Magnesium sulfide

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Magnesium sulfide
Magnesium-sulfide-3D-ionic.png
Names
Other names
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.031.597 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 234-771-1
PubChem CID
UNII
  • InChI=1S/Mg.S/q+2;-2 X mark.svgN
    Key: QENHCSSJTJWZAL-UHFFFAOYSA-N X mark.svgN
  • InChI=1/Mg.S/q+2;-2
    Key: QENHCSSJTJWZAL-UHFFFAOYAO
  • [Mg+2].[S-2]
Properties
MgS
Molar mass 56.38 g/mol
Appearancewhite to reddish brown powder
Density 2.84 g/cm3
Melting point 2,000 °C (3,630 °F; 2,270 K) approx.
decomposes
Structure
Halite (cubic), cF8
Fm3m, No. 225
cubic
Thermochemistry
45.6 J/mol K
Std molar
entropy
(S298)
50.3 J/mol K
-347 kJ/mol
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Source of H2S
Related compounds
Other anions
Magnesium oxide
Other cations
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Magnesium sulfide is an inorganic compound with the formula Mg S. It is a white crystalline material but often is encountered in an impure form that is brown and non-crystalline powder. It is generated industrially in the production of metallic iron.

Contents

Preparation and general properties

MgS is formed by the reaction of sulfur or hydrogen sulfide with magnesium. It crystallizes in the rock salt structure as its most stable phase, its zinc blende [1] and wurtzite [2] structures can be prepared by molecular beam epitaxy. The chemical properties of MgS resemble those of related ionic sulfides such as those of sodium, barium, or calcium. It reacts with oxygen to form the corresponding sulfate, magnesium sulfate. MgS reacts with water to give hydrogen sulfide and magnesium hydroxide. [3]

Applications

In the BOS steelmaking process, sulfur is the first element to be removed. Sulfur is removed from the impure blast furnace iron by the addition of several hundred kilograms of magnesium powder by a lance. Magnesium sulfide is formed, which then floats on the molten iron and is removed. [4]

MgS is a wide band-gap direct semiconductor of interest as a blue-green emitter, a property that has been known since the early 1900s. [5] The wide-band gap property also allows the use of MgS as photo-detector for short wavelength ultraviolet light. [6]

Occurrence

Aside from being a component of some slags, MgS is a rare nonterrestrial mineral niningerite detected in some meteorites. It is also a solid solution component along with CaS and FeS in oldhamite. MgS is also found in the circumstellar envelopes of certain evolved carbon stars, i. e., those with C/O > 1. [7]

Safety

MgS evolves hydrogen sulfide upon contact with moisture.

Related Research Articles

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Sulfur (also spelled sulphur in British English) is a chemical element; it has symbol S and atomic number 16. It is abundant, multivalent and nonmetallic. Under normal conditions, sulfur atoms form cyclic octatomic molecules with the chemical formula S8. Elemental sulfur is a bright yellow, crystalline solid at room temperature.

<span class="mw-page-title-main">Sphalerite</span> Zinc-iron sulfide mineral

Sphalerite is a sulfide mineral with the chemical formula (Zn, Fe)S. It is the most important ore of zinc. Sphalerite is found in a variety of deposit types, but it is primarily in sedimentary exhalative, Mississippi-Valley type, and volcanogenic massive sulfide deposits. It is found in association with galena, chalcopyrite, pyrite, calcite, dolomite, quartz, rhodochrosite, and fluorite.

Sulfide (also sulphide in British English ) is an inorganic anion of sulfur with the chemical formula S2− or a compound containing one or more S2− ions. Solutions of sulfide salts are corrosive. Sulfide also refers to large families of inorganic and organic compounds, e.g. lead sulfide and dimethyl sulfide. Hydrogen sulfide (H2S) and bisulfide (SH) are the conjugate acids of sulfide.

<span class="mw-page-title-main">Epitaxy</span> Crystal growth process relative to the substrate

Epitaxy refers to a type of crystal growth or material deposition in which new crystalline layers are formed with one or more well-defined orientations with respect to the crystalline seed layer. The deposited crystalline film is called an epitaxial film or epitaxial layer. The relative orientation(s) of the epitaxial layer to the seed layer is defined in terms of the orientation of the crystal lattice of each material. For most epitaxial growths, the new layer is usually crystalline and each crystallographic domain of the overlayer must have a well-defined orientation relative to the substrate crystal structure. Epitaxy can involve single-crystal structures, although grain-to-grain epitaxy has been observed in granular films. For most technological applications, single-domain epitaxy, which is the growth of an overlayer crystal with one well-defined orientation with respect to the substrate crystal, is preferred. Epitaxy can also play an important role while growing superlattice structures.

<span class="mw-page-title-main">Zinc oxide</span> White powder insoluble in water

Zinc oxide is an inorganic compound with the formula ZnO. It is a white powder which is insoluble in water. ZnO is used as an additive in numerous materials and products including cosmetics, food supplements, rubbers, plastics, ceramics, glass, cement, lubricants, paints, sunscreens, ointments, adhesives, sealants, pigments, foods, batteries, ferrites, fire retardants, semi conductors, and first-aid tapes. Although it occurs naturally as the mineral zincite, most zinc oxide is produced synthetically.

<span class="mw-page-title-main">Zinc sulfide</span> Inorganic compound

Zinc sulfide is an inorganic compound with the chemical formula of ZnS. This is the main form of zinc found in nature, where it mainly occurs as the mineral sphalerite. Although this mineral is usually black because of various impurities, the pure material is white, and it is widely used as a pigment. In its dense synthetic form, zinc sulfide can be transparent, and it is used as a window for visible optics and infrared optics.

<span class="mw-page-title-main">Cadmium sulfide</span> Chemical compound

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<span class="mw-page-title-main">Sulfur cycle</span> Biogeochemical cycle of sulfur

The important sulfur cycle is a biogeochemical cycle in which the sulfur moves between rocks, waterways and living systems. It is important in geology as it affects many minerals and in life because sulfur is an essential element (CHNOPS), being a constituent of many proteins and cofactors, and sulfur compounds can be used as oxidants or reductants in microbial respiration. The global sulfur cycle involves the transformations of sulfur species through different oxidation states, which play an important role in both geological and biological processes. Steps of the sulfur cycle are:

<span class="mw-page-title-main">Copper monosulfide</span> Chemical compound

Copper monosulfide is a chemical compound of copper and sulfur. It was initially thought to occur in nature as the dark indigo blue mineral covellite. However, it was later shown to be rather a cuprous compound, formula Cu3S(S2). CuS is a moderate conductor of electricity. A black colloidal precipitate of CuS is formed when hydrogen sulfide, H2S, is bubbled through solutions of Cu(II) salts. It is one of a number of binary compounds of copper and sulfur (see copper sulfide for an overview of this subject), and has attracted interest because of its potential uses in catalysis and photovoltaics.

<span class="mw-page-title-main">Sulfur water</span> Water exposed to hydrogen sulfide gas

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<span class="mw-page-title-main">Gallium(III) sulfide</span> Chemical compound

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References

  1. Bradford, C.; O'Donnell, C. B.; Urbaszek, B.; Balocchi, A.; Morhain, C.; Prior, K. A.; Cavenett, B. C. (2000). "Growth of zinc blende MgS/ZnSe single quantum wells by molecular-beam epitaxy using ZnS as a sulphur source". Appl. Phys. Lett. 76 (26): 3929. Bibcode:2000ApPhL..76.3929B. doi:10.1063/1.126824.
  2. Lai, Y. H.; He, Q. L.; Cheung, W. Y.; Lok, S. K.; Wong, K. S.; Ho, S. K.; Tam, K. W.; Sou, I. K. (2013). "Molecular beam epitaxy-grown wurtzite MgS thin films for solar-blind ultra-violet detection". Applied Physics Letters. 102 (17): 171104. Bibcode:2013ApPhL.102q1104L. doi:10.1063/1.4803000.
  3. Holleman, A. F.; Wiberg, E. "Inorganic Chemistry" Academic Press: San Diego, 2001. ISBN   0-12-352651-5.
  4. Irons, G. A.; Guthrie, R. I. L. "Kinetic aspects of magnesium desulfurization of blast furnace iron" Ironmaking and Steelmaking (1981), volume 8, pp.114-21.
  5. Tiede, E. "Reindarstellung von Magnesiumsulfid und seine Phosphorescenz. I (Preparation of pure magnesium sulfide and its phosphorescence. I)" Berichte der Deutschen Chemischen Gesellschaft (1916), volume 49, pages 1745-9.
  6. Hoi Lai, Ying; Cheung, Wai-Yip; Lok, Shu-Kin; Wong, George K.L.; Ho, Sut-Kam; Tam, Kam-Weng; Sou, Iam-Keong (2012). "Rocksalt MgS solar blind ultra-violet detectors". AIP Advances. 2 (1): 012149. Bibcode:2012AIPA....2a2149L. doi: 10.1063/1.3690124 .
  7. Goebel, J. H.; Moseley, S. H. (1985). "MgS Grain Component in Circumstellar Shells". Astrophysical Journal Letters. 290: L35. Bibcode:1985ApJ...290L..35G. doi:10.1086/184437.