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Si 2 Al 2 O 5 ( OH ) 4 [ kaolinite ] + 5 H 2 O ¤ 2 Al ( OH ) 3 [ gibbsite ] + 2 Si ( OH ) 4
[ orthosilicic acid ] with log K = 2log [ Si ( OH ) 4 ] .
The equilibrium only involves the silica content. Specialists early
knew this kind of transformation occurs in Ferralsols in tropical
environment (Sieffermann et al . 1968).
￿ The direct transformation of anorthite to gibbsite is described
by:
CaAl 2 Si 2 O 8 [ anorthite ] + 6 H 2 O + 2 H + ¤ 2 Al ( OH ) 3 [ gibbsite ] +
2 H 4 SiO 4 [ orthosilicic acid ] + Ca ++
giving log K = log [ Ca ++ ] - 2log [ H + ] + 2log [ H 4 SiO 4 ]
or again log K = log [ Ca ++ ]/[ H + ] 2 + 2log [ H 4 SiO 4 ]
In the latter type of equation, the Ca ++ / H + ratio and the silica content
are simultaneously involved.
When all calculations have been done, Figure 3.10 is obtained.
log [
Ca ++
[]
]
H +2
20
Anorthite
Ca-Montmorillonite
15
Gibbsite
Kaolinite
Waters
of
dry zones
10
Waters of
the temperate
zone
Waters
of hot
countries
5
ppm of SiO 2
1
10
100
-5
- 4
-3
log [H SiO ]
4
4
Fig. 3.10
Diagram of the montmorillonite-kaolinite-gibbsite equilibrium (Tardy 1969).
Actually, considering what has been said above, the equilibrium
boundary between anorthite and kaolinite in a diagram with silica
on the abscissa and Ca ++ /H + on the ordinate, is a horizontal line. The
gibbsite/kaolinite boundary is a vertical line. The anorthite/gibbsite
boundary is oblique.
 
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