Ytterbium Oxide

Ytterbium Oxide

The production method of Ytterbium(III) Oxide is mainly oxalic acid precipitation, that is, taking ytterbium chloride or Ytterbium(III) Nitrate solution as raw material, adjusting the Ph value to 2 with oxalic acid, adding ammonia to precipitate ytterbium oxalate, heating, curing, separation, washing, drying at 110 ℃, and then burning at 900~1000 ℃ to form Ytterbium(III) oxide.

Ytterbium(III) oxide, Molecular formula: Yb2O3; Molecular weight: 394.08. The pure product is colorless powder, light brown or yellow when containing Thulium(III) oxide. Micro hygroscopicity, easy to absorb water and carbon dioxide from the air, becoming basic ytterbium carbonate. It is the weakest alkaline element in the yttrium group except for lutetium oxide. Insoluble in water and cold acids, soluble in hot dilute acids.

Application Area:

1. Used for making special alloys

2. Yb: YAG is used as a special scintillation crystal growth additive.

3. Used for special ceramic media.

4. Used for special glass additives.

5. Used for industrial luminescent carbon rods, catalysts, etc.

Product Series

PRODUCT Product Code SAFETY DATA TECHNICAL DATA
Ytterbium Oxide 99.9% ET-Yb-01


Ytterbium Oxide 99.9%
Ytterbium Oxide 99.99% ET-Yb-02 Ytterbium Oxide 99.99%

Ytterbium Oxide 99.999%

ET-Yb-03 Ytterbium Oxide 99.999%

Properties (Theoretical)

Compound Formula Yb2O3
Molecular Weight 394.08
Appearance White
Melting Point 4,271° F (2,355° C)
Boiling Point 7,358° F (4,070° C)
Density 9200 kg/m3
Solubility in H2O N/A
Exact Mass 189.934 g/mol
Monoisotopic Mass 395.862544 Da

Health & Safety Information

Signal Word Warning
Hazard Statements H315-H319-H335
Hazard Codes Xi
Precautionary Statements P261-P305 + P351 + P338
Flash Point Not applicable
Risk Codes 36/37/38
Safety Statements 26-36
RTECS Number N/A
Transport Information NONH
WGK Germany 3
GHS Pictograms

About Ytterbium Oxide
About Ytterbium Oxide

The production method of Ytterbium(III) Oxide is mainly oxalic acid precipitation, that is, taking ytterbium chloride or Ytterbium(III) Nitrate solution as raw material, adjusting the Ph value to 2 with oxalic acid, adding ammonia to precipitate ytterbium oxalate, heating, curing, separation, washing, drying at 110 ℃, and then burning at 900~1000 ℃ to form Ytterbium(III) oxide.

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