PROMOTION OF OXYGEN DESORPTION TO ENHANCE DIRECT NO DECOMPOSITION OVER TB-PT AL2O3 CATALYST/

Authors
Citation
Ssc. Chuang et Cd. Tan, PROMOTION OF OXYGEN DESORPTION TO ENHANCE DIRECT NO DECOMPOSITION OVER TB-PT AL2O3 CATALYST/, JOURNAL OF PHYSICAL CHEMISTRY B, 101(15), 1997, pp. 3000-3004
Citations number
16
Categorie Soggetti
Chemistry Physical
Journal title
JOURNAL OF PHYSICAL CHEMISTRY B
ISSN journal
15206106 → ACNP
Volume
101
Issue
15
Year of publication
1997
Pages
3000 - 3004
Database
ISI
SICI code
1089-5647(1997)101:15<3000:POODTE>2.0.ZU;2-A
Abstract
Promotion of oxygen desorption at low temperatures holds the key to th e development of an effective NO decomposition catalyst. Addition of T b oxide to Pt/Al2O3 allows oxygen from dissociated NO to desorb at 593 K, which is significantly lower than the reported oxygen desorption t emperatures for Pt catalysts. Combined temperature-programmed desorpti on/reaction with in situ infrared study reveals that desorbed oxygen i s produced from decomposition of chelating bidentate nitrate, which ma y result from the reaction of adsorbed oxygen on Pt and adsorbed NO on Tb oxide. The Tb-promoted Pt/Al2O3 catalyst which possesses oxygen de sorption capability at low temperatures shows the activity for decompo sition of NO to N-2, N2O, NO2, and O-2 under pulse and steady-state re action conditions at 773-923 K.