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Fig. 3.17 Mössbauer spectrum of a Fougèrite sample at 78 K (a) compared with the spectrum of
a synthetic oxidized green rust sample with the same Fe 3+ molar fraction x (b) Mössbauer
spectrum of a green rust related sample from Trébeurden (c) and the spectrum of a similar sample
from the Mont Saint Michel (d) (adapted from Ref. [ 307 ])
the bay of Mont Saint Michel (Normandy, France) [ 138 ] as can be seen from the
example shown in Fig. 3.17 d.
Structural studies on synthetic samples [ 133 ] suggest that long ranger order
appears for x = 1/3, x = 2/3 and x = 1 which is confirmed by magnetic mea-
surements showing a ferrimagnetic behavior for x = 1/3, x = 2/3 with Néel
temperatures of 5 and 20 K respectively and being ferromagnetic for x = 1 with a
Curie temperature around 80 K [ 139 ]. From these findings together with the
appearance of typical doublets in the Mössbauer spectra Génin et al. [ 138 ] suggest
that the intermediate samples consist in fact of topotaxically mixed domains of the
ordered definite compounds. Therefore the natural green rust related minerals must
be considered as a mixture of three basic minerals:
Fe 2 þ
4
Fe 3 2
O ð 12 CO 3 : 3H 2 O
ð
x ¼ 1 = 3
Þ ;
Fe 2 2 Fe 3 4
O ð 10 O 2 CO3 : 3H 2 O
ð
x ¼ 2 = 3
Þ and
Fe 3 þ
6
O ð 8 O 4 CO 3 : 3H 2 O
ð
x ¼ 1
Þ:
They suggest to redefine the first one as fougérite, whereas in the case of x = 2/3
and x = 1, the new mineral names ''trébeurdenite'' and ''mössbauerite'' are
respectively proposed [ 138 ].
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