scholarly journals The Study of Crystal Structure on Grossular–Andradite Solid Solution

Minerals ◽  
2019 ◽  
Vol 9 (11) ◽  
pp. 691
Author(s):  
Yichuan Wang ◽  
Qiang Sun ◽  
Dengfei Duan ◽  
Xinjian Bao ◽  
Xi Liu
Keyword(s):  
Solid Solution ◽  
Rotation Angle ◽  
Enthalpy Of Mixing ◽  
X Ray Diffraction ◽  
Binary Solid Solution ◽  
Distortion Parameter ◽  
X Ray ◽  
Dodecahedral Site ◽  
Diffraction Peaks ◽  
Octahedral Distortion

The effects of Al3+–Fe3+ substitution on 10 synthesized garnet samples along the grossular–andradite binary solid solution were investigated using both powder and single-crystal X-ray diffraction. Results showed that cell volume increased with andradite content. Small negative excess volume was observed in the Al-rich samples. By measuring the bond length, polyhedral volume, octahedral distortion parameter (σ), and tetrahedral rotation angle (α), we determined that the distortion occurred on the dodecahedral site. The width of the diffraction peaks was obviously related to the composition of the solid solution. Full width at half maximum of diffraction peaks was used to calculate the microstrain, which may have a relationship with enthalpy of mixing.

Solid solutions in the system Ag2S–Ag2Se

1992 ◽  
Vol 7 (8) ◽  
pp. 2219-2224 ◽  
Author(s):  
N.E. Pingitore ◽  
B.F. Ponce ◽  
M.P. Eastman ◽  
F. Moreno ◽  
C. Podpora
Keyword(s):  
Solid Solution ◽  
Solid Solutions ◽  
Type Structure ◽  
Solid Solution Series ◽  
X Ray Diffraction ◽  
Compositional Gradient ◽  
X Ray ◽  
Optical Electron ◽  
Discrete Phase ◽  
Diffraction Peaks

Optical, electron microprobe, and x-ray diffraction analysis of 88 samples of various compositions between Ag2S and Ag2Se synthesized at high temperature in sealed quartz tubing indicates the presence of two solid-solution series in this system at ambient (room) conditions. One series extends from Ag2S to approximately Ag2S0.4Se0.7 and has the Ag2S-III-type structure (monoclinic). The second series ranges from Ag2S0.3Se0.7 to Ag2Se and is characterized by the Ag2Se-II-type structure (orthorhombic). Members of both series, in appropriate proportions, characterize the apparent compositional gap between the two solid solutions. Gradual shifts in the locations of the x-ray diffraction peaks along the compositional gradient of each solid solution revealed an expansion of the d-spacing as the larger Se ion was substituted for S in the Ag2S-III-type structure and a contraction as S was substituted for Se in the Ag2Se-II-type structure. The reported discrete phase, Ag4SSe (aguilarite, orthorhombic), appears to be simply a member of the monoclinic Ag2S-III-type solid solution.

Phase equilibria in the BaTiO3–La2TiO5–TiO2 system

1998 ◽  
Vol 13 (5) ◽  
pp. 1327-1334 ◽  
Author(s):  
Srečo Škapin ◽  
Drago Kolar ◽  
Danilo Suvorov ◽  
Zoran Samardžija
Keyword(s):  
Solid Solution ◽  
Electron Probe ◽  
Ternary Solid Solution ◽  
Secondary Phases ◽  
X Ray Diffraction ◽  
Binary Solid Solution ◽  
Subsolidus Phase ◽  
X Ray ◽  
Tie Lines ◽  
Scanning Electron

Subsolidus phase relations in the BaTiO3–La2TiO5–TiO2 part of the ternary BaO–La2O3–TiO2 system at 1300 °C in air were determined. The phases were characterized by x-ray diffraction, scanning electron microscopy, and electron probe wavelength dispersive spectroscopic microanalysis. A combination of techniques was employed because of insensitivity in detecting secondary phases by x-ray diffraction. The location and extent of Ba6−xLa8+2x/3Ti18O54 ternary solid solution 0.2(1) ⩽ x ⩽ 2.3(1) and Ba1−yLayTi1−y/4 (VTi)y/4O3 binary solid solution 0 ⩽ y ⩽ 0.3 at 1300 °C was established. Tie lines between various barium polytitanates with a sequence of Ba6−xLa8+2x/3Ti18O54 solid solution regions were determined.

scholarly journals Lattice Strain Evolutions in Ni-W Alloys during a Tensile Test Combined with Synchrotron X-ray Diffraction

Materials ◽  
2020 ◽  
Vol 13 (18) ◽  
pp. 4027
Author(s):  
Tarik Sadat ◽  
Damien Faurie ◽  
Dominique Thiaudière ◽  
Cristian Mocuta ◽  
David Tingaud ◽  
...  
Keyword(s):  
Solid Solution ◽  
Tensile Test ◽  
Single Phase ◽  
Lattice Strain ◽  
Tensile Tests ◽  
X Ray Diffraction ◽  
X Ray ◽  
Significant Difference ◽  
Diffraction Peaks

Ni and Ni(W) solid solution of bulk Ni and Ni-W alloys (Ni-10W, Ni-30W, and Ni-50W) (wt%) were mechanically compared through the evolution of their {111} X-ray diffraction peaks during in situ tensile tests on the DiffAbs beamline at the Synchrotron SOLEIL. A significant difference in terms of strain heterogeneities and lattice strain evolution occurred as the plastic activity increased. Such differences are attributed to the number of brittle W clusters and the hardening due to the solid solution compared to the single-phase bulk Ni sample.

Control of the phase composition of advanced calcium phosphates using an x-ray diffractometer with a curved position-sensitive detector

2020 ◽  
Vol 86 (6) ◽  
pp. 29-35
Author(s):  
V. P. Sirotinkin ◽  
O. V. Baranov ◽  
A. Yu. Fedotov ◽  
S. M. Barinov
Keyword(s):  
Phase Composition ◽  
Calcium Phosphates ◽  
Position Sensitive Detector ◽  
Sensitive Detector ◽  
X Ray Diffraction ◽  
X Ray ◽  
Impurity Phases ◽  
Position Sensitive ◽  
Diffraction Peaks ◽  
Diffraction Patterns

The results of studying the phase composition of advanced calcium phosphates Ca10(PO4)6(OH)2, β-Ca3(PO4)2, α-Ca3(PO4)2, CaHPO4 · 2H2O, Ca8(HPO4)2(PO4)4 · 5H2O using an x-ray diffractometer with a curved position-sensitive detector are presented. Optimal experimental conditions (angular positions of the x-ray tube and detector, size of the slits, exposure time) were determined with allowance for possible formation of the impurity phases during synthesis. The construction features of diffractometers with a position-sensitive detector affecting the profile characteristics of x-ray diffraction peaks are considered. The composition for calibration of the diffractometer (a mixture of sodium acetate and yttrium oxide) was determined. Theoretical x-ray diffraction patterns for corresponding calcium phosphates are constructed on the basis of the literature data. These x-ray diffraction patterns were used to determine the phase composition of the advanced calcium phosphates. The features of advanced calcium phosphates, which should be taken into account during the phase analysis, are indicated. The powder of high-temperature form of tricalcium phosphate strongly adsorbs water from the environment. A strong texture is observed on the x-ray diffraction spectra of dicalcium phosphate dihydrate. A rather specific x-ray diffraction pattern of octacalcium phosphate pentahydrate revealed the only one strong peak at small angles. In all cases, significant deviations are observed for the recorded angular positions and relative intensity of the diffraction peaks. The results of the study of experimentally obtained mixtures of calcium phosphate are presented. It is shown that the graphic comparison of experimental x-ray diffraction spectra and pre-recorded spectra of the reference calcium phosphates and possible impurity phases is the most effective method. In this case, there is no need for calibration. When using this method, the total time for analysis of one sample is no more than 10 min.

scholarly journals Synthesis of Ce1−xPdxO2−δ Solid Solution in Molten Nitrate

Catalysts ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 640
Author(s):  
Hideaki Sasaki ◽  
Keisuke Sakamoto ◽  
Masami Mori ◽  
Tatsuaki Sakamoto
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Solid Solutions ◽  
Photoelectron Spectroscopy ◽  
Synthesis Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Co Precipitation ◽  
Ionic States

CeO2-based solid solutions in which Pd partially substitutes for Ce attract considerable attention, owing to their high catalytic performances. In this study, the solid solution (Ce1−xPdxO2−δ) with a high Pd content (x ~ 0.2) was synthesized through co-precipitation under oxidative conditions using molten nitrate, and its structure and thermal decomposition were examined. The characteristics of the solid solution, such as the change in a lattice constant, inhibition of sintering, and ionic states, were examined using X-ray diffraction (XRD), scanning electron microscopy–energy-dispersive X-ray spectroscopy (SEM−EDS), transmission electron microscopy (TEM)−EDS, and X-ray photoelectron spectroscopy (XPS). The synthesis method proposed in this study appears suitable for the easy preparation of CeO2 solid solutions with a high Pd content.

scholarly journals Structural and Raman Vibrational Studies ofCeO2-Bi2O3Oxide System

2009 ◽  
Vol 2009 ◽  
pp. 1-4 ◽  
Author(s):  
L. Bourja ◽  
B. Bakiz ◽  
A. Benlhachemi ◽  
M. Ezahri ◽  
J. C. Valmalette ◽  
...  
Keyword(s):  
Solid Solution ◽  
Raman Spectroscopy ◽  
Phase Changes ◽  
Phase System ◽  
X Ray Diffraction ◽  
X Ray ◽  
Vibrational Studies ◽  
Coprecipitation Route

A series of ceramics samples belonging to theCeO2-Bi2O3phase system have been prepared via a coprecipitation route. The crystallized phases were obtained by heating the solid precursors at600∘Cfor 6 hours, then quenching the samples. X-ray diffraction analyses show that forx<0.20a solid solutionCe1−xBixO2−x/2with fluorine structure is formed. For x ranging between 0.25 and 0.7, a tetragonalβ′phase coexisting with the FCC solid solution is observed. For x ranging between 0.8 and 0.9, a new tetragonalβphase appears. Theβ′phase is postulated to be a superstructure of theβphase. Finally, close tox=1, the classical monoclinicα Bi2O3structure is observed. Raman spectroscopy confirms the existence of the phase changes as x varies between 0 and 1.

Comparative Studies of Ultra Low-κ Porous Silica Films with 2-D Hexagonal and Disordered Pore Structures

2004 ◽  
Vol 812 ◽  
Author(s):  
Nobutoshi Fujii ◽  
Kazuhiro Yamada ◽  
Yoshiaki Oku ◽  
Nobuhiro Hata ◽  
Yutaka Seino ◽  
...  
Keyword(s):  
Pore Structure ◽  
Nonionic Surfactants ◽  
Porous Silica ◽  
Silica Film ◽  
X Ray Diffraction ◽  
Silica Films ◽  
X Ray ◽  
X Ray Scattering ◽  
Porous Silica Film ◽  
Diffraction Peaks

AbstractPeriodic 2-dimensional (2-D) hexagonal and the disordered pore structure silica films have been developed using nonionic surfactants as the templates. The pore structure was controlled by the static electrical interaction between the micelle of the surfactant and the silica oligomer. No X-ray diffraction peaks were observed for the disordered mesoporous silica films, while the pore diameters of 2.0-4.0 nm could be measured by small angle X-ray scattering spectroscopy. By comparing the properties of the 2-D hexagonal and the disordered porous silica films which have the same porosity, it is found that the disordered porous silica film has advantages in terms of the dielectric constant and Young's modulus as well as the hardness. The disordered porous silica film is more suitable for the interlayer dielectrics for ULSI.

Microstructure and wear resistance of Cuss-toughened Cr5Si3/CrSi metal silicide alloys

2005 ◽  
Vol 20 (5) ◽  
pp. 1122-1130 ◽  
Author(s):  
Y.X. Yin ◽  
H.M. Wang
Keyword(s):  
Solid Solution ◽  
Wear Resistance ◽  
Sliding Wear ◽  
Room Temperature ◽  
Wear Test ◽  
Melting Process ◽  
Dry Sliding Wear ◽  
Metal Silicide ◽  
X Ray Diffraction ◽  
X Ray

Wear-resistant Cu-based solid-solution-toughened Cr5Si3/CrSi metal silicide alloy with a microstructure consisting of predominantly the dual-phase primary dendrites with a Cr5Si3 core encapsulated by CrSi phase and a small amount of interdendritic Cu-based solid solution (Cuss) was designed and fabricated by the laser melting process using Cr–Si–Cu elemental powder blends as the precursor materials. The microstructure of the Cuss-toughened Cr5Si3/CrSi metal silicide alloy was characterized by optical microscopy, powder x-ray diffraction, and energy dispersive spectroscopy. The Cuss-toughened silicide alloys have excellent wear resistance and low coefficient of friction under room temperature dry sliding wear test conditions with hardened 0.45% C carbon steel as the sliding–mating counterpart.

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