New precursors to vanadium phosphorus oxide catalysts have been synthe
sized based on alteration of the layered structure found in the active
VPO catalysts. n-Alkyl amine intercalation compounds of vanadyl hydro
en phosphate hemihydrate have been prepared that are transformed into
active vanadyl pyrophosphate catalysts. Catalytic performance for sel
ective oxidation of n-butane to maleic anhydride improves with length
of alkyl chain. Vanadyl phosphonates and vanadyl phosphite have been p
repared containing vanadyl dimer structures that are thermally transfo
rmed into vanadyl pyrophosphate below 650 K for the phosphonates and 5
50 K for the phosphite. The VPO catalyst from the vanadyl phosphite pr
ecursor had a high surface area of 35 m(2)/g, and displayed better sel
ectivity for maleic anhydride from n-butane oxidation than the convent
ional unpromoted catalyst. Mixed vanadyl phosphite-phosphate materials
, which were found to be very reactive for intercalation of amines, we
re intercalated with 3-aminopropyltriethoxysilane and calcined to prod
uce the first thermally stable pillared VPO catalyst.