Preparation and Characterization of β-Eucryptite Glass Ceramics

2012 ◽  
Vol 624 ◽  
pp. 134-137 ◽  
Author(s):  
Ping Zhai ◽  
Xiao Feng Duan ◽  
Da Qian Chen ◽  
Chong Hai Wang
Keyword(s):  
Heat Treatment ◽  
Expansion Coefficient ◽  
Heat Treatment Temperature ◽  
Glass Ceramics ◽  
Treatment Temperature ◽  
Structure And Properties ◽  
X Ray Diffraction ◽  
Solid Reaction ◽  
X Ray

In this paper, β-eucryptite glass ceramics were synthesized by using solid reaction method. Phase constitution, structure and properties of the material were studied by X-ray diffraction (XRD) and differential thermal analysis (DTA). Furthermore, the effects of heat treatment temperature and preservation time on the thermal expansion coefficient were also analyzed. The results showed that the crystallization temperature of β-eucryptite glass ceramics was in the range of 810-860 °C and the content was more than 90%. With the increase of heat treatment temperature, the material expansion coefficient decreased.

Neodymium Incorporation in Zirconolite-Based Glass-Ceramics

2000 ◽  
Vol 663 ◽  
Author(s):  
P. Loiseau ◽  
D. Caurant ◽  
N. Baffier ◽  
C. Fillet
Keyword(s):  
Heat Treatment ◽  
Glass Ceramics ◽  
Fission Products ◽  
Treatment Temperature ◽  
Spent Fuel ◽  
X Ray Diffraction ◽  
Parent Glass ◽  
X Ray ◽  
Spin Resonance

ABSTRACTThe investigations on enhanced reprocessing of nuclear spent fuel, and notably on separating the long-lived minor actinides, such as Am and Cm, from the other fission products have led to the development of highly durable specific matrices such as glass-ceramics for their immobilization. This study deals with the characterization of zirconolite (CaZrTi2O7) based glass-ceramics synthesized by devitrification of an aluminosilicate parent glass. Trivalent actinide ions were simulated by neodymium, which is a paramagnetic local probe. Glass-ceramics with Nd2O3 contents ranging from 0 to 10 weight % were prepared by heat treatment of a parent glass at two different growth temperatures: 1050° and 1200°C. X-ray diffraction (XRD), energy dispersive X-ray analysis (EDX) and electron spin resonance (ESR) measurements clearly indicate that Nd3+ ions are partly incorporated in zirconolite crystals formed in the bulk of the glass-ceramic samples. The amount of neodymium in the crystalline phase was estimated using ESR results and was found to decrease with increasing either heat treatment temperature or total Nd2O3 content.

In Situ X-Ray Diffraction Studies of Crystallization Growth Behavior in ZnO-Bi2O3-B2O3 Glass as a Route to Functional Optical Devices

MRS Advances ◽  
2018 ◽  
Vol 3 (11) ◽  
pp. 563-567 ◽  
Author(s):  
Quentin Altemose ◽  
Katrina Raichle ◽  
Brittani Schnable ◽  
Casey Schwarz ◽  
Myungkoo Kang ◽  
...  
Keyword(s):  
Heat Treatment ◽  
Glass Ceramics ◽  
Treatment Temperature ◽  
Crystal Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
In Situ Xrd ◽  
Dsc Measurements ◽  
Transmission Window

ABSTRACTTransparent optical ZnO–Bi2O3–B2O3 (ZBB) glass-ceramics were created by the melt quenching technique. In this work, a melt of the glass containing stoichiometric ratios of Zn/Bi/B and As was studied. Differential scanning calorimeter (DSC) measurements was used to measure the thermal behavior. VIS/NIR transmission measurements were used to determine the transmission window. X-ray diffraction (XRD) was used to determine crystal phase. In this study, we explore new techniques and report a detailed study of in-situ XRD of the ZBB composition in order to correlate nucleation temperature, heat treatment temperature, and heat treatment duration with induced crystal phase.

Preparation and Catalytic Performance of Ti(SO4)2/γ-Al2O3 Catalysts for Oligomerization of 1-Butene

2013 ◽  
Vol 634-638 ◽  
pp. 696-700
Author(s):  
Lin Jiu Xiao ◽  
Peng Li ◽  
Yong Gang Sheng
Keyword(s):  
Heat Treatment ◽  
Physicochemical Properties ◽  
Heat Treatment Temperature ◽  
Catalytic Performance ◽  
Treatment Temperature ◽  
Impregnation Method ◽  
X Ray Diffraction ◽  
Isothermal Adsorption ◽  
X Ray ◽  
Adsorption Desorption

A series of Ti(SO4)2/γ-Al2O3 catalysts were prepared by impregnation method and the catalytic performance of these catalysts in 1-butene oligomerization was investigated. The heat treatment temperature played great influences on the catalytic performance of these catalysts in the oligomerization. 90.1 wt.% conversion of 1-butene and 92.2 wt.% selectivity of dimers were obtained on Ti(SO4)2/γ-Al2O3(450) catalyst at 80 °C, 1.0 Mpa and LHSV=0.6 h−1. The heat treatment temperature determined the crystallinity of TiOSO4 and specific surface area of these catalysts, which affected the catalytic performance of these catalysts in 1-butene oligomerization. In addition, the physicochemical properties of these catalysts were comparatively characterized by powder X-ray diffraction (XRD), N2 isothermal adsorption-desorption techniques.

scholarly journals Influence of Different Heat Treatment Temperatures on the Microstructure, Corrosion, and Mechanical Properties Behavior of Fe-Based Amorphous/Nanocrystalline Coatings

Coatings ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 858
Author(s):  
Shenglin Liu ◽  
Yongsheng Zhu ◽  
Xinyue Lai ◽  
Xueping Zheng ◽  
Runnan Jia ◽  
...  
Keyword(s):  
Heat Treatment ◽  
Corrosion Resistance ◽  
Heat Treatment Temperature ◽  
Annealing Treatment ◽  
Treatment Temperature ◽  
X Ray Diffraction ◽  
Crystalline Phases ◽  
X Ray ◽  
Different Temperatures ◽  
Sprayed Coating

Fe-based amorphous/nanocrystalline coatings with smooth, compact interior structure and low porosity were fabricated via supersonic plasma spraying (SPS). The coatings showed outstanding corrosion resistance in a 3.5% NaCl solution at room temperature. In order to analyze the effect of annealing treatment on the microstructure, corrosion resistance and microhardness, the as-sprayed coating was annealed for 1 h under different temperatures such as 350, 450, 550 and 650 °C, respectively. The results showed that the number of oxides and cracks in the coatings presented an obvious increase with increasing annealing temperature, and the corrosion resistance of the coatings showed an obvious reduction. However, the microhardness of coatings showed an important increase. The microhardness of the coating could reach 1018 HV when the heat treatment temperature reached 650 °C. The X-ray diffraction (XRD) results showed that there appeared a number of crystalline phases in the coating when the heat treatment temperature was at 650 °C. The crystalline phases led to the increase of the microhardness.

scholarly journals Fabrication and Crystallization of ZnO-SLS Glass Derived Willemite Glass-Ceramics as a Potential Material for Optics Applications

2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Mohd Hafiz Mohd Zaid ◽  
Khamirul Amin Matori ◽  
Sidek Hj. Abdul Aziz ◽  
Halimah Mohamed Kamari ◽  
Wan Mahmood Mat Yunus ◽  
...  
Keyword(s):  
Heat Treatment ◽  
Glass Ceramic ◽  
Glass Ceramics ◽  
Structural Evolution ◽  
Linear Shrinkage ◽  
Treatment Temperature ◽  
Isothermal Heat Treatment ◽  
X Ray Diffraction ◽  
X Ray ◽  
Zinc Orthosilicate

Willemite glass-ceramics were successfully derived from conventional melt-quench ZnO-SLS precursor glass by an isothermal heat treatment process. The effect of heat treatment temperatures on the physical properties was investigated by Archimedes principle and linear shrinkage. The generation of willemite crystal phase and morphology with increase in heat treatment temperature was examined by X-ray diffraction (XRD), Fourier transform infrared (FTIR), and field emission scanning electron microscopy (FESEM) techniques. X-ray diffraction revealed that the metastableβ-Zn2SiO4and thermodynamically stable zinc orthosilicateα-Zn2SiO4phases can be observed at temperatures above 700°C. The experimental results indicated that the density and shrinkage of the glass-ceramic vary with increasing the sintering temperature. FTIR studies showed that the structure of glass-ceramic consists of SiO2and ZnO4units and exhibits the structural evolution of willemite glass-ceramics. The characteristic of strong vibrational bands can be related to theSiO44-tetrahedron corresponding to reference spectra of willemite.

Effect of MnFe2O4 and the Heat Treatment Temperature on the Bioactive Glass Properties

2016 ◽  
Vol 690 ◽  
pp. 137-142
Author(s):  
Thanaporn Boonchoo ◽  
Pratthana Intawin ◽  
Wilaiwan Leenakul
Keyword(s):  
Electron Microscopy ◽  
Heat Treatment ◽  
Magnetic Properties ◽  
Bioactive Glass ◽  
Glass Ceramics ◽  
Treatment Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Diffraction Peaks

In this study, the effects of heat treatment temperatures on structural and magnetic properties in MnFe2O4(MF)/SiO2-Na2O-CaO-P2O5 (bioglass) bioactive glass ceramics were investigated. The MF/SiO2-Na2O-CaO-P2O5 bioactive glass ceramics were fabricated under various heat treatment temperatures in a range of 600-1000 °C. X-ray diffraction (XRD) technique, the scanning electron microscopy (SEM) and transmission electron microscopy (TEM) are used to characterize phase and microstructure. The magnetic properties were determined from Vibrating Sample Magnetometer (VSM). The X-ray diffraction peaks presented two major crystalline phases: MnFe2O4 and Na2Ca2Si3O9. It was found that the heat treatment temperatures are the most influential parameter on microstructure and magnetic properties of the bioactive glass ceramics. The highest magnetic properties of studied ceramics were found in the sample heated at 1000 °C with adding 20 wt%. MF. The microstructural properties of the studies samples were investigated and the results were then correlated with the characteristics of heat treatment temperatures as well as the microstructure of the bioactive glass ceramic.

Nanoporosity in Ceramics from Polymeric Precursors

1994 ◽  
Vol 346 ◽  
Author(s):  
A.W. Reid ◽  
B. Rand ◽  
R.J.P. Emsley
Keyword(s):  
Heat Treatment ◽  
Pore Volume ◽  
Heat Treatment Temperature ◽  
Gas Adsorption ◽  
Treatment Temperature ◽  
X Ray Diffraction ◽  
Carbon Phase ◽  
Volume Increase ◽  
X Ray ◽  
Adsorption Analysis

ABSTRACTIt is shown that ceramics derived from polycarbosilane polymers may develop an open nanoporous network after heat treatment to a temperatures between 1300 and 1550°C in argon. The resulting SiC-based ceramics were characterised by N2 gas adsorption analysis and X-ray diffraction. The apparent surface area, and pore volume increase with increasing heat treatment temperature, reaching values of 170 m2g-1 and 0.12 cm3-1 respectively. The pore network develops as the SiC crystals grow and as carbon is ejected from the structure. It is thought that the porosity may reside within the carbon phase, but this remains to be confirmed.

Characterization of Glass Ceramics Produced from Natural and Waste Raw Materials

2018 ◽  
Vol 271 ◽  
pp. 23-27
Author(s):  
Uyat Bayarzul ◽  
Jadambaa Temuujin
Keyword(s):  
Crystallization Behavior ◽  
Cold Water ◽  
Raw Materials ◽  
Window Glass ◽  
Glass Ceramics ◽  
Hardness Test ◽  
Treatment Temperature ◽  
X Ray Diffraction ◽  
X Ray

Glass ceramics were prepared from fly ash, waste window glass and fluorite rawmaterials. Mixtures of raw materials were melted at 1300, 1400 and 1500 °C for 4 h and quenchedin cold water. The crystallization behavior of glass ceramics was investigated by differentialthermal analysis-thermogravimetry (DTA-TG). Crystallization at various temperatures (700, 800,900 and 1000 °C) for 30 min was used to obtain the glass ceramics. The obtained glass ceramicswere characterized by X-ray diffraction (XRD), light microscopy and hardness test. XRD studyrevealed that the crystallized phases were plagioclase-type minerals (diopside and albite). TheVickers hardness of the glass ceramics increased from 0.80±0.19 GPa to 6.35±0.35GPa and densityranged from 1.44 g/cm3 to 2.42 g/cm3 depending on the treatment temperature. Glass ceramicsprepared from fused glass melted at 1500 °C temperature showed the highest hardness comparedwith those melted at lower temperatures.

Characterization of NiTi Shape Memory Wires by Differential Scanning Calorimetry and Transmission X-ray Diffraction

1991 ◽  
Vol 246 ◽  
Author(s):  
Ming-Yuan Kao ◽  
Sepehr Fariabi ◽  
Paul E. Thoma ◽  
Husnu Ozkan ◽  
Louis Cartz
Keyword(s):  
Heat Treatment ◽  
Differential Scanning Calorimetry ◽  
Heat Treatment Temperature ◽  
Room Temperature ◽  
Cold Work ◽  
Treatment Temperature ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Niti Wires

AbstractThe reversible transformations between the Austenite (A) and Martensite (M) phases of NITI shape memory wires having a 78°C austenlte finish temperature (950°C annealed) were studied In the cold work and heat treatment ranges between 14 to 62% and 400 to 525°C respectively. The ranges of peak Transformation Temperatures (TI), determined by Differential Scanning Calorimetry (DSC) at a 10°C/min rate, were found to be 56 to 75°C, -28 to 33°C, and 38 to 52°C for the respective high temperature A, low temperature M, and the Intermediate Rhombohedral (R) phases. The degree of cold work and heat treatment had significant effects on the TT of NITI wires. The peak TT of A and M decreases with Increasing cold work. Except for the 14% cold worked wires, the peak TT Increases with Increasing heat treatment temperature for M, and Increases with Increasing heat treatment temperature for A for temperatures higher than 450°C. The peak IT of R Increases with Increasing cold work and decreasing heat treat temperature.Using MoKα radiation, transmission x-ray diffraction analysis was utilized to determine the phases at room temperature on wires thinned down to 0.05 to 0.01 mm in diameter. The diffraction patterns of body-centered cubic austenite (132) and monodlinic martenslte (B19) for NITi were both Identified. In addition, extra diffraction lines observed for various samples were tentatively assigned to M and the Intermediate R-phase. Depending on the thermal history and the processing conditions, the NITI wires consist of either a pure M, a mixture of A and R, or a mixture of A, R, and M at room temperature.

Structural characterization of carbons obtained from polyparaphenylenes prepared by the Kovacic and Yamamoto methods

1998 ◽  
Vol 13 (7) ◽  
pp. 2023-2030 ◽  
Author(s):  
M. Endo ◽  
C. Kim ◽  
T. Hiraoka ◽  
T. Karaki ◽  
K. Nishimura ◽  
...  
Keyword(s):  
Heat Treatment ◽  
Layer Structure ◽  
Treatment Temperature ◽  
Li Ion Batteries ◽  
X Ray Diffraction ◽  
X Ray ◽  
Heat Treated ◽  
Crystallite Structure ◽  
Li Ion

The structure of polyparaphenylene (PPP)-based carbons prepared by the Kovacic and Yamamoto methods heat-treated at 650–3000 °C have been characterized comparatively by using x-ray diffraction, SEM, TEM, and Raman spectroscopy. Both kinds of carbons indicate not typical but poor graphitizing behavior, especially for the case of PPP Yamamoto samples, and much less for PPP Kovacic samples, by heat treatment up to 3000 °C. The Kovacic-based samples heat-treated at 600–2400 °C have a more developed layer structure than that of Yamamoto-based samples. In contrast, for HTT's (heat-treatment temperature) more than about 2400 °C, PPP Yamamoto-based carbons exhibit a more developed crystallite structure than PPP Kovacic-based carbons. At a given HTT, PPP Kovacic-based carbons have a much more quinoid-like structure and graphene-type structure than PPP Yamamoto-based carbons, as indicated by the carbon yield and Raman scattering measurements. It is suggested that the detailed structure of the starting polymers influences the texture as well as the microstructure of resultant carbons even though both are obtained from the same kinds of precursors. These microstructures also largely influence the anode performance when these carbons are used in Li ion batteries.

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