Aluminium molybdate

Last updated
Aluminium molybdate
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.035.607 OOjs UI icon edit-ltr-progressive.svg
PubChem CID
  • InChI=1S/2Al.3Mo.12O/q2*+3;;;;;;;;;;6*-1 Yes check.svgY
    Key: NKSYNYABFPVRNP-UHFFFAOYSA-N Yes check.svgY
  • InChI=1/2Al.3Mo.12O/q2*+3;;;;;;;;;;6*-1/r2Al.3MoO4/c;;3*2-1(3,4)5/q2*+3;3*-2
    Key: NKSYNYABFPVRNP-WODKIKDAAY
  • [Al+3].[Al+3].[O-][Mo](=O)(=O)[O-].[O-][Mo]([O-])(=O)=O.[O-][Mo]([O-])(=O)=O
Properties
Al2(MoO4)3
Molar mass 533.77 g mol−1
Appearancegrey, metallic solid/powder
odorless
Melting point 705 °C (1,301 °F; 978 K)
slightly soluble in water
Structure [1]
P21/a, No. 14
a = 15.3803(9) Å, b = 9.0443(1) Å, c = 17.888(1) Å
α = 90°, β = 125.382(3)°, γ = 90°
Hazards
NFPA 704 (fire diamond)
NFPA 704.svgHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability (red): no hazard codeInstability (yellow): no hazard codeSpecial hazards (white): no code
1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X mark.svgN  verify  (what is  Yes check.svgYX mark.svgN ?)

Aluminium molybdate is the chemical compound Al2(MoO4)3. It forms in certain hydrodesulfurization catalysts when alumina is doped with excess molybdenum. [2] When molybdates are used to inhibit corrosion in aluminum piping, the protective film formed is hydrated aluminum molybdate. [3] [4] Although small quantities of aluminum molybdate form during aluminothermic reduction of molybdia, mechanical activation inhibits their formation. [5]

Large-scale samples can be prepared via sol-gel synthesis, [6] and have been proposed for molybdenum-99 storage in nuclear medicine. [7]

The room temperature crystal structure was refined using time-of-flight powder neutron diffraction data. It is monoclinic and isostructural with Fe2(MoO4)3 and Cr2(MoO4)3. [1] At high temperatures, the crystal rearranges to βAl2(MoO4)3, isostructural with scandium tungstate. [8]

Aluminum molybdate has a very low thermal expansion coefficient near room temperature.

Related Research Articles

<span class="mw-page-title-main">Molybdenum</span> Chemical element, symbol Mo and atomic number 42

Molybdenum is a chemical element; it has symbol Mo and atomic number 42. The name derived from Ancient Greek Μόλυβδος molybdos, meaning lead, since its ores were confused with lead ores. Molybdenum minerals have been known throughout history, but the element was discovered in 1778 by Carl Wilhelm Scheele. The metal was first isolated in 1781 by Peter Jacob Hjelm.

<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.

<span class="mw-page-title-main">Wulfenite</span> Molybdate mineral

Wulfenite is a lead molybdate mineral with the formula PbMoO4. It can be most often found as thin tabular crystals with a bright orange-red to yellow-orange color, sometimes brown, although the color can be highly variable. In its yellow form it is sometimes called "yellow lead ore".

<span class="mw-page-title-main">Pitting corrosion</span> Form of insidious localized corrosion in which a pit develops at the anode site

Pitting corrosion, or pitting, is a form of extremely localized corrosion that leads to the random creation of small holes in metal. The driving power for pitting corrosion is the depassivation of a small area, which becomes anodic while an unknown but potentially vast area becomes cathodic, leading to very localized galvanic corrosion. The corrosion penetrates the mass of the metal, with a limited diffusion of ions.

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">Chromate conversion coating</span> Chemical treatment of metals

Chromate conversion coating or alodine coating is a type of conversion coating used to passivate steel, aluminium, zinc, cadmium, copper, silver, titanium, magnesium, and tin alloys. The coating serves as a corrosion inhibitor, as a primer to improve the adherence of paints and adhesives, as a decorative finish, or to preserve electrical conductivity. It also provides some resistance to abrasion and light chemical attack on soft metals.

Silver molybdate (Ag2MoO4), a chemical compound, is a yellow, cubic crystalline substance often used in glass. Its crystals present two types of electronic structure, depending on the pressure conditions to which the crystal is subjected. At room temperature, Ag2MoO4 exhibits a spinel-type cubic structure, known as β-Ag2MoO4, which is more stable in nature. However, when exposed to high hydrostatic pressure, the tetragonal α-Ag2MoO4 forms as a metastable phase.

A conversion coating is a chemical or electro-chemical treatment applied to manufactured parts that superficially converts the material into a thin adhering coating of an insoluble compound. These coatings are commonly applied to protect the part against corrosion, to improve the adherence of other coatings, for lubrication, or for aesthetic purposes.

<span class="mw-page-title-main">Lithium aluminate</span> Chemical compound

Lithium aluminate, also called lithium aluminium oxide, is an inorganic chemical compound, an aluminate of lithium. In microelectronics, lithium aluminate is considered as a lattice matching substrate for gallium nitride. In nuclear technology, lithium aluminate is of interest as a solid tritium breeder material, for preparing tritium fuel for nuclear fusion. Lithium aluminate is a layered double hydroxide (LDH) with a crystal structure resembling that of hydrotalcite. Lithium aluminate solubility at high pH is much lower than that of aluminium oxides. In the conditioning of low- and intermediate level radioactive waste (LILW), lithium nitrate is sometimes used as additive to cement to minimise aluminium corrosion at high pH and subsequent hydrogen production. Indeed, upon addition of lithium nitrate to cement, a passive layer of LiH(AlO
2
)
2
· 5 H
2
O
is formed onto the surface of metallic aluminium waste immobilised in mortar. The lithium aluminate layer is insoluble in cement pore water and protects the underlying aluminium oxide covering the metallic aluminium from dissolution at high pH. It is also a pore filler. This hinders the aluminium oxidation by the protons of water and reduces the hydrogen evolution rate by a factor of 10.

Lithium molybdate (Li2MoO4) is a chemical compound. It is mainly used as an inhibitor in some types of industrial air conditioning.

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

Zinc molybdate is an inorganic compound with the formula ZnMoO4. It is used as a white pigment, which that is also a corrosion inhibitor. A related pigment is sodium zinc molybdate, Na2Zn(MoO4)2. The material has also been investigated as an electrode material.

<span class="mw-page-title-main">Schikorr reaction</span> Transformation of Fe(OH)2 into Fe3O4 with hydrogen release

The Schikorr reaction formally describes the conversion of the iron(II) hydroxide (Fe(OH)2) into iron(II,III) oxide (Fe3O4). This transformation reaction was first studied by Gerhard Schikorr. The global reaction follows:

<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.

<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">Lindgrenite</span> Copper molybdate mineral

Lindgrenite is an uncommon copper molybdate mineral with formula: Cu3(MoO4)2(OH)2. It occurs as tabular to platey monoclinic green to yellow green crystals.

Langbeinites are a family of crystalline substances based on the structure of langbeinite with general formula M2M'2(SO4)3, where M is a large univalent cation, and M' is a small divalent cation. The sulfate group, SO2−4, can be substituted by other tetrahedral anions with a double negative charge such as tetrafluoroberyllate, selenate, chromate, molybdate, or tungstates. Although monofluorophosphates are predicted, they have not been described. By redistributing charges other anions with the same shape such as phosphate also form langbeinite structures. In these the M' atom must have a greater charge to balance the extra three negative charges.

Ichnusaite (pronounced iknusa-ait) is a very rarely found mineral. Ichnusaite is a natural compound of thorium and molybdenum with the formula Th(MoO4)2·3H2O. It was discovered in Su Seinargiu, Sarroch, Cagliari, Sardegna, Italy in 2013. The name is from the old Greek name of Sardinia, Ιχνουσσα, Ichnusa.
This locality is also a place of discovery of the second natural thorium molybdate - nuragheite.

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

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.

References

  1. 1 2 Harrison, W. T. A.; Cheetham, A. K.; Faber, J. (1988). "The crystal structure of aluminium molybdate". Journal of Solid State Chemistry. 76 (2): 328–333. Bibcode:1988JSSCh..76..328H. doi:10.1016/0022-4596(88)90226-5.
  2. Medema, J.; van Stam, C.; de Beer, V. H. J.; Konings, A. J. A.; Koningsberger, D. C. (2 May 1977). "Raman spectroscopic study of CoMo/γ-Al2O3 catalysts" (PDF). Journal of Catalysis (published 1978). 53: 386–400. doi:10.1016/0021-9517(78)90110-0 via Eindhoven University of Technology library.
  3. McCune, R. C.; Shilts, R. L.; Ferguson, S. M. (1982-01-01). "A study of film formation on aluminum in aqueous solutions using Rutherford backscattering spectroscopy". Corrosion Science. 22 (11): 1049–1065. doi:10.1016/0010-938X(82)90091-9. ISSN   0010-938X.
  4. Byrne, Christian E.; Quesada Cangahuala, Nereida V.; D'Alessandro, Oriana; Deyá, Cecilia (2023-07-10). "Cerium and aluminum molybdates as inhibitors of the aluminum AA1050 corrosion process in aqueous NaCl solutions". Materials and Corrosion. 75: 73–83. doi:10.1002/maco.202313940. ISSN   0947-5117. S2CID   259872397.
  5. Sheybani, K.; Paydar, M. H.; Shariat, M. H. (2019-08-01). "Effect of mechanical activation on aluminothermic reduction of molybdenum trioxide". International Journal of Refractory Metals and Hard Materials. 82: 245–254. doi:10.1016/j.ijrmhm.2019.04.015. ISSN   0263-4368. S2CID   149603638.
  6. Ari, Monica; Miller, Kimberly J.; Marinkovic, Bojan A.; Jardim, Paula M.; de Avillez, Roberto; Rizzo, Fernando; White, Mary Anne (19 October 2010) [19 November 2010]. "Rapid synthesis of the low thermal expansion phase of Al2Mo3O12 via a sol–gel method using polyvinyl alcohol". Journal of Sol-Gel Science and Technology. Springer (published 2011). 58: 121–125. doi:10.1007/s10971-010-2364-9. S2CID   97549526.
  7. Amin, M.; El-Amir, M. A.; Ramadan, H. E.; El-Said, H. (2018-11-01). "99Mo/99mTc generators based on aluminum molybdate gel matrix prepared by nano method". Journal of Radioanalytical and Nuclear Chemistry. 318 (2): 915–922. doi:10.1007/s10967-018-6141-5. ISSN   1588-2780. S2CID   106317533.
  8. Harrison, William T. A. (1995-11-01). "Crystal structures of paraelastic aluminum molybdate and ferric molybdate, β-Al2(MoO4)3 and β-Fe2(MoO4)3". Materials Research Bulletin. 30 (11): 1325–1331. doi:10.1016/0025-5408(95)00157-3. ISSN   0025-5408.