Synthesis of sinteractive single-phase microstructure yttrium disilicate precursor powder using hydrothermal processing
This paper is the first report of the synthesis of a sinteractive single-phase microstructure yttrium disilicate precursor powder using hydrothermal processing. The effect of the pH of the precursor chemicals on the ease of formation of a single-phase material was investigated using x-ray diffractio...
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Published in | Journal of materials research Vol. 13; no. 11; pp. 3135 - 3143 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
New York, USA
Cambridge University Press
01.11.1998
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Online Access | Get full text |
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Summary: | This paper is the first report of the synthesis of a sinteractive single-phase microstructure yttrium disilicate precursor powder using hydrothermal processing. The effect of the pH of the precursor chemicals on the ease of formation of a single-phase material was investigated using x-ray diffraction, TEM, and SEM. Under very acidic conditions (pH 1), the formation of yttrium chloride, in addition to the yttrium disilicate precursors, produced a powder that absorbed moisture, did not sinter well, and produced a two-phase interpenetrating microstructure after sintering. At pH 6, yttrium chloride no longer formed, but the interpenetrating network persisted after sintering. Only under basic conditions (pH 10) did single-phase yttrium disilicate form after sintering. This work is noteworthy because the calcination time of 1 h required for the formation of this ceramic at 1050 °C is over an order of magnitude lower than the calcination times of over 100 h required when calcined in the temperature range 900 °C to 1150 °C, as reported previously by other workers. |
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Bibliography: | istex:5258C120876E8EBBA5F1F8488DCC0537F69A3824 Currently at Unilever Research, Colworth House, Sharnbrook, Bedford MK44 ILQ, United Kingdom. ark:/67375/6GQ-LDQ9WT0N-5 ArticleID:04660 PII:S0884291400046604 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0884-2914 2044-5326 |
DOI: | 10.1557/JMR.1998.0426 |