The Formation of Y-Ba-Cu-O Phases During Solid State Reaction

1987 ◽  
Vol 99 ◽  
Author(s):  
T. S. Chin ◽  
T. W. Huang ◽  
W. T Lin ◽  
N. C. Wu ◽  
Y. H. Chou ◽  
...  
Keyword(s):  
Solid State ◽  
Solid State Reaction ◽  
High Temperature Superconductor ◽  
Molar Ratio ◽  
Continuous Heating ◽  
Isothermal Heating ◽  
High Tc ◽  
X Ray ◽  
Y123 Phase ◽  
Y211 Phase

ABSTRACTThe formation of Y-Ba-Cu-O phases, including the high Tc superconducting YBa2Cu3O7−x (Y123) phase, during solid state reaction of the mixture of Y2O3: BacO3: CuO, in molar ratio of 0.2:0.6:1 to conform the formula of the perovskite (Y0.4 Ba0.6)CuO3 composition was studied by means of DTA, DTG and X-ray difractometry(XRD). For continuous heating at 10 C/min, it was found that the Y123 phase exists at 790–995 C, and gradually disappears at higher temperatures. The insulating Y2BaCuO5 (Y211) phase exists at 985 to 1190 C, the maximum experiment temperature. While the semiconducting YBa3Cu2O7-y, (Y132) phase coexists with the Y123 phase. For isothermal heating, it was found that the most appropriate temperature and time for the formation of the Y123 phase is 900 C and 16 hours. Semiquantitative data on the amount of phases presented, including the above mentioned phases and other binary Ba-Y-O or Ba-Cu-O phases, during heating are also given. High temperature superconductor with a Tc of around 93 K can be synthesized reproducibly by the processes based on this study.

Synthesis and Characterization of Calcium Silicate from Rice Husk Ash and Shell of Snail Pomacea canaliculata by Solid State Reaction

2015 ◽  
Vol 1103 ◽  
pp. 1-7 ◽  
Author(s):  
Rimruthai Phuttawong ◽  
Napat Chantaramee ◽  
Pusit Pookmanee ◽  
Ratchadaporn Puntharod
Keyword(s):  
Solid State ◽  
Rice Husk ◽  
Solid State Reaction ◽  
Calcium Silicate ◽  
Rice Husk Ash ◽  
Fourier Transforms ◽  
Molar Ratio ◽  
Pomacea Canaliculata ◽  
X Ray ◽  
Agricultural Byproduct

Calcium silicate was successfully synthesized using agricultural byproduct such as rice husk ash and shell of snail namely Pomacea canaliculata by solid state reaction. Chemical composition of silica in rice husk ash and calcium oxide in shell were 91.50 and 98.25%, respectively by X-ray fluorescent determination. The rice husk ash and shell in molar ratio of 1:1 were milled for 5-8 hr and calcined at 800-1000 °C for 2 hr. The Fourier transforms infrared spectra and X-ray diffractometry pattern were confirmed the formation of calcium silicate as the milling time increased.

VARIATION OF Tc IN SINGLE PHASE Bi2Sr2Ca1Cu2O8−x SYSTEM

1991 ◽  
Vol 05 (24n25) ◽  
pp. 1645-1653
Author(s):  
M. NASIR KHAN ◽  
F.A. KHWAJA ◽  
RAANA FARID
Keyword(s):  
High Temperature ◽  
Solid State ◽  
Electron Density ◽  
Solid State Reaction ◽  
Single Phase ◽  
High Temperature Superconductor ◽  
Nominal Composition ◽  
X Ray Diffraction ◽  
Layer Spacing ◽  
X Ray

The variation of Tc in a single-phase high temperature superconductor Bi 2 Sr 2 Ca 1 Cu 2 O 8−x is studied using techniques like X-ray diffraction, magnetic and electric measurements. The samples of Bi-Sr-Ca-Cu-O (with nominal composition 2212) are synthesized by solid state reaction using appropriate amounts of Bi 2 O 3, SrCO 3, CaCO 3 and CuO powders. The Tc is found to vary from 92 K to 115 K in the quenched samples. These changes in the value of Tc have been related to the changes in the inter-layer spacing. It is concluded that an increase in the electron density due to shortening of the inter-layer increases the attractive interaction between pairs and is thus responsible for the high Tc in these superconductors.

X-ray Structure Refinement and Vibrational Spectroscopy of Ca8Gd2 (PO4)6 O2

2013 ◽  
Vol 12 (10) ◽  
pp. 719-726
Author(s):  
R. Ayadi ◽  
Mohamed Boujelbene ◽  
T. Mhiri
Keyword(s):  
Solid State ◽  
General Formula ◽  
Vibrational Spectroscopy ◽  
Powder Diffraction ◽  
Infrared Spectra ◽  
Solid State Reaction ◽  
Structure Refinement ◽  
Unit Cell ◽  
Cell Group ◽  
X Ray

The present paper is interested in the study of compounds from the apatite family with the general formula Ca10 (PO4)6A2. It particularly brings to light the exploitation of the distinctive stereochemistries of two Ca positions in apatite. In fact, Gd-Bearing oxyapatiteCa8 Gd2 (PO4)6O2 has been synthesized by solid state reaction and characterized by X-ray powder diffraction. The site occupancies of substituents is0.3333 in Gd and 0.3333 for Ca in the Ca(1) position and 0. 5 for Gd in the Ca (2) position.  Besides, the observed frequencies in the Raman and infrared spectra were explained and discussed on the basis of unit-cell group analyses.

scholarly journals NOTIZEN. Weitere Verbindungen vom Typ A3NO3: K3NO3 und Rb3NO3 / Further Compounds Typ A3NO3: K3NO3 and Rb3NO3

1980 ◽  
Vol 35 (2) ◽  
pp. 237-238 ◽  
Author(s):  
Martin Jansen
Keyword(s):  
Solid State ◽  
Crystal Structures ◽  
Solid State Reaction ◽  
X Ray

Abstract K3NO3 and RbsNO3 were prepared by solid state reaction of equimolar mixtures of K2O/KNO2 and Rb20/RbN02, respectively. According to X-ray powder photographs their crystal structures are derived from the perovs-kite structure. K3NO3 is isostructural with Na3NO3 (a = 521.7 pm, Z = 1), Rb3NO3 represents a tetragonally distorted variant with a = 770.5, c = 550.8 pm and Z = 2.

Relative Reactivity Trends OP High Temperature Superconductor Phases

1992 ◽  
Vol 275 ◽  
Author(s):  
David R. Riley ◽  
Ji-Ping Zhou ◽  
A. Manthiram ◽  
John T. McDevitt
Keyword(s):  
Electron Microscopy ◽  
Carbon Dioxide ◽  
High Temperature ◽  
High Temperature Superconductor ◽  
Relative Reactivity ◽  
Complete Understanding ◽  
High Tc ◽  
X Ray ◽  
The Common ◽  
Scanning Electron

ABSTRACTMany of the high temperature superconductor phases degrade rapidly when in the presence of water, acids, carbon dioxide or carbon monoxide. In order to foster more rapid developments in the area of high-Tc research, it will be necessary to acquire a more complete understanding of the surface chemistry of these superconducting materials. In this paper, the relative reactivity of the common cuprate phases toward water is reported. X-ray powder diffraction and scanning electron microscopy measurements are utilized here to establish the reactivity trends.

Preparation of Ultra–Fine La3NbO7 Powder by Solid State Reaction

2012 ◽  
Vol 512-515 ◽  
pp. 158-161 ◽  
Author(s):  
Ling Dai ◽  
Qiang Xu ◽  
Shi Zhen Zhu ◽  
Ling Liu
Keyword(s):  
Solid State ◽  
Solid State Reaction ◽  
Single Phase ◽  
Thermal Barrier ◽  
X Ray Diffraction ◽  
X Ray ◽  
Granular Particle ◽  
Fine Particle Size ◽  
Ultra Fine Particle ◽  
Different Temperatures

As a new candidate material for the ceramic layer in thermal barrier coatings (TBCs) system, La3NbO7 was synthesized with La2O3 powder and Nb2O5 powder by solid state reaction. The stating powders with a mole ratio of La to Nb of 3:1 were mixed and then the mixture was calcined under the different temperatures(800°C, 1000°C, 1200°C) and dwell times(2h, 6h, 10h). The phase structure of the powder was observed by X–ray diffraction(XRD), and the microstructure of the sample was observed by scanning electron microscope(SEM). The effect of calcination temperature and dwell Time on the phase formation were examined. The results indicate that the La3NbO7 powder with single phase can be synthesized successfully at 1200°C for 10h in air, and the La3NbOsub>7 powders synthesized have an ultra-fine particle size of 0.5˜1µm with a granular particle shape. With the temperature increasing, LaNbO4/sub> was synthesized firstly and then La3NbO7 was synthesized with a mole ratio of La2O3 to LaNbO4 of 1:1.

High Tc Oxide Solid State Reaction Kinetics Via Complex Impedance Spectroscopy

1989 ◽  
Vol 169 ◽  
Author(s):  
E. A. Cooper ◽  
T. O. Mason ◽  
U. Balachandran ◽  
M. L. Kullberg
Keyword(s):  
Activation Energy ◽  
Particle Size ◽  
Solid State ◽  
Solid State Reaction ◽  
Complex Impedance ◽  
Particle Size Effect ◽  
Large Temperature ◽  
Impedance Spectra ◽  
High Tc ◽  
Solid State Reaction Kinetics

AbstractImpedance spectra (5Hz ‐ 13MHz) were collected during the solid state reaction of Yba2Cu2O6+y from large monosized CuO particles imbedded in a finely divided Y2 O3 /BaCO3 matrix. No particle size effect was observed, but a large temperature effect was observed corresponding to an activation energy of approximately 1.8eV (175kJ/mol) over the range 700‐900°C.

SYNTHESIS, MORPHOLOGY AND STRUCTURAL PROPERTIES OF (GD,ND)SR2RUCU2O8 SAMPLES

2003 ◽  
Vol 17 (04n06) ◽  
pp. 899-904 ◽  
Author(s):  
A. VECCHIONE ◽  
M. GOMBOS ◽  
C. TEDESCO ◽  
A. IMMIRZI ◽  
L. MARCHESE ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Solid State ◽  
Powder Diffraction ◽  
Solid State Reaction ◽  
X Ray ◽  
Structure And Morphology ◽  
Polycrystalline Powder ◽  
Scanning Electron

NdSr 2 RuCu 2 O x material has been prepared as polycrystalline powder by solid state reaction. The compound has been investigated by synchrotron x-ray powder diffraction and scanning electron microscopy. The experimental results show that the average crystal structure is a disordered cubic perovskite with Nd and Sr cations occupying the same site and the same substitution is found for Cu and Ru atoms. A comparison between the crystal structure and morphology of this compound and the superconducting tetragonal GdSr 2 RuCu 2 O 8 is also discussed.

Thermal enhancement of 2H11/2→4I15/2 up-conversion luminescence of Er3+ doped K2Yb(PO4)(MoO4) phosphors

2021 ◽  
Author(s):  
Hongqiang Cui ◽  
Yongze Cao ◽  
Lei Zhang ◽  
Yuhang Zhang ◽  
Siying Ran ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Solid State ◽  
Solid State Reaction ◽  
Solid State Reaction Method ◽  
X Ray Diffraction ◽  
Orthorhombic Crystal ◽  
Orthorhombic Crystal Structure ◽  
Reaction Method ◽  
X Ray ◽  
Thermal Enhancement

Er3+ with different concentrations doped K2Yb(PO4)(MoO4) phosphors were prepared by a solid-state reaction method, and the layered orthorhombic crystal structure of the samples was confirmed by X-ray diffraction (XRD). Under...

Changes in Crystallite Size of Tricalcium Silicate during the Laboratory Grinding

2021 ◽  
Vol 321 ◽  
pp. 23-27
Author(s):  
Simona Ravaszová ◽  
Karel Dvořák
Keyword(s):  
Solid State ◽  
Crystallite Size ◽  
Solid State Reaction ◽  
Solid State Reaction Method ◽  
Tricalcium Silicate ◽  
Planetary Mill ◽  
X Ray Diffraction ◽  
Reaction Method ◽  
X Ray ◽  
Grinding Time

The paper is focused on one of the most important component of Portland clinker-on the tricalcium silicate. The study reported in this article is focuses on the changes in crystallite size of synthetic tricalcium silicate obtained using solid state reaction method. Crystallite size changes are monitored during the grinding in three types of laboratory mills in two different conditions. Changing in crystallite size at various grinding time up to 120 minutes are studied with the aid of X-ray diffraction and using the Scherrer equation. It has been found that the most efficient laboratory mill in terms of speed and fineness of the material was the planetary mill.

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