A progressive sintering of the porosity of both V-free and V-loaded AlPO4-5
samples is observed upon calcination in air at increasing temperatures. Th
is sintering leads to the coexistence of porous AlPO4-5 and dense tridymite
. As established by cristallinity and pore volume measurements, the presenc
e of vanadium decreases by 100 to 300 degrees C the threshold temperature a
t which this sintering begins, in spite of the low V amount in the samples
(V/(V+Al+P) atomic ratio of 0.5-1%). This threshold temperature depends on
the method used to introduce V (by hydrothermal synthesis, under static con
ditions or agitation, and/or by grinding vanadia with a V-free AlPO4-5) and
on the morphology of the AlPO4-5 crystals as observed by scanning electron
microscopy. These factors are related to the dispersion of the V species w
ithin the porosity. Since only very small amounts of intraporosity V-IV spe
cies (V-IV/V-T < 1%) are detected by ESR, whatever the extent of the sinter
ing which generates tridymite, it is concluded that the thermal stability o
f V-loaded AlPO4-5 is determined by the dispersion of V-V species within th
e porosity. This conclusion is in line with earlier propositions made to ex
plain the thermal behaviour of V-loaded zeolites and V-contamined FCC catal
ysts.