A piece of ytterbium metal
|Name, symbol||Ytterbium, Yb|
|Ytterbium in the periodic table|
|Standard atomic weight (Ar)||173.045(10)|
|Group, block||, f-block|
|Electron configuration||[Xe] 4f14 6s2|
|2, 8, 18, 32, 8, 2|
|Melting point||1097 K (824 °C, 1515 °F)|
|Boiling point||1469 K (1196 °C, 2185 °F)|
|Density near r.t.||6.90 g/cm3|
|when liquid, at||6.21 g/cm3|
|Heat of fusion||7.66 kJ/mol|
|Heat of||129 kJ/mol|
|Molar heat capacity||26.74 J/(mol·K)|
|Oxidation states||3, 2, 1 (a basic oxide)|
|Electronegativity||Pauling scale: 1.1|
1st: 603.4 kJ/mol |
2nd: 1174.8 kJ/mol
3rd: 2417 kJ/mol
|Atomic radius||empirical: 176 pm|
|Covalent radius||187±8 pm|
|Crystal structure||Face-centered cubic (fcc)|
|Speed of sound thin rod||1590 m/s (at 20 °C)|
|Thermal expansion||26.3 µm/(m·K) (β, poly)|
|Thermal conductivity||38.5 W/(m·K)|
|Electrical resistivity||2.5·-7 Ω·m (β, poly)|
|Young's modulus||23.9 GPa (β form)|
|Shear modulus||9.9 GPa (β form)|
|Bulk modulus||30.5 GPa (β form)|
|Poisson ratio||0.207 (β form)|
|Vickers hardness||205–250 MPa|
|Brinell hardness||340–440 MPa|
|CAS Registry Number||7440-64-4|
|Naming||After Ytterby (Sweden), where it was mined|
|Discovery||Jean Charles Galissard de Marignac (1878)|
|First isolation||Carl Auer von Welsbach (1906)|
Ytterbium is a lanthanide with the symbol Yb and atomic number 70. It is a hard, silvery metal, sometimes described as slightly brassy, that is about as reactive as magnesium. It is not a particularly interesting addition to the amateur chemist's lab, but it and its ytterbium(II) derivatives are powerful reducing agents that can be used in organic synthesis as an alternative to samarium and its samarium(II) derivatives.
Ytterbium is a slightly brassy metal, sometimes found darkened as it slowly tarnishes in air over the course of months or years. It exists in three allotropes: α-ytterbium, which exists in a hexagonal crystal structure is stable below -13 °C and is diamagnetic, β-ytterbium, which is stable at room temperature, paramagnetic and exists in a face-centered cubic structure, and γ-ytterbium, which exists above 795 °C and has a body centered cubic structure.
Ytterbium can be thought of as analogous to zinc in terms of its relation to the other lanthanides. Due to the filled f-shell, the metal has an unusually low melting and boiling point (824 °C and 1196 °C respectively), and is also less dense than most other lanthanides. Melting ytterbium (which must be done in an inert atmosphere to prevent ignition of the metal) will invariably cause some to boil off due to the narrow liquid range. This filled f-shell contributes to ytterbium's extremely low magnetism compared to rare earths such as gadolinium, terbium and dysprosium. However, fine ytterbium powder can be picked up by a neodymium magnet.
Ytterbium is also notoriously soft and sticky. Although filing ytterbium into powder is easy, it will leave traces of itself behind in the grooves of the file, and it is nearly impossible to remove once situated there. It is best to dedicate a file to ytterbium and use a different file for other elements.
Ytterbium is a reactive metal, but it does not tarnish quickly in air, taking months or years to do so, and unless stored with complete disregard for its properties, rarely corrodes to the oxide. It does, however, burn in air to form ytterbium(III) oxide. Ytterbium powder burns with a characteristic green flame, notably in compositions with hexachloroethane and PTFE.
Ytterbium reacts vigorously with dilute acids to form salts. Most of these salts are soluble in water except for the fluoride and oxalate. All of these salts are white in color. Ytterbium also reacts with the halogens to form trihalides. The metal reacts only slowly in cold water, but vigorously in hot water, to form ytterbium hydroxide, which is basic enough to absorb carbon dioxide from the air to form ytterbium carbonate.
Under reducing conditions, ytterbium(II) species is known to exist. This ion will reduce water to hydrogen gas and is therefore unstable in aqueous solution. It can be isolated in tetrahydrofuran. Ytterbium(II) compounds can be formed by reacting metallic ytterbium with ytterbium(III) compounds, but they disproportionate back to ytterbium metal and ytterbium(III) compounds at elevated temperatures.
In glacial acetic acid, ytterbium dissolves slowly and forms an orange solution, likely an ytterbium(II) acetato complex. Adding water considerably increases the rate of reaction and limits the formation of the orange species. The resulting ytterbium(III) acetate tetrahydrate forms rhombic crystals and has a weak teal fluorescence under 365 nm UV light.
Ytterbium is more common than iodine on Earth, but it is very hard to find and relatively expensive. One source for ytterbium, as well as other rare earth metals, is Metallium. It is sold in 5 gram and 20 gram sizes, as well as rods, ampoules, and coins. Ytterbium and its compounds are occasionally sold on eBay as well.
- Making and using ytterbium(II) compounds
- Green-burning energetic mixtures
Ytterbium compounds have not been investigated for their toxicity, and should be treated as mildly toxic. Ytterbium has no biological role but may stimulate metabolism. Salts of ytterbium, especially the halides, tend to hydrolyze at elevated temperatures and may emit noxious or strongly acidic vapors (commonly HCl in the case of ytterbium(III) chloride).
Ytterbium as small pieces will ignite in the presence of an open flame, and ytterbium dust and powder may ignite very easily. Ytterbium and thulium fires may be identified by their brilliant green flames. Class D fire extinguishers should be at hand. Water may aggravate burning ytterbium and should never be used to put out the flame.
Ytterbium should be stored in closed containers, away from any acids and oxidizing agents, particularly volatile ones. It is stable in air almost indefinitely, but does tarnish slowly.
Best to try to recycle it.
Relevant Sciencemadness threads
None as of yet - why not start some research on this element?