L. Alejo et al., PARTIAL OXIDATION OF METHANOL TO PRODUCE HYDROGEN OVER CU-ZN-BASED CATALYSTS, Applied catalysis. A, General, 162(1-2), 1997, pp. 281-297
In this work Cu/ZnO and Cu/ZnO/Al2O3 catalysts have been studied for t
he partial oxidation of methanol with oxygen to produce hydrogen. Thes
e Cu-Zn based catalysts showed high activity for the partial oxidation
of methanol and it was found that the catalytic activity is directly
related to the copper metal surface area. In the series Cu-Zn with cop
per relative content of 20-70 wt%, the catalyst Cu40Zn60 (Cu 40 wt% an
d Zn 60 wt%) which showed the highest copper area gave the best result
s for the partial oxidation of methanol. The activation energies and T
OF (turnover frequencies) varied with the Cu-Zn catalyst composition.
For catalysts with low copper loading very high E-a and TOF were obtai
ned (for Cu30Zn70Ea = 482 kJ/mol and TOF ca. 200 min(-1) at 497-499 K)
whereas for higher copper contents the E-a and TOF decreased tending
to constant values (for Cu70Zn30Ea = 71 kJ/mol and TOF = 160 min(-1) a
t 497-499 K). These results are discussed in terms of a possible effec
t of the Cu-ZnO interaction which depends on the catalyst composition.
Catalytic experiments with Cu40Zn55Al5 (Cu 40 wt%, Zn 55 wt% and Al 5
wt%) showed that the presence of aluminium has an inhibiting effect p
roducing slightly lower methanol conversion. On the other hand, higher
selectivities for H-2 and CO2 were obtained with only traces of the u
ndesirable carbon monoxide. Moreover, the Al is very important for cat
alyst stability and life-time experiments showed that Cu40Zn55Al5 is s
table during the partial oxidation of methanol with no significant cha
nge in activity and selectivity even after 110 h operation at 503 K. T
he catalyst Cu40Zn60 with no Al, deactivates rapidly after 20 h reacti
on at 503 K. Experiments using N2O as oxidant showed higher activity t
o convert methanol but producing large amounts of H2O and CO. The impr
egnation of catalyst with Na produced similar effect increasing the se
lectivity for H2O and CO. The results presented seem to indicate that
the copper metal is active for partial oxidation of methanol to H-2 an
d CO2 whereas Cu+1 favour the formation of H2O and CO. CU+2 as CuO sho
ws very low activity for methanol conversion producing only CO2 and H2
O. (C) 1997 Elsevier Science B.V.