B01J23/08

Methods for dehydrogenating hydrocarbons

According to one or more embodiments described herein, a method for dehydrogenating hydrocarbons may include passing a hydrocarbon feed comprising one or more alkanes or alkyl aromatics into a fluidized bed reactor, contacting the hydrocarbon feed with a dehydrogenation catalyst in the fluidized bed reactor to produce a dehydrogenated product and hydrogen, and contacting the hydrogen with an oxygen-rich oxygen carrier material in the fluidized bed reactor to combust the hydrogen and form an oxygen-diminished oxygen carrier material. In additional embodiments, a dual-purpose material may be utilized which has dehydrogenation catalyst and oxygen carrying functionality.

SUPPORTED METAL OXIDES AS DEPOLYMERIZATION CATALYSTS

Methods of depolymerizing polyolefin-based material into useful petrochemical products using supported metal oxides and heat are described. The supported metal oxides improve the depolymerization reaction by decreasing the half time for the depolymerization, which results in a higher depolymerization rate and a shorter residence time in the depolymerization unit, allowing for a predictable depolymerization reaction, and decreasing the branching or aromatic formations in the product.

DIRECT SYNTHESIS OF LIGHT OLEFINS FROM CARBON DIOXIDE USING YTTRIA-STABILIZED ZIRCONIA SUPPORT
20220135495 · 2022-05-05 ·

The present invention features a direct synthesis of light olefins through the hydrogenation of carbon dioxide. In.sub.2O.sub.3 supported on cubic phase yttria-stabilized zirconia is used as a catalyst and is mixed with a molecular sieve to perform the hydrogenation. The cubic crystal structure of the yttria-stabilized zirconium dioxide is an excellent support for indium oxide particles and prevents their deactivation during CO.sub.2 hydrogenation. This direct synthesis route promotes a stable and efficient method for producing light olefins.

DIRECT SYNTHESIS OF LIGHT OLEFINS FROM CARBON DIOXIDE USING YTTRIA-STABILIZED ZIRCONIA SUPPORT
20220135495 · 2022-05-05 ·

The present invention features a direct synthesis of light olefins through the hydrogenation of carbon dioxide. In.sub.2O.sub.3 supported on cubic phase yttria-stabilized zirconia is used as a catalyst and is mixed with a molecular sieve to perform the hydrogenation. The cubic crystal structure of the yttria-stabilized zirconium dioxide is an excellent support for indium oxide particles and prevents their deactivation during CO.sub.2 hydrogenation. This direct synthesis route promotes a stable and efficient method for producing light olefins.

CATALYST FOR PREPARING HYDROCARBONS FROM CARBON DIOXIDE BY ONE-STEP HYDROGENATION AND METHOD FOR PREPARING SAME

Disclosed are a catalyst for preparing hydrocarbons from carbon dioxide by one-step hydrogenation and a method for preparing same. The catalyst includes nano-metal oxides and hierarchical zeolites, where the mass fraction of the nano-metal oxides in the catalyst is 10%-90%, and the mass fraction of the hierarchical zeolites in the catalyst is 10%-90%. The catalyst has excellent catalytic performance, good reaction stability and high selectivity for desired products, and in the hydrocarbons, C.sub.2.sup.=-C.sub.4.sup.= reach up to 80%, C.sub.5+ reach up to 80%, and aromatics reach up to 65%.

CATALYST FOR PREPARING HYDROCARBONS FROM CARBON DIOXIDE BY ONE-STEP HYDROGENATION AND METHOD FOR PREPARING SAME

Disclosed are a catalyst for preparing hydrocarbons from carbon dioxide by one-step hydrogenation and a method for preparing same. The catalyst includes nano-metal oxides and hierarchical zeolites, where the mass fraction of the nano-metal oxides in the catalyst is 10%-90%, and the mass fraction of the hierarchical zeolites in the catalyst is 10%-90%. The catalyst has excellent catalytic performance, good reaction stability and high selectivity for desired products, and in the hydrocarbons, C.sub.2.sup.=-C.sub.4.sup.= reach up to 80%, C.sub.5+ reach up to 80%, and aromatics reach up to 65%.

Use of molten salt to separate carbon from a molten metal catalyst

The present invention relates to a method for molten metal pyrolysis of hydrocarbons to produce hydrogen gas and carbon. Liquid salt is used to separate produced carbon from the molten metal and to facilitate isolation of produced carbon.

Use of molten salt to separate carbon from a molten metal catalyst

The present invention relates to a method for molten metal pyrolysis of hydrocarbons to produce hydrogen gas and carbon. Liquid salt is used to separate produced carbon from the molten metal and to facilitate isolation of produced carbon.

TANDEM CATALYSIS FOR ALKANE AND ALCOHOL DEHYDROGENATION COUPLED TO SELECTIVE HYDROGEN COMBUSTION
20230241586 · 2023-08-03 ·

Tandem catalysts for the dehydrogenation of alkanes and/or alcohols in tandem with selective hydrogen combustion are provided. Also provided are methods of making the catalysts and methods of using the catalysis for the dehydrogenation of alkanes and/or alcohols. The catalysts include a support having a surface, dehydrogenation catalysts particles dispersed on the surface of the support, and a porous selective hydrogen combustion catalyst overcoat on the dehydration catalyst particles. The catalysts couple dehydrogenation with selective hydrogen combustion in a sequence of reactions occurring in tandem to shift the equilibrium of the dehydrogenation towards higher conversion.

TANDEM CATALYSIS FOR ALKANE AND ALCOHOL DEHYDROGENATION COUPLED TO SELECTIVE HYDROGEN COMBUSTION
20230241586 · 2023-08-03 ·

Tandem catalysts for the dehydrogenation of alkanes and/or alcohols in tandem with selective hydrogen combustion are provided. Also provided are methods of making the catalysts and methods of using the catalysis for the dehydrogenation of alkanes and/or alcohols. The catalysts include a support having a surface, dehydrogenation catalysts particles dispersed on the surface of the support, and a porous selective hydrogen combustion catalyst overcoat on the dehydration catalyst particles. The catalysts couple dehydrogenation with selective hydrogen combustion in a sequence of reactions occurring in tandem to shift the equilibrium of the dehydrogenation towards higher conversion.