B01J23/22

Denitration catalyst and method for producing the same

There is provided a catalyst that exhibits a high denitration efficiency at a relatively low temperature and does not cause oxidation of SO.sub.2 in a selective catalytic reduction reaction that uses ammonia as a reducing agent. A denitration catalyst is obtained by coating a substrate with a catalyst component. The catalyst component contains 43 wt % or more of vanadium pentoxide and has a BET specific surface area of 30 m.sup.2/g or more. The denitration catalyst is used for denitration at 200 C. or lower.

Denitration catalyst and method for producing the same

There is provided a catalyst that exhibits a high denitration efficiency at a relatively low temperature and does not cause oxidation of SO.sub.2 in a selective catalytic reduction reaction that uses ammonia as a reducing agent. A denitration catalyst is obtained by coating a substrate with a catalyst component. The catalyst component contains 43 wt % or more of vanadium pentoxide and has a BET specific surface area of 30 m.sup.2/g or more. The denitration catalyst is used for denitration at 200 C. or lower.

Method for recycling denitration catalyst

There is provided a method for recycling a catalyst that exhibits a high denitration efficiency at a relatively low temperature and does not cause oxidation of SO.sub.2 in a selective catalytic reduction reaction that uses ammonia as a reducing agent. A method for recycling a denitration catalyst includes a step of removing a used denitration catalyst from a denitration device and then coating the used denitration catalyst with a catalyst component. The catalyst component contains 43 wt % or more of vanadium pentoxide and has a BET specific surface area of 30 m.sup.2/g or more, and the denitration catalyst after recycling is used for denitration at 200 C. or lower.

Method for recycling denitration catalyst

There is provided a method for recycling a catalyst that exhibits a high denitration efficiency at a relatively low temperature and does not cause oxidation of SO.sub.2 in a selective catalytic reduction reaction that uses ammonia as a reducing agent. A method for recycling a denitration catalyst includes a step of removing a used denitration catalyst from a denitration device and then coating the used denitration catalyst with a catalyst component. The catalyst component contains 43 wt % or more of vanadium pentoxide and has a BET specific surface area of 30 m.sup.2/g or more, and the denitration catalyst after recycling is used for denitration at 200 C. or lower.

CATALYST SUPPORT STRUCTURE AND METHOD FOR MANUFACTURING SAME
20200254424 · 2020-08-13 ·

Provided are a mercury oxidation catalyst support structure with which a mercury oxidation reaction can be carried out while inhibiting the oxidation reaction for SO.sub.2 included in exhaust gas and a method for manufacturing the same. This mercury oxidation catalyst structure is characterized by vanadium being unevenly supported on the surface of the support structure. The method for manufacturing the mercury oxidation catalyst structure includes a step of incorporating an inactive support throughout from the inside to the surface of the structure using an inactive support-containing liquid and a step of immersing the structure having been subjected to the step in a liquid containing vanadium or applying the same liquid to the surface of the same structure, followed by drying and calcinating, thereby supporting vanadium on the inactive support present in the surface of the structure.

CATALYST SUPPORT STRUCTURE AND METHOD FOR MANUFACTURING SAME
20200254424 · 2020-08-13 ·

Provided are a mercury oxidation catalyst support structure with which a mercury oxidation reaction can be carried out while inhibiting the oxidation reaction for SO.sub.2 included in exhaust gas and a method for manufacturing the same. This mercury oxidation catalyst structure is characterized by vanadium being unevenly supported on the surface of the support structure. The method for manufacturing the mercury oxidation catalyst structure includes a step of incorporating an inactive support throughout from the inside to the surface of the structure using an inactive support-containing liquid and a step of immersing the structure having been subjected to the step in a liquid containing vanadium or applying the same liquid to the surface of the same structure, followed by drying and calcinating, thereby supporting vanadium on the inactive support present in the surface of the structure.

Honeycomb catalyst for removal of nitrogen oxides in flue and exhaust gasses and method of preparation thereof

A vanadium oxide based honeycomb SCR catalyst composed of a plurality of corrugated sheets stacked upon one another to form a plurality of flow through channels, the corrugated sheets are provided with an inert inner core layer and an outermost layer containing a SCR catalyst composition.

Honeycomb catalyst for removal of nitrogen oxides in flue and exhaust gasses and method of preparation thereof

A vanadium oxide based honeycomb SCR catalyst composed of a plurality of corrugated sheets stacked upon one another to form a plurality of flow through channels, the corrugated sheets are provided with an inert inner core layer and an outermost layer containing a SCR catalyst composition.

Method for in situ high activity ODH catalyst

A process for preparing an oxidative dehydrogenation catalyst or oxidative dehydrogenation catalyst precursor that includes mixing solutions of molybdenum and tellurium at a pH from about 3.3 to 7.5; adjusting the pH of the resulting solution back to about 5 and adding VOSO.sub.4 and adding a solution of Nb.sub.2O.sub.5 and oxalic acid and treating the resulting precursor slurry in a controlled pressure hydrothermal process to obtain the catalyst.

Method for in situ high activity ODH catalyst

A process for preparing an oxidative dehydrogenation catalyst or oxidative dehydrogenation catalyst precursor that includes mixing solutions of molybdenum and tellurium at a pH from about 3.3 to 7.5; adjusting the pH of the resulting solution back to about 5 and adding VOSO.sub.4 and adding a solution of Nb.sub.2O.sub.5 and oxalic acid and treating the resulting precursor slurry in a controlled pressure hydrothermal process to obtain the catalyst.