first aqueous mixed solution containing Mo, V, and Sb; a mixing step of mixing the first aqueous mixed solution with a support raw material comprising silica sol, and a Nb raw material to obtain a second aqueous mixed solution; a drying step of drying the second aqueous mixed solution to obtain a dry powder; and a calcination step of calcining the dry powder to obtain the oxide catalyst, wherein the support raw material comprises 25% by mass or more, based on SiO.sub.2, of the silica sol having an average primary particle size of 3.0 nm or larger and smaller than 11 nm based on a total amount of the support raw material, and the silica sol comprises 55% or more of silica sol particles having a primary particle size of smaller than 11 nm.

The present invention provides a method for producing an oxide catalyst comprising Mo, V, Sb, and Nb for use in a gas-phase catalytic oxidation reaction or a gas-phase catalytic ammoxidation reaction of propane or isobutane, the method comprising: a preparation step of preparing a first aqueous mixed solution containing Mo, V, and Sb; a mixing step of mixing the first aqueous mixed solution with a support raw material comprising silica sol, and a Nb raw material to obtain a second aqueous mixed solution; a drying step of drying the second aqueous mixed solution to obtain a dry powder; and a calcination step of calcining the dry powder to obtain the oxide catalyst, wherein the support raw material comprises 25% by mass or more, based on SiO.sub.2, of the silica sol having an average primary particle size of 3.0 nm or larger and smaller than 11 nm based on a total amount of the support raw material, and the silica sol comprises 55% or more of silica sol particles having a primary particle size of smaller than 11 nm.

The present invention relates to a catalyst for fixed bed aniline rectification residue recycling and preparation method thereof. Based on the total weight of the catalyst, the catalyst comprises the following components in percentage by weight: 5-40% of an active component, 2-30% of a first cocatalyst component, 10-30% of a second cocatalyst component and the balance of carrier, wherein the active component is NiO; the first cocatalyst component is one or more of Fe, Mo, Cr or Co oxide; and the second cocatalyst component is one or more of La, Zr, Y or Ce oxide. The catalyst is prepared through co-precipitation. The catalyst shows high activity and stability in the waste liquid treatment process, and can still maintain high rectification residue cracking rate after reaction of 200 hours.