Neodymium molybdate

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Neodymium molybdate
2.svg Nd3+.svg 3.svg Molybdat-Ion.svg
Identifiers
Properties
Nd2(MoO4)3
Appearanceblue solid [1]
insoluble[ citation needed ]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Neodymium molybdate is an inorganic compound, with the chemical formula of Nd2(MoO4)3.

Contents

Preparation

It can be prepared by reacting neodymium oxide and molybdenum trioxide at a high temperature: [2]

Nd2O3 + 3MoO3 → Nd2(MoO4)3

It can also be prepared by reacting neodymium nitrate and (NH4)6Mo7O24, treating the obtained precipitate at a high temperature. [1]

Properties

It reacts with sodium molybdate at a high temperature to obtain NaNd(MoO4)2. [3] It reacts at roughly 350°C to 700°C with hydrogen sulfide to obtain neodymium sulfide and molybdenum disulfide. [4] At roughly 780K to 870K, it can be reduced by hydrogen to obtain Nd2Mo3O9. [5]

Related Research Articles

<span class="mw-page-title-main">Molybdenite</span> Molybdenum disulfide mineral

Molybdenite is a mineral of molybdenum disulfide, MoS2. Similar in appearance and feel to graphite, molybdenite has a lubricating effect that is a consequence of its layered structure. The atomic structure consists of a sheet of molybdenum atoms sandwiched between sheets of sulfur atoms. The Mo-S bonds are strong, but the interaction between the sulfur atoms at the top and bottom of separate sandwich-like tri-layers is weak, resulting in easy slippage as well as cleavage planes. Molybdenite crystallizes in the hexagonal crystal system as the common polytype 2H and also in the trigonal system as the 3R polytype.

Neodymium(III) chloride or neodymium trichloride is a chemical compound of neodymium and chlorine with the formula NdCl3. This anhydrous compound is a mauve-colored solid that rapidly absorbs water on exposure to air to form a purple-colored hexahydrate, NdCl3·6H2O. Neodymium(III) chloride is produced from minerals monazite and bastnäsite using a complex multistage extraction process. The chloride has several important applications as an intermediate chemical for production of neodymium metal and neodymium-based lasers and optical fibers. Other applications include a catalyst in organic synthesis and in decomposition of waste water contamination, corrosion protection of aluminium and its alloys, and fluorescent labeling of organic molecules (DNA).

Molybdenum trioxide describes a family of inorganic compounds with the formula MoO3(H2O)n where n = 0, 1, 2. The anhydrous compound is produced on the largest scale of any molybdenum compound since it is the main intermediate produced when molybdenum ores are purified. The anhydrous oxide is a precursor to molybdenum metal, an important alloying agent. It is also an important industrial catalyst. It is a yellow solid, although impure samples can appear blue or green.

<span class="mw-page-title-main">Sodium molybdate</span> Chemical compound

Sodium molybdate, Na2MoO4, is useful as a source of molybdenum. This white, crystalline salt is often encountered as the dihydrate, Na2MoO4·2H2O.

<span class="mw-page-title-main">Ammonium perrhenate</span> Chemical compound

Ammonium perrhenate (APR) is the ammonium salt of perrhenic acid, NH4ReO4. It is the most common form in which rhenium is traded. It is a white salt; soluble in ethanol and water, and mildly soluble in NH4Cl. It was first described soon after the discovery of rhenium.

<span class="mw-page-title-main">Ammonium heptamolybdate</span> Chemical compound

Ammonium heptamolybdate is the inorganic compound whose chemical formula is (NH4)6Mo7O24, normally encountered as the tetrahydrate. A dihydrate is also known. It is a colorless solid, often referred to as ammonium paramolybdate or simply as ammonium molybdate, although "ammonium molybdate" can also refer to ammonium orthomolybdate, (NH4)2MoO4, and several other compounds. It is one of the more common molybdenum compounds.

Aluminium molybdate is the chemical compound Al2(MoO4)3. It forms in certain hydrodesulfurization catalysts when alumina is doped with excess molybdenum. When molybdates are used to inhibit corrosion in aluminum piping, the protective film formed is hydrated aluminum molybdate. Although small quantities of aluminum molybdate form during aluminothermic reduction of molybdia, mechanical activation inhibits their formation.

<span class="mw-page-title-main">Molybdate</span> Chemical compound of the form –O–MoO₂–O–

In chemistry, a molybdate is a compound containing an oxyanion with molybdenum in its highest oxidation state of 6: O−Mo(=O)2−O. Molybdenum can form a very large range of such oxyanions, which can be discrete structures or polymeric extended structures, although the latter are only found in the solid state. The larger oxyanions are members of group of compounds termed polyoxometalates, and because they contain only one type of metal atom are often called isopolymetalates. The discrete molybdenum oxyanions range in size from the simplest MoO2−
4
, found in potassium molybdate up to extremely large structures found in isopoly-molybdenum blues that contain for example 154 Mo atoms. The behaviour of molybdenum is different from the other elements in group 6. Chromium only forms the chromates, CrO2−
4
, Cr
2
O2−
7
, Cr
3
O2−
10
and Cr
4
O2−
13
ions which are all based on tetrahedral chromium. Tungsten is similar to molybdenum and forms many tungstates containing 6 coordinate tungsten.

Ammonium orthomolybdate is the inorganic compound with the chemical formula (NH4)2MoO4. It is a white solid that is prepared by treating molybdenum trioxide with aqueous ammonia. Upon heating these solutions, ammonia is lost, to give ammonium heptamolybdate ((NH4)6Mo7O24·4H2O).

<span class="mw-page-title-main">Manganese(II) molybdate</span> Inorganic compound

Manganese(II) molybdate is an inorganic compound with the chemical formula MnMoO4. α-MnMoO4 has a monoclinic crystal structure. It is also antiferromagnetic at low temperatures.

<span class="mw-page-title-main">Iron(II) molybdate</span> Chemical compound

Iron(II) molybdate is an inorganic compound with the chemical formula FeMoO4.

<span class="mw-page-title-main">Neodymium(III) acetate</span> Compound of neodymium

Neodymium(III) acetate is an inorganic salt composed of a neodymium atom trication and three acetate groups as anions where neodymium exhibits the +3 oxidation state. It has a chemical formula of Nd(CH3COO)3 although it can be informally referred to as NdAc because Ac is an informal symbol for acetate. It commonly occurs as a light purple powder.

<span class="mw-page-title-main">Neodymium compounds</span> Chemical compounds with at least one neodymium atom

Neodymium compounds are compounds formed by the lanthanide metal neodymium (Nd). In these compounds, neodymium generally exhibits the +3 oxidation state, such as NdCl3, Nd2(SO4)3 and Nd(CH3COO)3. Compounds with neodymium in the +2 oxidation state are also known, such as NdCl2 and NdI2. Some neodymium compounds have colors that vary based upon the type of lighting.

<span class="mw-page-title-main">Neodymium tantalate</span> Chemical compound

Neodymium tantalate is an inorganic compound with the chemical formula NdTaO4. It is prepared by reacting neodymium oxide and tantalum pentoxide at 1200 °C. It reacts with a mixture of tantalum pentoxide and chlorine gas at high temperature to obtain Nd2Ta2O7Cl2. It is ammonolyzed at high temperature to obtain oxynitrides of Nd-Ta.

<span class="mw-page-title-main">Neodymium perrhenate</span> Chemical compound

Neodymium perrhenate is an inorganic compound with the chemical formula Nd(ReO4)3, which exists in anhydrous and tetrahydrate. It can be obtained by reacting excess neodymium oxide with 240 g/L perrhenic acid solution. In its solution, NdReO42+ and Nd(ReO4)2+ can be observed with stability constants of 16.5 and 23.6, respectively.

<span class="mw-page-title-main">Praseodymium arsenate</span> Chemical compound

Praseodymium arsenate is the arsenate salt of praseodymium, with the chemical formula of PrAsO4. It has good thermal stability. Its ferroelectric transition temperature is 52°C.

<span class="mw-page-title-main">Europium compounds</span> Compounds with at least one europium atom

Europium compounds are compounds formed by the lanthanide metal europium (Eu). In these compounds, europium generally exhibits the +3 oxidation state, such as EuCl3, Eu(NO3)3 and Eu(CH3COO)3. Compounds with europium in the +2 oxidation state are also known. The +2 ion of europium is the most stable divalent ion of lanthanide metals in aqueous solution. Many europium compounds fluoresce under ultraviolet light due to the excitation of electrons to higher energy levels. Lipophilic europium complexes often feature acetylacetonate-like ligands, e.g., Eufod.

<span class="mw-page-title-main">Terbium compounds</span> Chemical compounds with at least one terbium atom

Terbium compounds are compounds formed by the lanthanide metal terbium (Tb). Terbium generally exhibits the +3 oxidation state in these compounds, such as in TbCl3, Tb(NO3)3 and Tb(CH3COO)3. Compounds with terbium in the +4 oxidation state are also known, such as TbO2 and BaTbF6. Terbium can also form compounds in the 0, +1 and +2 oxidation states.

Samarium(III) molybdate is an inorganic compound, with the chemical formula Sm2(MoO4)3. It is one of the compounds formed by the three elements samarium, molybdenum and oxygen. It can be obtained by reacting samarium nitrate and sodium molybdate in the pH range of 5.5~6.0. Its single crystal can be grown at 1085 °C by the Czochralski method. It can be reduced to the tetravalent molybdenum compound Sm2Mo3O9 by hydrogen at 500~650 °C.

References

  1. 1 2 Q Huang; J Xu; W Li (March 1989). "Preparation of tetragonal defect scheelite-type RE2(MoO4)3 (RE=La TO Ho) by precipitation method". Solid State Ionics. 32–33: 244–249. doi:10.1016/0167-2738(89)90228-2 . Retrieved 2022-07-02.
  2. Rode, E. Ya.; Lysanova, G. V.; Kuznetsov, V. G.; Gokhman, L. Z. Synthesis and physicochemical study of rare earth molybdates. Zhurnal Neorganicheskoi Khimii, 1968. 13 (5): 1295-1302. ISSN   0044-457X.
  3. Mokhosoev, M. V.; Get'man, E. I.; Kokot, I. F. Double sodium-neodymium molybdates. Izvestiya Akademii Nauk SSSR, Neorganicheskie Materialy, 1969. 5 (6): 1107-1112. ISSN   0002-337X.
  4. Yampol'skaya, V. V.; Serebrennikov, V. V. Interaction of rare earth molybdates with hydrogen sulfide at elevated temperatures. Tr. Tomsk. Univ., 1973. 240: 86-89. CAN80: 140751.
  5. Gopalakrishnan, Jagannatha; Manthiram, Araumugam. Topochemically controlled hydrogen reduction of scheelite-related rare earth metal molybdates. Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1981. 3: 668-672.