Preparation and Sintering of Perovskite-Type Compound Powders by the Hydrazine Method
肼法钙钛矿型复合粉体的制备与烧结
基本信息
- 批准号:06650969
- 负责人:
- 金额:$ 1.34万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (C)
- 财政年份:1994
- 资助国家:日本
- 起止时间:1994 至 1996
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Submicron powders consisting of various kinds of perovskite-type compounds (PbZrO_3, LaCrO_3, LaCr_<0.85>Mg_<0.15-x>Co_xO_3 (x=0,0.05,0.10) have been prepared by the hydrazine method. Characterization of powders have been performed using transmission electron microscopy, differential thermal analysis, thermal gravimetry, X-ray diffraction analysis, and BET method. LaCr_<0.85>Mg_<0.15-x>Co_xO_3 powders have been sintered. Electrical and thermal properties of the sintered ceramics have been evaluated.1) PbZrO_3 Metastable ZrO_2 solid solutions containing up to 50 mol% PbO are formed at low temperatures from as-prepared amorphous materials ; the tetragonal phase up to 30 mol% PbO and the cubic phase between 30 and 50 mol% PbO.The compound PbZrO_3 is formed at 615゚ to 690゚C by transformation of c-ZrO_2 solid solution.2) LaCrO<@D23@>D2 Metastable LaCrO<@D24@>D2 crystallizes at (]SYgtoreq[)530゚C from as-prepared materials. The compound LaCrO<@D23@>D2 consisting of submicron powders (0.2mum) … More is formed at 840゚C by transformation of LaCrO<@D24@>D2.3) LaCr<@D20.85@>D2Mg<@D20.15-x@>D2Co<@D2x@>D2O<@D23@>D2 (x=0,0.05,0.10) As the same result as LaCrO<@D23@>D2, metastable LaCrO<@D24@>D2 solid solutions crystallize at low temperatures ((]SYapprxeq[)480゚C) from as-prepared amorphous materials. LaCrO<@D24@>D2 solid solutions transform at(]SYapprxeq[)780゚C into the compounds LaCr<@D20.85@>D2Mg<@D20.15-x@>D2Co<@D2x@>D2O<@D23@>D2 (x=0,0.05,0.10) consisting of submicron powders ((]SYapprxeq[)0.12mum). After being calcined at 1000゚C for 1h, the powders compacted into pellets at 343 MPa have been sintered at 1600゚C for 2h. Well-densified compacts ((]SYapprxeq[) 95% of theoretical) can be obtained, although these compounds show poor sinterability. The LaCr<@D20.85@>D2Mg<@D20.15-x@>D2Co<@D2x@>D2O<@D23@>D2 ceramics obtained show high electric conductivity of (]SYapprxeq[)8.8S・cm<@D1-1@>D1 at 1000゚C ; this value is about ten times higher than that of LaCrO<@D23@>D2 ceramics reported. Thermal expansion coefficients of ceramics alpha are (]SYapprxeq[)11.3-12.0x10<@D1-6@>D1K<@D1-1@>D1 in the temperature range between room temperature and 1000゚C ; the values are the same as c-ZrO<@D22@>D2. These results reveal that the LaCr<@D20.85@>D2Mg<@D20.15-x@>D2Co<@D2x@>D2O<@D23@>D2 ceramics are suitable candidates for electrodes in solid oxide fuel cell (SOFC) composed of c-ZrO<@D22@>D2 as a solid electroloyte. Less
用肼法制备了各种钙钛矿型化合物(PbZrO_3,LaCrO_3,LaCr_<;0.85>;Mg_<;0.15-x>;Co_xO_3(x=0,0.05,0.10))组成的亚微米粉末。用透射电子显微镜、差热分析、热重分析、X射线衍射分析和BET方法对粉末进行了表征。对LaCr0.85>;0.15-x>;CoxO_3粉末进行了烧结。1)非晶态材料在低温下形成PbO含量高达50%的PbO_2亚稳态固溶体,PbO含量在30~50摩尔%PbO之间形成四方相,立方相在30~50摩尔%PbO之间。化合物PbZrO_3是在615゚~690゚C通过c-ZrO_2固溶体转变而形成的。2)Lacro<;@D23@>;D2亚稳态Lacro<;@D24@>;D2在()SYgtoreq[)530゚℃结晶。由(0.2um)…亚微米粉末组成的化合物Lacro<;@D23@&Gt;D2Lacro<;@D24@>;D2.3)LaCr<;@D20.85@>;D2Mg<;@D20.15-x@>;D2Co<;@D2x@>;D2O<;@D23@>;D2(x=0,0.05,0.10)在840゚℃转变形成更多,与Lacro<;@D23@>;D2,亚稳Lacro<;@D24@>;D2固溶体由所制备的非晶态材料在低温(SYapprxeq[)480゚C)下结晶。LaCr<;@D20.85@>;D2Mg<;@D20.15-x@>;D2Co<;@D2x@>;D2O<;@D23@>;D2(x=0,0.05,0.10)由亚微粉(SYapprxeq[)0.12um)组成的化合物゚(x=0,0.05,0.10)。在1000゚C下焙烧1h后,在343 Mpa下压制成球团,然后在1600゚C下烧结2小时。虽然这些化合物的烧结性较差,但可以获得致密性良好的压坯(()SYapprxeq[)理论上的95%)。得到的LaCr<;@D20.85@>;D2Mg<;@D20.15-x@>;D2Co<;@D2x@>;D2O<;@D23@>;D2陶瓷在1000゚℃下表现出()8.8s·cm<;@d1-1@>;d1的高电导率,这一值约为文献报道的Lacro<;@d23@>;d2陶瓷的10倍。α陶瓷的热膨胀系数在室温至1000ZrO℃之间的温度范围内为(]SYapprxeq[)11.3-12.0x10<;@D1-6@>;D1K<;@D1-1@>;D1,其值与c-゚;@D22@&Gt;D2相同。这些结果表明,LaCr<;@D20.85@>;D2Mg<;@D20.15-x@>;D2Co<;@D2x@>;D2O<;@D23@>;D2陶瓷适合作为固体氧化物燃料电池的电极材料,由c-ZrO<;@d22@>;d2组成。较少
项目成果
期刊论文数量(1)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
K. Hirota et al.: "Formation of PbZrO_3 by Transformation of Cubic ZrO_2 Solid Solution" J. Am. Ceram. Soc.78. 3163-3164 (1995)
K. Hirota 等人:“通过立方 ZrO_2 固溶体的转化形成 PbZrO_3”J. Am。
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- 影响因子:0
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HIROTA Ken其他文献
Additive Manufacturing of Ceramics Using a Fused Deposition Modeling (FDM)-Type 3D Printer and Their Microwave Sintering and HIP Treatment
使用熔融沉积成型 (FDM) 型 3D 打印机增材制造陶瓷及其微波烧结和 HIP 处理
- DOI:
10.2497/jjspm.67.431 - 发表时间:
2020 - 期刊:
- 影响因子:0
- 作者:
HIROTA Ken;NAKAMURA Ibuki;WATANABE Kazumasa;TANIGUCHI Tomoki;KATO Masaki;UESUGI Naoki;KIMURA Hideo;NAKATA Akiyuki - 通讯作者:
NAKATA Akiyuki
水酸化ニッケル-糖アルコール複合体ゾルを用いた薄膜の調製とクロミック特性
氢氧化镍-糖醇复合溶胶薄膜的制备及铬性能
- DOI:
- 发表时间:
2021 - 期刊:
- 影响因子:0
- 作者:
NGUYEN Thi Minh Phuong;HIROTA Ken;KATO Masaki;TSUKAGOSHI Kazuhiko;YAMADA Hirohisa;TERABE Atsuki;MIZUTANI Hideto;笹村悠真・小島隆・上川直文 - 通讯作者:
笹村悠真・小島隆・上川直文
Fabrication of High Density Soft Magnetic Fe-3mass%Si/ferrite Composites with a High Saturation Magnetization Density of 1.5 T
制造%20of%20高%20密度%20软%20磁性%20Fe-3mass%Si/铁氧体%20复合材料%20with%20a%20高%20饱和度%20磁化%20密度%20of%201.5%20T
- DOI:
10.2497/jjspm.68.356 - 发表时间:
2021 - 期刊:
- 影响因子:0
- 作者:
YOSHIDA Minori;KATO Masaki;HIROTA Ken - 通讯作者:
HIROTA Ken
Fabrication of Dense ZrO<sub>2</sub>-Al<sub>2</sub>O<sub>3</sub> Ceramics by Pressure-less Sintering Using Neutralization Co-Precipitated Powders with Cellulose Nano-Fiber
中和共沉淀纤维素纳米纤维粉体无压烧结制备致密ZrO<sub>2</sub>-Al<sub>2</sub>O<sub>3</sub>陶瓷
- DOI:
10.2497/jjspm.67.381 - 发表时间:
2020 - 期刊:
- 影响因子:0
- 作者:
YOSHIDA Minori;HIROTA Ken;KATO Masaki;ZINNO Kazuhito;HAYASHI Takayuki;KIMURA Hideo - 通讯作者:
KIMURA Hideo
塩化チタン溶液の2段階透析によるチタン酸化物-カルボン酸複合体の合成とフォトクロミック特性
氯化钛溶液两步渗析合成氧化钛-羧酸络合物及其光致变色性能
- DOI:
- 发表时间:
2022 - 期刊:
- 影响因子:0
- 作者:
HIROTA Ken;NAKAMURA Ibuki;WATANABE Kazumasa;TANIGUCHI Tomoki;KATO Masaki;UESUGI Naoki;KIMURA Hideo;NAKATA Akiyuki;菊地蓮・稲垣優吾・小島隆・上川直文 - 通讯作者:
菊地蓮・稲垣優吾・小島隆・上川直文
HIROTA Ken的其他文献
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{{ truncateString('HIROTA Ken', 18)}}的其他基金
Fabrication of bulk magnetic composite materials consisting of controlled nano-structures
由受控纳米结构组成的块体磁性复合材料的制造
- 批准号:
17360332 - 财政年份:2005
- 资助金额:
$ 1.34万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Fabrication and Evaluation of Composite Magnetic Materials
复合磁性材料的制备与评价
- 批准号:
09450248 - 财政年份:1997
- 资助金额:
$ 1.34万 - 项目类别:
Grant-in-Aid for Scientific Research (B).
Formation and Electric Properties of Lead Magnesium Niobate
铌镁酸铅的形成及电性能
- 批准号:
04680058 - 财政年份:1992
- 资助金额:
$ 1.34万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
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