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 inJournal of materials research Vol. 13; no. 11; pp. 3135 - 3143
Main Authors Trusty, P. A., Chan, K. C., Ponton, C. B.
Format Journal Article
LanguageEnglish
Published New York, USA Cambridge University Press 01.11.1998
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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.
Bibliography:istex:5258C120876E8EBBA5F1F8488DCC0537F69A3824
Currently at Unilever Research, Colworth House, Sharnbrook, Bedford MK44 ILQ, United Kingdom.
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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