Investigation of the aromatization of C6+ hydrocarbons on chromia/lanthana-zirconia catalyst: Part I. Catalytic experiments

Journal of Molecular Catalysis A: Chemical

Volumn 210, Issue 1-2, 2004, Pages 211-216

  Klepel, Olaf ^a   Breitkopf, Cornelia ^a   Standke, Mirko ^a  

^a UNIVERSITY OF LEIPZIG   (Germany)

Author keywords

Aromatization; Catalysis; Chromia lanthana zirconia; Reaction mechanism

Indexed keywords

AROMATIC COMPOUNDS; AROMATIZATION; CHEMICAL BONDS; ISOMERIZATION; MOLECULAR STRUCTURE; ZIRCONIA;

EDUCT STRUCTURE;

CATALYST ACTIVITY;

CARBENE; CHROMIUM DERIVATIVE; HYDROCARBON; LANTHANUM; METHYL GROUP; ZIRCONIUM OXIDE;

AROMATIZATION; ARTICLE; CALCULATION; CATALYSIS; CATALYST; CHEMICAL BOND; CHEMICAL STRUCTURE; ISOMERIZATION;

EID: 1642533510     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2003.09.019     Document Type: Article

References (36)

1. Lieske, H., Hoang, D.-L., German Patent DE-OS 196 12 (2000).
2. Trunschke A., Hoang D.-L., Radnik J., Lieske H. J. Catal. 191:2000;456.
3. Hoang D.L., Lieske H. Thermochim. Acta. 345:2000;93.
4. Hoang D.L., Trunschke A., Brückner A., Radnik J., Lieske H. Surf. Sci. Catal. 130:2000;2357.
5. D.L. Hoang, J.-P., Müller, A., Dittmar, J., Radnik, H., Lieske, in: Proceeding of the Ninth International Symposium, Varna, 2000, p. 567.
6. Brückner A., Radnik J., Hoang D.L., Lieske H. Catal. Lett. 60:1999;183.
7. Ehwald H., Leibnitz U., Lieske H. Catal. Lett. 70:2000;23.
8. Mills G.A., Heinemann H., Milliken T.H., Oblad A.G. Ind. Eng. Chem. 45:1953;134.
9. Paal Z. J. Catal. 105:1987;540.
10. Rozengart M.I., Mortikov E.S., Kazansky B.A. Dokl. Akad. Nauk. SSSR. 158:1966;911.
11. Rozengart M.I., Mortikov E.S., Kazansky B.A. Dokl. Akad. Nauk. SSSR. 166:1966;619.
12. Paal Z., Tetenyi P. Acta Chim. Acad. Sci. Hung. 53:1967;193.
13. Paal Z., Tetenyi P. Acta Chim. Acad. Sci. Hung. 54:1967;175.
14. Paal Z., Tetenyi P. Acta Chim. Acad. Sci. Hung. 58:1968;105.
15. Paal Z., Tetenyi P. J. Catal. 105:1987;540.
16. Iglesia E., Baumgarten J., Price G.L., Rose K.D., Robbins J.L. J. Catal. 125:1990;95.
17. Paal Z., Lun X. Appl. Catal. 43:1988;1.
18. Paal Z. Adv. Catal. 29:1981;273.
19. Price G., Egedy C. J. Catal. 84:1983;462.
20. Tetenyi P. Catal. Today. 17:1993;439.
21. Fogelberg L.-G., Gore R., Ranby B. Acta Chem. Scand. 21:1967;2041.
22. Kazansky B.A., Plate A.F. Ber. Dtsch. Chem. Ges. B. 69:1936;1862.
23. Kazansky B.A., Libermann A.L., Batuev M.I. Dokl. Akad. Nauk. SSSR. 61:1948;67.
24. Twigg G.H. Faraday Soc. 35:1934;1006.
25. Herrington E.F.G., Rideal E.K. Proc. R. Soc. A. 184:1945;434.
26. Fung J., Wang I. J. Catal. 164:1996;166.
27. Herrington E.F.G., Rideal E.K. Proc. R. Soc. A. 144:1945;447.
28. Burch R., Paal Z. Appl. Catal. A. 114(1):1994;9.
29. CERIUS2, ©MSI 1994.
30. Smith A.E., Linder H.J. J. Comp. Aid. Mol. Des. 5:1991;235.
31. Allinger N.L. Adv. Phys. Org. Chem. 13:1976;1.
32. Davis B.H. Catal. Today. 53:1999;443.
33. Shi B., Davis B.H. J. Catal. 147:1994;38.
34. Shi B., Davis B.H. J. Catal. 157:1995;626.
35. Shi B., Davis B.H. J. Catal. 168:1997;129.
36. Shi B., Davis B.H. J. Catal. 162:1996;134.