Crystallization behavior and microstructure of lithium-calcium aluminogermanate glasses

1997 ◽  
Vol 12 (11) ◽  
pp. 3158-3164
Author(s):  
Moo-Chin Wang
Keyword(s):  
Electron Microscopy ◽  
Crystallization Behavior ◽  
Xrd Analysis ◽  
Heating Process ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Scanning Transmission ◽  
Fibrillar Morphology ◽  
Two Stages ◽  
Kinetics Of

The crystallization behavior and microstructure of lithium-calcium aluminogermanate (LCAG) glasses have been studied by using differential thermal analysis (DTA), x-ray diffraction (XRD), scanning electron microscopy (SEM), scanning transmission electron microscopy (STEM), and electron diffraction (ED). Uniform crystallization of the LCAG glass was found to result from two stages of the heating process. The kinetics of crystallization of the LCAG glasses was studied by DTA using the nonisothermal method. The activation energy for 3CaO · Al2O3 · 3GeO2 crystal growth was 693 kJ/mol. The precipitated crystals determined by XRD analysis were mainly 3CaO · Al2O3 · 3GeO2, and minor phases of 2CaO · Al2O3 · GeO2 and Li2O · Al2O3 · 2GeO2. Morphology and microstructure of the glasses after heat treatment determined by SEM and STEM techniques are presented. Crystallization starts at the surface of the glass sample and then proceeds toward the interior of glass matrix. The morphology of 2CaO · Al2O3 · GeO2 is that of a subangular bell-shaped single crystal growing in a preferred orientation through the segregated phase matrix of fine dispersion of 3CaO · Al2O3 · 3GeO2 crystals. The Li2O · Al2O3 · 2GeO2 phase grows anisotropically in the fine fibrillar morphology and parallel to the [331].

Understanding the Growth Mechanisms of Tin Oxide Nanowires by Chemical Vapor Deposition

2021 ◽  
Vol 21 (4) ◽  
pp. 2538-2544
Author(s):  
Nguyen Minh Hieu ◽  
Nguyen Hoang Hai ◽  
Mai Anh Tuan
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Chemical Vapor Deposition ◽  
Vapor Deposition ◽  
Chemical Vapor ◽  
Chemical Mapping ◽  
X Ray Diffraction ◽  
Lattice Constants ◽  
Transmission Electron ◽  
Scanning Transmission

Tin oxides nanowires were prepared by chemical vapor deposition using shadow mask. X-ray diffraction indicated that the products were tetragonal having crystalline structure with lattice constants a = 0.474 nm and c = 0.318 nm. The high-resolution transmission electron microscopy revealed that inter planar spacing is 0.25 nm. The results chemical mapping in scanning transmission electron microscopy so that the two elements of Oxygen and Tin are distributed very homogeneously in nanowires and exhibit no apparent elements separation. A bottom-up mechanism for SnO2 growth process has been proposed to explain the morphology of SnO2 nanowires.

Effect of Au on the Performance of Porous Silicon/V2O5 Nanorods Heterojunctions to NO2 Gas

NANO ◽  
2016 ◽  
Vol 11 (07) ◽  
pp. 1650079 ◽  
Author(s):  
Wenjun Yan ◽  
Ming Hu ◽  
Jiran Liang ◽  
Dengfeng Wang ◽  
Yulong Wei ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Porous Silicon ◽  
Room Temperature ◽  
Au Nanoparticles ◽  
Analytical Techniques ◽  
Heating Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

A novel composite of Au-functionalized porous silicon (PS)/V2O5 nanorods (PS/V2O5:Au) was prepared to detect NO2 gas. PS/V2O5 nanorods were synthesized by a heating process of pure vanadium film on PS, and then the obtained PS/V2O5 nanorods were functionalized with dispersed Au nanoparticles. Various analytical techniques, such as field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), have been employed to investigate the properties of PS/V2O5:Au. Herein, the PS/V2O5:Au sample exhibited improved NO2-sensing performances in response, stability and selectivity at room temperature (25[Formula: see text]C), compared with the pure PS/V2O5 nanorods. These phenomena were closely related to not only the dispersed Au nanoparticles acting as a catalyst but also the p-n heterojunctions between PS and V2O5 nanorods. Whereas, more Au nanoparticles suppressed the improvement of response to NO2 gas.

Transformation kinetics for mullite in kaolin–Al2O3 ceramics

2003 ◽  
Vol 18 (6) ◽  
pp. 1355-1362 ◽  
Author(s):  
Yung-Feng Chen ◽  
Moo-Chin Wang ◽  
Min-Hsiung Hon
Keyword(s):  
Glassy Phase ◽  
Avrami Equation ◽  
Mullite Formation ◽  
Transformation Kinetics ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Energy Dispersion Spectrometry ◽  
Two Stages ◽  
Kinetics Of

Transformation kinetics of mullite formation in kaolin–Al2O3 ceramics was studied by x-ray diffraction, transmission electron microscopy, and energy dispersion spectrometry. The mullitization process of kaolin–Al2O3 ceramics is described by two stages; one is the primary mullite transformation at 1273 to 1573 K, and the other is the secondary mullite formation at 1573 to 1873 K. The activation energy of 1164.6 kJ mol-1 obtained for the secondary mullite formation is lower than 1356.9 kJ mol-1 for the primary mullite transformation by the general form of the Johnson–Mehl–Avrami equation. The lower value of growth morphology parameter strongly supports that in the secondary mullite formation the added alumina is dissolved into glassy phase and the mullite is then precipitated.

scholarly journals Synthesis, Characterization, and Photocatalytic Performance of Mesoporous α-Mn2O3 Microspheres Prepared via a Precipitation Route

2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Manoj Pudukudy ◽  
Zahira Yaakob
Keyword(s):  
Electron Microscopy ◽  
Uv Light ◽  
Thermal Transformation ◽  
Xrd Analysis ◽  
Structural Deformation ◽  
Blue Dye ◽  
X Ray Diffraction ◽  
Electron Microscopic ◽  
X Ray ◽  
Transmission Electron

α-Mn2O3 microspheres with high phase purity, crystallinity, and surface area were synthesized by the thermal decomposition of precipitated MnCO3 microspheres without the use of any structure directing agents and tedious reaction conditions. The prepared Mn2O3 microspheres were characterized by Fourier transform infrared (FTIR) spectroscopy, powder X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), and Brunauer-Emmett-Teller (BET) and photoluminescence (PL) studies. The complete thermal transformation of MnCO3 to Mn2O3 was clearly shown by the FTIR and XRD analysis. The electron microscopic images clearly confirmed the microsphere-like morphology of the products with some structural deformation for the calcined Mn2O3 sample. The mesoporous texture generated from the interaggregation of subnanoparticles in the microstructures is visibly evident from the TEM and BET studies. Moreover, the Mn2O3 microstructures showed a moderate photocatalytic activity for the degradation of methylene blue dye pollutant under UV light irradiation, using air as the potential oxidizing agent.

scholarly journals Hydrothermal Synthesis of MnWO4@GO Composite as Non-Precious Electrocatalyst for Urea Oxidation

Nanomaterials ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 85
Author(s):  
Patnamsetty Chidanandha Nagajyothi ◽  
Kisoo Yoo ◽  
Rajavaram Ramaraghavulu ◽  
Jaesool Shim
Keyword(s):  
Electron Microscopy ◽  
Hydrothermal Synthesis ◽  
Photoelectron Spectroscopy ◽  
Xrd Analysis ◽  
Morphological Characterization ◽  
Energy Storage And Conversion ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Density Values

In this study, manganese tungstate (MW) and MW/graphene oxide (GO) composites were prepared by a facile hydrothermal synthesis at pH values of 7 and 12. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy were used for the structural, compositional, and morphological characterization of the nanoparticles (NPs). The XRD analysis revealed that the formation of monoclinic MnWO4 did not have impurities. The SEM and TEM analyses showed that the synthesized NPs were rod-shaped and well-distributed on the GO. The as-synthesized samples can be used as electrocatalysts for the urea oxidation reaction (UOR). The MW@GO-12 electrocatalyst exhibited higher current density values compared to other electrocatalysts. This study provides a new platform for synthesizing inexpensive nanocomposites as promising electrocatalysts for energy storage and conversion applications.

Enhancement of durability of NIR emission of Ag2S@ZnS QDs in water

2017 ◽  
Vol 31 (32) ◽  
pp. 1750297 ◽  
Author(s):  
M. Karimipour ◽  
M. Bagheri ◽  
M. Molaei
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Xrd Analysis ◽  
Core Shell ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Nir Emission ◽  
Core Shell Structure ◽  
Phase Transmission

Stability of Ag2S@ZnS QDs in water is a crucial concern for their application in biology. In this work, both physical sustainability and emission stability of Ag2S QDs were enhanced using parameter optimization of a pulsed microwave irradiation (MI) method up to 105 days after their preparation. UV–Vis and photoluminescence spectroscopies depicted an absorption and emission about 817 nm and 878 nm, respectively. X-ray diffraction (XRD) analysis showed a growth of Ag2S acanthite phase. Transmission Electron Microscopy (TEM) images revealed a clear formation of Ag2S@ZnS core–shell structure.

scholarly journals New Insight on the Hydrogen Absorption Evolution of the Mg–Fe–H System under Equilibrium Conditions

Metals ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 967 ◽  
Author(s):  
Julián Puszkiel ◽  
M. Castro Riglos ◽  
José Ramallo-López ◽  
Martin Mizrahi ◽  
Thomas Gemming ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Formation Mechanism ◽  
X Ray Diffraction ◽  
Equilibrium Conditions ◽  
Edge Structure ◽  
X Ray ◽  
Solid Diffusion ◽  
Transmission Electron ◽  
Scanning Transmission

Mg2FeH6 is regarded as potential hydrogen and thermochemical storage medium due to its high volumetric hydrogen (150 kg/m3) and energy (0.49 kWh/L) densities. In this work, the mechanism of formation of Mg2FeH6 under equilibrium conditions is thoroughly investigated applying volumetric measurements, X-ray diffraction (XRD), X-ray absorption near edge structure (XANES), and the combination of scanning transmission electron microscopy (STEM) with energy-dispersive X-ray spectroscopy (EDS) and high-resolution transmission electron microscopy (HR-TEM). Starting from a 2Mg:Fe stoichiometric powder ratio, thorough characterizations of samples taken at different states upon hydrogenation under equilibrium conditions confirm that the formation mechanism of Mg2FeH6 occurs from elemental Mg and Fe by columnar nucleation of the complex hydride at boundaries of the Fe seeds. The formation of MgH2 is enhanced by the presence of Fe. However, MgH2 does not take part as intermediate for the formation of Mg2FeH6 and acts as solid-solid diffusion barrier which hinders the complete formation of Mg2FeH6. This work provides novel insight about the formation mechanism of Mg2FeH6.

Study on the Growth Mechanism of K2Ti4O9 Crystal

2018 ◽  
Vol 37 (5) ◽  
pp. 405-410
Author(s):  
Xuesong Zhou ◽  
Jing Fan ◽  
Xiaoli Wei ◽  
Yi Shen ◽  
Yanzhi Meng
Keyword(s):  
Electron Microscopy ◽  
Growth Mechanism ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
Calcination Temperatures ◽  
Transmission Electron ◽  
Transformation Reaction ◽  
Calcination Method ◽  
Potassium Hexatitanate ◽  
Parallel Action

AbstractPotassium hexatitanate (K2Ti4O9) whiskers were prepared by the kneading–drying–calcination method. After the preparation of products under different calcination temperatures and holding times, their morphology and structure were characterized by thermogravimetric and differential thermal, X-ray diffraction (XRD), scanning electron microscopy and transmission electron microscopy. The XRD analysis showed that the reaction mixture was completely converted to K2Ti4O9 crystals at 800 °C when the T/K ratio was 3. Based on the analysis of LS (liquid–solid) growth mechanism, the corresponding transformation reaction mechanism during the roasting was elucidated. K2Ti4O9 whiskers grow mainly through the parallel action at a low temperature. With the increase in temperature, the series effect is obvious.

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