Zr1−xYbxWMoO8−x/2 (x = 0, 0.04) ceramics fabricated by in situ synthesis from trigonal polymorph: preparation, sintering process, and negative thermal expansion properties

In this study, negative thermal expansion (NTE) Zr 1− x Yb x WMoO 8− x /2 ( x  = 0, 0.04) ceramics were fabricated by in situ synthesis from trigonal polymorphous precursors for the first time. Phase transition was studied by means of powder X-ray diffraction. Study on the sintering process of Zr 1−...

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Published inJournal of materials science Vol. 47; no. 23; pp. 8061 - 8066
Main Authors Zhao, Ruiqi, Chen, Xi, Ma, Hui, Wang, Xishu, Zhao, Xinhua
Format Journal Article
LanguageEnglish
Published Boston Springer US 01.12.2012
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Summary:In this study, negative thermal expansion (NTE) Zr 1− x Yb x WMoO 8− x /2 ( x  = 0, 0.04) ceramics were fabricated by in situ synthesis from trigonal polymorphous precursors for the first time. Phase transition was studied by means of powder X-ray diffraction. Study on the sintering process of Zr 1− x Yb x WMoO 8− x /2 ( x  = 0, 0.04) ceramics was performed by calcining a series of precursor pellets at 950, 980, and 1000 °C for different times, varying from 1 min to 1 h. The results indicate that the sintering process can be mainly divided into three stages: phase transition from trigonal precursors to cubic Zr 1− x Yb x WMoO 8− x /2 ( c -Zr 1− x Yb x WMoO 8− x /2 , 0–5 min), densification of c -Zr 1− x Yb x WMoO 8− x /2 (6–30 min), and the final sintering stage with little densification (>30 min). Densification reaches almost the maximum in the duration of ~30 min at assigned temperature. Temperature has little influence on densification of ZrWMoO 8 , but improves that of Zr 0.96 Yb 0.04 WMoO 7.98 evidently. In addition, densification of ZrWMoO 8 can be promoted markedly by introduction of Yb 3+ .
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
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content type line 23
ISSN:0022-2461
1573-4803
DOI:10.1007/s10853-012-6698-2