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Samarium(III) oxide
Names
	IUPAC name samarium(III) oxide
	Other names samarium sesquioxide, samaria
Identifiers
CAS Number	12060-58-1 ;
3D model (JSmol)	Interactive image; Interactive image;
ChemSpider	140199 ;
ECHA InfoCard	100.031.845
EC Number	235-043-6;
PubChem CID	159425;
UNII	91N8739X2N ;
CompTox Dashboard (EPA)	DTXSID30925575 DTXSID4051611, DTXSID30925575 ;
	InChI InChI=1S/3O.2Sm/q3-2;2+3 Key: FKTOIHSPIPYAPE-UHFFFAOYSA-N ;
	SMILES O=[Sm]O[Sm]=O; [Sm+3].[Sm+3].[O-2].[O-2].[O-2];
Properties
Chemical formula	Sm2O3
Molar mass	348.72 g/mol
Appearance	yellow-white crystals
Density	8.347 g/cm3
Melting point	2,335 °C (4,235 °F; 2,608 K)
Boiling point	Not Stated
Solubility in water	insoluble
Magnetic susceptibility (χ)	+1988.0·10−6 cm3/mol
Structure
Crystal structure	Cubic, cI80
Space group	Ia-3, No. 206
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H319, H410
Precautionary statements	P264, P273, P280, P305+P351+P338, P337+P313, P391, P501
Related compounds
Other anions	Samarium(III) chloride
Other cations	Promethium(III) oxide, Europium(III) oxide
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Samarium(III) oxide (Sm₂ O₃) is a chemical compound. Samarium oxide readily forms on the surface of samarium metal under humid conditions or temperatures in excess of 150°C in dry air. Similar to rust on metallic iron, this oxide layer spalls off the surface of the metal, exposing more metal to continue the reaction. The oxide is commonly white to off yellow in color and is often encountered as a highly fine dust like powder.

Uses

Samarium(III) oxide is used in optical and infrared absorbing glass to absorb infrared radiation. Also, it is used as a neutron absorber in control rods for nuclear power reactors. The oxide catalyzes the dehydration and dehydrogenation of primary and secondary alcohols.^[1] Another use involves preparation of other samarium salts.^[2]

Preparations

Samarium(III) oxide may be prepared by two methods:

1. thermal decomposition of samarium(III) carbonate, hydroxide, nitrate, oxalate or sulfate:

Sm₂(CO₃)₃ → Sm₂O₃ + 3 CO₂

2. by burning the metal in air or oxygen at a temperature above 150 °C:

4 Sm + 3 O₂ → 2 Sm₂O₃

Reactions

Samarium(III) oxide dissolves in mineral acids, forming salts upon evaporation and crystallization:

Sm₂O₃ + 6 HCl → 2 SmCl₃ + 3 H₂O

The oxide can be reduced to metallic samarium by heating with a reducing agent, such as hydrogen or carbon monoxide, at elevated temperatures.

References

^ Catalytic properties of samarium oxide with respect to the dehydrogenation and dehydration of alcohols and the dehydrogenation of tetralin. Bulletin of the Academy of Sciences of the USSR, Division of chemical science, January 1964, Volume 13, Issue 1, pp 6–9.
^ Pradyot Patnaik. Handbook of Inorganic Chemicals. McGraw-Hill, 2002, ISBN 0-07-049439-8