scholarly journals Synthesis of biomorphic SiC and SiO2 ceramics

2008 ◽  
Vol 73 (7) ◽  
pp. 745-751 ◽  
Author(s):  
Adela Egelja ◽  
Jelena Gulicovski ◽  
Aleksandar Devecerski ◽  
Biljana Babic ◽  
Miroslav Miljkovic ◽  
...  

Coniferous wood (fir) was transformed by pyrolysis into carbon preforms, which were subsequently converted into biomorphic ceramics by the pressure infiltration technique with colloidal silica. An in situ reaction between the silica and the carbon template occurred in the cellular wall at a high sintering temperature. Depending on the employed atmosphere, non-oxide (SiC) or oxide (SiO2) ceramics were obtained. The morphology of the resulting porous ceramics and their phase composition were investigated by scanning electron microscopy (SEM/EDX) and X-ray diffraction (XRD). The experimental results showed that the biomorphic cellular morphology of the wood maintained in both the SiC and silica ceramics, which consisted of only the b-SiC phase and SiO2, respectively. .

2009 ◽  
Vol 3 (4) ◽  
pp. 197-201
Author(s):  
Adela Egelja ◽  
Aleksandar Devecerski ◽  
Jelena Gulicovski ◽  
Milena Rosic ◽  
Biljana Babic ◽  
...  

Tilia wood was transformed by pyrolysis into carbon preform. This porous carbon preform was infiltrated with TEOS (Si(OC2H5)4), as a source of silica. In situ reaction between the silica and the carbon template occurred in the cellular wall at a hight temperature. Depending on the applied atmosphere, non-oxide (SiC) or oxide (SiO2) ceramics were obtained. Scanning electron microscopy (SEM), X-ray diffraction (XRD), infrared (IR) spectroscopy, mercury porosimetry and BET measurements were employed to characterize the phases and crystal structure of biomorphic ceramics. The experimental results showed that the biomorphic cellular morphology of the wood maintained in both the SiC and SiO2 ceramics, wich consisted of ?-SiC with trace of ?-SiC and SiO2, respectively. .


2008 ◽  
Vol 591-593 ◽  
pp. 430-435
Author(s):  
Adriana Scoton Antonio Chinelatto ◽  
R. Justus ◽  
Adilson Luiz Chinelatto ◽  
F.M.C.N. Nadal ◽  
E.A.T. Berg

The ceramic matrix composites (CMCs) can be fabricated by the pressure infiltration technique. In this work it was studied porous preforms of quartzite that were infiltrated with aluminum liquid. For to produce the more resistant preforms of quartzite, it was additioned different quantities of bentonite (5 and 10%) and the preforms were firing at 1100°C and 1200°C. For the composites production, the melted aluminum was introduced into preforms under a pressure of 7 MPa. The characterizations of the composites were made by X-ray diffraction, scanning electron microscopy, and flexure strength. All the preforms studied presented sufficient strength for support the pressing during the process of squeeze casting. The results of X-ray diffraction of composites showed the presence of alumina, silicon and aluminum and fully interpenetration aluminum-siliconalumina composites were obtained by infiltration.


2016 ◽  
Vol 697 ◽  
pp. 399-403 ◽  
Author(s):  
Xian Gong Deng ◽  
Jun Kai Wang ◽  
Hai Jun Zhang ◽  
Jiang Hao Liu ◽  
Shao Wei Zhang

Magnesium aluminate spinel (MgAl2O4) porous ceramics were in-situ synthesized by heating the mixture of Al2O3 and MgCO3 with MgCl2 salt at 1400~1600 °C for 3 h, and then characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The morphology of as-prepared MgAl2O4 porous ceramics was dependent on the addition of MgCl2, and it indicated that the MgCl2 molten salt not only acted as a template for pore formation of the porous ceramics, but also provided a liquid environment for the synthesis of MgAl2O4.


2007 ◽  
Vol 280-283 ◽  
pp. 1143-1146
Author(s):  
Shu Qiang Ding ◽  
Dong Liang Jiang ◽  
Su Min Zhu

A novel technique was developed to synthesize porous silica–matrix ceramics from silicon carbide and alumina with an Y2O3 addition, using pine sawdust as a pore former. The porous ceramics were fabricated at temperatures of 1300–1500 oC in air by a reaction–bonding process based on two reactions: (1)SiC+2O2→SiO2+CO2 (Oxidation) and (2)2SiO2+3Al2O3→3Al2O3·2SiO2 (Mullitization). Reaction–bonding behavior, mechanical property and open porosity were investigated as a function of Y2O3 content as well as sintering temperature and holding time. Moreover, phase composition and microstructure of the porous silica–matrix ceramics were studied by X–ray diffraction (XRD) and scanning electron microscopy (SEM).


2007 ◽  
Vol 353-358 ◽  
pp. 1572-1575 ◽  
Author(s):  
Cong Hoa Vu ◽  
Quoc Thai Phan ◽  
Do Won Seo ◽  
Jae Kyoo Lim

Porous SiC/Si3N4 composites were fabricated by reaction between Si3N4 and C powder in 0.5 MPa nitrogen atmosphere at 1700oC, 1800oC and 1900oC for 0.5h, 1h and 2h, respectively. The characteristics of in situ porous Si3N4/SiC composites were further investigated by X-ray diffraction (XRD) and scanning electronic microscopy (SEM). Results show that the SiC particles are very fine. And the transformation from α-Si3N4 to β-Si3N4 is obvious at 1800oC for 2h and at 1900oC. Otherwise, at 1700oC, the formation of rod-like β-Si3N4 is inhibited. The compressive test was conducted at a cross-head speed of 0.5 mm/min to get the basic mechanical performance of the porous ceramics. The highest value of strength of these composites was obtained when sintered at 1800oC for 1h.


Author(s):  
R. E. Herfert

Studies of the nature of a surface, either metallic or nonmetallic, in the past, have been limited to the instrumentation available for these measurements. In the past, optical microscopy, replica transmission electron microscopy, electron or X-ray diffraction and optical or X-ray spectroscopy have provided the means of surface characterization. Actually, some of these techniques are not purely surface; the depth of penetration may be a few thousands of an inch. Within the last five years, instrumentation has been made available which now makes it practical for use to study the outer few 100A of layers and characterize it completely from a chemical, physical, and crystallographic standpoint. The scanning electron microscope (SEM) provides a means of viewing the surface of a material in situ to magnifications as high as 250,000X.


2017 ◽  
Vol 72 (6) ◽  
pp. 355-364
Author(s):  
A. Kopp ◽  
T. Bernthaler ◽  
D. Schmid ◽  
G. Ketzer-Raichle ◽  
G. Schneider

2020 ◽  
Author(s):  
Chi-Toan Nguyen ◽  
Alistair Garner ◽  
Javier Romero ◽  
Antoine Ambard ◽  
Michael Preuss ◽  
...  

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