Phase Investigations of Copper Based CuZn38Al2MnFe Alloy

2006 ◽  
Vol 113 ◽  
pp. 537-540
Author(s):  
Marek Szkodo ◽  
M. Głowacka ◽  
M. Smajdor ◽  
Henryk Bugłacki

In the work phase investigations of special brass CuZn38Al2MnFe alloy are presented. The microstructure, chemical composition and phase identification of the investigated alloy were examined using scanning electron microscopy (Philips 30/ESEM), light microscopy Leica coupled with PC computer with installed MultiScan program, energy dispersive X-ray spectroscopy (EDX) and X-ray diffractometry (XRD), respectively. The investigation of volume fraction existing phases was carried out using image analysis. It was found in the test bend that presence of Fe4Mn77Si19 phase in microstructure caused an increase of brittleness of the tested alloy.

1989 ◽  
Vol 03 (11) ◽  
pp. 877-885
Author(s):  
C.Y. HUANG ◽  
H.H. TAI ◽  
M.K. WU

Scanning electron microscopy, energy dispersive X-ray spectroscopy, and polarized light microscopy have shown that the addition of AgO to the E uBa 2 Cu 3 O y and GdBa 2 Cu 3 O y systems results in the growth of very large grains. Distribution of silver particle appears to influence the grain formation and growth in the superconducting composites.


Metals ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 723 ◽  
Author(s):  
Sónia Simões ◽  
Carlos Tavares ◽  
Aníbal Guedes

Joining γ-TiAl alloy to Ni-based superalloy Hastelloy using Ag-Cu sputtered coated Ti foil as brazing filler was investigated in this study. Brazing experiments were performed at 900, 950, and 980 °C with a dwelling stage of 10 min in vacuum. The microstructure and the chemical composition of the resulting interfaces were analyzed by scanning electron microscopy (SEM) and by energy dispersive X-ray spectroscopy (EDS), respectively. Sound joints were produced after brazing at 980 °C, presenting a multilayered interface, consisting mainly of Ti-Al and Ti-Ni-Al intermetallics close to the γ-TiAl alloy, and of Ti-rich, Ti-Ni, and Cr-Ni-Mo rich phases near Hastelloy. The hardness of the interface, ranging from around 300 to 1100 HV0.01, is higher than both base materials, but no segregation of either Ag solid solution or coarse intermetallic particles was observed. Therefore, the developed brazing filler also avoids the need to perform post-brazing heat treatments that aim to eliminate detrimental extensive segregation of either soft phases or of hard and brittle compounds.


2015 ◽  
Vol 41 (1) ◽  
pp. 17-21 ◽  
Author(s):  
Mariana Lima da Costa Valente ◽  
Antonio Carlos Shimano ◽  
Elcio Marcantonio Junior ◽  
Andréa Candido dos Reis

The purpose of the study was to use scanning electron microscopy and energy dispersive x-ray spectrometry to assess possible morphologic and chemical changes after performing double-insertion and pullout tests of implants of different shapes and surface treatments. Four different types of implants were used—cylindrical machined-surface implants, cylindrical double-surface–treated porous implants, cylindrical surface-treated porous implants, and tapered surface-treated porous implants—representing a total of 32 screws. The implants were inserted into synthetic bone femurs, totaling 8 samples, before performing each insertion with standardized torque. After each pullout the implants were analyzed by scanning electron microscopy and energy dispersive x-ray spectrometry using a universal testing machine and magnified 35 times. No structural changes were detected on morphological surface characterization, only substrate accumulation. As for composition, there were concentration differences in the titanium, oxygen, and carbon elements. Implants with surface acid treatment undergo greater superficial changes in chemical composition than machined implants, that is, the greater the contact area of the implant with the substrate, the greater the oxide layer change. In addition, prior manipulation can alter the chemical composition of implants, typically to a greater degree in surface-treated implants.


IAWA Journal ◽  
2020 ◽  
Vol 41 (3) ◽  
pp. 356-389
Author(s):  
Nadeeshani Karannagoda ◽  
Antanas Spokevicius ◽  
Steven Hussey ◽  
Gerd Bossinger

Abstract The products of secondary xylem are of significant biological and commercial importance, and as a result, the biology of secondary growth and how intrinsic and extrinsic factors influence this process have been the subject of intense investigation. Studies into secondary xylem range in scale from the cellular to the forest stand level, with phenotypic analyses often involving the assessment of traits relating to cell morphology and cell wall chemical composition. While numerous techniques are currently available for phenotypic analyses of samples containing abundant amounts of secondary tissue, only a few of them (microanalytical techniques) are suitable when working with limiting amounts of secondary tissue or where a fine-scale resolution of morphological features or cell wall chemical composition is required. While polarised light microscopy, scanning electron microscopy, field emission-scanning electron microscopy and X-ray scattering and micro-tomography techniques serve as the most frequently used microanalytical techniques in morphotyping, techniques such as scanning ultraviolet microspectrophotometry, X-ray photoelectron spectroscopy, gas chromatography, Fourier-transform infrared spectroscopy and matrix-assisted laser desorption ionisation mass spectrometry serve as the most commonly used microanalytical techniques in chemotyping. Light microscopy, fluorescence microscopy, confocal laser scanning microscopy, transmission electron microscopy and Raman spectroscopy serve as dual micro morphotyping and chemotyping techniques. In this review, we summarise and discuss these techniques in the light of their applicability as microanalytical techniques to study secondary xylem.


2011 ◽  
Vol 311-313 ◽  
pp. 864-870
Author(s):  
Gen Zhe Huang ◽  
Zeng Hui Li

In the present work, effects of elements vanadium and niobium on the microstructure of the conventional indefinite chilled rolls made by small vertical centrifugal caster were investigated, using optical microscopy, Scanning Electron Microscopy (SEM, Jeol 6400), Energy Dispersive X-ray Spectroscopy (EDXS, Cu-K radiation) to identify the type, morphology, and to measure the volume fraction and the distribution of carbides and graphites formed during solidification. Microstructural analysis indicates that, the amount of graphite is dramatically reduced by adding V element. The volume fraction of the square-like carbides NbC increases with the Nb content increasing. However, if Nb content is over a critical point, large amount of the square-like NbC carbide can be seriously segregated in the out part of the section.


2020 ◽  
Vol 60 (6) ◽  
Author(s):  
Jan Loskot ◽  
Maciej Zubko ◽  
Zbigniew Janikowski

In the presented research, the methods of scanning electron microscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction and transmission electron microscopy were applied to analyse the powder waste obtained by cutting of AW-3103 aluminium alloy using a fibre laser. The scanning electron microscopy allows to analyse the morphology of the waste microparticles, the energy-dispersive X-ray spectroscopy revealed their chemical composition, which was compared with the composition of the original cut material. In the waste powder, mainly plate-like particles were observed that contain almost pure aluminium. X-ray powder diffraction measurements confirmed that the waste powder is composed of aluminium phase with only a slight presence of other phases (magnetite, austenite and graphite) and the transmission electron microscopy revealed the presence of nanoscale particles in this waste powder. Furthermore, it was found that the average size of the microparticles depends on the thickness of the cut material: particles obtained from a thicker workpiece were substantially bigger than those obtained from the thinner material. On the contrary, the dimensions of the workpiece have only a little impact on the particles’ shape and no significant influence on their chemical composition. The results also suggest that the microparticles could be used as an input material for powder metallurgy. But there is also a certain health risk connected with inhalation of such tiny particles, especially the nanoparticles, which can penetrate deep into the human pulmonary system.


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