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T ( ° C)
650
K 5 La(MoO 4 ) 4
K 5 Sm(MoO 4 ) 4
K 5 Sm(MoO 4 ) 4
KSm(MoO 4 ) 2
Sm 2 MoO 6
Sm 2 MoO 4
600
KSm(MoO 4 ) 2
Sm 2 MoO 6
KLa(MoO 4 ) 2
550
La(OH) 3
SmMoO 4 OH
500
LaMoO 4 OH
K 5 Gd(MoO 4 ) 4
Gd 2 MoO 6
K 5 Gd(MoO 4 ) 4
K 5 Ho(MoO 4 ) 4
600
KGd(MoO 4 ) 2
Ho 2 MoO 6
Ho 2 MoO 6 KHo(MoO 4 ) 2
Gd 2 MoO 6
550
K 5 Gd(MoO 4 ) 4
KGd(MoO 4 ) 2
Gd 2 MoO 4
KHo(MoO 4 ) 2
500
HoMoO 4 OH
GdMoO 4 OH
1:1
1:2
1:3
1:4
1:1
1:2
1:3
1:4
N(Ln 2 O 3 /MoO 3 )
N(Ln 2 O 3 /MoO 3 )
Figure 8.17 TN-diagram of crystallization in the system R 2 O 3 a K 2 MoO 4 a H 2 O.
for “dry” conditions. Figure 8.18 shows the photograph of an assembly of
γ
-Bi 2 MoO 6
single crystals obtained in NH 4 Fsolution.
Several oxymolybdates of 1:3 ratio have been obtained and the prominent ones
are Fe 2 (MoO 4 ) 3 ,In 2 (MoO 4 ) 3 , and Fe 2 (MoO 4 ) 3 obtained in 5
10 wt% LiCl solu-
500 C and P
tions at T
1000 atm.
Among the mixed rare earth molybdates, the prominent ones are M 1 R(MoO 4 ) 2
(M 1 5
5
400
5
400
61] . These double molybdates are
known for every series of rare earth elements (Ln
Li, Na, K); R
5
rare earth elements [59
Lu, Y). They are prepared
by crystallization from solution, in the melt, solid-phase synthesis, and by the
hydrothermal method. The entire series of compounds are isostructural
5
La
to the
600 C,
tetragonal scheelite, CaWO 4 . The experimental conditions are T 5
525
P 5
50 wt% of K 2 MoO 4 were used as
solvents and KOH was added to obtain the desired pH of the growth media. The
other molybdates are
1000
1500 atm. Aqueous solutions of 5
-KBi(MoO 4 ) 2 , KY(MoO 4 ) 2 ,K 5 R(MoO 4 ) 4 ,K 2 Pb(MoO 4 ) 2 ,
K 2 (K 0.5 R 0.5 )(MoO 4 ) 2 , LiLa(MoO 4 ) 2 , and so on [62] . The experimental conditions,
α
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