Synthesis and Characterization of Gadolinia-Doped Ceria with Manganese Addition

2012 ◽  
Vol 727-728 ◽  
pp. 1296-1301
Author(s):  
J.D. Yang ◽  
R.A. Rocha ◽  
R. Muccillo ◽  
E.N.S. Muccillo
Keyword(s):  
Single Phase ◽  
Powder Materials ◽  
Doped Ceria ◽  
X Ray Diffraction ◽  
Cation Complexation ◽  
Wide Range ◽  
Diffraction Patterns ◽  
Etched Surface

Ceria-based materials have been extensively studied due to their wide range of technological application. In this work, nanostructured powders of 20 mol% gadolinia-doped ceria pure and containing 1 mol% manganese were synthesized by the cation complexation technique. Powder materials were calcined at 600°C, uniaxially pressed and sintered in the 1200-1500°C range for soaking times of 1, 2 and 4 h. X-ray diffraction patterns evidenced a single-phase fluorite-like structure in all studied specimens. The evolution of grain sizes was evaluated by scanning electron microscopy on polished and thermally etched surface of sintered pellets. The relative density decreases for soaking times above 1300°C (with Mn) and 1400°C (without Mn). The grain size increases with manganese addition. The role of the additive on the electrical conductivity of gadolinia-doped ceria was evaluated by impedance spectroscopy measurements.

scholarly journals Structural, Dielectric, Magnetic and Optical Properties of Cerium Substituted Ni-Zn Mixed Ferrite

2017 ◽  
Vol 14 (2) ◽  
pp. 133-139 ◽  
Author(s):  
Lovely George ◽  
C. Viji ◽  
Haisel Mathew ◽  
E.M. Mohammed
Keyword(s):  
Single Phase ◽  
Sol Gel ◽  
Strain Effect ◽  
X Ray Diffraction ◽  
Semiconducting Materials ◽  
Octahedral Sites ◽  
In Doping ◽  
Wide Range ◽  
Diffraction Patterns ◽  
Lower Saturation

Ce3+ doped Nickel Zinc ferrites have been synthesised by sol-gel method followed by sintering at 4000C for 4 hours. Powder X-ray diffraction patterns of the prepared samples confirm the formation of single phase cubic spinel structure. Crystallite size of samples doped with Ce are smaller than that of undoped ferrite. The lattice parameters decrease with increase in doping concentration of Ce3+ ion. W-H plots are drawn to study the strain effect in crystal structure.SEM micrographs show formation of spherical shaped nanoparticles. The vibration bands corresponding to metal oxygen vibrations at tetrahedral and octahedral sites in the FTIR spectra are in the reported range suggesting Ce3+occupation on octahedral sites predominantly. The doped samples exhibited lower saturation magnetization. The relative permittivity is found to show a decreasing trend with increase in frequency for all the samples which is characteristic of normal ferrimagnetism. The AC conductivity initially increases with frequency then remains constant over a wide range of frequencies. The UV analyses give the band gap which is less than 2 eV for all the samples which show that these are semiconducting materials.

2D X-ray diffraction and molecular modelling of the crystalline structure of polyesters under uniaxial stress

2021 ◽  
pp. 096739112199822
Author(s):  
Ahmed I Abou-Kandil ◽  
Gerhard Goldbeck
Keyword(s):  
Crystalline Structure ◽  
Molecular Modelling ◽  
Three Dimensional ◽  
Uniaxial Stress ◽  
X Ray Diffraction ◽  
X Ray ◽  
Wide Range ◽  
Modelling Techniques ◽  
Diffraction Patterns

Studying the crystalline structure of uniaxially and biaxially drawn polyesters is of great importance due to their wide range of applications. In this study, we shed some light on the behaviour of PET and PEN under uniaxial stress using experimental and molecular modelling techniques. Comparing experiment with modelling provides insights into polymer crystallisation with extended chains. Experimental x-ray diffraction patterns are reproduced by means of models of chains sliding along the c-axis leading to some loss of three-dimensional order, i.e. moving away from the condition of perfect register of the fully extended chains in triclinic crystals of both PET and PEN. This will help us understand the mechanism of polymer crystallisation under uniaxial stress and the appearance of mesophases in some cases as discussed herein.

scholarly journals CRYOGLOBULIN TEST AND CRYOGLOBULINEMIA HEPATITIS C-VIRUS RELATED

2016 ◽  
Vol 9 (1) ◽  
pp. e2017007 ◽  
Author(s):  
Umberto Basile
Keyword(s):  
Hepatitis C Virus ◽  
Hepatitis C ◽  
Confounding Factor ◽  
Underlying Disease ◽  
Clinical Syndrome ◽  
Laboratory Techniques ◽  
Preanalytical Phase ◽  
Wide Range

Cryoglobulins are immunoglobulins that precipitate in serum at temperatures below 37°C and resolubilize upon warming. The clinical syndrome of cryoglobulinemia usually includes purpura, weakness, and arthralgia, but the underlying disease may also contribute other symptoms. Blood samples for cryoglobulin are collected, transported, clotted and spun at 37°C, before the precipitate is allowed to form when serum is stored at 4°C in a Wintrobe tube for at least seven days. The most critical and confounding factor affecting the cryoglobulin test is when the preanalytical phase is not fully completed at 37°C. The easiest way to quantify cryoglobulins is the cryocrit estimate. However, this approach has low accuracy and sensitivity. Furthermore, the precipitate should be resolubilized by warming to confirm that it is truly formed of cryoglobulins. The characterization of cryoglobulins requires the precipitate is several times washed, before performing immunofixation, a technique by which cryoglobulins can be classified depending on the characteristics of the detected immunoglobulins. These features imply a pathogenic role of these molecules which are consequently associated with a wide range of symptoms and manifestations. According to the Brouet classification, Cryoglobulins are grouped into three types by the immunochemical properties of immunoglobulins in the cryoprecipitate. The aim of this paper is to review the major aspects of cryoglobulinemia and the laboratory techniques used to detect and characterize cryoglobulins, taking into consideration the presence and consequences of cryoglobulinemia in Hepatitis C Virus (HCV) infection.

scholarly journals Perbaikan Kelarutan Albendazol Melalui Pembentukan Kristal Multikomponen dengan Asam Malat

2020 ◽  
Vol 6 (1) ◽  
pp. 114-123
Author(s):  
Fikri Alatas ◽  
Fahmi Abdul Azizsidiq ◽  
Titta Hartyana Sutarna ◽  
Hestyari Ratih ◽  
Sundani Nurono Soewandhi
Keyword(s):  
Phase Solubility ◽  
Crystal Formation ◽  
Solubility Curve ◽  
X Ray Diffraction ◽  
Ethanol Mixture ◽  
X Ray ◽  
Grinding Method ◽  
Diffraction Patterns ◽  
Phase Solubility Curve

An effort to improve the solubility of albendazole (ABZ), an anthelmintic drug has been successfully carried out through the formation of multicomponent crystal with dl-malic acid (MAL). Construction of phase solubility curve of ABZ in MAL solution and crystal morphological observations after recrystallization in the acetone-ethanol (9:1) mixture were performed for initial prediction of multicomponent crystal formation. ABZ-MAL multicomponent crystal was prepared by wet grinding or also known as solvent-drop grinding (SDG) with acetone-ethanol (9:1) mixture as a solvent followed by characterization of the multicomponent crystal formation by powder X-ray diffraction and Fourier transform infrared (FTIR) methods. The solubility of ABZ-MAL multicomponent crystal was tested in water at ambient temperature and in pH 1.2, 4.5 and 6.8 of buffered solutions at 37°C. The phase solubility curve of the ABZ in the MAL solution showed type Bs. The ABZ-MAL mixture has a different crystalline morphology than pure ABZ and MAL after recrystallization in the acetone-ethanol mixture (9:1). The powder X-ray diffraction pattern and the FTIR spectrum of ABZ-MAL from SDG different from intact ABZ and MAL powder X-ray diffraction patterns and these results can indicate the ABZ-MAL multicomponent crystal formation. The ABZ-MAL multicomponent crystal has better solubility than pure ABZ in all media used. These results can be concluded that ABZ-MAL multicomponent crystal can be prepared by solvent-drop grinding method with acetone-ethanol (9:1) mixture as a solvent and can increase the solubility of albendazole.

scholarly journals PECHINI SYNTHESIS AND CHARACTERIZATION OF Eu3+ DOPED ZnCo2O4 SPINELS

2005 ◽  
Vol 03 (2) ◽  
pp. 24-29
Author(s):  
P.M. PIMENTEL ◽  
A.M.G. PEDROSA ◽  
H.K.S. SOUZA ◽  
C.N.S. JÚNIOR ◽  
R.C.A. PINTO ◽  
...  
Keyword(s):  
Spinel Structure ◽  
Pechini Method ◽  
Synthesis Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Spinel Oxides ◽  
Diffraction Patterns ◽  
Pechini Synthesis ◽  
Spinel Structures

Spinel oxides with the composition ZnCo2O4 and ZnCo2O4:Eu3+ have been synthesized by the Pechini method and characterized by X-ray diffraction, infrared spectroscopy, thermal analysis and scanning electron microscopy. IR spectroscopy revealed the presence of n1 and n2 bands, typical of spinel structures. The formation of monophase cubic spinel structure was confirmed by X-ray diffraction patterns. Extra lines corresponding to other phase has been observed in the powders calcined at 900 ºC. The results showed the extremely lower synthesis temperature than those presents in conventional methods.

scholarly journals Ferromagnetic Order in the Intermetallic Alloys laNi5-xMgx

2012 ◽  
Vol 29 (1) ◽  
pp. 50
Author(s):  
D.N Ba ◽  
L.T Tai ◽  
N.T Trung ◽  
N.T Huy
Keyword(s):  
Magnetic Properties ◽  
Curie Temperature ◽  
Room Temperature ◽  
Single Phase ◽  
Chemical Doping ◽  
Intermetallic Alloys ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ferromagnetic Order ◽  
Diffraction Patterns

The influences of the substitution of Ni with Mg on crystallographic and magnetic properties of the intermetallic alloys LaNi5-xMgx (x ≤ 0.4) were investigated. The X-ray diffraction patterns showed that all samples were of single phase, and the lattice parameters, a and c, decreased slightly upon chemical doping. LaNi5 is well known as an exchange-enhanced Pauli paramagnet. Interestingly, in LaNi5-xMgx, the ferromagnetic order existed even with a small amount of dopants; the Curie temperature reached the value of room temperature for x = 0.2, and enhanced with increasing x.

scholarly journals Preparation and characterization of oleogels with tallow and partially hydrolyzed tallow as organogelators

2021 ◽  
Vol 72 (1) ◽  
pp. e388
Author(s):  
E. Keskin Uslu ◽  
E. Yılmaz
Keyword(s):  
Loss Modulus ◽  
Solid Fat Content ◽  
X Ray Diffraction ◽  
Shear Rates ◽  
Peroxide Values ◽  
Time Sweep ◽  
Diffraction Patterns ◽  
Time Sweep Test ◽  
Addition Level

The aim of this study was to evaluate the organogelation potential of tallow fat (TF) and partially hydrolyzed tallow fat (HTF) against saturated monoglyceride (MG) and a saturated monoglyceride + diglyceride mixture (MDG) as the organogelators. TF itself created oleogel at a 30% addition level, while HTF, MG and MDG oleogels were prepared at 10% addition levels. Fatty acid composition data showed that the oleogel of HTF (HTFO) was quite similar to those of MG and MDG oleogels. Solid fat content, free fatty acidity and peroxide values were found to be in acceptable ranges for HTFO. Thermal properties, crystal morphology and X-ray diffraction patterns were also evaluated. Rheological analyses indicated that all oleogels had higher storage modulus (G´) than loss modulus (G´´). The time-sweep test showed that after applying higher shear rates, the gels re-formed at rest. Further, all oleogels maintained their gelled consistency until around 54 °C. The results suggest that HTF could be a cheap, efficient, fast melting, safe and readily available organogelator.

scholarly journals Appearance of efficient luminescence energy transfer in doped orthovanadate nanocrystals

2017 ◽  
Vol 50 (3) ◽  
pp. 787-794 ◽  
Author(s):  
Swati Bishnoi ◽  
G. Swati ◽  
Paramjeet Singh ◽  
V. V. Jaiswal ◽  
Mukesh K. Sahu ◽  
...  
Keyword(s):  
Energy Transfer ◽  
Band Gap ◽  
Photoluminescence Intensity ◽  
X Ray Diffraction ◽  
Synthesis Mechanism ◽  
Enhanced Photoluminescence ◽  
Nir Absorption ◽  
Decay Parameters

This paper reports the detailed synthesis mechanism and the structural, morphological and optical characterization of ultraviolet (∼311 nm) excitable samarium doped gadolinium yttrium orthovanadate, (Gd,Y)VO4:Sm3+, nanocrystals. X-ray diffraction and Rietveld refinement studies confirmed that the synthesized samples crystallize in a tetragonal structure withI41/amdspace group. The enhanced photoluminescence intensity of (Gd,Y)VO4:Sm3+compared with the existing YVO4:Sm3+phosphor clearly indicates the significant role of Gd3+ions. This has been attributed to the sensitization of the6PJenergy level of Gd3+ions by energy transfer from orthovanadate (VO43−) ions and subsequent energy trapping by Sm3+ions. The energy transfer from VO43−to Sm3+viaGd3+ions as intermediates and concentration quenching of Gd3+luminescence are discussed in detail. The optical band gap of the as-prepared nanocrystals has been estimated using UV–vis–NIR absorption spectroscopy, which reveals a slightly higher band gap (3.75 eV) for YVO4as compared to GdYVO4(3.50 eV). Furthermore, confocal microcopy, decay parameters and Commission Internationale de l'Eclairage chromatic coordinates have supplemented these studies, which established the suitability of these nanophosphors for achieving spectral conversion in silicon solar cells.

Growth and Characterization of bulk GaN by Ga Vapor Transport

2004 ◽  
Vol 831 ◽  
Author(s):  
Phanikumar Konkapaka ◽  
Huaqiang Wu ◽  
Yuri Makarov ◽  
Michael G. Spencer
Keyword(s):  
Growth Rates ◽  
Vapor Transport ◽  
Spiral Growth ◽  
X Ray Diffraction ◽  
X Ray ◽  
Force Microscopy ◽  
Atomic Force ◽  
Bulk Gan ◽  
Diffraction Patterns

ABSTRACTBulk GaN crystals of dimensions 8.5 mm × 8.5 mm were grown at growth rates greater than 200μm/hr using Gallium Vapor Transport technique. GaN powder and Ammonia were used as the precursors for growing bulk GaN. Nitrogen is used as the carrier gas to transport the Ga vapor that was obtained from the decomposition of GaN powder. During the process, the source GaN powder was kept at 1155°C and the seed at 1180°C. Using this process, it was possible to achieve growth rates of above 200 microns/hr. The GaN layers thus obtained were characterized using X-Ray diffraction [XRD], scanning electron microscopy [SEM], and atomic force microscopy [AFM]. X-ray diffraction patterns showed that the grown GaN layers are single crystals oriented along c direction. AFM studies indicated that the dominant growth mode was dislocation mediated spiral growth. Electrical and Optical characterization were also performed on these samples. Hall mobility measurements indicated a mobility of 550 cm2/V.s and a carrier concentration of 6.67 × 1018/cm3

Single Crystal Wurtzitic Aluminum Nitride Growth on Silicon Using Supersonic Gas Jets

1995 ◽  
Vol 395 ◽  
Author(s):  
S. A. Ustin ◽  
L. Lauhon ◽  
K. A. Brown ◽  
D. Q. Hu ◽  
W. Ho
Keyword(s):  
Aluminum Nitride ◽  
Growth Rates ◽  
High Energy ◽  
X Ray Diffraction ◽  
Rutherford Back Scattering ◽  
X Ray ◽  
Supersonic Molecular Beam ◽  
Supersonic Beams ◽  
Wide Range

ABSTRACTHighly oriented aluminum nitride (0001) films have been grown on Si(001) and Si (111) substrates at temperatures between 550° C and 775° C with dual supersonic molecular beam sources. Triethylaluminum (TEA;[(C2H5)3Al]) and ammonia (NH3) were used as precursors. Hydrogen, helium, and nitrogen were used as seeding gases for the precursors, providing a wide range of possible kinetic energies for the supersonic beams due to the disparate masses of the seed gases. Growth rates of AIN were found to depend strongly on the substrate orientation and the kinetic energy of the incident precursor; a significant increase in growth rate is seen when seeding in hydrogen or helium as opposed to nitrogen. Growth rates were 2–3 times greater on Si(001) than on Si(111). Structural characterization of the films was done by reflection high energy electron diffraction (RHEED) and x-ray diffraction (XRD). X-ray rocking curve (XRC) full-width half-maxima (FWHM) were seen as small as 2.5°. Rutherford back scattering (RBS) was used to determine the thickness of the films and their chemical composition. Films were shown to be nitrogen rich, deviating from perfect stoichiometry by 10%–20%. Surface analysis was performed by Auger electron spectroscopy (AES).

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