Continuous ceramic fibres are finding applications as reinforcements in ceramic matrix composites, and yttrium aluminium garnet (YAG) is a particularly attractive candidate material on account of its creep resistance at high temperatures. A continuous, aligned, 5·5 μm diameter polycrystalline YAG fibre was manufactured from an aqueous sol-gel precursor which contained chlorine, and compared to a similar nitrate containing YAG precursor fibre we have reported previously. The precursor sol was found to be stable at a higher concentration than the nitrate containing sol, and this resulted in denser gel fibres which demonstrated better sintering at equivalent temperatures, giving a 98·5% sintered YAG fibre at 1550°C with a grain size of only 1 μm. However, on firing in air, the fibres formed fully crystalline YAG between 800 and 900°C, a temperature 100°C higher than the fibres containing nitrate, and they were weakened by the presence of many hemispherical faults. It was shown that both of these features were due to the retention of chlorine until the onset of formation of the crystalline YAG phase, and a series of steaming experiments were devised to remove the halide before this process could occur. It was found that steaming the precursor fibre from 200 to 500°C over 3 h, followed by firing to the required temperature in air, removed the chlorine and the problems it caused in the formation of the YAG phase without any change in the sintering characteristics or grain size. The steamed fibres were of a strength and quality comparable to fibres drawn from organometallic precursors. Empirical friability measurements showed the strength was maintained after firing to 1550°C, although there was a deterioration in apparent strain to break of the aligned blanket product above 1200°C. Conversely, the creep resistance, measured using the BSR test, improved with increase in temperature. The fibres fired to 1550°C were fully relaxed at temperatures 100-150°C below that of coarser, larger YAG fibres previously reported with a 3 μm grain size and 120 μm diameter. However, when allowance was made for grain size, the difference in creep rates was within the range obtained by extrapolating previous data using lattice diffusion and grain boundary effect models. Fibres fired to 1400°C were much finer grained but only slightly inferior to the 1550°C fibre in terms of creep. The alumina sol used in this work contained a significant level of sodium, and this suggests that the creep rates are effected by grain boundary impurities, especially sodium. A sodium free sol has been procured and further work is recommended to clarify the effect of impurities and improve fibre properties.

The sintering behaviour, mechanical properties and creep resistance of aligned polycrystalline yttrium aluminium garnet (YAG) fibres, produced from an aqueous sol-Gel precursor

Pullar R. C.;
1999-01-01

Abstract

Continuous ceramic fibres are finding applications as reinforcements in ceramic matrix composites, and yttrium aluminium garnet (YAG) is a particularly attractive candidate material on account of its creep resistance at high temperatures. A continuous, aligned, 5·5 μm diameter polycrystalline YAG fibre was manufactured from an aqueous sol-gel precursor which contained chlorine, and compared to a similar nitrate containing YAG precursor fibre we have reported previously. The precursor sol was found to be stable at a higher concentration than the nitrate containing sol, and this resulted in denser gel fibres which demonstrated better sintering at equivalent temperatures, giving a 98·5% sintered YAG fibre at 1550°C with a grain size of only 1 μm. However, on firing in air, the fibres formed fully crystalline YAG between 800 and 900°C, a temperature 100°C higher than the fibres containing nitrate, and they were weakened by the presence of many hemispherical faults. It was shown that both of these features were due to the retention of chlorine until the onset of formation of the crystalline YAG phase, and a series of steaming experiments were devised to remove the halide before this process could occur. It was found that steaming the precursor fibre from 200 to 500°C over 3 h, followed by firing to the required temperature in air, removed the chlorine and the problems it caused in the formation of the YAG phase without any change in the sintering characteristics or grain size. The steamed fibres were of a strength and quality comparable to fibres drawn from organometallic precursors. Empirical friability measurements showed the strength was maintained after firing to 1550°C, although there was a deterioration in apparent strain to break of the aligned blanket product above 1200°C. Conversely, the creep resistance, measured using the BSR test, improved with increase in temperature. The fibres fired to 1550°C were fully relaxed at temperatures 100-150°C below that of coarser, larger YAG fibres previously reported with a 3 μm grain size and 120 μm diameter. However, when allowance was made for grain size, the difference in creep rates was within the range obtained by extrapolating previous data using lattice diffusion and grain boundary effect models. Fibres fired to 1400°C were much finer grained but only slightly inferior to the 1550°C fibre in terms of creep. The alumina sol used in this work contained a significant level of sodium, and this suggests that the creep rates are effected by grain boundary impurities, especially sodium. A sodium free sol has been procured and further work is recommended to clarify the effect of impurities and improve fibre properties.
File in questo prodotto:
File Dimensione Formato  
19JECS1747.pdf

non disponibili

Tipologia: Versione dell'editore
Licenza: Accesso chiuso-personale
Dimensione 558.82 kB
Formato Adobe PDF
558.82 kB Adobe PDF   Visualizza/Apri

I documenti in ARCA sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10278/3740275
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 58
  • ???jsp.display-item.citation.isi??? 56
social impact