Morphology and orientated growth of second-phase precipitates in a Eu2+-doped equimolar KCl:KBr solid solution: an epifluorescence microscopy study by using the doping ion as a fluorochrome

Microscopy ◽  
2020 ◽  
Vol 69 (1) ◽  
pp. 17-25
Author(s):  
Adolfo Ernesto Cordero-Borboa ◽  
Rodrigo Unda-Angeles
Keyword(s):  
Solid Solution ◽  
Cross Sections ◽  
Microscopy Study ◽  
Host Lattice ◽  
Epifluorescence Microscopy ◽  
Second Phase ◽  
X Ray Diffraction ◽  
Single Plate ◽  
Lattice Space ◽  
Optical Spectrophotometry

Abstract The shape and orientation of second-phase precipitates in a Eu2+-doped equimolar KCl:KBr solid solution are reported in this paper as they were unveiled by epifluorescence microscopy. To make this, microscopy images of different optical cross sections of some precipitate fields and, also, of some representative precipitates in these fields, were recorded by using the Eu2+ ion itself as a fluorochrome. From these images, the corresponding precipitate fields and individual precipitates were electronically reconstructed into the host lattice space. Previously, the KCl:KBr:Eu2+ system was characterized by absorption and fluorescence optical spectrophotometry, to tailor properly the fluorescence mirror unit, as well as by powder and single-plate X-ray diffraction, to correlate the host lattice orientation with those of the observed precipitates. These are shaped as plates, with broad faces parallel to host lattice {100}, {110} or {120}planes (the {100}, {110} and {120} precipitates, respectively), and as rods, aligned with a host lattice ˂100> direction (the ˂100> precipitates). The {100}, {110}, {120}-precipitate broad faces are in the shapes of 72.6° rhomboids, rectangles and 59.5° rhomboids, with a side lying along host lattice <310>, <110> and <421> directions, respectively, and with another side lying along a <100> direction. A typical precipitate field and the spatial reconstructions of typical {100}, {110}, {120} and ˂100> precipitates, as well as their corresponding electronic 3D-geometrical models, are described in detail. It is discussed that four different europium precipitation states are responsible for the precipitation and that the precipitate lattices are spatially coherent with the host lattice.

Structural, Optical and Magnetic Properties of (1−x)Bi0.5Na0.5TiO3+xBaCoO3−δ Solid Solution Systems Prepared by the Sol–Gel Method

2021 ◽  
Vol 21 (4) ◽  
pp. 2604-2612
Author(s):  
Dang Duc Dung ◽  
Nguyen The Hung
Keyword(s):  
Solid Solution ◽  
Magnetic Properties ◽  
Sol Gel ◽  
Host Lattice ◽  
Ferroelectric Materials ◽  
X Ray Diffraction ◽  
Gel Method ◽  
Sol Gel Method ◽  
Lattice Materials ◽  
Rhombohedral Symmetry

A new solid solution, (1−x)Bi0.5Na0.5TiO3+xBaCoO3−δ materials, was fabricated using the sol–gel method. X-ray diffraction showed that the crystal structure of the compound exhibited rhombohedral symmetry and is similar to the crystal structures of host Bi0.5Na0.5TiO3 materials. Distortions in the structures and reduction in the optical band gaps of the Bi0.5Na0.5TiO3 materials were possibly due to the random incorporation of Ba and Co cations into host lattice materials. The magnetic properties of the Bi0.5Na0.5TiO3 materials were tuned by controlling the concentrations of BaCoO3−δ as the solid solution. We expect that our work will provide valuable information on current methods for integrating ferromagnetic properties into lead-free ferroelectric materials for the development of multiferroic materials.

Analytical Electron Microscopy Study of Second-Phase Particles in 7075 and 7475 Aluminum Alloys

1985 ◽  
Vol 43 ◽  
pp. 348-349
Author(s):  
M. Raghavan ◽  
J. Y. Koo ◽  
J. W. Steeds ◽  
B. K. Park
Keyword(s):  
Aluminum Alloys ◽  
Silicon Oxide ◽  
Analytical Electron Microscopy ◽  
Microscopy Study ◽  
Electron Microscopy Study ◽  
Partial Substitution ◽  
Second Phase ◽  
X Ray ◽  
Second Phase Particles ◽  
Almost All

X-ray microanalysis and Convergent Beam Electron Diffraction (CBD) studies were conducted to characterize the second phase particles in two commercial aluminum alloys -- 7075 and 7475. The second phase particles studied were large (approximately 2-5μm) constituent phases and relatively fine ( ∼ 0.05-1μn) dispersoid particles, Figures 1A and B. Based on the crystal structure and chemical composition analyses, the constituent phases found in these alloys were identified to be Al7Cu2Fe, (Al,Cu)6(Fe,Cu), α-Al12Fe3Si, Mg2Si, amorphous silicon oxide and the modified 6Fe compounds, in decreasing order of abundance. The results of quantitative X-ray microanalysis of all the constituent phases are listed in Table I. The data show that, in almost all the phases, partial substitution of alloying elements occurred resulting in small deviations from the published stoichiometric compositions of the binary and ternary compounds.

scholarly journals Polyurethane Composite Foams Synthesized Using Bio-Polyols and Cellulose Filler

Materials ◽  
2021 ◽  
Vol 14 (13) ◽  
pp. 3474
Author(s):  
Katarzyna Uram ◽  
Milena Leszczyńska ◽  
Aleksander Prociak ◽  
Anna Czajka ◽  
Michał Gloc ◽  
...  
Keyword(s):  
Cross Sections ◽  
Raw Materials ◽  
Polyurethane Foams ◽  
Degree Of Crystallinity ◽  
X Ray Diffraction ◽  
Polyurethane Composite ◽  
Composite Foams ◽  
Closed Cell ◽  
Ft Ir ◽  
The Fourier Transform

Rigid polyurethane foams were obtained using two types of renewable raw materials: bio-polyols and a cellulose filler (ARBOCEL® P 4000 X, JRS Rettenmaier, Rosenberg, Germany). A polyurethane system containing 40 wt.% of rapeseed oil-based polyols was modified with the cellulose filler in amounts of 1, 2, and 3 php (per hundred polyols). The cellulose was incorporated into the polyol premix as filler dispersion in a petrochemical polyol made using calenders. The cellulose filler was examined in terms of the degree of crystallinity using the powder X-ray diffraction PXRD -and the presence of bonds by means of the fourier transform infrared spectroscopy FT-IR. It was found that the addition of the cellulose filler increased the number of cells in the foams in both cross-sections—parallel and perpendicular to the direction of the foam growth—while reducing the sizes of those cells. Additionally, the foams had closed cell contents of more than 90% and initial thermal conductivity coefficients of 24.8 mW/m∙K. The insulation materials were dimensionally stable, especially at temperatures close to 0 °C, which qualifies them for use as insulation at low temperatures.

scholarly journals A Study on the Damping Capacities of Mg–Zn–Y-Based Alloys with Lamellar Long Period Stacking Ordered Phases by Preparation Process

Metals ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 79
Author(s):  
Ruopeng Lu ◽  
Kai Jiao ◽  
Yuhong Zhao ◽  
Kun Li ◽  
Keyu Yao ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Solid Solution ◽  
Damping Capacity ◽  
Second Phase ◽  
Preparation Process ◽  
Obvious Effect ◽  
Lpso Phase ◽  
Long Period ◽  
Lamellar Phases ◽  
Ordered Phases

Mg alloys with fine mechanical properties and high damping capacities are essential in engineering applications. In this work, Mg–Zn–Y based alloys with lamellar long period stacking ordered (LPSO) phases were obtained by different processes. The results show that a more lamellar second phase can be obtained in the samples with more solid solution atoms. The density of the lamellar LPSO phase has an obvious effect on the damping of the magnesium alloy. The compact LPSO phase is not conducive to dislocation damping, but sparse lamellar phases can improve the damping capacity without significantly reducing the mechanical properties. The Mg95.3Zn2Y2.7 alloy with lamellar LPSO phases and ~100 μm grain size exhibited a fine damping property of 0.110 at ε = 10–3.

On the nature of the phase transitions of aluminosilicate perrhenate sodalite

2020 ◽  
Vol 235 (6-7) ◽  
pp. 213-223
Author(s):  
Hilke Petersen ◽  
Lars Robben ◽  
Thorsten M. Gesing
Keyword(s):  
Raman Spectroscopy ◽  
Phase Transitions ◽  
Decomposition Temperature ◽  
Second Phase ◽  
Structure Property ◽  
X Ray Diffraction ◽  
Temperature Dependent ◽  
Two Phase ◽  
Structure Property Relationships ◽  
Heat Capacity Measurements

AbstractThe temperature-dependent structure-property relationships of the aluminosilicate perrhenate sodalite |Na8(ReO4)2|[AlSiO4]6 (ReO4-SOD) were analysed via powder X-ray diffraction (PXRD), Raman spectroscopy and heat capacity measurements. ReO4-SOD shows two phase transitions in the investigated temperature range (13 K < T < 1480 K). The first one at 218.6(1) K is correlated to the transition of dynamically ordered $P\overline{4}3n$ (> 218.6(1 K) to a statically disordered (<218.6(1) K) SOD template in $P\overline{4}3n$. The loss of the dynamics of the template anion during cooling causes an increase of disorder, indicated by an unusual intensity decrease of the 011-reflection and an increase of the Re-O2 bond length with decreasing temperature. Additionally, Raman spectroscopy shows a distortion of the ReO4 anion. Upon heating the thermal expansion of the sodalite cage originated in the tilt-mechanism causes the second phase transition at 442(1) K resulting in a symmetry-increase from $P\overline{4}3n$ to $Pm\overline{3}n$, the structure with the sodalites full framework expansion. Noteworthy is the high decomposition temperature of 1320(10) K.

scholarly journals Synthesis of Ce1−xPdxO2−δ Solid Solution in Molten Nitrate

Catalysts ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 640
Author(s):  
Hideaki Sasaki ◽  
Keisuke Sakamoto ◽  
Masami Mori ◽  
Tatsuaki Sakamoto
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Solid Solutions ◽  
Photoelectron Spectroscopy ◽  
Synthesis Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Co Precipitation ◽  
Ionic States

CeO2-based solid solutions in which Pd partially substitutes for Ce attract considerable attention, owing to their high catalytic performances. In this study, the solid solution (Ce1−xPdxO2−δ) with a high Pd content (x ~ 0.2) was synthesized through co-precipitation under oxidative conditions using molten nitrate, and its structure and thermal decomposition were examined. The characteristics of the solid solution, such as the change in a lattice constant, inhibition of sintering, and ionic states, were examined using X-ray diffraction (XRD), scanning electron microscopy–energy-dispersive X-ray spectroscopy (SEM−EDS), transmission electron microscopy (TEM)−EDS, and X-ray photoelectron spectroscopy (XPS). The synthesis method proposed in this study appears suitable for the easy preparation of CeO2 solid solutions with a high Pd content.

scholarly journals Effect of Rare Earth Ce on Deep Stamping Properties of High-Strength Interstitial-Free Steel Containing Phosphorus

Materials ◽  
2020 ◽  
Vol 13 (6) ◽  
pp. 1473
Author(s):  
Hao Wang ◽  
Yanping Bao ◽  
Chengyi Duan ◽  
Lu Lu ◽  
Yan Liu ◽  
...  
Keyword(s):  
Solid Solution ◽  
Grain Size ◽  
Rare Earth ◽  
High Strength ◽  
Rolling Process ◽  
P Element ◽  
Second Phase ◽  
Strengthening Effect ◽  
Interstitial Free ◽  
If Steel

The influence of rare earth Ce on the deep stamping property of high-strength interstitial-free (IF) steel containing phosphorus was analyzed. After adding 120 kg ferrocerium alloy (Ce content is 10%) in the steel, the inclusion statistics and the two-dimensional morphology of the samples in the direction of 1/4 thickness of slab and each rolling process were observed and compared by scanning electron microscope (SEM). After the samples in each rolling process were treated by acid leaching, the three-dimensional morphology and components of the second phase precipitates were observed by SEM and energy dispersive spectrometer (EDS). The microstructure of the sample was observed by optical microscope, and the grain size was compared. Meanwhile, the content and strength of the favorable texture were analyzed by X-ray diffraction (XRD). Finally, the mechanical properties of the product were analyzed. The results showed that: (1) The combination of rare earth Ce with activity O and S in steel had lower Gibbs free energy, and it was easy to generate CeAlO3, Ce2O2S, and Ce2O3. The inclusions size was obviously reduced, but the number of inclusions was increased after adding rare earth. The morphology of inclusions changed from chain and strip to spherical. The size of rare earth inclusions was mostly about 2–5 μm, distributed and dispersed, and their elastic modulus was close to that of steel matrix, which was conducive to improving the structure continuity of steel. (2) The rare earth compound had a high melting point. As a heterogeneous nucleation point, the nucleation rate was increased and the solidification structure was refined. The grade of grain size of products was increased by 1.5 grades, which is helpful to improve the strength and plasticity of metal. (3) Rare earth Ce can inhibit the segregation of P element at the grain boundary and the precipitation of Fe(Nb+Ti)P phase. It can effectively increase the solid solution amount of P element in steel, improve the solid solution strengthening effect of P element in high-strength IF steel, and obtain a large proportion of {111} favorable texture, which is conducive to improving the stamping formability index r90 value.

scholarly journals Structural and Raman Vibrational Studies ofCeO2-Bi2O3Oxide System

2009 ◽  
Vol 2009 ◽  
pp. 1-4 ◽  
Author(s):  
L. Bourja ◽  
B. Bakiz ◽  
A. Benlhachemi ◽  
M. Ezahri ◽  
J. C. Valmalette ◽  
...  
Keyword(s):  
Solid Solution ◽  
Raman Spectroscopy ◽  
Phase Changes ◽  
Phase System ◽  
X Ray Diffraction ◽  
X Ray ◽  
Vibrational Studies ◽  
Coprecipitation Route

A series of ceramics samples belonging to theCeO2-Bi2O3phase system have been prepared via a coprecipitation route. The crystallized phases were obtained by heating the solid precursors at600∘Cfor 6 hours, then quenching the samples. X-ray diffraction analyses show that forx<0.20a solid solutionCe1−xBixO2−x/2with fluorine structure is formed. For x ranging between 0.25 and 0.7, a tetragonalβ′phase coexisting with the FCC solid solution is observed. For x ranging between 0.8 and 0.9, a new tetragonalβphase appears. Theβ′phase is postulated to be a superstructure of theβphase. Finally, close tox=1, the classical monoclinicα Bi2O3structure is observed. Raman spectroscopy confirms the existence of the phase changes as x varies between 0 and 1.

Nanostructured TiO2-Based Composites for Light Absorption

2014 ◽  
Vol 975 ◽  
pp. 207-212
Author(s):  
Dayse I. dos Santos ◽  
Olayr Modesto Jr. ◽  
Luis Vicente A. Scalvi ◽  
Americo S. Tabata
Keyword(s):  
Metal Oxide ◽  
Light Absorption ◽  
Structural Characteristics ◽  
Sol Gel ◽  
Second Phase ◽  
X Ray Diffraction ◽  
Two Phase ◽  
X Ray ◽  
Oxide Powders

Metal oxide nanocomposites were prepared by two different routes: polyol and sol-gel. Characterization by X ray diffraction showed that the first process produces directly a two-phase material, while the sol-gel powder never showed second phase below 600°C. Light spectroscopy of the treated powders indicated similarities for the processed materials. Although the overall material compositions are about the same, different structural characteristics are found for each processing. With the exception of Ti-Zn materials, all the double metal oxide powders showed higher absorbance than either TiO2 powder.

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