Thermodynamic Calculations of Phase Equilibria and Phase Fractions of a β-Solidifying TiAl Alloy using the CALPHAD Approach

2012 ◽  
Vol 1516 ◽  
pp. 59-64 ◽  
Author(s):  
Robert Werner ◽  
Martin Schloffer ◽  
Emanuel Schwaighofer ◽  
Helmut Clemens ◽  
Svea Mayer
Keyword(s):  
Phase Equilibria ◽  
Industrial Development ◽  
Tial Alloy ◽  
Thermodynamic Calculations ◽  
Nominal Composition ◽  
Calphad Approach ◽  
Scanning Electron Micrographs ◽  
X Ray Diffraction ◽  
Tial Alloys ◽  
X Ray

ABSTRACTThe CALPHAD (CALculation of PHAse Diagrams) method is widely recognized as a powerful tool in both scientific and industrial development of new materials and processes. For the implementation of consistent databases, where each phase is described separately, models are used which are based on physical principles and parameters assessed from experimental data. Such a database makes it possible to perform realistic calculations of thermodynamic properties of multi-component systems. However, a commercial available TiAl database can be applied for thermodynamic calculations to both conventional Ti-base alloys and complex intermetallic TiAl alloys to describe experimentally evaluated phase fractions as a function of temperature. In the present study calculations were done for a β-solidifying TiAl alloy with a nominal composition of Ti-43.5Al-4Nb-1Mo-0.1B (in at. %), termed TNMTM alloy. At room temperature this alloy consists of ordered γ-TiAl, α2-Ti3Al and β0-TiAl phases. At a certain temperature α2 and β0 disorder to α and β, respectively. Using the commercial database the thermodynamic calculations reflect only qualitative trends of phase fractions as a function of temperature. For more exact quantitative calculations the commercial available thermodynamic database had to be improved for TiAl alloys with high Nb (and Mo) contents, as recently reported for Nb-rich γ-TiAl alloys. Therefore, the database was modified by experimentally evaluated phase fractions obtained from quantitative microstructure analysis of light-optical and scanning electron micrographs as well as conventional X-ray diffraction after long-term heat treatments and by means of in-situ highenergy X-ray diffraction experiments. Based on the CALPHAD-conform thermodynamic assessment, the optimized database can now be used to correctly predict the phase equilibria of this multi-component alloying system, which is of interest for applications in automotive and aircraft engine industry.

The microstructure of an oxidized γ-TiAl+Cr alloy

1992 ◽  
Vol 50 (1) ◽  
pp. 166-167
Author(s):  
J.A. Sutliff ◽  
S.C. Huang ◽  
D.W. McKee
Keyword(s):  
Tial Alloy ◽  
Ion Beam ◽  
Intermetallic Phase ◽  
Analytical Electron Microscopy ◽  
Aircraft Engine ◽  
Oxide Surface ◽  
Nominal Composition ◽  
Tial Alloys ◽  
X Ray ◽  
Analytical Electron

Alloys based on the intermetallic phase γ-TiAl are considered good candidates for some high temperature aircraft engine applications. While a tremendous effort has been made to understand the mechanical properties of γ-TiAl, relatively little effort has been made to understand its oxidation behavior. Two of the authors have studied oxidation of several γ-TiAl alloys containing ternary and quaternary additions including Cr, Mn, Nb, Ta, and W. In this paper, we present some of the microstructural observations on an oxidized γ-TiAl alloy.An oxidized γ-TiAl alloy with a nominal composition of 50 at% Al and 2 at% Cr was examined using analytical electron microscopy. Oxidation of polished pieces occurred in air at 850°C for 6 hours. The pieces were ground from the unpolished side to a thickness of ∼75 μm and 3 mm disks were punched. The disks were electropolished in a perchloric/methanol solution. Electropolishing was done from the metal side only until “perforation” of the metal substrate. This resulted in a sample with an oxide ‘window’. The samples were further thinned by ion beam milling (5kV/500μA Ar+) from the oxide surface toward the oxide/metal interface. The sample was examined in a Philips EM430 TEM operated at 300 kV and x-ray spectra collected with an EDAX energy dispersive x-ray spectrometer having a windowless Si(Li) detector.

Diffusion brazing of γ-TiAl-alloys: Investigations of the joint by electron microscopy and high-energy X-ray diffraction

2013 ◽  
Vol 1516 ◽  
pp. 215-220 ◽  
Author(s):  
Katja Hauschildt ◽  
Andreas Stark ◽  
Uwe Lorenz ◽  
Norbert Schell ◽  
Torben Fischer ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Tial Alloy ◽  
Potential Method ◽  
High Energy ◽  
Substrate Material ◽  
X Ray Diffraction ◽  
Tial Alloys ◽  
X Ray ◽  
Diffusion Brazing ◽  
Synchrotron Facility

ABSTRACTDiffusion brazing is a potential method to repair parts made from TiAl-alloys. Two different brazing materials with varying contents of titanium, iron and nickel were investigated. The phases present in the brazed zone were identified by high energy X-ray diffraction (HEXRD) at the material science beamline HEMS at the PETRA III synchrotron facility at DESY in Hamburg, Germany, and the microstructure was characterised by scanning electron microscopy (SEM). The braze zone itself is composed of one to two transitional layers from the substrate material to the middle of the joint. Near the substrate material the phase constitution reassembles a TiAl-alloy while the middle of the joint is similar to α/β-titanium alloys. Besides phases commonly encountered in TiAl-alloys such as γ, α2 and β, additional phases, which are related to the presence of nickel or iron as melting point depressing elements are present. The microstructure of the brazed zone changes significantly during a subsequent heat treatment.

Electron Microscopy/Diffraction Study of the Ternary Mn-Er-S System

1990 ◽  
Vol 48 (1) ◽  
pp. 76-77
Author(s):  
A. R. Landa Canovas ◽  
L.C. Otero Diaz ◽  
T. White ◽  
B.G. Hyde
Keyword(s):  
Electron Microscopy ◽  
Gas Flow ◽  
Graphite Crucible ◽  
Nominal Composition ◽  
X Ray Diffraction ◽  
Alumina Crucible ◽  
X Ray ◽  
Intermediate Phases ◽  
Twin Band ◽  
Ar Gas

X-Ray diffraction revealed two intermediate phases in the system MnS+Er2S3,:MnEr2S4= MnS.Er2S3, and MnEr4S7= MnS.2Er2S3. Their structures may be described as NaCl type, chemically twinned at the unit cell level, and isostructural with CaTi2O4, and Y5S7 respectively; i.e. {l13} NaCl twin band widths are (4,4) and (4,3).The present study was to search for structurally-related (twinned B.) structures and or possible disorder, using the more sensitive and appropiate technigue of electron microscopy/diffraction.A sample with nominal composition MnEr2S4 was made by heating Mn3O4 and Er2O3 in a graphite crucible and a 5% H2S in Ar gas flow at 1500°C for 4 hours. A small amount of this material was thenannealed, in an alumina crucible, contained in sealed evacuated silica tube, for 24 days at 1100°C. Both samples were studied by X-ray powder diffraction, and in JEOL 2000 FX and 4000 EX microscopes.

scholarly journals Stable and Metastable Phase Equilibria Involving the Cu6Sn5 Intermetallic

2021 ◽  
Author(s):  
A. Leineweber ◽  
M. Löffler ◽  
S. Martin
Keyword(s):  
Phase Equilibria ◽  
Electron Backscatter Diffraction ◽  
Metastable Phase ◽  
Stable Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Heat Treated ◽  
Ordered Phases ◽  
Backscatter Diffraction ◽  
Kinetics Of

Abstract Cu6Sn5 intermetallic occurs in the form of differently ordered phases η, η′ and η′′. In solder joints, this intermetallic can undergo changes in composition and the state of order without or while interacting with excess Cu and excess Sn in the system, potentially giving rise to detrimental changes in the mechanical properties of the solder. In order to study such processes in fundamental detail and to get more detailed information about the metastable and stable phase equilibria, model alloys consisting of Cu3Sn + Cu6Sn5 as well as Cu6Sn5 + Sn-rich melt were heat treated. Powder x-ray diffraction and scanning electron microscopy supplemented by electron backscatter diffraction were used to investigate the structural and microstructural changes. It was shown that Sn-poor η can increase its Sn content by Cu3Sn precipitation at grain boundaries or by uptake of Sn from the Sn-rich melt. From the kinetics of the former process at 513 K and the grain size of the η phase, we obtained an interdiffusion coefficient in η of (3 ± 1) × 10−16 m2 s−1. Comparison of this value with literature data implies that this value reflects pure volume (inter)diffusion, while Cu6Sn5 growth at low temperature is typically strongly influenced by grain-boundary diffusion. These investigations also confirm that η′′ forming below a composition-dependent transus temperature gradually enriches in Sn content, confirming that Sn-poor η′′ is metastable against decomposition into Cu3Sn and more Sn-rich η or (at lower temperatures) η′. Graphic Abstract

scholarly journals First Report on the Geologic Occurrence of Natural Na–A Zeolite and Associated Minerals in Cretaceous Mudstones of the Paja Formation of Vélez (Santander), Colombia

Crystals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 218
Author(s):  
Carlos Alberto Ríos-Reyes ◽  
German Alfonso Reyes-Mendoza ◽  
José Antonio Henao-Martínez ◽  
Craig Williams ◽  
Alan Dyer
Keyword(s):  
Natural Zeolite ◽  
Scanning Electron Micrographs ◽  
Total Sulfur ◽  
Zeolite A ◽  
X Ray Diffraction ◽  
X Ray ◽  
Mineral Phases ◽  
The World ◽  
Porosity And Permeability ◽  
First Time

This study reports for the first time the geologic occurrence of natural zeolite A and associated minerals in mudstones from the Cretaceous Paja Formation in the urban area of the municipality of Vélez (Santander), Colombia. These rocks are mainly composed of quartz, muscovite, pyrophyllite, kaolinite and chlorite group minerals, framboidal and cubic pyrite, as well as marcasite, with minor feldspar, sulphates, and phosphates. Total organic carbon (TOC), total sulfur (TS), and millimeter fragments of algae are high, whereas few centimeters and not biodiverse small ammonite fossils, and other allochemical components are subordinated. Na–A zeolite and associated mineral phases as sodalite occur just beside the interparticle micropores (honeycomb from framboidal, cube molds, and amorphous cavities). It is facilitated by petrophysical properties alterations, due to processes of high diagenesis, temperatures up to 80–100 °C, with weathering contributions, which increase the porosity and permeability, as well as the transmissivity (fluid flow), allowing the geochemistry remobilization and/or recrystallization of pre-existing silica, muscovite, kaolinite minerals group, salts, carbonates, oxides and peroxides. X-ray diffraction analyses reveal the mineral composition of the mudstones and scanning electron micrographs show the typical cubic morphology of Na–A zeolite of approximately 0.45 mμ in particle size. Our data show that the sequence of the transformation of phases is: Poorly crystalline aluminosilicate → sodalite → Na–A zeolite. A literature review shows that this is an unusual example of the occurrence of natural zeolites in sedimentary marine rocks recognized around the world.

scholarly journals Characterization of ferrite nanoparticles for preparation of biocomposites

2017 ◽  
Vol 8 ◽  
pp. 1257-1265 ◽  
Author(s):  
Urszula Klekotka ◽  
Magdalena Rogowska ◽  
Dariusz Satuła ◽  
Beata Kalska-Szostko
Keyword(s):  
Chemical Method ◽  
Ferrite Nanoparticles ◽  
Chemical Activity ◽  
Nominal Composition ◽  
X Ray Diffraction ◽  
Wet Chemical Method ◽  
X Ray ◽  
Transmission Electron ◽  
Wet Chemical

Ferrite nanoparticles with nominal composition Me0.5Fe2.5O4 (Me = Co, Fe, Ni or Mn) have been successfully prepared by the wet chemical method. The obtained particles have a mean diameter of 11–16 ± 2 nm and were modified to improve their magnetic properties and chemical activity. The surface of the pristine nanoparticles was functionalized afterwards with –COOH and –NH2 groups to obtain a bioactive layer. To achieve our goal, two different modification approaches were realized. In the first one, glutaraldehyde was attached to the nanoparticles as a linker. In the second one, direct bonding of such nanoparticles with a bioparticle was studied. In subsequent steps, the nanoparticles were immobilized with enzymes such as albumin, glucose oxidase, lipase and trypsin as a test bioparticles. The characterization of the nanoparticles was acheived by transmission electron microscopy, X-ray diffraction, energy dispersive X-ray and Mössbauer spectroscopy. The effect of the obtained biocomposites was monitored by Fourier transform infrared spectroscopy. The obtained results show that in some cases the use of glutaraldehyde was crucial (albumin).

scholarly journals In Situ High-Energy X-ray Diffraction during Hot-Forming of a Multiphase TiAl Alloy

Metals ◽  
2015 ◽  
Vol 5 (4) ◽  
pp. 2252-2265 ◽  
Author(s):  
Andreas Stark ◽  
Marcus Rackel ◽  
Aristide Tchouaha Tankoua ◽  
Michael Oehring ◽  
Norbert Schell ◽  
...  
Keyword(s):  
Tial Alloy ◽  
High Energy ◽  
Hot Forming ◽  
X Ray Diffraction ◽  
X Ray

scholarly journals Mn-Induced Thermal Stability of L10 Phase in Fept Magnetic Nanoscale Ribbons

Nanomaterials ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 1278
Author(s):  
Alina Daniela Crisan ◽  
Aurel Leca ◽  
Dan Pantelica ◽  
Ioan Dan ◽  
Ovidiu Crisan
Keyword(s):  
Rare Earth ◽  
Single Phase ◽  
Permanent Magnets ◽  
Magnetic Hysteresis ◽  
Ternary Alloys ◽  
Large Temperature ◽  
Nominal Composition ◽  
X Ray Diffraction ◽  
X Ray ◽  
Operation Conditions

Magnetic nanoscale materials exhibiting the L10 tetragonal phase such as FePt or ternary alloys derived from FePt show most promising magnetic properties as a novel class of rare earth free permanent magnets with high operating temperature. A granular alloy derived from binary FePt with low Pt content and the addition of Mn with the nominal composition Fe57Mn8Pt35 has been synthesized in the shape of melt-spun ribbons and subsequently annealed at 600 °C and 700 °C for promoting the formation of single phase, L10 tetragonal, hard magnetic phase. Proton-induced X-ray emission spectroscopy PIXE has been utilized for checking the compositional effect of Mn addition. Structural properties were analyzed using X-ray diffraction and diffractograms were analyzed using full profile Rietveld-type analysis with MAUD (Materials Analysis Using Diffraction) software. By using temperature-dependent synchrotron X-ray diffraction, the disorder–order phase transformation and the stability of the hard magnetic L10 phase were monitored over a large temperature range (50–800 °C). A large interval of structural stability of the L10 phase was observed and this stability was interpreted in terms of higher ordering of the L10 phase promoted by the Mn addition. It was moreover found that both crystal growth and unit cell expansion are inhibited, up to the highest temperature investigated (800 °C), proving thus that the Mn addition stabilizes the formed L10 structure further. Magnetic hysteresis loops confirmed structural data, revealing a strong coercive field for a sample wherein single phase, hard, magnetic tetragonal L10 exists. These findings open good perspectives for use as nanocomposite, rare earth free magnets, working in extreme operation conditions.

Phase relationships in the join Ca(OH)2–CaCO3–Ca3(PO4)2–H2O at 1000 bars

1969 ◽  
Vol 37 (285) ◽  
pp. 75-82 ◽  
Author(s):  
G. M. Biggar
Keyword(s):  
Phase Equilibria ◽  
Water Content ◽  
X Ray Diffraction ◽  
X Ray ◽  
Synthetic Hydroxyapatite ◽  
Diffraction Patterns ◽  
Phase Relationships

SummaryPhase equilibria involving calcite, apatite, portlandite, liquid, and vapour were determined at 1000 bars. Calcite, apatite, and portlandite melt at 654 °C to form a liquid of composition (wt %), Ca(OH)2 53 %, CaCO3 46 %, Ca3(PO4)2 1 %. With water present melting occurs at 635 °C to form a similar liquid with a low water content. The X-ray diffraction patterns of the equilibrium apatites were not significantly different from synthetic hydroxyapatite.

scholarly journals Supplementary X-ray studies of the Ni-Sn-Bi system

2007 ◽  
Vol 43 (2) ◽  
pp. 141-150 ◽  
Author(s):  
G.P. Vassilev ◽  
K.I. Lilova ◽  
J.C. Gachon
Keyword(s):  
Electron Microscope ◽  
Scanning Electron Microscope ◽  
Phase Equilibria ◽  
Ternary Compound ◽  
Approximate Formula ◽  
Ternary Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Diffraction Peaks ◽  
Scanning Electron

Phase equilibria were studied in the system Ni-Sn-Bi. Special attention has been paid to the identification of the recently found ternary phase. For this purpose samples were synthesized using intimately mixed powders. After annealing and quenching, all alloys were analyzed by scanning electron microscope and by X-ray diffraction. The results give evidences about the existence of a ternary compound with approximate formula Ni6Sn2Bi to Ni7Sn2Bi. Overlapping of some neighboring diffraction peaks of this phase with NiBi and Ni3Sn_LT is the reason for the difficulties related to the X-ray diffraction identification of the ternary phase.

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