Comparison between Solid State Reaction and Coprecipitation Method of Titanium Oxide Addition on the YBa2Cu3Oδ Ceramics

2020 ◽  
Vol 1010 ◽  
pp. 187-193
Author(s):  
Ali Arlina ◽  
Nadiah Ameram ◽  
Nik Alnur Auli
Keyword(s):  
Solid State ◽  
Solid State Reaction ◽  
Single Phase ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
Orthorhombic Crystal ◽  
Sem Images ◽  
Orthorhombic Crystal Structure ◽  
Oxide Addition ◽  
Co Precipitation

In this work, comparison of TiO2 additions on the physical properties of YBa2Cu3Oδ superconductor system with nominal starting compositions at x= 0, 1, 2, and 5 wt.% was studied derived via solid state reaction and co-precipitation method. The samples were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The result from XRD shown that all the samples were polycrystalline for solid state reaction, while single phase appear for co-precipitation methods. The intensity of the peak become higher with increasing amount of TiO2 addition indicating the presence of increased amount of the unreacted in the samples. The refine lattice parameters indicated that all the samples have an orthorhombic crystal structure without occurrence of orthorhombic-tetragonal phase transformation. Furthermore, from SEM images for solid state reaction and co-precipitation method showed that the grain size of the samples decreased with TiO2 increased. Small addition of TiO2 derived from co-precipitation method enhanced the YBCO microstructures.

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...

scholarly journals Comparative Study on AC Susceptibility of YBa2Cu3O7−δ Added with BaZrO3 Nanoparticles Prepared via Solid-State and Co-Precipitation Method

Crystals ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 655 ◽  
Author(s):  
Nurhidayah Mohd Hapipi ◽  
Jee Lim ◽  
Soo Chen ◽  
Oon Lee ◽  
Abdul Shaari ◽  
...  
Keyword(s):  
Grain Size ◽  
Solid State ◽  
Grain Boundaries ◽  
Ac Susceptibility ◽  
Precipitation Method ◽  
Orthorhombic Crystal ◽  
Orthorhombic Crystal Structure ◽  
Weight Percentage ◽  
Average Grain Size ◽  
Co Precipitation

Polycrystalline samples of YBa2Cu3O7−δ (Y-123) added with x mol% of BaZrO3 (BZO) nanoparticles (x = 0.0, 2.0, 5.0, and 7.0) were synthesized using co-precipitation (COP) and solid-state (SS) method. X-ray diffraction (XRD) patterns showed the formation of Y-123 and Y-211 as the major and minor phases, respectively. The samples prepared using COP method showed higher weight percentage of Y-123 phase (≤98%) compared to the SS samples (≤93%). A peak corresponding to BZO was also found in the samples added with BZO nanoparticles. The increasing intensity of the BZO peak as the BZO amount increased showed the increasing amount of the unreacted nanoparticles in the samples. Refinement of unit cell lattice parameters indicated that all the samples have an orthorhombic crystal structure and there is no orthorhombic-tetragonal phase transformation. As observed using scanning electron microscopy (SEM), all the samples showed randomly distributed grains with irregular shape. The average grain size for the pure sample prepared using COP method is smaller (0.30 µm) compared with that of the pure SS sample (1.24 µm). Addition of 7.0 mol% BZO led to an increase of average grain size to 0.50 μm and 2.71 μm for the COP and SS samples, respectively, indicating grain growth. AC susceptibility (ACS) measurement showed a decrease in the onset critical temperature, Tc-onset with BZO addition. Comparatively, Tc-onset for the COP samples is higher than that of the SS samples. The value of Josephson’s current, Io increased up to 2.0 mol% BZO addition, above which the Io decreased more drastically for the SS samples. The value of Io is 53.95 μA and 32.08 μA for the 2.0 mol% BZO added SS and COP samples, respectively. The decrease of Io is attributed to the distribution of BZO particles at the grain boundaries as also reflected in the drastic decrease of phase lock-in temperature, Tcj. As a result of smaller average grain size, the presence of more grain boundaries containing insulating BZO particles led to lower Io in the COP samples.

Structural, Dielectric and Electrical Studies of Ba4CaRTi3Nb7O30 (R = Eu, Dy) Ferroelectric System

2013 ◽  
Vol 547 ◽  
pp. 41-48 ◽  
Author(s):  
Prasun Ganguly ◽  
A.M. Biradar ◽  
A.K. Jha
Keyword(s):  
Single Phase ◽  
Microstructural Analysis ◽  
Tungsten Bronze ◽  
Negative Temperature ◽  
Xrd Analysis ◽  
Solid State Reaction Method ◽  
X Ray Diffraction ◽  
Orthorhombic Crystal ◽  
Paraelectric Phase Transition ◽  
Orthorhombic Crystal Structure

The polycrystalline samples of Ba4CaRTi3Nb7O30 (R = Eu, Dy), members of tungsten-bronze family, were prepared by high-temperature solid state reaction method and studied for their dielectric and electrical properties. X-ray diffraction (XRD) analysis reveals the formation of single-phase compounds having orthorhombic crystal structure at room temperature. Microstructural analysis by scanning electron microscope (SEM) shows that the compounds have well defined grains, which are distributed uniformly throughout the sample. Detailed dielectric properties of the compounds as a function of frequency and temperature show that the compounds undergo non-relaxor kind of ferroelectric-paraelectric phase transition of diffuse nature. Ferroelectric, piezoelectric and pyroelectric studies of the compounds have been discussed in this paper. The temperature dependence of dc conductivity of the compounds have been investigated. The conductivity study over a wide temperature range suggests that the compounds have negative temperature coefficient of resistance (NTCR) behaviour.

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.

The Preparation and Characterization of LiFe0.98Mn0.02PO4/C by Spray-Drying and Low Temperature Reduction Route

2012 ◽  
Vol 581-582 ◽  
pp. 525-528
Author(s):  
Jia Feng Zhang ◽  
Bao Zhang ◽  
Xue Yi Guo ◽  
He Zhang Chen ◽  
Jian Long Wang ◽  
...  
Keyword(s):  
Low Temperature ◽  
Spray Drying ◽  
Xrd Analysis ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
Sem Images ◽  
Temperature Reduction ◽  
Co Precipitation ◽  
Low Temperature Reduction

The LiFe0.98Mn0.02PO4/C was synthesized by spray-drying and low temperature reduction route using FePO4•2H2O as precursor, which was prepared by a simple co-precipitation method. The LiFe0.98Mn0.02PO4/C sample was characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) and electrochemical measurements. The XRD analysis and SEM images show that sample has the good ordered structure and spherical particle. The charge-discharge tests demonstrate that the powder has the better electrochemical properties, with an initial discharge capacity of 162.1 mAh•g−1 and 155.8 mAh•g−1 at current density of 0.1 C and 1C, respectively. The capacity retention reaches 99.4% after 100 cycles at 1C.

Luminescence Properties of Self-Activated M3(VO4)2 (M = Mg, Ca, Sr, and Ba) Phosphors Synthesized by Solid-State Reaction Method

2016 ◽  
Vol 16 (4) ◽  
pp. 3684-3689 ◽  
Author(s):  
Xin Min ◽  
Zhaohui Huang ◽  
Minghao Fang ◽  
Yan’gai Liu ◽  
Chao Tang ◽  
...  
Keyword(s):  
Solid State ◽  
Solid State Reaction ◽  
Single Phase ◽  
Uv Light ◽  
Solid State Reaction Method ◽  
X Ray Diffraction ◽  
Light Emitting ◽  
Reaction Method ◽  
X Ray ◽  
Yield Decrease

In this paper, M3(VO4)2 (M = Mg, Ca, Sr, and Ba) self-activated phosphors were prepared by a solid-state reaction method at 1,000 °C for 5 h. The phase formation and micrographs were analyzed by X-ray diffraction and scanning electron microscopy. The Ca3(VO4)2 phosphor does not show any emission peaks under excitation with ultraviolet (UV) light. However, the M3(VO4)2 (M = Mg, Sr, and Ba) samples are effectively excited by UV light chips ranging from 200 nm to 400 nm and exhibit broad emission bands due to the charge transfer from the oxygen 2p orbital to the vacant 3d orbital of the vanadium in the VO4. The color of these phosphors changes from yellow to light blue via blue-green with increasing ionic radius from Mg to Sr to Ba. The luminescence lifetimes and quantum yield decrease with the increasing unit cell volume and V–V distance, in the order of Mg3(VO4)2 to Sr3(VO4)2 to Ba3(VO4)2. The emission intensity decreases with the increase of temperatures, but presents no color shift. This confirms that these self-activated M3(VO4)2 phosphors can be suggested as candidates of the single-phase phosphors for light using UV light emitting diodes (LEDs).

Synthesis, Phase Formation and Characterization of Co4Nb2O9 Powders Synthesized by Solid-State Reaction

2008 ◽  
Vol 55-57 ◽  
pp. 873-876 ◽  
Author(s):  
N. Chaiyo ◽  
R. Muanghlua ◽  
A. Ruangphanit ◽  
Wanwilai C. Vittayakorn ◽  
Naratip Vittayakorn
Keyword(s):  
Electron Microscopy ◽  
Solid State ◽  
Solid State Reaction ◽  
Dwell Time ◽  
Single Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Xrd Techniques ◽  
Scanning Electron

A corundum-type structure of cobalt niobate (Co4Nb2O9) has been synthesized by a solid-state reaction. The formation of the Co4Nb2O9 phase in the calcined powders was investigated as a function of calcination conditions by differential thermal analysis (DTA) and X-ray diffraction (XRD) techniques. Morphology and particle size have been determined by scanning electron microscopy (SEM). It was found that the minor phases of unreacted Co3O4 tend to form together with the columbite CoNb2O6 phase at a low calcination temperature and short dwell time. It seems that the single-phase of Co4Nb2O9 in a corundum phase can be obtained successfully at the calcination conditions of 900°C for 60 min, with heating/cooling rates of 20°C /min.

Physical and Optical Properties of Indium Oxide: Tin Nanoparticles Synthesized by Co-Precipitation Method

2015 ◽  
Vol 659 ◽  
pp. 604-608 ◽  
Author(s):  
Jiruntanin Kanoksinwuttipong ◽  
Wisanu Pecharapa ◽  
Russameeruk Noonuruk ◽  
Wicharn Techitdheera
Keyword(s):  
Optical Properties ◽  
Single Phase ◽  
Precipitation Method ◽  
Synthesis Process ◽  
X Ray Diffraction ◽  
Optical Absorbance ◽  
Molar Ratios ◽  
Tin Nanoparticles ◽  
Ion Substitution ◽  
Co Precipitation

Indium oxide:tin nanoparticles were synthesized by co-precipitation method using InCl3 and SnCl4·5H2O as starting precursor with different molar ratios of Sn:In. The crystalline structure, optical properties, chemical bonding and morphologies of all samples were characterized by X-ray diffraction (XRD), UV–vis spectrometer, Raman spectroscopy and field emission scanning electron microscope, respectively. The XRD results show that the crystallinity of as-synthesized powders was initially amorphous phase. After calcination at 400 °C for 2 h, a single phase ITO powder with 10% (mol%) SnO2 was obtained. The particle size of each sample is approximately 20-25 nm. The color of indium oxide:tin nanopowders after heat treatment changed from white to yellow due to the substitution of oxygen vacancies in the sample. After calcination, the intensity of Raman peak significantly decreased with increasing amount of Sn loading. This phenomenon indicates that ion substitution may occur during the synthesis process. Moreover, it is noticed that the optical absorbance of obviously changed with increasing Sn loading.

scholarly journals PREPARATION AND CHARACTERIZATION OF CALCIUM FLUORIDE NANO PARTICLES FOR DENTAL APPLICATIONS

2018 ◽  
Vol 6 (1) ◽  
pp. 338-346 ◽  
Author(s):  
Mohammad S. Al-Ajely ◽  
Kareema M. Ziadan ◽  
Rafed. M. Al-Bader
Keyword(s):  
Elemental Composition ◽  
Calcium Fluoride ◽  
Structural Characteristics ◽  
Nano Particles ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
Sem Images ◽  
Glass Type ◽  
Co Precipitation ◽  
Dental Applications

The aim of the present study was to prepare a calcium fluoride (CaF2NP) Nano particle which is used in dental composites as dental filling compo glass type. CaF2 Nano powders were prepared using a Co-precipitation method using binary liquid. Crystal Structural characteristics and Elemental composition of (CaF2NP) Nanoparticles were predicted by X-ray diffraction (XRD), which showed crystalline peaks of   this material. Elemental composition was obtained from EDX analysis.  Morphology and diameters of the Nano fibers were studied by scanning electron Microscope (SEM). The size of the particles was also measured from SEM images about 58 ± 21 nm.

Quaternary Chalcogenide Nanocrystals: Synthesis of Cu2ZnSnSe4 by Solid State Reaction and their Thermoelectric Properties

2013 ◽  
Vol 1543 ◽  
pp. 137-142 ◽  
Author(s):  
Umme Farva ◽  
Chan Park
Keyword(s):  
Solid State ◽  
Thermoelectric Properties ◽  
Solid State Reaction ◽  
Single Phase ◽  
Cost Effective ◽  
Solid State Reaction Method ◽  
Milling Process ◽  
Alloying Effect ◽  
Sem Images ◽  
Uniform Size

ABSTRACTIn this paper, synthesis of Cu2ZnSnSe4 (CZTSe) materials by using simple and cost-effective solid state reaction method from the elemental Cu, ZnO, SnO and elemental Se powders are carried out. The SEM images show spherical, non-uniform size with aggregation of nanopowders. The phase separation and thermal analysis of the milled powders suggested that most of the starting powders reacted because of a mechanical alloying effect during milling process. After the solid state reaction at above 500 °C, the nanopowders crystallized into stannite single phase, which are confirm by XRD spectra. The thermoelectric properties of synthesized powder are under study.

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