Relationship between the synthesis and structure of ceramic precursors of the TiO 2‒CeO 2‒ZrO2 system

Author(s):  
O. Yu. Kurapova ◽  
S. N. Golubev ◽  
A. G. Glukharev ◽  
V. G. Konakov
Keyword(s):  
Author(s):  
T.R. Dinger ◽  
G. Thomas

The use of Si3N4, alloys for high temperature, high stress structural applications has prompted numerous studies of the oxynitride glasses which exist as intergranular phases in their microstructures. Oxynitride glasses have been investigated recently in their bulk form in order to understand their crystallization behavior for subsequent Si3N4 applications and to investigate their worth as glass-ceramic precursors. This research investigates the crystallization sequence of a glass having a normalized composition of Y26Si30Al11 ON11 and lying in the A1N-Y2O3-SiO2 section of the Y-Si-Al-O-N system. Such glasses exist as intergranular phases in the technologically important Y2O3/Al2O3-fluxed Si3N4 alloys.


Author(s):  
J.M. Schwartz ◽  
L.F. Francis ◽  
L.D. Schmidt ◽  
P.S. Schabes-Retchkiman

Ceramic thin films and coatings are of interest for electrical, optical, magnetic and thermal barrier applications. Critical for improved properties in thin films is the development of specific microstructures during processing. To this end, the sol-gel method is advantageous as a versatile processing route. The sol-gel process involves depositing a solution containing metalorganic or colloidal ceramic precursors onto a substrate and heating the deposited layer to form a crystalline or non-crystalline ceramic coating. This route has several advantages, including the ability to create tailored microstructures and properties, to coat large or small areas, simple or complex shapes, and to more easily prepare multicomponent ceramics. Sol-gel derived coatings are amorphous in the as-deposited state and develop their crystalline structure and microstructure during heat-treatment. We are particularly interested in studying the amorphous to crystalline transformation, because many key features of the microstructure such as grain size and grain size distribution may be linked to this transformation.


1994 ◽  
Vol 371 ◽  
Author(s):  
Jun Liu ◽  
Jud W. Virden ◽  
Anthony Y. Kim ◽  
Bruce C. Bunker

AbstractRecently we proposed that heterogenous nucleation is an important phenomenon for the preparation of ordered mesoporous materials. In this paper we further investigate the effect of colloidal particles on the nucleation process of mesoporous materials. Based on the change of the electrical mobilities of the particles in the surfactant solution, we suggest that the adsorption and co-adsorption of surfactant and ceramic precursors changes local structural and chemistry on the particle surfaces, and favors the nucleation events within these regions.


2006 ◽  
Vol 40 (16) ◽  
pp. 5077-5083 ◽  
Author(s):  
Kaimin Shih ◽  
Tim White ◽  
James O. Leckie

2021 ◽  
Vol 322 ◽  
pp. 54-59
Author(s):  
Iva Rozsypalová ◽  
Petr Daněk ◽  
Pavla Rovnaníková ◽  
Zbyněk Keršner

The paper deals with selected alkali-activated aluminosilicate (AAAS) composites based on ceramic precursors in terms of their characterization by mechanical fracture parameters. Composites made of brick dust as a precursor and an alkaline activator with a silicate modulus of Ms = 0.8, 1.0, 1.2, 1.4 and 1.6 were investigated. The filler employed with one set of composites was quartz sand, while for the other set it was crushed brick. The test specimens had nominal dimensions of 40 × 40 × 160 mm and were provided with notches at midspan of up to 1/3 of the height of the specimens after 28 days. 6 samples from each composite were tested. The specimens were subjected to three-point bending tests in which force vs. displacement (deflection at midspan) diagrams (F–d diagrams) and force vs. crack mouth opening (F–CMOD) diagrams were recorded. After the correction of these diagrams, static modulus of elasticity, effective fracture toughness, effective toughness and specific fracture energy values were determined using the Effective Crack Model and the Work-of-Fracture method. After the fracture experiments, informative compressive strength values were determined from one of the parts. All of the evaluations included the determination of arithmetic means and standard deviations. The silicate modulus values and type of filler of the AAAS composites significantly influenced their mechanical fracture parameters.


1992 ◽  
pp. 378-382
Author(s):  
S. Piantelli ◽  
G. Maccauro ◽  
P. Fassina ◽  
A. Bukat

Author(s):  
Weigang Zhang ◽  
Changming Xie ◽  
Min Ge ◽  
Xi Wei

Two-dimensional C/C-ZrB2-ZrC-SiC composites with three phases of ultra high temperature ceramics (UHTCs) are fabricated for the first time using blending pre-ceramic polymeric precursors through the traditional polymer infiltration and pyrolysis (PIP) technique, in which a porous carbon fiber reinforced pyrolytic carbon (C/C) with a porosity of about 60% is prepared as preforms. The fabricated composite possesses a matrix of 20ZrB2-30ZrC-50SiC, which is obtained by co-pyrolysis of three pre-ceramic polymers solution in xylene with certain molar ratios. Pyrolysis of these ZrB2-ZrC-SiC pre-ceramic precursors is studied with XRD characterization of the residual solids. The gas phase products are analysized with an on-line GC-MS-FTIR coupling technique, which confirms the formation of crystalline ZrC and ZrB2 from these precursors at temperatures above 1400°C. Possible mechanisms of pyrolysis and formation of pure ZrB2 from the precursors with various B/Zr molar ratios are suggested. The densification process and microstructures of the fabricated composite are studied. It is found that a composite with a bulk density of 2.06 g/cm3 and open porosity of 9.6% can be obtained after 16 PIP cycles. The formed matrix exhibits homogeneous dispersion of three matrix ceramics without any oxide impurities, i.e., the nano sized ZrB2 and ZrC particles dispersed in a continuous SiC ceramic with clean crystalline boundaries and particle dimensions less than 200 nm. No erosion or interface reaction occurs upon the carbon fiber reinforcement, which therefore avoids a dramatic deterioration of mechanical strength of carbon fiber and the composite. Improvement of PIP benefits from two aspects; firstly, the dense pyrolytic carbon interphase deposited on fiber surface by CVI serves as barrier coating and secondly, pyrolysis of the novel organic polymeric precursors does not release corrosive by-products such as hydrogen chloride.


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