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Rubidium azide
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IUPAC name
Rubidium(1+);azide
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Other names
Rubidium azide
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Identifiers | |
3D model (JSmol)
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ChemSpider |
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PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
RbN3 | |
Molar mass | 127.49 g⋅mol−1 |
Appearance | Colorless needles |
Density | 2.79 g⋅cm−3 |
Melting point | 317–321 °C (603–610 °F; 590–594 K) |
Boiling point | Decomposes |
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Solubility | 0.182 g/100 g (16 °C, ethanol) |
Thermochemistry | |
Std enthalpy of
formation (ΔfH⦵298) |
−0.1 kcal⋅mol−1 |
Hazards | |
NFPA 704 (fire diamond) | |
Related compounds | |
Other anions
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Rubidium nitrate |
Other cations
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Lithium azide Sodium azide Potassium azide Silver azide Ammonium azide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Rubidium azide is an inorganic compound with the formula RbN3. It is the rubidium salt of the hydrazoic acid HN3. Like most azides, it is explosive.
Preparation
Rubidium azide can be created by the reaction between rubidium sulfate and barium azide which results in formation of easily separated insoluble barium sulfate:
- Rb2SO4 + Ba(N3)2 → 2 RbN3 + BaSO4
In at least one study, rubidium azide was produced by the reaction between butyl nitrite, hydrazine monohydrate, and rubidium hydroxide in the presence of ethanol:
- C4H9ONO + N2H4·H2O + RbOH → RbN3 + C4H9OH + 3 H2O
This formula is typically used to synthesize potassium azide from caustic potash.
Uses
Rubidium azide has been investigated for possible use in alkali vapor cells, which are components of atomic clocks, atomic magnetometers and atomic gyroscopes. Azides are desirable starting materials because they decompose into rubidium metal and nitrogen gas when exposed to UV light. According to one publication:
Among the different techniques used to fill microfabricated alkali vapor cell [sic], UV decomposition of rubidium azide (RbN3) into metallic Rb and nitrogen in Al2O3 coated cells is a very promising approach for low-cost wafer-level fabrication.
Structure
At room temperature, rubidium azide has the same structure as potassium hydrogen fluoride; a distorted cesium chloride structure. At 315 °C and 1 atm, rubidium azide will transition to the normal cesium chloride structure. The II/I transition temperature of rubidium azide is within 2 °C of its melting point.
Rubidium azide has a high pressure structure transition, which occurs at about 4.8 kilobars of pressure at 0 °C. The transition boundary of the II/III transition can be defined by the relationship , where is the pressure in kilobars and is the temperature in degrees Celsius.
Reactions
As with all azides, it will decompose and release nitrogen gas when heated or severely shocked:
- 2 RbN3 → 2 Rb + 3 N2
Discharge rubidium azide in nitrogen gas will produce rubidium nitride.
Hazards
At 4.1 kilobars of pressure and about 460 °C, rubidium azide will explosively decompose. Under normal circumstances, it explodes at 395 °C. It also decomposes upon exposure to ultraviolet light.
Rubidium azide is very sensitive to mechanical shock, with an impact sensitivity comparable to that of TNT.
Like all azides, rubidium azide is toxic.
Rubidium compounds
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Salts and covalent derivatives of the azide ion
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