Jump to content

Magnesium oxide

From Wikipedia, the free encyclopedia
(Redirected from ATCvet code QA06AD02)

Magnesium oxide
Names
IUPAC name
Magnesium oxide
Other names
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.013.793 Edit this at Wikidata
EC Number
  • 215-171-9
E number E530 (acidity regulators, ...)
KEGG
RTECS number
  • OM3850000
UNII
  • InChI=1S/Mg.O
    Key: CPLXHLVBOLITMK-UHFFFAOYSA-N
  • O=[Mg]
Properties
MgO
Molar mass 40.304 g/mol[1]
Appearance White powder
Odor Odorless
Density 3.6 g/cm3[1]
Melting point 2,852 °C (5,166 °F; 3,125 K)[1]
Boiling point 3,600 °C (6,510 °F; 3,870 K)[1]
Solubility Soluble in acid, ammonia
insoluble in alcohol
Electrical resistivity Dielectric[a]
Band gap 7.8 eV[2]
−10.2·10−6 cm3/mol[3]
Thermal conductivity 45–60 W·m−1·K−1[4]
1.7355
6.2 ± 0.6 D
Structure
Halite (cubic), cF8
Fm3m, No. 225
a = 4.212Å
Octahedral (Mg2+); octahedral (O2−)
Thermochemistry
37.2 J/mol K[8]
26.95 ± 0.15 J·mol−1·K−1[9]
−601.6 ± 0.3 kJ·mol−1[9]
-569.3 kJ/mol[8]
Pharmacology
A02AA02 (WHO) A06AD02 (WHO), A12CC10 (WHO)
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
 Metal fume fever, Irritant
GHS labelling:
GHS07: Exclamation mark
Warning
H315, H319, H335
P261, P264, P271, P273, P280, P302+P352, P304+P340, P305+P351+P338, P312, P333+P313, P337+P313, P362, P363, P391, P403+P233, P405
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
0
0
Flash point Non-flammable
NIOSH (US health exposure limits):
PEL (Permissible)
 TWA 15 mg/m3 (fume)[10]
REL (Recommended)
 None designated[10]
IDLH (Immediate danger)
 750 mg/m3 (fume)[10]
Safety data sheet (SDS) ICSC 0504
Related compounds
Other anions
 Magnesium sulfide
Magnesium selenide
Other cations
 Beryllium oxide
Calcium oxide
Strontium oxide
Barium oxide
Related compounds
 Magnesium hydroxide
Magnesium nitride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Magnesium oxide (MgO), or magnesia, is a white hygroscopic solid mineral that occurs naturally as periclase and is a source of magnesium (see also oxide). It has an empirical formula of MgO and consists of a lattice of Mg2+ ions and O2− ions held together by ionic bonding. Magnesium hydroxide forms in the presence of water (MgO + H2O → Mg(OH)2), but it can be reversed by heating it to remove moisture.

Magnesium oxide was historically known as magnesia alba (literally, the white mineral from Magnesia), to differentiate it from magnesia nigra, a black mineral containing what is now known as manganese.

[edit]

While "magnesium oxide" normally refers to MgO, the compound magnesium peroxide MgO2 is also known. According to evolutionary crystal structure prediction,[11] MgO2 is thermodynamically stable at pressures above 116 GPa (gigapascals), and a semiconducting suboxide Mg3O2 is thermodynamically stable above 500 GPa. Because of its stability, MgO is used as a model system for investigating vibrational properties of crystals.[12]

Electric properties

[edit]

Pure MgO is not conductive and has a high resistance to electric current at room temperature. The pure powder of MgO has a relative permittivity inbetween 3.2 to 9.9 with an approximate dielectric loss of tan(δ) > 2.16x103 at 1kHz.[5][6][7]

Production

[edit]

Magnesium oxide is produced by the calcination of magnesium carbonate or magnesium hydroxide. The latter is obtained by the treatment of magnesium chloride MgCl
2 solutions, typically seawater, with limewater or milk of lime.[13]

Mg2+ + Ca(OH)2 → Mg(OH)2 + Ca2+

Calcining at different temperatures produces magnesium oxide of different reactivity. High temperatures 1500 – 2000 °C diminish the available surface area and produces dead-burned (often called dead burnt) magnesia, an unreactive form used as a refractory. Calcining temperatures 1000 – 1500 °C produce hard-burned magnesia, which has limited reactivity and calcining at lower temperature, (700–1000 °C) produces light-burned magnesia, a reactive form, also known as caustic calcined magnesia. Although some decomposition of the carbonate to oxide occurs at temperatures below 700 °C, the resulting materials appear to reabsorb carbon dioxide from the air.[citation needed]

Applications

[edit]

Refractory insulator

[edit]

MgO is prized as a refractory material, i.e. a solid that is physically and chemically stable at high temperatures. It has the useful attributes of high thermal conductivity and low electrical conductivity. According to a 2006 reference book:[14]

By far the largest consumer of magnesia worldwide is the refractory industry, which consumed about 56% of the magnesia in the United States in 2004, the remaining 44% being used in agricultural, chemical, construction, environmental, and other industrial applications.

MgO is used as a refractory material for crucibles. It is also used as an insulator in heat-resistant electrical cable.

Biomedical

[edit]

Among metal oxide nanoparticles, magnesium oxide nanoparticles (MgO NPs) have distinct physicochemical and biological properties, including biocompatibility, biodegradability, high bioactivity, significant antibacterial properties, and good mechanical properties, which make it a good choice as a reinforcement in composites. [15]

Heating elements

[edit]

It is used extensively as an electrical insulator in tubular construction heating elements as in electric stove and cooktop heating elements. There are several mesh sizes available and most commonly used ones are 40 and 80 mesh per the American Foundry Society. The extensive use is due to its high dielectric strength and average thermal conductivity. MgO is usually crushed and compacted with minimal airgaps or voids.

Cement

[edit]

MgO is one of the components in Portland cement in dry process plants.

Sorel cement uses MgO as the main component in combination with MgCl2 and water.

Fertilizer

[edit]

MgO has an important place as a commercial plant fertilizer[16] and as animal feed.[17]

Fireproofing

[edit]

It is a principal fireproofing ingredient in construction materials. As a construction material, magnesium oxide wallboards have several attractive characteristics: fire resistance, termite resistance, moisture resistance, mold and mildew resistance, and strength, but also a severe downside as it attracts moisture and can cause moisture damage to surrounding materials.[18][14][1]

Medical

[edit]

Magnesium oxide is used for relief of heartburn and indigestion, as an antacid, magnesium supplement, and as a short-term laxative. It is also used to improve symptoms of indigestion. Side effects of magnesium oxide may include nausea and cramping.[19] In quantities sufficient to obtain a laxative effect, side effects of long-term use may rarely cause enteroliths to form, resulting in bowel obstruction.[20]

Waste treatment

[edit]

Magnesium oxide is used extensively in the soil and groundwater remediation, wastewater treatment, drinking water treatment, air emissions treatment, and waste treatment industries for its acid buffering capacity and related effectiveness in stabilizing dissolved heavy metal species.[according to whom?]

Many heavy metals species, such as lead and cadmium, are least soluble in water at mildly basic conditions (pH in the range 8–11). Solubility of metals increases their undesired bioavailability and mobility in soil and groundwater. Granular MgO is often blended into metals-contaminating soil or waste material, which is also commonly of a low pH (acidic), in order to drive the pH into the 8–10 range. Metal-hydroxide complexes tend to precipitate out of aqueous solution in the pH range of 8–10.

MgO is packed in bags around transuranic waste in the disposal cells (panels) at the Waste Isolation Pilot Plant, as a CO2 getter to minimize the complexation of uranium and other actinides by carbonate ions and so to limit the solubility of radionuclides. The use of MgO is preferred over CaO since the resulting hydration product (Mg(OH)
2) is less soluble and releases less hydration heat. Another advantage is to impose a lower pH value (about 10.5) in case of accidental water ingress into the dry salt layers, in contast to the more soluble Ca(OH)
2 which would create a higher pH of 12.5 (strongly alkaline conditions). The Mg2+
 cation being the second most abundant cation in seawater and in rocksalt, the potential release of magnesium ions dissolving in brines intruding the deep geological repository is also expected to minimize the geochemical disruption.[21]

Niche uses

[edit]
Unpolished MgO crystal
  • As a food additive, it is used as an anticaking agent. It is known to the US Food and Drug Administration for cacao products; canned peas; and frozen dessert.[22] It has an E number of E530.
  • As a reagent in the installation of the carboxybenzyl (Cbz) group using benzyl chloroformate in EtOAc for the N-protection of amines and amides.[23]
  • Doping MgO (about 1–5% by weight) into hydroxyapatite, a bioceramic mineral, increases the fracture toughness by migrating to grain boundaries, where it reduces grain size and changes the fracture mode from intergranular to transgranular.[24][25]
  • Pressed MgO is used as an optical material. It is transparent from 0.3 to 7 μm. The refractive index is 1.72 at 1 μm and the Abbe number is 53.58. It is sometimes known by the Eastman Kodak trademarked name Irtran-5, although this designation is obsolete. Crystalline pure MgO is available commercially and has a small use in infrared optics.[26]
  • An aerosolized solution of MgO is used in library science and collections management for the deacidification of at-risk paper items. In this process, the alkalinity of MgO (and similar compounds) neutralizes the relatively high acidity characteristic of low-quality paper, thus slowing the rate of deterioration.[27]
  • Magnesium oxide is used as an oxide barrier in spin-tunneling devices. Owing to the crystalline structure of its thin films, which can be deposited by magnetron sputtering, for example, it shows characteristics superior to those of the commonly used amorphous Al2O3. In particular, spin polarization of about 85% has been achieved with MgO[28] versus 40–60 % with aluminium oxide.[29] The value of tunnel magnetoresistance is also significantly higher for MgO (600% at room temperature and 1,100 % at 4.2 K[30]) than Al2O3 (ca. 70% at room temperature[31]).
  • MgO is a common pressure transmitting medium used in high pressure apparatuses like the multi-anvil press.[32]

Brake lining

[edit]

Magnesia is used in brake linings for its heat conductivity and intermediate hardness.[33] It helps dissipate heat from friction surfaces, preventing overheating, while minimizing wear on metal components.[34] Its stability under high temperatures ensures reliable and durable braking performance in automotive and industrial applications.[35]

Thin film transistors

[edit]

In thin film transistors(TFTs), MgO is often used as a dielectric material or an insulator due to its high thermal stability, excellent insulating properties, and wide bandgap.[36] Optimized IGZO/MgO TFTs demonstrated an electron mobility of 1.63 cm²/Vs, an on/off current ratio of 10⁶, and a subthreshold swing of 0.50 V/decade at −0.11 V.[37] These TFTs are integral to low-power applications, wearable devices, and radiation-hardened electronics, contributing to enhanced efficiency and durability across diverse domains.[38][39]

Historical uses

[edit]

Precautions

[edit]

Inhalation of magnesium oxide fumes can cause metal fume fever.[41]

See also

[edit]

Notes

[edit]
  1. ^ At room temperature.[5][6][7]

References

[edit]
  1. ^ a b c d Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). Boca Raton, FL: CRC Press. p. 4.74. ISBN 1-4398-5511-0.
  2. ^ Taurian, O.E.; Springborg, M.; Christensen, N.E. (1985). "Self-consistent electronic structures of MgO and SrO" (PDF). Solid State Communications. 55 (4): 351–5. Bibcode:1985SSCom..55..351T. doi:10.1016/0038-1098(85)90622-2. Archived from the original (PDF) on 2016-03-03. Retrieved 2012-03-27.
  3. ^ Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). Boca Raton, FL: CRC Press. p. 4.133. ISBN 1-4398-5511-0.
  4. ^ Application of magnesium compounds to insulating heat-conductive fillers Archived 2013-12-30 at the Wayback Machine. konoshima.co.jp
  5. ^ a b A P, Johnson (November 1986). Structural and electrical properties of magnesium oxide powders (Masters). Durham University.
  6. ^ a b Subramanian, M. A.; Shannon, R. D.; Chai, B. H. T.; Abraham, M. M.; Wintersgill, M. C. (November 1989). "Dielectric constants of BeO, MgO, and CaO using the two-terminal method". Physics and Chemistry of Minerals. 16 (8): 741–746. Bibcode:1989PCM....16..741S. doi:10.1007/BF00209695. ISSN 0342-1791. S2CID 95280958.
  7. ^ a b Hornak, Jaroslav; Trnka, Pavel; Kadlec, Petr; Michal, Ondřej; Mentlík, Václav; Šutta, Pavol; Csányi, Gergely; Tamus, Zoltán (2018-05-30). "Magnesium Oxide Nanoparticles: Dielectric Properties, Surface Functionalization and Improvement of Epoxy-Based Composites Insulating Properties". Nanomaterials. 8 (6): 381. doi:10.3390/nano8060381. ISSN 2079-4991. PMC 6027305. PMID 29848967.
  8. ^ a b Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). Boca Raton, FL: CRC Press. p. 5.15. ISBN 1-4398-5511-0.
  9. ^ a b Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). Boca Raton, FL: CRC Press. p. 5.2. ISBN 1-4398-5511-0.
  10. ^ a b c NIOSH Pocket Guide to Chemical Hazards. "#0374". National Institute for Occupational Safety and Health (NIOSH).
  11. ^ Zhu, Qiang; Oganov A.R.; Lyakhov A.O. (2013). "Novel stable compounds in the Mg-O system under high pressure" (PDF). Phys. Chem. Chem. Phys. 15 (20): 7696–7700. Bibcode:2013PCCP...15.7696Z. doi:10.1039/c3cp50678a. PMID 23595296. Archived from the original (PDF) on 2013-12-03. Retrieved 2013-11-06.
  12. ^ Mei, AB; O. Hellman; C. M. Schlepütz; A. Rockett; T.-C. Chiang; L. Hultman; I. Petrov; J. E. Greene (2015). "Reflection Thermal Diffuse X-Ray Scattering for Quantitative Determination of Phonon Dispersion Relations". Physical Review B. 92 (17): 174301. Bibcode:2015PhRvB..92q4301M. doi:10.1103/physrevb.92.174301.
  13. ^ Margarete Seeger; Walter Otto; Wilhelm Flick; Friedrich Bickelhaupt; Otto S. Akkerman. "Magnesium Compounds". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a15_595.pub2. ISBN 978-3527306732.
  14. ^ a b Mark A. Shand (2006). The chemistry and technology of magnesia. John Wiley and Sons. ISBN 978-0-471-65603-6. Retrieved 10 September 2011.
  15. ^ Saberi A, Baltatu MS, Vizureanu P (May 2024). "Recent Advances in Magnesium-Magnesium Oxide Nanoparticle Composites for Biomedical Applications". Bioengineering. 11 (5): 508. doi:10.3390/bioengineering11050508. PMC 11117911. PMID 38790374.
  16. ^ Nutrient Science. fertilizer101.org. Retrieved on 2017-04-26.
  17. ^ Magnesium oxide for the Animal Feed Industry. lehvoss.de
  18. ^ Mármol, Gonzalo; Savastano, Holmer (July 2017). "Study of the degradation of non-conventional MgO-SiO 2 cement reinforced with lignocellulosic fibers". Cement and Concrete Composites. 80: 258–267. doi:10.1016/j.cemconcomp.2017.03.015.
  19. ^ Magnesium Oxide. MedlinePlus. Last reviewed 02/01/2009
  20. ^ Tatekawa Y, Nakatani K, Ishii H, et al. (1996). "Small bowel obstruction caused by a medication bezoar: report of a case". Surgery Today. 26 (1): 68–70. doi:10.1007/BF00311997. PMID 8680127. S2CID 24976010.
  21. ^ wipp.energy.gov Step-By-Step Guide for Waste Handling at WIPP. Waste Isolation Pilot Plant. wipp.energy.gov
  22. ^ "Compound Summary for CID 14792 – Magnesium Oxide". PubChem.
  23. ^ Dymicky, M. (1989-02-01). "Preparation of Carbobenzoxy-L-Tyrosine Methyl and Ethyl Esters and of the Corresponding Carbobenzoxy Hydrazides". Organic Preparations and Procedures International. 21 (1): 83–90. doi:10.1080/00304948909356350. ISSN 0030-4948.
  24. ^ Tan, C.Y.; Yaghoubi, A.; Ramesh, S.; Adzila, S.; Purbolaksono, J.; Hassan, M.A.; Kutty, M.G. (December 2013). "Sintering and mechanical properties of MgO-doped nanocrystalline hydroxyapatite" (PDF). Ceramics International. 39 (8): 8979–8983. doi:10.1016/j.ceramint.2013.04.098. Archived from the original (PDF) on 2017-03-12. Retrieved 2015-08-08.
  25. ^ Tan, Chou Yong; Singh, Ramesh; Tolouei, R.; Sopyan, Iis; Teng, Wan Dung (2011). "Synthesis of High Fracture Toughness of Hydroxyapatite Bioceramics". Advanced Materials Research. 264–265: 1849–1855. doi:10.4028/www.scientific.net/amr.264-265.1849. ISSN 1662-8985. S2CID 137578750.
  26. ^ Stephens, Robert E. & Malitson, Irving H. (1952). "Index of Refraction of Magnesium Oxide". Journal of Research of the National Bureau of Standards. 49 (4): 249–252. doi:10.6028/jres.049.025.
  27. ^ "Mass Deacidification: Saving the Written Word". Library of Congress. Retrieved 26 September 2011.
  28. ^ Parkin, S. S. P.; Kaiser, C.; Panchula, A.; Rice, P. M.; Hughes, B.; Samant, M.; Yang, S. H. (2004). "Giant tunnelling magnetoresistance at room temperature with MgO (100) tunnel barriers". Nature Materials. 3 (12): 862–867. Bibcode:2004NatMa...3..862P. doi:10.1038/nmat1256. PMID 15516928. S2CID 33709206.
  29. ^ Monsma, D. J.; Parkin, S. S. P. (2000). "Spin polarization of tunneling current from ferromagnet/Al2O3 interfaces using copper-doped aluminum superconducting films". Applied Physics Letters. 77 (5): 720. Bibcode:2000ApPhL..77..720M. doi:10.1063/1.127097.
  30. ^ Ikeda, S.; Hayakawa, J.; Ashizawa, Y.; Lee, Y. M.; Miura, K.; Hasegawa, H.; Tsunoda, M.; Matsukura, F.; Ohno, H. (2008). "Tunnel magnetoresistance of 604% at 300 K by suppression of Ta diffusion in CoFeB/MgO/CoFeB pseudo-spin-valves annealed at high temperature". Applied Physics Letters. 93 (8): 082508. Bibcode:2008ApPhL..93h2508I. doi:10.1063/1.2976435. S2CID 122271110.
  31. ^ Wang, D.; Nordman, C.; Daughton, J. M.; Qian, Z.; Fink, J. (2004). "70% TMR at Room Temperature for SDT Sandwich Junctions with CoFeB as Free and Reference Layers". IEEE Transactions on Magnetics. 40 (4): 2269. Bibcode:2004ITM....40.2269W. CiteSeerX 10.1.1.476.8544. doi:10.1109/TMAG.2004.830219. S2CID 20439632.
  32. ^ Wang, Haikuo; He, Duanwei; Yan, Xiaozhi; Xu, Chao; Guan, Junwei; Tan, Ning; Wang, Wendan (December 2011). "Quantitative measurements of pressure gradients for the pyrophyllite and magnesium oxide pressure-transmitting mediums to 8 GPa in a large-volume cubic cell". High Pressure Research. 31 (4): 581–591. doi:10.1080/08957959.2011.614238. ISSN 0895-7959.
  33. ^ "Magnesium Oxide Ceramic Materials - An Overview". Advanced Ceramic Materials. Aug 8, 2024. Retrieved Sep 15, 2024.
  34. ^ CN patent 105087849A 
  35. ^ WO patent 2020122684A1 
  36. ^ Green, Julissa (Apr 24, 2024). "Magnesium Oxide Target in Thin-Film Transistors Production". Sputter Targets. Stanford Advanced Materials. Retrieved Oct 30, 2024.
  37. ^ Su, Zhan; Zhang, Xiao (2024). "Effect of substrate temperature on growth mechanism and properties of PEALD-MgO dielectric films for amorphous-IGZO TFTs". Surface and Coatings Technology. 483: 130819. doi:10.1016/j.surfcoat.2024.130819.
  38. ^ Yu, Fangzhou; Hong, Wen (2021). "MgZnO-Based Negative Capacitance Transparent Thin-Film Transistor Built on Glass". IEE Journal of the Electron Devices Society. 9: 798–803. doi:10.1109/JEDS.2021.3108904.
  39. ^ Zhao, Cheng; Li, Jun (2017). "Mg Doping to Simultaneously Improve the Electrical Performance and Stability of MgInO Thin-Film Transistors". IEEE Transactions on Electron Devices. 64 (5): 2216–2220. doi:10.1109/TED.2017.2678544.
  40. ^ Tellex, Peter A.; Waldron, Jack R. (1955). "Reflectance of Magnesium Oxide". JOSA. 45 (1): 19. Bibcode:1955JOSA...45...19T. doi:10.1364/JOSA.45.000019.
  41. ^ Magnesium Oxide. National Pollutant Inventory, Government of Australia.
[edit]
Retrieved from "https://en.wikipedia.org/w/index.php?title=Magnesium_oxide&oldid=1254205739"