A Rational Way to Prepare BaTiO3 Ceramics

2012 ◽  
Vol 535-537 ◽  
pp. 797-800
Author(s):  
Liang Luo ◽  
Yan Jun Zhu ◽  
Ling Ling Song ◽  
Xiao Bo Zhang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Phase Composition ◽  
Solid State ◽  
Field Emission ◽  
Solid State Reaction ◽  
X Ray Diffraction ◽  
One Pot ◽  
X Ray ◽  
Scanning Electron

A facile one-pot hydrothermal method has been developed for synthesis of porous and non-porous BaTiO3 ceramics using Ba(OH)2.8H2O, BaCO3 as barium source. In this paper, we research the effect of different barium source on the nanostructure of BaTiO3 ceramics in a solid state reaction, and the results indicated that the two different morphologies of BaTiO3 ceramics can be easily prepared by using these two different barium source. The phase composition and morphology of the as-obtained products were investigated by X-ray diffraction and field emission scanning electron microscopy (SEM).

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.

UTILIZATION OF FLY ASH AND CONCRETE RESIDUE IN THE PRODUCTION OF GEOPOLYMER BRICKS

2017 ◽  
Vol 12 (1) ◽  
pp. 63-77 ◽  
Author(s):  
Siriporn Sirikingkaew ◽  
Nuta Supakata
Keyword(s):  
Electron Microscopy ◽  
Mechanical Properties ◽  
Scanning Electron Microscopy ◽  
Compressive Strength ◽  
Phase Composition ◽  
Fly Ash ◽  
Industrial Waste ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

This study presents the development of geopolymer bricks synthetized from industrial waste, including fly ash mixed with concrete residue containing aluminosilicate compound. The above two ingredients are mixed according to five ratios: 100:0, 95:5, 90:10, 85:15, and 80:20. The mixture's physico-mechanical properties, in terms of water absorption and the compressive strength of the geopolymer bricks, are investigated according to the TIS 168-2546 standard. Scanning electron microscopy (SEM) and X-ray diffraction (XRD) analyses are used to investigate the microstructure and the elemental and phase composition of the brick specimens. The results indicate that the combination of fly ash and concrete residue represents a suitable approach to brick production, as required by the TIS 168–2546 standard.

scholarly journals Standard Hot Pressing as a Possible Solution to Obtain Dense K0.5Na0.5NbO3 Ceramic Doped by Er2O3 and Yb2O3

Materials ◽  
2019 ◽  
Vol 12 (24) ◽  
pp. 4171 ◽  
Author(s):  
Paweł Rutkowski ◽  
Jan Huebner ◽  
Adrian Graboś ◽  
Dariusz Kata ◽  
Dariusz Grzybek ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Rare Earth ◽  
Phase Composition ◽  
Powder Mixture ◽  
Hot Pressing ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ultrasonic Methods ◽  
Scanning Electron

In this study, the influence of the addition of rare earth oxides on the phase composition and density of KNN piezoelectric ceramics was investigated. The initial powders of Na2CO3 and K2CO3 were dried at 150 °C for 2 h. Then, a powder mixture for synthesis was prepared by adding a stoichiometric amount of Nb2O5 and 5 and 10 wt % overabundance of Na2CO3. All powders were mixed by ball-milling for 24 h and synthesized at 950 °C. The phase composition of the reaction bed was checked by means of X-ray diffraction (XRD). It had an appearance of tetragonal and monoclinic K0.5Na0.5NbO3 (KNN) phases. Then, 1 and 2 wt % of Er2O3 and Yb2O3, were added to the mixture. Green samples of 25 mm diameter and 3 mm thickness were prepared and sintered by hot pressing at 1000 °C for 2 h under 25 MPa pressure. The final samples were investigated via scanning electron microscopy (SEM)-energy-dispersive X-ray spectroscopy (EDS), XRD, Rietveld, and ultrasonic methods. Phase analysis showed tetragonal and orthorhombic KNN phases, and a contamination of (K2CO3·1.5H2O) was present. The obtained KNN polycrystals had a relative density above 95%. Texturing of the material was confirmed as a result of hot pressing.

Microstructure and Phase Composition of AlN/Al Composite Fabricated by Directed Melt Nitridation

2008 ◽  
Vol 368-372 ◽  
pp. 977-979
Author(s):  
Sheng Li Jin ◽  
Ya Wei Li ◽  
Jing Liu ◽  
Yuan Bing Li ◽  
Lei Zhao ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Phase Composition ◽  
Sandwich Structure ◽  
Ceramic Composite ◽  
Growth Direction ◽  
X Ray Diffraction ◽  
X Ray ◽  
Al Composite ◽  
Scanning Electron

AlN/Al ceramic composite was fabricated by directed melt nitridation of pure Al block covered with 10wt% Mg powder at 1300°C in a high purity flowing N2. Microstructure and phase composition of the composite were investigated by scanning electron microscopy with energy dispersive spectroscopy and X-ray diffraction. Results showed that AlN is the main phase in the composite and its lattice parameters of a and c are 3.1110Å and 4.9806Å, respectively. The phase composition of the composite changes along the growth direction and a gradient sandwich structure forms. The surface of the composite is made up of a dense and thin nodular AlN layer, underneath which an AlN/Al layer appears, followed by an AlN/Al/MgAl2O4 layer. Thermodynamic calculations predicted the formation of possible phases with the addition of Mg. It suggested that the content of Mg at the reaction frontier of nitridation is considerably lower to 0.15wt% where MgAl2O4 was stable, because of escape and reaction exhaustion of Mg. Once Mg is lower than 0.05wt%, only a dense AlN layer can exist, which prevents the further nitridation of Al melt.

scholarly journals Nickel-Doped Cerium Oxide Nanoparticles: Green Synthesis Using Stevia and Protective Effect against Harmful Ultraviolet Rays

Molecules ◽  
2019 ◽  
Vol 24 (24) ◽  
pp. 4424 ◽  
Author(s):  
Mehrdad Khatami ◽  
Mina Sarani ◽  
Faride Mosazadeh ◽  
Mohammadreza Rajabalipour ◽  
Alireza Izadi ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Cerium Oxide ◽  
Field Emission ◽  
Cerium Oxide Nanoparticles ◽  
Oxide Nanoparticles ◽  
X Ray Diffraction ◽  
Ni Doping ◽  
X Ray ◽  
Scanning Electron

Nanoparticles of cerium oxide CeO2 are important nanomaterials with remarkable properties for use in both industrial and non-industrial fields. In a general way, doping of oxide nanometric with transition metals improves the properties of nanoparticles. In this study, nickel- doped cerium oxide nanoparticles were synthesized from Stevia rebaudiana extract. Both doped and non-doped nanoparticles were characterized by X-ray diffraction, Field Emission Scanning Electron Microscopy, Energy Dispersive X-ray, Raman spectroscopy, and Vibrating-Sample Magnetometry analysis. According to X-ray diffraction, Raman and Energy Dispersive X-ray crystalline and single phase of CeO2 and Ni doped CeO2 nanoparticles exhibiting fluorite structure with F2g mode were synthesized. Field Emission Scanning Electron Microscopy shows that CeO2 and Ni doped nanoparticles have spherical shape and sizes ranging of 8 to 10 nm. Ni doping of CeO2 results in an increasing of magnetic properties. The enhancement of ultraviolet protector character via Ni doping of CeO2 is also discussed.

Biomorphic SiC Prepared from Carbonized Millet by Sol-Gel and Carbothermal Reduction Processing

2010 ◽  
Vol 152-153 ◽  
pp. 1683-1686
Author(s):  
Qing Wang ◽  
Ya Hui Zhang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Silicon Carbide ◽  
Phase Composition ◽  
Carbothermal Reduction ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Carbon Template ◽  
Scanning Electron

Biomorphic silicon carbide (bioSiC) was prepared by high temperature pyrolysis and sol-gel and carbothermal reduction processing at 1600 oC. The morphology and microstructure of carbon-silica composites and purified bioSiC samples were characterized by scanning electron microscopy. The phase composition of the resulting sample was analyzed by X-ray diffraction. The results suggest that the bioSiC mainly consists of cubic ß-SiC, and principally replicates the shape and microstructure of the carbon template.

Biomorphic TiO2 Ceramics Prepared from Cotton Stalk

2012 ◽  
Vol 602-604 ◽  
pp. 526-529
Author(s):  
Qing Wang ◽  
Lin Zhang ◽  
Ya Hui Zhang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Phase Composition ◽  
High Temperature ◽  
Sol Gel ◽  
Cotton Stalk ◽  
X Ray Diffraction ◽  
X Ray ◽  
Carbon Template ◽  
Scanning Electron

Biomorphic TiO2 was prepared by high temperature pyrolysis and a modified sol-gel route. The morphology and microstructure of TiO2 samples were characterized by scanning electron microscopy. The phase composition of the resulting sample was analyzed by X-ray diffraction. The results suggest that the biomorphic TiO2 mainly consists of rutile TiO2, and replicates the shape and part microstructure of the carbon template.

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.

scholarly journals Evolution of Free Volumes in Polycrystalline BaGa2O4 Ceramics Doped with Eu3+ Ions

Crystals ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 1515
Author(s):  
Halyna Klym ◽  
Ivan Karbovnyk ◽  
Andriy Luchechko ◽  
Yuriy Kostiv ◽  
Viktorija Pankratova ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Phase Composition ◽  
Grain Boundaries ◽  
Solid Phase ◽  
X Ray Diffraction ◽  
Spectroscopy Technique ◽  
X Ray ◽  
Positron Annihilation Lifetime ◽  
Scanning Electron

BaGa2O4 ceramics doped with Eu3+ ions (1, 3 and 4 mol.%) were obtained by solid-phase sintering. The phase composition and microstructural features of ceramics were investigated using X-ray diffraction and scanning electron microscopy in comparison with energy-dispersive methods. Here, it is shown that undoped and Eu3+-doped BaGa2O4 ceramics are characterized by a developed structure of grains, grain boundaries and pores. Additional phases are mainly localized near grain boundaries creating additional defects. The evolution of defect-related extended free volumes in BaGa2O4 ceramics due to the increase in the content of Eu3+ ions was studied using the positron annihilation lifetime spectroscopy technique. It is established that the increase in the number of Eu3+ ions in the basic BaGa2O4 matrix leads to the agglomeration of free-volume defects with their subsequent fragmentation. The presence of Eu3+ ions results in the expansion of nanosized pores and an increase in their number with their future fragmentation.

Nanostructured CaWO4, CaWO4:Eu3+ and CaWO4:Tb3+ Particles: Sonochemical Synthesis and Luminescent Properties

2008 ◽  
Vol 8 (3) ◽  
pp. 1183-1190 ◽  
Author(s):  
Chunxia Li ◽  
Cuikun Lin ◽  
Xiaoming Liu ◽  
Jun Lin
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Field Emission ◽  
Spherical Particles ◽  
X Ray Diffraction ◽  
Blue Emission Band ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

Nanostructured CaWO4, CaWO4:Eu3+, and CaWO4:Tb3+ phosphor particles were synthesized via a facile sonochemical route. X-ray diffraction, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, transmission electron microscopy, photoluminescence, low voltage cathodoluminescence spectra, and photoluminescence lifetimes were used to characterize the as-obtained samples. The X-ray diffraction results indicate that the samples are well crystallized with the scheelite structure of CaWO4. The transmission electron microscopy and field emission scanning electron microscopy images illustrate that the powders consist of spherical particles with sizes from 120 to 160 nm, which are the aggregates of even smaller nanoparticles ranging from 10 to 20 nm. Under UV light or electron beam excitation, the CaWO4 powder exhibited a blue emission band with a maximum at 430 nm originating from the WO2−4 groups, while the CaWO4:Eu3+ powder showed red emission dominated by 613 nm ascribed to the 5D0 → 7F2 of Eu3+, and the CaWO4:Tb3+ powders showed emission at 544 nm, ascribed to the 5D4 → 7F5 transition of Tb3+. The PL excitation and emission spectra suggest that the energy is transferred from WO2−4 to Eu3+CaWO4:Eu3+ and to Tb3+ in CaWO4:Tb3+. Moreover, the energy transfer from WO2−4 to Tb3+ in CaWO4:Tb3+ is more efficient than that from WO2−4 to Eu3+ in CaWO4:Eu3+. This novel and efficient pathway could open new opportunities for further investigating the novel properties of tungstate materials.

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