Fluorine

Fluorine, 9F
Small sample of pale yellow liquid fluorine condensed in liquid nitrogen
Liquid fluorine (F2 at extremely low temperature)
Fluorine
Pronunciation
Allotropesalpha, beta (see Allotropes of fluorine)
Appearancegas: very pale yellow
liquid: bright yellow
solid: alpha is opaque, beta is transparent
Standard atomic weight Ar°(F)
Fluorine in the periodic table
Hydrogen Helium
Lithium Beryllium Boron Carbon Nitrogen Oxygen Fluorine Neon
Sodium Magnesium Aluminium Silicon Phosphorus Sulfur Chlorine Argon
Potassium Calcium Scandium Titanium Vanadium Chromium Manganese Iron Cobalt Nickel Copper Zinc Gallium Germanium Arsenic Selenium Bromine Krypton
Rubidium Strontium Yttrium Zirconium Niobium Molybdenum Technetium Ruthenium Rhodium Palladium Silver Cadmium Indium Tin Antimony Tellurium Iodine Xenon
Caesium Barium Lanthanum Cerium Praseodymium Neodymium Promethium Samarium Europium Gadolinium Terbium Dysprosium Holmium Erbium Thulium Ytterbium Lutetium Hafnium Tantalum Tungsten Rhenium Osmium Iridium Platinum Gold Mercury (element) Thallium Lead Bismuth Polonium Astatine Radon
Francium Radium Actinium Thorium Protactinium Uranium Neptunium Plutonium Americium Curium Berkelium Californium Einsteinium Fermium Mendelevium Nobelium Lawrencium Rutherfordium Dubnium Seaborgium Bohrium Hassium Meitnerium Darmstadtium Roentgenium Copernicium Nihonium Flerovium Moscovium Livermorium Tennessine Oganesson


F

Cl
oxygenfluorineneon
Atomic number (Z)9
Groupgroup 17 (halogens)
Periodperiod 2
Block  p-block
Electron configuration[He] 2s2 2p5[3]
Electrons per shell2, 7
Physical properties
Phase at STPgas
Melting point(F2) 53.48 K ​(−219.67 °C, ​−363.41 °F)[4]
Boiling point(F2) 85.03 K ​(−188.11 °C, ​−306.60 °F)[4]
Density (at STP)1.696 g/L[5]
when liquid (at b.p.)1.505 g/cm3[6]
Triple point53.48 K, ​.252 kPa[7]
Critical point144.41 K, 5.1724 MPa[4]
Heat of vaporization6.51 kJ/mol[5]
Molar heat capacityCp: 31 J/(mol·K)[6] (at 21.1 °C)
Cv: 23 J/(mol·K)[6] (at 21.1 °C)
Vapor pressure
P (Pa) 1 10 100 1 k 10 k 100 k
at T (K) 38 44 50 58 69 85
Atomic properties
Oxidation states−1, 0[8] (oxidizes oxygen)
ElectronegativityPauling scale: 3.98[3]
Ionization energies
  • 1st: 1681 kJ/mol
  • 2nd: 3374 kJ/mol
  • 3rd: 6147 kJ/mol
  • (more)[9]
Covalent radius64 pm[10]
Van der Waals radius135 pm[11]
Color lines in a spectral range
Spectral lines of fluorine
Other properties
Natural occurrenceprimordial
Crystal structurecubic
Cubic crystal structure for fluorine
Thermal conductivity0.02591 W/(m⋅K)[12]
Magnetic orderingdiamagnetic (−1.2×10−4)[13][14]
CAS Number7782-41-4[3]
History
Namingafter the mineral fluorite, itself named after Latin fluo (to flow, in smelting)
DiscoveryAndré-Marie Ampère (1810)
First isolationHenri Moissan[3] (June 26, 1886)
Named by
Isotopes of fluorine
Main isotopes Decay
abun­dance half-life (t1/2) mode pro­duct
18F trace 109.734 min β+ 18O
19F 100% stable
 Category: Fluorine
| references

Fluorine is a chemical element; it has symbol F and atomic number 9. It is the lightest halogen[note 1] and exists at standard conditions as a highly toxic, pale yellow diatomic gas. Fluorine is extremely reactive, as it reacts with all other elements except for the light inert gases.

Among the elements, fluorine ranks 24th in universal abundance and 13th in terrestrial abundance. Fluorite, the primary mineral source of fluorine which gave the element its name, was first described in 1529; as it was added to metal ores to lower their melting points for smelting, the Latin verb fluo meaning 'to flow' gave the mineral its name. Proposed as an element in 1810, fluorine proved difficult and dangerous to separate from its compounds, and several early experimenters died or sustained injuries from their attempts. Only in 1886 did French chemist Henri Moissan isolate elemental fluorine using low-temperature electrolysis, a process still employed for modern production. Industrial production of fluorine gas for uranium enrichment, its largest application, began during the Manhattan Project in World War II.

Owing to the expense of refining pure fluorine, most commercial applications use fluorine compounds, with about half of mined fluorite used in steelmaking. The rest of the fluorite is converted into corrosive hydrogen fluoride en route to various organic fluorides, or into cryolite, which plays a key role in aluminium refining. Molecules containing a carbon–fluorine bond often have very high chemical and thermal stability; their major uses are as refrigerants, electrical insulation and cookware, and PTFE (Teflon). Pharmaceuticals such as atorvastatin and fluoxetine contain C−F bonds. The fluoride ion from dissolved fluoride salts inhibits dental cavities, and so finds use in toothpaste and water fluoridation. Global fluorochemical sales amount to more than US$15 billion a year.

Fluorocarbon gases are generally greenhouse gases with global-warming potentials 100 to 23,500 times that of carbon dioxide, and SF6 has the highest global warming potential of any known substance. Organofluorine compounds often persist in the environment due to the strength of the carbon–fluorine bond. Fluorine has no known metabolic role in mammals; a few plants and marine sponges synthesize organofluorine poisons (most often monofluoroacetates) that help deter predation.[16]

  1. ^ "Standard Atomic Weights: Fluorine". CIAAW. 2021.
  2. ^ Prohaska, Thomas; Irrgeher, Johanna; Benefield, Jacqueline; Böhlke, John K.; Chesson, Lesley A.; Coplen, Tyler B.; Ding, Tiping; Dunn, Philip J. H.; Gröning, Manfred; Holden, Norman E.; Meijer, Harro A. J. (4 May 2022). "Standard atomic weights of the elements 2021 (IUPAC Technical Report)". Pure and Applied Chemistry. doi:10.1515/pac-2019-0603. ISSN 1365-3075.
  3. ^ a b c d Jaccaud et al. 2000, p. 381.
  4. ^ a b c Haynes 2011, p. 4.121.
  5. ^ a b Jaccaud et al. 2000, p. 382.
  6. ^ a b c Compressed Gas Association 1999, p. 365.
  7. ^ "Triple Point | The Elements Handbook at KnowledgeDoor". KnowledgeDoor.
  8. ^ Himmel, D.; Riedel, S. (2007). "After 20 Years, Theoretical Evidence That 'AuF7' Is Actually AuF5·F2". Inorganic Chemistry. 46 (13). 5338–5342. doi:10.1021/ic700431s.
  9. ^ Dean 1999, p. 4.6.
  10. ^ Dean 1999, p. 4.35.
  11. ^ Matsui 2006, p. 257.
  12. ^ Yaws & Braker 2001, p. 385.
  13. ^ Mackay, Mackay & Henderson 2002, p. 72.
  14. ^ Cheng et al. 1999.
  15. ^ Chisté & Bé 2011.
  16. ^ Lee et al. 2014.


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