Heteropolyacid supported on acidic clay: A novel efficient catalyst for alkylation of ethylbenzene with dilute ethanol to diethylbenzene in presence of C8 aromatics

Journal of Molecular Catalysis A: Chemical

Volumn 285, Issue 1-2, 2008, Pages 155-161

  Bokade, Vijay V ^a,b   Yadav, Ganapati D ^a  

^a INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

^b NATIONAL CHEMICAL LABORATORY   (India)

Author keywords

Alkylation; Diethylbenzene; Heteropolyacid; Kinetics; Solid acids

Indexed keywords

ALKYLATION; CATALYSTS; ETHANOL; ETHYLBENZENE; KINETIC PARAMETERS; REDUCTION; VAPORS;

DIETHYLBENZENE; HETEROPOLYACID; KINETIC MODELS; SOLID ACIDS;

CLAY;

EID: 42649139970     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2007.11.018     Document Type: Article

References (33)

1. Olah G.A. Fried-Crafts Reaction (1966), Wiley Interscience, New York
2. Yadav G.D., and Goel P.K. Clean Tech. Environ. Policy 4 (2002) 165-170
3. Pope M.T. In Heteropoly and Isopoly Oxometalates (1983), Springer-Verlag, Berlin
4. Misono M. Catal. Rev. Sci. Eng. 29 (1987) 269-321
5. Ono Y. In: Thomas J.M., and Zamaraev K.I. (Eds). Perspectives in Catalysis (1992), Blackwell, London 431-465
6. Izumi Y., Urabe K., and Onaka M. Zeolite, Clay and Heteropoly acid in Organic Reactions, Kodansha (1992), Tokyo-VCH, Weinheim
7. Okuhara T., Nishimura T., Watanabe H., and Misono M. J. Mol. Catal. 74 (1992) 247-256
8. Yadav G.D., and Kirthivasan N. J. Chem. Soc. Chem. Commun. 2 (1995) 203-204
9. Yadav G.D. Catal. Surv. Asia 9 2 (2005) 117-137
10. Yadav G.D., and Bokade V.V. Appl. Catal. A 147 (1996) 299-323
11. Yadav G.D., and Pujari A.A. Green Chem. 1 (1999) 69-74
12. Yadav G.D., and Goel P.K. Green Chem. 2 (2000) 71-77
13. Yadav G.D., Goel P.K., and Joshi A.V. Green Chem. 3 (2001) 92-99
14. Yadav G.D., and Doshi N.S. Org. Process. Res. Dev. 6 (2002) 263-272
15. Yadav G.D., and Asthana N.S. Appl. Catal. A 244 (2003) 341-357
16. Yadav G.D., Asthana N.S., and Kamble V.S. Appl. Catal. A 240 (2003) 53-69
17. Yadav G.D., Asthana N.S., and Kamble V.S. J. Catal. 217 (2003) 88-99
18. Yadav G.D., Salgaonkar S.S., and Asthana N.S. Appl. Catal. A 265 (2004) 153-159
19. Pardee W.A., and Dodge B.F. Ind. Eng. Chem. Res. 35 (1943) 273-278
20. Marks E.M., Almand J.M., and Reid E.E. J. Org. Chem. 9 (1944) 13-20
21. E.C. Britton, J.C. van der Weele, US patent 2,403,785 (1946).
22. R.H. Boundy, R.F. Boyer, Am. Chem. Soc. Monograph. Reinhold, New York, 15, 1952.
23. G.L. Hervert, C.B. Linn, US Patent 2,939,890 (1960).
24. G.L. Hervert, C.B. Linn, US Patent 3,068,301 (1962).
25. R.G. Hay, L.F. Meyer, C.M. Selwitz, US Patent 3,129,255 (1964).
26. W.L. Benedict, W.J. Mattox, US Patent 2,418,689 (1947).
27. E.F. Peters, US patent 2,773,108 (1956).
28. W. Schwerdtel, W. Kroenig, French Patent 1,341,111 (1963).
29. J.J. Wise, Ger. DE 1,468,982 (1973).
30. Olah G.A., Kaspi J., and Bukala J. J. Org. Chem. 42 (1977) 4187-4191
31. Devassy B.M., and Halligudi S.B. J. Mol. Catal. A: Chem. 253 (2006) 8-15
32. Folger H.S. Elements of Chemical Reaction Engineering. 3rd ed. (1999), Prentice Hall, New Jersey p. 636
33. Choi S., Wang Y., Nie Z., Liu J., and Peden C.H.F. Catal. Today 55 (2000) 117-124