The Effect of Calcination Temperatures on the Phase Formation and Microstructure of (Pb1-xSrx)TiO3 Powders

2009 ◽  
Vol 421-422 ◽  
pp. 243-246 ◽  
Author(s):  
R. Sumang ◽  
Theerachai Bongkarn
Keyword(s):  
Single Phase ◽  
Average Particle Size ◽  
Solid State Reaction Method ◽  
Lattice Parameter ◽  
Average Particle ◽  
Reaction Method ◽  
X Ray ◽  
Calcination Temperatures ◽  
Powder Samples ◽  
Scanning Electron

(Pb1-xSrx)TiO3 (PST) (x=0.25, 0.50) powders were synthesized by a mixed oxide solid-state reaction method under various calcination temperatures (600-1100oC). Powder samples were characterized using thermogravimetric (TGA), differential thermal analysis (DTA), x–ray diffractrometer (XRD) and scanning electron microscopy (SEM). The results showed that a single-phase of PST for x=0.25 and 0.50 powders was successfully obtained with a calcination condition of 950 oC for 2 h with a heating/cooling rate of 5oC/min. The TGA-DTA results corresponded to the XRD investigation. The lattice parameter a increased whilst the lattice parameter c decreased with increasing calcination temperatures. The tetragonality of powders decreased with an increase of calcination temperatures. The average particle size of the powders increased with the increase of calcination temperature.

scholarly journals Thermoelectric properties of LaFeO3 system with doped Ti, Co, Cu

2017 ◽  
Vol 126 (1B) ◽  
pp. 147
Author(s):  
Nguyen Thi Thuy
Keyword(s):  
Electron Microscope ◽  
Solid State ◽  
Room Temperature ◽  
Unit Cell Volume ◽  
Single Phase ◽  
Solid State Reaction Method ◽  
X Ray Diffraction ◽  
Reaction Method ◽  
X Ray ◽  
Scanning Electron

<p><strong>Abstract: </strong>LaFeO<sub>3</sub> system with doped Ti, Co, Cu was manufactured by solid state reaction method, it was sintered at 1250<sup>0</sup>C and 1290<sup>0</sup>C in 10 hours with a heating rate of 3<sup>0</sup>C/min. Using X-ray diffraction and Scanning Electron Microscope (SEM) to examine the structure, it reveals that samples are single-phase and orthogonal-perovskite structure describing by the Pnma space group, the unit cell volume of the samples increases when Ti, Co, Cu are doped to replace ion Fe<sup>+3</sup>. The size of particle increase while raising the temperature of sintering. Measuring the resistance which depends on temperature between the room temperature and 1000K, it can be seen that when doping Co, Cu with the nominal component La(Fe<sub>0,2</sub>Co<sub>0,2</sub>Ti<sub>0,6</sub>)O<sub>3</sub> and La(Fe<sub>0,4</sub>Cu<sub>0,1</sub>Ti<sub>0,5</sub>)O<sub>3 </sub>, the conductivity of samples increases respectively. Especially, the conductivity of Cu doped sample is higher than two other samples, and reach the highest conductivity at about 900<sup>0</sup>C, Seebeck coefficient S of La(Fe<sub>0.6</sub>Ti<sub>0.4</sub>)O<sub>3</sub> can be change from positive to negative at the temperature of around 700<sup>0</sup>C.</p>

Influences of Firing Temperatures on Phase and Morphology Evolution of (Ba0.25Sr0.75)(Zr0.75Ti0.25)O3 Ceramics Synthesized via Solid-State Reaction Method

2009 ◽  
Vol 421-422 ◽  
pp. 247-250 ◽  
Author(s):  
Atthakorn Thongtha ◽  
Kritsana Angsukased ◽  
Theerachai Bongkarn
Keyword(s):  
Solid State ◽  
Solid State Reaction ◽  
Perovskite Phase ◽  
Average Particle Size ◽  
Solid State Reaction Method ◽  
Lattice Parameter ◽  
Average Particle ◽  
Strontium Zirconate ◽  
Reaction Method ◽  
Average Grain Size

The effect of calcination (1000-1400 oC) and sintering temperatures (1400-1600 oC) on the phase formation and microstructure of barium strontium zirconate titanate [(Ba0.25Sr0.75)(Zr0.75Ti0.25)O3; BSZT] ceramics were investigated. BSZT powders were prepared by the solid-state reaction method. Higher calcination temperatures increased the percentage of the perovskite phase, but decreased the lattice parameter a of BSZT powders. The pure perovskite phase of BSZT powders was detected above the calcination temperature of 1350 oC. The microstructure of BSZT powders exhibited an almost-spherical morphology and had a porous agglomerated form. The average particle size and the average grain size of the ceramics were increased with the increase of calcination and sintering temperatures. The highest density of the samples was 5.42 g/cm3 which was obtained from ceramic sintered at 1550 oC for 2 h.

scholarly journals Effect of Co-Ti Substitution on Magnetic Properties of Nanocrystalline BaFe12O19

2016 ◽  
Vol 1 (1) ◽  
Author(s):  
Erfan Handoko
Keyword(s):  
Magnetic Properties ◽  
Single Phase ◽  
Solid State Reaction Method ◽  
X Ray Diffraction ◽  
Polycrystalline Structure ◽  
Reaction Method ◽  
X Ray ◽  
Ti Substitution ◽  
Scanning Electron ◽  
Microstructure And Magnetic Properties

<p>The synthesis of nanocrystalline BaFe<sub>12-2x</sub>Co<sub>x</sub>Ti<sub>x</sub>O<sub>19</sub> with variations of x (x = 0, 1, 2, and 3) have been investigated. The formation of polycrystalline samples that the cationic of Co<sup>2+</sup> and Ti<sup>4+</sup> in Co-Ti substituted Fe in BaFe<sub>12</sub>O<sub>19</sub> ferrites structure were prepared by solid state reaction method. The crystal structure, microstructure, and magnetic properties were characterized using powder X-ray diffraction, scanning electron microscope (SEM) and permagraph meter, respectively. The results show that the nanocrystalline BaFe<sub>12-2x</sub>Co<sub>x</sub>Ti<sub>x</sub>O<sub>19</sub> has single phase with polycrystalline structure, the grain size decrease by doping, the coercivity (Hc) and saturation magnetization (Ms) decrease with increasing Co-Ti substitutions. </p>

Effect of Calcination Temperatures on Microstructure and Phase Formation of Ba(Zr0.25Ti0.75)O3 Powders

2008 ◽  
Vol 55-57 ◽  
pp. 205-208 ◽  
Author(s):  
Theerachai Bongkarn ◽  
N. Phungjitt ◽  
Naratip Vittayakorn
Keyword(s):  
Phase Formation ◽  
Perovskite Phase ◽  
Solid State Reaction Method ◽  
Lattice Parameter ◽  
Average Particle ◽  
Particle Sizes ◽  
Reaction Method ◽  
Calcination Temperatures ◽  
Pure Perovskite Phase ◽  
Second Phases

In this work, the effect of calcination temperatures on the microstructure and phase formation of Ba(Zr0.25Ti0.75)O3 (BZT) powders were investigated. The BZT powders were prepared via the solid state reaction method under various calcination temperatures. It was found that the second phases such as BaCO3, ZrO2, BaZrO3 and Ba2ZrO4 existed in samples with calcination temperature below 1200 oC. Homogeneity and a highly pure perovskite phase of the BZT powders were obtained with calcination condition at 1300 oC for 4 h. Lattice parameter a and the percentage of cubic perovskite phase tended to increase with increasing calcination temperatures. The TG-DTA results corresponded to the XRD investigation. The microstructures of calcined powders exhibited an almost-spherical morphology and had a porous agglomerated form in all samples. The average particle sizes were increased from 0.2 to 1.1mµ when calcination temperatures were increased from 800 to 1350 oC.

Synthesis and Dielectric Properties of Ba(Ti,Y)O3 Solid Solutions to Ba3Ti2YO8.5-BaTiO3 Composites

2011 ◽  
Vol 194-196 ◽  
pp. 109-112
Author(s):  
Min Huang ◽  
Yun Wu Wang
Keyword(s):  
Single Phase ◽  
Xrd Analysis ◽  
Solid State Reaction Method ◽  
Nominal Composition ◽  
X Ray Diffraction ◽  
Reaction Method ◽  
X Ray ◽  
Microstructure Observation ◽  
Ceramic Samples ◽  
Scanning Electron

Ceramic samples with the nominal composition (1-x) BaTiO3 + x Ba3Ti2YO8.5 (x = 0 - 0.4) were prepared by the solid-state reaction method. The X-ray diffraction (XRD) analysis and the lattice parameters determination indicate that the samples with x≤ 0.16 exhibit a single phase cubic perovskite structure. When x > 0.16, the system is of biphasic composites, which consist of Ba(Ti0.911Y0.089)O3 and Ba3Ti2YO8.5. The microstructure observation by Scanning Electron Microscopy (SEM) supports the XRD result. For the biphasic composites, the dielectric constant follows the Lichtenecker relation in a wide temperature range.

Effects of Calcination Temperatures on Phase and Morphology Evolution of (Ba0.25Sr0.75)(Zr0.75Ti0.25)O3 Powders Synthesized via Solid-State Reaction and Combustion Technique

2008 ◽  
Vol 55-57 ◽  
pp. 197-200 ◽  
Author(s):  
Atthakorn Thongtha ◽  
Kritsana Angsukased ◽  
Theerachai Bongkarn
Keyword(s):  
Solid State ◽  
Solid State Reaction ◽  
Perovskite Phase ◽  
Solid State Reaction Method ◽  
Lattice Parameter ◽  
Average Particle ◽  
Strontium Zirconate ◽  
Reaction Method ◽  
Calcination Temperatures ◽  
Combustion Technique

The effect of calcination temperatures (1000-1400 oC) on the phase formation and microstructure of barium strontium zirconate titanate [(Ba0.25Sr0.75)(Zr0.75Ti0.25)O3 ; BSZT] powders were investigated. BSZT powders were prepared and compared by the solid state reaction method and the combustion technique. The higher calcination temperatures increased the percentage of the perovskite phase, but decreased the lattice parameter a. The same crystallographic pure perovskite phase of BSZT powders, which were prepared via the combustion technique were detected above 1300 oC ; which was lower than the calcinations temperature of mixed oxide method by 50 oC. The TGA-DTA results corresponded to XRD investigation. The microstructure of BSZT powders, which were prepared using both techniques, exhibited an almost-spherical morphology and had a porous agglomerated form. The average particle sizes of BSZT powders prepared via the combustion technique (0.13-0.30 µm) and the solid state reaction method (0.18-0.38 µm) were increased with the increase of calcinations temperatures

Effect of Co-Ti Substitution on Magnetic Properties of Nanocrystalline BaFe12O19

2016 ◽  
Vol 1 ◽  
Author(s):  
Erfan Handoko
Keyword(s):  
Magnetic Properties ◽  
Single Phase ◽  
Solid State Reaction Method ◽  
X Ray Diffraction ◽  
Polycrystalline Structure ◽  
Reaction Method ◽  
X Ray ◽  
Ti Substitution ◽  
Scanning Electron ◽  
Microstructure And Magnetic Properties

<p>The synthesis of nanocrystalline BaFe<sub>12-2x</sub>Co<sub>x</sub>Ti<sub>x</sub>O<sub>19</sub> with variations of x (x = 0, 1, 2, and 3) have been investigated. The formation of polycrystalline samples that the cationic of Co<sup>2+</sup> and Ti<sup>4+</sup> in Co-Ti substituted Fe in BaFe<sub>12</sub>O<sub>19</sub> ferrites structure were prepared by solid state reaction method. The crystal structure, microstructure, and magnetic properties were characterized using powder X-ray diffraction, scanning electron microscope (SEM) and permagraph meter, respectively. The results show that the nanocrystalline BaFe<sub>12-2x</sub>Co<sub>x</sub>Ti<sub>x</sub>O<sub>19</sub> has single phase with polycrystalline structure, the grain size decrease by doping, the coercivity (Hc) and saturation magnetization (Ms) decrease with increasing Co-Ti substitutions. </p>

Influence of Excess Bi2O3 and Na2Co3 on Crystal Structure and Microstructure of Bismuth Sodium Titanate Ceramics

2011 ◽  
Vol 474-476 ◽  
pp. 1711-1714 ◽  
Author(s):  
Panadda Sittiketkron ◽  
Arrak Klinbumrung ◽  
Theerachai Bongkarn
Keyword(s):  
Crystal Structure ◽  
Dielectric Properties ◽  
Perovskite Phase ◽  
Average Particle Size ◽  
Sodium Titanate ◽  
Solid State Reaction Method ◽  
Lattice Parameter ◽  
Rhombohedral Structure ◽  
Average Particle ◽  
Average Grain Size

This study investigated the influence of excess Bi2O3 and Na2CO3 on the crystal structure, microstructure and dielectric properties of (Bi0.5Na0.5)TiO3 (BNT) ceramics. The BNT ceramics were synthesized using the solid-state reaction method with various excess Bi2O3 and Na2CO3 levels (0, 1, 2, 3 and 4 mol%). The X-ray characterization revealed that all samples had a rhombohedral structure. A pure perovskite phase was obtained in all samples. The lattice parameter a tended to increase with increased excess Bi2O3 and Na2CO3 content in the calcined powders and sintered ceramics. The average particle size increased while, the average grain size tended to decreased with increased of excess Bi2O3 and Na2CO3 content. The depolarization temperature (Td) and the Curie temperature (Tc) were slightly decreased with the increase of excess Bi2O3 and Na2CO3 content. The dielectric properties were related to the density.

scholarly journals Investigations of M3Al8O15:Eu3+,Dy3+ (M = Ba, Ca, Mg) phosphors

2016 ◽  
Vol 34 (2) ◽  
pp. 412-417
Author(s):  
Esra Öztürk
Keyword(s):  
Electron Microscopy ◽  
Solid State Reaction Method ◽  
Morphological Characterization ◽  
X Ray Diffraction ◽  
Reaction Method ◽  
X Ray ◽  
Three Samples ◽  
Scanning Electron ◽  
The Eu

AbstractIn this work, aluminate type phosphorescence materials were synthesized via the solid state reaction method and the photoluminescence (PL) properties, including excitation and emission bands, were investigated considering the effect of trace amounts of activator (Eu3+) and co-activator (Dy3+). The estimated thermal behavior of the samples at certain temperatures (> 1000 °C) during heat treatment was characterized by differential thermal analysis (DTA) and thermogravimetry (TG). The possible phase formation was characterized by X-ray diffraction (XRD). The morphological characterization of the samples was performed by scanning electron microscopy (SEM). The PL analysis of three samples showed maximum emission bands at around 610 nm, and additionally near 589 nm, 648 nm and 695 nm. The bands were attributed to typical transitions of the Eu3+ ions.

scholarly journals Pengaruh Suhu Sintering Terhadap Sintesis Silicon Carbide (SiC) Berbahan Dasar Abu Sekam Padi dan Grafit Pensil 2B

2015 ◽  
Vol 5 (01) ◽  
pp. 31
Author(s):  
Resky Irfanita ◽  
Asnaeni Ansar ◽  
Ayu Hardianti Pratiwi ◽  
Jasruddin J ◽  
Subaer S
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Silicon Carbide ◽  
Rice Husk Ash ◽  
Sintering Temperature ◽  
Solid State Reaction Method ◽  
X Ray Diffraction ◽  
Reaction Method ◽  
X Ray ◽  
Scanning Electron

The objective of this study is to investigate the effect of sintering temperature on the synthesis of SiC produced from rice husk ash (RHA) and 2B graphite pencils. The SiC was synthesized by using solid state reaction method sintered at temperatures of 750°C, 1000°C and 1200°C for 26 hours, 11.5 hours and 11.5 hours, respectively. The quantity and crystallinity level of SiC phase were measured by means of Rigaku MiniFlexII X-Ray Diffraction (XRD). The microstructure of SiC was examined by using Tescan Vega3SB Scanning Electron Microscopy (SEM). The XRD results showed that the concentration (wt%) of SiC phase increases with the increasing of sintering temperature. SEM results showed that the crystallinity level of SiC crystal is improving as the sintering temperature increases

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