Phase Equilibria and Dielectric Properties in Perovskite-like (1 − x)LaCa0.5Zr0.5O3–xATiO3 (A = Ca, Sr) Ceramics

2002 ◽  
Vol 17 (7) ◽  
pp. 1729-1734 ◽  
Author(s):  
Igor Levin ◽  
Terrell A. Vanderah ◽  
Rachel Coutts ◽  
Steven M. Bell

Phase equilibria and dielectric properties were analyzed for selected compositions in both LaCa0.5Zr0.5O3–CaTiO3 (LCZ-CT) and LaCa0.5Zr0.5O3–SrTiO3 (LCZ–ST) systems using x-ray powder diffraction and transmission electron microscopy. The end-member LaCa0.5Zr0.5O3 does not occur as a single phase but rather as a mixture of a perovskite-type phase with approximate composition La0.94Ca0.53Zr0.53O3 plus a minor amount of La2O3. This perovskite phase exhibited a combination of 1:1 ordering of Ca and Zr on the B-sites and octahedral tilting. In the (1 – x)LCZ– xCT system, the compositions x = 1/3 and x = 1/2 yielded single phases with perovskite-like structures featuring similar 1:1 B-site ordering superimposed onto octahedral tilting. The x = 1/2 composition in the LCZ–ST system resides in a two-phase field and contains a major perovskite phase and La2O3; the B-cations in the perovskite phase remain disordered at all temperatures. The approximate boundaries of perovskite-like phase fields in the La2O3–ATiO3–CaZrO3 (A = Ca, Sr) systems were outlined, as well as a schematic diagram for perovskite B-cation ordering transitions in the LCZ–CT system. The dielectric properties of the compositions investigated were measured at microwave frequencies and were correlated with the observed structural behavior.

1994 ◽  
Vol 365 ◽  
Author(s):  
Michael D. Sacks ◽  
Gary W. Scheiffele ◽  
Mohamed Saleem ◽  
Gregory A. Staab ◽  
Augusto A. Morrone ◽  
...  

ABSTRACTFine-diameter (∼ 10–15 µm), polymer-derived SiC fibers were characterized. The average tensile strength of the fibers was ∼ 2.8 GPa, although some lots had average strengths exceeding 3.5 GPa. Microstructure observations showed that fibers had fine grain sizes (mostly ∼0.05–0.2 µm), high densities (∼3.1–3.2 g'cm3), and small residual pore sizes (≤0.1 µm). Elemental analysis showed that fibers had near-stoichiometric composition. Electron and X-ray diffraction analyses indicated that fibers were primarily beta silicon carbide, with a minor amount of the alpha phase. A small amount of graphitic carbon was detected in some samples using high resolution transmission electron microscopy. The residual oxygen content in the fibers was ≤0.1 wt%. Fibers exhibited good thermomechanical stability, as heat treatment at 1800°C for 4h in argon resulted in only an ∼ 8% decrease in strength.


2020 ◽  
Vol 9 (5) ◽  
pp. 558-566 ◽  
Author(s):  
Jiamao Li ◽  
Chuimin Zhang ◽  
Hui Liu ◽  
Tai Qiu ◽  
Chuangang Fan

Abstract A rapid and facile approach was developed for the synthesis of ultrafine SmAlO3 powders through the combustion of stearic acid precursors. The obtained products were characterized by typical techniques including X-ray diffraction (XRD), Fourier Transform Infrared (FT-IR), thermogravimetric and differential thermal analysis (TG-DTA), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) to analyze the phase composition and microstructure. The dielectric characteristics of SmAlO3 microwave ceramics, using the as-obtained products as original materials, were also studied. Compared with the conventional solid-state reaction method, the synthesis temperature was dramatically reduced to 750 °C. The large-size sheet structure was composed of a number of micro/nano-scale crystallites, which were mostly irregular in shape due to the mutual growth and overlapping shapes of adjacent grains. The SmAlO3 ceramics with high density and uniform microstructure were obtained after sintering at 1500 °C for 4 h due to the favorable sintering activity of the as-synthesized powders. In addition, desired dielectric properties at microwave frequencies (dielectric constant εr = 20.22, quality factor Q·f = 74110 GHz, and a temperature coefficient of resonant frequency τf = −74.6 ppm/°C) were achieved.


2008 ◽  
Vol 1128 ◽  
Author(s):  
Jörg M. K. Wiezorek ◽  
Andreas K. Kulovits

AbstractWhile only a minor phase constituent, the deformation behavior of the hexagonal α2-Ti3Al phase, significantly affects the mechanical properties of two-phase TiAl based alloys. We have used conventional and high-resolution transmission electron microscopy to investigate the fine structure of pyramidal plane glide dislocations, with Burgers vectors of the type b=<2c+a>, in α2-Ti3Al after room temperature compression of binary polysynthetically twinned TiAl normal to the lamellar interfaces to nominal plastic strains of 1%-7%. We report atomic resolution observations of non-co-planar dislocation core configurations for <2c+a>-dislocations and show that translamellar deformation twins active in the majority γ-TiAl phase play an important role in facilitating pyramidal plane slip in α2-Ti3Al in the lamellar two-phase alloys.


Nanomaterials ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 769 ◽  
Author(s):  
Igor Mashkovsky ◽  
Pavel Markov ◽  
Galina Bragina ◽  
Galina Baeva ◽  
Alexander Rassolov ◽  
...  

Formation of PdIn intermetallic nanoparticles supported on α-Al2O3 was investigated by X-ray powder diffraction (XRD), transmission electron microscopy (TEM), and hydrogen temperature-programmed desorption (H2-TPD) methods. The metals were loaded as heterobimetallic Pd(μ-O2CMe)4In(O2CMe) complex to ensure intimate contact between Pd and In. Reduction in H2 at 200 °C resulted in Pd-rich PdIn alloy as evidenced by XRD and the disappearance of Pd hydride. A minor amount of Pd1In1 intermetallic phase appeared after reduction at 200 °C and its formation was accomplished at 400 °C. Neither monometallic Pd or in nor other intermetallic structures were found after reduction at 400–600 °C. Catalytic performance of Pd1In1/α-Al2O3 was studied in the selective liquid-phase diphenylacetylene (DPA) hydrogenation. It was found that the reaction rate of undesired alkene hydrogenation is strongly reduced on Pd1In1 nanoparticles enabling effective kinetic control of the hydrogenation, and the catalyst demonstrated excellent selectivity to alkene.


2017 ◽  
Vol 24 (2) ◽  
pp. 185-194 ◽  
Author(s):  
Ramaswami Sachidanandan Ernest Ravindran ◽  
Paramanandam Thomas ◽  
Sahadevan Renganathan

AbstractNylon 6,9/CaCu3Ti4O12 (CCTO) nanocrystal composites with relatively high dielectric permittivity (220 at 100 Hz) were fabricated by melt mixing followed by hot pressing. The CCTO nanoceramics were synthesized using the oxalate precursor route, and the transmission electron microscopy studies exhibited that the crystallites are in the range of 20–200 nm. The nanocomposites were characterized using X-ray diffraction, scanning electron microscopy, thermogravimetric analysis, differential scanning calorimetry, and impedance analyzer to study their structural, thermal, and dielectric properties. The introduction of CCTO nanoparticles into the matrix had influenced the thermal properties. The effective dielectric permittivity of the nanocomposite increased by the augmentation of CCTO content in the Nylon 6,9. Our experimental outcomes showed that the fixed dielectric permittivity of such two-phase composite was established above 200 when the CCTO concentration was closer to its percolation threshold. The room temperature dielectric permittivity as high as 220 at 100 Hz has been achieved when the CCTO content increased to 58 vol% in the polymer and this was increased to 3845 at 150°C. The increase in AC conductivity with the increase in the CCTO content in the polymer matrix supported the hopping of the charge carrier conduction mechanism.


2020 ◽  
Vol 16 ◽  
Author(s):  
Alliya Qamar ◽  
Rehana Zia ◽  
Madeeha Riaz

Background: Hydroxyapatite is similar to bone mineral in chemical composition, has good biocompatibility with host tissue and bone. Objective: This work aims to tailor the mechanical and dielectric properties of hydroxyapatite with zinc sudstitution, to improve wearability of implant and accelerate the healing process. Method: Pure and zinc incorporated hydroxyapatite Ca10(PO4)6(OH)2 samples have been successfully prepared by means of the chemical precipitation method. Results: The results showed that hydroxyapatite(Hap) having hexagonal structure was the major phase identified in all the samples. It was found that secondary phase of β-tricalcium phosphate (β-TCP) formed due to addition of Zinc resulting in biphasic structure BCP (Hap + β-TCP). A minor phase of ZnO also formed for higher concentration of Zn (Zn ≥ 2mol%) doping. It was found that the Zn incorporation to Hap enhanced both mechanical and dielectric properties without altering the bioactive properties. The microhardness increased upto 0.87 GPa for Zn concentration equal to 1.5mol%, which is comparable to the human bone ~0.3 - 0.9 GPa. The dielectric properties evaluated in the study showed that 1.5 mol% Zn doped hydroxyapatite had highest dielectric constant. Higher values of dielectric constant at low frequencies signifies its importance in healing processes and bone growth due to polarization of the material under the influence of electric field. Conclusion: Sample Z1.5 having 1.5 mol% Zn doping showed the most optimized properties suitable for bone regeneration applications.


Minerals ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 727
Author(s):  
Shiyun Jin ◽  
Huifang Xu ◽  
Seungyeol Lee

The enigmatic Bøggild intergrowth in iridescent labradorite crystals was revisited in light of recent work on the incommensurately modulated structures in the intermediated plagioclase. Five igneous samples and one metamorphic labradorite sample with various compositions and lamellar thicknesses were studied in this paper. The lamellar textures were characterized with conventional transmission electron microscopy (TEM) and scanning transmission electron microscopy (STEM). The compositions of individual lamellae were analyzed with high-resolution energy-dispersive X-ray spectroscopy (EDS) mapping and atom probe tomography (APT). The average structure states of the studied samples were also compared with single-crystal X-ray diffraction data (SC-XRD). The Na-rich lamellae have a composition of An44–48, and the Ca-rich lamellae range from An56 to An63. Significant differences between the lamellar compositions of different samples were observed. The compositions of the Bøggild intergrowth do not only depend on the bulk compositions, but also on the thermal history of the host rock. The implications on the subsolidus phase relationships of the plagioclase feldspar solid solution are discussed. The results cannot be explained by a regular symmetrical solvus such as the Bøggild gap, but they support an inclined two-phase region that closes at low temperature.


Author(s):  
Nadine S. Rögner ◽  
Veronika Mall ◽  
Martin Steinhaus

AbstractAn odorant screening by gas chromatography–olfactometry (GC–O) and a crude aroma extract dilution analysis (AEDA) applied to the volatiles isolated from a light and a dark liquid malt extract (LME) by solvent extraction and solvent-assisted flavour evaporation (SAFE) identified 28 odorants. Fifteen major odorants were subsequently quantitated and odour activity values (OAVs) were calculated as ratio of the concentration to the respective odour threshold value (OTV). Important odorants in the light LME included 3-(methylsulfanyl)propanal (OAV 1500), (E)-β-damascenone (OAV 430), and 4-ethenyl-2-methoxyphenol (OAV 91). In the dark LME, sotolon (OAV 780), 3-(methylsulfanyl)propanal (OAV 550), (E)-β-damascenone (OAV 410), acetic acid (OAV 160), and maltol (OAV 120) were of particular importance. To get an insight into the changes during malt extract production, the quantitations were extended to the malt used as the starting material for both LMEs. Addition of a minor amount of water to malt before volatile extraction was shown to be effective to cover the free as well as the bound malt odorants. Results showed that some LME odorants originated from the starting material whereas others were formed during processing. Important process-induced LME odorants included (E)-β-damascenone and 4-ethenyl-2-methoxyphenol in the light LME as well as maltol, sotolon, (E)-β-damascenone, and 2-methoxyphenol in the dark LME. In summary, the odorant formation during LME production was shown to be more important than the transfer of odorants from the malt.


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