The deposition of Mo on γ-alumina by the equilibrium adsorption
method starting from ammonium
heptamolybdate has been studied. Spectroscopic results converge to
indicate that a previously unrecognized species,
i.e., the Anderson-type heteropolymolybdate
[Al(OH)6Mo6O18]3-,
plays a major role in this type of synthesis as it
is quantitatively formed in the solution within a few hours, by
reaction of the heptamolybdate with dissolved aluminic
species. This results in a considerable increase of alumina
solubility in conditions generally thought to be
nonaggressive. Furthermore, this species is also present in the
solid catalyst after deposition, although it is harder
to observe than in the liquid phase. A parallel is drawn with a
well-known idea from the field of geochemistry, i.e.,
ligand-promoted oxide dissolution. The relevance of this
phenomenon in catalyst preparation is evaluated in
realistic
conditions corresponding to published studies and/or industrial
procedures. It is concluded that strong metal−support interaction in the deposition stage by surface dissolution
followed by reaction in the liquid phase is most
likely to be an important phenomenon, not only for cationic metal
precursors as previously known but also for
anionic precursors such as molybdates.