Hexagonal mesoporous. silica (HMS), AI-HMS, MCM-41, as well as ZrO2 modifie
d HMS supported cobalt and small amount of MnO promoted cobalt catalysts ar
e investigated by using X-ray diffraction, N-2 adsorption, transmission ele
ctron microscopy, and temperature programmed reduction techniques, and by t
esting their catalytic properties in Fischer-Tropsch synthesis. Cobalt oxid
es are dispersed highly on the surface of these mesoporous supports. Howeve
r, their BET surface area, pore volume, and pore size decrease, and pore wa
ll thickness increases a little. The main hydrocarbon products obtained ove
r these catalysts are the long chain hydrocarbons (wax). Comparing with MCM
-41 and Al-HMS, the HMS supported Co catalyst shows better catalytic activi
ty and C-5(+) selectivity, which is due to its smaller domain size with sho
rter channels and larger textural mesoporosity. With increasing Co loading
on the HMS support, the reduction temperature of cobalt oxides increases a
little, but the activity apparently increases, which is caused by more acti
ve sites in the channels of HMS. When AI-HMS is used as a support, the inte
raction between Co species and AI-HMS support caused by the acid properties
on the surface of Al-HMS, leads to a decrease of available Co metal sites
and a decrease of activity and C-5(+) selectivity. The pre-impregnated ZrO2
on the surface of HMS support favors the reduction of cobalt oxides and in
creases the activity and C-5(+) selectivity. The addition of small amount o
f Mn (less than or equal to2 wt.%) to Co/HMS catalyst, high yield of wax (3
6.2%) is obtained, which might be ascribed to that MnO segregates partially
the active Co sites and prevents the formation of methane at high reaction
temperature. (C) 2001 Elsevier Science B.V. All rights reserved.