Ni-exchanged AlMCM-41 - An efficient bifunctional catalyst for ethylene oligomerization

Journal of Catalysis

Volumn 225, Issue 1, 2004, Pages 213-222

  Hulea, Vasile ^a   Fajula, François ^a  

^a LABORATOIRE DE MATÉRIAUX CATALYTIQUES ET CATALYSE EN CHIMIE ORGANIQUE   (France)

Author keywords

Acidity; Ethylene; Ni AlMCM 41; Nickel; Oligomerization

Indexed keywords

ETHYLENE; HEPTANE; METAL; NICKEL; NITROGEN; SOLVENT;

ACIDITY; ARTICLE; CATALYST; CHEMICAL ANALYSIS; CHEMICAL REACTION; DESORPTION; OLIGOMERIZATION; SYNTHESIS; TEMPERATURE; X RAY DIFFRACTION;

EID: 2542428254     PISSN: 00219517     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jcat.2004.04.018     Document Type: Article

References (30)

1. Al-Jarallah A.M., Anabtawi J.A., Siddiqui A.A.B., Aitani A.M., Alsadoun A.W. Catal. Today. 14:1992;1
2. Yashima T., Ushida Y., Ebisawa M., Hara N. J. Catal. 36:1975;320
3. Bonneviot L., Olivier D., Che M. J. Mol. Catal. 21:1983;415
4. Elev J.V., Shelinov B.N., Kazansky V.B. J. Catal. 89:1984;470
5. Heveling J., van der Beek A., de Pender M. Appl. Catal. 42:1988;325
6. Nkosi B., Ng F.T.T., Rempel G.L. Appl. Catal. A. 158:1997;225
7. Ng F.T.T., Creaser D.C. Appl. Catal. A. 119:1994;327
8. Zhang L., Wang G., Bai X. Stud. Surf. Sci. Catal. 28:1986;965
9. Zhang Q., Kantcheva M., Dalla Lana I.G. Ind. Eng. Chem. Res. 36:1997;3433
10. Zhang Q., Dalla Lana I.G. Chem. Eng. Sci. 21/22:1997;4187
11. Heydenrych M.D., Nicolaides C.P., Scurrell M.S. J. Catal. 197:2001;49
12. Cai T. Catal. Today. 51:1999;153
13. Espinoza R.L., Korf C.J., Nicolaides C.P., Snel R. Appl. Catal. 29:1987;175
14. Espinoza R.L., Nicolaides C.P., Korf C.J., Snel R. Appl. Catal. 31:1987;259
15. Heveling J., Nicolaides C.P., Scurrell M.S. Appl. Catal. A. 173:1998;1
16. Nicolaides C.P., Scurrell M.S., Semano P.M. Appl. Catal. A. 245:2003;45
17. Bonneviot L., Che M., Dyrek K., Schollner R., Wendt G. J. Phys. Chem. 90:1986;2379
18. Kermarec M., Lepetit C., Cai F.X., Olivier D. J. Chem. Soc., Faraday Trans. I. 85:1989;1991
19. Cai T., Cao D., Song Z., Li L. Appl. Catal. A. 95:1993;L1
20. Beck J.S., Vartuli J.C., Roth W.J., Leonowicz M.E., Kresge C.T., Schmit K.D., Chu C.T.-W., Olson D.H., Sheppared E.W., McCullen S.B., Higgins J.B., Schlenker J.L. J. Am. Chem. Soc. 114:1992;10834
21. Hartmann M., Poppl A., Kevan L. J. Phys. Chem. 100:1996;9906
22. Desplantier-Giscard D., Galarneau A., Di Renzo F., Fajula F. Stud. Surf. Sci. Catal. 135:2001;06-P-27
23. Sing K.S.W., Everett D.H., Haul R.A.W., Moscou L., Pierotti R.A., Rouquérol J., Siemieniewska T. Pure Appl. Chem. 57:1985;603
24. Minchev C., Zubkov S.A., Valtchev V., Minkov V., Micheva N., Kanazirev V. Appl. Catal. A. 119:1994;195
25. Planck C.S. Proceedings of Third International Congress Catalysis, Amsterdam, vol. 1. 1965;727
26. Mosqueda-Jiménez B.I., Jentys A., Seshan K., Lercher J.A. Appl. Catal. B. 46:2003;189
27. Lewandowska A., Monteversdi S., Bettahar M., Ziolek M. J. Mol. Catal. A. 188:2002;85
28. Heveling J., Nicolaides C.P., Scurrell M.S. Appl. Catal. A. 248:2003;239
29. Davydov A.A., Kantcheva M., Chepotko M.L. Catal. Lett. 83:2002;97
30. Espinoza R.L., Snel R., Korf C.J., Nicolaides C.P. Appl. Catal. 29:1987;295