scholarly journals Study on the nonexistence of liquid miscibility gap in the Ce-Mn system

2007 ◽  
Vol 43 (1) ◽  
pp. 21-28 ◽  
Author(s):  
C. Tang ◽  
Y. Du ◽  
H. Xu ◽  
S. Hao ◽  
L. Zhang

To ascertain whether the liquid miscibility gap exists in the Ce-Mn system, 3 key alloys are prepared by arc melting the pure elements, annealed at specified temperature for 20 minutes, quenched in ice water and then subjected to X-ray diffraction (XRD) analysis for phase identification and to scanning electron microscopy (SEM) with energy dispersive X-ray analysis for microstructure observation and composition analysis. The XRD examination indicated that terminal solutions based on Ce and Mn exist in the water-quenched alloys. No compound was detected. Microstructure observation and composition analysis indicate the nonexistence of the liquid miscibility gap. The newly assessed Ce-Mn phase diagram was presented. .

2016 ◽  
Vol 850 ◽  
pp. 21-26
Author(s):  
Chao Fan Zhu ◽  
Shi Dong Lin ◽  
Jiang Wang ◽  
Mao Hua Rong ◽  
Guang Hui Rao ◽  
...  

In this work, eleven Mn-La alloys were investigated experimentally by means of thermal analysis. The temperatures of the invariant reactions in the Mn-La binary system were determined. To confirm whether the liquid miscibility gap exists in the Mn-La system, one key alloy (Mn72La28) was prepared and then checked by X-ray diffraction (XRD) analysis and scanning electron microscopy (SEM) equipped with energy dispersive X-ray spectroscopy (EDS). Microstructure observation and composition analysis indicated the nonexistence of the liquid miscibility gap. Based on the experimental results obtained in the present work and the critical review of the available experimental data in the published literature, a set of self-consistent thermodynamic parameters for the Mn-La system was obtained using the CALPHAD method by thermodynamic optimization of the selected experimental data.


Nanomaterials ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1969
Author(s):  
Riccardo Scarfiello ◽  
Elisabetta Mazzotta ◽  
Davide Altamura ◽  
Concetta Nobile ◽  
Rosanna Mastria ◽  
...  

The surface and structural characterization techniques of three atom-thick bi-dimensional 2D-WS2 colloidal nanocrystals cross the limit of bulk investigation, offering the possibility of simultaneous phase identification, structural-to-morphological evaluation, and surface chemical description. In the present study, we report a rational understanding based on X-ray photoelectron spectroscopy (XPS) and structural inspection of two kinds of dimensionally controllable 2D-WS2 colloidal nanoflakes (NFLs) generated with a surfactant assisted non-hydrolytic route. The qualitative and quantitative determination of 1T’ and 2H phases based on W 4f XPS signal components, together with the presence of two kinds of sulfur ions, S22− and S2−, based on S 2p signal and related to the formation of WS2 and WOxSy in a mixed oxygen-sulfur environment, are carefully reported and discussed for both nanocrystals breeds. The XPS results are used as an input for detailed X-ray Diffraction (XRD) analysis allowing for a clear discrimination of NFLs crystal habit, and an estimation of the exact number of atomic monolayers composing the 2D-WS2 nanocrystalline samples.


2014 ◽  
Vol 08 (02) ◽  
pp. 211-215 ◽  
Author(s):  
Yeliz Guven ◽  
Elif Bahar Tuna ◽  
Muzaffer Emin Dincol ◽  
Oya Aktoren

ABSTRACT Objective: The purpose of this study was to investigate and compare the crystalline structures of recently released MTA Plus (MTA-P), MTA Angelus (MTA-A), DiaRoot BioAggregate (BA) by X-ray diffraction (XRD) analysis. Materials and Methods: Phase analysis was carried out on powder and set forms of tested materials. The powder specimens placed into sample holders that were packed with a glass slide and the set samples prepared according to the manufacturer's instructions were placed into molds. The samples after being set for three days at 37°C and 100% humidity in an incubator were mounted onto the XRD machine and phase identification was accomplished using a search-match software program. Results: XRD findings indicated that major constituents of MTA-P were bismuth oxide, portlandite, dicalcium silicate and tricalcium silicate. The crystal structure of MTA-A were similar to those of MTA-P except for the absence of portlandite. Additionally, MTA-A had tricalcium aluminate differing from MTA-P. BA mainly differed from MTA-P and MTA-A by the radiopacifier (tantalum oxide-TO) in its composition. Conclusions: The majority of constituents of the tested materials have shown similarity except for the presence of tricalcium aluminate in MTA-A and the inclusion of TO in BA. In addition, set MTA-P showed a strong peak of portlandite.


2010 ◽  
Vol 177 ◽  
pp. 92-95 ◽  
Author(s):  
Ming Yi Wang ◽  
Zong De Liu ◽  
Li Ping Zhao

This paper reports an investigation of the effect of Nb additions on the microstructure of TiC–Ni cermets, which is prepared by plasma cladding technique. The composition of the cermets cladding layer was observed by scanning electron microscope (SEM) in combination with energy dispersive spectrometer (EDS), and X-ray diffraction (XRD) analysis was carried out for phase identification. The microstructure has a trend to become finer with the increase of Nb additions, however, when the Nb addition goes to 15 wt%, the ceramic particles become much bigger and cause large amounts of cracks. Then the component variation of different parts of the ceramic particle was analyzed using the EDS, and explained the reason of the variation and why the rim structure wasn't formed.


Author(s):  
Asif Ali ◽  
Yi Wai Chiang ◽  
Rafael M. Santos

For many decades, X-ray diffraction (XRD) has been used for material characterization. With the recent development in material science understanding and technology, various new materials are being developed, which requires upgrading the existing analytical techniques such that intricate problems can be solved. Although, XRD is a well-established non-destructive technique, it still requires further improvements in its characterization capabilities, especially when dealing with complex mineral structures. The present review conducts comprehensive discussions on atomic crystal structure, XRD principle, its applications, uncertainty during XRD analysis, and required safety precautions, all in one place. It further discusses the future research directions, especially the use of artificial intelligence and machine learning tools for improving the effectiveness and accuracy of XRD technique for mineral characterization. It has been focused that how XRD patterns can be utilized for a thorough understanding of the crystalline structure, size, and orientation, dislocation density, phase identification, quantification, and transformation, information about lattice parameters, residual stress, and strain, and thermal expansion coefficient of materials. All these important discussions on XRD for mineral characterization are compiled in this short yet comprehensive review that would benefit specialists and engineers in the chemical, mining, iron, metallurgy, and steel industries.


2011 ◽  
Vol 194-196 ◽  
pp. 109-112
Author(s):  
Min Huang ◽  
Yun Wu Wang

Ceramic samples with the nominal composition (1-x) BaTiO3 + x Ba3Ti2YO8.5 (x = 0 - 0.4) were prepared by the solid-state reaction method. The X-ray diffraction (XRD) analysis and the lattice parameters determination indicate that the samples with x≤ 0.16 exhibit a single phase cubic perovskite structure. When x > 0.16, the system is of biphasic composites, which consist of Ba(Ti0.911Y0.089)O3 and Ba3Ti2YO8.5. The microstructure observation by Scanning Electron Microscopy (SEM) supports the XRD result. For the biphasic composites, the dielectric constant follows the Lichtenecker relation in a wide temperature range.


TAPPI Journal ◽  
2011 ◽  
Vol 10 (1) ◽  
pp. 17-23
Author(s):  
KEVIN TAYLOR ◽  
RICH ADDERLY ◽  
GAVIN BAXTER

Over time, performance of tubular backpulse pressure filters in kraft mills deteriorates, even with regular acid washing. Unscheduled filter replacement due to filter plugging results in significant costs and may result in mill downtime. We identified acid-insoluble filter-plugging materials by scanning electron microscope/energy-dispersion X-ray spectroscopy (SEM/EDS) and X-ray diffraction (XRD) analysis in both polypropylene and Gore-Tex™ membrane filter socks. The major filter-plugging components were calcium sulfate (gypsum), calcium phosphate (hydroxylapatite), aluminosilicate clays, metal sulfides, and carbon. We carried out detailed sample analysis of both the standard acid-washing procedure and a modified procedure. Filter plugging by gypsum and metal sulfides appeared to occur because of the acid-washing procedure. Gypsum formation on the filter resulted from significant hydrolysis of sulfamic acid solution at temperatures greater than 130°F. Modification of the acid-washing procedure greatly reduced the amount of gypsum and addition of a surfactant to the acid reduced wash time and mobilized some of the carbon from the filter. With surfactant, acid washing was 95% complete after 40 min.


2019 ◽  
Author(s):  
Landon Williamson ◽  
◽  
Nicolas Perdrial ◽  
John M. Hughes ◽  
Mae Kate Campbell ◽  
...  

Author(s):  
Erdoğan Karip ◽  
Mehtap Muratoğlu

People are exposed to different kinds of diseases or various accidents in life. Hydroxyapatite (HA) has been widely employed for bone treatment applications. In this study, HA was extracted from sheep bones. Bio-composites were doped with 1, 5, and 10 wt.% of expanded perlite and 5 wt.% of ZrO2–MgO-P2O5. The bio-composites were prepared by the cold isostatic pressing method (250 MPa) and sintered at 900°C for 1 h. In order to evaluate the characteristics of the bio-composites, microhardness, density, X-ray diffraction (XRD), Fourier transform infra-red spectroscopy (FT-IR), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS) analyses were carried out on them. Additionally, the specimens whose characteristics were determined were kept in synthetic body fluid (SBF), and their in vitro behavior was examined. As a result, it was observed that microhardness increased as both the weight and the grain size of the expanded perlite were increased. Calcium silicate, tri-calcium phosphate, and hydroxyapatite were observed in the XRD analysis of all samples, and the formation of apatite structures was increased by addition of ZrO2–MgO–P2O5.


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