Subsolidus phase relations of the Dy-Fe-Al system

2011 ◽  
Vol 26 (1) ◽  
pp. 9-15
Author(s):  
Y. Q. Chen ◽  
J. K. Liang ◽  
J. Luo ◽  
J. B. Li ◽  
G. H. Rao

The subsolidus phase relations of the Dy-Fe-Al system have been investigated by means of X-ray powder diffraction. There are 5 ternary compounds, 10 binary compounds, and 21 three-phase regions in this system. The solid-solution regions of Dy(Fe1−xAlx)2, DyFe3−xAlx, Dy2(Fe1−xAlx)17, and DyFe12−xAlx have been determined based on the dependence of their unit-cell parameters on the Al content.

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Myroslava Horiacha ◽  
Galyna Nychyporuk ◽  
Rainer Pöttgen ◽  
Vasyl Zaremba

Abstract Phase formation in the solid solution TbNiIn1−x Ga x at 873 K was investigated in the full concentration range by means of powder X-ray diffraction and EDX analysis. The samples were synthesized by arc-melting of the pure metals with subsequent annealing at 873 K for one month. The influence of the substitution of indium by gallium on the type of structure and solubility was studied. The solubility ranges have been determined and changes of the unit cell parameters were calculated on the basis of powder X-ray diffraction data: TbNiIn1–0.4Ga0–0.6 (ZrNiAl-type structure, space group P 6 ‾ 2 m $P‾{6}2m$ , a = 0.74461(8)–0.72711(17) and c = 0.37976(5)–0.37469(8) nm); TbNiIn0.2–0Ga0.8–1.0 (TiNiSi-type structure, space group Pnma, а = 0.68950(11)–0.68830(12), b = 0.43053(9)–0.42974(6), с = 0.74186(10)–0.73486(13) nm). The crystal structures of TbNiGa (TiNiSi type, Pnma, a = 0.69140(5), b = 0.43047(7), c = 0.73553(8) nm, wR2=0.0414, 525 F 2 values, 21 variables), TbNiIn0.83(1)Ga0.17(1) (ZrNiAl type, P 6 ‾ 2 m $P‾{6}2m$ , a = 0.74043(6), c = 0.37789(3) nm, wR2 = 0.0293, 322 F 2 values, 16 variables) and TbNiIn0.12(2)Ga0.88(2) (TiNiSi type, Pnma, a = 0.69124(6), b = 0.43134(9), c = 0.74232(11) nm, wR2 = 0.0495, 516 F 2 values, 21 variables) have been determined. The characteristics of the solid solutions and the variations of the unit cell parameters are briefly discussed.


2007 ◽  
Vol 130 ◽  
pp. 97-100 ◽  
Author(s):  
Małgorzata Karolus ◽  
Edward Rówiński ◽  
Eugeniusz Łągiewka

Electrolytical layers of Ni-Mo alloys with polypyrrole, polytiofene and polyethylene were deposited on steel substrate (St3S, 4 cm2). After structural analyses of as quenched samples performed by X-ray diffraction it was noticed that the solid solution of Mo in Ni is observed. After annealing in an argon atmosphere the solid solution of Mo in Ni is becomeing more stable and crystalites are growing to the size of 200 – 300 Å. After annealing in an air atmosphere X-ray diffraction patterns show presence of phases: NiO, MoO, NiCO3, Mo2N. The unit cell parameters of solid solution after annealing are smaller than parameters of as quenched samples what means that the solid solution has been decomposing.


1999 ◽  
Vol 14 (4) ◽  
pp. 274-275 ◽  
Author(s):  
X. L. Chen ◽  
W. Eysel

The subsolidus phase relations in the ternary system La2O3–Bi2O3–CuO at 900 °C were investigated by X-ray powder diffraction. A new binary compound, Bi2La4O9, was found, as well as a binary and a ternary solid solution series, Bi1−xLaxO1.5 (0.16≤x≤0.33) and La2−xBixCuO4 (0≤x≤0.11), respectively.


2013 ◽  
Vol 28 (4) ◽  
pp. 269-275
Author(s):  
Sytle M. Antao

Twenty-seven scapolite samples from various localities and with compositions between Me6–93 were obtained using electron microprobe analysis (EMPA). Their unit-cell parameters were obtained using synchrotron high-resolution powder X-ray diffraction (HRPXRD) data and Rietveld structure refinements using space group P42/n. The EMPA data show the well-known discontinuity at Me75. In addition, the unit-cell parameters, especially c, show a discontinuity at Me75 (=five Al atoms per formula unit, apfu), ideally NaCa3[Al5Si7O24](CO3), where the scapolite solid solution is divided into two (Me% = [Ca/(Ca + Na + K)] × 100). A maximum c parameter value occurs at Me37.5 (=four Al apfu ideally), where complete Al–Si, Na–Ca, and Cl–CO3 order occurs. The unit-cell volume, V, varies smoothly with Me% and Al apfu across the series.


1997 ◽  
Vol 12 (4) ◽  
pp. 259-263 ◽  
Author(s):  
J. M. Loezos ◽  
T. A. Vanderah ◽  
J. P. Cline

X-ray powder diffraction data and refined unit cell parameters for three compounds found during experimental determination of the BaO:Fe2O3:TiO2 phase diagram are reported here. All three phases crystallize in space group C2/m (No. 12). Ba2Fe2Ti4O13 (“2:1:4”) is isostructural with K2Ti6O13 and Ba2ZnTi5O13: a=15.1939(9), b=3.8912(3), c=9.1244(5) Å, β=98.456(5)°; Z=2, ρcalc=4.890 g/cc. Ba3Fe10TiO20 (“3:5:1”) is structurally analogous to its aluminum congener Ba3Al10TiO20: a=15.336(1), b=11.7986(9), c=5.1700(4) Å, β=91.220(6)° (I2/m setting); Z=2, ρcalc=4.750 g/cc. Ba4Fe2Ti10O27 (“4:1:10”) is also isostructural with its aluminum analog Ba4Al2Ti10O27: a=19.799(1), b=11.4324(6), c=9.8936(6) Å, β=109.146(4)° (C2/m); Z=4, ρcalc=4.934 g/cc. The 2:1:4 and 3:5:1 compounds adopt open-framework type structures while the 4:1:10 phase exhibits an eight-layer close-packed arrangement.


Author(s):  
Joanna Kulaszewska ◽  
Sandra Dann ◽  
Peter Warwick ◽  
Caroline Kirk

Mineral phases which can be thought of as members of a metatorbernite–metazeunerite solid solution (Cu(UO 2 ) 2 (PO 4 ) 2− x (AsO 4 ) x .8H 2 O have been identified in radioactive samples from spoil heaps at the uranium mine site in South Terras, Cornwall (grid reference SW935523) . A complete solid solution (0 <  x  < 2) was synthesized by precipitation from solution using uranium (VI) nitrate and copper (II) chloride and phosphoric acid/arsenic acid in the appropriate molar proportions. Refined unit cell parameters determined by Pawley fitting of powder X-ray diffraction data showed a linear variation in the a unit cell parameter according to Vegard's Law, allowing the composition of the natural mineral phases found at South Terras to be determined from measurement of their unit cell parameters. High-resolution variable-temperature synchrotron powder X-ray diffraction studies were carried out at the Diamond Light Source on three members of this solid solution ( x  = 0, 1, 2) and showed different structural behaviour as a function of composition and temperature. Metatorbenite ( x  = 0) retains its tetragonal symmetry at low temperatures and dehydrates to an amorphous phase at 473 K, whereas metazeunrite ( x  = 2) transforms to an orthorhombic phase at low temperatures, regains its tetragonal symmetry on heating to 323 K and undergoes a further transition to an, as yet, unidentified phase at 473 K. This article is part of the theme issue ‘Fifty years of synchrotron science: achievements and opportunities’.


2004 ◽  
Vol 19 (4) ◽  
pp. 320-324 ◽  
Author(s):  
G. B. Song ◽  
J. K. Liang ◽  
F. S. Liu ◽  
L. T. Yang ◽  
J. Luo ◽  
...  

Pr1+xBa2−xCu3O7±δ solid solution was investigated by means of X-ray powder diffraction and Rietveld analysis. Single-phase PrBa2Cu3O7±δ (Pr123) can be synthesized under a Pr-rich condition by sintering at 950 °C in air. The solubility of Pr1+xBa2−xCu3O7±δ solid solution is 0.08≤x≤0.80. The structure of Pr1+xBa2−xCu3O7±δ is orthorhombic for 0.08≤x<0.30, and transforms into tetragonal for 0.30≤x≤0.80. To form single-phase Pr123, the Ba sites in the Pr123 structure are partially occupied by excess Pr ions, and the smallest amount of excess Pr is x=0.08. Meanwhile, all Ba ions stay in the Ba sites.


2011 ◽  
Vol 7 (3) ◽  
pp. 1399-1412
Author(s):  
I. Bechibani ◽  
H. Litaiem ◽  
S. Garcia Granda ◽  
M. Dammak ◽  
L. Ktari

The Tl2HAsO4.Te(OH)6 (TlAsTe) compound crystallizes in the triclinic system P1 with unit cell parameters: a= 7.100(10) Å, b= 7.281(13) Å, c= 8.383(11) Å, α= 76.91(1)°, β= 87.16(1)°, γ= 66.96(2)°, Z= 2 and V= 388.19(1) Å3. This new structure can be described as a lamellar one with the atomic arrangement being built by planes of Te(OH)6 octahedra alterning with planes of arsenate tetrahedra. Raman and infrared spectra recorded at room temperature confirm the presence of As  and Te  groups and characterize the hydrogen bonds present in the crystal lattice. Differential scanning calorimerty shows the presence of three-phase transitions at 396 K, 408 K and 430 K present in the title compound. Typical thermal analyses, such as differential thermal analysis and thermogravimetry show that the decomposition of this material starts at about T= 445 K. Magnetization curve of Tl2HAsO4·Te(OH)6 substance have revealed a diamagnetic response overall temperature range studied.


1996 ◽  
Vol 11 (1) ◽  
pp. 2-4
Author(s):  
Mohamed Ezahri ◽  
Georges Coffy ◽  
Bernard F. Mentzen

X-ray powder diffraction data are reported for the [(NH4)3Al1−xFex/2Crx/2(C2O4)3]·3H2O solid solution. The crystal system is triclinic with space group P1. Refined unit-cell parameters are given for the compositions x=0.10, 0.50 and 0.80.


2013 ◽  
Vol 11 (4) ◽  
pp. 604-609 ◽  
Author(s):  
Mariya Dzevenko ◽  
Andriy Hamyk ◽  
Yuriy Tyvanchuk ◽  
Yaroslav Kalychak

AbstractIsothermal section of the Er-Co-In system at T = 870 K was constructed by means of X-ray powder diffraction, microstructure, and EDX-analyses. Twelve ternary compounds, namely ErCoIn5 (HoCoGa5-type), Er6Co17.92In14 (Lu6Co17.92In14-type), ErCo4In (MgCu4Sn-type), Er2CoIn8 (Ho2CoGa8-type), Er10Co9In20 (Ho10Ni9In20-type), Er3Co1.87In4 (Lu3Co1.87In4-type), ErCoIn, Er11Co4In9 (Nd11Pd4In9-type), Er11Co3In6, Er8CoIn3 (Pr8CoGa3-type), Er6Co2.19In0.81 (Ho6Co2Ga-type), and Er13.83Co2.88In3.10 (Lu14Co2In3-type) exist in the Er-Co-In system at this temperature. The crystal structure of the Er8CoIn3 compound was determined by means of X-ray powder method (Pr8CoGa3-type, P63mc space group, a = 1.02374(2) nm, c = 0.68759(2) nm). Almost none of the binary compounds dissolve the third component. The exception is the existence of the solid solution based on ErCo3 binary compound, which dissolves up to 8 at.% of In.


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