scholarly journals Phase Equilibria in the Nb-Rich Region of Al-Nb-Sn at 900 and 1200 °C

Materials ◽  
2019 ◽  
Vol 12 (17) ◽  
pp. 2759 ◽  
Author(s):  
Ioannis Papadimitriou ◽  
Claire Utton ◽  
Panos Tsakiropoulos
Keyword(s):  
Crystal Structure ◽  
Phase Equilibria ◽  
Ternary Phase ◽  
X Ray Diffraction ◽  
High Solubility ◽  
Rich Region ◽  
X Ray ◽  
Heat Treated ◽  
Aero Engine ◽  
Scanning Electron

The Al-Nb-Sn phase diagram was studied experimentally in the Nb-rich region to provide important phase equilibria information for alloy design of Nb-silicide based materials for aero engine applications. Three alloys were produced: Nb-17Al-17Sn, Nb-33Al-13Sn and Nb-16Al-20Sn (at.%). As-cast and heat-treated alloys (900 and 1200 °C) were analysed using XRD (X-ray diffraction) and SEM/EDS (scanning electron microscopy/ electron dispersive x-ray spectroscopy). Tin showed a high solubility in Nb2Al, reaching up to 21 at.% in the Sn-rich areas, substituting for Al atoms. Tin and Al also substituted for each other in the A15 phases (Nb3Al and Nb3Sn). Tin showed limited solubility in NbAl3, not exceeding 3.6 at.% as it substituted Al atoms. The solubility of Al in NbSn2 varied from 4.8 to 6.8 at.%. A ternary phase, Nb5Sn2Al with the tI32 W5Si3 crystal structure, was found to be stable. This phase was observed in the 900 °C heat-treated samples, but not in the 1200 °C heated samples.

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.

Isothermal Sections of the U-Fe-Sb Ternary System

2012 ◽  
Vol 194 ◽  
pp. 21-25 ◽  
Author(s):  
Margarida S. Henriques ◽  
Thomas Malnoe ◽  
Olivier Tougait ◽  
Rui Vilar ◽  
Antonio Pereira Gonçalves
Keyword(s):  
Crystal Structure ◽  
Electron Microscopy ◽  
Solid Solution ◽  
Scanning Electron Microscopy ◽  
Ternary Phase ◽  
Energy Dispersive Spectrometry ◽  
X Ray Diffraction ◽  
Isothermal Sections ◽  
X Ray ◽  
Scanning Electron

A systematic study on the ternary uranium-iron-antimony was made at 700 and 750°C through powder X-ray diffraction and Scanning Electron Microscopy coupled with Energy Dispersive Spectrometry. The assessed sections confirmed the existence and crystal structure of the binary intermetallic compounds as well as the ternary phase UFeSb2. Moreover it was found that UFeSb2 is part of a solid solution, UFe1-xSb2, stable for 193Fe3-xSb4, crystallizing in the cubic type Y3Au3Sb4 and stable for 22

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

X-ray powder diffraction data of LaNi0.5Ti0.45Co0.05O3, LaNi0.45Co0.05Ti0.5O3, and LaNi0.5Ti0.5O3 perovskites

2021 ◽  
pp. 1-6
Author(s):  
Mariana M. V. M. Souza ◽  
Alex Maza ◽  
Pablo V. Tuza
Keyword(s):  
Crystal Structure ◽  
Rietveld Method ◽  
Pechini Method ◽  
Powder Diffraction Data ◽  
X Ray Diffraction ◽  
Unit Cell Parameters ◽  
X Ray ◽  
Cell Parameters ◽  
Modified Pechini Method ◽  
Scanning Electron

In the present work, LaNi0.5Ti0.45Co0.05O3, LaNi0.45Co0.05Ti0.5O3, and LaNi0.5Ti0.5O3 perovskites were synthesized by the modified Pechini method. These materials were characterized using X-ray fluorescence, scanning electron microscopy, and powder X-ray diffraction coupled to the Rietveld method. The crystal structure of these materials is orthorhombic, with space group Pbnm (No 62). The unit-cell parameters are a = 5.535(5) Å, b = 5.527(3) Å, c = 7.819(7) Å, V = 239.2(3) Å3, for the LaNi0.5Ti0.45Co0.05O3, a = 5.538(6) Å, b = 5.528(4) Å, c = 7.825(10) Å, V = 239.5(4) Å3, for the LaNi0.45Co0.05Ti0.5O3, and a = 5.540(2) Å, b = 5.5334(15) Å, c = 7.834(3) Å, V = 240.2(1) Å3, for the LaNi0.5Ti0.5O3.

Study on the Properties of Doped La in BaBi4Ti4O15 Ceramic

2007 ◽  
Vol 26-28 ◽  
pp. 243-246
Author(s):  
Xing Hua Yang ◽  
Jin Liang Huang ◽  
Xiao Wang ◽  
Chun Wei Cui
Keyword(s):  
Crystal Structure ◽  
Grain Size ◽  
Electron Microscope ◽  
Scanning Electron Microscope ◽  
Sintering Temperature ◽  
Solid Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Lanthanum Content ◽  
Scanning Electron

BaBi4-xLaxTi4O15 (BBLT) ceramics were prepared by conventional solid phase sintering ceramics processing technology. The crystal structure and the microstructure were detected by X-ray diffraction (XRD) and scanning electron microscope (SEM). The XRD analyses show that La3+ ions doping did not change the crystal structure of BBT ceramics. The sintering temperature increased from 1120°C to 1150°C with increasing Lanthanum content from 0 to 0.5, but it widened the sintering temperature range from 20°C to 50°C and refined the grain size of the BBT ceramic. Additionally, polarization treatment was performed and finally piezoelectric property was measured. As a result, the piezoelectric constant d33 of the 0.1at.% doped BBLT ceramics reached its highest value about 22pc/N at polarizing electric field of 8kV/mm and polarizing temperature of 120°C for 30min.

High-performance electrical properties of La-based perovskite ceramics for the functional phase of thick film resistors

2020 ◽  
Author(s):  
Yongcheng Lu ◽  
Yuanxun Li ◽  
Daming Chen ◽  
Rui Peng ◽  
Qinghui Yang ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Electrical Properties ◽  
Thick Film ◽  
High Performance ◽  
Composite Ceramics ◽  
X Ray Diffraction ◽  
X Ray ◽  
Alternative Material ◽  
Perovskite Ceramics ◽  
Scanning Electron

Abstract In order to explore an economical functional phase alternative material for thick film resistors, the crystal structure, microstructure, and electrical properties of (1-x)LSCN + xLCNZ (x = 0.0–1.0) composite ceramics were studied through solid-state reaction experiments. The composite ceramics were characterized by x–ray diffraction, scanning electron microscopy, energy dispersive x–ray spectroscopy, and DC four–probe method. Results suggested that the main phases of LSCN and LCNZ were formed, along with a small part of impurity phases. The addition of LCNZ to LSCN decreased the electrical conductivity and changed the TCR from positive to negative. Zero TCR could be achieved around 0.6 < x < 0.8 and relatively low absolute TCR values could be obtained for the samples of 0.4 ≤ x ≤ 0.8. The ceramic of 0.6LSCN + 0.4LCNZ showed the optimal performances of conductivity = 1923 S/cm, TCR = 379.54 ppm/℃, and relative density = 95.05%.

Tribological Performance Optimization of Electroless Nickel Coatings Under Lubricated Condition

2018 ◽  
pp. 250-280 ◽  
Author(s):  
Santanu Duari ◽  
Arkadeb Mukhopadhyay ◽  
Tapan Kumar Barman ◽  
Prasanta Sahoo
Keyword(s):  
Performance Optimization ◽  
Friction And Wear ◽  
Electroless Nickel ◽  
Heat Treating ◽  
Wear Depth ◽  
X Ray Diffraction ◽  
X Ray ◽  
Heat Treated ◽  
Electroless Ni ◽  
Scanning Electron

The present chapter aims to determine optimal tribo-testing condition for minimum coefficient of friction and wear depth of electroless Ni-P, Ni-P-W and Ni-P-Cu coatings under lubrication using grey relational analysis. Electroless Ni-P, Ni-P-W and Ni-P-Cu coatings are deposited on AISI 1040 steel substrates. They are heat treated at suitable temperatures to improve their hardness. Coating characterization is done using scanning electron microscope, energy dispersive X-Ray analysis and X-Ray diffraction techniques. Typical nodulated surface morphology is observed in the scanning electron micrographs of all the three coatings. Phase transformation on heat treating the deposits is captured through the use of X-Ray diffraction technique. Vicker's microhardness of the coatings in their as-deposited and heat treated condition is determined. Ni-P-W coatings are seen to exhibit the highest microhardness. Friction and wear tests under lubricated condition are carried out following Taguchi's experimental design principle. Finally, the predominating wear mechanism of the coatings is discussed.

Nanocrystalline Barium Zirconium Titanate Synthesized by the Sonochemical Process

2013 ◽  
Vol 802 ◽  
pp. 119-123
Author(s):  
Supamas Wirunchit ◽  
Rangson Muanghlua ◽  
Supamas Wirunchit ◽  
Wanwilai Vittayakorn ◽  
Naratip Vittayakorn
Keyword(s):  
Crystal Structure ◽  
Electron Microscopy ◽  
Reaction Time ◽  
Single Phase ◽  
Zirconium Titanate ◽  
X Ray Diffraction ◽  
X Ray ◽  
Large Particles ◽  
Barium Zirconium Titanate ◽  
Scanning Electron

Nanocrystalline barium zirconium titanate, BaZr0.4Ti0.6O3, was synthesized successfully via the sonochemical process. The effects of reaction time on the precipitation of Ba(Zr,Ti)O3 particles were investigated briefly. The crystal structure as well as molecular vibrations and morphology were investigated. X-ray diffraction indicated that the powders exhibited a single phase perovskite structure, without the presence of pyrochlore or unwanted phases at the reaction time of 60 min. Nanocrystals were formed before being oriented and aggregated into large particles in aqueous solution under ultrasonic irradiation. A scanning electron microscopy (SEM) photograph showed the BZT powder as spherical in shape with uniform nanosized features.

The Effect of Water Content on the Formation of TiO2 Nanotubes in Ethylene Glycol

2010 ◽  
Vol 173 ◽  
pp. 102-105 ◽  
Author(s):  
Khairul Arifah Saharudin ◽  
Srimala Sreekantan
Keyword(s):  
Crystal Structure ◽  
Aspect Ratio ◽  
Ethylene Glycol ◽  
Water Content ◽  
Anatase Phase ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Degradation Of Methyl Orange ◽  
Scanning Electron

In this paper, anodization of Ti foil was carried out in ethylene glycol (EG) containing 5 wt% NH4F solution and 0 to 1.5 wt% of water at 50 V for 60 min. The pH of the bath was kept constant at ~pH7. The crystal structure was studied by X-Ray Diffraction (XRD) analysis, and the morphology was observed via field emission scanning electron microscopy (FESEM). TiO2 nanotube with aspect ratio of 100 was obtained in EG containing less than 1wt % water. The nanotubes wall was very smooth. Increasing the water content > 1wt % results in short nanotubes of approximately 6.2μm with aspect ratio of 62. As anodized, nanotubes were amorphous and annealed at 400 °C promote 100 % anatase phase. Photocatalytic activity of the nanotubes produced at different water content was also evaluated by the degradation of methyl orange and the detail of the observation was discussed thoroughly in this paper.

Crystallization of a SiO2-MgO-Al2O3-K2O-Fe2O3-F Glass

2007 ◽  
Vol 336-338 ◽  
pp. 1829-1832 ◽  
Author(s):  
Qing Bo Tian ◽  
Yue Wang ◽  
Xue Tao Yue ◽  
Yan Sheng Yin ◽  
Su Hua Fan
Keyword(s):  
Phase Separation ◽  
Electron Probe ◽  
X Ray Diffraction ◽  
Crystalline Phases ◽  
Present Glass ◽  
X Ray ◽  
Heat Treated ◽  
Mica Crystal ◽  
Step Heat Treatment ◽  
Scanning Electron

The phase-separation and the crystallization of SiO2-MgO-Al2O3-K2O-Fe2O3-F glass were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM) and electron probe of microanalyzers (EPMA). The results reveal that the varieties and the morphology of crystalline phases formed depend sensitively on the thermal treatment schedules. During the isothermal treatments, the crystalline phases of mica, mica and iron oxide (FeFeO4), and FeFeO4 as major crystals are precipitated in the glass samples heat-treated at 900, 1000 and 1050°C respectively. However, the two-step heat treatment beginning at 900°C for 1h and subsequently followed at 1050°C for 1h leads to the precipitation of mica crystal and no any signs of FeFeO4 crystalline phase is observed. Also the morphology of sample is different from that of the isothermally treated glass at 1050°C, but is similar from that of sample at 900°C. A “worm”-shaped phase-separation is observed in the sample heated at 800°C for 0.5h, which exhibits different morphology from that of droplet- or globule-shape conventionally discerned. EPMA results show that the incorporation of Fe2O3 accelerates accumulation of fluorine element, promoting the phase-separation and the crystallization of the present glass.

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