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cerium magnesium

中文名称
——
中文别名
——
英文名称
cerium magnesium
英文别名
——
cerium magnesium化学式
CAS
——
化学式
CeMg
mdl
——
分子量
164.425
InChiKey
WZVKOPWAFSEFRX-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -0.92
  • 重原子数:
    2.0
  • 可旋转键数:
    0.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0.0
  • 氢给体数:
    0.0
  • 氢受体数:
    0.0

反应信息

  • 作为反应物:
    描述:
    cerium magnesium氢气 以 neat (no solvent) 为溶剂, 生成 cerium trihydride
    参考文献:
    名称:
    Kost, M. E.; Kuznetsov, N. T.; Shilov, A. L., Doklady Chemistry, 1987, vol. 292 - 297, p. 32 - 34
    摘要:
    DOI:
  • 作为产物:
    描述:
    氢化铈 (CeH3)magnesium 以 melt 为溶剂, 生成 cerium magnesium
    参考文献:
    名称:
    氮化镁化学
    摘要:
    摘要 已经在 RE-Mg-N(RE=La、Ce、Gd)系统中进行了实验,以探索使用 Mg 作为反应熔体合成氮化物的可能性,并扩展已知的含 Mg 氮化物化合物的数量。由于这些实验仅产生二元氮化物,我们探索了混合 Na/Mg 熔体的使用,并发现了四元氮化物 BaMg 3.33 Nb 0.67 N 4 ( 1 )、BaMg 3.33 Ta 0.67 N 4 ( 2 ) 和 Eu 4 TaMgN 5 ( 3 ) ,通过单晶结构分析表征。BaMg 3.33 M 0.67 N 4 化合物与 UCr 4 C 4 同型 [RK Behrens, W. Jeitschko, Monatsh. 化学 118 (1987) 43–50](填充的 MoNi 4 型 [D. Harker, J. Chem. Phys. 12 (1944) 315–317])并在空间群 I 4/ m (#87) 中结晶,具有晶格参数
    DOI:
    10.1016/s0925-8388(00)01413-4
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文献信息

  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: Mg: MVol.A2, 39, page 302 - 305
    作者:
    DOI:——
    日期:——
  • TEM study of real precipitation behavior of an Mg–0.5at%Ce age-hardened alloy
    作者:Kaichi Saito、Hiroshi Kaneki
    DOI:10.1016/j.jallcom.2013.05.131
    日期:2013.10
    Precipitates formed in an Mg-0.5at%Ce alloy during age-hardening at certain temperatures ranging between 180 degrees C and 250 degrees C have been thoroughly investigated by a combined technique of TEM and HAADF-STEM. The precipitation sequence can be presented as Mg-solid solution -> GP-zone -> beta(1) (Mg-3-Ce; BiF3-type) -> beta (Mg12Ce; Mn12Th-type). At an early stage of aging (180 degrees C for 2 h), fine precipitates of planar GP-zone with an ordered structure appear in parallel to (100)(m) planes of the Mg-matrix, having a thickness of sub-nm and an extension of 5-15 nm. With an advance of aging, the GP-zones increasingly grow larger and combine with the neighbors. When the GP-zones have reached as large as approximately 20 nm in diameter, the age-hardening effect is maximized (180 degrees C for 70 h). After the top-aging, the GP-zones begin to decompose and disappear, and instead precipitates of two other phases, i.e. the beta(1)- and the beta-phase come into sight in the matrix with definite crystallographic orientation relations of [0 0 1](m)// [1 1 0](beta 1)//[1 0 0](beta) and (1 1 0)(m)//(1 1 1)(beta 1)//(0 1 0)(beta), finally completing the aging effect with full of coarse beta-precipitates. (c) 2013 Elsevier B.V. All rights reserved.
  • Oxidation resistance of B2 rare earth–magnesium intermetallic compounds
    作者:B. Stumphy、Y. Mudryk、A. Russell、D. Herman、K. Gschneidner
    DOI:10.1016/j.jallcom.2007.06.067
    日期:2008.7
    The oxidation behaviors of YMg and CeMg were rneasured in flowing air using the thermal gravimetric analysis technique. Negligible oxidation is observed at room temperature in both compounds. At elevated temperatures, the rare earth metals oxidize preferentially, while the underlying materials transform into Mg-rich intermetallics before the Mg oxidizes to MgO. The oxidation resistance of YMg is several orders of magnitude greater than that of CeMg. The oxidation of YMg follows parabolic kinetics with an activation energy of 104 kJ/mol while that of CeMg obeys a linear law with an activation energy of 136 kJ/mol. (C) 2007 Elsevier B.V. All rights reserved.
  • Vogel, R., Zeitschrift fur anorganische Chemie, <hi>1915</hi>, vol. 91, p. 277 - 277
    作者:Vogel, R.
    DOI:——
    日期:——
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