Samarium(III) oxide
| _oxide.jpg) | |
| Names | |
|---|---|
| Other names samarium sesquioxide | |
| Identifiers | |
| 12060-58-1  | |
| ChemSpider | 140199  | 
| EC Number | 235-043-6 | 
| Jmol interactive 3D | Image | 
| PubChem | 159425 | 
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| Properties | |
| 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) | 
| insoluble | |
| Structure | |
| cubic | |
| Hazards | |
| EU classification (DSD) | not listed | 
| 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). | |
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| Infobox references | |
Samarium(III) oxide (Sm2O3) is a chemical compound.
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 dehydration of acyclic primary alcohols to aldehydes and ketones. Another use involves preparation of other samarium salts. [1]
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
- ↑ Pradyot Patnaik. Handbook of Inorganic Chemicals. McGraw-Hill, 2002, ISBN 0-07-049439-8
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