Catalyst regeneration processes that include measures for controlling emissions generated during the regeneration are described. The present invention further relates to catalytic processes for producing various chlorinated aromatic compounds that include provisions for controlling emissions during catalyst regeneration.

Catalyst regeneration processes that include measures for controlling emissions generated during the regeneration are described. The present invention further relates to catalytic processes for producing various chlorinated aromatic compounds that include provisions for controlling emissions during catalyst regeneration.

This application relates to preparation of mono and bimetallic group V, VI, and VII containing carbide catalysts and the methods of using the carbide catalysts in hydroprocessing applications. A method of producing a carbide catalyst comprising: depositing a precursor metal, an acid or an amine, and an organic compound on a support thereby forming an impregnated support, wherein the organic compound has a carbon number of 10 or greater; and carbonizing the impregnated support thereby forming a carbide phase on the support.

A SCR catalyst for removing nitrogen oxides comprises: a carrier prepared from a support in which Ti-PILC is mixed with titania; and a catalyst material on the carrier, wherein the catalyst material contains an active material of a vanadium component and a co-catalyst of a tungsten component. On the basis of the total weight of the catalyst, the support Ti-PILC is contained at 0.01-40 wt %, and the support titania is contained at 50 to 90 wt %. In addition, a method for producing a SCR catalyst for removing nitrogen oxides comprises the steps of: preparing a carrier by using a support in which Ti-PILC is mixed with titania; and supporting a catalyst material on the carrier. The present disclosure provides: a SCR catalyst for removing nitrogen oxides, which has an excellent nitrogen oxide removing performance and a high producing convenience; and a method for producing the same.

A SCR catalyst for removing nitrogen oxides comprises: a carrier prepared from a support in which Ti-PILC is mixed with titania; and a catalyst material on the carrier, wherein the catalyst material contains an active material of a vanadium component and a co-catalyst of a tungsten component. On the basis of the total weight of the catalyst, the support Ti-PILC is contained at 0.01-40 wt %, and the support titania is contained at 50 to 90 wt %. In addition, a method for producing a SCR catalyst for removing nitrogen oxides comprises the steps of: preparing a carrier by using a support in which Ti-PILC is mixed with titania; and supporting a catalyst material on the carrier. The present disclosure provides: a SCR catalyst for removing nitrogen oxides, which has an excellent nitrogen oxide removing performance and a high producing convenience; and a method for producing the same.

A process for the removal of nitrous oxide (N.sub.2O) contained in a process off-gas in an axial flow reactor. The process includes the steps of (a) adding an amount of reducing agent into the process off-gas; (b) in a first stage passing in axial flow direction the process off-gas admixed with the reducing agent through a first monolithic shaped catalyst active in decomposing nitrous oxide by reaction with the reducing agent to provide a gas with a reduced amount of nitrous oxide and residual amounts of reducing agent; and (c) in a second stage passing the gas with a reduced amount of nitrous oxide and residual amounts of the reducing agent in axial flow direction through a second monolithic shaped catalyst active in oxidation of the residual amounts of the reducing agent.

A process for the removal of nitrous oxide (N.sub.2O) contained in a process off-gas in an axial flow reactor. The process includes the steps of (a) adding an amount of reducing agent into the process off-gas; (b) in a first stage passing in axial flow direction the process off-gas admixed with the reducing agent through a first monolithic shaped catalyst active in decomposing nitrous oxide by reaction with the reducing agent to provide a gas with a reduced amount of nitrous oxide and residual amounts of reducing agent; and (c) in a second stage passing the gas with a reduced amount of nitrous oxide and residual amounts of the reducing agent in axial flow direction through a second monolithic shaped catalyst active in oxidation of the residual amounts of the reducing agent.

Disclosed is a catalyst for producing the olefin. The catalyst includes a support including alumina and a sub-support component, and a metal oxide impregnated on the support. The metal oxide includes anyone selected from an oxide of chromium, vanadium, manganese, iron, cobalt, molybdenum, copper, zinc, cerium and nickel; and the sub-support component includes anyone selected from zirconium, zinc and platinum.

A method for preparing a sol comprising TiO.sub.2 and ZrO.sub.2 and/or hydrated forms of TiO.sub.2 and ZrO.sub.2. The method includes mixing a material which includes metatitanic acid in an aqueous phase with a zirconyl compound or with a mixture of several zirconyl compounds. The material is provided either as a suspension or as a filter cake from the sulfate method. The material includes a H.sub.2SO.sub.4 content of 3 to 15 wt.-% relative to a quantity of TiO.sub.2 in the material. The zirconyl compound or the mixture of several zirconyl compounds is mixed in a quantity that is sufficient to provide the sol depending on the H.sub.2SO.sub.4 content.

A denitrification catalyst using ceramic nanotubes grown on a porous metal structure, including: a porous metal structure having a plurality of pores formed between metal supports such that exhaust gas penetrates through the pores in multiple directions; ceramic nanotubes grown on the porous metal structure through anodic oxidation; and an active material uniformly and highly dispersed as a nano-thin film layer on inner and outer surfaces of the ceramic nanotubes through a deposition or supporting process.