The gas-phase oxidative dehydrogenation of cyclohexanol with air using ETS-
10 and related materials is studied. At reaction temperatures below 200 deg
reesC, ETS-10 was 100% selective to cyclohexanone and 75% cyclohexanol conv
ersion was achieved. Catalyst deactivation was attributed to pore blockage.
The catalyst is completely regenerated by calcination at 400 degreesC. Cyc
lohexanol conversion increases with temperature and oxygen/cyclohexanol fee
d ratios. The introduction of Cr, Fe, K, or Cs in ETS-10 affects stability
and decreases conversion and selectivity towards cyclohexanone. For compari
son, some results on TS-1, zeolites NaX, and mordenite are also presented.
(C) 2001 Academic Press.