A. Hulsmans et al., The transformation of andalusite to mullite and silica: Part II. Transformation mechanisms in [100](A) and [010](A) directions, AM MINERAL, 85(7-8), 2000, pp. 987-992
The transformation of an andalusite (Al2O3. SiO2 = A) single-crystal to 3:2
-mullite (3Al(2)O(3). 2SiO(2) = M) and non-crystalline silica (SiO2) was in
vestigated at the (100)(A) and (010)(A) faces using electron microscopy. Th
e transformation starts topotactically at the surfaces producing a dense la
yer of mullite and vitreous silica on the surface and underneath the mullit
e layer. Next, the reaction proceeds by dissolution of andalusite in the vi
treous silica and by diffusional transport of alumina to mullite crystals o
ccasionally nucleated at the dissolving andalusite. Transformation along [1
00](A) proceeds twice as fast as along [010](A). which is explained by the
higher stability of the (010)(A) face against dissolution. Transformation b
y dissolution and precipitation is one order of magnitude slower than the t
opotactic transformation along [001](A). The transformation reaction of and
alusite to mullite and silica is highly anisotropic. Combining the results
along the directions [100](A), [010](A), and [001](A) predicts the type of
transformation which will take place at an arbitrary andalusite face. Only
if the c(A) axis is oriented more than 80 degrees off the surface normal, w
ill the reaction proceed by the dissolution-precipitation process, whereas
for all other orientations andalusite transforms by the fast topotactic rea
ction along the c(A) axis.