X-ray diffraction based on the comparison of experimental and calculat
ed powder profiles enabled the determination of the structural charact
eristics of hydrated and dehydrated Tunisian nacrite. Using the concep
t describing the structure of natural nacrite, the stacking mode of th
e layers in the hydrated and dehydrated nacrite has been determined. T
he hydrate is characterized by an 8.42 Angstrom basal distance; one wa
ter molecule per Si2Al2O5(OH)(4) is intercalated in the interlamellar
space, located above the vacant octahedral site of the layer at z = 6.
5 Angstrom and inserted inside the ditrigonal cavity of the tetrahedra
l sheet of the upper layer. The dehydrated nacrite obtained by heating
of the hydrate at 423 K has the same interlayer shift t = -0.35a as t
he natural nacrite. Coherence domain sizes along c and in the nb plan
e are the same as those in the hydrate but different from those of the
natural mineral. After dehydration, 5% of the layers had an interlaye
r shift similar to that obtained from the hydrate.