Reaction Behavior of Phosphorus in CaO-SiO2-FeOx Low Basicity Slag

2011 ◽  
Vol 282-283 ◽  
pp. 129-132
Author(s):  
Chang Su ◽  
Jing Kun Yu ◽  
Ning Ning Lv
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Scanning Electron Microscopy ◽  
Condensed Phase ◽  
Molten Slag ◽  
Heating Temperature ◽  
Holding Time ◽  
Reaction Behavior ◽  
X Ray ◽  
Scanning Electron

For investigating the reaction behavior of phosphorus in CaO–SiO2–FeOx low basicity slag, the CaO–SiO2–FeOx slag containing various amount of CaO particles was heated at 1623K and 1673K, respectively for 10 to 600s, and the products formed at the interface of the CaO particles and molten slag were observed by scanning electron microscopy (SEM) with energy dispersive X-ray (EDX). The research results showed that the solid solution containing P2O5 increased with the increasing of the heating temperature, and the formation of condensed phase was promoted by increasing the holding time and the CaO solid proportion.

Effect of TiC on coarsening and macrosegregation of Al–Bi alloys

2020 ◽  
Vol 111 (7) ◽  
pp. 607-615
Author(s):  
Congmin Li ◽  
Yanguo Yin ◽  
Ming Xu ◽  
Jianfeng Cheng ◽  
Lan Shen ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Heterogeneous Nucleation ◽  
Self Assembly ◽  
Holding Time ◽  
Energy Dispersive ◽  
Melt Temperature ◽  
X Ray ◽  
Minority Phase ◽  
Scanning Electron

Abstract The microstructures of an Al-Bi immiscible alloy and the corresponding composites containing TiC (1 wt.% and 2 wt.%) were explored for melt temperatures of 800 °C, 850 °C, and 900°C. It was demonstrated that serious coarsening and macrosegregation of Bi-rich minority phase particles occurred, which was slightly alleviated by increasing the melt temperature from 800 °C to 900 °C. By adding TiC particles, the coarsening and macrosegregation of Bi-rich minority phase particles were significantly impeded. Scanning electron microscopy and energy-dispersive X-ray spectroscopy revealed that TiC particles were located inside and on the surface of Bi-rich minority phase particles, exhibiting heterogeneous nucleation and self-assembly behaviour. By properly increasing the holding time of the melt, finer and more uniform Bi-rich minority phase particles were obtained.

Effect of Heat Treatments on Wettability of Nacre

2020 ◽  
Vol 985 ◽  
pp. 86-90
Author(s):  
Andi Muhammad Anshar ◽  
Sengo Kobayashi ◽  
Satoshi Okano
Keyword(s):  
Electron Microscopy ◽  
Thermal Analysis ◽  
Scanning Electron Microscopy ◽  
Heating Temperature ◽  
Pearl Oyster ◽  
Heat Treatments ◽  
Organic Substances ◽  
Water Contact ◽  
X Ray ◽  
Scanning Electron

The surface wettability of biomaterials influences on osteoblast behavior and bone formation. In this research, the variation of wettability of nacre by heat treatments was examined. Plates of the nacre were fabricated from shells of the Akoya pearl oyster. The specimens were heated at 100, 200, 300, 400, 500, and 600 °C. Characterizations of the specimens during and after heat treatments were carried out using scanning electron microscopy, X-ray diffractometry, and thermogravimetry-differential thermal analysis. The water contact angle (WCA) of the specimen was measured to evaluate wettability. The color of nacre changed from iridescent color to brownish weak-iridescence by the heating at and over 300 °C. The nacre heated at and over 300 °C became brittle because organic substances in nacre, which acts as the glue between the aragonite platelets were evaporated by the heating. The WCA of the specimen was decreased with increasing heating temperature, which should be related to the decrease in the number of organic substances in nacre by the heating.

Synthesis of Ti3Si0.4Al0.8C1.8 Solid Solution

2008 ◽  
Vol 368-372 ◽  
pp. 995-997
Author(s):  
Cui Wei Li ◽  
Hong Xiang Zhai ◽  
Yang Zhou ◽  
Shi Bo Li ◽  
Zhi Li Zhang
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Scanning Electron Microscopy ◽  
Single Phase ◽  
Lattice Parameters ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
Powder Mixtures ◽  
X Ray ◽  
Scanning Electron

In this study, free Ti/Si/Al/C powder mixtures with molar ratio of 3:0.4:0.8:1.8 were heated in Argon with various schedules, in order to reveal the possibility for the synthesis of Ti3Si0.4Al0.8C1.8 solid solution powder. X-ray diffraction (XRD) was used for the evaluation of phase identities of the powder after different treatments. Scanning electron microscopy (SEM) was used to observe the morphology of the Ti3Si0.4Al0.8C1.8 solid solution. XRD results showed that predominantly single phase samples of Ti3Si0.4Al0.8C1.8 was prepared after heating at 1400oC for 5 min in Argon and the lattice parameters of Ti3Si0.4Al0.8C1.8 lay between those of Ti3SiC2 and Ti3AlC2.

Effects of V2O5 on the synthesis of Ba2Ti9O20 powders

2005 ◽  
Vol 20 (10) ◽  
pp. 2741-2744 ◽  
Author(s):  
Huixing Lin ◽  
Wei Chen ◽  
Lan Luo
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Scanning Electron Microscopy ◽  
Single Phase ◽  
X Ray Diffraction ◽  
Eutectic Liquid ◽  
X Ray ◽  
Intermediate Phases ◽  
Phase Pure ◽  
Scanning Electron

Phase-pure Ba2Ti9O20 powders were made by doping 3 wt% of V2O5 to a Ba:Ti = 2:9 molar composition, and the effects of the dopant on the phase formation were investigated. The study shows that BaTiO3, BaTi2O5, and BaTi4O9 were the intermediate phases before the formation of Ba2Ti9O20 for samples with or without V2O5. However, with V2O5 doping, the temperature at which Ba2Ti9O20 occurred were lowered from 1150 to 1050 °C and single phase Ba2Ti9O20 powders was easily obtained at 1150 °C for 2 h. Microstructure of the powders was examined by field emission scanning electron microscopy. No evidence of V2O5–Ba2Ti9O20 solid-solution was found by x-ray diffraction and energy-dispersive spectroscopy. The benefit of V2O5 to facilitate the Ba2Ti9O20 synthesis is most probably due to a vanadium-containing eutectic liquid phase which accelerates the migration of reactant species.

scholarly journals Joining of γ-TiAl Alloy to Ni-Based Superalloy Using Ag-Cu Sputtered Coated Ti Brazing Filler Foil

Metals ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 723 ◽  
Author(s):  
Sónia Simões ◽  
Carlos Tavares ◽  
Aníbal Guedes
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Scanning Electron Microscopy ◽  
Chemical Composition ◽  
Tial Alloy ◽  
Energy Dispersive ◽  
X Ray ◽  
Base Materials ◽  
Intermetallic Particles ◽  
Scanning Electron

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.

Microwave-Assisted Preparation of Cu2O Octahedral Microcrystals

2011 ◽  
Vol 284-286 ◽  
pp. 746-749
Author(s):  
Chong Hai Deng ◽  
Han Mei Hu ◽  
Ming Di Yang
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Scanning Electron Microscopy ◽  
Growth Mechanism ◽  
X Ray Diffraction ◽  
Chemical Route ◽  
X Ray ◽  
Microwave Assisted ◽  
Morphology And Structure ◽  
Scanning Electron

In this paper, we reported a facile microwave-assisted green chemical route to prepare pure, uniform, and monodispersed Cu2O octahedron wrapped by the {111} faces by using glucose as a reducing agent. X-ray diffraction (XRD), energy dispersive X-ray spectrometry(EDX) and field emission scanning electron microscopy (FESEM) were used to characterize the as-synthesized products. It was found that the morphology and structure of Cu2O crystals were greatly affected by the concentration of NaOH. A solid-solution-solid growth mechanism was possibly proposed on the basis of the comparative experimental results.

Carbothermal Synthesis of Cr3C2-WC-Ni Nanocomposite Powders

2013 ◽  
Vol 661 ◽  
pp. 3-6 ◽  
Author(s):  
Yong Zhong Jin ◽  
Fa Ming Ye ◽  
Xian Guang Zeng ◽  
Rui Song Yang
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Scanning Electron Microscopy ◽  
Carbothermal Reduction ◽  
X Ray Diffraction ◽  
X Ray ◽  
Carbothermal Synthesis ◽  
Unit Cells ◽  
Nanocomposite Powders ◽  
Scanning Electron

Cr3C2-WC-Ni nanocomposite powders with ~50-100 nm were synthesized from precursors by vacuum-aided carbothermal reduction at only 750 °C for 2 h. The phase composition and microstructure of the synthesized products were investigated by X-ray diffraction (XRD) and scanning electron microscopy (SEM), respectively. The present study shows that Cr3C2-WC-Ni nanocomposite powders contain two kinds of solid-solution phases, namely Ni and (Cr, W)3C2solid solution, respectively. WC and W2C phases do not appear inreaction products due to the dissolution of tungsten atoms into Ni and Cr3C2unit cells. Especially, there is a change of the crystalline structure for (Cr, W)3C2phase from 750 °C to 800 °C.

Investigation on the Structural Properties of a New Prepared 0.2PZS-0.8PLZT Ceramics

2013 ◽  
Vol 856 ◽  
pp. 197-200
Author(s):  
Adel Sakri ◽  
Ahmed Boutarfaia
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Scanning Electron Microscopy ◽  
Smart Materials ◽  
Sintering Temperature ◽  
Human Life ◽  
Advanced Technology ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

View of the importance that has the development in the field of advanced technology transmission in human life, smart materials draws the attention of many researchers. In this contribution, we are interested in synthesizing a new smart material of the ceramic type based on Pb, Zr, Ti (PZT) doped La in the site A, and Sb, Zn in site B from a solid solution of pure oxides. The synthesized samples are thermally treated at 800°C. The techniques of x-ray diffraction (XRD) and SEM (scanning electron microscopy) are used to characterize the microstructure (the crystallographic phase), and the densities of the obtained samples were determined from their weights and volumes. The effect of sintering temperature on the microstructure properties was studied.

Microstructural and Dielectrical Properties for Ceramics and Thin Films of the xPbTiO3-(1−x)SrTiO3 Solid Solution

2001 ◽  
Vol 688 ◽  
Author(s):  
E. Martínez ◽  
A. Fundora ◽  
O. Blanco ◽  
S. García ◽  
E. Heredia ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Scanning Electron Microscopy ◽  
Dielectric Properties ◽  
Integrated Circuit ◽  
X Ray Diffraction ◽  
X Ray ◽  
Analysis Technique ◽  
Dielectrical Properties ◽  
Scanning Electron

AbstractSrTiO3 and PbTiO3 perovskites are combined to form the xPbTiO3-(1−x)SrTiO3 (PST) solid solution. The effect of the PbTiO3 content on the microstructural and dielectric properties is studied for different compositions (x=0.1,0.3,0.5,0.7, and 0.9). Microstructural features of the PST system are studied by X-Ray Diffraction (XRD) and Scanning Electron Microscopy (SEM) techniques. Electrical properties are studied by the thermoelectric analysis technique at both fixed frequency and varying frequency to study the behavior of the dielectric constant and dielectric loss.Films of 0.5PbTiO3-0.5SrTiO3 (PST50) have been obtained by RF ion sputtering on different substrates. We investigate the relation between the crystalline structure and the dielectric properties of PST50 films deposited on different metallic films. Scanning Electron Microscopy (SEM) and X-Ray Diffraction were used for the structural analysis of the PST50/TiN/Si and PST50/RuO2/TiN /Si systems. The dielectric properties of the PST50 films were measured for TiN/PST50/TiN/Si, and RuO2/PST50/RuO2/TiN/Si capacitors and the results were correlated to the structure and composition. The charge storage capabilities of the PST50 films are evaluated for possible application in integrated circuit technology.

Zirconolite-Based Ceramic Formulations for Immobilization of Zr-REE-Actinide Fraction of HLW

2004 ◽  
Vol 824 ◽  
Author(s):  
A.V. Ochkin ◽  
S.V. Stefanovsky ◽  
A.G. Ptashkin ◽  
N.S. Mikhailenko ◽  
O.I. Kirjanova
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Scanning Electron Microscopy ◽  
High Level Waste ◽  
X Ray Diffraction ◽  
Controlled Cooling ◽  
X Ray ◽  
Transmission Electron ◽  
High Level ◽  
Scanning Electron

AbstractTwo ceramics for immobilization of a Zr-REE-actinide fraction of high level waste (HLW) based on zirconolite or/and pyrochlore structures with minor brannerite/lucasite, and fluorite-structured dioxide-based solid solution, were synthesized and characterized. The samples were produced by melting of oxide mixtures at 1500 °C followed by controlled cooling for crystallization. Phase compositions of the samples obtained and waste elements partitioning among co-existing phases were investigated in detail using powder X-ray diffraction, scanning electron microscopy with energy dispersive spectroscopy, and transmission electron microscopy. Cerium enters cerianite-based solid solution, lucasite (if present), and to a lesser extent, pyrochlore and zirconolite. Europium and gadolinium enter predominantly zirconolite and pyrochlore. The highest uranium concentrations were found in a uraninite-based cubic solid solution or pyrochlore and zirconolite.

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