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Contents

   



(Top)
 


1 Preparation  





2 Reactions  





3 Structure  





4 Uses  





5 References  














Manganese(II,III) oxide






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Manganese(II,III) oxide
Names
IUPAC name

manganese(II) dimanganese(III) oxide

Other names

Manganese tetroxide; Manganese oxide, Manganomanganic oxide, Trimanganese tetraoxide, Trimanganese tetroxide[1]

Identifiers

CAS Number

3D model (JSmol)

ECHA InfoCard 100.013.879 Edit this at Wikidata

PubChem CID

RTECS number
  • OP0895000
UNII

CompTox Dashboard (EPA)

  • InChI=1S/3Mn.4O

    Key: GVNFAUMGUISVJW-UHFFFAOYSA-N

  • [Mn]=O.O=[Mn]O[Mn]=O

Properties

Chemical formula

Mn3O4

MnO·Mn2O3

Molar mass 228.812 g/mol
Appearance brownish-black powder[1]
Density 4.86 g/cm3
Melting point 1,567 °C (2,853 °F; 1,840 K)
Boiling point 2,847 °C (5,157 °F; 3,120 K)

Solubility in water

insoluble
Solubility soluble in HCl

Magnetic susceptibility (χ)

+12,400·10−6cm3/mol
Structure

Crystal structure

Spinel (tetragonal), tI28

Space group

I41/amd, No. 141
Hazards
NIOSH (US health exposure limits):

PEL (Permissible)

C 5 mg/m3[1]

REL (Recommended)

None established[1]

IDLH (Immediate danger)

N.D.[1]
Thermochemistry

Std molar
entropy
(S298)

149 J·mol−1·K−1[2]

Std enthalpy of
formation
fH298)

−1387 kJ·mol−1[2]

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

checkY verify (what is checkY☒N ?)

Infobox references

Manganese(II,III) oxide is the chemical compound with formula Mn3O4. Manganese is present in two oxidation states +2 and +3 and the formula is sometimes written as MnO·Mn2O3. Mn3O4 is found in nature as the mineral hausmannite.

Preparation[edit]

Mn3O4 formed when any manganese oxide is heated in air above 1000 °C.[3] Considerable research has centred on producing nanocrystalline Mn3O4 and various syntheses that involve oxidation of MnII or reduction of MnVI.[4][5][6]

Reactions[edit]

Mn3O4 has been found to act as a catalyst for a range of reactions e.g. the oxidation of methane and carbon monoxide;[7][8] the decomposition of NO,[9] the reduction of nitrobenzene[10] and the catalytic combustion of organic compounds.[11]

Structure[edit]

Mn3O4 has the spinel structure, where the oxide ions are cubic close packed and the MnII occupy tetrahedral sites and the MnIII octahedral sites.[3] The structure is distorted due to the Jahn–Teller effect.[3] At room temperature Mn3O4isparamagnetic, below 41-43 K, it is ferrimagnetic[12] although this has been reported as reducing in nanocrystalline samples to around 39 K.[13]

Uses[edit]

Mn3O4 is sometimes used as a starting material in the production of soft ferrites e.g. manganese zinc ferrite,[14] and lithium manganese oxide, used in lithium batteries.[15]

Manganese tetroxide can also be used as a weighting agent while drilling reservoir sections in oil and gas wells.[citation needed]

References[edit]

  1. ^ a b c d e NIOSH Pocket Guide to Chemical Hazards. "#0381". National Institute for Occupational Safety and Health (NIOSH).
  • ^ a b Zumdahl, Steven S. (2009). Chemical Principles 6th Ed. Houghton Mifflin Company. p. A22. ISBN 978-0-618-94690-7.
  • ^ a b c Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  • ^ Hausmannite Mn3O4 nanorods: synthesis, characterization and magnetic properties Jin Du et al. Nanotechnology, (2006),17 4923-4928, doi:10.1088/0957-4484/17/19/024
  • ^ One-step synthesis of Mn3O4 nanoparticles: Structural and magnetic study Vázquez-Olmos A., Redón R, Rodríguez-Gattorno G., Mata-Zamora M.E., Morales-Leal F, Fernández-Osorio A.L, Saniger J.M. Journal of Colloid and Interface Science, 291, 1, (2005), 175-180 doi:10.1016/j.jcis.2005.05.005
  • ^ Use of Carbonaceous Polysaccharide Microspheres as Templates for Fabricating Metal Oxide Hollow Spheres Xiaoming Sun, Junfeng Liu, Yadong Li, Chemistry - A European Journal,(2005), 12, 7, 2039 – 2047, doi:10.1002/chem.200500660
  • ^ The reduction and oxidation behaviour of manganese oxides Stobhe E.R, de Boer A.D., Geus J.W., Catalysis Today. (1999), 47, 161–167. doi:10.1016/S0920-5861(98)00296-X
  • ^ An in situ XRD investigation of singly and doubly promoted manganese oxide methane coupling catalysts.Moggridge G.D, Rayment T, Lambert R.M. Journal of Catalysis, (1992), 134, 242–252, doi:10.1016/0021-9517(92)90225-7
  • ^ NO Decomposition over Mn2O3 and Mn3O4. Yamashita T, Vannice A., Journal of Catalysis (1996),163, 158–168, doi:10.1006/jcat.1996.0315
  • ^ Selective reduction of nitrobenzene to nitrosobenzene over different kinds of trimanganese tetroxide catalysts.Wang W.M., Yang Y.N., Zhang J.Y., Applied Catalysis A. (1995), 133, 1, 81–93 doi:10.1016/0926-860X(95)00186-7
  • ^ Catalytic combustion of C3 hydrocarbons and oxygenates over Mn3O4. Baldi M, Finocchio E, Milella F, Busca G., Applied Catalysis B. (1998), 16, 1, 43–51, doi:10.1016/S0926-3373(97)00061-1
  • ^ Magnetic Structure of Mn3O4 by Neutron Diffraction Boucher B., Buhl R., Perrin M., J. Appl. Phys. 42, 1615 (1971); doi:10.1063/1.1660364
  • ^ Synthesis of superparamagnetic Mn3O4 nanocrystallites by ultrasonic irradiation I.K. Gopalakrishnan, N. Bagkar, R. Ganguly and S.K. Kulshreshtha Journal of Crystal Growth 280, 3-4, (2005), 436-441, doi:10.1016/j.jcrysgro.2005.03.060
  • ^ Method of making manganese-zinc ferrite U.S Patent number: 4093688 (1978) Arthur Withop, Roger Emil Travagli
  • ^ Process for preparing lithium manganese oxides, U.S Patent number: 6706443,(2004), Horst Krampitz, Gerhard Wohner

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Manganese(II,III)_oxide&oldid=1228203366"

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