NOx storage reduction over Pt-Ba/gamma-Al2O3 catalyst

Citation
L. Lietti et al., NOx storage reduction over Pt-Ba/gamma-Al2O3 catalyst, J CATALYSIS, 204(1), 2001, pp. 175-191
Citations number
21
Categorie Soggetti
Physical Chemistry/Chemical Physics","Chemical Engineering
Journal title
JOURNAL OF CATALYSIS
ISSN journal
00219517 → ACNP
Volume
204
Issue
1
Year of publication
2001
Pages
175 - 191
Database
ISI
SICI code
0021-9517(20011115)204:1<175:NSROPC>2.0.ZU;2-R
Abstract
A transient study on the NOx storage-reduction properties of a Pt-BaO/gamma -Al2O3 catalyst is performed by using a synthetic exhaust gas containing o xygen and nitrogen oxides (storage phase) and a reducing gas containing hyd rogen (reduction phase). The influence of water and carbon dioxide is also investigated. It is found that (i) NOx is stored in the form of nitrites an d nitrates; (ii) during storage nitrites are oxidized to nitrates, and nitr ates are most abundant when the storage process is completed; (iii) 0.3-3% CO2 has a marked inhibiting effect on the storage of NOx, particularly at l ow temperature, whereas 1% H2O has a promoting effect at low temperature an d an inhibiting effect at high temperature. In the presence of 0.3-3% CO2 1% H2O the process is inhibited at any temperature; (iv) the storage of NO x occurs preferentially in the order at BaO, Ba(OH)(2), and BaCO3. The abun dance of the different Ba sites at the catalyst surface depends on the comp osition of the exhaust gas and of the reducing gas; (v) considerable amount s of NOx are stored up to catalyst saturation and up to the NOx, breakthrou gh in He + 3% O-2 atmosphere that correspond to 24% Ba and 13-15% Ba to the best, respectively; (vi) in the presence of 0.3-3% CO2 and 1% H2O in the e xhaust these quantities diminish by 20-40% for NOx stored up to catalyst sa turation and by 50% for NOx stored up to the NOx breakthrough; (vii) the re duction of the stored NOx is fast and is limited by the concentration of th e reducing agent at any temperature in He + 2000 ppm H-2; (Viii) the reduct ion of the stored NOx is very selective to N-2 (95-100%); (ix) the reductio n is slower in the presence of 0.3-3% CO2 and 0.3-3% CO2 + 1% H2O; (x) once all the stored reactive NOx groups have been reduced, in the presence of 0 .3-3% CO2 and at sufficiently high temperature (T greater than or equal to 300 degreesC) CO is formed through the reverse WGS reaction. This reaction, however, is of lesser importance when water is present in the exhaust due to thermodynamic constraints. The complete set of reactions involved in the storage-reduction cycle is identified and used to account quantitatively f or the bulk of experimental data and to provide a comprehensive chemistry o f the process. (C) 2001 Academic Press.