Alumina-supported nickel catalysts are widely used in industry. The synthes
is of these catalysts often proceeds through coprecipitation: following the
precipitation of nickel salts and drying, the material is calcined, reduce
d, and passivated. Each of these steps may influence the catalyst ultimatel
y obtained. In the present study, the synthesis conditions were systematica
lly investigated. Following precipitation, a hydrotalcite is formed. Starti
ng from hydrotalcite precursors with varying Ni/Al ratios, the conversion t
o the ultimate Ni-on-alumina catalyst was studied, using TEM, TPR, XRD, and
chemisorption. In particular, we examined the effect of water vapour and a
cidic gases-liberated during calcination-on the morphology of the catalyst
ultimately obtained. Two competing mechanisms for the formation of the ulti
mate catalyst morphology are suggested. (C) 2001 Academic Press.