Microstructural analysis in the depth direction of a heteroepitaxial AlN thick film grown on a trench-patterned template by nanobeam X-ray diffraction

2018 ◽  
Vol 123 (16) ◽  
pp. 161563 ◽  
Author(s):  
K. Shida ◽  
S. Takeuchi ◽  
T. Tohei ◽  
H. Miyake ◽  
K. Hiramatsu ◽  
...  
Keyword(s):  
Thick Film ◽  
Microstructural Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Depth Direction

scholarly journals Effect of Molybdenum Content on the Corrosion and Microstructure of Low-Ni, Co-Free Maraging Steels

Metals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 852
Author(s):  
Asiful H. Seikh ◽  
Hossam Halfa ◽  
Mahmoud S. Soliman
Keyword(s):  
Corrosion Resistance ◽  
Electrochemical Impedance ◽  
Microstructural Analysis ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
Alloying Element ◽  
X Ray ◽  
Maraging Steels ◽  
Eds Analysis ◽  
Electroslag Refining

Molybdenum (Mo) is an important alloying element in maraging steels. In this study, we altered the Mo concentration during the production of four cobalt-free maraging steels using an electroslag refining process. The microstructure of the four forged maraging steels was evaluated to examine phase contents by optical microscopy, scanning electron microscopy (SEM), and X-ray diffraction (XRD) analysis. Additionally, we assessed the corrosion resistance of the newly developed alloys in 3.5% NaCl solution and 1 M H2SO4 solution through potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) techniques. Furthermore, we performed SEM and energy-dispersive spectroscopy (EDS) analysis after corrosion to assess changes in microstructure and Raman spectroscopy to identify the presence of phases on the electrode surface. The microstructural analysis shows that the formation of retained austenite increases with increasing Mo concentrations. It is found from corrosion study that increasing Mo concentration up to 4.6% increased the corrosion resistance of the steel. However, further increase in Mo concentration reduces the corrosion resistance.

Synthesis and Characterization of New Refractory Coatings Based on Talc, Cordierite, Zircon and Mullite Fillers for Lost Foam Casting Process

2014 ◽  
Vol 59 (1) ◽  
pp. 89-95 ◽  
Author(s):  
A. Prstić ◽  
Z. Aćimović-Pavlović ◽  
A. Terzić ◽  
L. Pavlović
Keyword(s):  
Microstructural Analysis ◽  
Casting Process ◽  
Lost Foam Casting ◽  
X Ray Diffraction ◽  
X Ray ◽  
Software Application ◽  
Design And Optimization ◽  
Refractory Coatings ◽  
Particle Size And Shape ◽  
Lost Foam

Abstract Refractory coatings based on different refractory fillers (talc, cordierite, zircon and mullite) for application in Lost Foam casting process were investigated. Design and optimization of the coatings composition with controlled, rheological properties included, and consequently synthesis were achieved by application of different coating components, namely different suspension agents and fillers and by alteration of the coating production procedure. Morphologic and microstructural analysis of fillers was carried out by means of scanning electronic microscope. X-ray diffraction analysis by means of X-ray diffractometer was applied in determination and monitoring the phase composition changes of the refractory fillers. An analysis of the particle size and shape was carried out by means of the PC software application package OZARIA 2.5. To assess the effects of application of individual refractory coatings, a detailed investigation of structural and mechanical properties of the moldings obtained was performed. Highlight was placed on revealing and analyzing surface and volume defects present on moldings. Radiographic molding tests were carried out by means of the X-ray device SAIFORT type-S200. Attained results are essential for the synthesis of refractory coatings based on high-temperature fillers and their applications in Lost Foam casting process for manufacturing of moldings with in-advance-set properties.

High-performance electrical properties of La-based perovskite ceramics for the functional phase of thick film resistors

2020 ◽  
Author(s):  
Yongcheng Lu ◽  
Yuanxun Li ◽  
Daming Chen ◽  
Rui Peng ◽  
Qinghui Yang ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Electrical Properties ◽  
Thick Film ◽  
High Performance ◽  
Composite Ceramics ◽  
X Ray Diffraction ◽  
X Ray ◽  
Alternative Material ◽  
Perovskite Ceramics ◽  
Scanning Electron

Abstract In order to explore an economical functional phase alternative material for thick film resistors, the crystal structure, microstructure, and electrical properties of (1-x)LSCN + xLCNZ (x = 0.0–1.0) composite ceramics were studied through solid-state reaction experiments. The composite ceramics were characterized by x–ray diffraction, scanning electron microscopy, energy dispersive x–ray spectroscopy, and DC four–probe method. Results suggested that the main phases of LSCN and LCNZ were formed, along with a small part of impurity phases. The addition of LCNZ to LSCN decreased the electrical conductivity and changed the TCR from positive to negative. Zero TCR could be achieved around 0.6 < x < 0.8 and relatively low absolute TCR values could be obtained for the samples of 0.4 ≤ x ≤ 0.8. The ceramic of 0.6LSCN + 0.4LCNZ showed the optimal performances of conductivity = 1923 S/cm, TCR = 379.54 ppm/℃, and relative density = 95.05%.

scholarly journals Synthesis and Ring-Opening Metathesis Polymerization of a New Norbornene Dicarboximide with a Pendant Carbazole Moiety

2019 ◽  
Vol 2019 ◽  
pp. 1-10
Author(s):  
Stefania Pragliola ◽  
Antonio Botta ◽  
Rubina Troiano ◽  
Veronica Paradiso ◽  
Fabia Grisi
Keyword(s):  
Ring Opening ◽  
Microstructural Analysis ◽  
Fluorescence Analysis ◽  
Dsc Analysis ◽  
X Ray Diffraction ◽  
Ring Opening Metathesis Polymerization ◽  
Metathesis Polymerization ◽  
X Ray ◽  
Excimer Formation ◽  
Film Polymer

A new norbornene dicarboximide presenting a pendant carbazole moiety linked by a p-methylene benzyl spacer is synthesized. This carbazole-functionalized monomer is polymerized via ring-opening metathesis polymerization using Grubbs third-generation catalyst. Microstructural analysis of resulting polymers performed by Nuclear Magnetic Resonance (NMR) shows that they are stereoirregular. Wide-angle X-ray diffraction (WAXD) and thermal (DSC) analysis indicate that polymers are also amorphous. With respect to the fluorescence analysis, both solution and film polymer samples exhibit only “normal structured” carbazole fluorescence, while excimer formation by overlap of carbazole groups is not detected.

Effect of nano Al2O3 coated Ag reinforced Cu matrix nanocomposites on mechanical and tribological behavior synthesis by P/M technique

2020 ◽  
Vol 54 (30) ◽  
pp. 4921-4928
Author(s):  
A Mohamed ◽  
MM Mohammed ◽  
AF Ibrahim ◽  
Omyma A El-Kady
Keyword(s):  
Wear Behavior ◽  
Composite Coatings ◽  
Microstructural Analysis ◽  
Wear Test ◽  
Test Results ◽  
X Ray Diffraction ◽  
X Ray ◽  
Average Hardness ◽  
Ag Particles ◽  
Matrix Nanocomposites

In this study, copper powder was reinforced with different weight percentages of Al2O3 particles (0, 5, 10, and 15 wt.% Al2O3 coated Ag) to produce Cu-Al2O3 composites by mechanical alloying and uniaxial cold pressing/sintering route. Electro-less deposition was used to coat Al2O3 particles with Ag. The microstructure of the consolidated samples was investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX) elemental mapping. The porosity, microhardness, and wear behavior of the consolidated samples were also investigated as a function of Al2O3 content. The EDX mapping images reveal that the Al2O3 reinforcement particles were homogeneously distributed into the Cu matrix. Microstructural analysis shows that the addition of Al2O3 coated Ag particles improves density of the composites coating. SEM micrographs result shows that slight porosities exist in the composites produced. Furthermore, the average hardness of the composite coatings varies from 72.3 to 187.6 HV as Al2O3 content increases from 0 to 15 wt.%. The wear test results showed that the composite with higher Al2O3 content 15 wt.% showed the best wear resistance.

X-ray diffraction Warren–Averbach mullite analysis in whiteware porcelains: influence of kaolin raw material

Clay Minerals ◽  
2018 ◽  
Vol 53 (3) ◽  
pp. 471-485 ◽  
Author(s):  
Angel Sanz ◽  
Joaquín Bastida ◽  
Angel Caballero ◽  
Marek Kojdecki
Keyword(s):  
Crystallite Size ◽  
Firing Temperature ◽  
Microstructural Analysis ◽  
Stoichiometric Composition ◽  
Raw Material ◽  
Size Distributions ◽  
X Ray Diffraction ◽  
X Ray ◽  
Different Temperatures ◽  
Crystallite Sizes

ABSTRACTCompositional and microstructural analysis of mullites in porcelain whitewares obtained by the firing of two blends of identical triaxial composition using a kaolin B consisting of ‘higher-crystallinity’ kaolinite or a finer halloysitic kaolin M of lower crystal order was performed. No significant changes in the average Al2O3 contents (near the stoichiometric composition 3:2) of the mullites were observed. Fast and slow firing at the same temperature using B or M kaolin yielded different mullite contents. The Warren–Averbach method showed increase of the D110 mullite crystallite size and crystallite size distributions with small shifts to greater values with increasing firing temperature for the same type of firing (slow or fast) using the same kaolin, as well as significant differences between fast and slow firing of the same blend at different temperatures for each kaolin. The higher maximum frequency distribution of crystallite size observed at the same firing temperature using blends with M kaolin suggests a clearer crystallite growth of mullite in this blend. The agreement between thickening perpendicular to prism faces and mean crystallite sizes <D110> of mullite were not always observed because the direction perpendicular to 110 planes is not preferred for growth.

scholarly journals Enhancement of Acetone Gas-Sensing Responses of Tapered WO3 Nanorods through Sputtering Coating with a Thin SnO2 Coverage Layer

Nanomaterials ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 864 ◽  
Author(s):  
Yuan-Chang Liang ◽  
Yu Chao
Keyword(s):  
Gas Sensing ◽  
Microstructural Analysis ◽  
Xrd Analysis ◽  
Thin Layers ◽  
Elemental Distribution ◽  
Distribution Analysis ◽  
Acetone Vapor ◽  
X Ray Diffraction ◽  
X Ray ◽  
Composite Nanorods

WO3–SnO2 composite nanorods were synthesized by combining hydrothermal growth of tapered tungsten trioxide (WO3) nanorods and sputter deposition of thin SnO2 layers. Crystalline SnO2 coverage layers with thicknesses in the range of 13–34 nm were sputter coated onto WO3 nanorods by controlling the sputtering duration of the SnO2. The X-ray diffraction (XRD) analysis results demonstrated that crystalline hexagonal WO3–tetragonal SnO2 composite nanorods were formed. The microstructural analysis revealed that the SnO2 coverage layers were in a polycrystalline feature. The elemental distribution analysis revealed that the SnO2 thin layers homogeneously covered the surfaces of the hexagonally structured WO3 nanorods. The WO3–SnO2 composite nanorods with the thinnest SnO2 coverage layer showed superior gas-sensing response to 100–1000 ppm acetone vapor compared to other composite nanorods investigated in this study. The substantially improved gas-sensing responses to acetone vapor of the hexagonally structured WO3 nanorods coated with the SnO2 coverage layers are discussed in relation to the thickness of SnO2 coverage layers and the core–shell configuration of the WO3–SnO2 composite nanorods.

Determination of Biaxial Texture of Thick Film EuBa2Cu3O7-δHomo-substrate by X-ray Diffraction

2006 ◽  
Vol 45 (2A) ◽  
pp. 983-988 ◽  
Author(s):  
Sheng-Qi Wang ◽  
Jian-Zhong Zhang ◽  
Roberta A. Bigelow ◽  
Robert S. Markiewicz ◽  
Bill C. Giessen
Keyword(s):  
Thick Film ◽  
X Ray Diffraction ◽  
X Ray ◽  
Biaxial Texture

Microstructural analysis of high-pressure compressed C60

2001 ◽  
Vol 16 (7) ◽  
pp. 1960-1966 ◽  
Author(s):  
K. Miyazawa ◽  
H. Satsuki ◽  
M. Kuwabara ◽  
M. Akaishi
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
High Pressure ◽  
High Resolution ◽  
Microstructural Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Hardness Tests ◽  
Lattice Planes

The structure and hardness of C60 bulk specimens compressed under 5.5 GPa at room temperature to 600 °C are investigated by high-resolution transmission electron microscopy, x-ray diffraction, and micro-Vickers hardness tests. A strong accumulation of the [1 1 0]tr orientation of high-pressure-treated C60 specimens was developed along the compression axis, and stacking faults and nano-sized deformation twins were introduced into the C60 specimens compressed at 450–600 °C. Curved lattice planes indicating a polymerization of C60 were observed by high resolution transmission electron microscopy (HRTEM). The polymerization of the high-pressure-compressed C60 is also supported by the computer simulation of HRTEM images.

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