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dicobalt titanide | 12052-50-5

中文名称
——
中文别名
——
英文名称
dicobalt titanide
英文别名
Cobalt;titanium;cobalt;titanium
dicobalt titanide化学式
CAS
12052-50-5
化学式
Co2Ti
mdl
——
分子量
165.866
InChiKey
ILKLNWONSJJVNS-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):
    -0.01
  • 重原子数:
    3
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    cobalt titanidedicobalt titanide 以 neat (no solvent) 为溶剂, 生成
    参考文献:
    名称:
    Amorphization by mechanical alloying: The role of mixtures of intermetallics
    摘要:
    DOI:
    10.1016/0022-5088(88)90369-4
  • 作为产物:
    描述:
    四氢化物钛 以 melt 为溶剂, 生成 dicobalt titanide
    参考文献:
    名称:
    Er-{Fe,Co}-{Ti,V} 系统和 ErFe2−xMx (M=Ti, V, Cr, Mn, Co, Ni, Cu, Mo) 合金的氢化性能
    摘要:
    摘要 已经通过 X 射线分析研究了 Er-{Fe,Co}-{Ti,V} 系统相图的等温截面。Er M 12 - x M ' x (M = Fe, Co; M' = Ti, V) 三元化合物(ThMn 12 结构类型,空间群I 4/ mmm )的存在已被证实,并确定了它们的均质范围。观察到基于ErM 2 的固溶体Er M 2 - x M ' x (MgCu 2 结构类型,空间群Fd -3 m )的形成。已经研究了 ErFe 2- x M x (M = Ti、V、Cr、Mn、Co、Ni、Cu、Mo) 合金的吸氢。
    DOI:
    10.1016/j.jallcom.2007.01.126
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文献信息

  • The Er–{Fe,Co}–{Ti,V} systems and hydrogenation properties of the ErFe2−xMx (M=Ti, V, Cr, Mn, Co, Ni, Cu, Mo) alloys
    作者:B. Kotur、О. Мyakush、I. Zavaliy
    DOI:10.1016/j.jallcom.2007.01.126
    日期:2007.9
    phase diagrams of the Er–Fe,Co}–Ti,V} systems have been investigated by means of X-ray analysis. Existence of the Er M 12 − x M ′ x (M = Fe, Co; M′ = Ti, V) ternary compounds (ThMn 12 structure type, space group I 4/ mmm ) have been confirmed and their homogeneity ranges were determined. Formation of the ErM 2 -based solid solutions Er M 2 − x M ′ x (MgCu 2 structure type, space group Fd -3 m ) was
    摘要 已经通过 X 射线分析研究了 Er-Fe,Co}-Ti,V} 系统相图的等温截面。Er M 12 - x M ' x (M = Fe, Co; M' = Ti, V) 三元化合物(ThMn 12 结构类型,空间群I 4/ mmm )的存在已被证实,并确定了它们的均质范围。观察到基于ErM 2 的固溶体Er M 2 - x M ' x (MgCu 2 结构类型,空间群Fd -3 m )的形成。已经研究了 ErFe 2- x M x (M = Ti、V、Cr、Mn、Co、Ni、Cu、Mo) 合金的吸氢。
  • Svatovskaya, L. B.; Sychev, M. M.; Ryabinina, G. A., Journal of applied chemistry of the USSR, 1981, vol. 54, p. 576 - 580
    作者:Svatovskaya, L. B.、Sychev, M. M.、Ryabinina, G. A.、Korneeva, T. A.
    DOI:——
    日期:——
  • On Friauf-Laves phases in the Zr1−xAlxT2, Zr1−xSixT2 and Zr1−xTixT2 (T ≡ Mn, Fe, Co) systems
    作者:Ž. Blažina、R. Trojko
    DOI:10.1016/0022-5088(87)90238-4
    日期:1987.7
  • Preparation of CoTi intermetallics by self-propagating combustion synthesis
    作者:C.L. Yeh、C.C. Yeh
    DOI:10.1016/j.jallcom.2005.01.013
    日期:2005.6
    The production of B2-type cobalt titanide (CoTi) from elemental powder compacts was conducted by self-propagating high-temperature synthesis (SHS) in this study. Effects of the initial sample density, particle size of the reactants, and initial sample temperature on the combustion characteristics, as well as on the composition of final products were studied. Unlike most of the intermetallic reactions, the combustion of the Co-Ti powder compact is self-sustained upon initiation even without any preheating prior to ignition, implying that the reaction is highly exothermic. The combustion process was preceded by fast propagation of the flame front, followed by vigorous bulk combustion. The flame-front propagation velocity and combustion temperature were found to increase with increasing sample green density and initial sample temperature. The degree of conversion to produce the CoTi phase was enhanced by increasing the sample green density or by preheating the sample prior to ignition. The use of fine particles of Co (2 mu m) in the green compact was also proved to be beneficial in improving the phase conversion, in comparison with the coarse Co powders (-325 mesh). Based upon the measured data of this study, the activation energy with a value of 67.95 kJ/mol was deduced for the synthesis of CoTi by SHS. (c) 2005 Elsevier B.V. All rights reserved.
  • Amorphization by mechanical alloying: The role of mixtures of intermetallics
    作者:P.Y Lee、J Jang、C.C Koch
    DOI:10.1016/0022-5088(88)90369-4
    日期:1988.6
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