scholarly journals Synthesis, Crystal Structure Refinement, and Electrical Conductivity of Pb(8−x)Na2Smx(VO4)6O(x/2)

2014 ◽  
Vol 2014 ◽  
pp. 1-7
Author(s):  
Tatiana M. Savankova ◽  
Lev G. Akselrud ◽  
Lyudmyla I. Ardanova ◽  
Alexey V. Ignatov ◽  
Eugeni I. Get’man ◽  
...  

Solid solutions of Pb(8−x)Na2Smx(VO4)6O(x/2)were studied using X-ray diffraction analysis including Rietveld refinement and scanning electron microscopy and by measuring their electrical conductivity. Crystal structure of the solid solutions was refined and the solubility region0≤x≤0.2was determined for samarium substitution for lead under the scheme2Pb2++□→2Sm3++O2-. The influence of degree of substitution on the electrical conductivity of solid solutions was established.

Author(s):  
Francisco Javier Serrano ◽  
Noemí Montoya ◽  
José Luis Pizarro ◽  
María Mercedes Reventós ◽  
Marek Andrzej Kojdecki ◽  
...  

Co2+-containing cordierite glasses, of nominal compositions (Mg1−xCox)2Al4Si5O18(withx= 0, 0.2, 0.4, 0.6, 0.8 and 1), were prepared by melting colloidal gel precursors. After isothermal heating at 1273 K for around 28 h, a single-phase α-cordierite (high-temperature hexagonal polymorph) was synthesized. All materials were investigated using X-ray powder diffraction and field-emission scanning electron microscopy. The crystal structure and microstructure were determined from X-ray diffraction patterns. Rietveld refinement confirmed the formation of magnesium–cobalt cordierite solid solutions. The unit-cell volume increased with the increase of cobalt content in the starting glass. The crystalline microstructure of the cordierites was interpreted using a mathematical model of a polycrystalline material and characterized by prevalent crystallite shape, volume-weighted crystallite size distribution and second-order crystalline lattice-strain distribution. Hexagonal prismatic was the prevalent shape of α-cordierite crystallites. Bimodality in the size distribution was observed and interpreted as a consequence of two paths of the crystallization: the nucleation from glass of μ-cordierite, which transformed into α-cordierite with annealing, or the nucleation of α-cordierite directly from glass at high temperatures. Scanning electron microscopy images agreed well with crystalline microstructure characteristics determined from the X-ray diffraction line-profile analysis.


2017 ◽  
Vol 23 (S1) ◽  
pp. 934-935
Author(s):  
R. Rodriguez-Mijangos ◽  
O. Hernández-Negrete ◽  
R. C. Carrillo-Torres ◽  
F. J. Carrillo-Pesqueira ◽  
M. E. Alvarez-Ramos ◽  
...  

2014 ◽  
Vol 602-603 ◽  
pp. 947-950
Author(s):  
Zhen Wang ◽  
Hai Yan Chen ◽  
Lin Qiang Gao ◽  
Xin Zou

BiFeO3 nanoparticles were successfully synthesized by a hydrothermal method by a mineralizer (KNO3). Structural characterization was performed by thermal analysis, powder X-ray diffraction (XRD) and scanning electron microscopy (TEM).The results showed that the products were perovskite structure BiFeO3 powders. Optimal conditions for the synthesis of single-phase BiFeO3 ceramics were obtained.


2022 ◽  
Vol 92 (3) ◽  
pp. 435
Author(s):  
А.М. Камалов ◽  
В.В Kодолова-Чухонцева ◽  
E.Н Дресвянина ◽  
T.П Масленникова ◽  
И.П Добровольская ◽  
...  

Using the methods of X-ray diffraction and scanning electron microscopy, the structure of composite films based on chitosan and single-wall carbon tubes has been studied. It is shown that the introduction of carbon nanotubes leads to the ordering of the chitosan structure. Increase in concentration of nanotubes (from 0 to 3%) causes rise in the value of storage modulus from 3 to 4 GPa (DMA data), increase in electrical conductivity of samples (from 10-11 to 102 S/m), and some changes in their dielectric permittivity (from 5.5. to 26 at an electrical field frequency of 1kHz). Data on the ionic and electronic components of the conductivity of the composite film are presented.


2021 ◽  
Vol 19 (3) ◽  
pp. 56-61
Author(s):  
Bilal Ahmed Omar ◽  
Rabab Shakour Ali

The ferritic nanocomposite which prepared has the chemical formula of (Co0.25𝑁𝑖0.25Zn0.5LaxFe2−xO4), for different values of (X= 0, 0. 25, 0. 5, 0. 75), by using the spontaneous combustion-gel method, where calcination had been at temperature of (700˚C) for two hours; then studied the structural properties of the resulting ferrite via X-Ray diffraction (XRD), and Scanning Electron Microscopy (SEM) The results denote that the ferrite has a unique phase with a spinal-shaped crystal structure and a granular size are (23-36) nm, with increase in lattice constant of decrease in porosity, and electrical properties were also take in to consideration, like value of dielectric constant, the loss coefficient also observed via increase the frequency. The alternating electrical conductivity (σa.c) increases with increasing frequency.


2017 ◽  
Vol 891 ◽  
pp. 473-477
Author(s):  
Renáta Verbová ◽  
Viktor Kavečanský ◽  
Pavel Diko ◽  
Samuel Piovarči

Crystalline barium cerate was synthesized by oxalate coprecipitation from nitrates of barium and cerium [1]. The oxalate precursor prepared by chemical methods was calcined at different temperatures up to 950°C. The barium cerate was studied by X-ray diffraction (XRD) and scanning electron microscopy (SEM). X-ray diffraction investigation enables the determination of the phases that originate at different stages of synthesis and the crystal structure of final barium cerate, as well. From XRD patterns the average size of coherent regions was estimated by using Halder-Wagner method [2]. Both size and shape of crystallites were also studied by scanning electron microscopy. It was found that crystallites of barium cerate arise within the initial particles of the oxalate precursor.


2015 ◽  
Vol 71 (2) ◽  
pp. 89-92
Author(s):  
Ali Hejrani-Dalir ◽  
Masumeh Tabatabaee ◽  
Ali Sheibani

2-Amino-3-hydroxypyridinium dioxido(pyridine-2,6-dicarboxylato-κ3O2,N,O6)vanadate(V), (C5H7N2O)[V(C7H3NO4)O2] or [H(amino-3-OH-py)][VO2(dipic)], (I), was prepared by the reaction of VCl3with dipicolinic acid (dipicH2) and 2-amino-3-hydroxypyridine (amino-3-OH-py) in water. The compound was characterized by elemental analysis, IR spectroscopy and X-ray structure analysis, and consists of an anionic [VO2(dipic)]−complex and an H(amino-3-OH-py)+counter-cation. The VVion is five-coordinated by oneO,N,O′-tridentate dipic dianionic ligand and by two oxide ligands. Thermal decomposition of (I) in the presence of polyethylene glycol led to the formation of nanoparticles of V2O5. Powder X-ray diffraction (PXRD) and scanning electron microscopy (SEM) were used to characterize the structure and morphology of the synthesized powder.


2013 ◽  
Vol 785-786 ◽  
pp. 697-700
Author(s):  
Mei Mei Wu ◽  
Wei Wang ◽  
Zi Jun Wang ◽  
Rong Deng Liu

Bi0.9Pr0.1Fe1-xTixO3 ceramics were prepared by a rapid liquid sintering method. The structure of samples was confirmed by X-ray diffraction and scanning electron microscopy. Ti substitution leads to some changes in the crystal structure of Bi0.9Pr0.1FeO3, which also significantly affects the dielectric constant and loss.


Materials ◽  
2020 ◽  
Vol 13 (24) ◽  
pp. 5841
Author(s):  
Bruno Caio Chaves Fernandes ◽  
Kassio Ferreira Mendes ◽  
Ananias Francisco Dias Júnior ◽  
Vinícius Patrício da Silva Caldeira ◽  
Taliane Maria da Silva Teófilo ◽  
...  

Pyrolysis conditions directly influence biochar properties and, consequently, influence the potential use of biochar. In this study, we evaluated the effects of different pyrolysis temperatures (450, 550, 650, 750, 850, and 950 °C) on the hydrogen potential, electrical conductivity, ash content, yield, volatile matter content, elemental analysis, Fourier-transform infrared spectroscopy results, X-ray diffraction results, scanning electron microscopy results, specific surface area, and micropore volume of eucalyptus wood-derived biochar. The degree of linear association between pyrolysis temperatures and biochar properties was examined using the Pearson correlation coefficient. The results showed a positive correlation of the pyrolysis temperature with the hydrogen potential value, electrical conductivity, and elemental carbon. There was a negative correlation of the pyrolysis temperature with the yield, volatile matter content, elemental oxygen, elemental hydrogen, surface area, aromaticity, hydrophilicity, and polarity indexes. The Fourier-transform infrared spectroscopy data indicated an increase in aromaticity and a decrease in the polarity of high-temperature biochar. The increased pyrolysis temperature caused the loss of cellulose and crystalline mineral components, as indicated by X-ray diffraction analysis and scanning electron microscopy images. These results indicated that changing the pyrolysis temperature enables the production of biochar from the same raw material with a wide range of physicochemical properties, which allows its use in various types of agricultural and environmental activities.


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