The polymorphic phase transition III-IV in ammonium nitrate is well kn
own to be catalysed by water. Owing to this predominant role of water,
it has been suggested in the literature that this transition proceeds
via dissolution and crystallization occurring at a disordered phase b
oundary or even in a ''bulk'' layer of solution. A systematic study on
the similarity between projections of specific (hkl)III and (hkl)IV f
aces predicts various orientation relationships between both phases. S
everal of these (hkl) faces and orientation relationships are confirme
d by microscopic observations of the III --> IV and IV --> III transit
ions, by texture goniometry results, as well as by microscopic observa
tions reported in literature. The combined experimental and theoretica
l results substaintiate the existence of a solid-solid transition mech
anism especially for single crystal. The transition is supposed to be
continuously catalysed from the surface of the crystals by solvent mol
ecules. The presence of a solution layer at the transition front would
be unlikely in view of the proposed solid-solid mechanism which impli
es a greater restriction than just a set of parallel faces, namely the
requirement of matching of faces.