B01J37/18

FLUIDIZABLE VANADIUM CATALYST FOR OXIDATIVE DEHYDROGENATION OF ALKANES TO OLEFINS IN A GAS PHASE OXYGEN FREE ENVIRONMENT

Fluidizable catalysts for the gas phase oxygen-free oxidative dehydrogenation of alkanes, such as propane, to corresponding olefins, such as propylene. The catalysts comprise 5-20% by weight per total catalyst weight of one or more vanadium oxides (VO.sub.x), such as V.sub.2O.sub.5. The dehydrogenation catalysts are disposed on an alumina support that is modified with calcium oxide to influence characteristics of lattice oxygen at the catalyst surface. Various methods of preparing and characterizing the catalyst as well as methods for the gas phase oxygen free oxidative dehydrogenation of alkanes, such as propane, to corresponding olefins, such as propylene, with improved alkane conversion and olefin product selectivity are also disclosed.

FLUIDIZABLE VANADIUM CATALYST FOR OXIDATIVE DEHYDROGENATION OF ALKANES TO OLEFINS IN A GAS PHASE OXYGEN FREE ENVIRONMENT

Fluidizable catalysts for the gas phase oxygen-free oxidative dehydrogenation of alkanes, such as propane, to corresponding olefins, such as propylene. The catalysts comprise 5-20% by weight per total catalyst weight of one or more vanadium oxides (VO.sub.x), such as V.sub.2O.sub.5. The dehydrogenation catalysts are disposed on an alumina support that is modified with calcium oxide to influence characteristics of lattice oxygen at the catalyst surface. Various methods of preparing and characterizing the catalyst as well as methods for the gas phase oxygen free oxidative dehydrogenation of alkanes, such as propane, to corresponding olefins, such as propylene, with improved alkane conversion and olefin product selectivity are also disclosed.

Control of nanostructure and activity by alloying and/or segregation

A method for synthesis of PtNi smooth surface core/shell particles or Nano cages and porous nanocages from segregated nanoparticles.

RED MUD COMPOSITIONS AND METHODS RELATED THERETO

This disclosure relates to red mud compositions. This disclosure also relates to methods of making red mud compositions. This disclosure additionally relates to methods of using red mud compositions.

RED MUD COMPOSITIONS AND METHODS RELATED THERETO

This disclosure relates to red mud compositions. This disclosure also relates to methods of making red mud compositions. This disclosure additionally relates to methods of using red mud compositions.

RUTHENIUM OXIDE AND CATALYST COMPRISING SAME
20230182118 · 2023-06-15 ·

The present disclosure relates to a novel ruthenium oxide, a method of preparing the same, and a catalyst for selective hydrogenation of an aromatic compound or an unsaturated compound including the ruthenium oxide.

Carbide-derived carbons having incorporated metal chloride or metallic nanoparticles

Carbide-derived carbons are provided that have high dynamic loading capacity for high vapor pressure gasses such as H.sub.2S, SO.sub.2, or NH.sub.3. The carbide-derived carbons can have a plurality of metal chloride or metallic nanoparticles entrapped therein. Carbide-derived carbons are provided by extracting a metal from a metal carbide by chlorination of the metal carbide to produce a porous carbon framework having residual metal chloride nanoparticles incorporated therein, and annealing the porous carbon framework with H.sub.2 to remove residual chloride by reducing the metal chloride nanoparticles to produce the metallic nanoparticles entrapped within the porous carbon framework. The metals can include Fe, Co, Mo, or a combination thereof. The carbide-derived carbons are provided with an ammonia dynamic loading capacity of 6.9 mmol g.sup.−1 to 10 mmol g.sup.−1 at a relative humidity of 0% RH to 75% RH.

Carbide-derived carbons having incorporated metal chloride or metallic nanoparticles

Carbide-derived carbons are provided that have high dynamic loading capacity for high vapor pressure gasses such as H.sub.2S, SO.sub.2, or NH.sub.3. The carbide-derived carbons can have a plurality of metal chloride or metallic nanoparticles entrapped therein. Carbide-derived carbons are provided by extracting a metal from a metal carbide by chlorination of the metal carbide to produce a porous carbon framework having residual metal chloride nanoparticles incorporated therein, and annealing the porous carbon framework with H.sub.2 to remove residual chloride by reducing the metal chloride nanoparticles to produce the metallic nanoparticles entrapped within the porous carbon framework. The metals can include Fe, Co, Mo, or a combination thereof. The carbide-derived carbons are provided with an ammonia dynamic loading capacity of 6.9 mmol g.sup.−1 to 10 mmol g.sup.−1 at a relative humidity of 0% RH to 75% RH.

METHOD FOR PREPARING CATALYST
20170341070 · 2017-11-30 · ·

[Problem to be Solved]

To provide a method for preparing a catalyst that has high activity and exhibits high durability with reduced elution of a catalyst metal when a liquid-phase oxidation reaction is brought about without combined use of an alkali; and a method for producing an oxide highly efficiently by use of the catalyst.

The method for preparing a catalyst has the following Steps 1, 2 and 3.

Step 1: preparing an aqueous dispersion of a catalyst carrying Pt on activated carbon;

Step 2: preparing an aqueous solution containing Bi in an ionic state; and

Step 3: adding the aqueous dispersion obtained in Step 1 to the aqueous solution obtained in Step 2.

METHOD FOR PREPARING CATALYST
20170341070 · 2017-11-30 · ·

[Problem to be Solved]

To provide a method for preparing a catalyst that has high activity and exhibits high durability with reduced elution of a catalyst metal when a liquid-phase oxidation reaction is brought about without combined use of an alkali; and a method for producing an oxide highly efficiently by use of the catalyst.

The method for preparing a catalyst has the following Steps 1, 2 and 3.

Step 1: preparing an aqueous dispersion of a catalyst carrying Pt on activated carbon;

Step 2: preparing an aqueous solution containing Bi in an ionic state; and

Step 3: adding the aqueous dispersion obtained in Step 1 to the aqueous solution obtained in Step 2.