完整後設資料紀錄
DC 欄位語言
dc.contributor.authorLin, Chien-Chengen_US
dc.contributor.authorChang, Yao-Wenen_US
dc.contributor.authorLin, Kun-Linen_US
dc.contributor.authorLin, Kun-Fungen_US
dc.date.accessioned2014-12-08T15:11:12Z-
dc.date.available2014-12-08T15:11:12Z-
dc.date.issued2008-07-01en_US
dc.identifier.issn0002-7820en_US
dc.identifier.urihttp://dx.doi.org/10.1111/j.1551-2916.2008.02428.xen_US
dc.identifier.urihttp://hdl.handle.net/11536/8589-
dc.description.abstractVarious Y(2)O(3)/ZrO(2) samples were fabricated by hot pressing, whereby Y(2)O(3) was mutually dissolved or reacted with ZrO(2) as a solid solution or Zr(3)Y(4)O(12). Hot-pressed samples were allowed to react with Ti melt at 1700 degrees C for 10 min in argon. Microstructural characterization was conducted using X-ray diffraction and analytical electron microscopy. The Y(2)O(3)/ZrO(2) samples became more stable with increasing Y(2)O(3) because Y(2)O(3) was hardly reacted and dissolved with Ti melt. The incorporation of more than 30 vol% Y(2)O(3) could effectively suppress the reactions in the Ti side, where only a very small amount of alpha-Ti and beta'-Ti was found. When ZrO(2) was dissolved into Ti on the zirconia side near the original interfaces, Y(2)O(3) reprecipitated in the samples containing 30%-70 vol% Y(2)O(3), because the solubility of Y(2)O(3) in Ti was very low. In the region far from the original interface, alpha-Zr, Y(2)O(3), and/or residual Zr(3)Y(4)O(12) were found in the samples containing more than 50 vol% Y(2)O(3) and the amount of alpha-Zr decreased with increasing Y(2)O(3).en_US
dc.language.isoen_USen_US
dc.titleEffect of yttria on interfacial reactions between titanium melt and hot-pressed yttria/zirconia composites at 1700 degrees Cen_US
dc.typeArticleen_US
dc.identifier.doi10.1111/j.1551-2916.2008.02428.xen_US
dc.identifier.journalJOURNAL OF THE AMERICAN CERAMIC SOCIETYen_US
dc.citation.volume91en_US
dc.citation.issue7en_US
dc.citation.spage2321en_US
dc.citation.epage2327en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000257709100038-
dc.citation.woscount5-
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