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(a)
(b)
(c)
A
RbNd P 4 O 12
RbNd (PO 3 ) -II
A
A
5
10
KND P 4 O 12
2
4
3
2
1
8
6
4
2
0
RbNd(PO 3 ) -I
CsNd(PO 3 ) 4
K ND (PO 3 ) 4
Nd P 5 O 14
1
Nd P 5 O 14
Nd P 5 O 14
Nd (PO 3 ) 3
Nd (PO 3 ) 3
Nd (PO 3 ) 3
B
B
B
0
2.6
3.2
3.8
3
4
5
6
1
2
P 2 O 5 /Cs 2 O + Nd 2 O 3
P 2 O 5 /K 2 O + Nd 2 O 3
P 2 O 5 /Rb 2 O + Nd 2 O 3
Figure 7.56 AB diagram of crystallization in (a) Cs 2 O a Nd 2 O 3 a P 2 O 5 a H 2 O, (b)
K 2 O a Nd 2 O 3 a P 2 O 5 a H 2 O, and (c) Rb 2 O a Nd 2 O 3 a P 2 O 5 a H 2 O systems [253] .
Figure 7.57 Phase
transformation with reference
to the changes in PT
conditions [254] .
700
500
300
0.5
1
2
P H 2 O (atm)
3
4
5
Figure 7.58 Phase
transformation with reference
to the changes in PT conditions
[254] .
700
500
NdPO 4
NdP 5 O 14
NdP 3 O 9
0.5
1
2
3
4
5
P H 2 O (atm)
MNdP 4 O 12 !
NdP 3 O 9 !
NdPO 4
ð
7
:
16
Þ
NdP 5 O 14 !
NdP 3 O 9 !
NdPO 4
Using these results, Byrappa et al. [253] reported on the hydrothermal growth of
TmP 5 O 14 crystals under mild hydrothermal conditions. The crystal size was much
higher and crystals were well faceted than the crystals obtained by Yoshimura
et al. [251] . The important aspect of this work is the growth of ultraphosphates
under mild hydrothermal conditions (T
240 C, P
100 bar). The autoclaves
used were simple Morey type provided with Teflon liners. The crystallization was
carried out through spontaneous nucleation.
5
5,
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