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trisodium orthophosphate

中文名称
——
中文别名
——
英文名称
trisodium orthophosphate
英文别名
trisodium orthophosphate Na3PO4, α;Sodium;phosphate
trisodium orthophosphate化学式
CAS
——
化学式
3Na*O4P
mdl
——
分子量
163.941
InChiKey
AJPJDKMHJJGVTQ-UHFFFAOYSA-K
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):
    -5.82
  • 重原子数:
    6
  • 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:
    86.2
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    gallium phosphatetrisodium orthophosphate 以 neat (no solvent, solid phase) 为溶剂, 生成
    参考文献:
    名称:
    Zimina; Slivko; Smirnova, Russian Journal of Inorganic Chemistry, 2003, vol. 48, # 3, p. 401 - 402
    摘要:
    DOI:
  • 作为产物:
    描述:
    sodium phosphate monobasic monohydrate 以 neat (no solvent, solid phase) 为溶剂, 生成 trisodium orthophosphate
    参考文献:
    名称:
    New Complex Phosphate Cation-Conducting Materials in Ternary System Li3PO4-Na3PO4-InPO4
    摘要:
    Phase equilibrium in ternary system Li3PO4-Na3PO4-InPO4 and formation of heterovalent Zr-substituted solid solutions (up to 15 mol%) for In3+ in Li3In2(PO4)(3) and Na3In2(PO4)(3) complex phosphates were studied by the cross-section method at 950 degrees C. Samples obtained were investigated by X-ray powder diffraction and impedance spectroscopy. Ionic conductivity of Na3In2(PO4)(3) and Li3In2(PO4)(3) complex phosphates is about 10(-2) S/cm at 300 degrees C. Heterovalent substitution was performed according to the scheme: In3+ = Zr4+ + v, where v is a vacancy in cationic sublattice. Zr-substituted (15 mol%) Na3In2(PO4)(3) and Li3In2(PO4)(3) have ionic conductivity of about 10(-1) S/cm at 300 degrees C.
    DOI:
    10.1111/j.1551-2916.2011.04454.x
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文献信息

  • Contribution a l'etude de la conductivite ionique de l'orthophosphate Na3PO4
    作者:Jean-François Brice、Brahim Majidi、Henri Kessler
    DOI:10.1016/0025-5408(82)90140-4
    日期:1982.2
    concerned with the ionic conductivity of pure trisodium orthophosphate Na3PO4, devoid of any trace of hydroxide NaOH. At the allotropic transition (330°C), we observe a jump of the ionic conductivity and a slight decrease in the activation energy (ΔE = 0,70 ± 0,02 eV for the quadratic variety and ΔE = 0,60 ± 0,04 eV for cubic γ-Na3PO4). Na3PO4 can be considered to be an electrolytic solid with medium conductivity
    摘要 目前的工作涉及纯正磷酸 Na3PO4 的离子电导率,不含任何痕量的氢氧化钠。在同素异形转变 (330°C) 时,我们观察到离子电导率的跳跃和活化能的轻微下降(二次变体的 ΔE = 0,70 ± 0,02 eV 和 ΔE = 0,60 ± 0, 04 eV(立方 γ-Na3PO4)。Na3PO4 可以被认为是一种具有中等电导率的电解固体(σ = 1.10 -4 Ω -1 cm -1 在 370°C 下)。
  • Spectroscopic characterization of pure and cation-stabilized sodium phosphate
    作者:R. S. Cole、Roger Frech
    DOI:10.1063/1.480971
    日期:2000.3
    was conducted of pure Na3PO4 and solid solutions of Na3PO4 doped with Mg2+ and Zn2+. Na3PO4 has two solid phases: a low-temperature tetragonal phase and a high-temperature cubic phase. A factor group analysis of the two phases yielded the expected number of modes and their symmetry-based assignments. A temperature-dependent Raman spectroscopic study was then performed for the pure compound. Analysis
    对纯Na3PO4和掺杂Mg2+和Zn2+的Na3PO4固溶体进行了系统研究。Na3PO4 有两个固相:低温四方相和高温立方相。两个阶段的因子组分析产生了预期的模式数量及其基于对称性的分配。然后对纯化合物进行温度依赖性拉曼光谱研究。掺杂 Na3PO4 的分析还提供了对立方结构中存在的局部结构变形的另一种描述。
  • Wiench, D. M.; Jansen, M., Zeitschrift fur Anorganische und Allgemeine Chemie
    作者:Wiench, D. M.、Jansen, M.
    DOI:——
    日期:——
  • Investigation of the basis of catalytic activity of solid state phosphate complexes in the Knoevenagel condensation
    作者:Jamal Bennazha、Mohamed Zahouilly、Ali Boukhari、Elizabeth M Holt
    DOI:10.1016/s1381-1169(03)00208-5
    日期:2003.8
    The Knoevenagel condensation of benzaldehyde and ethyl cyanoacetate in ethanol at ambient temperature was catalyzed with range of mono-, meta- and diphosphate complexes. Comparison of the results shows that the catalytic activity of those phosphates is related to the electropositivity of the cation present in the structure and to the availability of the phosphate moiety to serve as a base. (C) 2003 Elsevier Science B.V. All rights reserved.
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