nickel molybdate

• 分子结构分类: 无机化合物 - 混合金属/非金属化合物 - 过渡金属有机体
• 英文名称: nickel molybdate
• 英文别名: Molybdenum;nickel;tetrahydrate；molybdenum;nickel;tetrahydrate
• 化学式: MoNiO₄
• 分子量: 218.628
• InChiKey: JIOHJKXOGPQOGJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -3.3
• 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：
  4
• 氢给体数：
  4
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  nickel molybdate 以 neat (no solvent) 为溶剂， 生成 nickel molybdate
  参考文献：
  名称：

  Mono-disperse MMoO3·2H2O (M=Mn, Co, Ni) compound nanocrystals: Syntheses, characterization and luminescent properties

  摘要：

  Mono-disperse MMoO(3)(.)2H(2)O (M = Mn, Co, Ni) compound nanocrystals were synthesized by a low-temperature hydrothermal reaction route using (N2H4H2O)-H-. as a reduction reagent as well as a structure-directed reagent. The physical characterizations were carried out by TGA, XRD, XPS, SEM and Photo RE The data of XRD indicate a single phase of monocline symmetry. Nanostructures of MMoO3.2H(2)O (M = Mn, Co, Ni) samples in zero, one or two dimensions were observed from SEM images, respectively. Furthermore, MMoO3-2H(2)O are luminescent, which is different from composite oxides with ordinary structure. (c) 2006 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.jallcom.2006.06.078
• 作为产物：
  描述：

  nickel(II) chloride hexahydrate 、 五氯化钼 在 尿素 作用下， 以 乙醇 为溶剂， 生成 nickel molybdate
  参考文献：
  名称：

  Ni2 Mo3 N上的表面氧化物富集活化层（SOAL），用于快速且持久的放氧反应。

  摘要：

  氧气释放反应（OER）是可再生能源技术的关键，例如水电解和金属空气电池。但是，与质子偶联的电子转移相关的多个步骤会导致OER动力学下降，因此需要催化剂。在这里，我们证明了一种新型的氮化物Ni 2 Mo 3 N是一种高活性的OER催化剂，其性能优于基准材料RuO 2。Ni 2 Mo 3 N在0.1 m的额定超电势为270 mV时 表现出10 mA cm -2的电流密度KOH具有出色的催化循环性和耐久性。结构表征和计算研究表明，出色的活性源自表面富氧化物活化层（SOAL）的形成。表面上的次级Mo原子充当电子泵，稳定含氧物质并促进反应的连续性。这一发现将刺激具有氧化物表面层的三元氮化物作为电化学能量装置的有效OER催化剂的进一步发展。

  DOI：

  10.1002/anie.202008116

文献信息

• Interstitial nitrides revisited – A simple synthesis of M Mo3N (M = Fe, Co, Ni)
  作者：Jack O. Conway、Timothy J. Prior

  DOI：10.1016/j.jallcom.2018.09.307

  日期：2019.2

  Abstract The efficient synthesis of polycrystalline filled beta-Mn structured Ni2Mo3N, and the eta-carbides Fe3Mo3N and Co3Mo3N, by a single heating of metal powders at 975 °C under a hydrogen-nitrogen mixture is reported. Rietveld analysis of high-resolution X-ray powder diffraction data shows that the reduction-nitridation of NiMoO4 produces Ni2Mo3N and nickel; Ni3Mo3N is not obtained in this way

  摘要 报道了通过在 975 °C 下在氢-氮混合物下对金属粉末进行单次加热，有效合成了多晶填充的 β-Mn 结构的 Ni2Mo3N 以及 eta-碳化物 Fe3Mo3N 和 Co3Mo3N。高分辨率 X 射线粉末衍射数据的 Rietveld 分析表明，NiMoO4 的还原氮化生成 Ni2Mo3N 和镍；Ni3Mo3N 不是这样得到的，它的存在被否定了。
• Hybrid-atom-doped NiMoO₄ nanotubes for oxygen evolution reaction
  作者：Zhuoxun Yin、Shu Zhang、Wei Chen、Ma Xinzhi、Yang Zhou、Zhuanfang Zhang、Xin Wang、Jinlong Li

  DOI：10.1039/d0nj02305a

  日期：——

  Doping with hybrid atoms can narrow the band gap of NiMoO₄ nanotubes, improving their performance in the oxygen evolution reaction.

  掺杂混合原子可以缩小NiMoO₄纳米管的带隙，提高其在氧发生反应中的性能。
• Hydrogenation of oxo aldehydes to oxo alcohols in the presence of a nickel-molybdenum catalyst
  申请人：Saleh Yanni Ramzi

  公开号：US20050065384A1

  公开（公告）日：2005-03-24

  A reduced or partially reduced nickel-molybdenum catalyst prepared by a process having the steps of 1) reacting nickel carbonate and molybdenum oxide precursors to form nickel molybdate and 2) treating the nickel molybdate under reducing conditions to form the reduced or partially reduced nickel-molybdenum catalyst. There is also a process for making the catalyst. There is also a process for using the catalyst in the hydrogenation of an oxo aldehyde, thereby forming an oxo alcohol of high selectivity. There is also a process for forming an oxo alcohol from the hydroformylation/hydrogenation of an olefinic feedstream. There is also a process for forming an oxo alcohol by contacting formates, dimers, trimers, and organic acids with hydrogen in the presence of a reduced or partially reduced nickel-molybdenum catalyst. The foregoing processes are also useful with a catalyst having the general formula Y x Z wherein Y is nickel and/or cobalt and Z is molybdenum and/or tungsten; and wherein x ranges between about 0.25 to about 4.0. There are also reduced or partially reduced catalysts of the general formula Ni x Mo or Y x Z wherein x ranges between about 0.25 to about 4.0 and wherein oxide precursors of the catalysts are substantially free of ammonium groups.

  一种经过以下步骤制备的减少或部分减少的镍钼催化剂：1）反应镍碳酸盐和钼氧化物前体形成镍钼酸盐；2）在还原条件下处理镍钼酸盐，形成减少或部分减少的镍钼催化剂。还有一种制备该催化剂的方法。还有一种使用该催化剂在氢化氧化醛反应中，从而形成高选择性的氧化醇的方法。还有一种从烯烃进料的羰基化/氢化反应中形成氧化醇的方法。还有一种通过在减少或部分减少的镍钼催化剂存在下，将甲酸盐、二聚体、三聚体和有机酸与氢气接触，形成氧化醇的方法。上述方法也适用于具有一般式YxZ的催化剂，其中Y是镍和/或钴，Z是钼和/或钨；x在约0.25至约4.0之间变化。还有一般式为NixMo或YxZ的减少或部分减少的催化剂，其中x在约0.25至约4.0之间变化，催化剂的氧化物前体基本上不含铵基。
• Synthesis and structure of ternary molybdenum oxides MMo8O10 (M = Li or Zn) having orthogonal nonintersecting octahedral cluster chains
  作者：Kwang-Hwa Lii、Robert E. McCarley、Sangsoo Kim、Robert A. Jacobson

  DOI：10.1016/0022-4596(86)90078-2

  日期：1986.10

  Single crystal structure determination shows that these compounds are constructed from infinite chains consisting of edge-shared octahedral cluster units. The structure can be viewed as a stacking along the c axis of layers consisting of parallel chains, with the chains in successive layers oriented alternately along the a and b axes. Intra- and interlayer crosslinking of the chains by MoOMo bonds

  新化合物LiMo 8 O 10（I）和ZnMo 8 O 10（II）是通过在密封的Motube中于1370–1450°C下在Li 2 MoO 4，MoO 3和Mo（3:16:29摩尔）之间反应制备的比例分别为ZnO，MoO 3和Mo（摩尔比为1：3：5）。同晶的化合物是四方晶系，空间群我4 1 MD，Ž = 4，用晶格常数一个= 5.8515（6），C ^ = 24.783（3）一种用于予，和一个= 5.8961（4），C ^根据Guinier X射线粉末图案确定的II = 24.840（3）Å 。单晶结构测定表明，这些化合物是由无限的链构成的，该链由边缘共享的八面体簇单元组成。可以将结构视为由平行链组成的层沿c轴的堆叠，连续层中的链沿a和b交替取向轴。通过MoOMo键进行的链内和层间交联在八面体簇亚基的连接式[[Mo2Mo42O62O43）O23]中表示。与包含此类链的类似化合物相比
• Phase equilibria and thermodynamic properties in the system Ni-Mo-O
  作者：K. T. Jacob、G. M. Kale、G. N. K. Iyengar

  DOI：10.1007/bf01132018

  日期：1987.12

  Coexisting phases in the Ni-Mo-O ternary system at 1373 K have been identified by X-ray diffraction, optical microscopy and scanning electron microscopy. The samples were equilibrated in evacuated quartz capsules. Only one ternary phase, NiMoO4, was found to exist in the system. The reversible e.m.f. values of the following solid-state galvanic cells were measured in the temperature range 900 to 1500

  已通过 X 射线衍射、光学显微镜和扫描电子显微镜确定了 1373 K 下 Ni-Mo-O 三元系统中的共存相。样品在真空石英胶囊中平衡。仅发现系统中存在一种三元相 NiMoO4。在 900 到 1500 K 的温度范围内测量了以下固态原电池的可逆电动势值： (I) Pt, Ni + NiO/(CaO) ZrO2/NiO + MoO2 + NiMoO4, Pt；(II) Pt, Mo + /(CaO) ZrO2/O2, Pt；(III) Pt, Mo + /(CaO) ZrO2/Ni-Mo + , Pt。NiMoO4 和 的吉布斯形成能和 Ni-Mo 合金中的活性来自电动势数据。对于反应〈NiO〉+〈 〉+2(02)→〈NiMoO4〉我们得到ΔGr0 = -201 195 + 69.70T (±400) J mol−1；对于〈Mo〉+(02)→〈 〉我们得到ΔGf0