The present invention relates to an ammonia decomposition catalyst that converts ammonia into hydrogen and nitrogen. The catalyst includes ruthenium (Ru) as an active catalytic component and a composite oxide solid solution (La.sub.xCe.sub.1-xO.sub.y) including lanthanum oxide and cerium oxide as a catalyst support. The present invention also relates to an ammonia decomposition method using the catalyst and a hydrogen production method using the catalyst.

PROBLEM TO BE SOLVED:

In an apparatus for synthesizing methane from carbon dioxide and hydrogen, a device which is capable to remove the reaction heat and lower the reaction temperature as the reaction progresses in order to increase the conversion ratio to methane has been desired.

SOLUTION:

In the present invention, powders of magnesium hydroxide and magnesium carbonate, which are chemical heat storage agents, are used as part of the fluidizing medium of the multi-stage fluidized bed in the temperature range where the methanation reaction proceeds. The heat generated during the methanation reaction can be absorbed and stored in the powder. At this time, carbon dioxide generated from magnesium carbonate can be used as a raw material gas for the methanation reaction. Furthermore, after discharging the magnesium oxide generated by endotherm, the powder can be regenerated with an external regenerating facility and then the storage heat can be released and recovered. The regenerated powder can be fed to the uppermost stage of the multi-stage fluidized bed at a temperature lower than the internal temperature of the reactor to lower inside temperature. This made it possible to lower the reaction temperature of ascending reaction gas in the reactor along with the reaction progress, and to increase the conversion ratio to the produced methane by this lowered temperature.

PROBLEM TO BE SOLVED:

In an apparatus for synthesizing methane from carbon dioxide and hydrogen, a device which is capable to remove the reaction heat and lower the reaction temperature as the reaction progresses in order to increase the conversion ratio to methane has been desired.

SOLUTION:

In the present invention, powders of magnesium hydroxide and magnesium carbonate, which are chemical heat storage agents, are used as part of the fluidizing medium of the multi-stage fluidized bed in the temperature range where the methanation reaction proceeds. The heat generated during the methanation reaction can be absorbed and stored in the powder. At this time, carbon dioxide generated from magnesium carbonate can be used as a raw material gas for the methanation reaction. Furthermore, after discharging the magnesium oxide generated by endotherm, the powder can be regenerated with an external regenerating facility and then the storage heat can be released and recovered. The regenerated powder can be fed to the uppermost stage of the multi-stage fluidized bed at a temperature lower than the internal temperature of the reactor to lower inside temperature. This made it possible to lower the reaction temperature of ascending reaction gas in the reactor along with the reaction progress, and to increase the conversion ratio to the produced methane by this lowered temperature.

An object of the present invention is to increase the reduction performance of nitrogen oxides compared to existing three-way catalysts; simultaneously inhibit the emission of ammonia and nitrous oxide; simplify a process by means of a method of further doping an iridium-ruthenium catalyst into a commercial three-way catalyst; and expand the scope of application. The present invention provides a catalyst for simultaneously inhibiting the emission of ammonia and nitrous oxide by doping an iridium-ruthenium catalyst component into a three-way catalyst (TWC), a diesel oxidation catalyst, or a lean NOx trap supported on a honeycomb support.

An object of the present invention is to increase the reduction performance of nitrogen oxides compared to existing three-way catalysts; simultaneously inhibit the emission of ammonia and nitrous oxide; simplify a process by means of a method of further doping an iridium-ruthenium catalyst into a commercial three-way catalyst; and expand the scope of application. The present invention provides a catalyst for simultaneously inhibiting the emission of ammonia and nitrous oxide by doping an iridium-ruthenium catalyst component into a three-way catalyst (TWC), a diesel oxidation catalyst, or a lean NOx trap supported on a honeycomb support.

A method of manufacturing a catalyst article, the method comprising: providing a complex of a humic acid or derivative thereof, and a PGM; providing a support material; applying the complex to the support material to form a loaded support material; disposing the loaded support material on a substrate; and heating the loaded support material to form nanoparticles of the PGM on the support material.

The present disclosure provides a method for co-production of hydrofluorocarbons, which includes the steps of: preheating a mixture of chlorinated olefin and hydrogen fluoride; transferring the mixture to the top of a reactor; simultaneously introducing 1,1,1,2,3,3-hexafluoropropene and dichloromethane to the middle of the reactor for reaction; dividing the reactor into three to six sections; filling each section with a catalyst; obtaining reaction products at an outlet of the reactor; and separating the reaction products to obtain various hydrofluorocarbon products, respectively. The present disclosure has the advantages of a high yield, an optimal selectivity and a low energy consumption.

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. Fe.sub.3O.sub.4). 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.

Catalyst compositions to perform selective alkyl-demethylation of C2+-hydrocarbyl-substituted aromatic hydrocarbon may exhibit a hydrogen chemisorption of at least 15% and comprise an oxide support material selected from the group consisting of an alkaline earth metal oxide, silica, a composite of an alkaline earth metal oxide and Al.sub.2O.sub.3, a composite of ZnO and Al.sub.2O.sub.3, a lanthanide oxide, a composite of a lanthanide oxide and Al.sub.2O.sub.3, and combinations and mixtures of two or more thereof; and a transition metal element dispersed upon the oxide support material. Alkyl-demethylation processes of a C6+ aromatic hydrocarbon-containing stream comprising C2+-hydrocarbyl-substituted aromatic hydrocarbons may comprise contacting the catalyst compositions in an alkyl-demethylation zone under alkyl-demethylation conditions to form an alkyl-demethylated aromatic hydrocarbon as an effluent exiting the alkyl-demethylation zone.

Disclosed are catalyst compositions comprising two or more metal elements with high performances for selective alkyl-demethylation of C2+-hydrocarbyl-substituted aromatics, processes for making such catalyst compositions, and alkyl-demethylation processes using same. Also disclosed are preferred processes for making alkyl-demethylation catalyst compositions including a high-temperature calcination step, and preferred alkyl-demethylation processes having a high H.sub.2/HC molar ratio.