完整後設資料紀錄
DC 欄位語言
dc.contributor.authorChen, SYen_US
dc.contributor.authorLee, SYen_US
dc.contributor.authorLin, YJen_US
dc.date.accessioned2014-12-08T15:40:58Z-
dc.date.available2014-12-08T15:40:58Z-
dc.date.issued2003-05-01en_US
dc.identifier.issn0955-2219en_US
dc.identifier.urihttp://dx.doi.org/10.1016/S0955-2219(02)00199-1en_US
dc.identifier.urihttp://hdl.handle.net/11536/27916-
dc.description.abstractOxide powders of Bi2O3, ZnO and Nb2O5 were used to investigate the phase transformation, reaction kinetics and microwave properties of both Bi-2(Zn1/3Nb2/3)(2)O-7 and (Bi1.5Zn0.5)(Zn0.5Nb1.5)O-7 phases in the Bi2O3-ZnO-Nb2O5 system. Kinetic studies indicate that the formation mechanism of Bi-2(Zn1/3Nb2/3)(2)O-7 phase belongs to diffusion controlled reaction with a zero nucleation rate. In contrast, (Bi1.5Zn0.5)(Zn0.5Nb1.5)O-7 phase was interpreted as diffusion controlled reaction with a constant nucleation rate with either Bi5Nb3O15 or BiNbO4 phases as the nuclei. Furthermore, a lower activation energy and formation temperature were observed in the (Bi1.5Zn0.5)(Zn0.5Nb1.5)O-7 than Bi-2(Zn1/3Nb2/3)(2)O-7 phase. Additionally, the (Bi1.5Zn0.5)(Zn0.5Nb1.5)O-7 phase exhibits a higher dielectric constant but a lower Q value as compared with Bi-2(Zn1/3Nb2/3)(2)O-7 phase. (C) 2002 Elsevier Science Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectBi2O3-ZnO-Nb2O5en_US
dc.subjectmicrowave characteristicsen_US
dc.subjectphase transformationen_US
dc.subjectreaction kineticsen_US
dc.titlePhase transformation, reaction kinetics and microwave characteristics of Bi2O3-ZnO-Nb2O5 ceramicsen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/S0955-2219(02)00199-1en_US
dc.identifier.journalJOURNAL OF THE EUROPEAN CERAMIC SOCIETYen_US
dc.citation.volume23en_US
dc.citation.issue6en_US
dc.citation.spage873en_US
dc.citation.epage881en_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:000181227500008-
dc.citation.woscount16-
顯示於類別:期刊論文


文件中的檔案:

  1. 000181227500008.pdf

若為 zip 檔案,請下載檔案解壓縮後,用瀏覽器開啟資料夾中的 index.html 瀏覽全文。