A Kinetic Model for the Selective Catalytic Reduction of NOx with NH3 over an Fe-zeolite Catalyst
Artikel i vetenskaplig tidskrift, 2010

The selective catalytic reduction of NOx with ammonia over all Fe-zeolite catalyst was investigated experimentally and a transient kinetic model was developed. The model includes reactions that describe ammonia storage and oxidation, NO oxidation, selective catalytic reduction (SCR) of NO and NO2, formation of N2O, ammonia inhibition and ammonium nitrate formation. The model call account for a broad range of experimental conditions in the presence of H2O, CO2 and O-2 at temperatures from 150 to 650 degrees C. The catalyst stores ammonia at temperatures up to 400 degrees C and shows ammonia oxidation activity from 350 degrees C. The catalyst is also active for the oxidation of NO to NO2 and the oxidation reaches equilibrium at 500 degrees C. The SCR of NO is already active at 150 degrees C and the introduction of equal amounts of NO and NO2 greatly enhances the conversion of NOx at temperatures up to 300 degrees C. The formation of N2O is negligible if small fractions of NO2 are fed to the reactor, but a significant amount of N2O is formed at high NO2 to NO ratios. An ammonia inhibition oil the SCR of NO is observed at 200 degrees C. This kinetic model contains 12 reactions and is able to describe the experimental results Well. The model was validated using short transient experiments and experimental conditions not used in the parameter estimation and predicted these new conditions adequately.

CUZSM5 CATALYST

DIESEL-ENGINE

EXHAUST AFTERTREATMENT

NITROUS-ACID

FE-ZSM-5 CATALYSTS

LOW-TEMPERATURES

EXCHANGED ZEOLITES

AST SCR REACTION

UREA-SCR

NITRIC-OXIDE

Författare

Hanna Maria Sjövall

Chalmers, Kemi- och bioteknik, Kemisk reaktionsteknik

Kompetenscentrum katalys (KCK)

Richard Blint

General Motors

A. Gopinath

General Motors

Louise Olsson

Kompetenscentrum katalys (KCK)

Chalmers, Kemi- och bioteknik, Kemisk reaktionsteknik

Industrial & Engineering Chemistry Research

0888-5885 (ISSN) 1520-5045 (eISSN)

Vol. 49 1 39-52

Ämneskategorier

Kemiteknik

DOI

10.1021/ie9003464

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Skapat

2017-10-08