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Mechanism of methano
Applied Catalysis, 30 (198’7) 333-338
Elsevier Science Publishers B.V., Amsterdam - Printed in The Netherlands
333
MECHANISM OF METHANOL SYNTHESIS FROM CO,/CO/H2 MIXTURES OVER COPPER/ZINC OXIDE/
ALUMINA CATALYSTS: USE OF 14C-LABELLED REACTANTS
G.C. CHINCHEN, P.J. DENNY, D.G. PARKERa, M.S. SPENCER*and D.A. NHAN
Imperial Chemical Industries, plc, Agricultural Division, Billingham, Cleveland
TS23 ILB, England.
aImperial Chemical Industries, plc, Advanced Materials Business Group, Hilton,
Cleveland, England.
(Received 1 September 1986, accepted 20 December 1986)
ABSTRACT
The addition of
14
CO or14C02 tracers to C02/CO/H2 reactant mixtures for methanol
svnthesis over a commercial coooer/zinc oxide/alumina catalvst was used to deter-
mine the origin of the carbon in the product.. For pCD2/pCO ratios from 0.02 to
1 the fraction of methanol made from carbon dioxide rises from %0.7 to $1, so
carbon dioxide is the major reactant under industrial conditions. There is no
carbon-containing surface intermediate common to methanol synthesis and the water-
gas shift reaction.
INTRODUCTION
In much of the discussion [I,21 on the mechanism of methanol synthesis over
copper/zinc oxide catalysts it has been tacitly assumed that carbon monoxide is
the main source of carbon for the product methanol. However, earlier Russian work
[3], some with C tracers, indicated that methanol was made from carbon dioxide
only and recent studies [4-71 also indicate that carbon dioxide is the primary
reactant. As methanol can be made from CO/H2 and C02/H2 mixtures [8,9], isotope-
labelling studies under industrially-relevant conditions are the best method
for determining the source of methanol in the reaction of C02/CO/H2 mixtures.
In this paper both labelled CO and CO2 were used over a range of feed compositions
in a flow system with an industrial copper/zinc oxide/alumina catalyst.
EXPERIMENTAL
The industrial methanol synthesis catalyst, made by co-precipitation [IO] and
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