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偏磷酸锂 | 13762-75-9

中文名称
偏磷酸锂
中文别名
偏磷酸锶
英文名称
lithium metaphosphate
英文别名
——
偏磷酸锂化学式
CAS
13762-75-9
化学式
LiO3P
mdl
——
分子量
85.913
InChiKey
MRVHOJHOBHYHQL-UHFFFAOYSA-M
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

物化性质

  • 熔点:
    656℃ [AES93]
  • 密度:
    2.46 g/mL at 25 °C(lit.)
  • 溶解度:
    不溶于水

计算性质

  • 辛醇/水分配系数(LogP):
    -3.56
  • 重原子数:
    5
  • 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:
    57.2
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 危险品标志:
    Xn
  • 安全说明:
    S26,S36
  • 危险类别码:
    R22,R36/37/38
  • 储存条件:
    存放于惰性气体中,并避免接触湿气(吸湿)。

SDS

SDS:d7dd3991635b3ef5f2a65289a39d982d
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制备方法与用途

用途:用作絮凝剂和分析试剂。

反应信息

  • 作为反应物:
    描述:
    偏磷酸锂 在 NH4Cl 作用下, 以 not given 为溶剂, 生成
    参考文献:
    名称:
    Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: NH4: MVol.2, 8.16, page 467 - 475
    摘要:
    DOI:
  • 作为产物:
    参考文献:
    名称:
    VOLKOV, B. G.;NIKITIN, V. G.;FEDOTOV, V. V.;STOLYAROVA, L. N.
    摘要:
    DOI:
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文献信息

  • Crystal structures and electronic properties for the over-lithiated and Li–Ag substituted phases of Li9V3(P2O7)3(PO4)2 insertion electrode system
    作者:Masashige Onoda、Makoto Inagaki、Hiroaki Saito
    DOI:10.1016/j.jssc.2014.07.040
    日期:2014.11
    For the Li9V3(P2O7)3(PO4)2 insertion electrode system with a multiple-electron reaction, the over-lithiated phase LixV3(P2O7)3(PO4)2 with 9
    对于具有多电子反应的Li 9 V 3(P 2 O 7)3(PO 4)2插入电极系统,过锂化相Li x V 3(P 2 O 7)3(PO 4)2具有9
  • Synthesis, crystal structure and lithium ion conduction of Li<sub>3</sub>BP<sub>2</sub>O<sub>8</sub>
    作者:Toru Hasegawa、Hisanori Yamane
    DOI:10.1039/c3dt52917g
    日期:——
    group P (no. 2)). In the crystal structure of Li3BP2O8, BO4 and PO4 tetrahedra share O atoms and form one-dimensional 1∞[BP2O8]3− chains along the c-axis direction. A polycrystalline Li3BP2O8 bulk sample was synthesized by the solid state reaction of Li4P2O7 and LiPO3 prepared from the starting materials in advance with H3BO3 at 923 K. The lithium ion conductivities measured for the polycrystalline sample
    李的单晶3 BP 2 ö 8通过加热起始材料的混合物制备的锂:11::B:22 P摩尔比在13 933 K的空气,并通过在-10ķh的速率冷却- 1。用三斜晶胞参数对单晶的X射线衍射(XRD)反射进行索引:a = 5.1888(5)Å,b = 7.4118(7)Å,c = 7.6735(7)Å,α = 101.18(1) °,β = 105.07(1)°,γ = 90.34(1)°(空间群P(编号2))。在Li 3 BP 2 O 8,BO 4的晶体结构中和PO 4四面体共享O原子和形式的一维1 ∞ [BP 2 ö 8 ] 3-沿着链Ç轴方向。通过预先由原料制备的Li 4 P 2 O 7和LiPO 3与H 3 BO 3在923 K下进行固相反应,合成了多晶Li 3 BP 2 O 8块状样品。交流阻抗和直流方法测得的多晶样品为1.5×10 -5 S cm-1在583 K和6.0×10 -8小号厘米-1在423
  • Effects of LiPON Incorporation on the Structures and Properties of Mixed Oxy-Sulfide-Nitride Glassy Solid Electrolytes
    作者:Victor Torres、Steve W. Martin
    DOI:10.1021/acs.inorgchem.3c00756
    日期:2023.5.29
    determine the Tg and Tc values of these glasses. Fourier transformation-infrared, Raman, and magic angle spinning nuclear magnetic resonance spectroscopies were used to examine the short-range order structures of these materials. X-ray photoelectron spectroscopy was conducted on the glasses to further understand the bonding environments of the doped nitrogen. Finally, N and S elemental analyses were used to
    玻璃态固体电解质 (GSE) 是全固态电池开发中很有前途的固体电解质。混合氧硫化物氮化物 (MOSN) GSE 结合了硫化物玻璃的高离子电导率、氧化物玻璃的优异化学稳定性以及氮化物玻璃的电化学稳定性。然而,关于这些新型含氮电解质的合成和表征的报道非常有限。因此,在玻璃合成过程中系统地加入 LiPON 用于探索氮和氧添加对MOSN GSE 的玻璃化转变 ( Tg )和结晶温度 ( Tc )原子级结构的影响。MOSN GSE系列 58.3Li 2 S + 31.7SiS 2+ 10[(1 – x )Li 0.67 PO 2.83 + x LiPO 2.53 N 0.314 ], x = 0.0, 0.06, 0.12, 0.2, 0.27, 0.36,通过熔融淬火合成制备。使用差示扫描量热法测定Tg和Tc这些眼镜的价值。傅里叶变换红外、拉曼和魔角旋转核磁共振波谱法用于检查这些材料的短程有序结构。对玻璃进行了
  • Phase relation of Li2O–CoO–P2O5 ternary system and electrochemical behaviors of Co-base polyphosphates within this system
    作者:Xinghao Lin、Yanming Zhao、Zhiyong Liang、Danlin Yan、Xudong Liu、Mingming Wen、Youzhong Dong、Quan Kuang
    DOI:10.1016/j.jallcom.2015.06.179
    日期:2015.10
    The subsolidus phase relations in the Li2O-CoO-P2O5 system have been systematically investigated by means of X-ray diffraction (XRD) pattern. The results have confirmed 6 binary compounds, 5 ternary compounds and 17 three-phase regions. In this system, the solid-state synthesized process (under Ar/H-2 atmosphere) of LiCoPO4 using the Li2CO3, Co3O4 and NH4H2PO4 as raw materials has been investigated. The result indicates that the single-phase LiCoPO4 compound can be formed stably within the temperature range between 350 degrees C and 700 degrees C, while several intermediate or decomposition compounds have been detected outside this sintering temperature range. The electrochemical properties of these purephase LiCoPO4 powders obtained at different temperature are compared by galvanostatic charge/discharge mode and at the meantime, we also demonstrated for the first time that Li6Co5(P2O7)(4) electrode is electrochemically active. (C) 2015 Elsevier B.V. All rights reserved.
  • Bagieu-Beucher, M.; Masse, R., Zeitschrift fur Kristallographie
    作者:Bagieu-Beucher, M.、Masse, R.
    DOI:——
    日期:——
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