P. Ruterana et al., MICROSTRUCTURE AND EVOLUTION OF A MAGNESIUM LITHIUM ALUMINOSILICATE MATRIX COMPOSITE, Journal of Microscopy, 177, 1995, pp. 272-278
The microstructure of a magnesium lithium aluminosilicate glass cerami
c composite has been investigated by scanning electron microscopy and
analytical transmission electron microscopy. Attention was focused on
the as-received material, showing that there is a non-uniform distribu
tion of the major silicate phases inside the matrix. The largest part
is made of spodumene-type crystals containing more than 4wt% Mg. A min
or part of the matrix is made of micrometre-sized crystallites of spod
umene and cordierite. The spodumene is always sensitive to the electro
n beam irradiation. The morphology of the amorphized spodumene areas i
ndicates that it may have crystallized during a later stage of the mat
rix formation, filling the gaps between cordierite crystallites. The t
hird component of the matrix is made of carbon-rich areas. They can be
as large as 10 mu m and they always include amorphous Mg-rich silicat
es. However, they are mainly small (a few tens of nanometres in width)
when located at grain boundaries of spodumene crystals. In this case
the turbostratic carbon patches are also intimately mixed with an Mg-r
ich amorphous silicate. The interface between the matrix and the fibre
s has also been analysed, its thickness changes from one to the other,
and it is sometimes empty due to decohesion. When it is filled, its o
uter part contains mainly tubostratic carbon and the inner part is a m
ixture of silicon oxide and probably carbon. After creep at 1373 K, th
e spodumene-type crystals are larger and they are no longer sensitive
to the electron beam. The cordierite areas appear to shrink and the am
orphous patches which were mixed with carbon transform into small crys
tallites (1-10 mu m). The areas next to the fibres are found to extend
irregularly into the matrix, probably as a result of a chemical reduc
tion.