Effect of Glass Addition on the Properties of CaCu3Ti4O12 Ceramics

2016 ◽  
Vol 840 ◽  
pp. 52-56 ◽  
Author(s):  
Julie Juliewatty Mohamed ◽  
Mohd Fariz Ab Rahman ◽  
Mohd Fadzil Ain ◽  
Zainal Arifin Ahmad
Keyword(s):  
Raw Materials ◽  
Secondary Phase ◽  
Xrd Analysis ◽  
Solid State Reaction Method ◽  
Glass Addition ◽  
Reaction Method ◽  
X Ray ◽  
Fine Powders ◽  
Glass Additive ◽  
Ccto Sample

The effect of glass addition on the properties of CaCu3Ti4O12 (CCTO) ceramics was studied. CCTO ceramics with BaO-SrO-Nb2O5-B2O3-SiO2 (BSNBS) glass additive were prepared using solid state reaction method. The raw materials of CCTO and BSNBS were wet mixed separately for 24 hours, dried overnight and subsequently the BSNBS powders was melted at 1450°C for 2 hours while CCTO powders was calcined at 900°C for 12 hours. BSNBS glass then was grinded to form a fine powders. Different weight percentages of BSNBS powder were added into CCTO and the powders were wet mixed at 24 hours. The mixtures were dried, compacted at 250 MPa and then sintered at 1050°C for 10 hours. X-Ray Diffractometer (XRD) analysis showed the formation of CCTO phase for all sintered samples while secondary phase of CuO phase was identified for sintered BSNBS 1.0 sample. Observation on Scanning Electron Microscopy (SEM) micrographs showed abnormal grain growth was seen in CCTO sample and grain size of the samples become finer with increasing the concentration glass addition. CCTO sample obtained the highest dielectric constant (8670) while the lowest dielectric loss (0.38) was recorded by BSNBS 0.10 sample, measured at 1 MHz.

Synthesis of Nb2AlC Material by High Temperature Solid State Reaction Method

2015 ◽  
Vol 655 ◽  
pp. 240-243 ◽  
Author(s):  
Yu Chen Wang ◽  
Zhen Hua Liang ◽  
Gui Hua Peng ◽  
Jian Guang Xu
Keyword(s):  
High Temperature ◽  
Solid State ◽  
Solid State Reaction ◽  
Raw Materials ◽  
Heating Temperature ◽  
Solid State Reaction Method ◽  
Atomic Ratio ◽  
Reaction Method ◽  
X Ray ◽  
Scanning Electron

The Nb2AlC powders were synthesized by high temperature solid state reaction method ,in which, the mixed powders of niobium (Nb), aluminum (Al) , graphite (C) were used as raw materials in an atomic ratio of 2.0:1.1:1.0, respectively. And the heating temperature was adjusted in a range of 1600–1650°C in order to investigate the effects of different preparing conditions on the synthesis of Nb2AlC .The phase composition and morphology of the products were analyzed by X-ray powder diffraction (XRD), scanning electron microscopy (SEM) respectively. The results indicated that all the XRD peaks can be indexed as Nb2AlC with improved crystallization at 1610°C.And the SEM photographs show that the products are layered morphology.The reaction mechanism of Nb2AlC synthesis was also studied.

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.

Synthesis and Structural Characterization of La0.8Sr0.2MO3 (M=Mn, Fe, Co and Cr) Solid Ionic Material for Catalyst Application

2016 ◽  
Vol 840 ◽  
pp. 48-51
Author(s):  
Muhammad Nor Azri Aziz ◽  
Johar Banjuraizah ◽  
Shing Fhan Khor ◽  
Zainal Arifin Ahmad
Keyword(s):  
Crystal Structure ◽  
Electron Microscopy ◽  
Raw Materials ◽  
Solid State Reaction Method ◽  
Cold Isostatic Pressing ◽  
X Ray Diffraction ◽  
Reaction Method ◽  
X Ray ◽  
Scanning Electron

La0.8Sr0.2MO3+δ, (M=Mn, Fe, Cr, Co) ceramics were prepared by using solid state reaction method. All raw materials were mixed and ground using mortar. Homogenized powders were calcined at 900°C for three hour followed by grounding and uniaxial pressed at 100MPa. Compacted pellets were further pressed using cold isostatic pressing machine at 2600kg/m.s and sintered at 1300°C with heating rate 5°C/min for 4 hour. Crystal structure and phase transformation of sintered samples were obtained using X-ray diffraction. Density and porosity are measured by using Archimedes principle. The morphology of sintered samples is observed using scanning electron microscopy, while elemental analysis using the EDX.

Magnetic Properties of Bulk Zn0.95-XMnXFe0.05O2 Prepared by Sol-Gel Method and Subsequent Hot Pressing

2011 ◽  
Vol 268-270 ◽  
pp. 356-359 ◽  
Author(s):  
Wen Song Lin ◽  
C. H. Wen ◽  
Liang He
Keyword(s):  
Magnetic Properties ◽  
Photoelectron Spectroscopy ◽  
Raw Materials ◽  
Sol Gel ◽  
Secondary Phase ◽  
X Ray Diffraction ◽  
Gel Method ◽  
X Ray ◽  
Sol Gel Method ◽  
Doped Zno

Mn, Fe doped ZnO powders (Zn0.95-xMnxFe0.05O2, x≤0.05) were synthesized by an ameliorated sol-gel method, using Zn(CH3COO)2, Mn(CH3COO)2and FeCl2as the raw materials, with the addition of vitamin C as a kind of chemical reducer. The resulting powder was subsequently compacted under pressure of 10 MPa at the temperature of 873K in vacuum. The crystal structure and magnetic properties of Zn0.95-xMnxFe0.05O2powder and bulk samples have been investigated by X-ray diffraction (XRD) and vibrating sample magnetometer (VSM). X-ray photoelectron spectroscopy (XPS) was used to study chemical valence of manganese, iron and zinc in the samples. The x-ray diffraction (XRD) results showed that Zn0.95-xMnxFe0.05O (x≤0.05) samples were single phase with the ZnO-like wurtzite structure. No secondary phase was found in the XRD spectrum. X-ray photoelectron spectroscopy (XPS) showed that Fe and Mn existed in Zn0.95-xMnxFe0.05O2samples in Fe2+and Mn2+states. The results of VSM experiment proved the room temperature ferromagnetic properties (RTFP) of Mn, Fe co-doped ZnO samples.

scholarly journals Dielectric and impedance analysis of Li0.5La0.5Ti1-xZrxO3(x = 0.05 and 0.1) ceramics as improved electrolyte material for lithium-ion batteries

2016 ◽  
Vol 34 (3) ◽  
pp. 605-616 ◽  
Author(s):  
K. Vijaya Babu ◽  
V. Veeraiah
Keyword(s):  
Ionic Conductivity ◽  
Lithium Ion Batteries ◽  
Electric Modulus ◽  
Lithium Ion ◽  
Impedance Analysis ◽  
Solid State Reaction Method ◽  
High Ionic Conductivity ◽  
Conductivity Relaxation ◽  
Reaction Method ◽  
X Ray

AbstractThe most attractive property of Li0.5La0.5TiO3 (LLTO) electrolytes is their high ionic conductivity. Studies have shown that LLTO is capable of existing in a state with an ionic conductivity of 10-3 S/cm, which is comparable to liquid electrolytes. In addition to the high ionic conductivity of the material, LLTO is electrochemically stable and able to withstand hundreds of cycles. So, the studies of the solid electrolyte material are very important for the development of lithium-ion batteries. In the present paper, Li0.5La0.5Ti1-xZrxO3 (x = 0.05 and 0.1) have been prepared by a solid-state reaction method at 1300 °C for 6 hours to improve electrolyte materials for lithium-ion batteries. The phase identified by X-ray diffractometry and crystal structure corresponds to pm3m (2 2 1) space group (Z = 1). The frequency and temperature dependence of impedance, dielectric permittivity, dielectric loss and electric modulus of the Li0.5La0.5Ti1-xZrxO3 (x = 0.05 and 0.1) have been investigated. The dielectric and impedance properties have been studied over a range of frequency (42 Hz to 5 MHz) and temperatures (30 °C to 100 °C). The frequency dependent plot of modulus shows that the conductivity relaxation is of non-Debye type.

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

scholarly journals Structure and electric properties of cerium substituted SrBi1.8Ce0.2Nb2O9 and SrBi1.8Ce0.2Ta2O9 ceramics

2016 ◽  
Vol 10 (3) ◽  
pp. 183-188 ◽  
Author(s):  
Mohamed Afqir ◽  
Amina Tachafine ◽  
Didier Fasquelle ◽  
Mohamed Elaatmani ◽  
Jean-Claude Carru ◽  
...  
Keyword(s):  
Dielectric Constant ◽  
Solid State ◽  
Room Temperature ◽  
Single Phase ◽  
Solid State Reaction Method ◽  
X Ray Diffraction ◽  
Reaction Method ◽  
X Ray ◽  
Lcr Meter ◽  
Curie Temperature Tc

SrBi1.8Ce0.2Nb2O9 (SBCN) and SrBi1.8Ce0.2Ta2O9 (SBCT) powders were prepared via solid-state reaction method. X-ray diffraction analysis reveals that the SBCN and SBCT powders have the single phase orthorhom-bic Aurivillius structure at room temperature. The contribution of Raman scattering and FTIR spectroscopy of these samples were relatively smooth and resemble each other. The calcined powders were uniaxially pressed and sintered at 1250?C for 8 h to obtaine dense ceramics. Dielectric constant, loss tangent and AC conductivity of the sintered Ce-doped SrBi2Nb2O9 and SrBi2Ta2O9 ceramics were measured by LCR meter. The Ce-doped SBN (SBCN) ceramics have a higher Curie temperature (TC) and dielectric constant at TC (380?C and ?? ~3510) compared to the Ce-doped SBT (SBCT) ceramics (330?C and ?? ~115) when measured at 100Hz. However, the Ce-doped SBT (SBCT) ceramics have lower conductivity and dielectric loss.

Synthetic Processes via Complex Precursors of Rare Earth Manganites with the Perovskite and its Related Structures

2004 ◽  
Vol 449-452 ◽  
pp. 725-728 ◽  
Author(s):  
A. Shimono ◽  
Hirohisa Sato ◽  
K. Kawada-Wada ◽  
Yasuo Ito ◽  
Naoki Kamegashira
Keyword(s):  
Rare Earth ◽  
Single Phase ◽  
Solid State Reaction Method ◽  
Rare Earth Complex ◽  
Normal Process ◽  
Composition Region ◽  
Synthetic Process ◽  
Reaction Method ◽  
X Ray ◽  
Rare Earth Manganites

A development of synthetic process via rare earth complex precursors was applied to a formation of rare earth manganites which can not be easily formed by conventional (normal) process. Several compounds of rare earth manganites with various structures were successfully synthesized by this method and their crystal structures were identified by powder X-ray diffractometry. Both of the orthorhombic and rhombohedral LaMnO3phases were prepared. LnMn2O5phase was more easily prepared by this method than by another method. The solid solution of (Sr,La)2MnO4phase for various compositions were tried to prepare a single phase, especially for a composition region Sr/La ratio < 1. since this phase is normally formed for only region of Sr/La ratio .. 1 by the solid state reaction method.

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...

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