The Use of Organometallic Precursors to Silicon Nitride as Binders

1988 ◽  
Vol 121 ◽  
Author(s):  
Stuart T. Schwab ◽  
Cheryl R. Blanchard-Ardid

ABSTRACTCurrent techniques of advanced ceramic component fabrication are based on pressureless green body consolidation technology in which voids often remain in the final microstructure. Much of this residual porosity is created when the organic binder used to consolidate the ceramic powder burns off on sintering. A new concept in the field of ceramic processing is the use of an organometallic binder material which will pyrolyze on sintering and convert into a predetermined ceramic. Silicon nitride (Si3N4) is a ceramic material in great demand for elevated temperature applications because of its excellent high temperature properties. At the present time, silicon nitride cannot be successfully processed without the use of costly pressure sintering (e.g., hot pressing), or the addition of a glassy phase, which degrades the high temperature properties.Various preceramic polymers to be used as binders for cold pressing operations have been synthesized and studied. It has been demonstrated that these polymers may be dissolved in an appropriate organic solvent and mixed with a powder. Removal of the solvent yields homogeneous mixtures which may be consolidated into highly dense (> 66% of theoretical) green bodies. The ceramic yields of these polymers have also been determined.

2012 ◽  
Vol 32 (9) ◽  
pp. 1893-1899 ◽  
Author(s):  
Ulrich Degenhardt ◽  
Frank Stegner ◽  
Christian Liebscher ◽  
Uwe Glatzel ◽  
Karl Berroth ◽  
...  

2006 ◽  
Vol 317-318 ◽  
pp. 425-428 ◽  
Author(s):  
Yoshinobu Yamamoto ◽  
Toshiyuki Nishimura ◽  
Naoto Hirosaki ◽  
S. Guo ◽  
J. Cao ◽  
...  

High-temperature properties of silicon nitride ceramics with Lu-silicon-oxynitride grain boundary phases were investigated. Si3N4 powder with 1.2 mol% (SN12) and 4.8 mol% (SN48) of Lu2O3 were gas-pressure hot-pressed at 1950°C for 2 h under 20 MPa in 1 MPa N2. SN12 consisted of elongated β-Si3N4 and a secondary phase, Lu4Si2O7N2, whilst SN48 consisted of elongated β-Si3N4 and Lu4Si2O7N2 + Lu2SiO5. At 1500°C and 1600°C, the stress-strain curve of SN48 was nonlinear, whilst that of SN12 was linear, indicating that SN12 broke as a brittle fracture at these temperatures. SN12 had excellent oxidation resistance and weight gain during the oxidation at 1500°C for 1000 h was 4 g/m2. Creep lifetime of SN12 at 1500°C under tensile stress of 137 MPa exceeded 1678.5 h.


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