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Originally known as eka-caesium, francium was discovered in 1939 by Marguerite Perey ( [link] ) of the Curie Institute in Paris, France when she purified a sample of actinium-227, which had been reported to have a decay energy of 220 keV. However, Perey noticed decay particles with an energy level below 80 keV. Perey thought this decay activity was caused by a previously unidentified element, which exhibited chemical properties of an alkali metal. This led Perey to believe that it was element 87, caused by the alpha decay of actinium-227. Perey named the new isotope actinium-K (now referred to as francium-223) and in 1946, she proposed the name catium for her newly discovered element, however, she subsequently suggested francium, after France.

French physicist Marguerite Catherine Perey (1909 - 1975), a student of Marie Curie, and the first woman to be elected to the French Académie des Sciences.


The abundance of the alkali metals is given in [link] . Sodium’s high abundance is due mainly to large underground deposits of rock salt (NaCl). However, sodium is also more abundant in seawater (10,800 ppm) as compared to potassium (380 ppm).

Abundance of alkali metal elements.
Element Terrestrial abundance (ppm)
Li 20 (Earth’s crust), 40 (soil), 0.17 (sea water)
Na 23,000 (Earth’s crust), 10,500 (sea water)
K 21,000 (Earth’s crust), 14 (soil), 380 (sea water)
Rb 90 (Earth’s crust), 30 - 250 (soil), 0.1 (sea water)
Cs 3 (Earth’s crust), 0.0001 (soil), 0.0003 (sea water)
Fr Essentially nil


The naturally abundant isotopes of the alkali metals are listed in [link] . All of the isotopes of francium are radioactive. Lithium-7 and sodium-23 are both useful NMR nucleus having I = 1 / 2 .

Abundance of the major isotopes of the alkali metals.
Isotope Natural abundance (%)
Lithium-6 7.5
Lithium-7 92.5
Sodium-23 100
Potassium-39 93
Potassium-40 0.0118
Potassium-41 6.9
Caesium-133 100

Potassium has three isotopes ( [link] ), of which potassium-40 is radioactive and provides the basis for the determination of the age of rocks between 10 5 and 10 9 years old, i.e., those formed in proterozoic and cenozoic periods of geological time. The decay of potassium-40 occurs with a half life of 1.31 x 10 9 years, by two routes. That associated with a beta particle decay accounts for 89% of the decay:

While that associated with an electron capture and by positron emission decay accounts for 11% of the decay to give argon-40. Since many rocks contain potassium containing minerals the decay of potassium-40 after solidification of the rock will result in the formation of argon trapped in the rock. The argon-40 content is determined by mass spectrometry, while the potassium content is determined by flame spectrophotometry. The ratio of the two, [link] , will allow for the determination of the elapsed time since the rock solidified.

Caesium has at least 39 known isotopes (more than any other element except francium) ranging from caesium-112 caesium-151; however, caesium-133 is the only naturally occurring stable isotope. The other isotopes have half-lives from a few days to fractions of a second. The radiogenic isotope caesium-137 is produced from the detonation of nuclear weapons and is produced in nuclear power plants, and was released to the atmosphere most notably from the 1986 Chernobyl accident.

Physical properties

Many of the physical properties of the alkali metals ( [link] ) are typical of metals, e.g., thermal and electrical conductivity. However, due to the relatively weak inter-atomic forces (weak M-M bonding) they are soft and readily cut with a knife.

Selected physical properties of the alkali metal elements.
Element Mp (°C) Bp (°C) Density (g/cm 3 ) Electrical resistivity (Ω·cm)
Li 453 1615 0.534 12.17 @ 86 °C
Na 370 1156 0.968 5.23 @ 29 °C
K 336 1032 0.89 7.01 @ 22.8 °C
Rb 312 961 1.532 12.53 @ 53 °C
Cs 301 944 1.93 37.38 @ 28.1 °C


All the alkali metals are highly reactive and are as a consequence of the stability of the M + ion are strong reducing agents ( [link] ). The metals react readily with hydrogen and oxygen.

Electrochemical reduction potential for alkali metals.
Reduction Reduction potential (V)
Li + + e - → Li -3.045
Na + + e - → Na -2.7109
K + + e - → K -2.924
Rb + + e - → Rb -2.925
Cs + + e - → Cs -2.923

All of the alkali metals react with water to liberate hydrogen.

The reactions of alkali metals with water are exothermic and the heat generated is sufficient to ignite the hydrogen. In addition the solutions formed are highly alkaline. Caution should be taken when handling alkali metals and storage should always be under mineral oil.

A similar, but less violent, reaction is also observed with ammonia when catalyzed by transition metal ions.

In the absence of a catalyst, the Group 1 metals dissolve in liquid ammonia to form solutions with characteristic properties.

  • Highly reducing.
  • Blue color.
  • ESR signal due to solvated electrons.

As an example, the dissolution of sodium in liquid ammonia results in the formation of solvated Na + cations and electrons.

The solvated electrons are stable in liquid ammonia and form a complex: [e - (NH 3 ) 6 ]. It is this solvated electron that gives the strong reducing properties of the solution as well as the characteristic signal in the ESR spectrum associated with a single unpaired electron. The blue color of the solution is often ascribed to these solvated electrons; however, their absorption is in the far infra-red region of the spectrum. A second species, Na - (solv) , is actually responsible for the blue color of the solution.

The formation of the sodium anion is confirmed by complexation of the cation with a cryptan ligand (“C”) such as a crown ether.

The resulting complex is found to be isostructural to the iodide analog in the solid state.

Vapor phase

All the alkali metals form M 2 dimers in the vapor phase in an analogous manner to hydrogen. As with dihydrogen the bonding is associated with the molecular orbital combination of the two valence s-orbitals ( [link] ).

Molecular orbital diagram for the formation of M 2 .

Sodium vapor is commonly used for lighting in a gas discharge lamp, which uses sodium in an excited state to produce light ( [link] ). There are two varieties of such lamps: low pressure and high pressure.

A low pressure sodium streetlamp.

Questions & Answers

are nano particles real
Missy Reply
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Maira Reply
nanopartical of organic/inorganic / physical chemistry , pdf / thesis / review
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Maira Reply
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Even nanotechnology is pretty much all about chemistry... Its the chemistry on quantum or atomic level
no nanotechnology is also a part of physics and maths it requires angle formulas and some pressure regarding concepts
Preparation and Applications of Nanomaterial for Drug Delivery
Hafiz Reply
Application of nanotechnology in medicine
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Jyoti Reply
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Crow Reply
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RAW Reply
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Brian Reply
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industrial application...? mmm I think on the medical side as drug carrier, but you should go deeper on your research, I may be wrong
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scanning tunneling microscope
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Do u think that Graphene and Fullrene fiber can be used to make Air Plane body structure the lightest and strongest. Rafiq
what is differents between GO and RGO?
what is simplest way to understand the applications of nano robots used to detect the cancer affected cell of human body.? How this robot is carried to required site of body cell.? what will be the carrier material and how can be detected that correct delivery of drug is done Rafiq
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Any one who tell me about Preparation and application of Nanomaterial for drug Delivery
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Bob Reply
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The nanotechnology is as new science, to scale nanometric
nanotechnology is the study, desing, synthesis, manipulation and application of materials and functional systems through control of matter at nanoscale
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Damian Reply
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Mahar Reply

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Source:  OpenStax, Chemistry of the main group elements. OpenStax CNX. Aug 20, 2010 Download for free at http://cnx.org/content/col11124/1.25
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