CYCLOHEXANE OXIDATION CATALYZED BY TITANIUM SILICALITE (TS-1) - OVEROXIDATION AND COMPARISON WITH OTHER OXIDATION SYSTEMS

Citation
Ev. Spinace et al., CYCLOHEXANE OXIDATION CATALYZED BY TITANIUM SILICALITE (TS-1) - OVEROXIDATION AND COMPARISON WITH OTHER OXIDATION SYSTEMS, Journal of catalysis, 157(2), 1995, pp. 631-635
Citations number
18
Categorie Soggetti
Chemistry Physical
Journal title
ISSN journal
00219517
Volume
157
Issue
2
Year of publication
1995
Pages
631 - 635
Database
ISI
SICI code
0021-9517(1995)157:2<631:COCBTS>2.0.ZU;2-K
Abstract
At 100 degrees C cyclohexanol and cyclohexanone, obtained in the TS-1 catalyzed oxidation of cyclohexane, are further oxidized in uncatalyze d and TS-1 catalyzed reactions, Cyclohexanol is very selectively oxidi zed to cyclohexanone inside the porous system of TS-1 and unselectivel y oxidized to several oxidation products on the external surface. This unselective oxidation can be suppressed by the addition of 2,6-di-ter t-butyl-4-methylphenol (BHT), which does not enter the molecular sieve pore system and which efficiently reduces uncatalyzed oxidation, Cycl ohexanone oxidation is mostly uncatalyzed, forming predominantly dicar boxylic acids, and is not influenced by BHT, The products of the TS-1 catalyzed cyclohexanone oxidation are partially retained in the porous system, thus explaining the deactivation of the catalyst. Comparison with other systems shows that the turnover frequency of the TS-1 catal yzed cyclohexane oxidation is very similar to that of the radical-chai n process, thus suggesting that the rate-determining step of the TS-1 catalyzed reaction is also the homolytic cleavage of a C-H bond. (C) 1 995 Academic Press, Inc.