scholarly journals Synthesis, Microstructure and Crystal Structure of Perovskite-Type CeMO3 (M=Al, Ga) by Arc-Melting Method with Horizontal-Traveling Hearth

1998 ◽  
Vol 106 (1233) ◽  
pp. 509-513 ◽  
Author(s):  
Toetsu SHISHIDO ◽  
Yutong THENG ◽  
Akihiro SAITO ◽  
Hiroyuki HOIUCHI ◽  
Toshitsugu TAKAHASHI ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Melting Method ◽  
Arc Melting ◽  
Perovskite Type

scholarly journals Crystal structure and Mössbauer study of FeAl2O4

Nukleonika ◽  
2015 ◽  
Vol 60 (1) ◽  
pp. 47-49 ◽  
Author(s):  
Ilona Jastrzębska ◽  
Jacek Szczerba ◽  
Paweł Stoch ◽  
Artur Błachowski ◽  
Krzysztof Ruebenbauer ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Spinel Structure ◽  
Approximate Formula ◽  
Argon Atmosphere ◽  
Mossbauer Effect ◽  
Mössbauer Study ◽  
Melting Method ◽  
X Ray ◽  
Octahedral Sites ◽  
Arc Melting

Abstract In this work the synthesis of hercynite from Fe2O3 and Al2O3 powders was carried out by arc-melting method under the protective argon atmosphere. The obtained material was characterized with the use of powder X-ray diffractometry (XRD) and Mössbauer spectroscopy (MS). A Mössbauer effect in hercynite obtained by the arc-melting method indicated the cations distribution in the spinel structure among the tetrahedral and octahedral interstices. The presence of Fe2+ ions was detected in both tetrahedral and octahedral sites while Fe3+ ions occupied only the octahedral interstices. The approximate formula of the obtained iron-aluminate spinel was as follows (Fe2+0.77Al3+0.23) (Fe3+0.07Fe2+0.05Al0.88)2O4.

XRD STUDY OF THE Er1-xDyxNi2B2C SYSTEM MAGNETIC SUPERCONDUCTORS

2005 ◽  
Vol 19 (26) ◽  
pp. 3945-3950
Author(s):  
XIAOLING QIN ◽  
SHIXUN CAO ◽  
LIMING YU ◽  
JINCANG ZHANG ◽  
KATSUHIKO NISHIMURA ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Ionic Radius ◽  
Magnetic Moments ◽  
Powder Xrd ◽  
Melting Method ◽  
Arc Melting ◽  
Xrd Study ◽  
Superconducting Compound ◽  
Change Of Microstructure ◽  
Ionic Radius Difference

The magnetic superconducting samples of the intermetallic Er 1-x Dy x Ni 2 B 2 C system are prepared by the arc melting method. Powder XRD measurements are systematically conducted and analyzed. The change of microstructure reflects the contribution of the different magnetic moments and the ionic radius difference of Er and Dy to the crystal structure in the substitution of Er 1-x Dy x Ni 2 B 2 C system. The element substitution of Dy for Er in the magnetic superconducting compound is verified commendably in microstructure level by the powder XRD experiment.

Crystal structure and X-ray powder diffraction pattern of Ti2ZrAl

2000 ◽  
Vol 15 (3) ◽  
pp. 189-190 ◽  
Author(s):  
D. Sornadurai ◽  
B. Panigrahi ◽  
V. S. Sastry ◽  
Ramani
Keyword(s):  
Crystal Structure ◽  
Diffraction Pattern ◽  
Powder Diffraction ◽  
Single Phase ◽  
Xrd Analysis ◽  
Melting Method ◽  
X Ray ◽  
Structure Space ◽  
Arc Melting ◽  
Phase Pure

We report precision X-ray powder-diffraction (XRD) data of single phase pure Ti2ZrAl. Ti2ZrAl samples were prepared by an arc melting method and annealed at 1000 °C for 30 days. XRD analysis was carried out on these samples and it was found that Ti2ZrAl has a DO19 structure (space group P63/mmc, No. 194). The lattice parameters are found to be a=5.961±0.001 Å and c=4.793±0.001 Å.

Effect of Complexing Agent on Morphology and Crystal Structure of La1-xCexCoO3 (x=0, 0.2, and 0.4) Perovskite-Type Mixed Oxides Catalyst Prepared by Sol-Gel Method

2010 ◽  
Vol 658 ◽  
pp. 29-32 ◽  
Author(s):  
Kanit Soongprasit ◽  
Duangdao Aht-Ong ◽  
Viboon Sricharoenchaikul ◽  
Duangduen Atong
Keyword(s):  
Crystal Structure ◽  
Polyvinyl Alcohol ◽  
Mixed Oxides ◽  
Sol Gel ◽  
Value Added ◽  
Molar Ratio ◽  
Complexing Agent ◽  
Nitrate Hexahydrate ◽  
Mixed Oxide Catalysts ◽  
Perovskite Type

. La1-xCexCoO3 (x=0, 0.2, and 0.4) perovskite-type mixed oxides using polyvinyl alcohol (PVA) as complexing agent at two molar ratio of metal ion to PVA (1:1 and 1:2) were successfully prepared by sol-gel process. The precursor included lanthanum (II) nitrate hexahydrate, cerium (II) nitrate hexahydrate, and cobalt (II) nitrate hexahydrate where polyvinyl alcohol was added as complexing agent. The suitable condition of Cerium (Ce) substitution and PVA molar ratio were established for further application in hydrocarbon conversion to high value added products. TGA thermogram of as-prepared precursor showed that PVA absolutely decomposed at temperature higher than 500°C. XRD patterns of calcined catalyst showed both LaCoO3 rhombohedral and CeO2 cubic structures that confirmed the formation of mixed crystal structure. Nevertheless, Co3O4 slightly appeared with low peak intensity which came from the oxidation reaction of as-prepared catalyst during calcinations. XRD showed that PVA did not effect to crystal structure of synthesized catalyst. Higher PVA content added in the precursor cause the reduction of crystal growth of catalyst in calcinations step. In contrast, morphology of catalyst is directly related with PVA content such that the spongy and sheet-like structure were formed with increasing PVA content which prevented the agglomeration of particles. The results showed that PVA content play an important role in morphology of perovskite-type mixed oxide catalysts but did not affected to their crystal structures.

scholarly journals CRYSTAL STRUCTURE OF THE NEW SILICIDE Lu3Ni11.74(2)Si4

2020 ◽  
Vol 86 (5) ◽  
pp. 3-12
Author(s):  
Bohdana Belan ◽  
Mykola Manyako ◽  
Mariya Dzevenko ◽  
Dorota Kowalska ◽  
Roman Gladyshevskii
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Type Structure ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
Arc Melting ◽  
Pearson Symbol ◽  
Ternary Silicide

The new ternary silicide Lu3Ni11.74(2)Si4 was synthesized from the elements by arc-melting and its crystal structure was determined by the single-crystal X-ray diffraction. The compound crystallizes in the Sc3Ni11Ge4-type: Pearson symbol hP37.2, space group P63/mmc (No. 194), a = 8.0985(16), c = 8.550(2) Å, Z = 2; R = 0.0244, wR = 0.0430 for 244 reflections. The silicide Lu3Ni11.74(2)Si4 is new member of the EuMg5.2-type structure family.

scholarly journals Effect of Nd, Pr substitutional atoms on the magnetic and magnetostrictive properties in (Tb-Dy)(Fe-Co)2 Laves phases

2021 ◽  
Vol 2103 (1) ◽  
pp. 012196
Author(s):  
G A Politova ◽  
M A Ganin ◽  
A B Mikhailova ◽  
D A Morozov ◽  
K E Pankov ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Magnetic Properties ◽  
Laves Phase ◽  
Type Structure ◽  
Partial Substitution ◽  
Laves Phases ◽  
Temperature Range ◽  
Homogenizing Annealing ◽  
Arc Melting ◽  
Magnetostrictive Materials

Abstract Polycrystalline TbxDy1-xR0.1Fe2-zCoz (R = Nd, Pr, x = 0.2, 0.3; z = 0, 1.3) cubic Laves phase alloys with MgCu2-type structure were prepared by arc melting followed by homogenizing annealing. The crystal structure, magnetic properties, and magnetostriction have been investigated. Compounds with high values of magnetostrictive susceptibility were found in the temperature range 150-300 K. Compounds with partial substitution of cobalt for iron demonstrate a change in the sign of anisotropic magnetostriction. This work continues the search for magnetostrictive materials with inexpensive neodymium and praseodymium.

Crystal Structure of the Dy3Ni11.83Si3.98 Compound

2019 ◽  
Vol 289 ◽  
pp. 77-81
Author(s):  
Bohdana Belan ◽  
Mykola Manyako ◽  
Katarzyna Pasinska ◽  
Marta Demchyna ◽  
Roman E. Gladyshevskii
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Large Family ◽  
Type Structure ◽  
Single Crystal Diffraction ◽  
Space Group ◽  
X Ray ◽  
Arc Melting ◽  
Pearson Symbol ◽  
Ternary Silicide

The new ternary silicide Dy3Ni11.83(1)Si3.98(1)was synthesized from the elements by arc-melting and its crystal structure was determined by X-ray single-crystal diffraction. The compound crystallizes in a Sc3Ni11Ge4-type structure: Pearson symbolhP38, space groupP63/mmc(No. 194),a= 8.1990(7),c= 8.6840(7) Å,Z= 2;R= 0.0222, wR= 0.0284 for 365 reflections. The structure belongs to a large family of structures related to the EuMg5.2type, with representatives among ternary aluminides, silicides, germanides,etc.

The X-Ray Powder Diffraction Patterns and Crystal Structure for Al2M3Y(M=Cu, Ni)

2014 ◽  
Vol 950 ◽  
pp. 48-52
Author(s):  
De Gui Li ◽  
Ming Qin ◽  
Liu Qing Liang ◽  
Zhao Lu ◽  
Shu Hui Liu ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
Hexagonal Structure ◽  
Argon Atmosphere ◽  
X Ray Diffraction ◽  
High Quality ◽  
X Ray ◽  
Arc Melting ◽  
Diffraction Patterns

The Al2M3Y(M=Cu, Ni) compound was synthesized by arc melting under argon atmosphere. The high-quality powder X-ray diffraction data of Al2M3Y have been presented. The refinement of the X-ray diffraction patterns for the Al2M3Y compound show that the Al2M3Y has hexagonal structure, space groupP6/mmm(No.191), with a = b = 5.1618(2) Å, c = 4.1434(1) Å,V= 95.6 Å3,Z= 1,ڑx= 5.7922 g/cm3,F30= 155.5(0.0057, 34), RIR = 2.31 for Al2Cu3Y, and with a = b = 5.0399(1) Å, c = 4.0726(1) Å,V= 89.59 Å3,Z= 1,ڑx= 5.9118 g/cm3,F30= 135.7(0.0072, 30), RIR = 2.54 for Al2Ni3Y.

Preparation, Crystal Structure, and Properties of the Lanthanoid Carbides Ln4C7 with Ln = Ho, Er, Tm, and Lu

1996 ◽  
Vol 51 (5) ◽  
pp. 646-654 ◽  
Author(s):  
Ralf Czekalla ◽  
Wolfgang Jeitschko ◽  
Rolf-Dieter Hoffmann ◽  
Helmut Rabeneck
Keyword(s):  
Crystal Structure ◽  
Rietveld Method ◽  
Magnetic Ordering ◽  
Monoclinic Crystal ◽  
X Ray ◽  
Neutron Powder Diffraction Data ◽  
Monoclinic Crystal Structure ◽  
Arc Melting ◽  
Structure Factors ◽  
Hydrolysis Of

The isotypic carbides Ln4C7 (Ln = Ho, Er, Tm, Lu) were prepared by arc-melting of the elemental components, followed by annealing at 1300 °C. The positions of the metal and of some carbon atoms of the monoclinic crystal structure of LU4C7 were determined from X-ray powder data, and the last carbon positions were found and refined from neutron powder diffraction data: P21/c, a = 360.4(1), b = 1351.4(3), c = 629.0(2) pm, β = 104.97(2)°, Z = 2, R = 0.026 for 429 structure factors and 15 positional parameters. The structure contains isolated carbon atoms with octahedral lutetium coordination and linear C3-units, with C-C bond lengths of 132(1) and 135(1) pm. This carbide may therefore be considered as derived from methane and propadiene. The hydrolysis of LU4C7 with distilled water yields mainly methane and propine, while the hydrolyses of the corresponding holmium and erbium carbides resulted in relatively large amounts of saturated and unsaturated C2-hydrocarbons in addition to the expected products methane and propine. The structure comprises two-dimensionally infinite NaCl-type building elements, which are separated by the C3-units. It may be described as a stacking variant of a previously reported structure of HO4C7, now designated as the a-modification. The Lu4C7-type β -modification was obtained at higher temperatures. Its structure was refined by the Rietveld method from X-ray powder data to a residual R = 0.037 for 320 F values and 15 positional parameters. Lu4C7 is Pauli paramagnetic; β -HO4C7 and Er4C7 show Curie-Weiss behavior with magnetic ordering temperatures of less than 20 K.

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