KIT | KIT-Bibliothek | Impressum | Datenschutz

Catalytic activation of ceramic filter elements for combined particle separation, NOx removal and VOC total oxidation

Nacken, M.; Heidenreich, S.; Hackel, M. 1; Schaub, G. 1
1 Universität Karlsruhe (TH)

Abstract:

The development of a catalytically active filter element for combined particle separation and NOx removal or VOC total oxidation, respectively, is presented. For NOx removal by selective catalytic reduction (SCR) a catalytic coating based on a TiO2–V2O5–WO3 catalyst system was developed on a ceramic filter element. Different TiO2 sols of tailor-made mean particle size between 40 and 190 nm were prepared by the sol–gel process and used for the impregnation of filter element cylinders by the incipient wetness technique. The obtained TiO2-impregnated sintered filter element cylinders exhibit BET surface areas in the range between 0.5 and 1.3 m2/g. Selected TiO2-impregnated filter element cylinders of high BET surface area were catalytically activated by impregnation with a V2O5 and WO3 precursor solution. The obtained catalytic filter element cylinders show high SCR activity leading to 96% NO conversion at 300 °C, a filtration velocity of 2 cm/s and an NO inlet concentration of 500 vol.-ppm. The corresponding differential pressures fulfill the requirements for typical hot gas filtration applications. For VOC total oxidation, a TiO2-impregnated filter element support was catalytically activated with a Pt/V2O5 system. ... mehr


Originalveröffentlichung
DOI: 10.1016/j.apcatb.2006.02.030
Scopus
Zitationen: 87
Web of Science
Zitationen: 72
Dimensions
Zitationen: 81
Zugehörige Institution(en) am KIT Engler-Bunte-Institut (EBI)
Publikationstyp Zeitschriftenaufsatz
Publikationsjahr 2007
Sprache Englisch
Identifikator ISSN: 0926-3373
KITopen-ID: 1000050243
Erschienen in Applied Catalysis. B: Environmental
Verlag Elsevier
Band 70
Heft 1-4
Seiten 370-376
Nachgewiesen in Scopus
Web of Science
Dimensions
KIT – Die Forschungsuniversität in der Helmholtz-Gemeinschaft
KITopen Landing Page