The preparation of vanadium phosphorus oxide catalysts for the oxidati
on on n butane to maleic anhydride is discussed. In particular the pre
paration route based on the reduction of VOPO4 . 2H(2)O with alcohols
is described in detail and contrasted with two other preparation metho
ds: (i) using aqueous HCl as a reductant for V2O5 and (ii) using isobu
tanol as reductant and solvent for V2O5. The catalytic performance of
final catalysts prepared by in situ transformation under the reaction
conditions is contrasted. It is found that catalysts derived from the
reduction of VOPO4 . 2H(2)O with 1-alcohols tend to give high activity
catalysts by virtue of the high surface area material (typically 40 m
(2) g(-1)) generated by this synthetic method. The preparation of VO(H
2PO4)(2) by two routes is also described and it is shown that when thi
s material is used as a catalyst precursor, final catalysts are ultra-
selective for formation of maleic anhydride, together with furan. The
characterisation of all these catalysts using various electron microsc
opy techniques is described and the morphology of the active catalysts
is discussed.