scholarly journals Single Crystals of Cubic Rare-Earth Pyrochlore Germanates: RE2Ge2O7 (RE = Yb and Lu) Grown by a High-Temperature Hydrothermal Technique

2018 ◽  
Vol 57 (20) ◽  
pp. 12456-12460 ◽  
Author(s):  
Liurukara D. Sanjeewa ◽  
Kate A. Ross ◽  
Colin L. Sarkis ◽  
Harikrishnan S. Nair ◽  
Colin D. McMillen ◽  
...  
1994 ◽  
Vol 49 (9) ◽  
pp. 1277-1281 ◽  
Author(s):  
Ch. Rabbow ◽  
Hk. Müller-Buschbaum

High temperature reactions of BaCO3/MnO/Er2O3 (3:1:1) led to single crystals of Ba3ErMn2O9. The product shows the structure of the hexagonal precious metal oxides Ba3LnRu2O9, but crystallizes with orthorhombic symmetry, space group C122v-Cmc21, a = 5.823 Å, b - 10.099 Å, c = 14.409 Å; Z = 4. The crystal structure is characterized by ErO6 octahedra, Mn2O9 face shared double octahedra and Ba2+ within cuboctahedral and anticuboctahedral coordination by O2-, respectively. In contrast to precious metal oxides the Mn-Mn distances inside the Mn2O9 double octahedra are elongated


2009 ◽  
Vol 176 ◽  
pp. 012010 ◽  
Author(s):  
Nikolay Leonyuk ◽  
Victor Maltsev ◽  
Elena Volkova ◽  
Elizaveta Koporulina ◽  
Larisa Nekrasova ◽  
...  

1977 ◽  
Vol 32 (5) ◽  
pp. 495-498 ◽  
Author(s):  
W. Muschick ◽  
Hk. Müller-Buschbaum

Single crystals of 1—x Ho2O3 : xCaO (x = 0.07), CaHoO2.5 (A) and Ca0.5Ho1.5O2.75 (B) were prepared by high temperature reaction and investigated with X-ray single crystal data. It can be shown that small amounts of CaO stabilize the monoclinic B-Typ of rare earth oxides. Phase (A) and (B) cannot be seen as a stabilized B-type crystal because they have an new crystal structure with space groupC22h–P 21/m, a = 656.6, b = 356.7, c = 529.4 pm, β = 92.3°; a = 650.2, b = 352.4, c = 584.5, β = 92.3°.


2020 ◽  
Vol 49 (14) ◽  
pp. 4323-4335
Author(s):  
Tiffany M. Smith Pellizzeri ◽  
Liurukara D. Sanjeewa ◽  
Steven Pellizzeri ◽  
Colin D. McMillen ◽  
V. Ovidiu Garlea ◽  
...  

Two new alkali vanadate carbonates with divalent transition metals have been synthesized as large single crystals via a high-temperature (600 °C) hydrothermal technique.


2006 ◽  
Vol 988 ◽  
Author(s):  
Samuel J. Mugavero III ◽  
William R Gemmill ◽  
Hans-Conrad zur Loye

AbstractThe growth of new phases out of high temperature hydroxide solutions as a means of discovering new materials is discussed. We have succeeded in solubilizing rare earth cations and platinum group metal cations in molten hydroxides and have grown single crystals with a large number of new compositions and new structure types. The use of sealed silver tubes has enabled us to control the water content and, hence, the acidity of the hydroxide melts, and thereby to grow crystals via slow cooling. The synthetic conditions and structures of several new oxides including Ln1-xNa1+xIrO4 (Ln = Gd-Er, Y; x = 0.04-0.26), Ln3RuO7 (Ln = La, Sm, Eu), LnNaPd6O8 (Ln = Tb-Lu, Y) and La9RbIr4O24 are presented.


Author(s):  
A. Garg ◽  
R. D. Noebe ◽  
R. Darolia

Small additions of Hf to NiAl produce a significant increase in the high-temperature strength of single crystals. Hf has a very limited solubility in NiAl and in the presence of Si, results in a high density of G-phase (Ni16Hf6Si7) cuboidal precipitates and some G-platelets in a NiAl matrix. These precipitates have a F.C.C structure and nucleate on {100}NiAl planes with almost perfect coherency and a cube-on-cube orientation-relationship (O.R.). However, G-phase is metastable and after prolonged aging at high temperature dissolves at the expense of a more stable Heusler (β'-Ni2AlHf) phase. In addition to these two phases, a third phase was shown to be present in a NiAl-0.3at. % Hf alloy, but was not previously identified (Fig. 4 of ref. 2 ). In this work, we report the morphology, crystal-structure, O.R., and stability of this unknown phase, which were determined using conventional and analytical transmission electron microscopy (TEM).Single crystals of NiAl containing 0.5at. % Hf were grown by a Bridgman technique. Chemical analysis indicated that these crystals also contained Si, which was not an intentional alloying addition but was picked up from the shell mold during directional solidification.


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