Characterization of Glass Ceramics Produced from Natural and Waste Raw Materials

2018 ◽  
Vol 271 ◽  
pp. 23-27
Author(s):  
Uyat Bayarzul ◽  
Jadambaa Temuujin

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.

2000 ◽  
Vol 663 ◽  
Author(s):  
P. Loiseau ◽  
D. Caurant ◽  
N. Baffier ◽  
C. Fillet

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.


2012 ◽  
Vol 624 ◽  
pp. 134-137 ◽  
Author(s):  
Ping Zhai ◽  
Xiao Feng Duan ◽  
Da Qian Chen ◽  
Chong Hai Wang

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.


MRS Advances ◽  
2018 ◽  
Vol 3 (11) ◽  
pp. 563-567 ◽  
Author(s):  
Quentin Altemose ◽  
Katrina Raichle ◽  
Brittani Schnable ◽  
Casey Schwarz ◽  
Myungkoo Kang ◽  
...  

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.


2013 ◽  
Vol 834-836 ◽  
pp. 309-314
Author(s):  
Zi Fan Xiao ◽  
Jin Shu Cheng ◽  
Jun Xie

A glass-ceramic belonging to the CaO-Al2O3-SiO2(CAS) system with different composition of spodumene and doping the Li2O with amount between 0~2.5 % (mass fraction) were prepared by onestage heat treatment, under sintering and crystallization temperature at 1120 °C for two hours. In this paper, differential thermal analysis, X-ray diffraction, scanning electron microscopy, energy dispersive spectrometry and bending strength test were employed to investigate the microstructure and properties of all samples. β-wollastonite crystals were identified as the major crystalline phases, and increasing Li2O was found to be benefit for the crystallization and tiny crystalline phases remelting, resulting in the content of major crystalline phases increased first and then decreased with increasing the expense of spodumene. Meanwhile, the crystal size can be positively related with the content of Li2O. The preferable admixed dosage of spodumene can be obtained, besides the strength of glass-ceramics can be more than 90 MPa.


2014 ◽  
Vol 1035 ◽  
pp. 263-267
Author(s):  
Xiu Quan Zhao ◽  
Zheng Cao ◽  
Yu Teng Wu ◽  
Hong Jiang ◽  
Chang Jiu Li ◽  
...  

Glass-ceramic materials of the Li2O-ZnO-SiO2 system, with various amounts of TiO2 added, have been prepared. The appropriate heat treatment temperatures were selected according to the information provided by the differential thermal analysis (DTA). X-ray diffraction (XRD) analysis demonstrated that in the LZS glass-ceramics system, the main phases are Li2ZnSiO4, cristobalite, tridymite and quartz. The scanning electron microscopy (SEM) revealed that crystals appear as lamellar and spherical particles in the glass-ceramics samples. In addition, the average coefficient of the thermal expansion (CTE) values first decreased, then increased and finally tended to flatten. When the content of TiO2 increased to 6%, the CTE value decreased to 9.15×10-6/K, reached the lowest value. When the content of TiO2 increased to 10%, the CTE value reached highest value 13.90×10-6/K.


2010 ◽  
Vol 92 ◽  
pp. 131-137 ◽  
Author(s):  
Qiu Hua Yuan ◽  
Pei Xin Zhang ◽  
Li Gao ◽  
Hai Lin Peng ◽  
Xiang Zhong Ren ◽  
...  

The crystallization behavior of MgO-Al2O3-SiO2 glass-ceramics by sol-gel technology was investigated by using x-ray diffraction (XRD), differential thermal analysis (DTA), Scanning electron microscopy (SEM). The results showed that: (1)α-cordierite phase was precipitated when the green body was calcined at 1050°C, and α-cordierite of high purity and stability could be formed at 1100°C; (2) Adding an appropriate amount of low melting point glass powder into the green body may provide liquid-phase environment during the sintering process, which will help enhance the tightness density of glass-ceramic, and thus improve its flexural strength.


2012 ◽  
Vol 554-556 ◽  
pp. 18-22
Author(s):  
Supakorn Silakate ◽  
Anucha Wannagon ◽  
Apinon Nuntiya

The objectives of this study were to prepare leadless crystalline glazes from iron oxide by using low temperature firing (1,100°C) and to study the effect of concentration of iron oxide on the phase composition of the glaze raw materials on phase transformation in leadless iron oxide crystalline glaze. The crystalline phases were investigated by using the DTA, X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. The composition of the glaze raw materials compose of nepheline syenite, colemanite, pottery stone, bentonite, ZnO, Li2CO3, SiOSubscript text2 and 10, 15 and 20%(w/w) iron oxide (Fe2O3). The glaze raw materials were ground for homogeneous mixtures by ball milling for 24h. The average particle size of the mixture was 3.86 µm. The glaze bodies were carried to firing at 1,100°C at the heating rate of 2°C/min and soaking for 0.5h. Then, the glaze bodies were cooled at the cooling rate of 1°C/min and maintained at 1,080°C for 3h and then maintained at 980°C for 1h, respectively. From the experiment results, it was found that the crystallization temperatures (Tc) of franklinite (ZnFe2O4) and anorthite (CaAl2Si2O8) depend on the concentration of iron oxide content.


2011 ◽  
Vol 66-68 ◽  
pp. 65-69
Author(s):  
Long Feng Li ◽  
Yuan Gao ◽  
Mao Lin Zhang

Ca-Mg-Al hydrotalcite-like compounds (CaMgAl-HTLcs) were synthesized by a hydrothermal method, and characterized by X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and differential thermal analysis (DTA) techniques. The effects of the medium pH value, the molar ratio of the raw materials, the reaction temperature and the reaction time on the structure of CaMgAl-HTLcs were studied. The results showed that increasing treatment temperature and reaction time could improve the crystallinity and monodispersity of hydrotalcite-like compound particles. And well-defined CaMgAl-HTLcs could be prepared at a pH value of 10~11 with n(Zn+Mg+Ca):n(Al) =2. The products synthesized were applied to PVC to improve the thermal stability of PVC.


2006 ◽  
Vol 514-516 ◽  
pp. 843-847 ◽  
Author(s):  
Cristina Borges Correia ◽  
João C. Bordado

Polyurethane adhesives provide excellent flexibility, impact resistance and durability. Polyurethanes are formed through the reaction of an isocyanate component with polyether or polyester polyols or other active hydrogen compounds. This paper refers to polyurethane adhesives made from polyester polyols with long aliphatic chains (up to 36 carbon atoms) and MDI (diphenylmethane-4,4’-diisocyanate). The polyester polyols have been made from dimer acids obtained from renewable sources and short chain diols. The polyols that were used presented different degrees of unsaturation. The influence of the different raw materials in the adhesives performance is studied. The polyurethanes were produced by reaction between quasi-stoichiometric quantities of polyol and MDI, at several temperatures. The reaction was carried under inert atmosphere and at temperatures below 100°C. Performance of the adhesives was tested by carrying adhesion, hardness and water absorption tests. Characterization of both the polyester polyols and polyurethane adhesives was carried by Fourier Transform Infrared Spectroscopy (FTIR), Differential Scanning Calorimetry (DSC), Magnetic Nuclear Resonance (NMR), X-Ray Diffraction (WAXD), Scanning RMN Imaging of 1H of Stray- Field b (MRI) and Brookfield viscometry.


Clay Minerals ◽  
2019 ◽  
Vol 54 (3) ◽  
pp. 277-281 ◽  
Author(s):  
Cristiana Costa ◽  
António Fortes ◽  
Fernando Rocha ◽  
Angela Cerqueira ◽  
Delfim Santos ◽  
...  

AbstractPortuguese gypsum deposits utilized by the cement industry were characterized mineralogically, chemically and technologically for possible application in dermocosmetics. The deposits studied (Loulé, Óbidos and Soure) correspond to small outcrops in diapiric anticline areas. In principle, they represent gypsites which are white, and generally of higher quality for traditional applications (e.g. white cement), or greyish, and generally not adequate for cements and mortars. The analytical methods used to characterize the materials were wet sieving and X-ray sedimentation, X-ray diffraction, X-ray fluorescence spectrometry and assessment of abrasiveness, plasticity, texturometrics (adhesivity and firmness), oil absorption and cooling rate. The Óbidos gypsum displayed greater mineralogical and chemical quality (almost pure calcium sulfate) and had a finer grain size (<63 μm), whereas Loulé and Soure gypsums contain mineralogical impurities (mainly quartz). The Óbidos gypsum shows good characteristics in general for application in dermocosmetics because of its absorption, plasticity, adhesivity, firmness and low abrasiveness.


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