Subsolidus phase relations and structures of solid solutions in the systems K2MoO4–Na2MoO4–MMoO4 (M = Mn, Zn)

2019 ◽  
Vol 272 ◽  
pp. 148-156 ◽  
Author(s):  
Oksana A. Gulyaeva ◽  
Zoya A. Solodovnikova ◽  
Sergey F. Solodovnikov ◽  
Vasiliy N. Yudin ◽  
Evgeniya S. Zolotova ◽  
...  
1965 ◽  
Vol 2 (6) ◽  
pp. 596-621 ◽  
Author(s):  
A. D. Edgar

The extent of melilite solid solutions has been determined for the systems gehlenite–soda melilite, akermanite–soda melilite, and gehlenite–akermanite–soda melilite at 800 °C and 1 000 kg/cm2[Formula: see text] Approximately 50 weight % NaCaAlSi2O7 will form melilite solid solutions with both gehlenite and akermanite but the extent of complete solid solutions in the gehlenite–akermanite–soda melilite system is very limited at this temperature. Lattice parameter determinations of melilite solid solutions indicate that there is a small but significant change in both a and c parameters with increasing soda melilite in the gehlenite–soda melilite system. In the gehlenite–akermanite–soda melilite system, although the range of complete solid solution is very limited, melilites form more than 90% of the products in most compositions and their lattice parameters can be correlated approximately with their bulk compositions, A rapid X-ray method has been developed to determine the approximate compositions of melilites in this system. Comparison is made between the synthetic samples and natural melilites.A reconnaissance of subsolidus phase relations indicates that phase relations are very complex and that only over a very small compositional range can these systems be considered binary or ternary. These studies also indicate that the relations reported by Nurse and Midgley in 1953 should probably be modified. Although the composition NaCaAlSi2O7 does not synthesize only a melilite under the conditions used in this study, it is believed that this is the correct composition of the sodium-bearing end-member.


Author(s):  
Luke L. Y. Chang

SummarySubsolidus phase relations in the systems ZnWO4-MnWO4, ZnWO4-ZnMoO4, MnMoO4-ZnMoO4, and MnWO4-MnMoO4, were investigated by using the quenching technique. A complete series of solid solutions forms in the system ZnWO4-MnWO4 above 840° C, whereas limited solid solubilities were found in the other three. The various limits of solubility are, at 620° C, 4·0 mole % ZnMoO4 in ZnWO4 and 4·0 mole % ZnWO4 in ZnMoO4, 13·0 mole % ZnMoO4 in MnMoO4 and 12·0 mole % MnMoO4 in ZnMoO4, 9·0 mole % MnMoO4 in MnWO4 and 6·0 mole % in MnWO4 in MnMoO4; and at 1000° C, 15·0 mole % ZnMoO4 in ZnWO4 and 15·0 mole % ZnWO4 in ZnMoO4, 36·0 mole % ZnMoO4 in MnMoO4 and 29·0 mole % MnMoO4 in ZnMoO4, 15·0 mole % MnMoO4 in MnWO4 and 27·0 mole % MnWO4 in MnMoO4.Subsolidus phase relations in the system ZnWO4-ZnMoO4-MnWO4-MnMoO4 were studied at 900° C. The solubility of molybdenum in the (Zn,Mn)WO4 series increases from both end members to a maximum of 27·0 mole % at the composition Mn35Zn65. Both molybdates also have limited ranges of solid solutions, and a three-phase region occupies the central portion of the system defined by three points with compositions of 41 mole % ZnMoO4, 26 mole % MnMoO4, 33 mole % MnWO4; 57 mole % ZnMoO4, 10 mole % MnMoO4, 35 mole % MnWO4; and 27 mole % ZnMoO4, 34 mole % MnWO4, 39 mole % ZnWO4.


2010 ◽  
Vol 46 (9) ◽  
pp. 1019-1024 ◽  
Author(s):  
G. D. Nipan ◽  
V. A. Ketsko ◽  
T. N. Kol’tsova ◽  
M. A. Kop’eva ◽  
A. I. Stognii ◽  
...  

1966 ◽  
Vol 3 (2) ◽  
pp. 211-222 ◽  
Author(s):  
S. Somanchi

Phase relations were determined in the Ag–Sb system through the temperature range 500° to 300 °C to permit a better understanding of the origin of certain silver ores and to provide a base for the study of more complex sulfosalt systems. The Sb-rich solvus for the ε phase (Ag6 ± xSb) at 500°, 450°, 350°, and 300 °C occurs at 18.2, 17.75, 17.75, and 17.7 weight percent Sb, respectively. The Ag-rich solvus of the ε′ phase (dyscrasite) occurs at 22.5% Sb at 500 °C and 22.9% at 450°, 400°, 350°, and 300 °C. The Sb-rich solvus of this phase occurs at 27.2% Sb at 500°, 450°, 400°, and 350 °C. Therefore the atomic silver to antimony ratio ranges from nearly 4 to 3, and the formula may be written Ag7 ± xSb2. An order–disorder transition of ε′ to a third phase, ε″, reported to occur at about 440° to 449 °C, was not observed. The compositions of the solid solutions relate to high angle X-ray powder reflections through the following functions: for ε phase, d = 0.000150x + 0.79743, and for ε′ phase, d = 0.00160x + 0.76608, where d is the specific interplanar spacing in Ångstroms and x is the weight percent antimony.


1997 ◽  
Vol 252 (1-2) ◽  
pp. 143-147 ◽  
Author(s):  
Y Jinling ◽  
L Jingkui ◽  
T Weihua ◽  
S Ying ◽  
C Xiaolong ◽  
...  

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