Reactivity of nitrogen containing organic intermediates in the selective catalytic reduction of NO(x) with organic compounds: A model study with tert-butyl substituted nitrogen compounds

Applied Catalysis B: Environmental

Volumn 19, Issue 1, 1998, Pages 9-22

  Obuchi, Akira ^a,b   Wögerbauer, Clemens ^a   Köppel, René ^a   Baiker, Alfons ^a  

^a ETH ZURICH   (Switzerland)

^b NATL INST FOR RSRC AND ENVIRON   (Japan)

Author keywords

Alumina; Cyanide; Isocyanate; Mechanism; Nitrile N oxide; NO(x); Selective reduction

Indexed keywords

ALUMINA; CYANIDES; MIXTURES; NITROGEN OXIDES; ORGANIC COMPOUNDS; REDUCTION;

ISOCYANATE; SELECTIVE CATALYSIS;

CATALYSIS;

EID: 0032569686     PISSN: 09263373     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0926-3373(98)00053-8     Document Type: Article

References (29)

1. Iwamoto M., Yahiro H. Catal. Today. 22:1994;5.
2. Amiridis M.D., Zhang T., Farrauto R.J. Appl. Catal. B. 10:1996;203.
3. Armor J.N. Catal. Today. 26:1995;99.
4. Burch R., Millington P.J. Catal. Today. 26:1995;185.
5. Yokoyama C., Misono M. J. Catal. 150:1994;9.
6. Beutel T., Adelman B.J., Lei G.-D., Sachtler W.M.H. Catal. Lett. 32:1995;83.
7. Bamwenda G.R., Ogata A., Obuchi A., Oi J., Mizuno K., Skrzypek J. Appl. Catal. B. 6:1995;311.
8. N.W. Hayes, W. Grunert, G.J. Hutchings, R.W. Joyner, E.S. Shpiro, J. Chem. Soc., Chem. Commun. (1994) 531.
9. C. Li, K.A. Bethke, H.H. Kung, M.C. Kung, J. Chem. Soc., Chem. Commun. (1995) 813.
10. Ukisu Y., Sato S. Appl. Catal. B. 2:1993;147.
11. Radtke F., Köppel R.A., Baiker A. Appl. Catal. A. 107:1994;L125.
12. Radtke F., Köppel R.A., Baiker A. Catal. Lett. 28:1994;131.
13. F. Radtke, R.A. Köppel, A. Baiker, J. Chem. Soc., Chem. Commun. (1995) 427.
14. Takeda H., Iwamoto M. Catal. Lett. 38:1996;21.
15. H. Yasuda, T. Miyamoto, M. Misono, ACS Symposium Series 587, Reduction of Nitrogen Oxide Emissions, American Chemical Society, 1995, p. 110.
16. Li Y., Slager T.L., Armor J.N. J. Catal. 150:1994;388.
17. Lukyanov D.B., Lombardo E.A., Sill G.A., d'Itri J.L., Hall W.K. J. Catal. 163:1996;447.
18. Cant N.W., Cowan A.D. Catal. Today. 35:1997;89.
19. Cant N.W., Cowan A.D., Doughty A., Haynes B.S., Nelson P.F. Catal. Lett. 46:1997;212.
20. Lombardo E.A., Sill G.A., d'Itri J.L., Hall W.K. J. Catal. 173:1998;440.
21. C. Grundmann, Methoden der organischen Chemie, Bd. E5, Carbonsäuren und Carbonsäure-Derivate, Georg Thieme Verlag, Stuttgart, 1985, p. 1601.
22. Zinner G., Guenther H. Angew. Chem. 76:1964;440.
23. Yamakawa M., Kubota T., Akazawa H. Theoret. Chim. Acta (Berl.). 15:1969;244.
24. Califano N.S., Scarpati R., Speroni G. Lincei - Rend. Sc. Fis. Mat. Nat. 23:1957;263.
25. Curran D.P., Scanga S.A., Fenk J.C. J. Org. Chem. 49:1984;3474.
26. Radtke F., Köppel R.A., Baiker A. Catal. Today. 26:1995;159.
27. Cowan A.D., Cant N.W., Haynes B.S., Nelson P.F. J. Catal. 176:1998;329.
28. M. Windholz et al. (Eds.), The Merck Index, 9th ed., Merck & Co., 1976, p. ONR-90, and literature cited therein.
29. Lukyanov D.B., d'Itri J.L., Sill G., Hall W.K. Stud. Surf. Sci. Catal. 101:1996;651.