Study of Microstructure in 0.9PMNTa-0.1PT Ceramics

2000 ◽  
Author(s):  
Jin T. Wang ◽  
Feng Tang
Keyword(s):  
Grain Size ◽  
Lead Titanate ◽  
Lead Magnesium Niobate ◽  
Scanning Electron Micrographs ◽  
X Ray Diffraction ◽  
X Ray ◽  
Chemical Content ◽  
Lead Magnesium ◽  
Ta Doping ◽  
Scanning Electron

Abstract Ta-Doping effect on the microstructure of lead magnesium niobate-lead titanate crystalline solutions 0.9PbMg1/3(Nb(1−x)Tax)2/3O3-0.1PbTiO3(PMN-PT) have been firstly investigated in this paper. Scanning Electron Micrographs (SEM) were taken from fractured surfaces of the samples with different additives of x = 0.0, 0.1, 0.2, 0.3 and 1.0 by Hitachi F-2460N microscope operating at an accelerating voltage of 25kV. The chemical content analysis for the synthesized samples performed on JEOL Super Prob733 Energy Perspective Spectrum. The x-ray diffraction was carried out with a Siemens D5000 Dual Diffraction Meter. It is clearly evident that doping Ta in PMNTa-PT can affect the grain size and density of the compounds. Smaller grain size (3.1μm) is formed in the specimens with the additives of x = 0.1, 0.2 and 0.3 in comparison with those of the specimens without doping (6.6μm) or over doping (6.4μm). The porosity at grain intersections increase with increasing of additive tantalum for niobium site in 0.9PMNTa-0.1PT. Larger grain size (6.4μm), greater non-uniformity and more inter-granular voids are found in the compound, if tantalum completely substitutes niobium (x = 1). No non-reacted starting regents were observed in any of the compositions mentioned above.

Single crystal x-ray diffraction of lead magnesium niobate-lead titanate in the transmission mode

2006 ◽  
Vol 89 (9) ◽  
pp. 092903 ◽  
Author(s):  
Alp Sehirlioglu ◽  
David A. Payne ◽  
Scott R. Wilson ◽  
Pengdi Han
Keyword(s):  
Single Crystal ◽  
Lead Titanate ◽  
Lead Magnesium Niobate ◽  
Transmission Mode ◽  
X Ray Diffraction ◽  
X Ray ◽  
Magnesium Niobate ◽  
Lead Magnesium

The Synthesis of Cu0.81Ni0.19 Intermetallics by Mechanical Alloying

2012 ◽  
Vol 496 ◽  
pp. 379-382
Author(s):  
Rui Song Yang ◽  
Ming Tian Li ◽  
Chun Hai Liu ◽  
Xue Jun Cui ◽  
Yong Zhong Jin
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Grain Size ◽  
Mechanical Alloying ◽  
Milling Time ◽  
Elemental Powder ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scherrer Equation ◽  
Scanning Electron

The Cu0.81Ni0.19 has been synthesized directly from elemental powder of nickel and copper by mechanical alloying. The alloyed Cu0.81Ni0.19 alloy powders are prepared by milling of 8h. The grain size calculated by Scherrer equation of the NiCu alloy decreased with the increasing of milling time. The end-product was analyzed by X-ray diffraction (XRD), scanning electron microscopy (SEM)

Hydrothermal Synthesis of Lead Titanate Epitaxial Film for Non-Volatile Memory Device Application

2013 ◽  
Vol 652-654 ◽  
pp. 1846-1850
Author(s):  
Thin Thin Thwe ◽  
Than Than Win ◽  
Yin Maung Maung ◽  
Ko Ko Kyaw Soe
Keyword(s):  
Electron Microscopy ◽  
Silicon Dioxide ◽  
Lead Titanate ◽  
Conduction Mechanism ◽  
Epitaxial Film ◽  
Memory Device ◽  
X Ray Diffraction ◽  
X Ray ◽  
Non Volatile Memory ◽  
Scanning Electron

Hydrothermal synthesized lead titanate (PbTiO3¬) powder was prepared in a Teflon-lined stainless steel bomb at different bath temperatures. X-ray diffraction was performed to examine the phase assignment and crystallographic properties of hydrothermal synthesized lead titanate powder. Silicon dioxide (SiO2) was thermally deposited and adapted as intermediate layer on p-Si (100) substrates for MFIS (Metal/Ferroelectric/ Insulator/Semi-conductor) design. The microstructures of PbTiO3 film for both MFS and MFIS designs were observed by scanning electron microscopy (SEM). Charge conduction mechanism was also interpreted by C-2-V relationship. Polarization and electric field characteristics were measured by Sawyer-Tower circuit and good hysteresis nature was formed for both structures of the films. The loop of MFIS was wider than that of MFS cell. Also, the higher value of polarization (Ps=3.21E-03µC/cm2) for MFIS could be explained on the basis of higher dipole moment in this SiO2 buffer layer.

Study on the Properties of Doped La in BaBi4Ti4O15 Ceramic

2007 ◽  
Vol 26-28 ◽  
pp. 243-246
Author(s):  
Xing Hua Yang ◽  
Jin Liang Huang ◽  
Xiao Wang ◽  
Chun Wei Cui
Keyword(s):  
Crystal Structure ◽  
Grain Size ◽  
Electron Microscope ◽  
Scanning Electron Microscope ◽  
Sintering Temperature ◽  
Solid Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Lanthanum Content ◽  
Scanning Electron

BaBi4-xLaxTi4O15 (BBLT) ceramics were prepared by conventional solid phase sintering ceramics processing technology. The crystal structure and the microstructure were detected by X-ray diffraction (XRD) and scanning electron microscope (SEM). The XRD analyses show that La3+ ions doping did not change the crystal structure of BBT ceramics. The sintering temperature increased from 1120°C to 1150°C with increasing Lanthanum content from 0 to 0.5, but it widened the sintering temperature range from 20°C to 50°C and refined the grain size of the BBT ceramic. Additionally, polarization treatment was performed and finally piezoelectric property was measured. As a result, the piezoelectric constant d33 of the 0.1at.% doped BBLT ceramics reached its highest value about 22pc/N at polarizing electric field of 8kV/mm and polarizing temperature of 120°C for 30min.

scholarly journals Photocatalytic Degradation of Nitro and Chlorophenols Using Doped and Undoped Titanium Dioxide Nanoparticles

2011 ◽  
Vol 2011 ◽  
pp. 1-8 ◽  
Author(s):  
Hassan Ilyas ◽  
Ishtiaq A. Qazi ◽  
Wasim Asgar ◽  
M. Ali Awan ◽  
Zahir-ud-din Khan
Keyword(s):  
Photocatalytic Degradation ◽  
Crystallite Size ◽  
Model Compound ◽  
Titanium Dioxide Nanoparticles ◽  
Xrd Analysis ◽  
Scanning Electron Micrographs ◽  
X Ray Diffraction ◽  
X Ray ◽  
Liquid Impregnation ◽  
Scanning Electron

Pure and Ag-TiO2nanoparticles were synthesized, with the metallic doping being done using the Liquid Impregnation (LI) method. The resulting nanoparticles were characterized by analytical methods such as scanning electron micrographs (SEMs), Energy Dispersive Spectroscopy (EDS), and X-ray diffraction (XRD). XRD analysis indicated that the crystallite size ofTiO2was 27 nm to 42 nm while the crystallite size of Ag-TiO2was 11.27 nm to 42.52 nm. The photocatalytic activity of pureTiO2and silver dopedTiO2was tested by photocatalytic degradation ofp-nitrophenol as a model compound. Ag-TiO2nanoparticles exhibited better results (98% degradation) as compared to pureTiO2nanoparticles (83% degradation) in 1 hour for the degradation ofp-nitrophenol. Ag-TiO2was further used for the photocatalytic degradation of 2,4-dichlorphenol (99% degradation), 2,5-dichlorophenol (98% degradation), and 2,4,6-trichlorophenol (96% degradation) in 1 hour. The degree of mineralization was tested by TOC experiment indicating that 2,4-DCP was completely mineralized, while 2,5-DCP was mineralized upto 95 percent and 2,4,6-TCP upto 86 percent within a period of 2 hours.

Light Burning Condition of Preparing Dolomite Clinker Using Natural Dolomite

2018 ◽  
Vol 281 ◽  
pp. 156-162
Author(s):  
Wang Nian Zhang ◽  
Xi Tang Wang ◽  
Zhou Fu Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Grain Size ◽  
Sintering Process ◽  
X Ray Diffraction ◽  
Burning Temperature ◽  
X Ray ◽  
Temperature Range ◽  
Scanning Electron

The influence of the light burning temperature on the sintering property of nature dolomite has been investigated by two-step sintering process in the temperature range 1500 °C to 1600 °C. The resulting bulk densities and apparent porosities of the sintered dolomite samples were examined, and analyzing the sintered dolomite by scanning electron microscopy and X-ray diffraction were performed. The results showed light burned at 850 °C for 3 h, the main phases of the dolomite with 3-5 grain size were MgO, CaO and little CaCO3, and then fired at 1600 °C,the density of sintering dolomite reached to 3.38 g/cm3, the apparent property was 1.2 %, the size of MgO grain up to 3.75 μm . However when dolomite light burned at 1050 °C for 3 h, the main phases were MgO and CaO, and then fired at 1600 °C,the density of sintering dolomite only was 3.30 g/cm3, the apparent property was 2.3 %, the size of MgO only was 3.05 μm .

The Effects of Al-Ca Compounds on Grain Refinement of Mg-Ca Alloys

2011 ◽  
Vol 686 ◽  
pp. 348-354 ◽  
Author(s):  
Shu Tao Xiong ◽  
Fu Sheng Pan ◽  
Bin Jiang ◽  
Xiao Ke Li
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Grain Size ◽  
Grain Refinement ◽  
X Ray Diffraction ◽  
X Ray ◽  
Metallic Compound ◽  
Scanning Electron ◽  
Main Factor

In the present work, Al-Ca metallic compound was prepared in Mg-Ca alloys and the effects of Al-Ca metallic compound and different Al/Ca values on the grain refinement of Mg-Ca alloys were investigated by scanning electron microscopy and X-ray diffraction, and the mechanism of grain refinement of Mg-Ca alloys was discussed. The results showed that the grain size of Mg-0.5Ca alloy was obviously reduced from 550μm to 230μm due to the addition of Al. Al2Ca phase existed in these alloys and its morphology evolved from granular to rod-like. It is regarded as the main factor for the grain refinement.

Synthesis, Structural Characterization and Morphological Studies of Nanocrystalline CdO by Wet-Chemical Method

2018 ◽  
Vol 24 (8) ◽  
pp. 5519-5522
Author(s):  
Israr Ul Hassan ◽  
Liji John ◽  
R. Selwin Joseyphus ◽  
I. Hubert Joe ◽  
R. S Amritha ◽  
...  
Keyword(s):  
Grain Size ◽  
Chemical Method ◽  
Cadmium Oxide ◽  
X Ray Diffraction ◽  
Wet Chemical Method ◽  
X Ray ◽  
Morphological Studies ◽  
Oxide Particles ◽  
Wet Chemical ◽  
Scanning Electron

Synthesis of nanocrystalline cadmium oxide particles were explored by the reaction of inorganic precursor (cadmium chloride) and alkali (sodium hydroxide) via modified wet-chemical method followed by annealing at various temperatures (250, 500 and 750 °C). The structural, optical and morphological studies of cadmium oxide samples were carried out by X-ray diffraction, infrared, ultraviolet-visible, and scanning electron microscope techniques. From X-ray diffraction analysis, it was confirmed that cadmium oxide particles furnish a face centred cubic phase structure and revealing a grain size of around 59 nm. The scanning electron microscope micrographs admit that cadmium oxide samples are agglomerated and have spherical shapes. The bonding deformation and stretching frequency results of cadmium oxide samples were obtained from infrared spectra. The corresponding increase in calcination temperatures has shown an increase in particle size while as no change was found in band gape. These results attribute that the variation in annealing temperature has a significant role on the crystalline nature, grain size and its optical properties. Furthermore, the synthesized cadmium oxide samples were examined for bioactivity analysis.

Processing of Nano Hydroxyapatite from Eggshell and Seashell

2010 ◽  
Vol 659 ◽  
pp. 159-164 ◽  
Author(s):  
Gréta Gergely ◽  
Ferenc Wéber ◽  
Mihály Tóth ◽  
Attila Lajos Tóth ◽  
Zsolt E. Horváth ◽  
...  
Keyword(s):  
Heat Treatment ◽  
Grain Size ◽  
Ball Milling ◽  
Milling Process ◽  
Effect Of Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Attrition Milling ◽  
Milling Method ◽  
Scanning Electron

Hydroxyapatite (HAp) was successfully produced from recycled eggshell, seashell and phosphoric acid by using two different type of milling method (attrition milling and ball milling). According to the analysis, the attrition milling resulted nanosize HAp even after milling, while the ball milling process provided HAp only after a 400oC, 2 h long heat treatment. The grain size in both cases were approximately preserved during the heat treatment. The effect of temperature on stoichiometry, morphology and crystallinity of HAp powders were investigated. The structures of the HAp were characterized by X-ray diffraction and Scanning Electron Microsopy.

Influence of Annealing Time on Microstructure of Ni-W Alloys

2013 ◽  
Vol 747-748 ◽  
pp. 613-618
Author(s):  
Qiao Zhang ◽  
Shu Hua Liang ◽  
Chen Zhang ◽  
Jun Tao Zou
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Grain Size ◽  
Grain Boundaries ◽  
Annealing Time ◽  
Single Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Average Grain Size ◽  
Scanning Electron

The as-cast Ni-W alloys with 15wt%W, 25wt%W and 30wt%W were annealed in hydrogen at 1100. The effect of the annealing time on the microstructure of Ni-W alloys was studied, and the phase constituents and microstructure of annealed Ni-W alloys were characterized by the X-ray diffraction (XRD) and scanning electron microscopy (SEM). The results showed that no any phase changed for Ni-15%W, Ni-25%W and Ni-30%W alloys annealed for 60 min, 90 min and 150 min, which were still consisted of single-phase Ni (W) solid solution. However, microstructure had a significant change after annealing. With increase of annealing time, the microstructure of Ni-15%W alloy became more uniform after annealing for 90 min, and the average grain size was 95μm, whereas the grain size of Ni-15%W alloy increased significantly after annealing for 150 min. For Ni-25%W and Ni-30%W, there was no obvious change on the grain size with increase of annealing time, and the amount of oxides at grain boundaries gradually reduced. After annealing for 150 min, the impurities at grain boundaries almost disappeared. Subsequently, the annealing at 1100 for 150 min was beneficial for the desired microstructure of Ni-25%W and Ni-30%W alloys.

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