邢献然
冶金和材料热力学与网络数据库、新材料制备和稀土材料物理化学以及相图与相结构等方面
个性化签名
- 姓名:邢献然
- 目前身份:
- 担任导师情况:
- 学位:
-
学术头衔:
博士生导师, 优秀教师/优秀教育工作者
- 职称:-
-
学科领域:
材料科学基础学科
- 研究兴趣:冶金和材料热力学与网络数据库、新材料制备和稀土材料物理化学以及相图与相结构等方面
邢献然,北京科技大学教授,博士生导师,物理化学系主任,国家人事部百千万人才工程一、二层次人选、教育部高校青年教师奖获得者,教育部高等学校优秀骨干教师。兼任中国稀土学会理事,稀有金属冶金学术委员会、全国相图委员会、X射线粉末衍射委员会委员,《中国稀土学报》编委等。
一直从事材料物理化学教学科研工作。在冶金和材料热力学与网络数据库、新材料制备和稀土材料物理化学以及相图与相结构等方面,取得若干创新性成果;获省部级科技进步奖3项,发表学术论文50余篇,被SCI或EI收录40篇(次),申请发明专利2项,参加撰写教材2部。
-
主页访问
2081
-
关注数
0
-
成果阅读
354
-
成果数
8
-
55浏览
-
0点赞
-
0收藏
-
0分享
-
154下载
-
0评论
-
引用
【期刊论文】Phase evolution of barium titanate from alkoxide gel-derived precursor
邢献然
,-0001,():
-1年11月30日
-
44浏览
-
0点赞
-
0收藏
-
0分享
-
331下载
-
0评论
-
引用
【期刊论文】Thermal expansion of lattice parameter of (powder) silicon up to 1473 K
邢献然
,-0001,():
-1年11月30日
-
46浏览
-
0点赞
-
0收藏
-
0分享
-
763下载
-
0评论
-
引用
邢献然, Xianran Xing* and Zhenqi Zhu, Xinping Qiu
,-0001,():
-1年11月30日
The main phase ZrV2O7 material, doped with zirconia and vanadium (V) oxide, was synthesized by solid state reaction and sol-gel methods. X-ray power diffraction patterns show that it is cubic structure. Thermal mechanic analysis measurements present a zero-thermal expansion of this material above 150℃. As well the heat capacity dependent on temperature, determined by differential scanning calorimetry, keeps in constant almost in the same temperature range. The relation between unusual thermal expansion and abnormal heat capacity is discussed with quantum mechanics.
ZrV2O7,, zero-thermal expansion,, heat capacity,, Gr
-
28浏览
-
0点赞
-
0收藏
-
0分享
-
514下载
-
0评论
-
引用
【期刊论文】Solid solution Pb1-xSrxTiO3 and its thermal expansion
邢献然, Xianran Xing*, Jun Chen, Jinxia Deng, Guirong Liu
Journal of Alloys and Compounds 360(2003)286-289,-0001,():
-1年11月30日
The solid solution limit of Pb1-xSrxTiO3 was determined in the composition range of 0≤x≤1.0 at room temperature (RT). The phases 12x x 3 were isolated and indexed in a tetragonal system with x<0.5 and in a cubic one with x≥0.5. The cell parameters of Pb1-xSrxTiO3 continuously, but nonlinearly, change with solubility x. The intrinsic thermal expansions of the solid solution compounds Pb1-xSrxTiO3 (x=0, 0.15, 0.20, 0.50, 0.90, 1.0) were obtained in the temperature range from RT to 1173K with high-temperature X-ray powder diffraction. Negative thermal expansion coefficients of Pb Sr TiO (x=0, 0.15, 0.20) were found below the Curie points. The thermal expansions of these titanate ceramics were highly correlated with the solubility in the solid solution Pb1-xSrxTiO3.
Lead strontium titanate, Phase transition, Thermal expansion, X-Ray diffraction
-
32浏览
-
0点赞
-
0收藏
-
0分享
-
155下载
-
0评论
-
引用
【期刊论文】Thermal expansions of ceramics in the system Pb1−x(La1/2K1/2)xTiO3
邢献然, Jun Chen, Xianran Xing*, Jinxia Deng, Guirong Liu
Journal of Alloys and Compounds 372(2004)259-266,-0001,():
-1年11月30日
The solid solution limit of Pb1−x(La1/2K1/2)xTiO3 was determined in the composition range of 0 ≤ x < 1. The compounds of Pb1−x(La1/2K1/2)xTiO3 were indexed in a tetragonal system for 0 ≤ x ≤ 0.4 and indexed in a cubic one for 0.45 ≤ x < 1 at room temperature. A tiny amount of La2Ti2O7 pyrochlore phase was detected in the sample Pb1−x(La1/2K1/2)xTiO3 for x=1.0. The lattice parameters of Pb1−x(La1/2K1/2)xTiO3 (x=0.1, 0.2, 0.3, 0.4, 0.6, 0.8) were determined by high temperature XRD, and their intrinsic thermal expansion coefficients were obtained in the temperature range from room temperature to 900℃. In the temperature range from room temperature to the Curie point, the compound Pb0.8(La1/2K1/2)0.2TiO3 has a low intrinsic thermal expansion coefficient (−7.1×10−6℃−1), which is the value closest to zero in all the investigated compounds. The (ferroelectric) Curie temperatures of Pb1−x(La1/2K1/2)xTiO3 could be predicted from our experimental results for 0≤x≤0.4.
Solid solution Pb1−x(, La1/, 2K1/, 2), xTiO3, Phase transition, High temperature X-ray powder diffractometry (, HTXRPD), , Thermal expansion, Curie temperature
-
70浏览
-
0点赞
-
0收藏
-
0分享
-
65下载
-
0评论
-
引用
【期刊论文】Solid solution Ba1-x PbxTiO3 and its thermal expansion
邢献然, Xianran Xing*, Jinxia Deng, Zhenqi Zhu, Guirong Liu
Journal of Alloys and Compounds 353(2003)1-4,-0001,():
-1年11月30日
The solid solution limit of Ba1-x PbxTiO3 was determined in the composition range of 0≤x≤1.0. All solid solution compounds were indexed in tetragonal symmetry with lead titanate structure type at room temperature. The cell parameters of Ba1-x PbxTiO3 continuously, but nonlinearly, change with x. The structure of Ba1-x PbxTiO3 is tetragonal in the temperature range RT–330℃ and in cubic system beyond 330℃ with HTXRPD. The intrinsic thermal expansion coefficients of Ba1-xPbxTiO3 (x=0, 0.5, 1.0) were obtained. The correlation between thermal expansion and ferroelectric properties is briefly discussed.
Solid solution Ba Pb TiO, Thermal expansion, Phase transition, High temperature X-ray powder diffractometry (, HTXRPD),
-
45浏览
-
0点赞
-
0收藏
-
0分享
-
91下载
-
0评论
-
引用
【期刊论文】Novel thermal expansion of lead titanate
邢献然, XING Xianran, DENG Jinxia, CHEN Jun and LIU Guirong
RARE METALS Vol. 22, No.4, Dec 2003, p. 1,-0001,():
-1年11月30日
Lattice parameters of lead titanate were precisely re-determined in the temperature range of −150-950℃ by high precision XRPD measurements. It was clarified that there was no any evidence for a new phase transition at low temperatures. Tetragonal distortion strain decreases with temperature increasing. A novel thermal expansion was observed, positive thermal expansion from −150℃ to room temperature (RT) and above 490℃, and the negative thermal expansion in the temperature range of RT-490℃. A big jump of thermal expansion coefficient is attributed to the tetragonal-cubic phase transition. A rationalization for the negative thermal expansion of PbTiO3 is due to the decrease of anion-anion repulsion as polyhedra become more regular at heating. The mechanisms of positive and negative thermal expansions were elucidated as the same nature in the homogenous tetragonal phase at present case.
metallurgical physical chemistry, thermal expansion, X-ray powder diffraction (, XRPD), , lead titanate, phase transition.,
-
34浏览
-
0点赞
-
0收藏
-
0分享
-
332下载
-
0评论
-
引用