New X-ray powder diffraction data for Mo2.85Al1.91Si4.81

2006 ◽  
Vol 21 (3) ◽  
pp. 238-240
Author(s):  
S. A. Tayebifard ◽  
K. Ahmadi ◽  
R. Yazdani-Rad ◽  
M. Doroudian
Keyword(s):  
High Temperature ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
The Self ◽  
Powder Diffraction Data ◽  
Temperature Synthesis ◽  
Automatic Indexing ◽  
X Ray ◽  
High Temperature Synthesis ◽  
Good Agreement

X-ray powder diffraction data for Mo2.85Al1.91Si4.81 are reported. The new Mo2.85Al1.91Si4.81 compound was successfully prepared using the self-propagating high-temperature synthesis (SHS) technique. The starting atomic mixture of reactant powders was Mo+2(1−x)Si+2xAl with x=0.3. The final powder compound obtained by the SHS technique was determined to be Mo2.85Al1.91Si4.81 by ICP-AES. X-ray powder diffraction pattern of Mo2.85Al1.91Si4.81 was recorded using an X-ray powder diffractometer, Cu Kα radiation, and analyzed by automatic indexing programs. Mo2.85Al1.91Si4.81 was found to be hexagonal with a=4.6929(2) Å and c=6.5515(4) Å. The XRD results are in good agreement with those of Mo2.85Ga2Si4.15.

scholarly journals Synthesis of the Tetragonal Phase of Zintl’s NaTl and Its Structure Determination from Powder Diffraction Data

Materials ◽  
2019 ◽  
Vol 12 (8) ◽  
pp. 1356 ◽  
Author(s):  
Susanne Tiefenthaler ◽  
Nikolaus Korber ◽  
Stefanie Gärtner
Keyword(s):  
High Temperature ◽  
Powder Diffraction ◽  
Liquid Ammonia ◽  
Powder Diffraction Data ◽  
Temperature Synthesis ◽  
High Temperature Synthesis ◽  
Structure Solution ◽  
Long Time ◽  
Original Procedure ◽  
Model Independent

A tetragonal distortion of the long-time known NaTl structure at 298 K was observed in different experimental setups, including Zintl’s original procedure of reducing Tl(I)-iodide by sodium liquid ammonia solutions. The powder diffraction pattern obtained by the high temperature synthesis using classical solid-state techniques allowed a model-independent unambiguous structure solution and refinement of tetragonal distorted NaTl (Rp = 0.0179, wRp = 0.0246, R = 0.0477, wR = 0.0527, GooF = 1.24).

A Study of Fe-Based Composite Coating Fabricated by the Self-Propagating High Temperature Synthesis

2012 ◽  
Vol 626 ◽  
pp. 138-142
Author(s):  
Saowanee Singsarothai ◽  
Vishnu Rachpech ◽  
Sutham Niyomwas
Keyword(s):  
High Temperature ◽  
Composite Coating ◽  
Steel Substrate ◽  
The Self ◽  
X Ray Diffraction ◽  
Temperature Synthesis ◽  
X Ray ◽  
High Temperature Synthesis ◽  
Precursor Powders ◽  
Scanning Electron

The steel substrate was coated by Fe-based composite using self-propagating high-temperature synthesis (SHS) reaction of reactant coating paste. The green paste was prepared by mixing precursor powders of Al, Fe2O3and Al2O3. It was coated on the steel substrate before igniting by oxy-acetylene flame. The effect of coating paste thickness and the additives on the resulted Fe-based composite coating was studied. The composite coating was characterized by X-ray diffraction (XRD) and scanning electron microscope (SEM) couple with dispersive X-ray (EDS).

X-ray powder diffraction data for the superconducting phase Tl0.5Pb0.5Sr2CaCu2O6.5+δ

1993 ◽  
Vol 8 (4) ◽  
pp. 249-250 ◽  
Author(s):  
Chan Park ◽  
Robert L. Snyder
Keyword(s):  
High Temperature ◽  
Molten Salt ◽  
Diffraction Pattern ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
Superconducting Phase ◽  
Powder Diffraction Data ◽  
X Ray ◽  
High Temperature Superconducting

The X-ray powder diffraction pattern for a sample of the high-temperature superconducting phase Tl0.5Pb0.5Sr2CaCu2O6.5+δ has been determined. The sample was prepared by a molten salt technique and had a Tc of 96 K.

Powder-diffraction data for several solid solutions with the compositions (CaxSr1−x)CuO2 and (CaxSr1−x)2CuO3

1995 ◽  
Vol 10 (4) ◽  
pp. 296-299 ◽  
Author(s):  
S. T. Misture ◽  
C. Park ◽  
R. L. Snyder ◽  
B. Jobst ◽  
B. Seebacher
Keyword(s):  
High Temperature ◽  
Solid State ◽  
Powder Diffraction ◽  
Solid Solutions ◽  
Diffraction Data ◽  
Solid State Reaction ◽  
High Temperature Superconductors ◽  
Powder Diffraction Data ◽  
X Ray ◽  
Diffraction Patterns

Several compositions of the solid solutions (CaxSr1−x)CuO2 and (CaxSr1−x)2CuO3, both of which are found as minor phases in the high-temperature superconductors, were prepared by solid-state reaction. X-ray powder-diffraction patterns for three compositions of (CaxSr1−x)CuO2 and two for (CaxSr1−x)2CuO3 are presented.

X-ray diffraction analysis of (Na0.6H0.4)(Ta0.7Nb0.3)O3

1999 ◽  
Vol 14 (3) ◽  
pp. 231-233 ◽  
Author(s):  
Raj P. Singh ◽  
Michael J. Miller ◽  
Jeffrey N. Dann
Keyword(s):  
High Temperature ◽  
Diffraction Analysis ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
Unit Cell ◽  
Type Structure ◽  
Powder Diffraction Data ◽  
X Ray Diffraction ◽  
X Ray

(Na0.6H0.4)(Ta0.7Nb0.3)O3 was synthesized by heating a tantalum/niobium scale containing two sodium tantalate/niobate phases :Na14(Ta0.7Nb0.3)12O37·31H2O and NaH2Ta0.7Nb0.3O4. Powder X-ray diffraction data for (Na0.6H0.4)(Ta0.7Nb0.3)O3 indicated it to be a cubic perovskite (ABO3/ReO3 type structure) with unit cell a0=3.894 Å. The compound is analogous to the mineral lueshite (NaNbO3), and to the high temperature forms of NaTaO3 and NaNbO3. Powder diffraction data for (Na0.6H0.4)(Ta0.7Nb0.3)O3 will be useful in the analysis of synthetic tantalum/niobium concentrates.

Self-Propagating High-Temperature Synthesis of Fe-W(B, C) Based Composite

2013 ◽  
Vol 748 ◽  
pp. 46-50 ◽  
Author(s):  
Saowanee Singsarothai ◽  
Sutham Niyomwas
Keyword(s):  
Electron Microscope ◽  
High Temperature ◽  
Scanning Electron Microscope ◽  
The Self ◽  
X Ray Diffraction ◽  
Temperature Synthesis ◽  
X Ray ◽  
High Temperature Synthesis ◽  
Flame Ignition ◽  
Scanning Electron

Fe-W based composite have successfully been prepared using natural resource. The ferberite (Fe (Mn, Sn)WO4) tailings mixed with aluminum, carbon and boron oxide powder were used as reactants. The reactants were pressed and followed by oxy-acetylene flame ignition. The products from the self-propagating high-temperature synthesis (SHS) reaction were characterized by X-ray diffraction (XRD) and scanning electron microscope (SEM) couple with dispersive X-ray (EDS).

X-ray powder diffraction data for rhombohedral AlPt

2006 ◽  
Vol 21 (4) ◽  
pp. 318-319
Author(s):  
Mark A. Rodriguez ◽  
David P. Adams
Keyword(s):  
Thin Film ◽  
High Temperature ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
Lattice Parameter ◽  
Unit Cell ◽  
Powder Diffraction Data ◽  
Space Group ◽  
X Ray ◽  
High Temperature Reactions

X-ray powder diffraction data for a rhombohedral AlPt phase formed by self-propagating, high-temperature reactions of Al∕Pt bi-layer films are reported. Multilayer Al∕Pt thin film samples, reacted in air or vacuum, transformed into rhombohedral AlPt with space group R-3(148). Indexing and lattice parameter refinement of AlPt powders (generated from thin-film samples) yielded trigonal/hexagonal unit-cell lattice parameters of a=15.623(6) Å and c=5.305(2) Å, Z=39, and V=1121.5 Å3.

X-ray powder diffraction data for high-temperature Al4Re(Ni)

2009 ◽  
Vol 24 (1) ◽  
pp. 29-31 ◽  
Author(s):  
B. Grushko
Keyword(s):  
High Temperature ◽  
Diffraction Pattern ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
Monoclinic Phase ◽  
Binary Alloys ◽  
Powder Diffraction Data ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray

A monoclinic phase isostructural to Al4W was revealed in Al–Ni–Re close to the Al–Re terminal. It is assumed to be a ternary extension of the high-temperature Al4Re phase usually transforming in binary alloys even by sharp quenching from the existence temperatures. The powder X-ray diffraction pattern of this phase of the Al77Ni2.5Re20.5 composition was indexed for the Cm space group with a=5.1538(12) Å, b=17.410(5) Å, c=5.1546(15) Å, and β=100.548(16)°.

Investigation on B, Cr Doped Ni3Al Alloy Prepared by Self-Propagation High-Temperature Synthesis and Hot Extrusion

2013 ◽  
Vol 747-748 ◽  
pp. 124-131 ◽  
Author(s):  
Li Yuan Sheng ◽  
Jian Ting Guo ◽  
Chao Yuan ◽  
F. Yang ◽  
G.S. Li ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Mechanical Properties ◽  
High Temperature ◽  
Hot Extrusion ◽  
The Self ◽  
Al Alloy ◽  
Temperature Synthesis ◽  
X Ray ◽  
High Temperature Synthesis ◽  
Transmission Electron

The Ni3Al and Ni3Al-B-Cr alloys were fabricated by the self-propagation high-temperature synthesis with hot extrusion method. Their microstructure and mechanical properties were studied by using combination of X-ray diffraction, optical microscopy, transmission electron microscopy and compression test. Analysis of X-ray spectra exhibited that the elemental powders had been transformed to the Ni3Al phase after the self-propagation high-temperature synthesis processing. Microstructure examination showed that the alloy without extrusion consisted of coarse and fine grains, but the subsequent hot extrusion procedure homogenized the grain size and densified the alloy obviously. Transmission electron microscopy observations on the Ni3Al alloy revealed that Ni3Al, γ-Ni and Al2O3 particles were the main phases. When the boron and chromium were added, besides the β-NiAl phase, α-Cr phase and some Cr7Ni3 particles with stacking faults inside were observed. In addition, a lot of substructure and high-density dislocation arrays were observed in the extruded part, which indicated that the subsequent extrusion had led to great deformation and partly recrystallizing in the alloy. Moreover, the subsequent extrusion procedure redistributed the Al2O3 particles and eliminated the γ-Ni. These changes were helpful to refine the microstructure and weaken the misorientation. The mechanical test showed that the self-propagation high-temperature synthesis with hot extrusion improved the mechanical properties of the Ni3Al alloy significantly. The addition of B and Cr in Ni3Al alloy increased the mechanical properties further, but the compressive strength of the alloy was still lower than that synthesized by combustion. Finally, the self-propagation high-temperature synthesis with hot extrusion was a good method to prepare Ni3Al alloy from powder.

Sign in / Sign up

Export Citation Format

Share Document