Characterisation of β Phase in WE54 Magnesium Alloy

2007 ◽  
Vol 130 ◽  
pp. 155-158 ◽  
Author(s):  
Tomasz Rzychoń ◽  
Andrzej Kiełbus ◽  
Bożena Bierska-Piech
Keyword(s):  
Electron Microscopy ◽  
Rare Earth ◽  
Volume Fraction ◽  
Ageing Time ◽  
Lattice Parameter ◽  
Rare Earth Alloys ◽  
X Ray Diffraction ◽  
X Ray ◽  
Β Phase ◽  
Transmission Electron

Precipitation hardened magnesium-rare earth alloys offer attractive properties for the aerospace and racing automotive industries. The most successful magnesium alloys developed to date have been those based on the Mg-Y-Nd system identified as WE54 (Mg-5.0wt%Y-4.1wt%RE-0.5wt%Zr) and WE43 (Mg-4.0wt%Y-3.3wt%RE-0.5wt%Zr), where RE represents neodymium-rich rare earth elements. Precipitations sequence in WE-system alloys involved the formation of phases designated β”, β’, β1 and β depending on the ageing temperature. WE54 alloy with the equilibrium β-phase exhibits good ductility and medium tensile strength. The β phase precipitated in Mg-Y-Nd alloy during ageing at 300 °C was studied using X-ray diffraction analysis and transmission electron microscopy. Precipitation at 300 °C for one hour causes formation of the equilibrium β phase. This phase has an f.c.c. structure (a = 2.2 nm), which makes it isomorphous with Mg5Gd. With the prolonged ageing time at 300 °C, the volume fraction of the β phase increases and lattice parameter of the solid solution of α-magnesium decreases.

Preparation and Property of Al87Ce3Ni8.5Mn1.5 Nanophase Amorphous Composites

2011 ◽  
Vol 412 ◽  
pp. 263-266
Author(s):  
Hong Wei Zhang ◽  
Li Li Zhang ◽  
Feng Rui Zhai ◽  
Jia Jin Tian ◽  
Can Bang Zhang
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Single Phase ◽  
Volume Fraction ◽  
Material Structure ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
Different Temperatures

The higher mechanical strength of Al87Ce3Ni8.5Mn1.5 nanophase amorphous composites has been obtained with two methods. The first nanophase amorphous composites are directly produced by the single roller spin quenching technology. The method taken for the second nanophase amorphous composites is at first to obtain amorphous single-phase alloy, followed by annealed at different temperatures .The formative condition, the microstructure, the particle size, the volume fraction of α-Al phase and microhardness of nanophase amorphous composites etc have been investigated and compared by X-ray diffraction (XRD) and transmission electron microscopy (TEM) and differential scanning calorimetry (DSC). The microstructure of composites produced by the second method is higher than the former, the fabricated material structure of the system is more uniform and the process is easier to control.

Morphological and structural evolutions of nonequilibrium titanium-nitride alloy powders produced by reactive ball milling

1992 ◽  
Vol 7 (4) ◽  
pp. 888-893 ◽  
Author(s):  
M. Sherif El-Eskandarany ◽  
K. Sumiyama ◽  
K. Aoki ◽  
K. Suzuki
Keyword(s):  
Electron Microscopy ◽  
Titanium Nitride ◽  
Gas Flow ◽  
Lattice Parameter ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Nitrogen Gas ◽  
X Ray ◽  
Grain Sizes ◽  
Transmission Electron

Nonequilibrium titanium-nitride alloy powders have been fabricated by a high energetic ball mill under nitrogen gas flow at room temperature and characterized by means of x-ray diffraction, scanning electron microscopy, transmission electron microscopy, and differential scanning calorimetry. Initial hcp titanium is completely transformed to nonequilibrium-fcc Ti–N after 720 ks of the milling time. The fcc Ti–N phase is stable at relatively low temperature and transforms at 855 K to Ti2N and δ phases. At the final stage of milling, the particle- and grain-sizes of alloy powders are 1 mm and 5 nm, respectively, and the lattice parameter is 0.419 nm.

Phase Transformation in Binary Titanium-Base Alloys with Metals of the I, IV−VIII Groups

2007 ◽  
Vol 546-549 ◽  
pp. 1349-1354 ◽  
Author(s):  
A.V. Dobromyslov
Keyword(s):  
Electron Microscopy ◽  
Structural Information ◽  
Eutectoid Decomposition ◽  
X Ray Diffraction ◽  
Minimum Concentration ◽  
X Ray ◽  
Β Phase ◽  
Ω Phase ◽  
Α Phase ◽  
Transmission Electron

Martensitic β→α′(α″) transformation, β→ω transformation and eutectoid decomposition in a series of Ti-base alloys with d transition metals of Groups I, IV-VIII have been investigated using the techniques of X-ray diffraction, optical and transmission electron microscopy. Phase and structural information is given on the non-equilibrium and metastable modifications occurring in these alloys after quenching from high-temperature β-field and aging. The conditions of the orthorhombic α″-phase, ω-phase and metastable β-phase formation in binary titanium–base alloys with d-metals of V-VIII groups were investigated. It was established that the position of the alloying metal in the Periodic Table defines the presence or absence of the α″-phase in the alloy after quenching and the minimum concentration of the alloying metal necessary for formation of the α″-phase, ω-phase and metastable β-phase.

Research on Solution and Aging Treatment of Mg-7Zn-3Al Alloy

2007 ◽  
Vol 561-565 ◽  
pp. 247-250
Author(s):  
Jing Zhang ◽  
Fu Sheng Pan ◽  
Ru Lin Zuo
Keyword(s):  
Electron Microscopy ◽  
Grain Boundary ◽  
Volume Fraction ◽  
Solution Treatment ◽  
Aging Treatment ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Quantitative Image ◽  
The Matrix

Effect of solution and aging treatment on the microstructure of Mg-7Zn-3Al alloy is studied by using optical microscopy, scanning electron microscopy, X-ray diffraction, transmission electron microscopy and quantitative image analysis. The results show that the as-aged microstructure is composed of α-Mg matrix, grain boundary τ (Mg32(Al,Zn)49 ) phase, and fine dispersed τ particles inside the grain. The solution degree has significant effects on the formation, morphology, and size of the grain boundary τ phase. The volume fraction and the size of the undissolved eutectic τ phase decrease with the increase of solution time treated at 325°C. Through sufficient solution treatment, discontinuous eutectic τ phase retains fine strip morphology after aging, in contrast to the microstructure in sample undergone insufficient solution which manifests as-cast feature, while at the same time nano-sized particles precipitate out from the matrix. The precipitates display paralleled short bar, having certain orientation relationship with the matrix.

Novel Process for Synthesizing Nano-Ceramics Powder: Mechanical & Thermal Activation Processing

2007 ◽  
Vol 280-283 ◽  
pp. 581-586 ◽  
Author(s):  
Xiao Long Cui ◽  
Li Shan Cui
Keyword(s):  
Electron Microscopy ◽  
Mechanical Activation ◽  
Thermal Activation ◽  
Processing Time ◽  
Lattice Parameter ◽  
Synthesis Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

A novel process for synthesizing nano-ceramics powders, named Mechanical & Thermal Activation Processing, is discussed in the present paper. Dissimilar with the tradition processing of mechanical activation or mechanochemistry, the processing is based on thermal activation in liquid phase (molten salt) after mechanical activation. The synthesizing of nanometer sized TiC particles by the method was investigated. The end product has been analyzed by X-ray diffraction (XRD),transmission electron microscope (TEM), scanning electron microscopy (SEM) and energy dispersion X-ray (EDX). The results show that nano-meter sized particles were formed, and the lattice parameter of TiC is close to the value of non-oxygen TiC. Compared with usually methods, the whole processing time needed is shortened; moreover, the synthesis temperature could be reduced 500°C. The mechanism for mechanical & yhermal activation is discussed.

Effects of Ho-Doping on Crystal Structure and Microstructure of La0.7Sr0.3MnO3 Ceramics

2013 ◽  
Vol 745-746 ◽  
pp. 96-101 ◽  
Author(s):  
Ben Zhe Sun ◽  
Si Lang Zhou ◽  
Tie Shen
Keyword(s):  
Crystal Structure ◽  
Electron Microscopy ◽  
Perovskite Structure ◽  
Volume Fraction ◽  
Partial Substitution ◽  
X Ray Diffraction ◽  
Doping Amount ◽  
X Ray ◽  
Transmission Electron ◽  
Structure And Microstructure

Crystal structure and microstructure of La0.7-xHoxSr0.3MnO3 (x=0.2,0.6) prepared by usual ceramic techniques and grinding procedure were investigated using X-ray diffraction (XRD) and transmission electron microscopy (TEM). When doping amount x equals to 0.2, incorporation of Ho atoms contributed to phase separation and coexistence of rhombohedral (La0.7Sr0.3MnO3) and hexagonal (HoMnO3) phases. La0.7Sr0.3MnO3 phase is of typical perovskite structure, whereas, HoMnO3 phase is non-perovskite structure. As x reaches 0.6, the volume fraction of HoMnO3 phase was significantly increasing. Meanwhile, an orthorhombic lattice with perovskite structure and space group Pnma can be observed. It prevented from partial substitution of La 3+ or Sr2+ by Ho3+ and the distortion of Mn-O octahedra.

scholarly journals Phase Formation of Mg-Zn-Gd Alloys on the Mg-rich Corner

Materials ◽  
2018 ◽  
Vol 11 (8) ◽  
pp. 1351 ◽  
Author(s):  
Lan Luo ◽  
Yong Liu ◽  
Meng Duan
Keyword(s):  
Electron Microscopy ◽  
Phase Diagram ◽  
Lattice Parameter ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Set Up ◽  
Cast Magnesium ◽  
Binary Compounds ◽  
Fcc Structure

The phase constitutions of as-cast magnesium (Mg)-Zn-Gd alloys (Zn/Gd = 0.25~60, Zn 0~10 at.%, Gd 0~2 at.%, 48 samples) were investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The Mg-Zn-Gd phase diagram focused on the Mg-rich corner (with up to 20 at.% Zn, 10 at.% Gd) has been set up. Five regions can be classified as follows: (I) α-Mg+W-phase+(binary compounds), (II) α-Mg+W-phase+I-phase(+binary compounds), (III) α-Mg+I-phase(+binary compounds), (IV) α-Mg+binary compounds, and (V) α-Mg. The phase diagram has been verified by solidification behaviors observation using differential thermal analysis (DTA). Moreover, the structures of I-phase and W-phase in the alloy were explored in details. In terms of the Hume-Rothery rules, I-phase is confirmed as FK-type quasicrystalline with a chemical stoichiometry as Mg30±1Zn62Gd8±1 (at.%). The composition and lattice parameter a W-phase (fcc structure, m3¯m) are affected by the composition of Mg-Zn-Gd alloys, especially by the Zn/Gd ratio of alloys. This work would be instructive for the design of Mg-Zn-Gd alloys to obtain the phase components, and then selected the strengthening ways, which could adjust its mechanical properties.

A High Resolution Study of G.P. Zones in Aluminum - 4.2 at % Silver

1982 ◽  
Vol 40 ◽  
pp. 722-723 ◽  
Author(s):  
R. Gronsky
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
High Resolution ◽  
Computer Simulations ◽  
Structural Characteristics ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Resolution Study

The phenomenon of clustering in Al-Ag alloys has been extensively studied since the early work of Guinierl, wherein the pre-precipitation state was characterized as an assembly of spherical, ordered, silver-rich G.P. zones. Subsequent x-ray and TEM investigations yielded results in general agreement with this model. However, serious discrepancies were later revealed by the detailed x-ray diffraction - based computer simulations of Gragg and Cohen, i.e., the silver-rich clusters were instead octahedral in shape and fully disordered, atleast below 170°C. The object of the present investigation is to examine directly the structural characteristics of G.P. zones in Al-Ag by high resolution transmission electron microscopy.

Identification of calcium oxalate crystals in dried or fixed tobacco leaf

1984 ◽  
Vol 42 ◽  
pp. 288-289
Author(s):  
Vicki L. Baliga ◽  
Mary Ellen Counts
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Calcium Oxalate ◽  
Growth And Development ◽  
Polarized Light ◽  
Calcium Oxalate Crystals ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

Calcium is an important element in the growth and development of plants and one form of calcium is calcium oxalate. Calcium oxalate has been found in leaf seed, stem material plant tissue culture, fungi and lichen using one or more of the following methods—polarized light microscopy (PLM), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and x-ray diffraction.Two methods are presented here for qualitatively estimating calcium oxalate in dried or fixed tobacco (Nicotiana) leaf from different stalk positions using PLM. SEM, coupled with energy dispersive x-ray spectrometry (EDS), and powder x-ray diffraction were used to verify that the crystals observed in the dried leaf with PLM were calcium oxalate.

The Effect of the Microstructure of Diffusion Barriers on the Palladium Activation for Electroless Copper Deposition

2002 ◽  
Vol 716 ◽  
Author(s):  
Seok Woo Hong ◽  
Yong Sun Lee ◽  
Ki-Chul Park ◽  
Jong-Wan Park
Keyword(s):  
Electron Microscopy ◽  
Diffusion Barriers ◽  
Copper Deposition ◽  
X Ray Diffraction ◽  
Plan View ◽  
X Ray ◽  
Transmission Electron ◽  
Electroless Copper ◽  
Sheet Resistance Measurement ◽  
Scanning Electron

AbstractThe effect of microstructure of dc magnetron sputtered TiN and TaN diffusion barriers on the palladium activation for autocatalytic electroless copper deposition has been investigated by using X-ray diffraction, sheet resistance measurement, field emission scanning electron microscopy (FE-SEM) and plan view transmission electron microscopy (TEM). The density of palladium nuclei on TaN diffusion barrier increases as the grain size of TaN films decreases, which was caused by increasing nitrogen content in TaN films. Plan view TEM results of TiN and TaN diffusiton barriers showed that palladium nuclei formed mainly on the grain boundaries of the diffusion barriers.

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