Phase Equilibria among γ-Fe, γ-Fe and Fe2Mo Phases and Stability of the Laves Phase in Fe-Mo-Ni Ternary System at Elevated Temperatures

2006 ◽  
Vol 980 ◽  
Author(s):  
Shigehiro Ishikawa ◽  
Takashi Matsuo ◽  
Masao Takeyama

AbstractPhase equilibria among the bcc Fe(α), fcc Fe(γ) and Fe2Mo(λ)_phases in Fe-Mo-Ni ternary system, particularly paying attention to the existence of the γ+λ two-phase region, have been examined at elevated temperatures below Tc (1200 K), the peritectoid reaction temperature in Fe-Mo binary system: λ?α+Fe7Mo6 (μ). At 1173 K the α+γ+μ three-phase coexisting region exists near the Fe-Mo binary edge and no λ phase region was identified. At 1073 K the λ phase in equilibrium with α and γ phases exists, although the composition homogeneity region of the ternary λ phase was limited to its binary edge toward the equi-nickel concentration direction up to about 3at % Ni. Instead, large two-phase region of γ+μ was extended along the same direction up to 20 at% Ni. The γ+λ two-phase region appears below Tc through a transition peritectoid reaction: α+μ¨γ+λ. The γ phase in equilibrium with λ phase is stable only at elevated temperatures, and it transforms martensitically to α phase during cooling. The addition of Ni stabilizes γ and μ phases against α and λ phases, thereby decreasing the relative stability of the λ phase.

2004 ◽  
Vol 842 ◽  
Author(s):  
Masao Takeyama ◽  
Nobuyuki Gomi ◽  
Sumio Morita ◽  
Takashi Matsuo

ABSTRACTPhase equilibria in Fe-Ni-Nb ternary system at elevated temperatures have been examined, in order to identify the two-phase region of γ-Fe (austenite) and ε-Fe2Nb (C14). The ε single phase region exists in the range of 27.5 to 35.5 at.% Nb in the Fe-Nb binary system, and it extends toward the equi-niobium concentration direction up to 44 at.% Ni in the ternary system at 1473 K, indicating that more than half of the Fe atoms in Fe2Nb can be replaced with Ni. Thus, the γ+ε two-phase region exists extensively, and the solubility of Nb in γ phase increases from 1.5 to 6.0 at.% with increase in Ni content. The lattice parameters of a and c in the C14 Laves phase decrease with increasing Ni content. The change in a axis is in good agreement with calculation based on Vegard's law, whereas that of c axis is much larger than the calculated value. The result suggests that atomic size effect is responsible for a-axis change and the binding energy is dominant factor for the c-axis change. To extend these findings to development of new class of austenitic steels strengthened by Laves phase, an attempt has been made to control the c/a ratio by alloying. The addition of Cr is effective to make the c/a ratio close to the cubic symmetry value (1.633).


2007 ◽  
Vol 561-565 ◽  
pp. 435-438 ◽  
Author(s):  
Tomoaki Sugiura ◽  
Shigehiro Ishikawa ◽  
Takashi Matsuo ◽  
Masao Takeyama

The phase equilibria among α-Fe, γ-Fe and Fe2Ti phases in Fe-Ti-Ni ternary system at 1473 K and 1373 K with Ni (γ former element) addition were examined, by paying attention to the γ+Fe2Ti two-phase region. The Fe2Ti single-phase region extends toward the equal-titanium concentration direction up to about 30 at% Ni, and the Laves phase becomes in equilibrium with γ-Fe by 12 at% Ni addition, but the γ+Fe2Ti two-phase region is limited because of the formation of liquid phase by further Ni addition at 1473 K. With decreasing temperature, a ternary eutectic reaction (L→γ-Fe+Fe2Ti+Ni3Ti) occurs, making the two-phase region wider just below the invariant reaction at 1373 K, and the region becomes narrower again by the enlargement of the three-phases region toward Fe-rich side.


2011 ◽  
Vol 1295 ◽  
Author(s):  
Y. Hasebe ◽  
K. Hashimoto ◽  
T. Matsuo ◽  
M. Takeyama

ABSTRACTPhase equilibria among γ-Fe, ε-Fe2Nb Laves and δ-Ni3Nb phases in Fe-Ni-Nb ternary system at 1473 K and 1373 K were experimentally examined, and also assessed by calculation in order to calculate the phase equilibria among these phases at 973 K. A ternary compound with hP24 structure with its limited composition range of Fe-21.5Nb- (56.8-59.8) Ni exists between Fe2Nb and Ni3Nb phase regions at both temperatures. Including the hP24 phase, the calculated isotherms at both temperatures are in good agreement with experimental ones. By using the optimized interaction parameters among the three elements in each phase, the isothermal section calculated at 973 K revealed a γ-Fe+ Fe2Nb + Ni3Nb three-phase coexisting region extended to Fe-rich composition of 80 at. % Fe. This suggests a possibility to develop austenitic heatresistant steels strengthened by both intermetallics phases.


Materials ◽  
2019 ◽  
Vol 12 (3) ◽  
pp. 444
Author(s):  
Wenchao Yang ◽  
Moumiao Liu ◽  
Junli Feng ◽  
Jingwu Wu ◽  
Jun Mao ◽  
...  

A complete understanding of the solid-state phase equilibria of the ternary Al–Sn–Y system is essential for the development of both Al-based structural materials and Sn-based lead-free solders. In this work, the phase relationships in the Al–Sn–Y ternary system at 473 K were investigated mainly by means of X-ray powder diffraction (XRD), differential scanning calorimetry (DSC) and scanning electron microscopy (SEM) with energy disperse spectroscopy (EDS) analysis. The existence of 12 binary compounds, namely Sn3Y, Sn5Y2, Sn2Y, Sn10Y11, Sn4Y5, Sn3Y5, AlY2, Al3Y5, Al2Y3, AlY, Al2Y and α–Al3Y, was confirmed. Controversial phases (Sn5Y2 and Al3Y5) were found in this work. This isothermal section consisted of 15 single-phase regions, 27 two-phase regions and 13 three-phase regions. No ternary compounds were found and none of the other phases in this system revealed a remarkable solid solution at 473 K.


Processes ◽  
2021 ◽  
Vol 9 (3) ◽  
pp. 413
Author(s):  
Sandra Lopez-Zamora ◽  
Jeonghoon Kong ◽  
Salvador Escobedo ◽  
Hugo de Lasa

The prediction of phase equilibria for hydrocarbon/water blends in separators, is a subject of considerable importance for chemical processes. Despite its relevance, there are still pending questions. Among them, is the prediction of the correct number of phases. While a stability analysis using the Gibbs Free Energy of mixing and the NRTL model, provide a good understanding with calculation issues, when using HYSYS V9 and Aspen Plus V9 software, this shows that significant phase equilibrium uncertainties still exist. To clarify these matters, n-octane and water blends, are good surrogates of naphtha/water mixtures. Runs were developed in a CREC vapor–liquid (VL_ Cell operated with octane–water mixtures under dynamic conditions and used to establish the two-phase (liquid–vapor) and three phase (liquid–liquid–vapor) domains. Results obtained demonstrate that the two phase region (full solubility in the liquid phase) of n-octane in water at 100 °C is in the 10-4 mol fraction range, and it is larger than the 10-5 mol fraction predicted by Aspen Plus and the 10-7 mol fraction reported in the technical literature. Furthermore, and to provide an effective and accurate method for predicting the number of phases, a machine learning (ML) technique was implemented and successfully demonstrated, in the present study.


2016 ◽  
Vol 873 ◽  
pp. 18-22
Author(s):  
Ming Li Huang ◽  
Xue Shen ◽  
Hong Xiao Li

The equilibrium alloys closed to Mg-Nd side in the Mg-rich corner of the Mg-Zn-Nd system at 400°C have been investigated by scanning electron microscopy, electron probe microanalysis and X-ray diffraction. The binary solid solutions Mg12Nd and Mg3Nd with the solubility of Zn have been identified. The maximum solubility of Zn in Mg12Nd is 4.8at%, and Mg12Nd phase can be in equilibrium with Mg solid solution. However, only when the solubility range of Zn in 26at%~32.2at%, Mg3Nd can be in two-phase equilibrium with Mg solid solution. As the results, two two-phase regions as Mg+Mg12Nd and Mg+Mg3Nd and a three-phase region as Mg+Mg12Nd+Mg3Nd in Mg-Nd-Zn ternary isothermal section at 400°C have been identified.


1952 ◽  
Vol 44 (3) ◽  
pp. 609-615 ◽  
Author(s):  
H. H. Reamer ◽  
B. H. Sage ◽  
W. N. Lacey

2006 ◽  
Vol 59 (3) ◽  
pp. 225 ◽  
Author(s):  
Liang Gao ◽  
Tao Jiang ◽  
Buxing Han ◽  
Baoning Zong ◽  
Xiaoxin Zhang ◽  
...  

The oxidation of cyclohexane with H2O2 in a compressed CO2/acetic acid binary system was studied at 60.0 and 80.0°C, at pressures up to 18 MPa, and with the zeolite TS-1 as catalyst. The phase behaviour of the reaction system was also observed. There are three fluid phases in the reaction system at lower pressure but two at higher pressures. In the three-phase region the yields of the products, cyclohexanol and cyclohexanone, increase considerably with increasing pressure and reaches a maximum near the phase-separating pressure. CO2 can thus enhance the reaction effectively. However, the effect of pressure on the yield is very limited after the transition to a two-phase system.


1983 ◽  
Vol 27 ◽  
Author(s):  
D. I. Potter ◽  
M. Ahmed ◽  
S. Lamond

ABSTRACTThe chemical and microstructural changes caused by the direct implantation of solutes into metals are examined. The particular case involving Al+-ion implantation into nickel is treated in detail. Chemical composition profiles measured using Auger spectroscopy and Rutherford backscattering, and average near-surface chemical composition measured using an analytical electron microscope, are compared with model calculations. The microstructures that develop during implantation are investigated using transmission electron microscopy. For low fluences implanted near room temperature, these microstructures contain dislocations and dislocation loops. Dislocation loops, dislocations, and voids result from implantations at temperatures near 500°C. Higher fluences at these elevated temperatures produce precipitates when the composition of implanted solute lies in a two-phase region of the phase diagram. Implanted concentrations corresponding to intermetallic compounds produce continuous layers of these compounds. Room temperature, as compared to elevated temperature, implantation may produce the same phases at the appropriate concentrations, e.g. β'-NiAl, or different phases, depending on the relative stability of the phases involved.


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